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The New England Journal of Medicine|May 10, 2013
Ataxia, dementia, and hypogonadotropism caused by disordered ubiquitinationDavid H Margolin, Maria Kousi, Yee-Ming Chan, et al.
Biorxiv : the Preprint Server for Biology|March 30, 2023
Inferring compound heterozygosity from large-scale exome sequencing dataMichael H Guo, Laurent C Francioli, Sarah L Stenton, et al.
Nature Medicine|December 17, 2002
Cytokine traps: multi-component, high-affinity blockers of cytokine actionAris N Economides, Laura Rocco Carpenter, John S Rudge, et al.
Human Molecular Genetics|February 18, 2009
Use of a genetic isolate to identify rare disease variants: C7 on 5p associated with MSSuvi P Kallio, Eveliina Jakkula, Shaun Purcell, et al.
Molecular Psychiatry|September 20, 2017
The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disordersC B Pedersen, J Bybjerg-Grauholm, M G Pedersen, et al.
Science (New York, N.Y.)|March 26, 2016
Survey of variation in human transcription factors reveals prevalent DNA binding changesLuis A Barrera, Anastasia Vedenko, Jesse V Kurland, et al.
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