This is an in silico analysis of data available from genome-wide scans. Through analysis of QTL, genes and polymorphisms that regulate BMD, we identified 82 BMD QTL, 191 BMD-associated (BMDA) genes, and 83 genes containing known BMD-associated polymorphisms (BMDAP). The catalogue of all BMDA/BMDAP genes and relevant literatures are provided. In total, there are substantially more BMDA/BMDAP genes in regions of the genome where QTL have been identified than in non-QTL regions. Among 191 BMDA genes and 83 BMDAP genes, 133 and 58 are localized in QTL regions, respectively. The difference was still noticeable for the chromosome distribution of these genes between QTL and non-QTL regions. These results have allowed us to generate an int...
QTL analyses identified several chromosomal regions influencing skeletal phenotypes of the femur and...
Osteoporosis is a common aging-related disease diagnosed primarily using bone mineral density (BMD)....
International audienceThe genetic landscape of diseases associated with changes in bone mineral dens...
AbstractThis is an in silico analysis of data available from genome-wide scans. Through analysis of ...
Bone mineral density (BMD) is one of the strongest determinants of osteoporotic fracture risk. Over ...
Bone mineral density (BMD) is a heritable trait, and in mice, over 100 quantitative trait loci (QTLs...
ABSTRACT: BMD is highly heritable; however, little is known about the genes. To identify loci contro...
BMD is highly heritable; however, little is known about the genes. To identify loci controlling BMD,...
Identification of genes that regulate BMD will enhance our understanding of osteoporosis and could p...
Genetic analyses for loci regulating bone mineral density have been conducted in a cohort of F(2) mi...
Introduction: Previous studies have identified quantitative trait loci (QTL) that determine BMD in m...
Bone Mineral Density (BMD) is a complex trait likely determined by multiple genes. We attempted to i...
Osteoporosis, characterized by low levels of bone mineral density (BMD), is a prevalent medical cond...
The distal end of mouse chromosome 1 (Chr 1) harbors quantitative trait loci (QTLs) that regulate bo...
Osteoporosis, characterized by low levels of bone mineral density (BMD), is a prevalent medical cond...
QTL analyses identified several chromosomal regions influencing skeletal phenotypes of the femur and...
Osteoporosis is a common aging-related disease diagnosed primarily using bone mineral density (BMD)....
International audienceThe genetic landscape of diseases associated with changes in bone mineral dens...
AbstractThis is an in silico analysis of data available from genome-wide scans. Through analysis of ...
Bone mineral density (BMD) is one of the strongest determinants of osteoporotic fracture risk. Over ...
Bone mineral density (BMD) is a heritable trait, and in mice, over 100 quantitative trait loci (QTLs...
ABSTRACT: BMD is highly heritable; however, little is known about the genes. To identify loci contro...
BMD is highly heritable; however, little is known about the genes. To identify loci controlling BMD,...
Identification of genes that regulate BMD will enhance our understanding of osteoporosis and could p...
Genetic analyses for loci regulating bone mineral density have been conducted in a cohort of F(2) mi...
Introduction: Previous studies have identified quantitative trait loci (QTL) that determine BMD in m...
Bone Mineral Density (BMD) is a complex trait likely determined by multiple genes. We attempted to i...
Osteoporosis, characterized by low levels of bone mineral density (BMD), is a prevalent medical cond...
The distal end of mouse chromosome 1 (Chr 1) harbors quantitative trait loci (QTLs) that regulate bo...
Osteoporosis, characterized by low levels of bone mineral density (BMD), is a prevalent medical cond...
QTL analyses identified several chromosomal regions influencing skeletal phenotypes of the femur and...
Osteoporosis is a common aging-related disease diagnosed primarily using bone mineral density (BMD)....
International audienceThe genetic landscape of diseases associated with changes in bone mineral dens...