Showing results (71-80 of 168) with videos related to
Sort By:
Pageof 17
Molecular Neurobiology|January 6, 2019
Antisense Transcription in Loci Associated to Hereditary Neurodegenerative DiseasesSilvia Zucchelli, Stefania Fedele, Paolo Vatta, et al.Nucleic Acids Research|December 31, 2005
Pfam: clans, web tools and servicesRobert D Finn, Jaina Mistry, Benjamin Schuster-Böckler, et al.Scientific Reports|September 21, 2016
Transcriptome analysis of periodontitis-associated fibroblasts by CAGE sequencing identified DLX5 and RUNX2 long variant as novel regulators involved in periodontitisMasafumi Horie, Yoko Yamaguchi, Akira Saito, et al.Allergy|May 26, 2022
Remission of peanut allergy is associated with rewiring of allergen-driven T helper 2-related gene networksSarah E Ashley, Anya C Jones, Denise Anderson, et al.Plos One|July 5, 2012
FusionFinder: a software tool to identify expressed gene fusion candidates from RNA-Seq dataRichard W Francis, Katherine Thompson-Wicking, Kim W Carter, et al.BMC Genomics|August 13, 2015
Integrated analyses of zebrafish miRNA and mRNA expression profiles identify miR-29b and miR-223 as potential regulators of optic nerve regenerationPaula I Fuller-Carter, Kim W Carter, Denise Anderson, et al.BMC Genomics|January 13, 2018
Correction to: Relatively frequent switching of transcription start sites during cerebellar developmentPeter Zhang, Emmanuel Dimont, Thomas Ha, et al.Stem Cell Research & Therapy|December 4, 2023
Gene editing and cardiac disease modelling for the interpretation of genetic variants of uncertain significance in congenital heart diseaseVanessa S Fear, Catherine A Forbes, Nicole C Shaw, et al.Military Medicine|October 4, 2012
Writing, self-reflection, and medical school performance: the Human Context of Health CareMark B Stephens, Brian V Reamy, Denise Anderson, et al.Cell|March 23, 2019
A Diagnosis for All Rare Genetic Diseases: The Horizon and the Next FrontiersKym M Boycott, Taila Hartley, Leslie G Biesecker, et al.Pageof 17