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Plos Genetics|February 6, 2013
Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutationsKatherine R Bull, Andrew J Rimmer, Owen M Siggs, et al.Comparative and Functional Genomics|July 17, 2008
Three novel pigmentation mutants generated by genome-wide random ENU mutagenesis in the mouseVicky Tsipouri, John A Curtin, Pat M Nolan, et al.Genome Research|September 15, 2004
Organization and evolution of a gene-rich region of the mouse genome: a 12.7-Mb region deleted in the Del(13)Svea36H mouseAnn-Marie Mallon, Laurens Wilming, Joseph Weekes, et al.Cell|January 16, 2007
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humansDavid A Keays, Guoling Tian, Karine Poirier, et al.American Journal of Medical Genetics|July 14, 1999
Follow-up study on a susceptibility locus for schizophrenia on chromosome 6qM Martinez, L R Goldin, Q Cao, et al.Proceedings of the National Academy of Sciences of the United States of America|August 20, 2005
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screenDebora Bogani, Catherine Willoughby, Jennifer Davies, et al.Nature Genetics|July 2, 2003
Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31Philomena Mburu, Mirna Mustapha, Anabel Varela, et al.Plos One|February 6, 2013
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5Nellie Y Loh, Liz Bentley, Henrik Dimke, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|July 30, 2021
INFRAFRONTIER quality principles in systemic phenotypingHilke Ehlich, Heather L Cater, Ann M Flenniken, et al.Physiological Genomics|May 29, 2008
Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory studySilvia Mandillo, Valter Tucci, Sabine M Hölter, et al.Pageof 48