Analysis of serum biomarker profiles in DDH Hip osteoarthritis versus primary hip osteoarthritis: a prospective observational study in a recent arthroplasty cohort. [PDF]
Harsanyi S +6 more
europepmc +1 more source
Generation and characterization of a novel inducible Sost_P2A_CreERT2 mouse model with high specificity for osteocytes. [PDF]
Prideaux M +4 more
europepmc +1 more source
Meta-Analysis of Ocy-454 Showed Interrupted Osteocyte Maturation in Spaceflight Affects SOST Expression and Hypoxic Response. [PDF]
Honjo M +3 more
europepmc +1 more source
Establishment of a human osteocyte model to reveal mechanisms of chronic Staphylococcus epidermidis bone and joint infections. [PDF]
Siverino C +4 more
europepmc +1 more source
Life course adiposity and risk of incident osteoporosis: a prospective cohort study from the UK Biobank. [PDF]
Liu H, Zhu J, Zhang Q, Chen J, Huang R.
europepmc +1 more source
Reversing LRP 5-Dependent Osteoporosis and SOST Deficiency–Induced Sclerosing Bone Disorders by Altering WNT Signaling Activity [PDF]
The bone formation inhibitor sclerostin encoded by SOST binds in vitro to low-density lipoprotein receptor-related protein (LRP) 5/6 Wnt co-receptors, thereby inhibiting Wnt/β-catenin signaling, a central pathway of skeletal homeostasis.
Jonathan Gooi, Hansjoerg Keller
exaly +2 more sources
SOST/Sclerostin Improves Posttraumatic Osteoarthritis and Inhibits MMP2/3 Expression After Injury [PDF]
Patients with anterior cruciate ligament (ACL) rupture are two times as likely to develop posttraumatic osteoarthritis (PTOA). Annually, there are ∼900,000 knee injuries in the United States, which account for ∼12% of all osteoarthritis (OA) cases.
Gabriela Loots +2 more
exaly +2 more sources
Spatial-temporal regulation of bone morphogenetic protein (BMP) and Wnt activity is essential for normal cardiovascular development, and altered activity of these growth factors causes maldevelopment of the cardiac outflow tract and great arteries.
Rui Monteiro +2 more
exaly +2 more sources
Novel SOST gene mutation in a sclerosteosis patient and her parents
: Introduction Sclerosteosis (OMIM 269500) is a rare autosomal recessive condition characterized by increased bone density associated with syndactyly. It is linked to a genetic defect in the SOST gene coding for sclerostin.
Vandana Dhiman +2 more
exaly +1 more source
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