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Biorxiv : the Preprint Server for Biology|February 7, 2023
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.
Molecular Psychiatry|November 17, 2004
Support for involvement of neuregulin 1 in schizophrenia pathophysiologyT L Petryshen, F A Middleton, A Kirby, et al.
Nature Neuroscience|November 27, 2019
Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variantsF Kyle Satterstrom, Raymond K Walters, Tarjinder Singh, et al.
The FEBS Journal|July 24, 2013
Global characterization of signalling networks associated with tamoxifen resistance in breast cancerBrigid C Browne, Falko Hochgräfe, Jianmin Wu, et al.
Nature Genetics|March 22, 2016
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general populationElise B Robinson, Beate St Pourcain, Verneri Anttila, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 15, 2002
Global analysis of the Deinococcus radiodurans proteome by using accurate mass tagsMary S Lipton, Ljiljana Pasa-Tolic', Gordon A Anderson, et al.
Cell Reports|June 23, 2015
Integrated Genomics of Crohn's Disease Risk Variant Identifies a Role for CLEC12A in Antibacterial AutophagyJakob Begun, Kara G Lassen, Humberto B Jijon, et al.
Nature Genetics|December 9, 2008
Genome-wide association analysis of metabolic traits in a birth cohort from a founder populationChiara Sabatti, Susan K Service, Anna-Liisa Hartikainen, et al.
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