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The Journal of Clinical Endocrinology and Metabolism|August 24, 2018
Heterozygous Mutations in TBX1 as a Cause of Isolated HypoparathyroidismDong Li, Christopher T Gordon, Myriam Oufadem, et al.
Physiological Genomics|April 28, 2005
Definition of the unique human extraocular muscle allotype by expression profilingM Dominik Fischer, Murat T Budak, Marina Bakay, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 21, 2010
Targeting stents with local delivery of paclitaxel-loaded magnetic nanoparticles using uniform fieldsMichael Chorny, Ilia Fishbein, Benjamin B Yellen, et al.
Plos One|September 19, 2018
CLEC16A regulates splenocyte and NK cell function in part through MEK signalingRahul Pandey, Marina Bakay, Heather S Hain, et al.
Human Molecular Genetics|January 13, 2006
Loss of emerin at the nuclear envelope disrupts the Rb1/E2F and MyoD pathways during muscle regenerationGisela Melcon, Serguei Kozlov, Dedra A Cutler, et al.
Journal of the National Cancer Institute|February 26, 2020
Mitochondrial DNA Haplogroups and Susceptibility to NeuroblastomaXiao Chang, Marina Bakay, Yichuan Liu, et al.
Scientific Reports|April 30, 2021
Inducible knockout of Clec16a in mice results in sensory neurodegenerationHeather S Hain, Rahul Pandey, Marina Bakay, et al.
Cell|June 21, 2014
The diabetes susceptibility gene Clec16a regulates mitophagyScott A Soleimanpour, Aditi Gupta, Marina Bakay, et al.
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