Mosaic tetrasomy 20p associated with osteoporosis and recurrent fractures
ASA Maziad, LH Seaver - … Journal of Medical Genetics Part A, 2015 - Wiley Online Library
Tetrasomy 20p is a very rare chromosome abnormality, with only two single cases
previously reported in the literature, both fetuses with multiple congenital anomalies …
previously reported in the literature, both fetuses with multiple congenital anomalies …
[引用][C] Aus der Orthopädischen Klinik und Poliklinik der Universität Würzburg Direktor: Professor Dr. med. Maximilian Rudert
LS Kramer
Senyvo amžiaus žmonių vitamino D, kaulų mineralų tankio ir fizinio pajėgumo sąsajos bei VDR geno BsmI polimorfizmo ryšys su sunkia pomenopauzine osteoporoze
V Strazdienė - 2013 - epublications.vu.lt
Abstract [eng] There is conflicting evidence as to whether vitamin D deficiency contributes to
physical performance and muscle mass. Many studies have shown that the heritability of …
physical performance and muscle mass. Many studies have shown that the heritability of …
[PDF][PDF] Searching for the Molecular Pathways Regulating Bone Mineral Density in the Proteome and RNA Interference Era
FA Saad - J Orthopedics Rheumatol, 2013 - pdfs.semanticscholar.org
Osteoporosis is a polygenic disorder associated with low bone mineral density and
deterioration of bone microarchitecture with increased chance of bone fractures. Although …
deterioration of bone microarchitecture with increased chance of bone fractures. Although …
Family-based genetic analysis of osteoporosis
S Nguyen - 2014 - unsworks.unsw.edu.au
Osteoporosis is a common disease affecting a significant proportion of older people. Its
primary endpoint, fracture, results in severe outcomes including increased morbidity and …
primary endpoint, fracture, results in severe outcomes including increased morbidity and …
Identification of genes for complex diseases by integrating multiple types of genomic data
Combining multi-types of genomic data for integrative analyses can take advantage of
complementary information and thus can have higher power to identify genes/variables that …
complementary information and thus can have higher power to identify genes/variables that …
Decreased Expression of the Human Urea Transporter SLC14A1 in Bone is Induced by Cytokines and Stimulates Adipogenesis of Mesenchymal Progenitor Cells
M Komrakova, M Blaschke, ML Ponce… - Experimental and …, 2020 - thieme-connect.com
The human urea transporter SLC14A1 (HUT11/UT-B) has been suggested as a marker for
the adipogenic differentiation of bone cells with a relevance for bone diseases. We …
the adipogenic differentiation of bone cells with a relevance for bone diseases. We …
Charakterisierung des Einflusses von Estrogenrezeptoren auf mechanoresponsive Reporter
LS Kramer - 2021 - opus.bibliothek.uni-wuerzburg.de
Osteoporose wird definiert als erworbene, generalisierte Skeletterkrankung, die durch eine
verminderte Knochenfestigkeit und einen pathologischen Knochenverlust charakterisiert …
verminderte Knochenfestigkeit und einen pathologischen Knochenverlust charakterisiert …
Whole exome sequencing in identifying genetic factors in musculoskeletal diseases
S Skarp - 2019 - oulurepo.oulu.fi
Osajulkaisut Osajulkaisut eivät sisälly väitöskirjan elektroniseen versioon. Skarp, S.,
Kämäräinen, O.-P., Wei, G.-H., Jakkula, E., Kiviranta, I., Kröger, H.,… Männikkö, M.(2018) …
Kämäräinen, O.-P., Wei, G.-H., Jakkula, E., Kiviranta, I., Kröger, H.,… Männikkö, M.(2018) …