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Nature Communications|November 7, 2023
Transcriptional reprogramming by mutated IRF4 in lymphomaNikolai Schleussner, Pierre Cauchy, Vedran Franke, et al.American Journal of Human Genetics|August 20, 2019
Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related EncephalopathyClara D M van Karnebeek, Rúben J Ramos, Xiao-Yan Wen, et al.Nature Communications|May 15, 2023
Integrative genomic analyses in adipocytes implicate DNA methylation in human obesity and diabetesLiam McAllan, Damir Baranasic, Sergio Villicaña, et al.Human Molecular Genetics|November 13, 2013
DNAJC13 mutations in Parkinson diseaseCarles Vilariño-Güell, Alex Rajput, Austen J Milnerwood, et al.The Journal of Experimental Medicine|July 31, 2025
ASXL1 deficiency causes epigenetic dysfunction, combined immunodeficiency, and EBV-associated lymphomaMaggie P Fu, Mehul Sharma, Pariya Yousefi, et al.Genome Biology|February 28, 2015
Gateways to the FANTOM5 promoter level mammalian expression atlasMarina Lizio, Jayson Harshbarger, Hisashi Shimoji, et al.Plos Genetics|May 10, 2006
Transcript annotation in FANTOM3: mouse gene catalog based on physical cDNAsNorihiro Maeda, Takeya Kasukawa, Rieko Oyama, et al.Nature Genetics|May 24, 2016
NANS-mediated synthesis of sialic acid is required for brain and skeletal developmentClara D M van Karnebeek, Luisa Bonafé, Xiao-Yan Wen, et al.Cell|May 15, 2018
Interfaces of Malignant and Immunologic Clonal Dynamics in Ovarian CancerAllen W Zhang, Andrew McPherson, Katy Milne, et al.The New England Journal of Medicine|April 11, 2019
Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLSAndré B P van Kuilenburg, Maja Tarailo-Graovac, Phillip A Richmond, et al.Pageof 41