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Nature Communications|November 7, 2019
The long noncoding RNA lncNB1 promotes tumorigenesis by interacting with ribosomal protein RPL35Pei Y Liu, Andrew E Tee, Giorgio Milazzo, et al.
European Journal of Human Genetics : EJHG|August 15, 2022
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysisLisa J Ewans, Andre E Minoche, Deborah Schofield, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2007
Association of a common complement receptor 2 haplotype with increased risk of systemic lupus erythematosusHui Wu, Susan A Boackle, Punchong Hanvivadhanakul, et al.
Cell|February 24, 2018
A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and SeizuresVincenzo A Gennarino, Elizabeth E Palmer, Laura M McDonell, et al.
Nature Communications|January 25, 2020
The Medical Genome Reference Bank contains whole genome and phenotype data of 2570 healthy elderlyMark Pinese, Paul Lacaze, Emma M Rath, et al.
American Journal of Human Genetics|August 9, 2020
Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic DataSimon Easteal, Ruth M Arkell, Renzo F Balboa, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 26, 2015
Analysis of 13 cell types reveals evidence for the expression of numerous novel primate- and tissue-specific microRNAsEric Londin, Phillipe Loher, Aristeidis G Telonis, et al.
Nucleic Acids Research|October 31, 2016
RNAcentral: a comprehensive database of non-coding RNA sequences, Anton I Petrov, Simon J E Kay, et al.
Nature Immunology|September 20, 2019
Denisovan, modern human and mouse TNFAIP3 alleles tune A20 phosphorylation and immunityNathan W Zammit, Owen M Siggs, Paul E Gray, et al.
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