Functional relevance of the BMD-associated polymorphism rs312009: Novel Involvement of RUNX2 in LRP5 transcriptional regulation-Reference-Cited by-同舟云学术

Functional relevance of the BMD-associated polymorphism rs312009: Novel Involvement of RUNX2 in LRP5 transcriptional regulation

Published:2011-05 Issue:5 Volume:26 Page:1133-1144
ISSN:0884-0431
Container-title:Journal of Bone and Mineral Research
language:en
Short-container-title:J Bone Miner Res

Author:

Agueda Lídia,Velázquez-Cruz Rafael,Urreizti Roser,Yoskovitz Guy,Sarrión Patricia,Jurado Susana,Güerri Roberto,Garcia-Giralt Natàlia,Nogués Xavier,Mellibovsky Leonardo,Díez-Pérez Adolfo,Marie Pierre J,Balcells Susana,Grinberg Daniel

Publisher

Wiley

Subject

Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference41 articles.

1. LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development;Gong;Cell.,2001

2. A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait;Little;Am J Hum Genet.,2002

3. Genetic regulation of bone mass and susceptibility to osteoporosis;Ralston;Genes Dev.,2006

4. Regulation of bone mass by Wnt signaling;Krishnan;J Clin Invest.,2006

5. Transcriptional control of skeletogenesis;Karsenty;Annu Rev Genomics Hum Genet.,2008

Cited by 14 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. Polymorphisms in the Runx2 and osteocalcin genes affect BMD in postmenopausal women: a systematic review and meta-analysis;Endocrine;2023-12-06

2. WNT signaling in skeletal homeostasis and diseases;Marcus and Feldman's Osteoporosis;2021

3. The importance of the Wnt/β-catenin pathway and LRP5 protein in bone metabolism of postmenopausal women;Advances in Clinical and Experimental Medicine;2019-02-28

4. Light-Controlled BMSC Sheet–Implant Complexes with Improved Osteogenesis via an LRP5/β-Catenin/Runx2 Regulatory Loop;ACS Applied Materials & Interfaces;2017-09-26

5. New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss;Human Mutation;2017-08-01