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Development (Cambridge, England)|February 7, 2019
Lineage-specific reorganization of nuclear peripheral heterochromatin and H3K9me2 domainsKelvin See, Yemin Lan, Joshua Rhoades, et al.Brain Research|December 18, 2019
Genome-wide synthetic lethal CRISPR screen identifies FIS1 as a genetic interactor of ALS-linked C9ORF72Noori Chai, Michael S Haney, Julien Couthouis, et al.Genome Research|September 4, 2003
Retrotransposons and their recognition of pol II promoters: a comprehensive survey of the transposable elements from the complete genome sequence of Schizosaccharomyces pombeNathan J Bowen, I King Jordan, Jonathan A Epstein, et al.Wound Repair and Regeneration : Official Publication of the Wound Healing Society [And] the European Tissue Repair Society|April 15, 2005
MRL mice fail to heal the heart in response to ischemia-reperfusion injuryIbrahim Abdullah, John J Lepore, Jonathan A Epstein, et al.Genesis (New York, N.Y. : 2000)|March 25, 2005
Identification of a hypaxial somite enhancer element regulating Pax3 expression in migrating myoblasts and characterization of hypaxial muscle Cre transgenic miceChristopher B Brown, Kurt A Engleka, Jennifer Wenning, et al.Nature|July 26, 2023
CAR T therapy beyond cancer: the evolution of a living drugDaniel J Baker, Zoltan Arany, Joseph A Baur, et al.Development (Cambridge, England)|July 1, 2004
Cardiac outflow tract defects in mice lacking ALK2 in neural crest cellsVesa Kaartinen, Marek Dudas, Andre Nagy, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|February 28, 2013
Resolution of defective dorsal aortae patterning in Sema3E-deficient mice occurs via angiogenic remodelingStryder M Meadows, Lyndsay A Ratliff, Manvendra K Singh, et al.Neuromuscular Disorders : NMD|March 6, 2014
Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophyJulien Couthouis, Alya R Raphael, Carly Siskind, et al.Biorxiv : the Preprint Server for Biology|February 8, 2024
TDP-43 nuclear loss in FTD/ALS causes widespread alternative polyadenylation changesYi Zeng, Anastasiia Lovchykova, Tetsuya Akiyama, et al.Pageof 36