Activation of RANK/RANKL/OPG Pathway Is Involved in the Pathophysiology of Fibrous Dysplasia and Associated With Disease Burden-Reference-Cited by-同舟云学术

Activation of RANK/RANKL/OPG Pathway Is Involved in the Pathophysiology of Fibrous Dysplasia and Associated With Disease Burden

Published:2018-11-29 Issue:2 Volume:34 Page:290-294
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

de Castro Luis F¹,Burke Andrea B¹²,Wang Howard D¹³,Tsai Jeffrey¹²,Florenzano Pablo¹⁴,Pan Kristen S¹³,Bhattacharyya Nisan¹,Boyce Alison M¹,Gafni Rachel I¹,Molinolo Alfredo A⁵,Robey Pamela G⁶,Collins Michael T¹

Affiliation:

1. Skeletal Disorders and Mineral Homeostasis SectionNational Institute of Dental and Craniofacial ResearchNational Institutes of HealthBethesdaMDUSA

2. Department of Oral and Maxillofacial SurgeryUniversity of Washington School of DentistrySeattleWAUSA

3. Medical Research Scholars Program (MRSP)National Institutes of HealthBethesdaMDUSA

4. Department of EndocrinologySchool of MedicinePontificia Universidad Catolica de ChileSantiagoChile

5. Biorepository and Tissue Technology Shared ResourceMoores Cancer CenterUniversity of CaliforniaSan Diego, La JollaCAUSA

6. Skeletal Biology SectionNational Institute of Dental and Craniofacial ResearchNational Institutes of HealthBethesdaMDUSA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jbmr.3602

Reference20 articles.

1. Activating Mutations of the Stimulatory G Protein in the McCune–Albright Syndrome

2. Fibrous Dysplasia as a Stem Cell Disease

3. The histopathology of fibrous dysplasia of bone in patients with activating mutations of the Gs? gene: site-specific patterns and recurrent histological hallmarks

4. An Instrument to Measure Skeletal Burden and Predict Functional Outcome in Fibrous Dysplasia of Bone

5. Transfer, Analysis and Reversion of the Fibrous Dysplasia Cellular Phenotype in Human Skeletal Progenitors

Cited by 72 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Craniomaxillofacial Fibro-osseous Lesions in Children;Oral and Maxillofacial Surgery Clinics of North America;2024-08

2. A Mathematical Model for Fibrous Dysplasia: The Role of the Flow of Mutant Cells;Bulletin of Mathematical Biology;2024-07-15

3. Rankl genetic deficiency and functional blockade undermine skeletal stem and progenitor cell differentiation;Stem Cell Research & Therapy;2024-07-06

4. Vitamin D Attenuates Fibrotic Properties of Fibrous Dysplasia-Derived Cells for the Transit towards Osteocytic Phenotype;International Journal of Molecular Sciences;2024-05-01

5. Transcriptomic Signature and Pro-Osteoclastic Secreted Factors of Abnormal Bone-Marrow Stromal Cells in Fibrous Dysplasia;Cells;2024-04-30