Oxidative-stress-related genes in osteoporosis: a systematic review

G León-Reyes, AD Argoty-Pantoja, A Becerra-Cervera… - Antioxidants, 2023 - mdpi.com
Osteoporosis is characterized by a decline in bone mineral density (BMD) and increased
fracture risk. Free radicals and antioxidant systems play a central role in bone remodeling …

The insulin-like growth factor-I gene and osteoporosis: a critical appraisal

T Niu, CJ Rosen - Gene, 2005 - Elsevier
Osteoporosis, a disorder of skeletal fragility, is common in the elderly, and its prevalence is
increasing as more individuals with low bone mineral density (BMD), the strongest predictor …

How is mRNA expression predictive for protein expression? A correlation study on human circulating monocytes

Y Guo, P Xiao, S Lei, F Deng, GG Xiao… - Acta biochimica et …, 2008 - Wiley Online Library
A key assumption in studying mRNA expression is that it is informative in the prediction of
protein expression. However, only limited studies have explored the mRNA‐protein …

Linkage of Osteoporosis to Chromosome 20p12 and Association to BMP2

U Styrkarsdottir, JB Cazier, A Kong, O Rolfsson… - PLoS …, 2003 - journals.plos.org
Osteoporotic fractures are a major cause of morbidity and mortality in ageing populations.
Osteoporosis, defined as low bone mineral density (BMD) and associated fractures, have …

Genome-wide copy-number-variation study identified a susceptibility gene, UGT2B17, for osteoporosis

TL Yang, XD Chen, Y Guo, SF Lei, JT Wang… - The American Journal of …, 2008 - cell.com
Osteoporosis, a highly heritable disease, is characterized mainly by low bone-mineral
density (BMD), poor bone geometry, and/or osteoporotic fractures (OF). Copy-number …

Danon's disease as a cause of hypertrophic cardiomyopathy: a systematic survey

P Charron, E Villard, P Sebillon, P Laforêt… - Journal of Medical …, 2004 - jmg.bmj.com
Background: Hypertrophic cardiomyopathy (HCM) is an autosomal dominant disease
caused by mutations in sarcomeric genes. However, extensive genetic screening failed to …

Heterozygous Mutations in the LDL Receptor‐Related Protein 5 (LRP5) Gene Are Associated With Primary Osteoporosis in Children

H Hartikka, O Mäkitie, M Männikkö… - Journal of bone and …, 2005 - academic.oup.com
Three of 20 patients with juvenile osteoporosis were found to have a heterozygous mutation
in the LRP5 gene. No mutations were found in the type I collagen genes. Mutations in the …

Mutations in the insulin‐like factor 3 receptor are associated with osteoporosis

A Ferlin, A Pepe, L Gianesello, A Garolla… - Journal of Bone and …, 2008 - academic.oup.com
Abstract Introduction: Insulin‐like factor 3 (INSL3) is produced primarily by testicular Leydig
cells. It acts by binding to its specific G protein–coupled receptor RXFP2 (relaxin family …

The insulin-like growth factor system in bone: basic and clinical implications

M Kawai, CJ Rosen - Endocrinology and metabolism clinics of North …, 2012 - Elsevier
The insulin-like growth factor (IGF) regulatory system is critical for skeletal growth and
maintenance. Initially there was great hope that the recombinant IGFs might be used …

Genetics of osteoporosis: accelerating pace in gene identification and validation

WF Li, SX Hou, B Yu, MM Li, C Férec, JM Chen - Human genetics, 2010 - Springer
Osteoporosis is characterized by low bone mineral density and structural deterioration of
bone tissue, leading to an increased risk of fractures. It is the most common metabolic bone …