-
1
-
-
0037385299
-
Neurological aspects of osteopetrosis
-
DOI 10.1046/j.1365-2990.2003.00474.x
-
Steward CG. Neurological aspects of osteopetrosis. Neuropathol Appl Neurobiol 2003; 29: 87-97. (Pubitemid 36408327)
-
(2003)
Neuropathology and Applied Neurobiology
, vol.29
, Issue.2
, pp. 87-97
-
-
Steward, C.G.1
-
2
-
-
0344578061
-
Type II autosomal dominant osteopetrosis (Albers-Schönberg disease): Clinical and radiological manifestations in 42 patients
-
Benichou OD, Laredo JD, de Vernejoul MC. Type II autosomal dominant osteopetrosis (Albers-Schönberg disease): clinical and radiological manifestations in 42 patients. Bone 2000; 26: 87-93.
-
(2000)
Bone
, vol.26
, pp. 87-93
-
-
Benichou, O.D.1
Laredo, J.D.2
De Vernejoul, M.C.3
-
3
-
-
33645789497
-
Clinical, genetic, and cellular analysis of 49 osteopetrotic patients: Implications for diagnosis and treatment
-
Del Fattore A, Peruzzi B, Rucci N et al. Clinical, genetic, and cellular analysis of 49 osteopetrotic patients: implications for diagnosis and treatment. J Med Genet 2006; 43: 315-325.
-
(2006)
J Med Genet
, vol.43
, pp. 315-325
-
-
Del Fattore, A.1
Peruzzi, B.2
Rucci, N.3
-
4
-
-
18244403197
-
Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease
-
Balemans W, Patel N, Ebeling M et al. Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease. J Med Genet 2002; 39: 91-97. (Pubitemid 34146376)
-
(2002)
Journal of Medical Genetics
, vol.39
, Issue.2
, pp. 91-97
-
-
Balemans, W.1
Patel, N.2
Ebeling, M.3
Van Hul, E.4
Wuyts, W.5
Lacza, C.6
Dioszegi, M.7
Dikkers, F.G.8
Hildering, P.9
Willems, P.J.10
Verheij, J.B.G.M.11
Lindpaintner, K.12
Vickery, B.13
Foernzler, D.14
Van Hul, W.15
-
5
-
-
0035282968
-
Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)
-
Balemans W, Ebeling M, Patel N et al. Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST). Hum Mol Genet 2001; 10: 537-543. (Pubitemid 32184286)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.5
, pp. 537-543
-
-
Balemans, W.1
Ebeling, M.2
Patel, N.3
Van Hul, E.4
Olson, P.5
Dioszegi, M.6
Lacza, C.7
Wuyts, W.8
Van Den, E.J.9
Willems, P.10
Paes-Alves, A.F.11
Hill, S.12
Bueno, M.13
Ramos, F.J.14
Tacconi, P.15
Dikkers, F.G.16
Stratakis, C.17
Lindpaintner, K.18
Vickery, B.19
Foernzler, D.20
Van Hul, W.21
more..
-
6
-
-
0037373341
-
Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions with an increased bone density
-
DOI 10.1086/368277
-
Van Wesenbeeck L, Cleiren E, Gram J et al. Six novel missense mutations in the LDL receptor-related protein 5 (LRP5) gene in different conditions withan increased bone density. Am J Hum Genet 2003; 72: 763-771. (Pubitemid 36255977)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.3
, pp. 763-771
-
-
Van Wesenbeeck, L.1
Cleiren, E.2
Gram, J.3
Beals, R.K.4
Benichou, O.5
Scopelliti, D.6
Key, L.7
Renton, T.8
Bartels, C.9
Gong, Y.10
Warman, M.L.11
De Vernejoul, M.-C.12
Bollerslev, J.13
Van Hul, W.14
-
7
-
-
56349162283
-
Lrp5 controls bone formation by inhibiting serotonin synthesis in the duodenum
-
Yadav VK, Ryu JH, Suda N et al. Lrp5 controls bone formation by inhibiting serotonin synthesis in the duodenum. Cell 2008; 135: 825-837.
-
(2008)
Cell
, vol.135
, pp. 825-837
-
-
Yadav, V.K.1
Ryu, J.H.2
Suda, N.3
-
8
-
-
18244389008
-
Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the CICN7 chloride channel gene
-
Cleiren E, Benichou O, Van Hul E et al. Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene. Hum Mol Genet 2001; 10: 2861-2867. (Pubitemid 34030917)
-
(2001)
Human Molecular Genetics
, vol.10
, Issue.25
, pp. 2861-2867
-
-
Cleiren, E.1
Benichou, O.2
Van Hul, E.3
Gram, J.4
Bollerslev, J.5
Singer, F.R.6
Beaverson, K.7
Aledo, A.8
Whyte, M.P.9
Yoneyama, T.10
De Vernejoul, M.-C.11
Van Hul, W.12
-
10
-
-
58149308297
-
Infantile malignant, autosomal recessive osteopetrosis: The rich and the poor
-
Villa A, Guerrini MM, Cassani B et al. Infantile malignant, autosomal recessive osteopetrosis: the rich and the poor. Calcif Tissue Int 2009; 84: 1-12.
-
(2009)
Calcif Tissue Int
, vol.84
, pp. 1-12
-
-
Villa, A.1
Guerrini, M.M.2
Cassani, B.3
-
11
-
-
24644501631
-
Lessons from osteopetrotic mutations in animals: Impact on our current understanding of osteoclast biology
-
DOI 10.1615/CritRevEukaryotGeneExpr.v15.i2.40
-
Van Wesenbeeck L, Van Hul W. Lessons from osteopetrotic mutations in animals: impact on our current understanding of osteoclast biology. Crit Rev Eukaryot Gene Expr 2005; 15: 133-162. (Pubitemid 41277408)
-
(2005)
Critical Reviews in Eukaryotic Gene Expression
, vol.15
, Issue.2
, pp. 133-162
-
-
Van Wesenbeeck, L.1
Van Hul, W.2
-
12
-
-
0001690310
-
Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification
-
Sly WS, Hewett-Emmett D, Whyte MP et al. Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification. Proc Natl Acad Sci U S A 1983; 80: 2752-2756. (Pubitemid 13093387)
-
(1983)
Proceedings of the National Academy of Sciences of the United States of America
, vol.80
, Issue.9 I
, pp. 2752-2756
-
-
Sly, W.S.1
Hewett, E.D.2
Whyte, M.P.3
-
14
-
-
0028217372
-
Carbonic anhydrase II deficiency: Single-base deletion in exon 7 is the predominant mutation in Caribbean Hispanic patients
-
Hu PY, Ernst AR, Sly WS et al. Carbonic anhydrase II deficiency: single-base deletion in exon 7 is the predominant mutation in Caribbean Hispanic patients. Am J Hum Genet 1994; 54: 602-608. (Pubitemid 24089599)
-
(1994)
American Journal of Human Genetics
, vol.54
, Issue.4
, pp. 602-608
-
-
Hu, P.Y.1
Ernst, A.R.2
Sly, W.S.3
Venta, P.J.4
Skaggs, L.A.5
Tashian, R.E.6
-
15
-
-
0033946477
-
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis
-
DOI 10.1038/77131
-
Frattini A, Orchard PJ, Sobacchi C et al. Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis. Nat Genet 2000; 25: 343-346. (Pubitemid 30437326)
-
(2000)
Nature Genetics
, vol.25
, Issue.3
, pp. 343-346
-
-
Frattini, A.1
Orchard, P.J.2
Sobacchi, C.3
Giliani, S.4
Abinun, M.5
Mattsson, J.P.6
Keeling, D.J.7
Andersson, A.-K.8
Wallbrandt, P.9
Zecca, L.10
Notarangelo, L.D.11
Vezzoni, P.12
Villa, A.13
-
16
-
-
0034641590
-
+-ATPase cause infantile malignant osteopetrosis
-
Kornak U, Schulz A, Friedrich W et al. Mutations in the a3 subunit of the vacuolar H(+)-ATPase cause infantile malignant osteopetrosis. Hum Mol Genet 2000; 9: 2059-2063. (Pubitemid 30642671)
-
(2000)
Human Molecular Genetics
, vol.9
, Issue.13
, pp. 2059-2063
-
-
Kornak, U.1
Schulz, A.2
Friedrich, W.3
Uhlhaas, S.4
Kremens, B.5
Voit, T.6
Hasan, C.7
Bode, U.8
Jentsch, T.J.9
Kubisch, C.10
-
17
-
-
0034708665
-
+-ATPase. Preferential expression of the a3 isoform during osteoclast differentiation
-
DOI 10.1074/jbc.275.12.8760
-
Toyomura T, Oka T, Yamaguchi C et al. Three subunit a isoforms of mouse vacuolar H(+)-ATPase. Preferential expression of the a3 isoform during osteoclast differentiation. J Biol Chem 2000; 275: 8760-8765. (Pubitemid 30180229)
-
(2000)
Journal of Biological Chemistry
, vol.275
, Issue.12
, pp. 8760-8765
-
-
Toyomura, T.1
Oka, T.2
Yamaguchi, C.3
Wada, Y.4
Futai, M.5
-
18
-
-
0035951282
-
Loss of the CIC-7 chloride channel leads to osteopetrosis in mice and man
-
DOI 10.1016/S0092-8674(01)00206-9
-
Kornak U, Kasper D, Bosl MR et al. Loss of the ClC-7 chloride channel leads to osteopetrosis in mice and man. Cell 2001; 104: 205-215. (Pubitemid 32174837)
-
(2001)
Cell
, vol.104
, Issue.2
, pp. 205-215
-
-
Kornak, U.1
Kasper, D.2
Bosl, M.R.3
Kaiser, E.4
Schweizer, M.5
Schulz, A.6
Friedrich, W.7
Delling, G.8
Jentsch, T.J.9
-
19
-
-
0037393446
-
Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human
-
DOI 10.1038/nm842
-
Chalhoub N, Benachenhou N, Rajapurohitam V et al. Grey-lethal mutation induces severe malignant autosomal recessive osteopetrosis in mouse and human. Nat Med 2003; 9: 399-406. (Pubitemid 36460073)
-
(2003)
Nature Medicine
, vol.9
, Issue.4
, pp. 399-406
-
-
Chalhoub, N.1
Benachenhou, N.2
Rajapurohitam, V.3
Pata, M.4
Ferron, M.5
Frattini, A.6
Villa, A.7
Vacher, J.8
-
20
-
-
33745507483
-
Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement
-
DOI 10.1359/jbmr.060403
-
Pangrazio A, Poliani PL, Megarbane A et al. Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement. J Bone Miner Res 2006; 21: 1098-1105. (Pubitemid 43962838)
-
(2006)
Journal of Bone and Mineral Research
, vol.21
, Issue.7
, pp. 1098-1105
-
-
Pangrazio, A.1
Poliani, P.L.2
Megarbane, A.3
Lefranc, G.4
Lanino, E.5
Di, R.M.6
Rucci, F.7
Lucchini, F.8
Ravanini, M.9
Facchetti, F.10
Abinun, M.11
Vezzoni, P.12
Villa, A.13
Frattini, A.14
-
21
-
-
33644861728
-
ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function
-
DOI 10.1038/nature04535, PII N04535
-
Lange PF, Wartosch L, Jentsch TJ. ClC-7 requires Ostm1 as a beta-subunit to support bone resorption and lysosomal function. Nature 2006; 440: 220-223. (Pubitemid 43372100)
-
(2006)
Nature
, vol.440
, Issue.7081
, pp. 220-223
-
-
Lange, P.F.1
Wartosch, L.2
Jentsch, T.J.3
Fuhrmann, J.C.4
-
22
-
-
2342632645
-
Identification of a Novel Mutation in the Coding Region of the Grey-Lethal Gene OSTM1 in Human Malignant Infantile Osteopetrosis
-
DOI 10.1002/humu.20028
-
Ramirez A, Faupel J, Goebel I et al. Identification of a novel mutation in the coding region of the greylethal gene OSTM1 in human malignant infantile osteopetrosis. Hum Mutat 2004; 23: 471-476. (Pubitemid 38569220)
-
(2004)
Human Mutation
, vol.23
, Issue.5
, pp. 471-476
-
-
Ramirez, A.1
Faupel, J.2
Goebel, I.3
Stiller, A.4
Beyer, S.5
Stockle, C.6
Hasan, C.7
Bode, U.8
Kornak, U.9
Kubisch, C.10
-
23
-
-
34147150205
-
Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans
-
DOI 10.1172/JCI30328
-
Van Wesenbeeck L., Odgren PR, Coxon FP et al. Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans. J Clin Invest 2007; 117: 919-930. (Pubitemid 46556748)
-
(2007)
Journal of Clinical Investigation
, vol.117
, Issue.4
, pp. 919-930
-
-
Van Wesenbeeck, L.1
Odgren, P.R.2
Coxon, F.P.3
Frattini, A.4
Moens, P.5
Perdu, B.6
MacKay, C.A.7
Van Hul, E.8
Timmermans, J.-P.9
Vanhoenacker, F.10
Jacobs, R.11
Peruzzi, B.12
Teti, A.13
Helfrich, M.H.14
Rogers, M.J.15
Villa, A.16
Van Hul, W.17
-
24
-
-
39749179636
-
A new heterozygous mutation (R714C) of the osteopetrosis gene, Pleckstrin homolog domain containing family M (with run domain) member 1 (PLEKHM1), impairs vesicular acidification and increases TRACP secretion in osteoclasts
-
DOI 10.1359/jbmr.071107
-
Del Fattore A, Fornari R, Van WL et al. A new heterozygous mutation (R714C) of the osteopetrosis gene, pleckstrin homolog domain containing family M (with run domain) member 1 (PLEKHM1), impairs vesicular acidification and increases TRACP secretion in osteoclasts. J Bone Miner Res 2008; 23: 380-391. (Pubitemid 351304668)
-
(2008)
Journal of Bone and Mineral Research
, vol.23
, Issue.3
, pp. 380-391
-
-
Del, F.A.1
Fornari, R.2
Van Wesenbeeck, L.3
De Freitas, F.4
Timmermans, J.-P.5
Peruzzi, B.6
Cappariello, A.7
Rucci, N.8
Spera, G.9
Helfrich, M.H.10
Van Hul, W.11
Migliaccio, S.12
Teti, A.13
-
25
-
-
34547521058
-
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL
-
DOI 10.1038/ng2076, PII NG2076
-
Sobacchi C, Frattini A, Guerrini MM et al. Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKL. Nat Genet 2007; 39: 960-962. (Pubitemid 47185178)
-
(2007)
Nature Genetics
, vol.39
, Issue.8
, pp. 960-962
-
-
Sobacchi, C.1
Frattini, A.2
Guerrini, M.M.3
Abinun, M.4
Pangrazio, A.5
Susani, L.6
Bredius, R.7
Mancini, G.8
Cant, A.9
Bishop, N.10
Grabowski, P.11
Del, F.A.12
Messina, C.13
Errigo, G.14
Coxon, F.P.15
Scott, D.I.16
Teti, A.17
Rogers, M.J.18
Vezzoni, P.19
Villa, A.20
Helfrich, M.H.21
more..
-
26
-
-
46349084493
-
Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations
-
DOI 10.1016/j.ajhg.2008.06.015, PII S0002929708003637
-
Guerrini MM, Sobacchi C, Cassani B et al. Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutations. Am J Hum Genet 2008; 83: 64-76. (Pubitemid 351916706)
-
(2008)
American Journal of Human Genetics
, vol.83
, Issue.1
, pp. 64-76
-
-
Guerrini, M.M.1
Sobacchi, C.2
Cassani, B.3
Abinun, M.4
Kilic, S.S.5
Pangrazio, A.6
Moratto, D.7
Mazzolari, E.8
Clayton-Smith, J.9
Orchard, P.10
Coxon, F.P.11
Helfrich, M.H.12
Crockett, J.C.13
Mellis, D.14
Vellodi, A.15
Tezcan, I.16
Notarangelo, L.D.17
Rogers, M.J.18
Vezzoni, P.19
Villa, A.20
Frattini, A.21
more..
-
27
-
-
0026409519
-
Morphologic features of bone in human osteopetrosis
-
Helfrich MH, Aronson DC, Everts V et al. Morphologic features of bone in human osteopetrosis. Bone 1991; 12: 411-419.
-
(1991)
Bone
, vol.12
, pp. 411-419
-
-
Helfrich, M.H.1
Aronson, D.C.2
Everts, V.3
-
28
-
-
34249751708
-
Are nonresorbing osteoclasts sources of bone anabolic activity?
-
DOI 10.1359/jbmr.070109
-
Karsdal MA, Martin TJ, Bollerslev J et al. Are nonresorbing osteoclasts sources of bone anabolic activity? J Bone Miner Res 2007; 22: 487-494. (Pubitemid 47457424)
-
(2007)
Journal of Bone and Mineral Research
, vol.22
, Issue.4
, pp. 487-494
-
-
Karsdal, M.A.1
Martin, T.J.2
Bollerslev, J.3
Christiansen, C.4
Henriksen, K.5
-
29
-
-
46349084493
-
Human Osteoclast-Poor Osteopetrosis with Hypogammaglobulinemia due to TNFRSF11A (RANK) Mutations
-
DOI 10.1016/j.ajhg.2008.06.015, PII S0002929708003637
-
Guerrini MM, Sobacchi C, Cassani B et al. Human osteoclast-poor osteopetrosis with hypogammaglobulinemiadue to TNFRSF11A (RANK) mutations. Am J Hum Genet 2008; 83: 64-76. (Pubitemid 351916706)
-
(2008)
American Journal of Human Genetics
, vol.83
, Issue.1
, pp. 64-76
-
-
Guerrini, M.M.1
Sobacchi, C.2
Cassani, B.3
Abinun, M.4
Kilic, S.S.5
Pangrazio, A.6
Moratto, D.7
Mazzolari, E.8
Clayton-Smith, J.9
Orchard, P.10
Coxon, F.P.11
Helfrich, M.H.12
Crockett, J.C.13
Mellis, D.14
Vellodi, A.15
Tezcan, I.16
Notarangelo, L.D.17
Rogers, M.J.18
Vezzoni, P.19
Villa, A.20
Frattini, A.21
more..
-
30
-
-
37349108189
-
Genetics, pathogenesis and complications of osteopetrosis
-
Del Fattore A, Cappariello A, Teti A. Genetics, pathogenesis and complications of osteopetrosis. Bone 2008; 42:1 9-29.
-
(2008)
Bone
, vol.42
, pp. 19-29
-
-
Del Fattore, A.1
Cappariello, A.2
Teti, A.3
-
31
-
-
17144463459
-
Mechanisms of osteoclast dysfunction in human osteopetrosis: Abnormal osteoclastogenesis and lack of osteoclast-specific adhesion structures
-
Teti A, Migliaccio S, Taranta A et al. Mechanisms of osteoclast dysfunction in human osteopetrosis: abnormal osteoclastogenesis and lack of osteoclastspecific adhesion structures. J Bone Miner Res 1999; 14: 2107-2117. (Pubitemid 30026960)
-
(1999)
Journal of Bone and Mineral Research
, vol.14
, Issue.12
, pp. 2107-2117
-
-
Teti, A.1
Migliaccio, S.2
Taranta, A.3
Bernardini, S.4
De Rossi, G.5
Luciani, M.6
Iacobini, M.7
De Felice, L.8
Boldrini, R.9
Bosman, C.10
Corsi, A.11
Bianco, P.12
-
32
-
-
69349087894
-
Osteopetrosis with micro-lacunar resorption because of defective integrin organization
-
Blair HC, Yaroslavskiy BB, Robinson LJ et al. Osteopetrosis with micro-lacunar resorption because of defective integrin organization. Lab Invest 2009; 89: 1007-1017.
-
(2009)
Lab Invest
, vol.89
, pp. 1007-1017
-
-
Blair, H.C.1
Yaroslavskiy, B.B.2
Robinson, L.J.3
-
33
-
-
37049239211
-
Osteopetrosis cured by temporary parabiosis
-
Walker DG. Osteopetrosis cured by temporary parabiosis. Science 1973; 180: 875.
-
(1973)
Science
, vol.180
, pp. 875
-
-
Walker, D.G.1
-
34
-
-
0016811449
-
Bone resorption restored in osteopetrotic mice by transplants of normal bone marrow and spleen cells
-
Walker DG. Bone resorption restored in osteopetrotic mice by transplants of normal bone marrow and spleen cells. Science 1975; 190: 784-785.
-
(1975)
Science
, vol.190
, pp. 784-785
-
-
Walker, D.G.1
-
35
-
-
0018891088
-
Successful bone-marrow transplantation for infantile malignant osteopetrosis
-
Coccia PF, Krivit W, Cervenka J et al. Successful bone-marrow transplantation for infantile malignant osteopetrosis. N Engl J Med 1980; 302: 701-708. (Pubitemid 10132096)
-
(1980)
New England Journal of Medicine
, vol.302
, Issue.13
, pp. 701-708
-
-
Coccia, P.F.1
Krivit, W.2
Cervenka, J.3
-
36
-
-
0029809357
-
Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency
-
Gelb BD, Shi GP, Chapman HA, Desnick RJ. Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency. Science 1996; 273: 1236-1238.
-
(1996)
Science
, vol.273
, pp. 1236-1238
-
-
Gelb, B.D.1
Shi, G.P.2
Chapman, H.A.3
Desnick, R.J.4
-
37
-
-
38749144762
-
The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K
-
DOI 10.1016/j.bmcl.2007.12.047, PII S0960894X07015065
-
Gauthier JY, Chauret N, Cromlish W et al. The discovery of odanacatib (MK-0822), a selective inhibitor of cathepsin K. Bioorg Med Chem Lett 2008; 18: 923-928. (Pubitemid 351179363)
-
(2008)
Bioorganic and Medicinal Chemistry Letters
, vol.18
, Issue.3
, pp. 923-928
-
-
Gauthier, J.Y.1
Chauret, N.2
Cromlish, W.3
Desmarais, S.4
Duong, L.T.5
Falgueyret, J.-P.6
Kimmel, D.B.7
Lamontagne, S.8
Leger, S.9
LeRiche, T.10
Li, C.S.11
Masse, F.12
McKay, D.J.13
Nicoll-Griffith, D.A.14
Oballa, R.M.15
Palmer, J.T.16
Percival, M.D.17
Riendeau, D.18
Robichaud, J.19
Rodan, G.A.20
Rodan, S.B.21
Seto, C.22
Therien, M.23
Truong, V.-L.24
Venuti, M.C.25
Wesolowski, G.26
Young, R.N.27
Zamboni, R.28
Black, W.C.29
more..
-
38
-
-
30744432094
-
The role of chloride channels in osteoclasts: ClC-7 as a target for osteoporosis treatment
-
DOI 10.1358/dnp.2005.18.8.944546
-
Schaller S, Henriksen K, Sorensen MG, Karsdal MA. The role of chloride channels in osteoclasts: ClC-7 as a target for osteoporosis treatment. Drug News Perspect 2005; 18: 489-495. (Pubitemid 43094116)
-
(2005)
Drug News and Perspectives
, vol.18
, Issue.8
, pp. 489-495
-
-
Schaller, S.1
Henriksen, K.2
Sorensen, M.G.3
Karsdal, M.A.4
-
39
-
-
38449105080
-
Diphyllin, a novel and naturally potent V-ATPase inhibitor, abrogates acidification of the osteoclastic resorption lacunae and bone resorption
-
DOI 10.1359/jbmr.070613
-
Sørensen MG, Henriksen K, Neutzsky-Wulff AV et al. Diphyllin, a novel and naturally potent V-ATPase inhibitor, abrogates acidification of the osteoclastic resorption lacunae and bone resorption. J Bone Miner Res 2007; 22: 1640-1648. (Pubitemid 351229334)
-
(2007)
Journal of Bone and Mineral Research
, vol.22
, Issue.10
, pp. 1640-1648
-
-
Sorensen, M.G.1
Henriksen, K.2
Neutzsky-Wulff, A.V.3
Dziegiel, M.H.4
Karsdal, M.A.5
-
40
-
-
10244259169
-
Immature dendritic cell transdifferentiation into osteoclasts: A novel pathway sustained by the rheumatoid arthritis microenvironment
-
DOI 10.1182/blood-2004-01-0041
-
Rivollier A, Mazzorana M, Tebib J et al. Immature dendritic cell transdifferentiation into osteoclasts: a novel pathway sustained by the rheumatoid arthritis microenvironment. Blood 2004; 104: 4029-4037. (Pubitemid 39620153)
-
(2004)
Blood
, vol.104
, Issue.13
, pp. 4029-4037
-
-
Rivollier, A.1
Mazzorana, M.2
Tebib, J.3
Piperno, M.4
Aitsiselmi, T.5
Rabourdin-Combe, C.6
Jurdic, P.7
Servet-Delprat, C.8
|