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Genome Research|April 23, 2020
Suppressor mutations in Mecp2-null mice implicate the DNA damage response in Rett syndrome pathologyAdebola Enikanolaiye, Julie Ruston, Rong Zeng, et al.
American Journal of Human Genetics|July 18, 2017
CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic DeletionsMolly Gasperini, Gregory M Findlay, Aaron McKenna, et al.
Nature Communications|May 6, 2017
Quantification of differential gene expression by multiplexed targeted resequencing of cDNAPeer Arts, Jori van der Raadt, Sebastianus H C van Gestel, et al.
Elife|May 25, 2017
The dynamic three-dimensional organization of the diploid yeast genomeSeungsoo Kim, Ivan Liachko, Donna G Brickner, et al.
Nature Reviews. Genetics|September 28, 2011
Exome sequencing as a tool for Mendelian disease gene discoveryMichael J Bamshad, Sarah B Ng, Abigail W Bigham, et al.
Prenatal Diagnosis|April 5, 2013
Noninvasive fetal genome sequencing: a primerMatthew W Snyder, LaVone E Simmons, Jacob O Kitzman, et al.
American Journal of Human Genetics|September 17, 2018
A Multiplex Homology-Directed DNA Repair Assay Reveals the Impact of More Than 1,000 BRCA1 Missense Substitution Variants on Protein FunctionLea M Starita, Muhtadi M Islam, Tapahsama Banerjee, et al.
Nucleic Acids Research|May 6, 2015
Accurate identification of centromere locations in yeast genomes using Hi-CNelle Varoquaux, Ivan Liachko, Ferhat Ay, et al.
Aging Cell|August 6, 2013
Targeted enrichment and high-resolution digital profiling of mitochondrial DNA deletions in human brainSean D Taylor, Nolan G Ericson, Joshua N Burton, et al.
Biorxiv : the Preprint Server for Biology|March 18, 2024
Multi-condition and multi-modal temporal profile inference during mouse embryonic developmentRan Zhang, Chengxiang Qiu, Gala Filippova, et al.
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