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Human Molecular Genetics|May 26, 2019
Mendelian randomization analysis of celiac GWAS reveals a blood expression signature with diagnostic potential in absence of gluten consumptionNora Fernandez-Jimenez, Jose Ramon BilbaoHuman Molecular Genetics|May 26, 2019
PTEN modulates gene transcription by redistributing genome-wide RNA polymerase II occupancyAta Abbas, Roshan Padmanabhan, Todd Romigh, et al.Human Molecular Genetics|April 13, 2022
Role of non-coding RNAs on liver metabolism and NAFLD pathogenesisGene Qian, Núria MorralHuman Molecular Genetics|July 28, 2022
ETS1 loss in mice impairs cardiac outflow tract septation via a cell migration defect autonomous to the neural crestLizhu Lin, Antonella Pinto, Lu Wang, et al.Human Molecular Genetics|June 5, 2019
RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathwaysOlivia K Gardner, Lily Wang, Derek Van Booven, et al.Human Molecular Genetics|July 20, 2010
Genome-wide association analysis identifies multiple loci related to resting heart rateMark Eijgelsheim, Christopher Newton-Cheh, Nona Sotoodehnia, et al.Human Molecular Genetics|July 20, 2010
Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipidsAmel Bahloul, Vincent Michel, Jean-Pierre Hardelin, et al.Human Molecular Genetics|July 20, 2010
Locus category based analysis of a large genome-wide association study of rheumatoid arthritisJan Freudenberg, Annette T Lee, Katherine A Siminovitch, et al.Human Molecular Genetics|June 30, 2010
Clorgyline-mediated reversal of neurological deficits in a Complexin 2 knockout mouseDervila Glynn, Helen E Gibson, Michael K Harte, et al.Human Molecular Genetics|May 25, 2010
In vivo expression of polyglutamine-expanded huntingtin by mouse striatal astrocytes impairs glutamate transport: a correlation with Huntington's disease subjectsMathilde Faideau, Jinho Kim, Kerry Cormier, et al.Pageof 1,195