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European Journal of Cell Biology|January 4, 2015
Distribution of formins in cardiac muscle: FHOD1 is a component of intercalated discs and costameresAbdulatif Al Haj, Antonina J Mazur, Katarzyna Radaszkiewicz, et al.
EMBO Reports|July 10, 2023
RNA polymerase II CTD is dispensable for transcription and required for termination in human cellsYousra Yahia, Alexia Pigeot, Amal Zine El Aabidine, et al.
Genes & Development|April 18, 2013
In vivo live imaging of RNA polymerase II transcription factories in primary cellsAlireza Ghamari, Mariëtte P C van de Corput, Supat Thongjuea, 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.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|October 6, 2005
Reduced cisplatin sensitivity of head and neck squamous cell carcinoma cell lines correlates with mutations affecting the COOH-terminal nuclear localization signal of p53Robert Mandic, Chantal J Schamberger, Julia F Müller, et al.
Molecular Cell|November 26, 2018
Arginine Citrullination at the C-Terminal Domain Controls RNA Polymerase II TranscriptionPriyanka Sharma, Antonios Lioutas, Narcis Fernandez-Fuentes, et al.
Transcription|November 15, 2015
Site-specific methylation and acetylation of lysine residues in the C-terminal domain (CTD) of RNA polymerase IIKirsten Voss, Ignasi Forné, Nicolas Descostes, et al.
Antioxidants (Basel, Switzerland)|August 6, 2021
Integration of Cardiac Actin Mutants Causing Hypertrophic (p.A295S) and Dilated Cardiomyopathy (p.R312H and p.E361G) into Cellular StructuresConstanze Erdmann, Roua Hassoun, Sebastian Schmitt, et al.
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