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Genetics of osteoporosis: accelerating pace in gene identification and validation.

Genetics of osteoporosis: accelerating pace in gene identification and validation.

http://www.wikidata.org/entity/Q37681343

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Bone overgrowth-associated mutations in the LRP4 gene impair sclerostin facilitator function Functional relevance of the BMD-associated polymorphism rs312009: novel involvement of RUNX2 in LRP5 transcriptional regulation Gene expression profiling suggests a pathological role of human bone marrow-derived mesenchymal stem cells in aging-related skeletal diseases Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)Gender-specific DNA methylome analysis of a Han Chinese longevity population Association of LRP5 genotypes with osteoporosis in Tunisian post-menopausal women Synopsis and meta-analysis of genetic association studies in osteoporosis for the focal adhesion family genes: the CUMAGAS-OSTEOporosis information system.The transcriptional profile of mesenchymal stem cell populations in primary osteoporosis is distinct and shows overexpression of osteogenic inhibitors The genetics of bone loss: challenges and prospects Relationship between CATSPERB, NR5A2 gene polymorphisms and Peak Bone Mineral Density in College Students in China Gene expression changes in human mesenchymal stem cells from patients with osteoporosis.Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women.Value of rare low bone mass diseases for osteoporosis genetics.Genome-wide approaches for identifying genetic risk factors for osteoporosis.OPG rs2073617 polymorphism is associated with upregulated OPG protein expression and an increased risk of intervertebral disc degeneration Clinical impact of recent genetic discoveries in osteoporosis.Genetic factors influencing bone mineral content in a black South African population.A Candidate Gene Association Study of Bone Mineral Density in an Iranian Population.The role of midkine in skeletal remodelling.Pharmacogenetics of osteoporosis-related bone fractures: moving towards the harmonization and validation of polymorphism diagnostic tools.The Lrp4R1170Q Homozygous Knock-In Mouse Recapitulates the Bone Phenotype of Sclerosteosis in Humans.Connecting Bone and Fat: The Potential Role for Sclerostin.Polymorphisms in VDR gene in Tunisian postmenopausal women are associated with osteopenia phenotype.Association between vitamin D receptor gene polymorphisms and bone mineral density in Chinese women.The genetic profile of bone repair.Single nucleotide polymorphism 6q25.1 rs2046210 and increased risk of breast cancer.Replication study of three functional polymorphisms associated with bone mineral density in a cohort of Spanish women.Association of MTHFR C667T polymorphism with bone mineral density and fracture risk: an updated meta-analysis.MHC class II transactivator is an in vivo regulator of osteoclast differentiation and bone homeostasis co-opted from adaptive immunity.An Optimized Method to Generate Human Active Osteoclasts From Peripheral Blood Monocytes.Effects of Type 2 Diabetic Serum on Proliferation and Osteogenic Differentiation of Mesenchymal Stem Cells.Association of Vitamin D Receptor (FokI and BsmI) Gene Polymorphism with Bone Mineral Density and Their Effect on 25-Hydroxyvitamin D Level in North Indian Postmenopausal Women with Osteoporosis The Relationship between Polymorphisms in the Vitamin D Receptor Gene and Bone Mineral Density in Postmenopausal Women

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Genetics of osteoporosis: accelerating pace in gene identification and validation.

http://www.wikidata.org/entity/Q37681343

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 12 December 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Genetics of osteoporosis: accelerating pace in gene identification and validation.

@en

Genetics of osteoporosis: accelerating pace in gene identification and validation.

@nl

type

label

Genetics of osteoporosis: accelerating pace in gene identification and validation.

@en

Genetics of osteoporosis: accelerating pace in gene identification and validation.

@nl

prefLabel

Genetics of osteoporosis: accelerating pace in gene identification and validation.

@en

Genetics of osteoporosis: accelerating pace in gene identification and validation.

@nl

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Genetics of osteoporosis: accelerating pace in gene identification and validation.

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Bin Yu

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Claude Férec

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Jian-Min Chen

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Meng-Meng Li

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Shu-Xun Hou

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Wen-Feng Li

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P2860

Two single nucleotide polymorphisms in the CYP17 and COMT Genes--relation to bone mass and longitudinal bone changes in postmenopausal women with or without hormone replacement therapy. The Danish Osteoporosis Prevention Study.

Collaborative meta-analysis: associations of 150 candidate genes with osteoporosis and osteoporotic fracture.

Reduced inflammation and tissue damage in transgenic rabbits overexpressing 15-lipoxygenase and endogenous anti-inflammatory lipid mediators.

The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis.

Structure and function of claudins.

Eph receptors and ephrin signaling pathways: a role in bone homeostasis.

Roles of bone morphogenetic protein type I receptors and Smad proteins in osteoblast and chondroblast differentiation.

Diminished callus size and cartilage synthesis in alpha 1 beta 1 integrin-deficient mice during bone fracture healing.

Association of a single-nucleotide polymorphism in low-density lipoprotein receptor-related protein 5 gene with bone mineral density.

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10.1007/S00439-009-0773-Z

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