Differentially expressed genes in autosomal dominant osteopetrosis type II osteoclasts reveal known and novel pathways for osteoclast biology-Reference-Cited by-同舟云学术

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Differentially expressed genes in autosomal dominant osteopetrosis type II osteoclasts reveal known and novel pathways for osteoclast biology

Published:2013-12-16 Issue:3 Volume:94 Page:275-285
ISSN:0023-6837
Container-title:Laboratory Investigation
language:en
Short-container-title:Lab Invest

Author:

Coudert Amélie E,Del Fattore Andrea,Baulard Céline,Olaso Robert,Schiltz Corinne,Collet Corinne,Teti Anna,de Vernejoul Marie-Christine

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Pathology and Forensic Medicine

Link

http://www.nature.com/articles/labinvest2013140.pdf

Reference67 articles.

1. Del Fattore A, Cappariello A, Teti A . Genetics, pathogenesis and complications of osteopetrosis. Bone 2008;42:19–29.

2. de Vernejoul MC, Kornak U . Heritable sclerosing bone disorders: presentation and new molecular mechanisms. Ann N Y Acad Sci 2010;1192:269–277.

3. 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.

4. 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.

5. 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.

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