-
1
-
-
18044386744
-
LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development
-
DOI 10.1016/S0092-8674(01)00571-2
-
Gong Y, Slee RB, Fukai N, Rawadi G, Roman-Roman S, Reginato AM, Wang H, Cundy T, Glorieux FH, Lev D, Zacharin M, Oexle K, Marcelino J, Suwairi W, Heeger S, Sabatakos G, Apte S, Adkins WN, Allgrove J, Arslan-Kirchner M, Batch JA, Beighton P, Black GC, Boles RG, Boon LM, Borrone C, Brunner HG, Carle GF, Dallapiccola B, De Paepe A, Floege B, Halfhide ML, Hall B, Hennekam RC, Hirose T, Jans A, Juppner H, Kim CA, Keppler-Noreuil K, Kohlschuetter A, LaCombe D, Lambert M, Lemyre E, Letteboer T, Peltonen L, Ramesar RS, Romanengo M, Somer H, Steichen-Gersdorf E, Steinmann B, Sullivan B, Superti-Furga A, Swoboda W, van den Boogaard MJ, Van Hul W, Vikkula M, Votruba M, Zabel B, Garcia T, Baron R, Olsen BR, Warman ML,. LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development. Cell. 2001; 107 (4): 513-23. (Pubitemid 33152786)
-
(2001)
Cell
, vol.107
, Issue.4
, pp. 513-523
-
-
Gong, Y.1
Slee, R.B.2
Fukai, N.3
Rawadi, G.4
Roman-Roman, S.5
Reginato, A.M.6
Wang, H.7
Cundy, T.8
Glorieux, F.H.9
Lev, D.10
Zacharin, M.11
Oexle, K.12
Marcelino, J.13
Suwairi, W.14
Heeger, S.15
Sabatakos, G.16
Apte, S.17
Adkins, W.N.18
Allgrove, J.19
Arslan-Kirchner, M.20
Batch, J.A.21
Beighton, P.22
Black, G.C.M.23
Boles, R.G.24
Boon, L.M.25
Borrone, C.26
Brunner, H.G.27
Carle, G.F.28
Dallapiccola, B.29
De Paepe, A.30
Floege, B.31
Halfhide, M.L.32
Hall, B.33
Hennekam, R.C.34
Hirose, T.35
Jans, A.36
Juppner, H.37
Kim, C.A.38
Keppler-Noreuil, K.39
Kohlschuetter, A.40
LaCombe, D.41
Lambert, M.42
Lemyre, E.43
Letteboer, T.44
Peltonen, L.45
Ramesar, R.S.46
Romanengo, M.47
Somer, H.48
Steichen-Gersdorf, E.49
Steinmann, B.50
Sullivan, B.51
Superti-Furga, A.52
Swoboda, W.53
Van Den Boogaard, M.-J.54
Van Hul, W.55
Vikkula, M.56
Votruba, M.57
Zabel, B.58
Garcia, T.59
Baron, R.60
Olsen, B.R.61
Warman, M.L.62
more..
-
2
-
-
0036138175
-
A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait
-
DOI 10.1086/338450
-
Little RD, Carulli JP, Del Mastro RG, Dupuis J, Osborne M, Folz C, Manning SP, Swain PM, Zhao SC, Eustace B, Lappe MM, Spitzer L, Zweier S, Braunschweiger K, Benchekroun Y, Hu X, Adair R, Chee L, FitzGerald MG, Tulig C, Caruso A, Tzellas N, Bawa A, Franklin B, McGuire S, Nogues X, Gong G, Allen KM, Anisowicz A, Morales AJ, Lomedico PT, Recker SM, Van Eerdewegh P, Recker RR, Johnson ML,. A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait. Am J Hum Genet. 2002; 70 (1): 11-9. (Pubitemid 34031693)
-
(2002)
American Journal of Human Genetics
, vol.70
, Issue.1
, pp. 11-19
-
-
Little, R.D.1
Carulli, J.P.2
Del Mastro, R.G.3
Dupuis, J.4
Osborne, M.5
Folz, C.6
Manning, S.P.7
Swain, P.M.8
Zhao, S.C.9
Eustace, B.10
Lappe, M.M.11
Spitzer, L.12
Zweier, S.13
Braunschweiger, K.14
Benchekroun, Y.15
Hu, X.16
Adair, R.17
Chee, L.18
Fitzgerald, M.G.19
Tulig, C.20
Caruso, A.21
Tzellas, N.22
Bawa, A.23
Franklin, B.24
McGuire, S.25
Nogues, X.26
Gong, G.27
Allen, K.M.28
Anisowicz, A.29
Morales, A.J.30
Lomedico, P.T.31
Recker, S.M.32
Van Eerdewegh, P.33
Recker, R.R.34
Johnson, M.L.35
more..
-
3
-
-
0035999445
-
Localization of the gene causing autosomal dominant osteopetrosis type I to chromosome 11q12-13
-
Van Hul E, Gram J, Bollerslev J, Van Wesenbeeck L, Mathysen D, Andersen PE, Vanhoenacker F, Van Hul W,. Localization of the gene causing autosomal dominant osteopetrosis type I to chromosome 11q12-13. J Bone Miner Res. 2002; 17 (6): 1111-7. (Pubitemid 34535150)
-
(2002)
Journal of Bone and Mineral Research
, vol.17
, Issue.6
, pp. 1111-1117
-
-
Van Hul, E.1
Gram, J.2
Bollerslev, J.3
Van Wesenbeeck, L.4
Mathysen, D.5
Andersen, P.E.6
Vanhoenacker, F.7
Van Hul, W.8
-
4
-
-
17844391255
-
Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda
-
DOI 10.1210/jc.86.7.3233
-
Christie PT, Curley A, Nesbit MA, Chapman C, Genet S, Harper PS, Keeling SL, Wilkie AO, Winter RM, Thakker RV,. Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda. J Clin Endocrinol Metab. 2001; 86 (7): 3233-6. (Pubitemid 32673493)
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, Issue.7
, pp. 3233-3236
-
-
Christie, P.T.1
Curley, A.2
Nesbit, M.A.3
Chapman, C.4
Genet, S.5
Harper, P.S.6
Keeling, S.L.7
Wilkie, A.O.M.8
Winter, R.M.9
Thakker, R.V.10
-
5
-
-
26444528459
-
MO)
-
DOI 10.1172/JCI22900
-
Kennedy AM, Inada M, Krane SM, Christie PT, Harding B, Lopez-Otin C, Sanchez LM, Pannett AA, Dearlove A, Hartley C, Byrne MH, Reed AA, Nesbit MA, Whyte MP, Thakker RV,. MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO). J Clin Invest. 2005; 115 (10): 2832-42. (Pubitemid 41434410)
-
(2005)
Journal of Clinical Investigation
, vol.115
, Issue.10
, pp. 2832-2842
-
-
Kennedy, A.M.1
Inada, M.2
Krane, S.M.3
Christie, P.T.4
Harding, B.5
Lopez-Otin, C.6
Sanchez, L.M.7
Pannett, A.A.J.8
Dearlove, A.9
Hartley, C.10
Byrne, M.H.11
Reed, A.A.C.12
Nesbit, M.A.13
Whyte, M.P.14
Thakker, R.V.15
-
6
-
-
0033837092
-
The genetics of osteoporosis: Future diagnostic possibilities
-
Brown MA, Eisman JA,. The genetics of osteoporosis. Future diagnostic possibilities. Clin Lab Med. 2000; 20 (3): 527-47, vi-vii. (Pubitemid 30657510)
-
(2000)
Clinics in Laboratory Medicine
, vol.20
, Issue.3
, pp. 527-547
-
-
Brown, M.A.1
Eisman, J.A.2
-
7
-
-
84889301733
-
Assessment of bone mass and microarchitecture in rodents
-
Rosen C.J. editor. 7th ed. Washington, DC: American Society for Bone and Mineral Research
-
Blaine A, Christiansen, Bouxsein ML,. Assessment of bone mass and microarchitecture in rodents. In:, Rosen CJ, editor. Primer on the metabolic bone diseases and disorders of mineral metabolism, 7th ed. Washington, DC: American Society for Bone and Mineral Research; 2008. p. 38-45.
-
(2008)
Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism
, pp. 38-45
-
-
Blaine, A.1
Christiansen2
Bouxsein, M.L.3
-
8
-
-
84863399069
-
Animal models: Genetic manipulation
-
Rosen C.J. editor. 7th ed. Washington, DC: American Society for Bone and Mineral Research
-
Lyons K,. Animal models: genetic manipulation. In:, Rosen CJ, editor. Primer on the metabolic bone diseases and disorders of mineral metabolism, 7th ed. Washington, DC: American Society for Bone and Mineral Research; 2008. p. 45-51.
-
(2008)
Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism
, pp. 45-51
-
-
Lyons, K.1
-
9
-
-
84889366871
-
Animal models: Allelic determinants for BMD
-
Rosen C.J. editor. 7th ed. Washington, DC: American Society for Bone and Mineral Research
-
Wesley G, Beamer CJR,. Animal models: allelic determinants for BMD. In:, Rosen CJ, editor. Primer on the metabolic bone diseases and disorders of mineral metabolism, 7th ed. Washington, DC: American Society for Bone and Mineral Research; 2008. p. 51-6.
-
(2008)
Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism
, pp. 51-56
-
-
Wesley, G.1
Beamer, C.J.R.2
-
10
-
-
0024543742
-
Induction of specific locus mutations in mouse spermatogonial stem cells by combined chemical X-ray treatments
-
Cattanach BM, Peters J, Rasberry C,. Induction of specific locus mutations in mouse spermatogonial stem cells by combined chemical X-ray treatments. Mutat Res. 1989; 212 (1): 91-101. (Pubitemid 19116810)
-
(1989)
Mutation Research
, vol.212
, Issue.1
, pp. 91-101
-
-
Cattanach, B.M.1
Peters, J.2
Rasberry, C.3
-
11
-
-
0034425410
-
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse
-
DOI 10.1038/78140
-
Nolan PM, Peters J, Strivens M, Rogers D, Hagan J, Spurr N, Gray IC, Vizor L, Brooker D, Whitehill E, Washbourne R, Hough T, Greenaway S, Hewitt M, Liu X, McCormack S, Pickford K, Selley R, Wells C, Tymowska-Lalanne Z, Roby P, Glenister P, Thornton C, Thaung C, Stevenson JA, Arkell R, Mburu P, Hardisty R, Kiernan A, Erven A, Steel KP, Voegeling S, Guenet JL, Nickols C, Sadri R, Nasse M, Isaacs A, Davies K, Browne M, Fisher EM, Martin J, Rastan S, Brown SD, Hunter J,. A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse. Nat Genet. 2000; 25 (4): 440-3. (Pubitemid 32983439)
-
(2000)
Nature Genetics
, vol.25
, Issue.4
, pp. 440-443
-
-
Nolan, P.M.1
Peters, J.2
Strivens, M.3
Rogers, D.4
Hagan, J.5
Spurr, N.6
Gray, I.C.7
Vizor, L.8
Brooker, D.9
Whitehill, E.10
Washbourne, R.11
Hough, T.12
Greenaway, S.13
Hewitt, M.14
Liu, X.15
McCormack, S.16
Pickford, K.17
Selley, R.18
Wells, C.19
Tymowska-Lalanne, Z.20
Roby, P.21
Glenister, P.22
Thornton, C.23
Thaung, C.24
Stevenson, J.-A.25
Arkell, R.26
Mburu, P.27
Hardisty, R.28
Kiernan, A.29
Erven, A.30
Steel, K.P.31
Voegeling, S.32
Guenet, J.-L.33
Nickols, C.34
Sadri, R.35
Naase, M.36
Isaacs, A.37
Davies, K.38
Browne, M.39
Fisher, E.M.C.40
Martin, J.41
Rastan, S.42
Brown, S.D.M.43
Hunter, J.44
more..
-
12
-
-
0033860151
-
Implementation of a large-scale ENU mutagenesis program: Towards increasing the mouse mutant resource
-
DOI 10.1007/s003350010096
-
Nolan PM, Peters J, Vizor L, Strivens M, Washbourne R, Hough T, Wells C, Glenister P, Thornton C, Martin J, Fisher E, Rogers D, Hagan J, Reavill C, Gray I, Wood J, Spurr N, Browne M, Rastan S, Hunter J, Brown SD,. Implementation of a large-scale ENU mutagenesis program: towards increasing the mouse mutant resource. Mamm Genome. 2000; 11 (7): 500-6. (Pubitemid 30602213)
-
(2000)
Mammalian Genome
, vol.11
, Issue.7
, pp. 500-506
-
-
Nolan, P.M.1
Peters, J.2
Vizor, L.3
Strivens, M.4
Washbourne, R.5
Hough, T.6
Wells, C.7
Glenister, P.8
Thornton, C.9
Martin, J.10
Fisher, E.11
Rogers, D.12
Hagan, J.13
Reavill, C.14
Gray, I.15
Wood, J.16
Spurr, N.17
Browne, M.18
Rastan, S.19
Hunter, J.20
Brown, S.D.M.21
more..
-
13
-
-
40149105883
-
An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda
-
DOI 10.1152/physiolgenomics.00116.2007
-
Barbaric I, Perry MJ, Dear TN, Rodrigues Da Costa A, Salopek D, Marusic A, Hough T, Wells S, Hunter AJ, Cheeseman M, Brown SD,. An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda. Physiol Genomics. 2008; 32 (3): 311-21. (Pubitemid 351328554)
-
(2008)
Physiological Genomics
, vol.32
, Issue.3
, pp. 311-321
-
-
Barbaric, I.1
Perry, M.J.2
Dear, T.N.3
Da Costa, A.R.4
Salopek, D.5
Marusic, A.6
Hough, T.7
Wells, S.8
Hunter, A.J.9
Cheeseman, M.10
Brown, S.D.M.11
-
14
-
-
36048995717
-
Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2
-
DOI 10.1359/jbmr.070515
-
Hough TA, Polewski M, Johnson K, Cheeseman M, Nolan PM, Vizor L, Rastan S, Boyde A, Pritzker K, Hunter AJ, Fisher EM, Terkeltaub R, Brown SD,. Novel mouse model of autosomal semidominant adult hypophosphatasia has a splice site mutation in the tissue nonspecific alkaline phosphatase gene Akp2. J Bone Miner Res. 2007; 22 (9): 1397-407. (Pubitemid 351339684)
-
(2007)
Journal of Bone and Mineral Research
, vol.22
, Issue.9
, pp. 1397-1407
-
-
Hough, T.A.1
Polewski, M.2
Johnson, K.3
Cheeseman, M.4
Nolan, P.M.5
Vizor, L.6
Rastan, S.7
Boyde, A.8
Pritzker, K.9
Hunter, A.J.10
Fisher, E.M.C.11
Terkeltaub, R.12
Brown, S.D.M.13
-
15
-
-
0037634002
-
The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media
-
DOI 10.1007/s10162-002-3015-9
-
Hardisty RE, Erven A, Logan K, Morse S, Guionaud S, Sancho-Oliver S, Hunter AJ, Brown SD, Steel KP,. The deaf mouse mutant Jeff (Jf) is a single gene model of otitis media. J Assoc Res Otolaryngol. 2003; 4 (2): 130-8. (Pubitemid 36753764)
-
(2003)
JARO - Journal of the Association for Research in Otolaryngology
, vol.4
, Issue.2
, pp. 130-138
-
-
Hardisty, R.E.1
Erven, A.2
Logan, K.3
Morse, S.4
Guionaud, S.5
Sancho-Oliver, S.6
Hunter, A.J.7
Brown, S.D.M.8
Steel, K.P.9
-
16
-
-
48749090557
-
Role of the transcription factor sox4 in insulin secretion and impaired glucose tolerance
-
Goldsworthy M, Hugill A, Freeman H, Horner E, Shimomura K, Bogani D, Pieles G, Mijat V, Arkell R, Bhattacharya S, Ashcroft FM, Cox RD,. Role of the transcription factor sox4 in insulin secretion and impaired glucose tolerance. Diabetes. 2008; 57 (8): 2234-44.
-
(2008)
Diabetes.
, vol.57
, Issue.8
, pp. 2234-2244
-
-
Goldsworthy, M.1
Hugill, A.2
Freeman, H.3
Horner, E.4
Shimomura, K.5
Bogani, D.6
Pieles, G.7
Mijat, V.8
Arkell, R.9
Bhattacharya, S.10
Ashcroft, F.M.11
Cox, R.D.12
-
17
-
-
2542524743
-
A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene
-
DOI 10.2337/diabetes.53.6.1577
-
Toye AA, Moir L, Hugill A, Bentley L, Quarterman J, Mijat V, Hough T, Goldsworthy M, Haynes A, Hunter AJ, Browne M, Spurr N, Cox RD,. A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene. Diabetes. 2004; 53 (6): 1577-83. (Pubitemid 38697672)
-
(2004)
Diabetes
, vol.53
, Issue.6
, pp. 1577-1583
-
-
Toye, A.A.1
Moir, L.2
Hugill, A.3
Bentley, L.4
Quarterman, J.5
Mijat, V.6
Hough, T.7
Goldsworthy, M.8
Haynes, A.9
Hunter, A.J.10
Browne, M.11
Spurr, N.12
Cox, R.D.13
-
18
-
-
0034108294
-
Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorder
-
Mortier GR, Weis M, Nuytinck L, King LM, Wilkin DJ, De Paepe A, Lachman RS, Rimoin DL, Eyre DR, Cohn DH,. Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorder. J Med Genet. 2000; 37 (4): 263-71. (Pubitemid 30245931)
-
(2000)
Journal of Medical Genetics
, vol.37
, Issue.4
, pp. 263-271
-
-
Mortier, G.R.1
Weis, M.A.2
Nuytinck, L.3
King, L.M.4
Wilkin, D.J.5
De Paepe, A.6
Lachman, R.S.7
Rimoin, D.L.8
Eyre, D.R.9
Cohn, D.H.10
-
19
-
-
1642388383
-
Spondyloepiphyseal dysplasia congenita with absent femoral head
-
DOI 10.1097/00009957-200403000-00001
-
Jung SC, Mathew S, Li QW, Lee YJ, Lee KS, Song HR,. Spondyloepiphyseal dysplasia congenita with absent femoral head. J Pediatr Orthop B. 2004; 13 (2): 63-9. (Pubitemid 38380973)
-
(2004)
Journal of Pediatric Orthopaedics Part B
, vol.13
, Issue.2
, pp. 63-69
-
-
Jung, S.-C.1
Mathew, S.2
Li, Q.-W.3
Lee, Y.-J.4
Lee, K.-S.5
Song, H.-R.6
-
20
-
-
22144481004
-
The phenotypic spectrum of COL2A1 mutations
-
DOI 10.1002/humu.20179
-
Nishimura G, Haga N, Kitoh H, Tanaka Y, Sonoda T, Kitamura M, Shirahama S, Itoh T, Nakashima E, Ohashi H, Ikegawa S,. The phenotypic spectrum of COL2A1 mutations. Hum Mutat. 2005; 26 (1): 36-43. (Pubitemid 40980701)
-
(2005)
Human Mutation
, vol.26
, Issue.1
, pp. 36-43
-
-
Nishimura, G.1
Haga, N.2
Kitoh, H.3
Tanaka, Y.4
Sonoda, T.5
Kitamura, M.6
Shirahama, S.7
Itoh, T.8
Nakashima, E.9
Ohashi, H.10
Ikegawa, S.11
-
21
-
-
34249101894
-
A first familial G504S mutation of COL2A1 gene results in distinctive spondyloepiphyseal dysplasia congenita
-
DOI 10.1016/j.cca.2007.04.005, PII S0009898107002021
-
Xia X, Cui Y, Huang Y, Pan L, Wu Y, Zhang P, Jin B,. A first familial G504S mutation of COL2A1 gene results in distinctive spondyloepiphyseal dysplasia congenita. Clin Chim Acta. 2007; 382 (1-2): 148-50. (Pubitemid 46782744)
-
(2007)
Clinica Chimica Acta
, vol.382
, Issue.1-2
, pp. 148-150
-
-
Xia, X.1
Cui, Y.2
Huang, Y.3
Pan, L.4
Wu, Y.5
Zhang, P.6
Jin, B.7
-
22
-
-
0023231039
-
Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: Report of a pedigree with autosomal dominant inheritance
-
MacDermot KD, Roth SC, Hall C, Winter RM,. Epiphyseal dysplasia of the femoral head, mild vertebral abnormality, myopia, and sensorineural deafness: report of a pedigree with autosomal dominant inheritance. J Med Genet. 1987; 24 (10): 602-8. (Pubitemid 17149536)
-
(1987)
Journal of Medical Genetics
, vol.24
, Issue.10
, pp. 602-608
-
-
Macdermot, K.D.1
Roth, S.C.2
Hall, C.3
Winter, R.M.4
-
23
-
-
0031434686
-
Immunohistochemistry of collagen types II and X, and enzyme- histochemistry of alkaline phosphatase in the developing condylar cartilage of the fetal mouse mandible
-
DOI 10.1017/S0021878297002781
-
Shibata S, Fukada K, Suzuki S, Yamashita Y,. Immunohistochemistry of collagen types II and X, and enzyme-histochemistry of alkaline phosphatase in the developing condylar cartilage of the fetal mouse mandible. J Anat. 1997; 191 (Pt 4): 561-70. (Pubitemid 28022417)
-
(1997)
Journal of Anatomy
, vol.191
, Issue.4
, pp. 561-570
-
-
Shibata, S.1
Fukada, K.2
Suzuki, S.3
Yamashita, Y.4
-
24
-
-
0036011282
-
Pyrosequencing™: An accurate detection platform for single nucleotide polymorphisms
-
DOI 10.1002/humu.10078
-
Fakhrai-Rad H, Pourmand N, Ronaghi M,. Pyrosequencing: an accurate detection platform for single nucleotide polymorphisms. Hum Mutat. 2002; 19 (5): 479-85. (Pubitemid 34461621)
-
(2002)
Human Mutation
, vol.19
, Issue.5
, pp. 479-485
-
-
Fakhrai-Rad, H.1
Pourmand, N.2
Ronaghi, M.3
-
25
-
-
2542471328
-
Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome
-
DOI 10.1074/jbc.M401797200
-
Nesbit MA, Bowl MR, Harding B, Ali A, Ayala A, Crowe C, Dobbie A, Hampson G, Holdaway I, Levine MA, McWilliams R, Rigden S, Sampson J, Williams AJ, Thakker RV,. Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome. J Biol Chem. 2004; 279 (21): 22624-34. (Pubitemid 38679463)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.21
, pp. 22624-22634
-
-
Nesbit, M.A.1
Bowl, M.R.2
Harding, B.3
Ali, A.4
Ayala, A.5
Crowe, C.6
Dobbie, A.7
Hampson, G.8
Holdaway, I.9
Levine, M.A.10
McWilliams, R.11
Rigden, S.12
Sampson, J.13
Williams, A.J.14
Thakker, R.V.15
-
26
-
-
68049084873
-
Uromodulin mutations causing Familial Juvenile Hyperuricaemic Nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum
-
Williams SE, Reed AA, Galvanovskis J, Antignac C, Goodship T, Karet FE, Kotanko P, Lhotta K, Moriniere V, Williams P, Wong W, Rorsman P, Thakker RV,. Uromodulin mutations causing Familial Juvenile Hyperuricaemic Nephropathy lead to protein maturation defects and retention in the endoplasmic reticulum. Hum Mol Genet. 2009; 18 (16): 2963-74.
-
(2009)
Hum Mol Genet.
, vol.18
, Issue.16
, pp. 2963-2974
-
-
Williams, S.E.1
Reed, A.A.2
Galvanovskis, J.3
Antignac, C.4
Goodship, T.5
Karet, F.E.6
Kotanko, P.7
Lhotta, K.8
Moriniere, V.9
Williams, P.10
Wong, W.11
Rorsman, P.12
Thakker, R.V.13
-
27
-
-
0035491768
-
Characterization of immortalized human chondrocytes originated from osteoarthritis cartilage
-
Yoshimatsu T, Saitoh A, Ryu JN, Shima D, Handa H, Hiramoto M, Kawakami Y, Aizawa S,. Characterization of immortalized human chondrocytes originated from osteoarthritis cartilage. Int J Mol Med. 2001; 8 (4): 345-51.
-
(2001)
Int J Mol Med.
, vol.8
, Issue.4
, pp. 345-351
-
-
Yoshimatsu, T.1
Saitoh, A.2
Ryu, J.N.3
Shima, D.4
Handa, H.5
Hiramoto, M.6
Kawakami, Y.7
Aizawa, S.8
-
28
-
-
33847322639
-
SGCE missense mutations that cause myoclonus-dystonia syndrome impair ε-sarcoglycan trafficking to the plasma membrane: Modulation by ubiquitination and torsinA
-
DOI 10.1093/hmg/ddl472
-
Esapa CT, Waite A, Locke M, Benson MA, Kraus M, McIlhinney RA, Sillitoe RV, Beesley PW, Blake DJ,. SGCE missense mutations that cause myoclonus-dystonia syndrome impair epsilon-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA. Hum Mol Genet. 2007; 16 (3): 327-42. (Pubitemid 46323188)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.3
, pp. 327-342
-
-
Esapa, C.T.1
Waite, A.2
Locke, M.3
Benson, M.A.4
Kraus, M.5
McIlhinney, R.A.J.6
Sillitoe, R.V.7
Beesley, P.W.8
Blake, D.J.9
-
29
-
-
0019126423
-
Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S
-
DOI 10.1002/tera.1420220306
-
McLeod MJ,. Differential staining of cartilage and bone in whole mouse fetuses by alcian blue and alizarin red S. Teratology. 1980; 22 (3): 299-301. (Pubitemid 11209786)
-
(1980)
Teratology
, vol.22
, Issue.3
, pp. 299-301
-
-
McLeod, M.J.1
-
30
-
-
74049159081
-
Delta-EF1 is a negative regulator of Ihh in the developing growth plate
-
Bellon E, Luyten FP, Tylzanowski P,. delta-EF1 is a negative regulator of Ihh in the developing growth plate. J Cell Biol. 2009; 187 (5): 685-99.
-
(2009)
J Cell Biol.
, vol.187
, Issue.5
, pp. 685-699
-
-
Bellon, E.1
Luyten, F.P.2
Tylzanowski, P.3
-
31
-
-
1442358788
-
Sox5 and Sox6 are needed to develop and maintain source, columnar, and hypertrophic chondrocytes in the cartilage growth plate
-
DOI 10.1083/jcb.200312045
-
Smits P, Dy P, Mitra S, Lefebvre V,. Sox5 and Sox6 are needed to develop and maintain source, columnar, and hypertrophic chondrocytes in the cartilage growth plate. J Cell Biol. 2004; 164 (5): 747-58. (Pubitemid 38282958)
-
(2004)
Journal of Cell Biology
, vol.164
, Issue.5
, pp. 747-758
-
-
Smits, P.1
Dy, P.2
Mitra, S.3
Lefebvre, V.4
-
32
-
-
1242292280
-
Pancreatic β-cell granule peptides form heteromolecular complexes which inhibit islet amyloid polypeptide fibril formation
-
Jaikaran ET, Nilsson MR, Clark A,. Pancreatic beta-cell granule peptides form heteromolecular complexes which inhibit islet amyloid polypeptide fibril formation. Biochem J. 2004; 377 (Pt 3): 709-16. (Pubitemid 38221842)
-
(2004)
Biochemical Journal
, vol.377
, Issue.3
, pp. 709-716
-
-
Jaikaran, E.T.A.S.1
Nilsson, M.R.2
Clark, A.3
-
33
-
-
61849137831
-
Inhibiting Dickkopf-1 (Dkk1) removes suppression of bone formation and prevents the development of osteolytic bone disease in multiple myeloma
-
Heath DJ, Chantry AD, Buckle CH, Coulton L, Shaughnessy JD Jr, Evans HR, Snowden JA, Stover DR, Vanderkerken K, Croucher PI,. Inhibiting Dickkopf-1 (Dkk1) removes suppression of bone formation and prevents the development of osteolytic bone disease in multiple myeloma. J Bone Miner Res. 2009; 24 (3): 425-36.
-
(2009)
J Bone Miner Res.
, vol.24
, Issue.3
, pp. 425-436
-
-
Heath, D.J.1
Chantry, A.D.2
Buckle, C.H.3
Coulton, L.4
Shaughnessy Jr., J.D.5
Evans, H.R.6
Snowden, J.A.7
Stover, D.R.8
Vanderkerken, K.9
Croucher, P.I.10
-
34
-
-
6344279052
-
Musculoskeletal responses of 2-year-old Thoroughbred horses to early training. 8. Quantitative back-scattered electron scanning electron microscopy and confocal fluorescence microscopy of the epiphysis of the third metacarpal bone
-
Boyde A, Firth EC,. Musculoskeletal responses of 2-year-old Thoroughbred horses to early training. 8. Quantitative back-scattered electron scanning electron microscopy and confocal fluorescence microscopy of the epiphysis of the third metacarpal bone. N Z Vet J. 2005; 53 (2): 123-32. (Pubitemid 40529348)
-
(2005)
New Zealand Veterinary Journal
, vol.53
, Issue.2
, pp. 123-132
-
-
Boyde, A.1
Firth, E.C.2
-
35
-
-
0032971847
-
The mineralization density of iliac crest bone from children with osteogenesis imperfecta
-
DOI 10.1007/s002239900600
-
Boyde A, Travers R, Glorieux FH, Jones SJ,. The mineralization density of iliac crest bone from children with osteogenesis imperfecta. Calcif Tissue Int. 1999; 64 (3): 185-90. (Pubitemid 29107233)
-
(1999)
Calcified Tissue International
, vol.64
, Issue.3
, pp. 185-190
-
-
Boyde, A.1
Travers, R.2
Glorieux, F.H.3
Jones, S.J.4
-
36
-
-
0031149422
-
Inhibition of chondrogenesis by Wnt gene expression in vivo and in vitro
-
DOI 10.1006/dbio.1997.8536
-
Rudnicki JA, Brown AM,. Inhibition of chondrogenesis by Wnt gene expression in vivo and in vitro. Dev Biol. 1997; 185 (1): 104-18. (Pubitemid 27244221)
-
(1997)
Developmental Biology
, vol.185
, Issue.1
, pp. 104-118
-
-
Rudnicki, J.A.1
Brown, A.M.C.2
-
37
-
-
61349101373
-
Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation
-
Witte F, Dokas J, Neuendorf F, Mundlos S, Stricker S,. Comprehensive expression analysis of all Wnt genes and their major secreted antagonists during mouse limb development and cartilage differentiation. Gene Expr Patterns. 2009; 9 (4): 215-23.
-
(2009)
Gene Expr Patterns.
, vol.9
, Issue.4
, pp. 215-223
-
-
Witte, F.1
Dokas, J.2
Neuendorf, F.3
Mundlos, S.4
Stricker, S.5
-
38
-
-
0028856176
-
Transgenic mice with targeted inactivation of the Col2 alpha 1 gene for collagen II develop a skeleton with membranous and periosteal bone but no endochondral bone
-
Li SW, Prockop DJ, Helminen H, Fassler R, Lapvetelainen T, Kiraly K, Peltarri A, Arokoski J, Lui H, Arita M,. Transgenic mice with targeted inactivation of the Col2 alpha 1 gene for collagen II develop a skeleton with membranous and periosteal bone but no endochondral bone. Genes Dev. 1995; 9 (22): 2821-30.
-
(1995)
Genes Dev.
, vol.9
, Issue.22
, pp. 2821-2830
-
-
Li, S.W.1
Prockop, D.J.2
Helminen, H.3
Fassler, R.4
Lapvetelainen, T.5
Kiraly, K.6
Peltarri, A.7
Arokoski, J.8
Lui, H.9
Arita, M.10
-
39
-
-
33644639082
-
Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens
-
DOI 10.1007/s00335-005-0101-4
-
Keays DA, Clark TG, Flint J,. Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens. Mamm Genome. 2006; 17 (3): 230-8. (Pubitemid 43327654)
-
(2006)
Mammalian Genome
, vol.17
, Issue.3
, pp. 230-238
-
-
Keays, D.A.1
Clark, T.G.2
Flint, J.3
-
40
-
-
3142722961
-
Chondroptosis: A variant of apoptotic cell death in chondrocytes?
-
DOI 10.1023/B:APPT.0000025803.17498.26
-
Roach HI, Aigner T, Kouri JB,. Chondroptosis: a variant of apoptotic cell death in chondrocytes?. Apoptosis. 2004; 9 (3): 265-77. (Pubitemid 38981501)
-
(2004)
Apoptosis
, vol.9
, Issue.3
, pp. 265-277
-
-
Roach, H.I.1
Aigner, T.2
Kouri, J.B.3
-
41
-
-
0019391029
-
Disproportionate micromelia (Dmm): An incomplete dominant mouse dwarfism with abnormal cartilage matrix
-
Brown KS, Cranley RE, Greene R, Kleinman HK, Pennypacker JP,. Disproportionate micromelia (Dmm): an incomplete dominant mouse dwarfism with abnormal cartilage matrix. J Embryol Exp Morphol. 1981; 62: 165-82. (Pubitemid 11155712)
-
(1981)
Journal of Embryology and Experimental Morphology
, vol.62
, pp. 165-182
-
-
Brown, K.S.1
Cranley, R.E.2
Greene, R.3
-
42
-
-
10744233690
-
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis
-
DOI 10.1359/jbmr.2003.18.9.1612
-
Donahue LR, Chang B, Mohan S, Miyakoshi N, Wergedal JE, Baylink DJ, Hawes NL, Rosen CJ, Ward-Bailey P, Zheng QY, Bronson RT, Johnson KR, Davisson MT,. A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis. J Bone Miner Res. 2003; 18 (9): 1612-21. (Pubitemid 37022919)
-
(2003)
Journal of Bone and Mineral Research
, vol.18
, Issue.9
, pp. 1612-1621
-
-
Donahue, L.R.1
Chang, B.2
Mohan, S.3
Miyakoshi, N.4
Wergedal, J.E.5
Baylink, D.J.6
Hawes, N.L.7
Rosen, C.J.8
Ward-Bailey, P.9
Zheng, Q.Y.10
Bronson, R.T.11
Johnson, K.R.12
Davisson, M.T.13
-
43
-
-
0031034806
-
Disproportionate micromelia (Dmm) in mice caused by a mutation in the C- propeptide coding region of Col2a1
-
DOI 10.1002/(SICI)1097-0177(199701)208:1<25::AID-AJA3>3.0.CO;2-3
-
Pace JM, Li Y, Seegmiller RE, Teuscher C, Taylor BA, Olsen BR,. Disproportionate micromelia (Dmm) in mice caused by a mutation in the C-propeptide coding region of Col2a1. Dev Dyn. 1997; 208 (1): 25-33. (Pubitemid 27030481)
-
(1997)
Developmental Dynamics
, vol.208
, Issue.1
, pp. 25-33
-
-
Pace, J.M.1
Li, Y.2
Seegmiller, R.E.3
Teuscher, C.4
Taylor, B.A.5
Olsen, B.R.6
-
44
-
-
0242438182
-
Protein consequences of the Col2a1 C-propeptide mutation in the chondrodysplastic Dmm mouse
-
DOI 10.1016/S0945-053X(03)00077-5
-
Fernandes RJ, Seegmiller RE, Nelson WR, Eyre DR,. Protein consequences of the Col2a1 C-propeptide mutation in the chondrodysplastic Dmm mouse. Matrix Biol. 2003; 22 (5): 449-53. (Pubitemid 37393323)
-
(2003)
Matrix Biology
, vol.22
, Issue.5
, pp. 449-453
-
-
Fernandes, R.J.1
Seegmiller, R.E.2
Nelson, W.R.3
Eyre, D.R.4
-
46
-
-
54349105636
-
The heterozygous disproportionate micromelia (dmm) mouse: Morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype
-
Seegmiller RE, Bomsta BD, Bridgewater LC, Niederhauser CM, Montano C, Sudweeks S, Eyre DR, Fernandes RJ,. The heterozygous disproportionate micromelia (dmm) mouse: morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype. J Histochem Cytochem. 2008; 56 (11): 1003-11.
-
(2008)
J Histochem Cytochem.
, vol.56
, Issue.11
, pp. 1003-1011
-
-
Seegmiller, R.E.1
Bomsta, B.D.2
Bridgewater, L.C.3
Niederhauser, C.M.4
Montano, C.5
Sudweeks, S.6
Eyre, D.R.7
Fernandes, R.J.8
-
47
-
-
0035935618
-
Double heterozygosity for pseudoachondroplasia and spondyloepiphyseal dysplasia congenita
-
DOI 10.1002/ajmg.10062
-
Unger S, Korkko J, Krakow D, Lachman RS, Rimoin DL, Cohn DH,. Double heterozygosity for pseudoachondroplasia and spondyloepiphyseal dysplasia congenita. Am J Med Genet. 2001; 104 (2): 140-6. (Pubitemid 33062940)
-
(2001)
American Journal of Medical Genetics
, vol.104
, Issue.2
, pp. 140-146
-
-
Unger, S.1
Korkko, J.2
Krakow, D.3
Lachman, R.S.4
Rimoin, D.L.5
Cohn, D.H.6
-
48
-
-
0028863623
-
Stickler syndrome. A mutation in the nonhelical 3′ end of type II procollagen gene
-
Ahmad NN, Dimascio J, Knowlton RG, Tasman WS,. Stickler syndrome. A mutation in the nonhelical 3′ end of type II procollagen gene. Arch Ophthalmol. 1995; 113 (11): 1454-7.
-
(1995)
Arch Ophthalmol.
, vol.113
, Issue.11
, pp. 1454-1457
-
-
Ahmad, N.N.1
Dimascio, J.2
Knowlton, R.G.3
Tasman, W.S.4
-
49
-
-
18544362958
-
Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule
-
Richards AJ, Morgan J, Bearcroft PW, Pickering E, Owen MJ, Holmans P, Williams N, Tysoe C, Pope FM, Snead MP, Hughes H,. Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule. J Med Genet. 2002; 39 (9): 661-5. (Pubitemid 35001719)
-
(2002)
Journal of Medical Genetics
, vol.39
, Issue.9
, pp. 661-665
-
-
Richards, A.J.1
Morgan, J.2
Bearcroft, P.W.P.3
Pickering, E.4
Owen, M.J.5
Holmans, P.6
Williams, N.7
Tysoe, C.8
Pope, F.M.9
Snead, M.P.10
Hughes, H.11
-
50
-
-
0029871742
-
A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasia
-
Zabel B, Hilbert K, Stoss H, Superti-Furga A, Spranger J, Winterpacht A,. A specific collagen type II gene (COL2A1) mutation presenting as spondyloperipheral dysplasia. Am J Med Genet. 1996; 63 (1): 123-8.
-
(1996)
Am J Med Genet.
, vol.63
, Issue.1
, pp. 123-128
-
-
Zabel, B.1
Hilbert, K.2
Stoss, H.3
Superti-Furga, A.4
Spranger, J.5
Winterpacht, A.6
-
51
-
-
4344660043
-
Spondyloperipheral dysplasia is caused by truncating mutations in the C-propeptide of COL2A1
-
Zankl A, Zabel B, Hilbert K, Wildhardt G, Cuenot S, Xavier B, Ha-Vinh R, Bonafe L, Spranger J, Superti-Furga A,. Spondyloperipheral dysplasia is caused by truncating mutations in the C-propeptide of COL2A1. Am J Med Genet A. 2004; 129 (2): 144-8. (Pubitemid 39121280)
-
(2004)
American Journal of Medical Genetics
, vol.129
, Issue.2
, pp. 144-148
-
-
Zankl, A.1
Zabel, B.2
Hilbert, K.3
Wildhardt, G.4
Cuenot, S.5
Xavier, B.6
Ha-Vinh, R.7
Bonafe, L.8
Spranger, J.9
Superti-Furga, A.10
-
52
-
-
36348969441
-
Czech dysplasia metatarsal type: Another type II collagen disorder
-
DOI 10.1038/sj.ejhg.5201913, PII 5201913
-
Hoornaert KP, Marik I, Kozlowski K, Cole T, Le Merrer M, Leroy JG, Coucke PJ, Sillence D, Mortier GR,. Czech dysplasia metatarsal type: another type II collagen disorder. Eur J Hum Genet. 2007; 15 (12): 1269-75. (Pubitemid 350143184)
-
(2007)
European Journal of Human Genetics
, vol.15
, Issue.12
, pp. 1269-1275
-
-
Hoornaert, K.P.1
Marik, I.2
Kozlowski, K.3
Cole, T.4
Le Merrer, M.5
Leroy, J.G.6
Coucke, P.J.7
Sillence, D.8
Mortier, G.R.9
-
53
-
-
84882564866
-
Structure, biosynthesis and gene regulation of collagens in cartilage and bone
-
Markus Seibel S.R. Bilezikian J. editors. 2nd ed. New York: Elsevier
-
Mark Kvd,. Structure, biosynthesis and gene regulation of collagens in cartilage and bone. In:, Markus Seibel SR, Bilezikian J, editors. Dynamics of bone and cartilage metabolism, 2nd ed. New York: Elsevier; 2006. p. 3-40.
-
(2006)
Dynamics of Bone and Cartilage Metabolism
, pp. 3-40
-
-
Mark, K.1
-
54
-
-
17844373840
-
Procollagen trafficking, processing and fibrillogenesis
-
DOI 10.1242/jcs.01731
-
Canty EG, Kadler KE,. Procollagen trafficking, processing and fibrillogenesis. J Cell Sci. 2005; 118 (Pt 7): 1341-53. (Pubitemid 40585115)
-
(2005)
Journal of Cell Science
, vol.118
, Issue.7
, pp. 1341-1353
-
-
Canty, E.G.1
Kadler, K.E.2
-
55
-
-
33646405997
-
The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene
-
Hoornaert KP, Dewinter C, Vereecke I, Beemer FA, Courtens W, Fryer A, Fryssira H, Lees M, Mullner-Eidenbock A, Rimoin DL, Siderius L, Superti-Furga A, Temple K, Willems PJ, Zankl A, Zweier C, De Paepe A, Coucke P, Mortier GR,. The phenotypic spectrum in patients with arginine to cysteine mutations in the COL2A1 gene. J Med Genet. 2006; 43 (5): 406-13.
-
(2006)
J Med Genet.
, vol.43
, Issue.5
, pp. 406-413
-
-
Hoornaert, K.P.1
Dewinter, C.2
Vereecke, I.3
Beemer, F.A.4
Courtens, W.5
Fryer, A.6
Fryssira, H.7
Lees, M.8
Mullner-Eidenbock, A.9
Rimoin, D.L.10
Siderius, L.11
Superti-Furga, A.12
Temple, K.13
Willems, P.J.14
Zankl, A.15
Zweier, C.16
De Paepe, A.17
Coucke, P.18
Mortier, G.R.19
-
56
-
-
0036133536
-
Y-position collagen II mutation disrupts cartilage formation and skeletal development in a transgenic mouse model of spondyloepiphyseal dysplasia
-
Gaiser KG, Maddox BK, Bann JG, Boswell BA, Keene DR, Garofalo S, Horton WA,. Y-position collagen II mutation disrupts cartilage formation and skeletal development in a transgenic mouse model of spondyloepiphyseal dysplasia. J Bone Miner Res. 2002; 17 (1): 39-47. (Pubitemid 33150995)
-
(2002)
Journal of Bone and Mineral Research
, vol.17
, Issue.1
, pp. 39-47
-
-
Gaiser, K.G.1
Maddox, B.K.2
Bann, J.G.3
Boswell, B.A.4
Keene, D.R.5
Garofalo, S.6
Horton, W.A.7
-
57
-
-
0022444528
-
Chondrocalcin is identical with the C-propeptide of type II procollagen
-
Van der Rest M, Rosenberg LC, Olsen BR, Poole AR,. Chondrocalcin is identical with the C-propeptide of type II procollagen. Biochem J. 1986; 237 (3): 923-5. (Pubitemid 16003796)
-
(1986)
Biochemical Journal
, vol.237
, Issue.3
, pp. 923-925
-
-
Van Der Rest, M.1
Rosenberg, L.C.2
Olsen, B.R.3
Poole, A.R.4
-
58
-
-
0029742646
-
The C-propeptide of type II procollagen binds to the enhancer region of the type II procollagen gene and regulates its transcription
-
Nakata K, Miyamoto S, Bernier S, Tanaka M, Utani A, Krebsbach P, Rhodes C, Yamada Y,. The c-propeptide of type II procollagen binds to the enhancer region of the type II procollagen gene and regulates its transcription. Ann N Y Acad Sci. 1996; 785: 307-8. (Pubitemid 26302154)
-
(1996)
Annals of the New York Academy of Sciences
, vol.785
, pp. 307-308
-
-
Nakata, K.1
Miyamoto, S.2
Bernier, S.3
Tanaka, M.4
Utani, A.5
Krebsbach, P.6
Rhodes, C.7
Yamada, Y.8
-
59
-
-
0023656926
-
Assembly of collagen fibrils de novo by cleavage of the type i pC-collagen with procollagen C-proteinase. Assay of critical concentration demonstrates that collagen self-assembly is a classical example of an entropy-driven process
-
Kadler KE, Hojima Y, Prockop DJ,. Assembly of collagen fibrils de novo by cleavage of the type I pC-collagen with procollagen C-proteinase. Assay of critical concentration demonstrates that collagen self-assembly is a classical example of an entropy-driven process. J Biol Chem. 1987; 262 (32): 15696-701.
-
(1987)
J Biol Chem.
, vol.262
, Issue.32
, pp. 15696-15701
-
-
Kadler, K.E.1
Hojima, Y.2
Prockop, D.J.3
-
60
-
-
0037087610
-
Imaging of procollagen transport reveals COPI-dependent cargo sorting during ER-to-Golgi transport in mammalian cells
-
Stephens DJ, Pepperkok R,. Imaging of procollagen transport reveals COPI-dependent cargo sorting during ER-to-Golgi transport in mammalian cells. J Cell Sci. 2002; 115 (Pt 6): 1149-60. (Pubitemid 34272480)
-
(2002)
Journal of Cell Science
, vol.115
, Issue.6
, pp. 1149-1160
-
-
Stephens, D.J.1
Pepperkok, R.2
-
61
-
-
0019616433
-
Ultrastructural evidence of a functional heterogeneity among physeal chondrocytes in growing swine
-
Wilsman NJ, Farnum CE, Hilley HD, Carlson CS,. Ultrastructural evidence of a functional heterogeneity among physeal chondrocytes in growing swine. Am J Vet Res. 1981; 42 (9): 1547-53.
-
(1981)
Am J Vet Res.
, vol.42
, Issue.9
, pp. 1547-1553
-
-
Wilsman, N.J.1
Farnum, C.E.2
Hilley, H.D.3
Carlson, C.S.4
-
62
-
-
0024235472
-
Histochemical, immunofluorescence, and ultrastructural differences in fetal cartilage among three genetically distinct chondrodystrophic mice
-
DOI 10.1002/tera.1420380606
-
Seegmiller RE, Brown K, Chandrasekhar S,. Histochemical, immunofluorescence, and ultrastructural differences in fetal cartilage among three genetically distinct chondrodystrophic mice. Teratology. 1988; 38 (6): 579-92. (Pubitemid 19023777)
-
(1988)
Teratology
, vol.38
, Issue.6
, pp. 579-592
-
-
Seegmiller, R.E.1
Brown, K.2
Chandrasekhar, S.3
-
63
-
-
37149029397
-
Articular cartilage and biomechanical properties of the long bones in Frzb-knockout mice
-
DOI 10.1002/art.23137
-
Lories RJ, Peeters J, Bakker A, Tylzanowski P, Derese I, Schrooten J, Thomas JT, Luyten FP,. Articular cartilage and biomechanical properties of the long bones in Frzb-knockout mice. Arthritis Rheum. 2007; 56 (12): 4095-103. (Pubitemid 350262337)
-
(2007)
Arthritis and Rheumatism
, vol.56
, Issue.12
, pp. 4095-4103
-
-
Lories, R.J.U.1
Peeters, J.2
Bakker, A.3
Tylzanowski, P.4
Derese, I.5
Schrooten, J.6
Thomas, J.T.7
Luvten, F.P.8
|