[HTML][HTML] Long noncoding RNAs: a missing link in osteoporosis

AM Silva, SR Moura, JH Teixeira, MA Barbosa… - Bone research, 2019 - nature.com
Osteoporosis is a systemic disease that results in loss of bone density and increased
fracture risk, particularly in the vertebrae and the hip. This condition and associated …

Molecular genetics and economics

JP Beauchamp, D Cesarini, M Johannesson… - Journal of Economic …, 2011 - aeaweb.org
The costs of comprehensively genotyping human subjects have fallen to the point where
major funding bodies, even in the social sciences, are beginning to incorporate genetic and …

[HTML][HTML] Control of osteocyte dendrite formation by Sp7 and its target gene osteocrin

JS Wang, T Kamath, CM Mazur… - Nature …, 2021 - nature.com
Some osteoblasts embed within bone matrix, change shape, and become dendrite-bearing
osteocytes. The circuitry that drives dendrite formation during “osteocytogenesis” is poorly …

[HTML][HTML] An osteoporosis risk SNP at 1p36. 12 acts as an allele-specific enhancer to modulate LINC00339 expression via long-range loop formation

XF Chen, DL Zhu, M Yang, WX Hu, YY Duan… - The American Journal of …, 2018 - cell.com
Genome-wide association studies (GWASs) have reproducibly associated variants within
intergenic regions of 1p36. 12 locus with osteoporosis, but the functional roles underlying …

Endocrine crosstalk between muscle and bone

M Brotto, ML Johnson - Current osteoporosis reports, 2014 - Springer
The musculoskeletal system is a complex organ comprised of the skeletal bones, skeletal
muscles, tendons, ligaments, cartilage, joints, and other connective tissue that physically …

[HTML][HTML] MEF2C regulates osteoclastogenesis and pathologic bone resorption via c-FOS

T Fujii, K Murata, SH Mun, S Bae, YJ Lee, T Pannellini… - Bone Research, 2021 - nature.com
Osteoporosis is a metabolic bone disease with dysregulated coupling between bone
resorption and bone formation, which results in decreased bone mineral density. The …

Common variants at 12q15 and 12q24 are associated with infant head circumference

HR Taal, B St Pourcain, E Thiering, S Das… - Nature …, 2012 - nature.com
To identify genetic variants associated with head circumference in infancy, we performed a
meta-analysis of seven genome-wide association studies (GWAS)(N= 10,768 individuals of …

[HTML][HTML] A comprehensive overview of skeletal phenotypes associated with alterations in Wnt/β-catenin signaling in humans and mice

KA Maupin, CJ Droscha, BO Williams - Bone Research, 2013 - nature.com
The Wnt signaling pathway plays key roles in differentiation and development and
alterations in this signaling pathway are causally associated with numerous human …

Genome-wide association studies of skeletal phenotypes: what we have learned and where we are headed

YH Hsu, DP Kiel - The Journal of Clinical Endocrinology & …, 2012 - academic.oup.com
Context: The primary goals of genome-wide association studies (GWAS) are to discover new
molecular and biological pathways involved in the regulation of bone metabolism that can …

[HTML][HTML] Epigenetic mechanisms in bone

P Vrtačnik, J Marc, B Ostanek - Clinical Chemistry and Laboratory …, 2014 - degruyter.com
Epigenetics refers to the study of mechanisms able to influence gene expression in a stable
and potentially heritable manner without altering the DNA sequence. These mechanisms …