-
1
-
-
0028060362
-
The diagnosis of osteoporosis
-
Kanis J.A., Melton III L.J., Christiansen C., Johnston C.C., and Khaltaev N. The diagnosis of osteoporosis. J. Bone Miner. Res. 9 (1994) 1137-1141
-
(1994)
J. Bone Miner. Res.
, vol.9
, pp. 1137-1141
-
-
Kanis, J.A.1
Melton III, L.J.2
Christiansen, C.3
Johnston, C.C.4
Khaltaev, N.5
-
2
-
-
0842341476
-
Site and gender specificity of inheritance of bone mineral density
-
Duncan E.L., Cardon L.R., Sinsheimer J.S., Wass J.A., and Brown M.A. Site and gender specificity of inheritance of bone mineral density. J. Bone Miner. Res. 18 (2003) 1531-1538
-
(2003)
J. Bone Miner. Res.
, vol.18
, pp. 1531-1538
-
-
Duncan, E.L.1
Cardon, L.R.2
Sinsheimer, J.S.3
Wass, J.A.4
Brown, M.A.5
-
3
-
-
0023508467
-
Genetic determinants of bone mass in adults. A twin study
-
Pocock N.A., Eisman J.A., Hopper J.L., Yeates M.G., Sambrook P.N., and Eberl S. Genetic determinants of bone mass in adults. A twin study. J. Clin. Invest. 80 (1987) 706-710
-
(1987)
J. Clin. Invest.
, vol.80
, pp. 706-710
-
-
Pocock, N.A.1
Eisman, J.A.2
Hopper, J.L.3
Yeates, M.G.4
Sambrook, P.N.5
Eberl, S.6
-
4
-
-
0028866916
-
Segregation analysis and variance components analysis of bone mineral density in healthy families
-
Gueguen R., Jouanny P., Guillemin F., Kuntz C., Pourel J., and Siest G. Segregation analysis and variance components analysis of bone mineral density in healthy families. J. Bone Miner. Res. 10 (1995) 2017-2022
-
(1995)
J. Bone Miner. Res.
, vol.10
, pp. 2017-2022
-
-
Gueguen, R.1
Jouanny, P.2
Guillemin, F.3
Kuntz, C.4
Pourel, J.5
Siest, G.6
-
5
-
-
0031856655
-
Genetic and environmental contributions to the association between quantitative ultrasound and bone mineral density measurements: a twin study
-
Howard G.M., Nguyen T.V., Harris M., Kelly P.J., and Eisman J.A. Genetic and environmental contributions to the association between quantitative ultrasound and bone mineral density measurements: a twin study. J. Bone Miner. Res. 13 (1998) 1318-1327
-
(1998)
J. Bone Miner. Res.
, vol.13
, pp. 1318-1327
-
-
Howard, G.M.1
Nguyen, T.V.2
Harris, M.3
Kelly, P.J.4
Eisman, J.A.5
-
6
-
-
0037146578
-
Finding genes that underlie complex traits
-
Glazier A.M., Nadeau J.H., and Aitman T.J. Finding genes that underlie complex traits. Science 298 (2002) 2345-2349
-
(2002)
Science
, vol.298
, pp. 2345-2349
-
-
Glazier, A.M.1
Nadeau, J.H.2
Aitman, T.J.3
-
7
-
-
0242291131
-
The nature and identification of quantitative trait loci: a community's view
-
Abiola O., Angel J.M., Avner P., Bachmanov A.A., Belknap J.K., Bennett B., Blankenhorn E.P., Blizard D.A., Bolivar V., Brockmann G.A., Buck K.J., Bureau J.F., Casley W.L., Chesler E.J., Cheverud J.M., Churchill G.A., Cook M., Crabbe J.C., Crusio W.E., Darvasi A., de Haan G., Dermant P., Doerge R.W., Elliot R.W., Farber C.R., Flaherty L., Flint J., Gershenfeld H., Gibson J.P., Gu J., Gu W., Himmelbauer H., Hitzemann R., Hsu H.C., Hunter K., Iraqi F.F., Jansen R.C., Johnson T.E., Jones B.C., Kempermann G., Lammert F., Lu L., Manly K.F., Matthews D.B., Medrano J.F., Mehrabian M., Mittlemann G., Mock B.A., Mogil J.S., Montagutelli X., Morahan G., Mountz J.D., Nagase H., Nowakowski R.S., O'Hara B.F., Osadchuk A.V., Paigen B., Palmer A.A., Peirce J.L., Pomp D., Rosemann M., Rosen G.D., Schalkwyk L.C., Seltzer Z., Settle S., Shimomura K., Shou S., Sikela J.M., Siracusa L.D., Spearow J.L., Teuscher C., Threadgill D.W., Toth L.A., Toye A.A., Vadasz C., Van Zant G., Wakeland E., Williams R.W., Zhang H.G., and Zou F. The nature and identification of quantitative trait loci: a community's view. Nat. Rev., Genet. 4 (2003) 911-916
-
(2003)
Nat. Rev., Genet.
, vol.4
, pp. 911-916
-
-
Abiola, O.1
Angel, J.M.2
Avner, P.3
Bachmanov, A.A.4
Belknap, J.K.5
Bennett, B.6
Blankenhorn, E.P.7
Blizard, D.A.8
Bolivar, V.9
Brockmann, G.A.10
Buck, K.J.11
Bureau, J.F.12
Casley, W.L.13
Chesler, E.J.14
Cheverud, J.M.15
Churchill, G.A.16
Cook, M.17
Crabbe, J.C.18
Crusio, W.E.19
Darvasi, A.20
de Haan, G.21
Dermant, P.22
Doerge, R.W.23
Elliot, R.W.24
Farber, C.R.25
Flaherty, L.26
Flint, J.27
Gershenfeld, H.28
Gibson, J.P.29
Gu, J.30
Gu, W.31
Himmelbauer, H.32
Hitzemann, R.33
Hsu, H.C.34
Hunter, K.35
Iraqi, F.F.36
Jansen, R.C.37
Johnson, T.E.38
Jones, B.C.39
Kempermann, G.40
Lammert, F.41
Lu, L.42
Manly, K.F.43
Matthews, D.B.44
Medrano, J.F.45
Mehrabian, M.46
Mittlemann, G.47
Mock, B.A.48
Mogil, J.S.49
Montagutelli, X.50
Morahan, G.51
Mountz, J.D.52
Nagase, H.53
Nowakowski, R.S.54
O'Hara, B.F.55
Osadchuk, A.V.56
Paigen, B.57
Palmer, A.A.58
Peirce, J.L.59
Pomp, D.60
Rosemann, M.61
Rosen, G.D.62
Schalkwyk, L.C.63
Seltzer, Z.64
Settle, S.65
Shimomura, K.66
Shou, S.67
Sikela, J.M.68
Siracusa, L.D.69
Spearow, J.L.70
Teuscher, C.71
Threadgill, D.W.72
Toth, L.A.73
Toye, A.A.74
Vadasz, C.75
Van Zant, G.76
Wakeland, E.77
Williams, R.W.78
Zhang, H.G.79
Zou, F.80
more..
-
8
-
-
34248172950
-
Identification of mouse Duffy antigen receptor for chemokines (Darc) as a BMD QTL gene
-
Edderkaoui B., Baylink D.J., Beamer W.G., Wergedal J.E., Porte R., Chaudhuri A., and Mohan S. Identification of mouse Duffy antigen receptor for chemokines (Darc) as a BMD QTL gene. Genome Res. 17 (2007) 577-585
-
(2007)
Genome Res.
, vol.17
, pp. 577-585
-
-
Edderkaoui, B.1
Baylink, D.J.2
Beamer, W.G.3
Wergedal, J.E.4
Porte, R.5
Chaudhuri, A.6
Mohan, S.7
-
9
-
-
9144272249
-
Regulation of bone mass in mice by the lipoxygenase gene Alox15
-
Klein R.F., Allard J., Avnur Z., Nikolcheva T., Rotstein D., Carlos A.S., Shea M., Waters R.V., Belknap J.K., Peltz G., and Orwoll E.S. Regulation of bone mass in mice by the lipoxygenase gene Alox15. Science 303 (2004) 229-232
-
(2004)
Science
, vol.303
, pp. 229-232
-
-
Klein, R.F.1
Allard, J.2
Avnur, Z.3
Nikolcheva, T.4
Rotstein, D.5
Carlos, A.S.6
Shea, M.7
Waters, R.V.8
Belknap, J.K.9
Peltz, G.10
Orwoll, E.S.11
-
10
-
-
33846425795
-
Secreted frizzled-related protein 4 is a negative regulator of peak BMD in SAMP6 mice
-
Nakanishi R., Shimizu M., Mori M., Akiyama H., Okudaira S., Otsuki B., Hashimoto M., Higuchi K., Hosokawa M., Tsuboyama T., and Nakamura T. Secreted frizzled-related protein 4 is a negative regulator of peak BMD in SAMP6 mice. J. Bone Miner. Res. 21 (2006) 1713-1721
-
(2006)
J. Bone Miner. Res.
, vol.21
, pp. 1713-1721
-
-
Nakanishi, R.1
Shimizu, M.2
Mori, M.3
Akiyama, H.4
Okudaira, S.5
Otsuki, B.6
Hashimoto, M.7
Higuchi, K.8
Hosokawa, M.9
Tsuboyama, T.10
Nakamura, T.11
-
11
-
-
34548589037
-
The association of common polymorphisms in the QPCT gene with bone mineral density in the Chinese population
-
Huang Q.Y., and Kung A.W. The association of common polymorphisms in the QPCT gene with bone mineral density in the Chinese population. J. Hum. Genet. 52 (2007) 757-762
-
(2007)
J. Hum. Genet.
, vol.52
, pp. 757-762
-
-
Huang, Q.Y.1
Kung, A.W.2
-
12
-
-
41349095456
-
PGMapper: a web-based tool linking phenotype to genes
-
Xiong Q., Qiu Y., and Gu W. PGMapper: a web-based tool linking phenotype to genes. Bioinformatics 24 (2008) 1011-1013
-
(2008)
Bioinformatics
, vol.24
, pp. 1011-1013
-
-
Xiong, Q.1
Qiu, Y.2
Gu, W.3
-
13
-
-
0037303461
-
Congenic strains of mice for verification and genetic decomposition of quantitative trait loci for femoral bone mineral density
-
Shultz K.L., Donahue L.R., Bouxsein M.L., Baylink D.J., Rosen C.J., and Beamer W.G. Congenic strains of mice for verification and genetic decomposition of quantitative trait loci for femoral bone mineral density. J. Bone Miner. Res. 18 (2003) 175-185
-
(2003)
J. Bone Miner. Res.
, vol.18
, pp. 175-185
-
-
Shultz, K.L.1
Donahue, L.R.2
Bouxsein, M.L.3
Baylink, D.J.4
Rosen, C.J.5
Beamer, W.G.6
-
14
-
-
0032718183
-
Quantitative trait loci for bone density in C57BL/6J and CAST/EiJ inbred mice
-
Beamer W.G., Shultz K.L., Churchill G.A., Frankel W.N., Baylink D.J., Rosen C.J., and Donahue L.R. Quantitative trait loci for bone density in C57BL/6J and CAST/EiJ inbred mice. Mamm. Genome 10 (1999) 1043-1049
-
(1999)
Mamm. Genome
, vol.10
, pp. 1043-1049
-
-
Beamer, W.G.1
Shultz, K.L.2
Churchill, G.A.3
Frankel, W.N.4
Baylink, D.J.5
Rosen, C.J.6
Donahue, L.R.7
-
15
-
-
33846899009
-
Identification of novel RANK polymorphisms and their putative association with low BMD among postmenopausal women
-
Koh J.M., Park B.L., Kim D.J., Kim G.S., Cheong H.S., Kim T.H., Hong J.M., Shin H.I., Park E.K., Kim S.Y., and Shin H.D. Identification of novel RANK polymorphisms and their putative association with low BMD among postmenopausal women. Osteoporos. Int. 18 (2007) 323-331
-
(2007)
Osteoporos. Int.
, vol.18
, pp. 323-331
-
-
Koh, J.M.1
Park, B.L.2
Kim, D.J.3
Kim, G.S.4
Cheong, H.S.5
Kim, T.H.6
Hong, J.M.7
Shin, H.I.8
Park, E.K.9
Kim, S.Y.10
Shin, H.D.11
-
16
-
-
13544264662
-
Association of interleukin 10 haplotype with low bone mineral density in Korean postmenopausal women
-
Park B.L., Han I.K., Lee H.S., Kim L.H., Kim S.J., Shin J.S., Kim S.Y., and Shin H.D. Association of interleukin 10 haplotype with low bone mineral density in Korean postmenopausal women. J. Biochem. Mol. Biol. 37 (2004) 691-699
-
(2004)
J. Biochem. Mol. Biol.
, vol.37
, pp. 691-699
-
-
Park, B.L.1
Han, I.K.2
Lee, H.S.3
Kim, L.H.4
Kim, S.J.5
Shin, J.S.6
Kim, S.Y.7
Shin, H.D.8
-
17
-
-
33750087502
-
Identification of adiponectin and its receptors in human osteoblast-like cells and association of T45G polymorphism in exon 2 of adiponectin gene with lumbar spine bone mineral density in Korean women
-
Lee W.Y., Rhee E.J., Oh K.W., Kim S.Y., Jung C.H., Yun E.J., Baek K.H., Kang M.I., and Kim S.W. Identification of adiponectin and its receptors in human osteoblast-like cells and association of T45G polymorphism in exon 2 of adiponectin gene with lumbar spine bone mineral density in Korean women. Clin. Endocrinol. (Oxf.) 65 (2006) 631-637
-
(2006)
Clin. Endocrinol. (Oxf.)
, vol.65
, pp. 631-637
-
-
Lee, W.Y.1
Rhee, E.J.2
Oh, K.W.3
Kim, S.Y.4
Jung, C.H.5
Yun, E.J.6
Baek, K.H.7
Kang, M.I.8
Kim, S.W.9
-
18
-
-
34047274619
-
Attenuation of bone mass and increase of osteoclast formation in decoy receptor 3 transgenic mice
-
Tang C.H., Hsu T.L., Lin W.W., Lai M.Z., Yang R.S., Hsieh S.L., and Fu W.M. Attenuation of bone mass and increase of osteoclast formation in decoy receptor 3 transgenic mice. J Biol Chem 282 (2007) 2346-2354
-
(2007)
J Biol Chem
, vol.282
, pp. 2346-2354
-
-
Tang, C.H.1
Hsu, T.L.2
Lin, W.W.3
Lai, M.Z.4
Yang, R.S.5
Hsieh, S.L.6
Fu, W.M.7
-
19
-
-
48249091732
-
A novel dwarfism with gonadal dysfunction due to loss-of-function allele of the collagen receptor gene, Ddr2, in the mouse
-
Kano K., Marin de Evsikova C., Young J., Wnek C., Maddatu T.P., Nishina P.M., and Naggert J.K. A novel dwarfism with gonadal dysfunction due to loss-of-function allele of the collagen receptor gene, Ddr2, in the mouse. Mol. Endocrinol. 22 (2008) 1866-1880
-
(2008)
Mol. Endocrinol.
, vol.22
, pp. 1866-1880
-
-
Kano, K.1
Marin de Evsikova, C.2
Young, J.3
Wnek, C.4
Maddatu, T.P.5
Nishina, P.M.6
Naggert, J.K.7
-
20
-
-
44649092795
-
P2X7 receptors on osteoblasts couple to production of lysophosphatidic acid: a signaling axis promoting osteogenesis
-
Panupinthu N., Rogers J.T., Zhao L., Solano-Flores L.P., Possmayer F., Sims S.M., and Dixon S.J. P2X7 receptors on osteoblasts couple to production of lysophosphatidic acid: a signaling axis promoting osteogenesis. J. Cell Biol. 181 (2008) 859-871
-
(2008)
J. Cell Biol.
, vol.181
, pp. 859-871
-
-
Panupinthu, N.1
Rogers, J.T.2
Zhao, L.3
Solano-Flores, L.P.4
Possmayer, F.5
Sims, S.M.6
Dixon, S.J.7
-
21
-
-
0034968388
-
Quantitative trait loci for femoral and lumbar vertebral bone mineral density in C57BL/6J and C3H/HeJ inbred strains of mice
-
Beamer W.G., Shultz K.L., Donahue L.R., Churchill G.A., Sen S., Wergedal J.R., Baylink D.J., and Rosen C.J. Quantitative trait loci for femoral and lumbar vertebral bone mineral density in C57BL/6J and C3H/HeJ inbred strains of mice. J. Bone Miner. Res. 16 (2001) 1195-1206
-
(2001)
J. Bone Miner. Res.
, vol.16
, pp. 1195-1206
-
-
Beamer, W.G.1
Shultz, K.L.2
Donahue, L.R.3
Churchill, G.A.4
Sen, S.5
Wergedal, J.R.6
Baylink, D.J.7
Rosen, C.J.8
-
22
-
-
0036732410
-
SHIP-deficient mice are severely osteoporotic due to increased numbers of hyper-resorptive osteoclasts
-
Takeshita S., Namba N., Zhao J.J., Jiang Y., Genant H.K., Silva M.J., Brodt M.D., Helgason C.D., Kalesnikoff J., Rauh M.J., Humphries R.K., Krystal G., Teitelbaum S.L., and Ross F.P. SHIP-deficient mice are severely osteoporotic due to increased numbers of hyper-resorptive osteoclasts. Nat. Med. 8 (2002) 943-949
-
(2002)
Nat. Med.
, vol.8
, pp. 943-949
-
-
Takeshita, S.1
Namba, N.2
Zhao, J.J.3
Jiang, Y.4
Genant, H.K.5
Silva, M.J.6
Brodt, M.D.7
Helgason, C.D.8
Kalesnikoff, J.9
Rauh, M.J.10
Humphries, R.K.11
Krystal, G.12
Teitelbaum, S.L.13
Ross, F.P.14
-
23
-
-
33947370286
-
Inhibin a is an endocrine stimulator of bone mass and strength
-
Perrien D.S., Akel N.S., Edwards P.K., Carver A.A., Bendre M.S., Swain F.L., Skinner R.A., Hogue W.R., Nicks K.M., Pierson T.M., Suva L.J., and Gaddy D. Inhibin a is an endocrine stimulator of bone mass and strength. Endocrinology 148 (2007) 1654-1665
-
(2007)
Endocrinology
, vol.148
, pp. 1654-1665
-
-
Perrien, D.S.1
Akel, N.S.2
Edwards, P.K.3
Carver, A.A.4
Bendre, M.S.5
Swain, F.L.6
Skinner, R.A.7
Hogue, W.R.8
Nicks, K.M.9
Pierson, T.M.10
Suva, L.J.11
Gaddy, D.12
-
24
-
-
45749089286
-
Persistent expression of Pax3 in the neural crest causes cleft palate and defective osteogenesis in mice
-
Wu M., Li J., Engleka K.A., Zhou B., Lu M.M., Plotkin J.B., and Epstein J.A. Persistent expression of Pax3 in the neural crest causes cleft palate and defective osteogenesis in mice. J. Clin. Invest. 118 (2008) 2076-2087
-
(2008)
J. Clin. Invest.
, vol.118
, pp. 2076-2087
-
-
Wu, M.1
Li, J.2
Engleka, K.A.3
Zhou, B.4
Lu, M.M.5
Plotkin, J.B.6
Epstein, J.A.7
-
25
-
-
0033567213
-
Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation
-
St-Jacques B., Hammerschmidt M., and McMahon A.P. Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation. Genes Dev. 13 (1999) 2072-2086
-
(1999)
Genes Dev.
, vol.13
, pp. 2072-2086
-
-
St-Jacques, B.1
Hammerschmidt, M.2
McMahon, A.P.3
-
26
-
-
34548057008
-
Genetic dissection of mouse distal chromosome 1 reveals three linked BMD QTLs with sex-dependent regulation of bone phenotypes
-
Beamer W.G., Shultz K.L., Ackert-Bicknell C.L., Horton L.G., Delahunty K.M., Coombs H.F., Donahue L.R., Canalis E., and Rosen C.J. Genetic dissection of mouse distal chromosome 1 reveals three linked BMD QTLs with sex-dependent regulation of bone phenotypes. J. Bone Miner. Res. 22 (2007) 1187-1196
-
(2007)
J. Bone Miner. Res.
, vol.22
, pp. 1187-1196
-
-
Beamer, W.G.1
Shultz, K.L.2
Ackert-Bicknell, C.L.3
Horton, L.G.4
Delahunty, K.M.5
Coombs, H.F.6
Donahue, L.R.7
Canalis, E.8
Rosen, C.J.9
-
27
-
-
29644445238
-
Quantitative trait loci that determine BMD in C57BL/6J and 129S1/SvImJ inbred mice
-
Ishimori N., Li R., Walsh K.A., Korstanje R., Rollins J.A., Petkov P., Pletcher M.T., Wiltshire T., Donahue L.R., Rosen C.J., Beamer W.G., Churchill G.A., and Paigen B. Quantitative trait loci that determine BMD in C57BL/6J and 129S1/SvImJ inbred mice. J. Bone Miner. Res. 21 (2006) 105-112
-
(2006)
J. Bone Miner. Res.
, vol.21
, pp. 105-112
-
-
Ishimori, N.1
Li, R.2
Walsh, K.A.3
Korstanje, R.4
Rollins, J.A.5
Petkov, P.6
Pletcher, M.T.7
Wiltshire, T.8
Donahue, L.R.9
Rosen, C.J.10
Beamer, W.G.11
Churchill, G.A.12
Paigen, B.13
-
28
-
-
33749160469
-
Association of PLXNA2 polymorphisms with vertebral fracture risk and bone mineral density in postmenopausal Korean population
-
Hwang J.Y., Lee J.Y., Park M.H., Kim K.S., Kim K.K., Ryu H.J., Lee J.K., Han B.G., Kim J.W., Oh B., Kimm K., Park B.L., Shin H.D., Kim T.H., Hong J.M., Park E.K., Kim D.J., Koh J.M., Kim G.S., and Kim S.Y. Association of PLXNA2 polymorphisms with vertebral fracture risk and bone mineral density in postmenopausal Korean population. Osteoporos. Int. 17 (2006) 1592-1601
-
(2006)
Osteoporos. Int.
, vol.17
, pp. 1592-1601
-
-
Hwang, J.Y.1
Lee, J.Y.2
Park, M.H.3
Kim, K.S.4
Kim, K.K.5
Ryu, H.J.6
Lee, J.K.7
Han, B.G.8
Kim, J.W.9
Oh, B.10
Kimm, K.11
Park, B.L.12
Shin, H.D.13
Kim, T.H.14
Hong, J.M.15
Park, E.K.16
Kim, D.J.17
Koh, J.M.18
Kim, G.S.19
Kim, S.Y.20
more..
-
29
-
-
29644440844
-
Multiple genetic loci from CAST/EiJ chromosome 1 affect vBMD either positively or negatively in a C57BL/6J background
-
Edderkaoui B., Baylink D.J., Beamer W.G., Wergedal J.E., Dunn N.R., Shultz K.L., and Mohan S. Multiple genetic loci from CAST/EiJ chromosome 1 affect vBMD either positively or negatively in a C57BL/6J background. J. Bone Miner. Res. 21 (2006) 97-104
-
(2006)
J. Bone Miner. Res.
, vol.21
, pp. 97-104
-
-
Edderkaoui, B.1
Baylink, D.J.2
Beamer, W.G.3
Wergedal, J.E.4
Dunn, N.R.5
Shultz, K.L.6
Mohan, S.7
-
30
-
-
0034778616
-
Confirmation and fine mapping of chromosomal regions influencing peak bone mass in mice
-
Klein O.F., Carlos A.S., Vartanian K.A., Chambers V.K., Turner E.J., Phillips T.J., Belknap J.K., and Orwoll E.S. Confirmation and fine mapping of chromosomal regions influencing peak bone mass in mice. J. Bone Miner. Res. 16 (2001) 1953-1961
-
(2001)
J. Bone Miner. Res.
, vol.16
, pp. 1953-1961
-
-
Klein, O.F.1
Carlos, A.S.2
Vartanian, K.A.3
Chambers, V.K.4
Turner, E.J.5
Phillips, T.J.6
Belknap, J.K.7
Orwoll, E.S.8
-
31
-
-
0042665656
-
Quantitative trait loci for bone density in mice: the genes determining total skeletal density and femur density show little overlap in F2 mice
-
Masinde G.L., Li X., Gu W., Wergedal J., Mohan S., and Baylink D.J. Quantitative trait loci for bone density in mice: the genes determining total skeletal density and femur density show little overlap in F2 mice. Calcif. Tissue Int. 71 (2002) 421-428
-
(2002)
Calcif. Tissue Int.
, vol.71
, pp. 421-428
-
-
Masinde, G.L.1
Li, X.2
Gu, W.3
Wergedal, J.4
Mohan, S.5
Baylink, D.J.6
-
32
-
-
0031754518
-
Quantitative trait loci affecting peak bone mineral density in mice
-
Klein R.F., Mitchell S.R., Phillips T.J., Belknap J.K., and Orwoll E.S. Quantitative trait loci affecting peak bone mineral density in mice. J. Bone Miner. Res. 13 (1998) 1648-1656
-
(1998)
J. Bone Miner. Res.
, vol.13
, pp. 1648-1656
-
-
Klein, R.F.1
Mitchell, S.R.2
Phillips, T.J.3
Belknap, J.K.4
Orwoll, E.S.5
-
33
-
-
33645746691
-
A functional polymorphism in the PTHR1 promoter region is associated with adult height and BMD measured at the femoral neck in a large cohort of young caucasian women
-
Scillitani A., Jang C., Wong B.Y., Hendy G.N., and Cole D.E. A functional polymorphism in the PTHR1 promoter region is associated with adult height and BMD measured at the femoral neck in a large cohort of young caucasian women. Hum. Genet. 119 (2006) 416-421
-
(2006)
Hum. Genet.
, vol.119
, pp. 416-421
-
-
Scillitani, A.1
Jang, C.2
Wong, B.Y.3
Hendy, G.N.4
Cole, D.E.5
-
34
-
-
34848884285
-
PTHR1 polymorphisms influence BMD variation through effects on the growing skeleton
-
Vilarino-Guell C., Miles L.J., Duncan E.L., Ralston S.H., Compston J.E., Cooper C., Langdahl B.L., Maclelland A., Pols H.A., Reid D.M., Uitterlinden A.G., Steer C.D., Tobias J.H., Wass J.A., and Brown M.A. PTHR1 polymorphisms influence BMD variation through effects on the growing skeleton. Calcif. Tissue Int. 81 (2007) 270-278
-
(2007)
Calcif. Tissue Int.
, vol.81
, pp. 270-278
-
-
Vilarino-Guell, C.1
Miles, L.J.2
Duncan, E.L.3
Ralston, S.H.4
Compston, J.E.5
Cooper, C.6
Langdahl, B.L.7
Maclelland, A.8
Pols, H.A.9
Reid, D.M.10
Uitterlinden, A.G.11
Steer, C.D.12
Tobias, J.H.13
Wass, J.A.14
Brown, M.A.15
-
35
-
-
3042600009
-
Stat1 controls postnatal bone formation by regulating fibroblast growth factor signaling in osteoblasts
-
Xiao L., Naganawa T., Obugunde E., Gronowicz G., Ornitz D.M., Coffin J.D., and Hurley M.M. Stat1 controls postnatal bone formation by regulating fibroblast growth factor signaling in osteoblasts. J. Biol. Chem. 279 (2004) 27743-27752
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 27743-27752
-
-
Xiao, L.1
Naganawa, T.2
Obugunde, E.3
Gronowicz, G.4
Ornitz, D.M.5
Coffin, J.D.6
Hurley, M.M.7
-
36
-
-
19944431157
-
Insulin-like growth factor-binding protein-5 induces a gender-related decrease in bone mineral density in transgenic mice
-
Salih D.A., Mohan S., Kasukawa Y., Tripathi G., Lovett F.A., Anderson N.F., Carter E.J., Wergedal J.E., Baylink D.J., and Pell J.M. Insulin-like growth factor-binding protein-5 induces a gender-related decrease in bone mineral density in transgenic mice. Endocrinology 146 (2005) 931-940
-
(2005)
Endocrinology
, vol.146
, pp. 931-940
-
-
Salih, D.A.1
Mohan, S.2
Kasukawa, Y.3
Tripathi, G.4
Lovett, F.A.5
Anderson, N.F.6
Carter, E.J.7
Wergedal, J.E.8
Baylink, D.J.9
Pell, J.M.10
-
37
-
-
0142241272
-
Bone architecture and disc degeneration in the lumbar spine of mice lacking GDF-8 (myostatin)
-
Hamrick M.W., Pennington C., and Byron C.D. Bone architecture and disc degeneration in the lumbar spine of mice lacking GDF-8 (myostatin). J. Orthop. Res. 21 (2003) 1025-1032
-
(2003)
J. Orthop. Res.
, vol.21
, pp. 1025-1032
-
-
Hamrick, M.W.1
Pennington, C.2
Byron, C.D.3
-
38
-
-
33744536200
-
SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation
-
Dobreva G., Chahrour M., Dautzenberg M., Chirivella L., Kanzler B., Farinas I., Karsenty G., and Grosschedl R. SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation. Cell 125 (2006) 971-986
-
(2006)
Cell
, vol.125
, pp. 971-986
-
-
Dobreva, G.1
Chahrour, M.2
Dautzenberg, M.3
Chirivella, L.4
Kanzler, B.5
Farinas, I.6
Karsenty, G.7
Grosschedl, R.8
-
39
-
-
30344463802
-
Nuclear receptor coactivator-3 alleles are associated with serum bioavailable testosterone, insulin-like growth factor-1, and vertebral bone mass in men
-
Sheu Y.T., Zmuda J.M., Cauley J.A., Moffett S.P., Rosen C.J., Ishwad C., and Ferrell R.E. Nuclear receptor coactivator-3 alleles are associated with serum bioavailable testosterone, insulin-like growth factor-1, and vertebral bone mass in men. J. Clin. Endocrinol. Metab. 91 (2006) 307-312
-
(2006)
J. Clin. Endocrinol. Metab.
, vol.91
, pp. 307-312
-
-
Sheu, Y.T.1
Zmuda, J.M.2
Cauley, J.A.3
Moffett, S.P.4
Rosen, C.J.5
Ishwad, C.6
Ferrell, R.E.7
-
40
-
-
0842306340
-
Association of a polymorphism of the matrix metalloproteinase-9 gene with bone mineral density in Japanese men
-
Yamada Y., Ando F., Niino N., and Shimokata H. Association of a polymorphism of the matrix metalloproteinase-9 gene with bone mineral density in Japanese men. Metabolism 53 (2004) 135-137
-
(2004)
Metabolism
, vol.53
, pp. 135-137
-
-
Yamada, Y.1
Ando, F.2
Niino, N.3
Shimokata, H.4
-
41
-
-
33744997890
-
Carminerin contributes to chondrocyte calcification during endochondral ossification
-
Yamada T., Kawano H., Koshizuka Y., Fukuda T., Yoshimura K., Kamekura S., Saito T., Ikeda T., Kawasaki Y., Azuma Y., Ikegawa S., Hoshi K., Chung U.I., Nakamura K., Kato S., and Kawaguchi H. Carminerin contributes to chondrocyte calcification during endochondral ossification. Nat. Med. 12 (2006) 665-670
-
(2006)
Nat. Med.
, vol.12
, pp. 665-670
-
-
Yamada, T.1
Kawano, H.2
Koshizuka, Y.3
Fukuda, T.4
Yoshimura, K.5
Kamekura, S.6
Saito, T.7
Ikeda, T.8
Kawasaki, Y.9
Azuma, Y.10
Ikegawa, S.11
Hoshi, K.12
Chung, U.I.13
Nakamura, K.14
Kato, S.15
Kawaguchi, H.16
-
42
-
-
0034021980
-
Chromosomal mapping of osteopenia-associated quantitative trait loci using closely related mouse strains
-
Benes H., Weinstein R.S., Zheng W., Thaden J.J., Jilka R.L., Manolagas S.C., and Shmookler Reis R.J. Chromosomal mapping of osteopenia-associated quantitative trait loci using closely related mouse strains. J. Bone Miner. Res. 15 (2000) 626-633
-
(2000)
J. Bone Miner. Res.
, vol.15
, pp. 626-633
-
-
Benes, H.1
Weinstein, R.S.2
Zheng, W.3
Thaden, J.J.4
Jilka, R.L.5
Manolagas, S.C.6
Shmookler Reis, R.J.7
-
43
-
-
35548984468
-
P518/Qrfp sequence polymorphisms in SAMP6 osteopenic mouse
-
Zhang Q., Qiu P., Arreaza M.G., Simon J.S., Golovko A., Laverty M., Vassileva G., Gustafson E.L., Rojas-Triana A., Bober L.A., Hedrick J.A., Monsma Jr. F.J., Greene J.R., Bayne M.L., and Murgolo N.J. P518/Qrfp sequence polymorphisms in SAMP6 osteopenic mouse. Genomics 90 (2007) 629-635
-
(2007)
Genomics
, vol.90
, pp. 629-635
-
-
Zhang, Q.1
Qiu, P.2
Arreaza, M.G.3
Simon, J.S.4
Golovko, A.5
Laverty, M.6
Vassileva, G.7
Gustafson, E.L.8
Rojas-Triana, A.9
Bober, L.A.10
Hedrick, J.A.11
Monsma Jr., F.J.12
Greene, J.R.13
Bayne, M.L.14
Murgolo, N.J.15
-
44
-
-
30644465291
-
The G-protein-coupled receptor GPR103 regulates bone formation
-
Baribault H., Danao J., Gupte J., Yang L., Sun B., Richards W., and Tian H. The G-protein-coupled receptor GPR103 regulates bone formation. Mol. Cell. Biol. 26 (2006) 709-717
-
(2006)
Mol. Cell. Biol.
, vol.26
, pp. 709-717
-
-
Baribault, H.1
Danao, J.2
Gupte, J.3
Yang, L.4
Sun, B.5
Richards, W.6
Tian, H.7
-
45
-
-
2542506612
-
Associations between ABO blood groups and osteoporosis in postmenopausal women
-
Choi J.W., and Pai S.H. Associations between ABO blood groups and osteoporosis in postmenopausal women. Ann. Clin. Lab. Sci. 34 (2004) 150-153
-
(2004)
Ann. Clin. Lab. Sci.
, vol.34
, pp. 150-153
-
-
Choi, J.W.1
Pai, S.H.2
-
46
-
-
0345876776
-
Genetic loci determining bone density in mice with diet-induced atherosclerosis
-
Drake T.A., Schadt E., Hannani K., Kabo J.M., Krass K., Colinayo V., Greaser III L.E., Goldin J., and Lusis A.J. Genetic loci determining bone density in mice with diet-induced atherosclerosis. Physiol. Genomics 5 (2001) 205-215
-
(2001)
Physiol. Genomics
, vol.5
, pp. 205-215
-
-
Drake, T.A.1
Schadt, E.2
Hannani, K.3
Kabo, J.M.4
Krass, K.5
Colinayo, V.6
Greaser III, L.E.7
Goldin, J.8
Lusis, A.J.9
-
47
-
-
0030792031
-
Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system
-
Saftig P., Hartmann D., Lullmann-Rauch R., Wolff J., Evers M., Koster A., Hetman M., von Figura K., and Peters C. Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system. J. Biol. Chem. 272 (1997) 18628-18635
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 18628-18635
-
-
Saftig, P.1
Hartmann, D.2
Lullmann-Rauch, R.3
Wolff, J.4
Evers, M.5
Koster, A.6
Hetman, M.7
von Figura, K.8
Peters, C.9
-
48
-
-
0034920371
-
Impaired ossification in mice lacking the transcription factor Sp3
-
Gollner H., Dani C., Phillips B., Philipsen S., and Suske G. Impaired ossification in mice lacking the transcription factor Sp3. Mech. Dev. 106 (2001) 77-83
-
(2001)
Mech. Dev.
, vol.106
, pp. 77-83
-
-
Gollner, H.1
Dani, C.2
Phillips, B.3
Philipsen, S.4
Suske, G.5
-
49
-
-
33645776740
-
Single-nucleotide polymorphisms and haplotypes of bone morphogenetic protein genes and peripheral bone mineral density in young Korean men and women
-
Choi J.Y., Shin C.S., Hong Y.C., and Kang D. Single-nucleotide polymorphisms and haplotypes of bone morphogenetic protein genes and peripheral bone mineral density in young Korean men and women. Calcif. Tissue Int. 78 (2006) 203-211
-
(2006)
Calcif. Tissue Int.
, vol.78
, pp. 203-211
-
-
Choi, J.Y.1
Shin, C.S.2
Hong, Y.C.3
Kang, D.4
-
50
-
-
4243129131
-
Linkage of osteoporosis to chromosome 20p12 and association to BMP2
-
Styrkarsdottir U., Cazier J.B., Kong A., Rolfsson O., Larsen H., Bjarnadottir E., Johannsdottir V.D., Sigurdardottir M.S., Bagger Y., Christiansen C., Reynisdottir I., Grant S.F., Jonasson K., Frigge M.L., Gulcher J.R., Sigurdsson G., and Stefansson K. Linkage of osteoporosis to chromosome 20p12 and association to BMP2. PLoS Biol. 1 (2003) E69
-
(2003)
PLoS Biol.
, vol.1
-
-
Styrkarsdottir, U.1
Cazier, J.B.2
Kong, A.3
Rolfsson, O.4
Larsen, H.5
Bjarnadottir, E.6
Johannsdottir, V.D.7
Sigurdardottir, M.S.8
Bagger, Y.9
Christiansen, C.10
Reynisdottir, I.11
Grant, S.F.12
Jonasson, K.13
Frigge, M.L.14
Gulcher, J.R.15
Sigurdsson, G.16
Stefansson, K.17
-
51
-
-
33846921117
-
Associations of catalase gene polymorphisms with bone mineral density and bone turnover markers in postmenopausal women
-
Oh B., Kim S.Y., Kim D.J., Lee J.Y., Lee J.K., Kimm K., Park B.L., Shin H.D., Kim T.H., Park E.K., Koh J.M., and Kim G.S. Associations of catalase gene polymorphisms with bone mineral density and bone turnover markers in postmenopausal women. J. Med. Genet. 44 (2007) e62
-
(2007)
J. Med. Genet.
, vol.44
-
-
Oh, B.1
Kim, S.Y.2
Kim, D.J.3
Lee, J.Y.4
Lee, J.K.5
Kimm, K.6
Park, B.L.7
Shin, H.D.8
Kim, T.H.9
Park, E.K.10
Koh, J.M.11
Kim, G.S.12
-
52
-
-
34250697844
-
Linkage to chromosome 11p12 in two Maltese families with a highly penetrant form of osteoporosis
-
Vidal C., Galea R., Brincat M., and Anastasi A.X. Linkage to chromosome 11p12 in two Maltese families with a highly penetrant form of osteoporosis. Eur. J. Hum. Genet. 15 (2007) 800-809
-
(2007)
Eur. J. Hum. Genet.
, vol.15
, pp. 800-809
-
-
Vidal, C.1
Galea, R.2
Brincat, M.3
Anastasi, A.X.4
-
53
-
-
0033561039
-
TRAF6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling
-
Lomaga M.A., Yeh W.C., Sarosi I., Duncan G.S., Furlonger C., Ho A., Morony S., Capparelli C., Van G., Kaufman S., van der Heiden A., Itie A., Wakeham A., Khoo W., Sasaki T., Cao Z., Penninger J.M., Paige C.J., Lacey D.L., Dunstan C.R., Boyle W.J., Goeddel D.V., and Mak T.W. TRAF6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling. Genes Dev. 13 (1999) 1015-1024
-
(1999)
Genes Dev.
, vol.13
, pp. 1015-1024
-
-
Lomaga, M.A.1
Yeh, W.C.2
Sarosi, I.3
Duncan, G.S.4
Furlonger, C.5
Ho, A.6
Morony, S.7
Capparelli, C.8
Van, G.9
Kaufman, S.10
van der Heiden, A.11
Itie, A.12
Wakeham, A.13
Khoo, W.14
Sasaki, T.15
Cao, Z.16
Penninger, J.M.17
Paige, C.J.18
Lacey, D.L.19
Dunstan, C.R.20
Boyle, W.J.21
Goeddel, D.V.22
Mak, T.W.23
more..
-
54
-
-
0037947596
-
Targeted deletion of histidine decarboxylase gene in mice increases bone formation and protects against ovariectomy-induced bone loss
-
Fitzpatrick L.A., Buzas E., Gagne T.J., Nagy A., Horvath C., Ferencz V., Mester A., Kari B., Ruan M., Falus A., and Barsony J. Targeted deletion of histidine decarboxylase gene in mice increases bone formation and protects against ovariectomy-induced bone loss. Proc. Natl Acad. Sci. U. S. A. 100 (2003) 6027-6032
-
(2003)
Proc. Natl Acad. Sci. U. S. A.
, vol.100
, pp. 6027-6032
-
-
Fitzpatrick, L.A.1
Buzas, E.2
Gagne, T.J.3
Nagy, A.4
Horvath, C.5
Ferencz, V.6
Mester, A.7
Kari, B.8
Ruan, M.9
Falus, A.10
Barsony, J.11
-
55
-
-
34347208727
-
Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2
-
Johnson K.R., Marden C.C., Ward-Bailey P., Gagnon L.H., Bronson R.T., and Donahue L.R. Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2. Mol. Endocrinol. 21 (2007) 1593-1602
-
(2007)
Mol. Endocrinol.
, vol.21
, pp. 1593-1602
-
-
Johnson, K.R.1
Marden, C.C.2
Ward-Bailey, P.3
Gagnon, L.H.4
Bronson, R.T.5
Donahue, L.R.6
-
56
-
-
35748953461
-
Conditional deletion of gremlin causes a transient increase in bone formation and bone mass
-
Gazzerro E., Smerdel-Ramoya A., Zanotti S., Stadmeyer L., Durant D., Economides A.N., and Canalis E. Conditional deletion of gremlin causes a transient increase in bone formation and bone mass. J. Biol. Chem. 282 (2007) 31549-31557
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 31549-31557
-
-
Gazzerro, E.1
Smerdel-Ramoya, A.2
Zanotti, S.3
Stadmeyer, L.4
Durant, D.5
Economides, A.N.6
Canalis, E.7
-
57
-
-
0034007273
-
Disruption of the fibroblast growth factor-2 gene results in decreased bone mass and bone formation
-
Montero A., Okada Y., Tomita M., Ito M., Tsurukami H., Nakamura T., Doetschman T., Coffin J.D., and Hurley M.M. Disruption of the fibroblast growth factor-2 gene results in decreased bone mass and bone formation. J. Clin. Invest. 105 (2000) 1085-1093
-
(2000)
J. Clin. Invest.
, vol.105
, pp. 1085-1093
-
-
Montero, A.1
Okada, Y.2
Tomita, M.3
Ito, M.4
Tsurukami, H.5
Nakamura, T.6
Doetschman, T.7
Coffin, J.D.8
Hurley, M.M.9
-
58
-
-
25144448701
-
Dkk2 has a role in terminal osteoblast differentiation and mineralized matrix formation
-
Li X., Liu P., Liu W., Maye P., Zhang J., Zhang Y., Hurley M., Guo C., Boskey A., Sun L., Harris S.E., Rowe D.W., Ke H.Z., and Wu D. Dkk2 has a role in terminal osteoblast differentiation and mineralized matrix formation. Nat. Genet. 37 (2005) 945-952
-
(2005)
Nat. Genet.
, vol.37
, pp. 945-952
-
-
Li, X.1
Liu, P.2
Liu, W.3
Maye, P.4
Zhang, J.5
Zhang, Y.6
Hurley, M.7
Guo, C.8
Boskey, A.9
Sun, L.10
Harris, S.E.11
Rowe, D.W.12
Ke, H.Z.13
Wu, D.14
-
59
-
-
0032526145
-
Renal agenesis in mice homozygous for a gene trap mutation in the gene encoding heparan sulfate 2-sulfotransferase
-
Bullock S.L., Fletcher J.M., Beddington R.S., and Wilson V.A. Renal agenesis in mice homozygous for a gene trap mutation in the gene encoding heparan sulfate 2-sulfotransferase. Genes Dev. 12 (1998) 1894-1906
-
(1998)
Genes Dev.
, vol.12
, pp. 1894-1906
-
-
Bullock, S.L.1
Fletcher, J.M.2
Beddington, R.S.3
Wilson, V.A.4
-
60
-
-
0042807404
-
A common methylenetetrahydrofolate reductase (C677T) polymorphism is associated with low bone mineral density and increased fracture incidence after menopause: longitudinal data from the Danish osteoporosis prevention study
-
Abrahamsen B., Madsen J.S., Tofteng C.L., Stilgren L., Bladbjerg E.M., Kristensen S.R., Brixen K., and Mosekilde L. A common methylenetetrahydrofolate reductase (C677T) polymorphism is associated with low bone mineral density and increased fracture incidence after menopause: longitudinal data from the Danish osteoporosis prevention study. J. Bone Miner. Res. 18 (2003) 723-729
-
(2003)
J. Bone Miner. Res.
, vol.18
, pp. 723-729
-
-
Abrahamsen, B.1
Madsen, J.S.2
Tofteng, C.L.3
Stilgren, L.4
Bladbjerg, E.M.5
Kristensen, S.R.6
Brixen, K.7
Mosekilde, L.8
-
61
-
-
0033953774
-
Association of methylenetetrahydrofolate reductase (MTHFR) polymorphism with bone mineral density in postmenopausal Japanese women
-
Miyao M., Morita H., Hosoi T., Kurihara H., Inoue S., Hoshino S., Shiraki M., Yazaki Y., and Ouchi Y. Association of methylenetetrahydrofolate reductase (MTHFR) polymorphism with bone mineral density in postmenopausal Japanese women. Calcif. Tissue Int. 66 (2000) 190-194
-
(2000)
Calcif. Tissue Int.
, vol.66
, pp. 190-194
-
-
Miyao, M.1
Morita, H.2
Hosoi, T.3
Kurihara, H.4
Inoue, S.5
Hoshino, S.6
Shiraki, M.7
Yazaki, Y.8
Ouchi, Y.9
-
62
-
-
0037106438
-
Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women
-
Albagha O.M., Tasker P.N., McGuigan F.E., Reid D.M., and Ralston S.H. Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women. Hum. Mol. Genet. 11 (2002) 2289-2295
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2289-2295
-
-
Albagha, O.M.1
Tasker, P.N.2
McGuigan, F.E.3
Reid, D.M.4
Ralston, S.H.5
-
63
-
-
8644227628
-
Association between TNFRSF1B polymorphisms and bone mineral density, bone loss and fracture
-
Tasker P.N., Albagha O.M., Masson C.B., Reid D.M., and Ralston S.H. Association between TNFRSF1B polymorphisms and bone mineral density, bone loss and fracture. Osteoporos. Int. 15 (2004) 903-908
-
(2004)
Osteoporos. Int.
, vol.15
, pp. 903-908
-
-
Tasker, P.N.1
Albagha, O.M.2
Masson, C.B.3
Reid, D.M.4
Ralston, S.H.5
-
64
-
-
0034089081
-
Association of a polymorphism in the TNFR2 gene with low bone mineral density
-
Spotila L.D., Rodriguez H., Koch M., Adams K., Caminis J., Tenenhouse H.S., and Tenenhouse A. Association of a polymorphism in the TNFR2 gene with low bone mineral density. J. Bone Miner. Res. 15 (2000) 1376-1383
-
(2000)
J. Bone Miner. Res.
, vol.15
, pp. 1376-1383
-
-
Spotila, L.D.1
Rodriguez, H.2
Koch, M.3
Adams, K.4
Caminis, J.5
Tenenhouse, H.S.6
Tenenhouse, A.7
-
65
-
-
33744975547
-
Association of PLOD1 polymorphisms with bone mineral density in a population-based study of women from the UK
-
Tasker P.N., Macdonald H., Fraser W.D., Reid D.M., Ralston S.H., and Albagha O.M. Association of PLOD1 polymorphisms with bone mineral density in a population-based study of women from the UK. Osteoporos. Int. 17 (2006) 1078-1085
-
(2006)
Osteoporos. Int.
, vol.17
, pp. 1078-1085
-
-
Tasker, P.N.1
Macdonald, H.2
Fraser, W.D.3
Reid, D.M.4
Ralston, S.H.5
Albagha, O.M.6
-
66
-
-
0037223851
-
Association of the - 381T/C promoter variation of the brain natriuretic peptide gene with low bone-mineral density and rapid postmenopausal bone loss
-
Kajita M., Ezura Y., Iwasaki H., Ishida R., Yoshida H., Kodaira M., Suzuki T., Hosoi T., Inoue S., Shiraki M., Orimo H., and Emi M. Association of the - 381T/C promoter variation of the brain natriuretic peptide gene with low bone-mineral density and rapid postmenopausal bone loss. J. Hum. Genet. 48 (2003) 77-81
-
(2003)
J. Hum. Genet.
, vol.48
, pp. 77-81
-
-
Kajita, M.1
Ezura, Y.2
Iwasaki, H.3
Ishida, R.4
Yoshida, H.5
Kodaira, M.6
Suzuki, T.7
Hosoi, T.8
Inoue, S.9
Shiraki, M.10
Orimo, H.11
Emi, M.12
-
67
-
-
34248585741
-
Association of candidate gene polymorphisms with bone mineral density in community-dwelling Japanese women and men
-
Yamada Y., Ando F., and Shimokata H. Association of candidate gene polymorphisms with bone mineral density in community-dwelling Japanese women and men. Int. J. Mol. Med. 19 (2007) 791-801
-
(2007)
Int. J. Mol. Med.
, vol.19
, pp. 791-801
-
-
Yamada, Y.1
Ando, F.2
Shimokata, H.3
-
68
-
-
34249666244
-
Leptin receptor genotype at Gln223Arg is associated with body composition, BMD, and vertebral fracture in postmenopausal Danish women
-
Fairbrother U.L., Tanko L.B., Walley A.J., Christiansen C., Froguel P., and Blakemore A.I. Leptin receptor genotype at Gln223Arg is associated with body composition, BMD, and vertebral fracture in postmenopausal Danish women. J. Bone Miner. Res. 22 (2007) 544-550
-
(2007)
J. Bone Miner. Res.
, vol.22
, pp. 544-550
-
-
Fairbrother, U.L.1
Tanko, L.B.2
Walley, A.J.3
Christiansen, C.4
Froguel, P.5
Blakemore, A.I.6
-
69
-
-
33746641679
-
Functional knockout of the matrilin-3 gene causes premature chondrocyte maturation to hypertrophy and increases bone mineral density and osteoarthritis
-
van der Weyden L., Wei L., Luo J., Yang X., Birk D.E., Adams D.J., Bradley A., and Chen Q. Functional knockout of the matrilin-3 gene causes premature chondrocyte maturation to hypertrophy and increases bone mineral density and osteoarthritis. Am. J. Pathol. 169 (2006) 515-527
-
(2006)
Am. J. Pathol.
, vol.169
, pp. 515-527
-
-
van der Weyden, L.1
Wei, L.2
Luo, J.3
Yang, X.4
Birk, D.E.5
Adams, D.J.6
Bradley, A.7
Chen, Q.8
-
70
-
-
0033615959
-
Perlecan maintains the integrity of cartilage and some basement membranes
-
Costell M., Gustafsson E., Aszodi A., Morgelin M., Bloch W., Hunziker E., Addicks K., Timpl R., and Fassler R. Perlecan maintains the integrity of cartilage and some basement membranes. J. Cell Biol. 147 (1999) 1109-1122
-
(1999)
J. Cell Biol.
, vol.147
, pp. 1109-1122
-
-
Costell, M.1
Gustafsson, E.2
Aszodi, A.3
Morgelin, M.4
Bloch, W.5
Hunziker, E.6
Addicks, K.7
Timpl, R.8
Fassler, R.9
-
71
-
-
36849026384
-
Protein-tyrosine phosphatase H1 controls growth hormone receptor signaling and systemic growth
-
Pilecka I., Patrignani C., Pescini R., Curchod M.L., Perrin D., Xue Y., Yasenchak J., Clark A., Magnone M.C., Zaratin P., Valenzuela D., Rommel C., and Hooft van Huijsduijnen R. Protein-tyrosine phosphatase H1 controls growth hormone receptor signaling and systemic growth. J. Biol. Chem. 282 (2007) 35405-35415
-
(2007)
J. Biol. Chem.
, vol.282
, pp. 35405-35415
-
-
Pilecka, I.1
Patrignani, C.2
Pescini, R.3
Curchod, M.L.4
Perrin, D.5
Xue, Y.6
Yasenchak, J.7
Clark, A.8
Magnone, M.C.9
Zaratin, P.10
Valenzuela, D.11
Rommel, C.12
Hooft van Huijsduijnen, R.13
-
72
-
-
0142179020
-
Genetic effects for femoral biomechanics, structure, and density in C57BL/6J and C3H/HeJ inbred mouse strains
-
Koller D.L., Schriefer J., Sun Q., Shultz K.L., Donahue L.R., Rosen C.J., Foroud T., Beamer W.G., and Turner C.H. Genetic effects for femoral biomechanics, structure, and density in C57BL/6J and C3H/HeJ inbred mouse strains. J. Bone Miner. Res. 18 (2003) 1758-1765
-
(2003)
J. Bone Miner. Res.
, vol.18
, pp. 1758-1765
-
-
Koller, D.L.1
Schriefer, J.2
Sun, Q.3
Shultz, K.L.4
Donahue, L.R.5
Rosen, C.J.6
Foroud, T.7
Beamer, W.G.8
Turner, C.H.9
-
73
-
-
34249661230
-
Association of KIT gene polymorphisms with bone mineral density in postmenopausal Korean women
-
Kim S.Y., Lee J.Y., Kim H.Y., Oh B., Kimm K., Kim H.L., Park B.L., Shin H.D., Park E.K., Koh J.M., and Kim G.S. Association of KIT gene polymorphisms with bone mineral density in postmenopausal Korean women. J. Hum. Genet. 52 (2007) 502-509
-
(2007)
J. Hum. Genet.
, vol.52
, pp. 502-509
-
-
Kim, S.Y.1
Lee, J.Y.2
Kim, H.Y.3
Oh, B.4
Kimm, K.5
Kim, H.L.6
Park, B.L.7
Shin, H.D.8
Park, E.K.9
Koh, J.M.10
Kim, G.S.11
-
74
-
-
29244460361
-
CD38 is associated with premenopausal and postmenopausal bone mineral density and postmenopausal bone loss
-
Drummond F.J., Mackrill J.J., O'Sullivan K., Daly M., Shanahan F., and Molloy M.G. CD38 is associated with premenopausal and postmenopausal bone mineral density and postmenopausal bone loss. J. Bone Miner. Metab. 24 (2006) 28-35
-
(2006)
J. Bone Miner. Metab.
, vol.24
, pp. 28-35
-
-
Drummond, F.J.1
Mackrill, J.J.2
O'Sullivan, K.3
Daly, M.4
Shanahan, F.5
Molloy, M.G.6
-
75
-
-
33646875056
-
ALDH2 polymorphisms and bone mineral density in an elderly Japanese population
-
Yamaguchi J., Hasegawa Y., Kawasaki M., Masui T., Kanoh T., Ishiguro N., and Hamajima N. ALDH2 polymorphisms and bone mineral density in an elderly Japanese population. Osteoporos. Int. 17 (2006) 908-913
-
(2006)
Osteoporos. Int.
, vol.17
, pp. 908-913
-
-
Yamaguchi, J.1
Hasegawa, Y.2
Kawasaki, M.3
Masui, T.4
Kanoh, T.5
Ishiguro, N.6
Hamajima, N.7
-
76
-
-
33748954614
-
SULT1E1 genetic polymorphisms modified the association between phytoestrogen consumption and bone mineral density in healthy Korean women
-
Lee S.A., Choi J.Y., Shin C.S., Hong Y.C., Chung H., and Kang D. SULT1E1 genetic polymorphisms modified the association between phytoestrogen consumption and bone mineral density in healthy Korean women. Calcif. Tissue Int. 79 (2006) 152-159
-
(2006)
Calcif. Tissue Int.
, vol.79
, pp. 152-159
-
-
Lee, S.A.1
Choi, J.Y.2
Shin, C.S.3
Hong, Y.C.4
Chung, H.5
Kang, D.6
-
77
-
-
4043120646
-
Serum levels of matrix extracellular phosphoglycoprotein (MEPE) in normal humans correlate with serum phosphorus, parathyroid hormone and bone mineral density
-
Jain A., Fedarko N.S., Collins M.T., Gelman R., Ankrom M.A., Tayback M., and Fisher L.W. Serum levels of matrix extracellular phosphoglycoprotein (MEPE) in normal humans correlate with serum phosphorus, parathyroid hormone and bone mineral density. J. Clin. Endocrinol. Metab. 89 (2004) 4158-4161
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 4158-4161
-
-
Jain, A.1
Fedarko, N.S.2
Collins, M.T.3
Gelman, R.4
Ankrom, M.A.5
Tayback, M.6
Fisher, L.W.7
-
78
-
-
34247261472
-
Skeletal overgrowth is mediated by deficiency in a specific isoform of fibroblast growth factor receptor 3
-
Eswarakumar V.P., and Schlessinger J. Skeletal overgrowth is mediated by deficiency in a specific isoform of fibroblast growth factor receptor 3. Proc. Natl Acad. Sci. U. S. A. 104 (2007) 3937-3942
-
(2007)
Proc. Natl Acad. Sci. U. S. A.
, vol.104
, pp. 3937-3942
-
-
Eswarakumar, V.P.1
Schlessinger, J.2
-
79
-
-
43549121267
-
Bone sialoprotein plays a functional role in bone formation and osteoclastogenesis
-
Malaval L., Wade-Gueye N.M., Boudiffa M., Fei J., Zirngibl R., Chen F., Laroche N., Roux J.P., Burt-Pichat B., Duboeuf F., Boivin G., Jurdic P., Lafage-Proust M.H., Amedee J., Vico L., Rossant J., and Aubin J.E. Bone sialoprotein plays a functional role in bone formation and osteoclastogenesis. J. Exp. Med. 205 (2008) 1145-1153
-
(2008)
J. Exp. Med.
, vol.205
, pp. 1145-1153
-
-
Malaval, L.1
Wade-Gueye, N.M.2
Boudiffa, M.3
Fei, J.4
Zirngibl, R.5
Chen, F.6
Laroche, N.7
Roux, J.P.8
Burt-Pichat, B.9
Duboeuf, F.10
Boivin, G.11
Jurdic, P.12
Lafage-Proust, M.H.13
Amedee, J.14
Vico, L.15
Rossant, J.16
Aubin, J.E.17
-
80
-
-
10344262559
-
The AP1 transcription factor Fra2 is required for efficient cartilage development
-
Karreth F., Hoebertz A., Scheuch H., Eferl R., and Wagner E.F. The AP1 transcription factor Fra2 is required for efficient cartilage development. Development 131 (2004) 5717-5725
-
(2004)
Development
, vol.131
, pp. 5717-5725
-
-
Karreth, F.1
Hoebertz, A.2
Scheuch, H.3
Eferl, R.4
Wagner, E.F.5
-
81
-
-
0032918417
-
Osteopathy and resistance to vitamin D toxicity in mice null for vitamin D binding protein
-
Safadi F.F., Thornton P., Magiera H., Hollis B.W., Gentile M., Haddad J.G., Liebhaber S.A., and Cooke N.E. Osteopathy and resistance to vitamin D toxicity in mice null for vitamin D binding protein. J. Clin. Invest. 103 (1999) 239-251
-
(1999)
J. Clin. Invest.
, vol.103
, pp. 239-251
-
-
Safadi, F.F.1
Thornton, P.2
Magiera, H.3
Hollis, B.W.4
Gentile, M.5
Haddad, J.G.6
Liebhaber, S.A.7
Cooke, N.E.8
-
82
-
-
0035834738
-
Cloning and characterization of a novel protein kinase that impairs osteoblast differentiation in vitro
-
Kearns A.E., Donohue M.M., Sanyal B., and Demay M.B. Cloning and characterization of a novel protein kinase that impairs osteoblast differentiation in vitro. J. Biol. Chem. 276 (2001) 42213-42218
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 42213-42218
-
-
Kearns, A.E.1
Donohue, M.M.2
Sanyal, B.3
Demay, M.B.4
-
83
-
-
34248162417
-
Microphthalmia-associated transcription factor polymorphisms and association with bone mineral density of the proximal femur in postmenopausal women
-
Koh J.M., Kim G.S., Oh B., Lee J.Y., Park B.L., Shin H.D., Hong J.M., Kim T.H., Kim S.Y., and Park E.K. Microphthalmia-associated transcription factor polymorphisms and association with bone mineral density of the proximal femur in postmenopausal women. Mol. Cells 23 (2007) 246-251
-
(2007)
Mol. Cells
, vol.23
, pp. 246-251
-
-
Koh, J.M.1
Kim, G.S.2
Oh, B.3
Lee, J.Y.4
Park, B.L.5
Shin, H.D.6
Hong, J.M.7
Kim, T.H.8
Kim, S.Y.9
Park, E.K.10
-
84
-
-
35748963239
-
Genome-wide association with bone mass and geometry in the Framingham Heart Study
-
Kiel D.P., Demissie S., Dupuis J., Lunetta K.L., Murabito J.M., and Karasik D. Genome-wide association with bone mass and geometry in the Framingham Heart Study. BMC Med. Genet. 8 Suppl. 1 (2007) S14
-
(2007)
BMC Med. Genet.
, vol.8
, Issue.SUPPL. 1
-
-
Kiel, D.P.1
Demissie, S.2
Dupuis, J.3
Lunetta, K.L.4
Murabito, J.M.5
Karasik, D.6
-
85
-
-
33846026338
-
A functional single nucleotide polymorphism in the vitamin-K-dependent gamma-glutamyl carboxylase gene (Arg325Gln) is associated with bone mineral density in elderly Japanese women
-
Kinoshita H., Nakagawa K., Narusawa K., Goseki-Sone M., Fukushi-Irie M., Mizoi L., Yoshida H., Okano T., Nakamura T., Suzuki T., Inoue S., Orimo H., Ouchi Y., and Hosoi T. A functional single nucleotide polymorphism in the vitamin-K-dependent gamma-glutamyl carboxylase gene (Arg325Gln) is associated with bone mineral density in elderly Japanese women. Bone 40 (2007) 451-456
-
(2007)
Bone
, vol.40
, pp. 451-456
-
-
Kinoshita, H.1
Nakagawa, K.2
Narusawa, K.3
Goseki-Sone, M.4
Fukushi-Irie, M.5
Mizoi, L.6
Yoshida, H.7
Okano, T.8
Nakamura, T.9
Suzuki, T.10
Inoue, S.11
Orimo, H.12
Ouchi, Y.13
Hosoi, T.14
-
86
-
-
0036091476
-
The PERK eukaryotic initiation factor 2 alpha kinase is required for the development of the skeletal system, postnatal growth, and the function and viability of the pancreas
-
Zhang P., McGrath B., Li S., Frank A., Zambito F., Reinert J., Gannon M., Ma K., McNaughton K., and Cavener D.R. The PERK eukaryotic initiation factor 2 alpha kinase is required for the development of the skeletal system, postnatal growth, and the function and viability of the pancreas. Mol. Cell. Biol. 22 (2002) 3864-3874
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 3864-3874
-
-
Zhang, P.1
McGrath, B.2
Li, S.3
Frank, A.4
Zambito, F.5
Reinert, J.6
Gannon, M.7
Ma, K.8
McNaughton, K.9
Cavener, D.R.10
-
87
-
-
0033949961
-
Association of bone mineral density with polymorphism of the human matrix Gla protein locus in elderly women
-
Tsukamoto K., Orimo H., Hosoi T., Miyao M., Yoshida H., Watanabe S., Suzuki T., and Emi M. Association of bone mineral density with polymorphism of the human matrix Gla protein locus in elderly women. J. Bone Miner. Metab. 18 (2000) 27-30
-
(2000)
J. Bone Miner. Metab.
, vol.18
, pp. 27-30
-
-
Tsukamoto, K.1
Orimo, H.2
Hosoi, T.3
Miyao, M.4
Yoshida, H.5
Watanabe, S.6
Suzuki, T.7
Emi, M.8
-
88
-
-
13444295117
-
Decreased BMD and limb deformities in mice carrying mutations in both Lrp5 and Lrp6
-
Holmen S.L., Giambernardi T.A., Zylstra C.R., Buckner-Berghuis B.D., Resau J.H., Hess J.F., Glatt V., Bouxsein M.L., Ai M., Warman M.L., and Williams B.O. Decreased BMD and limb deformities in mice carrying mutations in both Lrp5 and Lrp6. J. Bone Miner. Res. 19 (2004) 2033-2040
-
(2004)
J. Bone Miner. Res.
, vol.19
, pp. 2033-2040
-
-
Holmen, S.L.1
Giambernardi, T.A.2
Zylstra, C.R.3
Buckner-Berghuis, B.D.4
Resau, J.H.5
Hess, J.F.6
Glatt, V.7
Bouxsein, M.L.8
Ai, M.9
Warman, M.L.10
Williams, B.O.11
-
89
-
-
9644303231
-
Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice
-
Sitara D., Razzaque M.S., Hesse M., Yoganathan S., Taguchi T., Erben R.G., Juppner H., and Lanske B. Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice. Matrix Biol. 23 (2004) 421-432
-
(2004)
Matrix Biol.
, vol.23
, pp. 421-432
-
-
Sitara, D.1
Razzaque, M.S.2
Hesse, M.3
Yoganathan, S.4
Taguchi, T.5
Erben, R.G.6
Juppner, H.7
Lanske, B.8
-
90
-
-
0036251217
-
Parathyroid hormone is essential for normal fetal bone formation
-
Miao D., He B., Karaplis A.C., and Goltzman D. Parathyroid hormone is essential for normal fetal bone formation. J. Clin. Invest. 109 (2002) 1173-1182
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 1173-1182
-
-
Miao, D.1
He, B.2
Karaplis, A.C.3
Goltzman, D.4
-
91
-
-
0035431807
-
The transcription factors L-Sox5 and Sox6 are essential for cartilage formation
-
Smits P., Li P., Mandel J., Zhang Z., Deng J.M., Behringer R.R., de Crombrugghe B., and Lefebvre V. The transcription factors L-Sox5 and Sox6 are essential for cartilage formation. Dev. Cell 1 (2001) 277-290
-
(2001)
Dev. Cell
, vol.1
, pp. 277-290
-
-
Smits, P.1
Li, P.2
Mandel, J.3
Zhang, Z.4
Deng, J.M.5
Behringer, R.R.6
de Crombrugghe, B.7
Lefebvre, V.8
-
92
-
-
33748168883
-
Association of polymorphisms in forkhead box C2 and perilipin genes with bone mineral density in community-dwelling Japanese individuals
-
Yamada Y., Ando F., and Shimokata H. Association of polymorphisms in forkhead box C2 and perilipin genes with bone mineral density in community-dwelling Japanese individuals. Int. J. Mol. Med. 18 (2006) 119-127
-
(2006)
Int. J. Mol. Med.
, vol.18
, pp. 119-127
-
-
Yamada, Y.1
Ando, F.2
Shimokata, H.3
-
93
-
-
33846147623
-
COL1A1, ESR1, VDR and TGFB1 polymorphisms and haplotypes in relation to BMD in Spanish postmenopausal women
-
Bustamante M., Nogues X., Enjuanes A., Elosua R., Garcia-Giralt N., Perez-Edo L., Caceres E., Carreras R., Mellibovsky L., Balcells S., Diez-Perez A., and Grinberg D. COL1A1, ESR1, VDR and TGFB1 polymorphisms and haplotypes in relation to BMD in Spanish postmenopausal women. Osteoporos. Int. 18 (2007) 235-243
-
(2007)
Osteoporos. Int.
, vol.18
, pp. 235-243
-
-
Bustamante, M.1
Nogues, X.2
Enjuanes, A.3
Elosua, R.4
Garcia-Giralt, N.5
Perez-Edo, L.6
Caceres, E.7
Carreras, R.8
Mellibovsky, L.9
Balcells, S.10
Diez-Perez, A.11
Grinberg, D.12
-
94
-
-
0037343809
-
Polymorphisms in the transforming growth factor beta 1 gene and osteoporosis
-
Langdahl B.L., Carstens M., Stenkjaer L., and Eriksen E.F. Polymorphisms in the transforming growth factor beta 1 gene and osteoporosis. Bone 32 (2003) 297-310
-
(2003)
Bone
, vol.32
, pp. 297-310
-
-
Langdahl, B.L.1
Carstens, M.2
Stenkjaer, L.3
Eriksen, E.F.4
-
95
-
-
41949128499
-
Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study
-
Langdahl B.L., Uitterlinden A.G., Ralston S.H., Trikalinos T.A., Balcells S., Brandi M.L., Scollen S., Lips P., Lorenc R., Obermayer-Pietsch B., Reid D.M., Armas J.B., Arp P.P., Bassiti A., Bustamante M., Husted L.B., Carey A.H., Perez Cano R., Dobnig H., Dunning A.M., Fahrleitner-Pammer A., Falchetti A., Karczmarewicz E., Kruk M., van Leeuwen J.P., Masi L., van Meurs J.B., Mangion J., McGuigan F.E., Mellibovsky L., Mosekilde L., Nogues X., Pols H.A., Reeve J., Renner W., Rivadeneira F., van Schoor N.M., and Ioannidis J.P. Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study. Bone 42 (2007) 969-981
-
(2007)
Bone
, vol.42
, pp. 969-981
-
-
Langdahl, B.L.1
Uitterlinden, A.G.2
Ralston, S.H.3
Trikalinos, T.A.4
Balcells, S.5
Brandi, M.L.6
Scollen, S.7
Lips, P.8
Lorenc, R.9
Obermayer-Pietsch, B.10
Reid, D.M.11
Armas, J.B.12
Arp, P.P.13
Bassiti, A.14
Bustamante, M.15
Husted, L.B.16
Carey, A.H.17
Perez Cano, R.18
Dobnig, H.19
Dunning, A.M.20
Fahrleitner-Pammer, A.21
Falchetti, A.22
Karczmarewicz, E.23
Kruk, M.24
van Leeuwen, J.P.25
Masi, L.26
van Meurs, J.B.27
Mangion, J.28
McGuigan, F.E.29
Mellibovsky, L.30
Mosekilde, L.31
Nogues, X.32
Pols, H.A.33
Reeve, J.34
Renner, W.35
Rivadeneira, F.36
van Schoor, N.M.37
Ioannidis, J.P.38
more..
-
96
-
-
11244262704
-
APOE haplotypes influence bone mineral density in Caucasian males but not females
-
Long J.R., Liu P.Y., Liu Y.J., Lu Y., Shen H., Zhao L.J., Xiong D.H., and Deng H.W. APOE haplotypes influence bone mineral density in Caucasian males but not females. Calcif. Tissue Int. 75 (2004) 299-304
-
(2004)
Calcif. Tissue Int.
, vol.75
, pp. 299-304
-
-
Long, J.R.1
Liu, P.Y.2
Liu, Y.J.3
Lu, Y.4
Shen, H.5
Zhao, L.J.6
Xiong, D.H.7
Deng, H.W.8
-
97
-
-
33750247815
-
Rescue of progeria in trichothiodystrophy by homozygous lethal Xpd alleles
-
Andressoo J.O., Jans J., de Wit J., Coin F., Hoogstraten D., van de Ven M., Toussaint W., Huijmans J., Thio H.B., van Leeuwen W.J., de Boer J., Egly J.M., Hoeijmakers J.H., van der Horst G.T., and Mitchell J.R. Rescue of progeria in trichothiodystrophy by homozygous lethal Xpd alleles. PLoS Biol. 4 (2006) e322
-
(2006)
PLoS Biol.
, vol.4
-
-
Andressoo, J.O.1
Jans, J.2
de Wit, J.3
Coin, F.4
Hoogstraten, D.5
van de Ven, M.6
Toussaint, W.7
Huijmans, J.8
Thio, H.B.9
van Leeuwen, W.J.10
de Boer, J.11
Egly, J.M.12
Hoeijmakers, J.H.13
van der Horst, G.T.14
Mitchell, J.R.15
-
98
-
-
33645815089
-
Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects
-
Desai J., Shannon M.E., Johnson M.D., Ruff D.W., Hughes L.A., Kerley M.K., Carpenter D.A., Johnson D.K., Rinchik E.M., and Culiat C.T. Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects. Hum. Mol. Genet. 15 (2006) 1329-1341
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 1329-1341
-
-
Desai, J.1
Shannon, M.E.2
Johnson, M.D.3
Ruff, D.W.4
Hughes, L.A.5
Kerley, M.K.6
Carpenter, D.A.7
Johnson, D.K.8
Rinchik, E.M.9
Culiat, C.T.10
-
99
-
-
0347721834
-
Osteoblast-specific knockout of the insulin-like growth factor (IGF) receptor gene reveals an essential role of IGF signaling in bone matrix mineralization
-
Zhang M., Xuan S., Bouxsein M.L., von Stechow D., Akeno N., Faugere M.C., Malluche H., Zhao G., Rosen C.J., Efstratiadis A., and Clemens T.L. Osteoblast-specific knockout of the insulin-like growth factor (IGF) receptor gene reveals an essential role of IGF signaling in bone matrix mineralization. J. Biol. Chem. 277 (2002) 44005-44012
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 44005-44012
-
-
Zhang, M.1
Xuan, S.2
Bouxsein, M.L.3
von Stechow, D.4
Akeno, N.5
Faugere, M.C.6
Malluche, H.7
Zhao, G.8
Rosen, C.J.9
Efstratiadis, A.10
Clemens, T.L.11
-
100
-
-
12544249249
-
Effect of CYP1A1 gene polymorphisms on estrogen metabolism and bone density
-
Napoli N., Villareal D.T., Mumm S., Halstead L., Sheikh S., Cagaanan M., Rini G.B., and Armamento-Villareal R. Effect of CYP1A1 gene polymorphisms on estrogen metabolism and bone density. J. Bone Miner. Res. 20 (2005) 232-239
-
(2005)
J. Bone Miner. Res.
, vol.20
, pp. 232-239
-
-
Napoli, N.1
Villareal, D.T.2
Mumm, S.3
Halstead, L.4
Sheikh, S.5
Cagaanan, M.6
Rini, G.B.7
Armamento-Villareal, R.8
-
101
-
-
0033714872
-
The oxidative metabolism of estradiol conditions postmenopausal bone density and bone loss
-
Leelawattana R., Ziambaras K., Roodman-Weiss J., Lyss C., Wagner D., Klug T., Armamento-Villareal R., and Civitelli R. The oxidative metabolism of estradiol conditions postmenopausal bone density and bone loss. J. Bone Miner. Res. 15 (2000) 2513-2520
-
(2000)
J. Bone Miner. Res.
, vol.15
, pp. 2513-2520
-
-
Leelawattana, R.1
Ziambaras, K.2
Roodman-Weiss, J.3
Lyss, C.4
Wagner, D.5
Klug, T.6
Armamento-Villareal, R.7
Civitelli, R.8
-
102
-
-
31544451065
-
Association study of semaphorin 7a (sema7a) polymorphisms with bone mineral density and fracture risk in postmenopausal Korean women
-
Koh J.M., Oh B., Lee J.Y., Lee J.K., Kimm K., Kim G.S., Park B.L., Cheong H.S., Shin H.D., Hong J.M., Kim T.H., Park E.K., and Kim S.Y. Association study of semaphorin 7a (sema7a) polymorphisms with bone mineral density and fracture risk in postmenopausal Korean women. J. Hum. Genet. 51 (2006) 112-117
-
(2006)
J. Hum. Genet.
, vol.51
, pp. 112-117
-
-
Koh, J.M.1
Oh, B.2
Lee, J.Y.3
Lee, J.K.4
Kimm, K.5
Kim, G.S.6
Park, B.L.7
Cheong, H.S.8
Shin, H.D.9
Hong, J.M.10
Kim, T.H.11
Park, E.K.12
Kim, S.Y.13
-
103
-
-
0034813396
-
The loss of Smad3 results in a lower rate of bone formation and osteopenia through dysregulation of osteoblast differentiation and apoptosis
-
Borton A.J., Frederick J.P., Datto M.B., Wang X.F., and Weinstein R.S. The loss of Smad3 results in a lower rate of bone formation and osteopenia through dysregulation of osteoblast differentiation and apoptosis. J. Bone Miner. Res. 16 (2001) 1754-1764
-
(2001)
J. Bone Miner. Res.
, vol.16
, pp. 1754-1764
-
-
Borton, A.J.1
Frederick, J.P.2
Datto, M.B.3
Wang, X.F.4
Weinstein, R.S.5
-
104
-
-
0043210538
-
Targeted disruption of a murine glucuronyl C5-epimerase gene results in heparan sulfate lacking L-iduronic acid and in neonatal lethality
-
Li J.P., Gong F., Hagner-McWhirter A., Forsberg E., Abrink M., Kisilevsky R., Zhang X., and Lindahl U. Targeted disruption of a murine glucuronyl C5-epimerase gene results in heparan sulfate lacking L-iduronic acid and in neonatal lethality. J. Biol. Chem. 278 (2003) 28363-28366
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 28363-28366
-
-
Li, J.P.1
Gong, F.2
Hagner-McWhirter, A.3
Forsberg, E.4
Abrink, M.5
Kisilevsky, R.6
Zhang, X.7
Lindahl, U.8
-
105
-
-
4444356016
-
The immune regulatory protein B7-H3 promotes osteoblast differentiation and bone mineralization
-
Suh W.K., Wang S.X., Jheon A.H., Moreno L., Yoshinaga S.K., Ganss B., Sodek J., Grynpas M.D., and Mak T.W. The immune regulatory protein B7-H3 promotes osteoblast differentiation and bone mineralization. Proc. Natl Acad. Sci. U. S. A. 101 (2004) 12969-12973
-
(2004)
Proc. Natl Acad. Sci. U. S. A.
, vol.101
, pp. 12969-12973
-
-
Suh, W.K.1
Wang, S.X.2
Jheon, A.H.3
Moreno, L.4
Yoshinaga, S.K.5
Ganss, B.6
Sodek, J.7
Grynpas, M.D.8
Mak, T.W.9
-
106
-
-
0037304076
-
Conventional and tissue-specific inactivation of the 25-hydroxyvitamin D-1alpha-hydroxylase (CYP27B1)
-
St-Arnaud R., Dardenne O., Prud'homme J., Hacking S.A., and Glorieux F.H. Conventional and tissue-specific inactivation of the 25-hydroxyvitamin D-1alpha-hydroxylase (CYP27B1). J. Cell. Biochem. 88 (2003) 245-251
-
(2003)
J. Cell. Biochem.
, vol.88
, pp. 245-251
-
-
St-Arnaud, R.1
Dardenne, O.2
Prud'homme, J.3
Hacking, S.A.4
Glorieux, F.H.5
-
107
-
-
33847174964
-
Detecting novel bone density and bone size quantitative trait loci using a cross of MRL/MpJ and CAST/EiJ inbred mice
-
Yu H., Mohan S., Edderkaoui B., Masinde G.L., Davidson H.M., Wergedal J.E., Beamer W.G., and Baylink D.J. Detecting novel bone density and bone size quantitative trait loci using a cross of MRL/MpJ and CAST/EiJ inbred mice. Calcif. Tissue Int. 80 (2007) 103-110
-
(2007)
Calcif. Tissue Int.
, vol.80
, pp. 103-110
-
-
Yu, H.1
Mohan, S.2
Edderkaoui, B.3
Masinde, G.L.4
Davidson, H.M.5
Wergedal, J.E.6
Beamer, W.G.7
Baylink, D.J.8
-
108
-
-
0042884446
-
Association between an insulin-like growth factor I gene promoter polymorphism and bone mineral density in the elderly: the Rotterdam Study
-
Rivadeneira F., Houwing-Duistermaat J.J., Vaessen N., Vergeer-Drop J.M., Hofman A., Pols H.A., Van Duijn C.M., and Uitterlinden A.G. Association between an insulin-like growth factor I gene promoter polymorphism and bone mineral density in the elderly: the Rotterdam Study. J. Clin. Endocrinol. Metab. 88 (2003) 3878-3884
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, pp. 3878-3884
-
-
Rivadeneira, F.1
Houwing-Duistermaat, J.J.2
Vaessen, N.3
Vergeer-Drop, J.M.4
Hofman, A.5
Pols, H.A.6
Van Duijn, C.M.7
Uitterlinden, A.G.8
-
109
-
-
0033638923
-
Insulin-like growth factors and bone mineral density in African American and White girls
-
Yanovski J.A., Sovik K.N., Nguyen T.T., and Sebring N.G. Insulin-like growth factors and bone mineral density in African American and White girls. J. Pediatr. 137 (2000) 826-832
-
(2000)
J. Pediatr.
, vol.137
, pp. 826-832
-
-
Yanovski, J.A.1
Sovik, K.N.2
Nguyen, T.T.3
Sebring, N.G.4
-
110
-
-
25444489016
-
Defective osteogenesis of the stromal stem cells predisposes CD18-null mice to osteoporosis
-
Miura Y., Miura M., Gronthos S., Allen M.R., Cao C., Uveges T.E., Bi Y., Ehirchiou D., Kortesidis A., Shi S., and Zhang L. Defective osteogenesis of the stromal stem cells predisposes CD18-null mice to osteoporosis. Proc. Natl Acad. Sci. U. S. A. 102 (2005) 14022-14027
-
(2005)
Proc. Natl Acad. Sci. U. S. A.
, vol.102
, pp. 14022-14027
-
-
Miura, Y.1
Miura, M.2
Gronthos, S.3
Allen, M.R.4
Cao, C.5
Uveges, T.E.6
Bi, Y.7
Ehirchiou, D.8
Kortesidis, A.9
Shi, S.10
Zhang, L.11
-
111
-
-
22744449169
-
Type XIII collagen strongly affects bone formation in transgenic mice
-
Ylonen R., Kyronlahti T., Sund M., Ilves M., Lehenkari P., Tuukkanen J., and Pihlajaniemi T. Type XIII collagen strongly affects bone formation in transgenic mice. J. Bone Miner. Res. 20 (2005) 1381-1393
-
(2005)
J. Bone Miner. Res.
, vol.20
, pp. 1381-1393
-
-
Ylonen, R.1
Kyronlahti, T.2
Sund, M.3
Ilves, M.4
Lehenkari, P.5
Tuukkanen, J.6
Pihlajaniemi, T.7
-
112
-
-
0030060372
-
Defective bone formation in Krox-20 mutant mice
-
Levi G., Topilko P., Schneider-Maunoury S., Lasagna M., Mantero S., Cancedda R., and Charnay P. Defective bone formation in Krox-20 mutant mice. Development 122 (1996) 113-120
-
(1996)
Development
, vol.122
, pp. 113-120
-
-
Levi, G.1
Topilko, P.2
Schneider-Maunoury, S.3
Lasagna, M.4
Mantero, S.5
Cancedda, R.6
Charnay, P.7
-
113
-
-
33845984911
-
Parathyroid-specific double knockout of Gq and G11 alpha-subunits leads to a phenotype resembling germline knockout of the extracellular Ca2+ -sensing receptor
-
Wettschureck N., Lee E., Libutti S.K., Offermanns S., Robey P.G., and Spiegel A.M. Parathyroid-specific double knockout of Gq and G11 alpha-subunits leads to a phenotype resembling germline knockout of the extracellular Ca2+ -sensing receptor. Mol. Endocrinol. 21 (2007) 274-280
-
(2007)
Mol. Endocrinol.
, vol.21
, pp. 274-280
-
-
Wettschureck, N.1
Lee, E.2
Libutti, S.K.3
Offermanns, S.4
Robey, P.G.5
Spiegel, A.M.6
-
114
-
-
18044388164
-
Association of a single nucleotide polymorphism in the lipoxygenase ALOX15 5′-flanking region (- 5229G/A) with bone mineral density
-
Urano T., Shiraki M., Fujita M., Hosoi T., Orimo H., Ouchi Y., and Inoue S. Association of a single nucleotide polymorphism in the lipoxygenase ALOX15 5′-flanking region (- 5229G/A) with bone mineral density. J. Bone Miner. Metab. 23 (2005) 226-230
-
(2005)
J. Bone Miner. Metab.
, vol.23
, pp. 226-230
-
-
Urano, T.1
Shiraki, M.2
Fujita, M.3
Hosoi, T.4
Orimo, H.5
Ouchi, Y.6
Inoue, S.7
-
115
-
-
33645337659
-
Human ALOX12, but not ALOX15, is associated with BMD in white men and women
-
Ichikawa S., Koller D.L., Johnson M.L., Lai D., Xuei X., Edenberg H.J., Klein R.F., Orwoll E.S., Hui S.L., Foroud T.M., Peacock M., and Econs M.J. Human ALOX12, but not ALOX15, is associated with BMD in white men and women. J. Bone Miner. Res. 21 (2006) 556-564
-
(2006)
J. Bone Miner. Res.
, vol.21
, pp. 556-564
-
-
Ichikawa, S.1
Koller, D.L.2
Johnson, M.L.3
Lai, D.4
Xuei, X.5
Edenberg, H.J.6
Klein, R.F.7
Orwoll, E.S.8
Hui, S.L.9
Foroud, T.M.10
Peacock, M.11
Econs, M.J.12
-
116
-
-
34447097190
-
Polymorphisms in ALOX12, but not ALOX15, are significantly associated with BMD in postmenopausal women
-
Mullin B.H., Spector T.D., Curtis C.C., Ong G.N., Hart D.J., Hakim A.J., Worthy T., and Wilson S.G. Polymorphisms in ALOX12, but not ALOX15, are significantly associated with BMD in postmenopausal women. Calcif. Tissue Int. 81 (2007) 10-17
-
(2007)
Calcif. Tissue Int.
, vol.81
, pp. 10-17
-
-
Mullin, B.H.1
Spector, T.D.2
Curtis, C.C.3
Ong, G.N.4
Hart, D.J.5
Hakim, A.J.6
Worthy, T.7
Wilson, S.G.8
-
117
-
-
0041971243
-
Association of genetic variation of the RIL gene, encoding a PDZ-LIM domain protein and localized in 5q31.1, with low bone mineral density in adult Japanese women
-
Omasu F., Ezura Y., Kajita M., Ishida R., Kodaira M., Yoshida H., Suzuki T., Hosoi T., Inoue S., Shiraki M., Orimo H., and Emi M. Association of genetic variation of the RIL gene, encoding a PDZ-LIM domain protein and localized in 5q31.1, with low bone mineral density in adult Japanese women. J. Hum. Genet. 48 (2003) 342-345
-
(2003)
J. Hum. Genet.
, vol.48
, pp. 342-345
-
-
Omasu, F.1
Ezura, Y.2
Kajita, M.3
Ishida, R.4
Kodaira, M.5
Yoshida, H.6
Suzuki, T.7
Hosoi, T.8
Inoue, S.9
Shiraki, M.10
Orimo, H.11
Emi, M.12
-
118
-
-
33845473304
-
SHBG gene promoter polymorphisms in men are associated with serum sex hormone-binding globulin, androgen and androgen metabolite levels, and hip bone mineral density
-
Eriksson A.L., Lorentzon M., Mellstrom D., Vandenput L., Swanson C., Andersson N., Hammond G.L., Jakobsson J., Rane A., Orwoll E.S., Ljunggren O., Johnell O., Labrie F., Windahl S.H., and Ohlsson C. SHBG gene promoter polymorphisms in men are associated with serum sex hormone-binding globulin, androgen and androgen metabolite levels, and hip bone mineral density. J. Clin. Endocrinol. Metab. 91 (2006) 5029-5037
-
(2006)
J. Clin. Endocrinol. Metab.
, vol.91
, pp. 5029-5037
-
-
Eriksson, A.L.1
Lorentzon, M.2
Mellstrom, D.3
Vandenput, L.4
Swanson, C.5
Andersson, N.6
Hammond, G.L.7
Jakobsson, J.8
Rane, A.9
Orwoll, E.S.10
Ljunggren, O.11
Johnell, O.12
Labrie, F.13
Windahl, S.H.14
Ohlsson, C.15
-
119
-
-
37449026264
-
Osteopenia in Sparc (osteonectin)-deficient mice: characterization of phenotypic determinants of femoral strength and changes in gene expression
-
Mansergh F.C., Wells T., Elford C., Evans S.L., Perry M.J., Evans M.J., and Evans B.A. Osteopenia in Sparc (osteonectin)-deficient mice: characterization of phenotypic determinants of femoral strength and changes in gene expression. Physiol. Genomics 32 (2007) 64-73
-
(2007)
Physiol. Genomics
, vol.32
, pp. 64-73
-
-
Mansergh, F.C.1
Wells, T.2
Elford, C.3
Evans, S.L.4
Perry, M.J.5
Evans, M.J.6
Evans, B.A.7
-
120
-
-
6344263668
-
Polymorphism in the growth hormone gene, weight in infancy, and adult bone mass
-
Dennison E.M., Syddall H.E., Rodriguez S., Voropanov A., Day I.N., and Cooper C. Polymorphism in the growth hormone gene, weight in infancy, and adult bone mass. J. Clin. Endocrinol. Metab. 89 (2004) 4898-4903
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 4898-4903
-
-
Dennison, E.M.1
Syddall, H.E.2
Rodriguez, S.3
Voropanov, A.4
Day, I.N.5
Cooper, C.6
-
121
-
-
0037384971
-
Growth hormone predicts bone density in elderly women
-
Dennison E.M., Hindmarsh P.C., Kellingray S., Fall C.H., and Cooper C. Growth hormone predicts bone density in elderly women. Bone 32 (2003) 434-440
-
(2003)
Bone
, vol.32
, pp. 434-440
-
-
Dennison, E.M.1
Hindmarsh, P.C.2
Kellingray, S.3
Fall, C.H.4
Cooper, C.5
-
122
-
-
33746634349
-
COL1A1 Sp1 polymorphism associates with bone density in early puberty
-
Suuriniemi M., Kovanen V., Mahonen A., Alen M., Wang Q., Lyytikainen A., and Cheng S. COL1A1 Sp1 polymorphism associates with bone density in early puberty. Bone 39 (2006) 591-597
-
(2006)
Bone
, vol.39
, pp. 591-597
-
-
Suuriniemi, M.1
Kovanen, V.2
Mahonen, A.3
Alen, M.4
Wang, Q.5
Lyytikainen, A.6
Cheng, S.7
-
123
-
-
0347297216
-
Relationship between bone mineral density and angiotensin converting enzyme polymorphism in hypertensive postmenopausal women
-
Perez-Castrillon J.L., Justo I., Silva J., Sanz A., Martin-Escudero J.C., Igea R., Escudero P., Pueyo C., Diaz C., Hernandez G., and Duenas A. Relationship between bone mineral density and angiotensin converting enzyme polymorphism in hypertensive postmenopausal women. Am. J. Hypertens. 16 (2003) 233-235
-
(2003)
Am. J. Hypertens.
, vol.16
, pp. 233-235
-
-
Perez-Castrillon, J.L.1
Justo, I.2
Silva, J.3
Sanz, A.4
Martin-Escudero, J.C.5
Igea, R.6
Escudero, P.7
Pueyo, C.8
Diaz, C.9
Hernandez, G.10
Duenas, A.11
-
124
-
-
8844261126
-
Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites
-
Uitterlinden A.G., Arp P.P., Paeper B.W., Charmley P., Proll S., Rivadeneira F., Fang Y., van Meurs J.B., Britschgi T.B., Latham J.A., Schatzman R.C., Pols H.A., and Brunkow M.E. Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites. Am. J. Hum. Genet. 75 (2004) 1032-1045
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 1032-1045
-
-
Uitterlinden, A.G.1
Arp, P.P.2
Paeper, B.W.3
Charmley, P.4
Proll, S.5
Rivadeneira, F.6
Fang, Y.7
van Meurs, J.B.8
Britschgi, T.B.9
Latham, J.A.10
Schatzman, R.C.11
Pols, H.A.12
Brunkow, M.E.13
-
125
-
-
85047689811
-
Impaired osteoblastic differentiation, reduced bone formation, and severe osteoporosis in noggin-overexpressing mice
-
Wu X.B., Li Y., Schneider A., Yu W., Rajendren G., Iqbal J., Yamamoto M., Alam M., Brunet L.J., Blair H.C., Zaidi M., and Abe E. Impaired osteoblastic differentiation, reduced bone formation, and severe osteoporosis in noggin-overexpressing mice. J. Clin. Invest. 112 (2003) 924-934
-
(2003)
J. Clin. Invest.
, vol.112
, pp. 924-934
-
-
Wu, X.B.1
Li, Y.2
Schneider, A.3
Yu, W.4
Rajendren, G.5
Iqbal, J.6
Yamamoto, M.7
Alam, M.8
Brunet, L.J.9
Blair, H.C.10
Zaidi, M.11
Abe, E.12
-
126
-
-
33750435875
-
Vitamin D deficiency associated with number of neurofibromas in neurofibromatosis 1
-
Lammert M., Friedman J.M., Roth H.J., Friedrich R.E., Kluwe L., Atkins D., Schooler T., and Mautner V.F. Vitamin D deficiency associated with number of neurofibromas in neurofibromatosis 1. J. Med. Genet. 43 (2006) 810-813
-
(2006)
J. Med. Genet.
, vol.43
, pp. 810-813
-
-
Lammert, M.1
Friedman, J.M.2
Roth, H.J.3
Friedrich, R.E.4
Kluwe, L.5
Atkins, D.6
Schooler, T.7
Mautner, V.F.8
-
127
-
-
5344238900
-
Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome
-
Haldeman R.J., Cooper L.F., Hart T.C., Phillips C., Boyd C., Lester G.E., and Wright J.T. Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome. Bone 35 (2004) 988-997
-
(2004)
Bone
, vol.35
, pp. 988-997
-
-
Haldeman, R.J.1
Cooper, L.F.2
Hart, T.C.3
Phillips, C.4
Boyd, C.5
Lester, G.E.6
Wright, J.T.7
-
128
-
-
0035999441
-
Role of inducible nitric oxide synthase in skeletal adaptation to acute increases in mechanical loading
-
Watanuki M., Sakai A., Sakata T., Tsurukami H., Miwa M., Uchida Y., Watanabe K., Ikeda K., and Nakamura T. Role of inducible nitric oxide synthase in skeletal adaptation to acute increases in mechanical loading. J. Bone Miner. Res. 17 (2002) 1015-1025
-
(2002)
J. Bone Miner. Res.
, vol.17
, pp. 1015-1025
-
-
Watanuki, M.1
Sakai, A.2
Sakata, T.3
Tsurukami, H.4
Miwa, M.5
Uchida, Y.6
Watanabe, K.7
Ikeda, K.8
Nakamura, T.9
-
129
-
-
28144460153
-
Contrasting skeletal phenotypes in mice with an identical mutation targeted to thyroid hormone receptor alpha1 or beta
-
O'Shea P.J., Bassett J.H., Sriskantharajah S., Ying H., Cheng S.Y., and Williams G.R. Contrasting skeletal phenotypes in mice with an identical mutation targeted to thyroid hormone receptor alpha1 or beta. Mol. Endocrinol. 19 (2005) 3045-3059
-
(2005)
Mol. Endocrinol.
, vol.19
, pp. 3045-3059
-
-
O'Shea, P.J.1
Bassett, J.H.2
Sriskantharajah, S.3
Ying, H.4
Cheng, S.Y.5
Williams, G.R.6
-
130
-
-
0035810951
-
Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization
-
Bi W., Huang W., Whitworth D.J., Deng J.M., Zhang Z., Behringer R.R., and de Crombrugghe B. Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization. Proc. Natl Acad. Sci. U. S. A. 98 (2001) 6698-6703
-
(2001)
Proc. Natl Acad. Sci. U. S. A.
, vol.98
, pp. 6698-6703
-
-
Bi, W.1
Huang, W.2
Whitworth, D.J.3
Deng, J.M.4
Zhang, Z.5
Behringer, R.R.6
de Crombrugghe, B.7
-
131
-
-
0011983514
-
Identification of peak bone mass QTL in a spontaneously osteoporotic mouse strain
-
Shimizu M., Higuchi K., Bennett B., Xia C., Tsuboyama T., Kasai S., Chiba T., Fujisawa H., Kogishi K., Kitado H., Kimoto M., Takeda N., Matsushita M., Okumura H., Serikawa T., Nakamura T., Johnson T.E., and Hosokawa M. Identification of peak bone mass QTL in a spontaneously osteoporotic mouse strain. Mamm. Genome 10 (1999) 81-87
-
(1999)
Mamm. Genome
, vol.10
, pp. 81-87
-
-
Shimizu, M.1
Higuchi, K.2
Bennett, B.3
Xia, C.4
Tsuboyama, T.5
Kasai, S.6
Chiba, T.7
Fujisawa, H.8
Kogishi, K.9
Kitado, H.10
Kimoto, M.11
Takeda, N.12
Matsushita, M.13
Okumura, H.14
Serikawa, T.15
Nakamura, T.16
Johnson, T.E.17
Hosokawa, M.18
-
132
-
-
33749531907
-
T-1213C polymorphism of estrogen receptor beta is associated with low bone mineral density and osteoporotic fractures
-
Kung A.W., Lai B.M., Ng M.Y., Chan V., and Sham P.C. T-1213C polymorphism of estrogen receptor beta is associated with low bone mineral density and osteoporotic fractures. Bone 39 (2006) 1097-1106
-
(2006)
Bone
, vol.39
, pp. 1097-1106
-
-
Kung, A.W.1
Lai, B.M.2
Ng, M.Y.3
Chan, V.4
Sham, P.C.5
-
133
-
-
27744506678
-
Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women
-
Ichikawa S., Koller D.L., Peacock M., Johnson M.L., Lai D., Hui S.L., Johnston C.C., Foroud T.M., and Econs M.J. Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women. J. Clin. Endocrinol. Metab. 90 (2005) 5921-5927
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, pp. 5921-5927
-
-
Ichikawa, S.1
Koller, D.L.2
Peacock, M.3
Johnson, M.L.4
Lai, D.5
Hui, S.L.6
Johnston, C.C.7
Foroud, T.M.8
Econs, M.J.9
-
134
-
-
38049175037
-
Effects of serum TSH and FT4 levels and the TSHR-Asp727Glu polymorphism on bone: the Rotterdam Study
-
van der Deure W.M., Uitterlinden A.G., Hofman A., Rivadeneira F., Pols H.A., Peeters R.P., and Visser T.J. Effects of serum TSH and FT4 levels and the TSHR-Asp727Glu polymorphism on bone: the Rotterdam Study. Clin. Endocrinol. (Oxf.) 68 (2008) 175-181
-
(2008)
Clin. Endocrinol. (Oxf.)
, vol.68
, pp. 175-181
-
-
van der Deure, W.M.1
Uitterlinden, A.G.2
Hofman, A.3
Rivadeneira, F.4
Pols, H.A.5
Peeters, R.P.6
Visser, T.J.7
-
135
-
-
10744226715
-
TSH is a negative regulator of skeletal remodeling
-
Abe E., Marians R.C., Yu W., Wu X.B., Ando T., Li Y., Iqbal J., Eldeiry L., Rajendren G., Blair H.C., Davies T.F., and Zaidi M. TSH is a negative regulator of skeletal remodeling. Cell 115 (2003) 151-162
-
(2003)
Cell
, vol.115
, pp. 151-162
-
-
Abe, E.1
Marians, R.C.2
Yu, W.3
Wu, X.B.4
Ando, T.5
Li, Y.6
Iqbal, J.7
Eldeiry, L.8
Rajendren, G.9
Blair, H.C.10
Davies, T.F.11
Zaidi, M.12
-
136
-
-
10744230206
-
Quantitative trait loci on chromosomes 2p, 4p, and 13q influence bone mineral density of the forearm and hip in Mexican Americans
-
Kammerer C.M., Schneider J.L., Cole S.A., Hixson J.E., Samollow P.B., O'Connell J.R., Perez R., Dyer T.D., Almasy L., Blangero J., Bauer R.L., and Mitchell B.D. Quantitative trait loci on chromosomes 2p, 4p, and 13q influence bone mineral density of the forearm and hip in Mexican Americans. J. Bone Miner. Res. 18 (2003) 2245-2252
-
(2003)
J. Bone Miner. Res.
, vol.18
, pp. 2245-2252
-
-
Kammerer, C.M.1
Schneider, J.L.2
Cole, S.A.3
Hixson, J.E.4
Samollow, P.B.5
O'Connell, J.R.6
Perez, R.7
Dyer, T.D.8
Almasy, L.9
Blangero, J.10
Bauer, R.L.11
Mitchell, B.D.12
-
137
-
-
20244363931
-
Loci for regulation of bone mineral density in men and women identified by genome wide linkage scan: the FAMOS study
-
Ralston S.H., Galwey N., MacKay I., Albagha O.M., Cardon L., Compston J.E., Cooper C., Duncan E., Keen R., Langdahl B., McLellan A., O'Riordan J., Pols H.A., Reid D.M., Uitterlinden A.G., Wass J., and Bennett S.T. Loci for regulation of bone mineral density in men and women identified by genome wide linkage scan: the FAMOS study. Hum. Mol. Genet. 14 (2005) 943-951
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 943-951
-
-
Ralston, S.H.1
Galwey, N.2
MacKay, I.3
Albagha, O.M.4
Cardon, L.5
Compston, J.E.6
Cooper, C.7
Duncan, E.8
Keen, R.9
Langdahl, B.10
McLellan, A.11
O'Riordan, J.12
Pols, H.A.13
Reid, D.M.14
Uitterlinden, A.G.15
Wass, J.16
Bennett, S.T.17
-
138
-
-
29044450387
-
Bone mineral density in men with genetic hemochromatosis and HFE gene mutation
-
Guggenbuhl P., Deugnier Y., Boisdet J.F., Rolland Y., Perdriger A., Pawlotsky Y., and Chales G. Bone mineral density in men with genetic hemochromatosis and HFE gene mutation. Osteoporos. Int. 16 (2005) 1809-1814
-
(2005)
Osteoporos. Int.
, vol.16
, pp. 1809-1814
-
-
Guggenbuhl, P.1
Deugnier, Y.2
Boisdet, J.F.3
Rolland, Y.4
Perdriger, A.5
Pawlotsky, Y.6
Chales, G.7
-
139
-
-
0036566575
-
Pallister-Hall syndrome phenotype in mice mutant for Gli3
-
Bose J., Grotewold L., and Ruther U. Pallister-Hall syndrome phenotype in mice mutant for Gli3. Hum. Mol. Genet. 11 (2002) 1129-1135
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 1129-1135
-
-
Bose, J.1
Grotewold, L.2
Ruther, U.3
-
140
-
-
35448993532
-
Family-based association study of ROR2 polymorphisms with an array of radiographic hand bone strength phenotypes
-
Ermakov S., Malkin I., Keter M., Kobyliansky E., and Livshits G. Family-based association study of ROR2 polymorphisms with an array of radiographic hand bone strength phenotypes. Osteoporos. Int. 18 (2007) 1683-1692
-
(2007)
Osteoporos. Int.
, vol.18
, pp. 1683-1692
-
-
Ermakov, S.1
Malkin, I.2
Keter, M.3
Kobyliansky, E.4
Livshits, G.5
-
141
-
-
33750301324
-
Wnt/beta-catenin signaling interacts differentially with Ihh signaling in controlling endochondral bone and synovial joint formation
-
Mak K.K., Chen M.H., Day T.F., Chuang P.T., and Yang Y. Wnt/beta-catenin signaling interacts differentially with Ihh signaling in controlling endochondral bone and synovial joint formation. Development 133 (2006) 3695-3707
-
(2006)
Development
, vol.133
, pp. 3695-3707
-
-
Mak, K.K.1
Chen, M.H.2
Day, T.F.3
Chuang, P.T.4
Yang, Y.5
-
142
-
-
29244488577
-
Variation in genes involved in the RANKL/RANK/OPG bone remodeling pathway are associated with bone mineral density at different skeletal sites in men
-
Hsu Y.H., Niu T., Terwedow H.A., Xu X., Feng Y., Li Z., Brain J.D., Rosen C.J., Laird N., and Xu X. Variation in genes involved in the RANKL/RANK/OPG bone remodeling pathway are associated with bone mineral density at different skeletal sites in men. Hum. Genet. 118 (2006) 568-577
-
(2006)
Hum. Genet.
, vol.118
, pp. 568-577
-
-
Hsu, Y.H.1
Niu, T.2
Terwedow, H.A.3
Xu, X.4
Feng, Y.5
Li, Z.6
Brain, J.D.7
Rosen, C.J.8
Laird, N.9
Xu, X.10
-
143
-
-
33748710617
-
Association of TNFSF11 gene promoter polymorphisms with bone mineral density in postmenopausal women
-
Mencej S., Prezelj J., Kocijancic A., Ostanek B., and Marc J. Association of TNFSF11 gene promoter polymorphisms with bone mineral density in postmenopausal women. Maturitas 55 (2006) 219-226
-
(2006)
Maturitas
, vol.55
, pp. 219-226
-
-
Mencej, S.1
Prezelj, J.2
Kocijancic, A.3
Ostanek, B.4
Marc, J.5
-
144
-
-
0037221067
-
Chondromodulin I is a bone remodeling factor
-
Nakamichi Y., Shukunami C., Yamada T., Aihara K., Kawano H., Sato T., Nishizaki Y., Yamamoto Y., Shindo M., Yoshimura K., Nakamura T., Takahashi N., Kawaguchi H., Hiraki Y., and Kato S. Chondromodulin I is a bone remodeling factor. Mol. Cell. Biol. 23 (2003) 636-644
-
(2003)
Mol. Cell. Biol.
, vol.23
, pp. 636-644
-
-
Nakamichi, Y.1
Shukunami, C.2
Yamada, T.3
Aihara, K.4
Kawano, H.5
Sato, T.6
Nishizaki, Y.7
Yamamoto, Y.8
Shindo, M.9
Yoshimura, K.10
Nakamura, T.11
Takahashi, N.12
Kawaguchi, H.13
Hiraki, Y.14
Kato, S.15
-
145
-
-
24144444524
-
Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency
-
Mohan S., Kapoor A., Singgih A., Zhang Z., Taylor T., Yu H., Chadwick R.B., Chung Y.S., Donahue L.R., Rosen C., Crawford G.C., Wergedal J., and Baylink D.J. Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency. J. Bone Miner. Res. 20 (2005) 1597-1610
-
(2005)
J. Bone Miner. Res.
, vol.20
, pp. 1597-1610
-
-
Mohan, S.1
Kapoor, A.2
Singgih, A.3
Zhang, Z.4
Taylor, T.5
Yu, H.6
Chadwick, R.B.7
Chung, Y.S.8
Donahue, L.R.9
Rosen, C.10
Crawford, G.C.11
Wergedal, J.12
Baylink, D.J.13
-
146
-
-
0034635966
-
Impaired endochondral ossification and angiogenesis in mice deficient in membrane-type matrix metalloproteinase I
-
Zhou Z., Apte S.S., Soininen R., Cao R., Baaklini G.Y., Rauser R.W., Wang J., Cao Y., and Tryggvason K. Impaired endochondral ossification and angiogenesis in mice deficient in membrane-type matrix metalloproteinase I. Proc. Natl Acad. Sci. U. S. A. 97 (2000) 4052-4057
-
(2000)
Proc. Natl Acad. Sci. U. S. A.
, vol.97
, pp. 4052-4057
-
-
Zhou, Z.1
Apte, S.S.2
Soininen, R.3
Cao, R.4
Baaklini, G.Y.5
Rauser, R.W.6
Wang, J.7
Cao, Y.8
Tryggvason, K.9
-
147
-
-
33846978104
-
Intraflagellar transport is essential for endochondral bone formation
-
Haycraft C.J., Zhang Q., Song B., Jackson W.S., Detloff P.J., Serra R., and Yoder B.K. Intraflagellar transport is essential for endochondral bone formation. Development 134 (2007) 307-316
-
(2007)
Development
, vol.134
, pp. 307-316
-
-
Haycraft, C.J.1
Zhang, Q.2
Song, B.3
Jackson, W.S.4
Detloff, P.J.5
Serra, R.6
Yoder, B.K.7
-
148
-
-
34347375328
-
Filamin B represses chondrocyte hypertrophy in a Runx2/Smad3-dependent manner
-
Zheng L., Baek H.J., Karsenty G., and Justice M.J. Filamin B represses chondrocyte hypertrophy in a Runx2/Smad3-dependent manner. J. Cell Biol. 178 (2007) 121-128
-
(2007)
J. Cell Biol.
, vol.178
, pp. 121-128
-
-
Zheng, L.1
Baek, H.J.2
Karsenty, G.3
Justice, M.J.4
-
149
-
-
0037633770
-
A thyrotoxic skeletal phenotype of advanced bone formation in mice with resistance to thyroid hormone
-
O'Shea P.J., Harvey C.B., Suzuki H., Kaneshige M., Kaneshige K., Cheng S.Y., and Williams G.R. A thyrotoxic skeletal phenotype of advanced bone formation in mice with resistance to thyroid hormone. Mol. Endocrinol. 17 (2003) 1410-1424
-
(2003)
Mol. Endocrinol.
, vol.17
, pp. 1410-1424
-
-
O'Shea, P.J.1
Harvey, C.B.2
Suzuki, H.3
Kaneshige, M.4
Kaneshige, K.5
Cheng, S.Y.6
Williams, G.R.7
-
150
-
-
0037609723
-
Mesenchymal progenitor self-renewal deficiency leads to age-dependent osteoporosis in Sca-1/Ly-6A null mice
-
Bonyadi M., Waldman S.D., Liu D., Aubin J.E., Grynpas M.D., and Stanford W.L. Mesenchymal progenitor self-renewal deficiency leads to age-dependent osteoporosis in Sca-1/Ly-6A null mice. Proc. Natl Acad. Sci. U. S. A. 100 (2003) 5840-5845
-
(2003)
Proc. Natl Acad. Sci. U. S. A.
, vol.100
, pp. 5840-5845
-
-
Bonyadi, M.1
Waldman, S.D.2
Liu, D.3
Aubin, J.E.4
Grynpas, M.D.5
Stanford, W.L.6
-
151
-
-
11144357428
-
ATF4 is a substrate of RSK2 and an essential regulator of osteoblast biology; implication for Coffin-Lowry Syndrome
-
Yang X., Matsuda K., Bialek P., Jacquot S., Masuoka H.C., Schinke T., Li L., Brancorsini S., Sassone-Corsi P., Townes T.M., Hanauer A., and Karsenty G. ATF4 is a substrate of RSK2 and an essential regulator of osteoblast biology; implication for Coffin-Lowry Syndrome. Cell 117 (2004) 387-398
-
(2004)
Cell
, vol.117
, pp. 387-398
-
-
Yang, X.1
Matsuda, K.2
Bialek, P.3
Jacquot, S.4
Masuoka, H.C.5
Schinke, T.6
Li, L.7
Brancorsini, S.8
Sassone-Corsi, P.9
Townes, T.M.10
Hanauer, A.11
Karsenty, G.12
-
152
-
-
33745219182
-
Long-lived growth hormone receptor knockout mice show a delay in age-related changes of body composition and bone characteristics
-
Bonkowski M.S., Pamenter R.W., Rocha J.S., Masternak M.M., Panici J.A., and Bartke A. Long-lived growth hormone receptor knockout mice show a delay in age-related changes of body composition and bone characteristics. J. Gerontol. A, Biol. Sci. Med. Sci. 61 (2006) 562-567
-
(2006)
J. Gerontol. A, Biol. Sci. Med. Sci.
, vol.61
, pp. 562-567
-
-
Bonkowski, M.S.1
Pamenter, R.W.2
Rocha, J.S.3
Masternak, M.M.4
Panici, J.A.5
Bartke, A.6
-
153
-
-
24344507232
-
A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis
-
Lemos M.C., Kotanko P., Christie P.T., Harding B., Javor T., Smith C., Eastell R., and Thakker R.V. A novel EXT1 splice site mutation in a kindred with hereditary multiple exostosis and osteoporosis. J. Clin. Endocrinol. Metab. 90 (2005) 5386-5392
-
(2005)
J. Clin. Endocrinol. Metab.
, vol.90
, pp. 5386-5392
-
-
Lemos, M.C.1
Kotanko, P.2
Christie, P.T.3
Harding, B.4
Javor, T.5
Smith, C.6
Eastell, R.7
Thakker, R.V.8
-
154
-
-
33644620327
-
TNFRSF11B gene variants and bone mineral density in postmenopausal women in Malta
-
Vidal C., Brincat M., and Xuereb Anastasi A. TNFRSF11B gene variants and bone mineral density in postmenopausal women in Malta. Maturitas 53 (2006) 386-395
-
(2006)
Maturitas
, vol.53
, pp. 386-395
-
-
Vidal, C.1
Brincat, M.2
Xuereb Anastasi, A.3
-
155
-
-
23744459835
-
DC-STAMP is essential for cell-cell fusion in osteoclasts and foreign body giant cells
-
Yagi M., Miyamoto T., Sawatani Y., Iwamoto K., Hosogane N., Fujita N., Morita K., Ninomiya K., Suzuki T., Miyamoto K., Oike Y., Takeya M., Toyama Y., and Suda T. DC-STAMP is essential for cell-cell fusion in osteoclasts and foreign body giant cells. J. Exp. Med. 202 (2005) 345-351
-
(2005)
J. Exp. Med.
, vol.202
, pp. 345-351
-
-
Yagi, M.1
Miyamoto, T.2
Sawatani, Y.3
Iwamoto, K.4
Hosogane, N.5
Fujita, N.6
Morita, K.7
Ninomiya, K.8
Suzuki, T.9
Miyamoto, K.10
Oike, Y.11
Takeya, M.12
Toyama, Y.13
Suda, T.14
-
156
-
-
0034647482
-
Role of the mouse ank gene in control of tissue calcification and arthritis
-
Ho A.M., Johnson M.D., and Kingsley D.M. Role of the mouse ank gene in control of tissue calcification and arthritis. Science 289 (2000) 265-270
-
(2000)
Science
, vol.289
, pp. 265-270
-
-
Ho, A.M.1
Johnson, M.D.2
Kingsley, D.M.3
-
157
-
-
19944433990
-
TIEG1 null mouse-derived osteoblasts are defective in mineralization and in support of osteoclast differentiation in vitro
-
Subramaniam M., Gorny G., Johnsen S.A., Monroe D.G., Evans G.L., Fraser D.G., Rickard D.J., Rasmussen K., van Deursen J.M., Turner R.T., Oursler M.J., and Spelsberg T.C. TIEG1 null mouse-derived osteoblasts are defective in mineralization and in support of osteoclast differentiation in vitro. Mol. Cell. Biol. 25 (2005) 1191-1199
-
(2005)
Mol. Cell. Biol.
, vol.25
, pp. 1191-1199
-
-
Subramaniam, M.1
Gorny, G.2
Johnsen, S.A.3
Monroe, D.G.4
Evans, G.L.5
Fraser, D.G.6
Rickard, D.J.7
Rasmussen, K.8
van Deursen, J.M.9
Turner, R.T.10
Oursler, M.J.11
Spelsberg, T.C.12
-
158
-
-
0030803396
-
Vitamin D-receptor gene polymorphisms and bone density in prepubertal American girls of Mexican descent
-
Sainz J., Van Tornout J.M., Loro M.L., Sayre J., Roe T.F., and Gilsanz V. Vitamin D-receptor gene polymorphisms and bone density in prepubertal American girls of Mexican descent. N. Engl. J. Med. 337 (1997) 77-82
-
(1997)
N. Engl. J. Med.
, vol.337
, pp. 77-82
-
-
Sainz, J.1
Van Tornout, J.M.2
Loro, M.L.3
Sayre, J.4
Roe, T.F.5
Gilsanz, V.6
-
159
-
-
34548008794
-
Association analysis of the polymorphisms of the VDR gene with bone mineral density and the occurrence of fractures
-
Horst-Sikorska W., Kalak R., Wawrzyniak A., Marcinkowska M., Celczynska-Bajew L., and Slomski R. Association analysis of the polymorphisms of the VDR gene with bone mineral density and the occurrence of fractures. J. Bone Miner. Metab. 25 (2007) 310-319
-
(2007)
J. Bone Miner. Metab.
, vol.25
, pp. 310-319
-
-
Horst-Sikorska, W.1
Kalak, R.2
Wawrzyniak, A.3
Marcinkowska, M.4
Celczynska-Bajew, L.5
Slomski, R.6
-
160
-
-
33747115419
-
The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis
-
Uitterlinden A.G., Ralston S.H., Brandi M.L., Carey A.H., Grinberg D., Langdahl B.L., Lips P., Lorenc R., Obermayer-Pietsch B., Reeve J., Reid D.M., Amedei A., Bassiti A., Bustamante M., Husted L.B., Diez-Perez A., Dobnig H., Dunning A.M., Enjuanes A., Fahrleitner-Pammer A., Fang Y., Karczmarewicz E., Kruk M., van Leeuwen J.P., Mavilia C., van Meurs J.B., Mangion J., McGuigan F.E., Pols H.A., Renner W., Rivadeneira F., van Schoor N.M., Scollen S., Sherlock R.E., and Ioannidis J.P. The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis. Ann. Intern. Med. 145 (2006) 255-264
-
(2006)
Ann. Intern. Med.
, vol.145
, pp. 255-264
-
-
Uitterlinden, A.G.1
Ralston, S.H.2
Brandi, M.L.3
Carey, A.H.4
Grinberg, D.5
Langdahl, B.L.6
Lips, P.7
Lorenc, R.8
Obermayer-Pietsch, B.9
Reeve, J.10
Reid, D.M.11
Amedei, A.12
Bassiti, A.13
Bustamante, M.14
Husted, L.B.15
Diez-Perez, A.16
Dobnig, H.17
Dunning, A.M.18
Enjuanes, A.19
Fahrleitner-Pammer, A.20
Fang, Y.21
Karczmarewicz, E.22
Kruk, M.23
van Leeuwen, J.P.24
Mavilia, C.25
van Meurs, J.B.26
Mangion, J.27
McGuigan, F.E.28
Pols, H.A.29
Renner, W.30
Rivadeneira, F.31
van Schoor, N.M.32
Scollen, S.33
Sherlock, R.E.34
Ioannidis, J.P.35
more..
-
161
-
-
0028080039
-
Bone mineral density in relation to polymorphism at the vitamin D receptor gene locus
-
Hustmyer F.G., Peacock M., Hui S., Johnston C.C., and Christian J. Bone mineral density in relation to polymorphism at the vitamin D receptor gene locus. J. Clin. Invest. 94 (1994) 2130-2134
-
(1994)
J. Clin. Invest.
, vol.94
, pp. 2130-2134
-
-
Hustmyer, F.G.1
Peacock, M.2
Hui, S.3
Johnston, C.C.4
Christian, J.5
-
162
-
-
38749086157
-
Wnt10b increases postnatal bone formation by enhancing osteoblast differentiation
-
Bennett C.N., Ouyang H., Ma Y.L., Zeng Q., Gerin I., Sousa K.M., Lane T.F., Krishnan V., Hankenson K.D., and MacDougald O.A. Wnt10b increases postnatal bone formation by enhancing osteoblast differentiation. J. Bone Miner. Res. 22 (2007) 1924-1932
-
(2007)
J. Bone Miner. Res.
, vol.22
, pp. 1924-1932
-
-
Bennett, C.N.1
Ouyang, H.2
Ma, Y.L.3
Zeng, Q.4
Gerin, I.5
Sousa, K.M.6
Lane, T.F.7
Krishnan, V.8
Hankenson, K.D.9
MacDougald, O.A.10
-
163
-
-
0033962445
-
Association of bone mineral density with polymorphism of the human calcium-sensing receptor locus
-
Tsukamoto K., Orimo H., Hosoi T., Miyao M., Ota N., Nakajima T., Yoshida H., Watanabe S., Suzuki T., and Emi M. Association of bone mineral density with polymorphism of the human calcium-sensing receptor locus. Calcif. Tissue Int. 66 (2000) 181-183
-
(2000)
Calcif. Tissue Int.
, vol.66
, pp. 181-183
-
-
Tsukamoto, K.1
Orimo, H.2
Hosoi, T.3
Miyao, M.4
Ota, N.5
Nakajima, T.6
Yoshida, H.7
Watanabe, S.8
Suzuki, T.9
Emi, M.10
-
164
-
-
34547687978
-
AHSG gene polymorphisms are associated with bone mineral density in Caucasian nuclear families
-
Yang Y.J., Wang Y.B., Lei S.F., Long J.R., Shen H., Zhao L.J., Jiang D.K., Xiao S.M., Chen X.D., Chen Y., and Deng H.W. AHSG gene polymorphisms are associated with bone mineral density in Caucasian nuclear families. Eur. J. Epidemiol. 22 (2007) 527-532
-
(2007)
Eur. J. Epidemiol.
, vol.22
, pp. 527-532
-
-
Yang, Y.J.1
Wang, Y.B.2
Lei, S.F.3
Long, J.R.4
Shen, H.5
Zhao, L.J.6
Jiang, D.K.7
Xiao, S.M.8
Chen, X.D.9
Chen, Y.10
Deng, H.W.11
-
165
-
-
0347379858
-
Osteocrin, a novel bone-specific secreted protein that modulates the osteoblast phenotype
-
Thomas G., Moffatt P., Salois P., Gaumond M.H., Gingras R., Godin E., Miao D., Goltzman D., and Lanctot C. Osteocrin, a novel bone-specific secreted protein that modulates the osteoblast phenotype. J. Biol. Chem. 278 (2003) 50563-50571
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 50563-50571
-
-
Thomas, G.1
Moffatt, P.2
Salois, P.3
Gaumond, M.H.4
Gingras, R.5
Godin, E.6
Miao, D.7
Goltzman, D.8
Lanctot, C.9
-
167
-
-
34548074165
-
Association between physical activity and BMD in young men is modulated by catechol-O-methyltransferase (COMT) genotype: the GOOD study
-
Lorentzon M., Eriksson A.L., Nilsson S., Mellstrom D., and Ohlsson C. Association between physical activity and BMD in young men is modulated by catechol-O-methyltransferase (COMT) genotype: the GOOD study. J. Bone Miner. Res. 22 (2007) 1165-1172
-
(2007)
J. Bone Miner. Res.
, vol.22
, pp. 1165-1172
-
-
Lorentzon, M.1
Eriksson, A.L.2
Nilsson, S.3
Mellstrom, D.4
Ohlsson, C.5
-
168
-
-
2942638110
-
Bone mineral density of the lumbar spine is associated with TNF gene polymorphisms in early postmenopausal Japanese women
-
Furuta I., Kobayashi N., Fujino T., Kobamatsu Y., Shirogane T., Yaegashi M., Sakuragi N., Cho K., Yamada H., Okuyama K., and Minakami H. Bone mineral density of the lumbar spine is associated with TNF gene polymorphisms in early postmenopausal Japanese women. Calcif. Tissue Int. 74 (2004) 509-515
-
(2004)
Calcif. Tissue Int.
, vol.74
, pp. 509-515
-
-
Furuta, I.1
Kobayashi, N.2
Fujino, T.3
Kobamatsu, Y.4
Shirogane, T.5
Yaegashi, M.6
Sakuragi, N.7
Cho, K.8
Yamada, H.9
Okuyama, K.10
Minakami, H.11
-
169
-
-
0036112495
-
TNF-alpha gene polymorphism and plasma TNF-alpha levels are related to lumbar spine bone area in healthy female Caucasian adolescents
-
Wennberg P., Nordstrom P., Lorentzon R., Lerner U.H., and Lorentzon M. TNF-alpha gene polymorphism and plasma TNF-alpha levels are related to lumbar spine bone area in healthy female Caucasian adolescents. Eur. J. Endocrinol. 146 (2002) 629-634
-
(2002)
Eur. J. Endocrinol.
, vol.146
, pp. 629-634
-
-
Wennberg, P.1
Nordstrom, P.2
Lorentzon, R.3
Lerner, U.H.4
Lorentzon, M.5
-
170
-
-
0035992658
-
Alleles of RUNX2/CBFA1 gene are associated with differences in bone mineral density and risk of fracture
-
Vaughan T., Pasco J.A., Kotowicz M.A., Nicholson G.C., and Morrison N.A. Alleles of RUNX2/CBFA1 gene are associated with differences in bone mineral density and risk of fracture. J. Bone Miner. Res. 17 (2002) 1527-1534
-
(2002)
J. Bone Miner. Res.
, vol.17
, pp. 1527-1534
-
-
Vaughan, T.1
Pasco, J.A.2
Kotowicz, M.A.3
Nicholson, G.C.4
Morrison, N.A.5
-
171
-
-
34848816852
-
Promoter 2 -1025 T/C polymorphism in the RUNX2 gene is associated with femoral neck bmd in Spanish postmenopausal women
-
Bustamante M., Nogues X., Agueda L., Jurado S., Wesselius A., Caceres E., Carreras R., Ciria M., Mellibovsky L., Balcells S., Diez-Perez A., and Grinberg D. Promoter 2 -1025 T/C polymorphism in the RUNX2 gene is associated with femoral neck bmd in Spanish postmenopausal women. Calcif. Tissue Int. 81 (2007) 327-332
-
(2007)
Calcif. Tissue Int.
, vol.81
, pp. 327-332
-
-
Bustamante, M.1
Nogues, X.2
Agueda, L.3
Jurado, S.4
Wesselius, A.5
Caceres, E.6
Carreras, R.7
Ciria, M.8
Mellibovsky, L.9
Balcells, S.10
Diez-Perez, A.11
Grinberg, D.12
-
172
-
-
27444437671
-
Polymorphisms of the CLCN7 gene are associated with BMD in women
-
Pettersson U., Albagha O.M., Mirolo M., Taranta A., Frattini A., McGuigan F.E., Vezzoni P., Teti A., van Hul W., Reid D.M., Villa A., and Ralston S.H. Polymorphisms of the CLCN7 gene are associated with BMD in women. J. Bone Miner. Res. 20 (2005) 1960-1967
-
(2005)
J. Bone Miner. Res.
, vol.20
, pp. 1960-1967
-
-
Pettersson, U.1
Albagha, O.M.2
Mirolo, M.3
Taranta, A.4
Frattini, A.5
McGuigan, F.E.6
Vezzoni, P.7
Teti, A.8
van Hul, W.9
Reid, D.M.10
Villa, A.11
Ralston, S.H.12
-
173
-
-
33645880137
-
Regulation of osteoclast function and bone mass by RAGE
-
Zhou Z., Immel D., Xi C.X., Bierhaus A., Feng X., Mei L., Nawroth P., Stern D.M., and Xiong W.C. Regulation of osteoclast function and bone mass by RAGE. J. Exp. Med. 203 (2006) 1067-1080
-
(2006)
J. Exp. Med.
, vol.203
, pp. 1067-1080
-
-
Zhou, Z.1
Immel, D.2
Xi, C.X.3
Bierhaus, A.4
Feng, X.5
Mei, L.6
Nawroth, P.7
Stern, D.M.8
Xiong, W.C.9
-
174
-
-
0035504102
-
Comparison of Pkd1-targeted mutants reveals that loss of polycystin-1 causes cystogenesis and bone defects
-
Lu W., Shen X., Pavlova A., Lakkis M., Ward C.J., Pritchard L., Harris P.C., Genest D.R., Perez-Atayde A.R., and Zhou J. Comparison of Pkd1-targeted mutants reveals that loss of polycystin-1 causes cystogenesis and bone defects. Hum. Mol. Genet. 10 (2001) 2385-2396
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2385-2396
-
-
Lu, W.1
Shen, X.2
Pavlova, A.3
Lakkis, M.4
Ward, C.J.5
Pritchard, L.6
Harris, P.C.7
Genest, D.R.8
Perez-Atayde, A.R.9
Zhou, J.10
-
175
-
-
0035085253
-
Discoidin domain receptor 1 tyrosine kinase has an essential role in mammary gland development
-
Vogel W.F., Aszodi A., Alves F., and Pawson T. Discoidin domain receptor 1 tyrosine kinase has an essential role in mammary gland development. Mol. Cell. Biol. 21 (2001) 2906-2917
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 2906-2917
-
-
Vogel, W.F.1
Aszodi, A.2
Alves, F.3
Pawson, T.4
-
176
-
-
34447519114
-
Smad4 is required for maintaining normal murine postnatal bone homeostasis
-
Tan X., Weng T., Zhang J., Wang J., Li W., Wan H., Lan Y., Cheng X., Hou N., Liu H., Ding J., Lin F., Yang R., Gao X., Chen D., and Yang X. Smad4 is required for maintaining normal murine postnatal bone homeostasis. J. Cell. Sci. 120 (2007) 2162-2170
-
(2007)
J. Cell. Sci.
, vol.120
, pp. 2162-2170
-
-
Tan, X.1
Weng, T.2
Zhang, J.3
Wang, J.4
Li, W.5
Wan, H.6
Lan, Y.7
Cheng, X.8
Hou, N.9
Liu, H.10
Ding, J.11
Lin, F.12
Yang, R.13
Gao, X.14
Chen, D.15
Yang, X.16
-
177
-
-
15544373018
-
Osteoclast deficiency results in disorganized matrix, reduced mineralization, and abnormal osteoblast behavior in developing bone
-
Dai X.M., Zong X.H., Akhter M.P., and Stanley E.R. Osteoclast deficiency results in disorganized matrix, reduced mineralization, and abnormal osteoblast behavior in developing bone. J. Bone Miner. Res. 19 (2004) 1441-1451
-
(2004)
J. Bone Miner. Res.
, vol.19
, pp. 1441-1451
-
-
Dai, X.M.1
Zong, X.H.2
Akhter, M.P.3
Stanley, E.R.4
-
178
-
-
15844384047
-
Leptin regulation of bone resorption by the sympathetic nervous system and CART
-
Elefteriou F., Ahn J.D., Takeda S., Starbuck M., Yang X., Liu X., Kondo H., Richards W.G., Bannon T.W., Noda M., Clement K., Vaisse C., and Karsenty G. Leptin regulation of bone resorption by the sympathetic nervous system and CART. Nature 434 (2005) 514-520
-
(2005)
Nature
, vol.434
, pp. 514-520
-
-
Elefteriou, F.1
Ahn, J.D.2
Takeda, S.3
Starbuck, M.4
Yang, X.5
Liu, X.6
Kondo, H.7
Richards, W.G.8
Bannon, T.W.9
Noda, M.10
Clement, K.11
Vaisse, C.12
Karsenty, G.13
-
179
-
-
20444423769
-
Association of polymorphisms in CYP17A1, MTP, and VLDLR with bone mineral density in community-dwelling Japanese women and men
-
Yamada Y., Ando F., and Shimokata H. Association of polymorphisms in CYP17A1, MTP, and VLDLR with bone mineral density in community-dwelling Japanese women and men. Genomics 86 (2005) 76-85
-
(2005)
Genomics
, vol.86
, pp. 76-85
-
-
Yamada, Y.1
Ando, F.2
Shimokata, H.3
-
180
-
-
0033537767
-
Abnormal morphogenesis but intact IKK activation in mice lacking the IKKalpha subunit of IkappaB kinase
-
Hu Y., Baud V., Delhase M., Zhang P., Deerinck T., Ellisman M., Johnson R., and Karin M. Abnormal morphogenesis but intact IKK activation in mice lacking the IKKalpha subunit of IkappaB kinase. Science 284 (1999) 316-320
-
(1999)
Science
, vol.284
, pp. 316-320
-
-
Hu, Y.1
Baud, V.2
Delhase, M.3
Zhang, P.4
Deerinck, T.5
Ellisman, M.6
Johnson, R.7
Karin, M.8
-
181
-
-
27744526420
-
Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22
-
Parsons C.A., Mroczkowski H.J., McGuigan F.E., Albagha O.M., Manolagas S., Reid D.M., Ralston S.H., and Shmookler Reis R.J. Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22. Hum. Mol. Genet. 14 (2005) 3141-3148
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3141-3148
-
-
Parsons, C.A.1
Mroczkowski, H.J.2
McGuigan, F.E.3
Albagha, O.M.4
Manolagas, S.5
Reid, D.M.6
Ralston, S.H.7
Shmookler Reis, R.J.8
-
182
-
-
34250026450
-
Farnesyl diphosphate synthase: a novel genotype association with bone mineral density in elderly women
-
Levy M.E., Parker R.A., Ferrell R.E., Zmuda J.M., and Greenspan S.L. Farnesyl diphosphate synthase: a novel genotype association with bone mineral density in elderly women. Maturitas 57 (2007) 247-252
-
(2007)
Maturitas
, vol.57
, pp. 247-252
-
-
Levy, M.E.1
Parker, R.A.2
Ferrell, R.E.3
Zmuda, J.M.4
Greenspan, S.L.5
-
183
-
-
0035043560
-
A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density
-
Ota N., Nakajima T., Nakazawa I., Suzuki T., Hosoi T., Orimo H., Inoue S., Shirai Y., and Emi M. A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density. J. Hum. Genet. 46 (2001) 267-272
-
(2001)
J. Hum. Genet.
, vol.46
, pp. 267-272
-
-
Ota, N.1
Nakajima, T.2
Nakazawa, I.3
Suzuki, T.4
Hosoi, T.5
Orimo, H.6
Inoue, S.7
Shirai, Y.8
Emi, M.9
-
184
-
-
0038647391
-
Association of interleukin-6 promoter variant with bone mineral density in pre-menopausal women
-
Chung H.W., Seo J.S., Hur S.E., Kim H.L., Kim J.Y., Jung J.H., Kim L.H., Park B.L., and Shin H.D. Association of interleukin-6 promoter variant with bone mineral density in pre-menopausal women. J. Hum. Genet. 48 (2003) 243-248
-
(2003)
J. Hum. Genet.
, vol.48
, pp. 243-248
-
-
Chung, H.W.1
Seo, J.S.2
Hur, S.E.3
Kim, H.L.4
Kim, J.Y.5
Jung, J.H.6
Kim, L.H.7
Park, B.L.8
Shin, H.D.9
-
185
-
-
0036785320
-
Klotho gene polymorphisms associated with bone density of aged postmenopausal women
-
Kawano K., Ogata N., Chiano M., Molloy H., Kleyn P., Spector T.D., Uchida M., Hosoi T., Suzuki T., Orimo H., Inoue S., Nabeshima Y., Nakamura K., Kuro-o M., and Kawaguchi H. Klotho gene polymorphisms associated with bone density of aged postmenopausal women. J. Bone Miner. Res. 17 (2002) 1744-1751
-
(2002)
J. Bone Miner. Res.
, vol.17
, pp. 1744-1751
-
-
Kawano, K.1
Ogata, N.2
Chiano, M.3
Molloy, H.4
Kleyn, P.5
Spector, T.D.6
Uchida, M.7
Hosoi, T.8
Suzuki, T.9
Orimo, H.10
Inoue, S.11
Nabeshima, Y.12
Nakamura, K.13
Kuro-o, M.14
Kawaguchi, H.15
-
186
-
-
12844263399
-
Association of polymorphisms of the androgen receptor and klotho genes with bone mineral density in Japanese women
-
Yamada Y., Ando F., Niino N., and Shimokata H. Association of polymorphisms of the androgen receptor and klotho genes with bone mineral density in Japanese women. J. Mol. Med. 83 (2005) 50-57
-
(2005)
J. Mol. Med.
, vol.83
, pp. 50-57
-
-
Yamada, Y.1
Ando, F.2
Niino, N.3
Shimokata, H.4
-
187
-
-
38449103748
-
Association of FLT3 polymorphisms with low BMD and risk of osteoporotic fracture in postmenopausal women
-
Koh J.M., Oh B., Lee J.Y., Lee J.K., Kimm K., Park B.L., Shin H.D., Lee I.K., Kim H.J., Hong J.M., Kim T.H., Kim G.S., Kim S.Y., and Park E.K. Association of FLT3 polymorphisms with low BMD and risk of osteoporotic fracture in postmenopausal women. J. Bone Miner. Res. 22 (2007) 1752-1758
-
(2007)
J. Bone Miner. Res.
, vol.22
, pp. 1752-1758
-
-
Koh, J.M.1
Oh, B.2
Lee, J.Y.3
Lee, J.K.4
Kimm, K.5
Park, B.L.6
Shin, H.D.7
Lee, I.K.8
Kim, H.J.9
Hong, J.M.10
Kim, T.H.11
Kim, G.S.12
Kim, S.Y.13
Park, E.K.14
-
188
-
-
22744444441
-
Association of the OSCAR promoter polymorphism with BMD in postmenopausal women
-
Kim G.S., Koh J.M., Chang J.S., Park B.L., Kim L.H., Park E.K., Kim S.Y., and Shin H.D. Association of the OSCAR promoter polymorphism with BMD in postmenopausal women. J. Bone Miner. Res. 20 (2005) 1342-1348
-
(2005)
J. Bone Miner. Res.
, vol.20
, pp. 1342-1348
-
-
Kim, G.S.1
Koh, J.M.2
Chang, J.S.3
Park, B.L.4
Kim, L.H.5
Park, E.K.6
Kim, S.Y.7
Shin, H.D.8
-
189
-
-
0348049687
-
Association of a polymorphism of the dopamine receptor D4 gene with bone mineral density in Japanese men
-
Yamada Y., Ando F., Niino N., and Shimokata H. Association of a polymorphism of the dopamine receptor D4 gene with bone mineral density in Japanese men. J. Hum. Genet. 48 (2003) 629-633
-
(2003)
J. Hum. Genet.
, vol.48
, pp. 629-633
-
-
Yamada, Y.1
Ando, F.2
Niino, N.3
Shimokata, H.4
-
190
-
-
33646119424
-
A new SNP in a negative regulatory region of the CYP19A1 gene is associated with lumbar spine BMD in postmenopausal women
-
Enjuanes A., Garcia-Giralt N., Supervia A., Nogues X., Ruiz-Gaspa S., Bustamante M., Mellibovsky L., Grinberg D., Balcells S., and Diez-Perez A. A new SNP in a negative regulatory region of the CYP19A1 gene is associated with lumbar spine BMD in postmenopausal women. Bone 38 (2006) 738-743
-
(2006)
Bone
, vol.38
, pp. 738-743
-
-
Enjuanes, A.1
Garcia-Giralt, N.2
Supervia, A.3
Nogues, X.4
Ruiz-Gaspa, S.5
Bustamante, M.6
Mellibovsky, L.7
Grinberg, D.8
Balcells, S.9
Diez-Perez, A.10
-
191
-
-
34147128192
-
CYP19A1 polymorphisms are associated with bone mineral density in Chinese men
-
Hong X., Hsu Y.H., Terwedow H., Arguelles L.M., Tang G., Liu X., Zhang S., Xu X., and Xu X. CYP19A1 polymorphisms are associated with bone mineral density in Chinese men. Hum. Genet. 121 (2007) 491-500
-
(2007)
Hum. Genet.
, vol.121
, pp. 491-500
-
-
Hong, X.1
Hsu, Y.H.2
Terwedow, H.3
Arguelles, L.M.4
Tang, G.5
Liu, X.6
Zhang, S.7
Xu, X.8
Xu, X.9
-
192
-
-
0036287198
-
Association of a polymorphism of the CC chemokine receptor-2 gene with bone mineral density
-
Yamada Y., Ando F., Niino N., and Shimokata H. Association of a polymorphism of the CC chemokine receptor-2 gene with bone mineral density. Genomics 80 (2002) 8-12
-
(2002)
Genomics
, vol.80
, pp. 8-12
-
-
Yamada, Y.1
Ando, F.2
Niino, N.3
Shimokata, H.4
-
193
-
-
0034641607
-
Evidence of a linkage disequilibrium between polymorphisms in the human estrogen receptor alpha gene and their relationship to bone mass variation in postmenopausal Italian women
-
Becherini L., Gennari L., Masi L., Mansani R., Massart F., Morelli A., Falchetti A., Gonnelli S., Fiorelli G., Tanini A., and Brandi M.L. Evidence of a linkage disequilibrium between polymorphisms in the human estrogen receptor alpha gene and their relationship to bone mass variation in postmenopausal Italian women. Hum. Mol. Genet. 9 (2000) 2043-2050
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2043-2050
-
-
Becherini, L.1
Gennari, L.2
Masi, L.3
Mansani, R.4
Massart, F.5
Morelli, A.6
Falchetti, A.7
Gonnelli, S.8
Fiorelli, G.9
Tanini, A.10
Brandi, M.L.11
-
194
-
-
0041808714
-
Association of 5′ estrogen receptor alpha gene polymorphisms with bone mineral density, vertebral bone area and fracture risk
-
van Meurs J.B., Schuit S.C., Weel A.E., van der Klift M., Bergink A.P., Arp P.P., Colin E.M., Fang Y., Hofman A., van Duijn C.M., van Leeuwen J.P., Pols H.A., and Uitterlinden A.G. Association of 5′ estrogen receptor alpha gene polymorphisms with bone mineral density, vertebral bone area and fracture risk. Hum. Mol. Genet. 12 (2003) 1745-1754
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 1745-1754
-
-
van Meurs, J.B.1
Schuit, S.C.2
Weel, A.E.3
van der Klift, M.4
Bergink, A.P.5
Arp, P.P.6
Colin, E.M.7
Fang, Y.8
Hofman, A.9
van Duijn, C.M.10
van Leeuwen, J.P.11
Pols, H.A.12
Uitterlinden, A.G.13
-
195
-
-
47249126240
-
Estrogen receptor alpha CA dinucleotide repeat polymorphism is associated with rate of bone loss in perimenopausal women and bone mineral density and risk of osteoporotic fractures in postmenopausal women
-
Lai B.M., Cheung C.L., Luk K.D., and Kung A.W. Estrogen receptor alpha CA dinucleotide repeat polymorphism is associated with rate of bone loss in perimenopausal women and bone mineral density and risk of osteoporotic fractures in postmenopausal women. Osteoporos. Int. 19 (2008) 571-579
-
(2008)
Osteoporos. Int.
, vol.19
, pp. 571-579
-
-
Lai, B.M.1
Cheung, C.L.2
Luk, K.D.3
Kung, A.W.4
-
196
-
-
36248987334
-
Polymorphisms and haplotypes of integrinalpha1 (ITGA1) are associated with bone mineral density and fracture risk in postmenopausal Koreans
-
Lee H.J., Kim S.Y., Koh J.M., Bok J., Kim K.J., Kim K.S., Park M.H., Shin H.D., Park B.L., Kim T.H., Hong J.M., Park E.K., Kim D.J., Oh B., Kimm K., Kim G.S., and Lee J.Y. Polymorphisms and haplotypes of integrinalpha1 (ITGA1) are associated with bone mineral density and fracture risk in postmenopausal Koreans. Bone 41 (2007) 979-986
-
(2007)
Bone
, vol.41
, pp. 979-986
-
-
Lee, H.J.1
Kim, S.Y.2
Koh, J.M.3
Bok, J.4
Kim, K.J.5
Kim, K.S.6
Park, M.H.7
Shin, H.D.8
Park, B.L.9
Kim, T.H.10
Hong, J.M.11
Park, E.K.12
Kim, D.J.13
Oh, B.14
Kimm, K.15
Kim, G.S.16
Lee, J.Y.17
-
197
-
-
15544370499
-
Bone mass effects of a BMP4 gene polymorphism in postmenopausal women
-
Ramesh Babu L., Wilson S.G., Dick I.M., Islam F.M., Devine A., and Prince R.L. Bone mass effects of a BMP4 gene polymorphism in postmenopausal women. Bone 36 (2005) 555-561
-
(2005)
Bone
, vol.36
, pp. 555-561
-
-
Ramesh Babu, L.1
Wilson, S.G.2
Dick, I.M.3
Islam, F.M.4
Devine, A.5
Prince, R.L.6
-
198
-
-
16644383500
-
Association of multiple nucleotide variations in the pituitary glutaminyl cyclase gene (QPCT) with low radial BMD in adult women
-
Ezura Y., Kajita M., Ishida R., Yoshida S., Yoshida H., Suzuki T., Hosoi T., Inoue S., Shiraki M., Orimo H., and Emi M. Association of multiple nucleotide variations in the pituitary glutaminyl cyclase gene (QPCT) with low radial BMD in adult women. J. Bone Miner. Res. 19 (2004) 1296-1301
-
(2004)
J. Bone Miner. Res.
, vol.19
, pp. 1296-1301
-
-
Ezura, Y.1
Kajita, M.2
Ishida, R.3
Yoshida, S.4
Yoshida, H.5
Suzuki, T.6
Hosoi, T.7
Inoue, S.8
Shiraki, M.9
Orimo, H.10
Emi, M.11
-
199
-
-
0032910962
-
A genome-wide scan for loci linked to forearm bone mineral density
-
Niu T., Chen C., Cordell H., Yang J., Wang B., Wang Z., Fang Z., Schork N.J., Rosen C.J., and Xu X. A genome-wide scan for loci linked to forearm bone mineral density. Hum. Genet. 104 (1999) 226-233
-
(1999)
Hum. Genet.
, vol.104
, pp. 226-233
-
-
Niu, T.1
Chen, C.2
Cordell, H.3
Yang, J.4
Wang, B.5
Wang, Z.6
Fang, Z.7
Schork, N.J.8
Rosen, C.J.9
Xu, X.10
-
200
-
-
13144252230
-
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q
-
Devoto M., Shimoya K., Caminis J., Ott J., Tenenhouse A., Whyte M.P., Sereda L., Hall S., Considine E., Williams C.J., Tromp G., Kuivaniemi H., Ala-Kokko L., Prockop D.J., and Spotila L.D. First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q. Eur. J. Hum. Genet. 6 (1998) 151-157
-
(1998)
Eur. J. Hum. Genet.
, vol.6
, pp. 151-157
-
-
Devoto, M.1
Shimoya, K.2
Caminis, J.3
Ott, J.4
Tenenhouse, A.5
Whyte, M.P.6
Sereda, L.7
Hall, S.8
Considine, E.9
Williams, C.J.10
Tromp, G.11
Kuivaniemi, H.12
Ala-Kokko, L.13
Prockop, D.J.14
Spotila, L.D.15
-
201
-
-
12144287023
-
LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density
-
Mizuguchi T., Furuta I., Watanabe Y., Tsukamoto K., Tomita H., Tsujihata M., Ohta T., Kishino T., Matsumoto N., Minakami H., Niikawa N., and Yoshiura K. LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density. J. Hum. Genet. 49 (2004) 80-86
-
(2004)
J. Hum. Genet.
, vol.49
, pp. 80-86
-
-
Mizuguchi, T.1
Furuta, I.2
Watanabe, Y.3
Tsukamoto, K.4
Tomita, H.5
Tsujihata, M.6
Ohta, T.7
Kishino, T.8
Matsumoto, N.9
Minakami, H.10
Niikawa, N.11
Yoshiura, K.12
-
202
-
-
14844298409
-
Influence of LRP5 polymorphisms on normal variation in BMD
-
Koay M.A., Woon P.Y., Zhang Y., Miles L.J., Duncan E.L., Ralston S.H., Compston J.E., Cooper C., Keen R., Langdahl B.L., MacLelland A., O'Riordan J., Pols H.A., Reid D.M., Uitterlinden A.G., Wass J.A., and Brown M.A. Influence of LRP5 polymorphisms on normal variation in BMD. J. Bone Miner. Res. 19 (2004) 1619-1627
-
(2004)
J. Bone Miner. Res.
, vol.19
, pp. 1619-1627
-
-
Koay, M.A.1
Woon, P.Y.2
Zhang, Y.3
Miles, L.J.4
Duncan, E.L.5
Ralston, S.H.6
Compston, J.E.7
Cooper, C.8
Keen, R.9
Langdahl, B.L.10
MacLelland, A.11
O'Riordan, J.12
Pols, H.A.13
Reid, D.M.14
Uitterlinden, A.G.15
Wass, J.A.16
Brown, M.A.17
-
203
-
-
34047262543
-
LRP5 coding polymorphisms influence the variation of peak bone mass in a normal population of French-Canadian women
-
Giroux S., Elfassihi L., Cardinal G., Laflamme N., and Rousseau F. LRP5 coding polymorphisms influence the variation of peak bone mass in a normal population of French-Canadian women. Bone 40 (2007) 1299-1307
-
(2007)
Bone
, vol.40
, pp. 1299-1307
-
-
Giroux, S.1
Elfassihi, L.2
Cardinal, G.3
Laflamme, N.4
Rousseau, F.5
-
204
-
-
33847720301
-
Association of a single-nucleotide variation (A1330V) in the low-density lipoprotein receptor-related protein 5 gene (LRP5) with bone mineral density in adult Japanese women
-
Ezura Y., Nakajima T., Urano T., Sudo Y., Kajita M., Yoshida H., Suzuki T., Hosoi T., Inoue S., Shiraki M., and Emi M. Association of a single-nucleotide variation (A1330V) in the low-density lipoprotein receptor-related protein 5 gene (LRP5) with bone mineral density in adult Japanese women. Bone 40 (2007) 997-1005
-
(2007)
Bone
, vol.40
, pp. 997-1005
-
-
Ezura, Y.1
Nakajima, T.2
Urano, T.3
Sudo, Y.4
Kajita, M.5
Yoshida, H.6
Suzuki, T.7
Hosoi, T.8
Inoue, S.9
Shiraki, M.10
Emi, M.11
-
205
-
-
0842283935
-
Association between a polymorphism affecting an AP1 binding site in the promoter of the TCIRG1 gene and bone mass in women
-
Sobacchi C., Vezzoni P., Reid D.M., McGuigan F.E., Frattini A., Mirolo M., Albhaga O.M., Musio A., Villa A., and Ralston S.H. Association between a polymorphism affecting an AP1 binding site in the promoter of the TCIRG1 gene and bone mass in women. Calcif. Tissue Int. 74 (2004) 35-41
-
(2004)
Calcif. Tissue Int.
, vol.74
, pp. 35-41
-
-
Sobacchi, C.1
Vezzoni, P.2
Reid, D.M.3
McGuigan, F.E.4
Frattini, A.5
Mirolo, M.6
Albhaga, O.M.7
Musio, A.8
Villa, A.9
Ralston, S.H.10
-
206
-
-
19044398852
-
A frequent regulatory variant of the estrogen-related receptor alpha gene associated with BMD in French-Canadian premenopausal women
-
Laflamme N., Giroux S., Loredo-Osti J.C., Elfassihi L., Dodin S., Blanchet C., Morgan K., Giguere V., and Rousseau F. A frequent regulatory variant of the estrogen-related receptor alpha gene associated with BMD in French-Canadian premenopausal women. J. Bone Miner. Res. 20 (2005) 938-944
-
(2005)
J. Bone Miner. Res.
, vol.20
, pp. 938-944
-
-
Laflamme, N.1
Giroux, S.2
Loredo-Osti, J.C.3
Elfassihi, L.4
Dodin, S.5
Blanchet, C.6
Morgan, K.7
Giguere, V.8
Rousseau, F.9
-
207
-
-
0037369088
-
Association of a haplotype (196Phe/532Ser) in the interleukin-1-receptor-associated kinase (IRAK1) gene with low radial bone mineral density in two independent populations
-
Ishida R., Emi M., Ezura Y., Iwasaki H., Yoshida H., Suzuki T., Hosoi T., Inoue S., Shiraki M., Ito H., and Orimo H. Association of a haplotype (196Phe/532Ser) in the interleukin-1-receptor-associated kinase (IRAK1) gene with low radial bone mineral density in two independent populations. J. Bone Miner. Res. 18 (2003) 419-423
-
(2003)
J. Bone Miner. Res.
, vol.18
, pp. 419-423
-
-
Ishida, R.1
Emi, M.2
Ezura, Y.3
Iwasaki, H.4
Yoshida, H.5
Suzuki, T.6
Hosoi, T.7
Inoue, S.8
Shiraki, M.9
Ito, H.10
Orimo, H.11
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