Genetics and Epigenetics

ba0005p233 | Genetics and Epigenetics

Differentially methylated regions in gene enhancers of mesenchymal stem cells from osteoporotic patients

ba0005p234 | Genetics and Epigenetics

SNP regulation of miRNA expression and its association with osteoporosis

ba0005p235 | Genetics and Epigenetics

Periostin serum levels and gene polymorphism are associated with bone microarchitecture

ba0005p236 | Genetics and Epigenetics

Interaction between periostin gene (Postn) and other gene polymorphism involved in periostin expression and activity on bone microstructure in humans

ba0005p237 | Genetics and Epigenetics

Association among oxidative stress, Wnt signaling and trabecular bone microstructure in osteoporosis and osteoarthritis

ba0005p238 | Genetics and Epigenetics

Genetic variants at the Wnt/β-catenin and oestrogen receptor signalling pathways are associated with low bone mineral density in dancers

ba0005p239 | Genetics and Epigenetics

Search for BMD-related variants of DKK1 and SOST by resequencing in the BARCOS cohort

ba0005p240 | Genetics and Epigenetics

Analysis of the polyalanine repeat polymorphism in the RUNX2 gene in relation to bone mineral density and fracture risk in Maltese postmenopausal women

ba0005p241 | Genetics and Epigenetics

Identification of a novel locus on 2q13 of large effect size which predisposes to clinical vertebral fractures independently of BMD: the GEFOS consortium

ba0005p242 | Genetics and Epigenetics

A family with Paget disease of bone caused by a novel mutation of hnRNPA2B1 gene

ba0005p243 | Genetics and Epigenetics

Geometric morphometrics: a mathematical tool to compare morphological traits based on SOST dysfunction in mice

ba0005p244 | Genetics and Epigenetics

NBAS is the gene mutated in two patients affected by Acrofrontofacionasal Dysostosis type 1

ba0005p245 | Genetics and Epigenetics

Circulating microRNAs in postmenopausal women with osteoporosis and vertebral fractures

ba0005p246 | Genetics and Epigenetics

In a population based association study: IAPP gene variants are not associated with bone phenotypes in elderly women

ba0005p247 | Genetics and Epigenetics

Common variants in Rspo 1,2 and 3 do not associate with BMD in stratified subpopulations of the Odense Androgen Study and mutations in these genes are not a common cause of craniotubular hyperostosis

ba0005p248 | Genetics and Epigenetics

Identification and functional validation of microRNA expression in human bone tissue

ba0005p249 | Genetics and Epigenetics

Identification of epigenomic regulators of osteoblast function

ba0005p250 | Genetics and Epigenetics

Advancing maternal age at childbirth is associated with less favourable trabecular bone mineral density and tibial cortical bone geometry in young adult male offspring

ba0005p251 | Genetics and Epigenetics

Polymorphism of vitamin D receptor gene, estrogen receptor gene and collagen type I α1 gene for osteoporosis in Ukrainian women

ba0005p256 | Genetics and Epigenetics

OPTN and CCDC3 share a bidirectional promoter region that is regulated by NfkB

ba0005p257 | Genetics and Epigenetics

Bone Abstracts

43rd Annual European Calcified Tissue Society Congress

Poster Presentations

Differentially methylated regions in gene enhancers of mesenchymal stem cells from osteoporotic patients

SNP regulation of miRNA expression and its association with osteoporosis

Periostin serum levels and gene polymorphism are associated with bone microarchitecture

Interaction between periostin gene (Postn) and other gene polymorphism involved in periostin expression and activity on bone microstructure in humans

Association among oxidative stress, Wnt signaling and trabecular bone microstructure in osteoporosis and osteoarthritis

Genetic variants at the Wnt/β-catenin and oestrogen receptor signalling pathways are associated with low bone mineral density in dancers

Search for BMD-related variants of DKK1 and SOST by resequencing in the BARCOS cohort

Analysis of the polyalanine repeat polymorphism in the RUNX2 gene in relation to bone mineral density and fracture risk in Maltese postmenopausal women

Identification of a novel locus on 2q13 of large effect size which predisposes to clinical vertebral fractures independently of BMD: the GEFOS consortium

A family with Paget disease of bone caused by a novel mutation of hnRNPA2B1 gene

Geometric morphometrics: a mathematical tool to compare morphological traits based on SOST dysfunction in mice

NBAS is the gene mutated in two patients affected by Acrofrontofacionasal Dysostosis type 1

Circulating microRNAs in postmenopausal women with osteoporosis and vertebral fractures

In a population based association study: IAPP gene variants are not associated with bone phenotypes in elderly women

Common variants in Rspo 1,2 and 3 do not associate with BMD in stratified subpopulations of the Odense Androgen Study and mutations in these genes are not a common cause of craniotubular hyperostosis

Identification and functional validation of microRNA expression in human bone tissue

Identification of epigenomic regulators of osteoblast function

Advancing maternal age at childbirth is associated with less favourable trabecular bone mineral density and tibial cortical bone geometry in young adult male offspring

Establishment of an in vivo model to examine the osteoanabolic epigenome

Mitochondrial DNA point mutation is associated with lower bone turnover markers

Investigating the osteoanabolic epigenome of aging-related bone loss in humans

Genetic risk factors for knee osteoarthritis in postmenopausal ukrainian women

Polymorphism of vitamin D receptor gene, estrogen receptor gene and collagen type I α1 gene for osteoporosis in Ukrainian women

OPTN and CCDC3 share a bidirectional promoter region that is regulated by NfkB

Comparative analysis of human and zebrafish OPTN: molecular and evolutionary perspectives

BiosciAbstracts