Genetic studies in osteoporosis: The end of the beginning


Autoria(s): Duncan, Emma L.; Brown, Matthew A.
Data(s)

12/09/2008

Resumo

Osteoporosis and disorders of bone fragility are highly heritable, but despite much effort the identities of few of the genes involved has been established. Recent developments in genetics such as genome-wide association studies are revolutionizing research in this field, and it is likely that further contributions will be made through application of next-generation sequencing technologies, analysis of copy number variation polymorphisms, and high-throughput mouse mutagenesis programs. This article outlines what we know about osteoporosis genetics to date and the probable future directions of research in this field.

Formato

application/pdf

Identificador

http://eprints.qut.edu.au/87867/

Publicador

BioMed Central

Relação

http://eprints.qut.edu.au/87867/1/87867.pdf

DOI:10.1186/ar2479

Duncan, Emma L. & Brown, Matthew A. (2008) Genetic studies in osteoporosis: The end of the beginning. Arthritis Research and Therapy, 10(5), Artical Number:-214.

Direitos

Copyright 2008 The Author(s)

Fonte

School of Biomedical Sciences; Faculty of Health; Institute of Health and Biomedical Innovation

Palavras-Chave #alkaline phosphatase #calcium sensing receptor #carbonate dehydratase II #cathepsin K #chloride channel #collagen type 1 #low density lipoprotein receptor related protein 5 #membrane protein #osteoprotegerin #oxygenase #procollagen lysine 2 oxoglutarate 5 dioxygenase #receptor activator of nuclear factor kappa B #sclerostin #bone fragility #gene number #gene technology #genetic association #genetic identification #genetic polymorphism #genetic susceptibility #genetic variability #high throughput screening #human #mutagenesis #nonhuman #osteoporosis #prevalence #review #sequence analysis #animal #clinical trial #genetic predisposition #genetics #Animals #Clinical Trials as Topic #Genetic Predisposition to Disease #Humans
Tipo

Journal Article