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Nature Communications|July 12, 2019
Paternal-age-related de novo mutations and risk for five disordersJacob L Taylor, Jean-Christophe P G Debost, Sarah U Morton, et al.Gut|February 10, 2009
Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitisE A M Festen, P Goyette, R Scott, et al.Nature Genetics|January 24, 2009
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosusRobert R Graham, Chris Cotsapas, Leela Davies, et al.Cell Stem Cell|July 22, 2020
Mesenchymal Niche-Derived Neuregulin-1 Drives Intestinal Stem Cell Proliferation and Regeneration of Damaged EpitheliumThierry Jardé, Wing Hei Chan, Fernando J Rossello, et al.The New England Journal of Medicine|January 11, 2008
Association between microdeletion and microduplication at 16p11.2 and autismLauren A Weiss, Yiping Shen, Joshua M Korn, et al.American Journal of Human Genetics|April 3, 2004
Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22F A Middleton, M T Pato, K L Gentile, et al.The Biochemical Journal|October 11, 2013
A robust methodology to subclassify pseudokinases based on their nucleotide-binding propertiesJames M Murphy, Qingwei Zhang, Samuel N Young, et al.Nature|November 4, 2014
Genetic and epigenetic fine mapping of causal autoimmune disease variantsKyle Kai-How Farh, Alexander Marson, Jiang Zhu, et al.Genome Research|May 15, 2024
A harmonized public resource of deeply sequenced diverse human genomesZan Koenig, Mary T Yohannes, Lethukuthula L Nkambule, et al.Breast Cancer Research : BCR|August 4, 2021
Evaluation of FGFR targeting in breast cancer through interrogation of patient-derived modelsNicole J Chew, Terry C C Lim Kam Sian, Elizabeth V Nguyen, et al.Pageof 163