Results 161 to 170 of about 10,314 (209)

Early Diagnosis and Follow-Up of a Novel Homozygous Mutation in <i>SOST</i> Gene in a Child with Recurrent Facial Palsy: A Case Report and Review of the Literature. [PDF]

open access: yesInt J Mol Sci
Acquaviva F   +11 more
europepmc   +1 more source

Wnt/β-Catenin Pathway and Hydraulic Calcium Silicate-Based Cements: A Narrative Review. [PDF]

open access: yesDent J (Basel)
Del Giudice C   +6 more
europepmc   +1 more source

Bone Mineral Density and Serum Levels of Bone Remodeling Markers in Ankylosing Spondylitis Treated with Anti TNF-α Agents. [PDF]

open access: yesMed Sci (Basel)
Alvarez-Ayala EG   +15 more
europepmc   +1 more source

Genetic evidence that SOST inhibits WNT signaling in the limb [PDF]

open access: yesDevelopmental Biology, 2010
SOST is a negative regulator of bone formation, and mutations in human SOST are responsible for sclerosteosis. In addition to high bone mass, sclerosteosis patients occasionally display hand defects, suggesting that SOST may function embryonically. Here we report that overexpression of SOST leads to loss of posterior structures of the zeugopod and ...
Gabriela Loots   +2 more
exaly   +4 more sources

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