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Genome Research|November 11, 2016
A systematic comparison reveals substantial differences in chromosomal versus episomal encoding of enhancer activityFumitaka Inoue, Martin Kircher, Beth Martin, et al.Nature Genetics|July 30, 2013
Massively parallel decoding of mammalian regulatory sequences supports a flexible organizational modelRobin P Smith, Leila Taher, Rupali P Patwardhan, et al.Human Mutation|April 30, 2014
A novel ZRS mutation leads to preaxial polydactyly type 2 in a heterozygous form and Werner mesomelic syndrome in a homozygous formJulia E VanderMeer, Reymundo Lozano, Miao Sun, et al.Pharmacogenomics|May 20, 2020
Noncoding SNPs associated with increased GDF15 levels located in a metformin-activated enhancer region upstream of GDF15Natália D Linhares, Daniela A Pereira, Izabela McA Conceição, et al.Nature Communications|December 22, 2015
A genome-wide association study identifies four novel susceptibility loci underlying inguinal herniaEric Jorgenson, Nadja Makki, Ling Shen, et al.Computational and Structural Biotechnology Journal|January 22, 2025
The topography of nullomer-emerging mutations and their relevance to human diseaseCandace S Y Chan, Ioannis Mouratidis, Austin Montgomery, et al.Disease Models & Mechanisms|September 1, 2025
The importance of imperfect pre-clinical models in adolescent idiopathic scoliosisDiane S Sepich, Ryan S Gray, Nadav Ahituv, et al.Journal of Lipid Research|July 18, 2008
A new mouse mutant for the LDL receptor identified using ENU mutagenesisKaren L Svenson, Nadav Ahituv, Rebecca S Durgin, et al.Plos Genetics|October 26, 2019
Dysregulation of STAT3 signaling is associated with endplate-oriented herniations of the intervertebral disc in Adgrg6 mutant miceZhaoyang Liu, Garrett W D Easson, Jingjing Zhao, et al.Plos Computational Biology|June 27, 2014
Integrating diverse datasets improves developmental enhancer predictionGenevieve D Erwin, Nir Oksenberg, Rebecca M Truty, et al.Pageof 18