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Journal of the Renin-Angiotensin-Aldosterone System : JRAAS|March 26, 2011
Polymorphisms of the angiotensin-converting enzyme and angiotensinogen gene in patients with atrial fibrillationNurdan Papila Topal, Beste Ozben, Veysel Sabri Hancer, et al.Cell Reports|February 2, 2017
Immune Escape via a Transient Gene Expression Program Enables Productive Replication of a Latent PathogenJessica A Linderman, Mariko Kobayashi, Vinayak Rayannavar, et al.Proceedings of the National Academy of Sciences of the United States of America|February 18, 2009
Rescuing Z+ agrin splicing in Nova null mice restores synapse formation and unmasks a physiologic defect in motor neuron firingMatteo Ruggiu, Ruth Herbst, Natalie Kim, et al.The Journal of Clinical Investigation|June 11, 2009
Patients with lung cancer and paraneoplastic Hu syndrome harbor HuD-specific type 2 CD8+ T cellsWendy K Roberts, Ilana J Deluca, Ashby Thomas, et al.Elife|February 8, 2013
Dendritic cells loaded with FK506 kill T cells in an antigen-specific manner and prevent autoimmunity in vivoDana E Orange, Nathalie E Blachere, John Fak, et al.Neuron|September 15, 2017
cTag-PAPERCLIP Reveals Alternative Polyadenylation Promotes Cell-Type Specific Protein Diversity and Shifts Araf Isoforms with Microglia ActivationHun-Way Hwang, Yuhki Saito, Christopher Y Park, et al.Cell|July 2, 2005
Antisense-mediated depletion reveals essential and specific functions of microRNAs in Drosophila developmentDan Leaman, Po Yu Chen, John Fak, et al.Elife|March 27, 2018
Differential 3' Processing of Specific Transcripts Expands Regulatory and Protein Diversity Across Neuronal Cell TypesSaša Jereb, Hun-Way Hwang, Eric Van Otterloo, et al.Journal of the Renin-Angiotensin-Aldosterone System : JRAAS|January 8, 2009
Angiotensin-converting enzyme gene polymorphism in arrhythmogenic right ventricular dysplasia: is DD genotype helpful in predicting syncope risk?Beste Ozben, Ibrahim Altun, Veysel Sabri Hancer, et al.Neuron|August 17, 2019
A Large Panel of Isogenic APP and PSEN1 Mutant Human iPSC Neurons Reveals Shared Endosomal Abnormalities Mediated by APP β-CTFs, Not AβDylan Kwart, Andrew Gregg, Claudia Scheckel, et al.Pageof 9