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Microbial Genomics|December 20, 2023
Characterization of the RofA regulon in the pandemic M1global and emergent M1UK lineages of Streptococcus pyogenesXiangyun Zhi, Ana Vieira, Kristin K Huse, et al.BMC Genomics|February 13, 2013
Combined ChIP-Seq and transcriptome analysis identifies AP-1/JunD as a primary regulator of oxidative stress and IL-1β synthesis in macrophagesRichard P Hull, Prashant K Srivastava, Zelpha D'Souza, et al.Plos One|March 15, 2019
Optimisation of laboratory methods for whole transcriptomic RNA analyses in human left ventricular biopsies and blood samples of clinical relevanceKerrie L Ford, Maryam Anwar, Rachael Heys, et al.British Journal of Haematology|May 31, 2013
Target enrichment and high-throughput sequencing of 80 ribosomal protein genes to identify mutations associated with Diamond-Blackfan anaemiaGareth Gerrard, Mikel Valgañón, Hui En Foong, et al.Molecular Genetics & Genomic Medicine|February 6, 2014
Identification and biochemical analysis of a novel APOB mutation that causes autosomal dominant hypercholesterolemiaEllen R A Thomas, Santosh S Atanur, Penny J Norsworthy, et al.Human Molecular Genetics|July 28, 2007
SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular colobomaCheryl Y Gregory-Evans, Mariya Moosajee, Matthew D Hodges, et al.British Journal of Haematology|February 24, 2005
Heterogeneity of the epsilon gamma delta beta-thalassaemias: characterization of three novel English deletionsHelen Rooks, Jean Bergounioux, Laurence Game, et al.Nature Cell Biology|October 25, 2011
Cdc14 phosphatase promotes segregation of telomeres through repression of RNA polymerase II transcriptionAndres Clemente-Blanco, Nicholas Sen, Maria Mayan-Santos, et al.Plos One|December 19, 2024
Correction: Low Dose Iron Treatments Induce a DNA Damage Response in Human Endothelial Cells within MinutesInês G Mollet, Dilipkumar Patel, Fatima S Govani, et al.Annals of the Rheumatic Diseases|January 20, 2018
Changes in macrophage transcriptome associate with systemic sclerosis and mediate GSDMA contribution to disease riskAida Moreno-Moral, Marta Bagnati, Surya Koturan, et al.Pageof 7