The Osteoclast—Not Always Guilty
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Physiology
Reference10 articles.
1. Successful Bone-Marrow Transplantation for Infantile Malignant Osteopetrosis
2. MACROPHAGE COLONY STIMULATING FACTOR RESTORESIN VIVOBONE RESORPTION IN THEOP/OPOSTEOPETROTIC MOUSE
3. Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis
4. OPGL is a key regulator of osteoclastogenesis, lymphocyte development and lymph-node organogenesis
5. Loss of the ClC-7 Chloride Channel Leads to Osteopetrosis in Mice and Man
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1. Deletion of Rheb1 in Osteocytes Leads to Osteopenia Characterized by Reduced Bone Formation and Enhanced Bone Resorption;DNA and Cell Biology;2022-07-01
2. A novel mutation in TNFRSF11A gene causes pediatric osteopetrosis: case report;BMC Surgery;2021-05-28
3. Osteoclastogenesis inhibition by mutated IGSF23 results in human osteopetrosis;Cell Proliferation;2019-09-27
4. Osteopetrosis: genetics, treatment and new insights into osteoclast function;Nature Reviews Endocrinology;2013-07-23
5. Targeting Bone Remodeling for the Treatment of Osteoporosis: Summary of the Proceedings of an ASBMR Workshop;Journal of Bone and Mineral Research;2009-03
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