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 …

[引用][C] Analyse der differentiellen Genexpression von humanen Stro1-positiven Zellen aus pulpalem Zahnkeimgewebe und Beckenkammspongiosa

D Oellerich - 2016 - Niedersächsische Staats-und …

[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 …

[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 …

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 …

Identification of genes for complex diseases by integrating multiple types of genomic data

H Cao, S Lei, HW Deng… - 2012 Annual International …, 2012 - ieeexplore.ieee.org
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 …

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 …

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 …

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) …