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Gene|April 15, 2020
From protein uptake to Dent disease: An overview of the CLCN5 geneLisa Gianesello, Dorella Del Prete, Monica Ceol, et al.
Thrombosis and Haemostasis|February 21, 2022
The Lesson Learned from the New c.2547-1G > T Mutation Combined with p.R854Q: When a Type 2N Mutation Reveals a Quantitative von Willebrand Factor DefectAlessandra Casonato, Maria Rita Cozzi, Silvia Ferrari, et al.
American Journal of Physiology. Endocrinology and Metabolism|August 24, 2006
T222P mutation of the insulin-like 3 hormone receptor LGR8 is associated with testicular maldescent and hinders receptor expression on the cell surface membraneNatalia V Bogatcheva, Alberto Ferlin, Shu Feng, et al.
Frontiers in Medicine|May 21, 2021
ACE2 and SARS-CoV-2 Infection Risk: Insights From Patients With Two Rare Genetic Tubulopathies, Gitelman's and Bartter's SyndromesLorenzo A Calò, Matteo Rigato, Luca Sgarabotto, et al.
Clinical Endocrinology|April 28, 2011
Androgens modulate osteocalcin release by human visceral adipose tissueCarlo Foresta, Giacomo Strapazzon, Luca De Toni, et al.
The Journal of Clinical Endocrinology and Metabolism|April 23, 2010
Evidence for osteocalcin production by adipose tissue and its role in human metabolismCarlo Foresta, Giacomo Strapazzon, Luca De Toni, et al.
International Journal of Molecular Sciences|January 21, 2023
Emerging Perspectives on the Rare Tubulopathy Dent Disease: Is Glomerular Damage a Direct Consequence of ClC-5 Dysfunction?Giovanna Priante, Monica Ceol, Lisa Gianesello, et al.
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