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Endocrinology|August 16, 2005
A mouse model of albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas geneEmily L Germain-Lee, William Schwindinger, Janet L Crane, et al.
Journal of Child Neurology|April 1, 2014
High-dose glucocorticoid therapy in the management of seizures in neonatal incontinentia pigmenti: a case reportDavid S Wolf, W Christopher Golden, Julie Hoover-Fong, et al.
American Journal of Epidemiology|February 1, 1984
Epidemiologic investigation of an oil-associated pneumonic paralytic eosinophilic syndrome in SpainJ G Rigau-Pérez, L Pérez-Alvarez, S Dueñas-Castro, et al.
The Journal of Clinical Endocrinology and Metabolism|September 14, 2013
Reduced insulin sensitivity in adults with pseudohypoparathyroidism type 1aRanganath Muniyappa, Mary A Warren, Xiongce Zhao, et al.
The Journal of Biological Chemistry|June 30, 2017
Activin receptor type 2A (ACVR2A) functions directly in osteoblasts as a negative regulator of bone massBrian C Goh, Vandana Singhal, Angelica J Herrera, et al.
Dalton Transactions (Cambridge, England : 2003)|September 26, 2012
Minimizing side reactions in chemoenzymatic dynamic kinetic resolution: organometallic and material strategiesCiara L Pollock, Kevin J Fox, Sophie D Lacroix, et al.
Morphologie : Bulletin De L'Association Des Anatomistes|July 18, 2016
Correlation between structural changes and acute thrombogenicity in transcatheter pericardium valves after crimping and balloon deploymentJ-M Bourget, R Zegdi, J Lin, et al.
Molecular Psychiatry|October 31, 2018
Alterations in sperm long RNA contribute to the epigenetic inheritance of the effects of postnatal traumaK Gapp, G van Steenwyk, P L Germain, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 21, 2020
Functional redundancy of type I and type II receptors in the regulation of skeletal muscle growth by myostatin and activin ASe-Jin Lee, Adam Lehar, Yewei Liu, et al.
Molecular Psychiatry|July 20, 2005
Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autismA Philippi, E Roschmann, F Tores, et al.
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