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Engagement of the Osteoclast Integrin α<sub>v</sub>β<sub>3</sub> by Osteopontin Stimulates Phosphatidylinositol 3-Hydroxyl Kinase Activity<sup>a</sup><sup>b</sup>.
- Published in:
- Annals of the New York Academy of Sciences, 1995, v. 760, n. 1, p. 151, doi. 10.1111/j.1749-6632.1995.tb44627.x
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- Publication type:
- Article
Multicentric carpotarsal osteolysis syndrome is caused by only a few domain-specific mutations in MAFB, a negative regulator of RANKL-induced osteoclastogenesis.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 9, p. 2287, doi. 10.1002/ajmg.a.36641
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- Publication type:
- Article
Dysosteosclerosis Presents as an "Osteoclast-Poor" Form of Osteopetrosis: Comprehensive Investigation of a 3-Year-Old Girl and Literature Review.
- Published in:
- 2010
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- Publication type:
- Case Study
ATRAID regulates the action of nitrogen-containing bisphosphonates on bone.
- Published in:
- Science Translational Medicine, 2020, v. 12, n. 544, p. 1, doi. 10.1126/scitranslmed.aav9166
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- Article
X‐Linked Hypophosphatemia: Uniquely Mild Disease Associated With PHEX 3′‐UTR Mutation c.*231A>G (A Retrospective Case–Control Study).
- Published in:
- Journal of Bone & Mineral Research, 2020, v. 35, n. 5, p. 920, doi. 10.1002/jbmr.3955
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- Publication type:
- Article
PHEX 3′-UTR c.*231A>G Near The Polyadenylation Signal is a Relatively Common, Mild, American Mutation That Masquerades as Sporadic or X-Linked Recessive Hypophosphatemic Rickets.
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- Journal of Bone & Mineral Research, 2015, v. 30, n. 1, p. 137, doi. 10.1002/jbmr.2307
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- Publication type:
- Article
Dysosteosclerosis: Clinical and Radiological Evolution Reflecting Genetic Heterogeneity.
- Published in:
- JBMR Plus, 2022, v. 6, n. 8, p. 1, doi. 10.1002/jbm4.10663
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- Publication type:
- Article