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Human Molecular Genetics|June 25, 2016
Cilia gene mutations cause atrioventricular septal defects by multiple mechanismsOzanna Burnicka-Turek, Jeffrey D Steimle, Wenhui Huang, et al.Nature Genetics|July 30, 2013
A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndromeChristie M Buchovecky, Stephen D Turley, Hannah M Brown, et al.Nature|August 18, 2009
Targeted capture and massively parallel sequencing of 12 human exomesSarah B Ng, Emily H Turner, Peggy D Robertson, et al.Science (New York, N.Y.)|August 4, 2022
The continuum of Drosophila embryonic development at single-cell resolutionDiego Calderon, Ronnie Blecher-Gonen, Xingfan Huang, et al.American Journal of Human Genetics|December 24, 2013
Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence dataZongxiao He, Brian J O'Roak, Joshua D Smith, et al.Nature|November 24, 2017
Corrigendum: The 4D nucleome projectJob Dekker, Andrew S Belmont, Mitchell Guttman, et al.Nature Cell Biology|April 24, 2026
The proteomic landscape and temporal dynamics of human and mouse gastruloid developmentRiddhiman K Garge, Valerie Lynch, Rose Fields, et al.American Journal of Human Genetics|June 3, 2017
Genetic-Variation-Driven Gene-Expression Changes Highlight Genes with Important Functions for Kidney DiseaseYi-An Ko, Huiguang Yi, Chengxiang Qiu, et al.Methods (San Diego, Calif.)|February 1, 2018
Using DNase Hi-C techniques to map global and local three-dimensional genome architecture at high resolutionWenxiu Ma, Ferhat Ay, Choli Lee, et al.Nature Methods|December 2, 2014
Fine-scale chromatin interaction maps reveal the cis-regulatory landscape of human lincRNA genesWenxiu Ma, Ferhat Ay, Choli Lee, et al.Pageof 47