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Investigative Ophthalmology & Visual Science|April 27, 2007
Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataractDavid Cohen, Udy Bar-Yosef, Jaime Levy, et al.
Frontiers in Psychology|April 1, 2021
"Motherese" Prosody in Fetal-Directed Speech: An Exploratory Study Using Automatic Social Signal ProcessingErika Parlato-Oliveira, Catherine Saint-Georges, David Cohen, et al.
Molecular Autism|August 27, 2013
Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndromeSylvie Tordjman, George M Anderson, David Cohen, et al.
The Journal of Trauma|February 13, 2004
Small volume albumin administration protects against hemorrhagic shock-induced bone marrow dysfunctionAdena J Osband, Ziad C Sifri, Lai Wang, et al.
JCI Insight|January 28, 2021
Neonatal hyperoxia inhibits proliferation and survival of atrial cardiomyocytes by suppressing fatty acid synthesisEthan David Cohen, Min Yee, George A Porter, et al.
Journal of Autism and Developmental Disorders|March 31, 2005
Specific genetic disorders and autism: clinical contribution towards their identificationDavid Cohen, Nadège Pichard, Sylvie Tordjman, et al.
Plos One|February 9, 2013
Developmental and environmental regulation of Aquaporin gene expression across Populus species: divergence or redundancy?David Cohen, Marie-Béatrice Bogeat-Triboulot, Silvère Vialet-Chabrand, et al.
Plant Molecular Biology|August 2, 2014
Expression and characterization of plasma membrane aquaporins in stomatal complexes of Zea maysRobert B Heinen, Gerd Patrick Bienert, David Cohen, et al.
Thyroid : Official Journal of the American Thyroid Association|October 18, 2006
Scanning electron microscopy of thyroid cells under fully hydrated conditions--a novel technique for a seasoned procedure: a brief observationOhad Cohen, Rachel Beery, Shmuel Levit, et al.
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