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Journal of Immunology (Baltimore, Md. : 1950)|July 19, 2015
Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food AllergyJin Li, Irene Fung, Joseph T Glessner, et al.Plos Genetics|October 8, 2011
A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated lociJonathan P Bradfield, Hui-Qi Qu, Kai Wang, et al.Brain : a Journal of Neurology|February 16, 2006
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regenerationMarina Bakay, Zuyi Wang, Gisela Melcon, et al.Human Molecular Genetics|June 16, 2018
Pathogenic variant in EPHB4 results in central conducting lymphatic anomalyDong Li, Tara L Wenger, Christoph Seiler, et al.Nature Communications|September 29, 2016
Genome-wide association study for acute otitis media in children identifies FNDC1 as disease contributing geneGijs van Ingen, Jin Li, André Goedegebure, et al.Nature Communications|January 16, 2020
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associationsYun Rose Li, Joseph T Glessner, Bradley P Coe, et al.Nature Communications|April 21, 2015
Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cellsJin Li, Silje F Jørgensen, S Melkorka Maggadottir, et al.Nature Communications|October 10, 2015
Genetic sharing and heritability of paediatric age of onset autoimmune diseasesYun R Li, Sihai D Zhao, Jin Li, et al.Nature Medicine|August 25, 2015
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseasesYun R Li, Jin Li, Sihai D Zhao, et al.Pageof 3