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Nature Communications|April 22, 2023
Transcription factor binding site orientation and order are major drivers of gene regulatory activityIlias Georgakopoulos-Soares, Chengyu Deng, Vikram Agarwal, et al.Human Mutation|March 11, 2018
Mutations in the fourth β-propeller domain of LRP4 are associated with isolated syndactyly with fusion of the third and fourth fingersRivka Sukenik Halevy, Huan-Chieh Chien, Bo Heinz, et al.NAR Genomics and Bioinformatics|April 27, 2023
Quasi-prime peptides: identification of the shortest peptide sequences unique to a speciesIoannis Mouratidis, Candace S Y Chan, Nikol Chantzi, et al.Science China. Life Sciences|March 15, 2020
Characterization of functional transposable element enhancers in acute myeloid leukemiaYingying Zeng, Yaqiang Cao, Rivka Sukenik Halevy, et al.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.Pageof 18