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Proceedings of the National Academy of Sciences of the United States of America|September 15, 1999
A homeobox gene, vax2, controls the patterning of the eye dorsoventral axisA M Barbieri, G Lupo, A Bulfone, et al.
Genomics|October 1, 1992
Exclusion of linkage between hypokalemic periodic paralysis (HOKPP) and three candidate lociW L Casley, M Allon, H K Cousin, et al.
The EMBO Journal|February 4, 2006
A unique set of SH3-SH3 interactions controls IB1 homodimerizationOle Kristensen, Sylvie Guenat, Imran Dar, et al.
Glia|April 5, 2013
Sh3tc2 deficiency affects neuregulin-1/ErbB signalingEstelle Arnaud Gouttenoire, Vincenzo Lupo, Eduardo Calpena, et al.
Neurobiology of Aging|March 12, 2014
Investigation of memory, executive functions, and anatomic correlates in asymptomatic FMR1 premutation carriersLoyse Hippolyte, Giovanni Battistella, Aline G Perrin, et al.
Journal of Biomolecular Screening|November 10, 2006
Homogeneous and nonradioactive high-throughput screening platform for the characterization of kinase inhibitors in cell lysatesSylvie Guenat, Nathalie Rouleau, Christelle Bielmann, et al.
Journal of Neuroinflammation|October 16, 2012
Carriers of the fragile X mental retardation 1 (FMR1) premutation allele present with increased levels of cytokine IL-10Diana Marek, Stephanie Papin, Kim Ellefsen, et al.
European Journal of Human Genetics : EJHG|July 22, 2010
Genetic male infertility and mutation of CATSPER ion channelsMichael S Hildebrand, Matthew R Avenarius, Marc Fellous, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|June 2, 2021
Paternal obesity and its transgenerational effects on gastrointestinal function in male rat offspringM P R Machado, L A Gama, A P S Beckmann, et al.
American Journal of Human Genetics|December 5, 1998
Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31H Feit, A Silbergleit, L B Schneider, et al.
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