المؤلفون: Joshua D Eaton, Jessica Board, Lee Davidson, Chris Estell, Steven West

المصدر: eLife, Vol 13 (2024)

مصطلحات موضوعية: Integrator, transcription, CDK9, RNA polymerase II, promoter, INTS11, Medicine, Science, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://elifesciences.org/articles/92764; https://doaj.org/toc/2050-084X

URL الوصول: https://doaj.org/article/2c3f24c7b7a5449b86eaae485b5c2a3b

المؤلفون: Chris Estell, Lee Davidson, Pieter C Steketee, Adam Monier, Steven West

المصدر: eLife, Vol 10 (2021)

مصطلحات موضوعية: transcription termination, non-coding transcription, integrator, exosome, enhancer, RNA polymerase II, Medicine, Science, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://elifesciences.org/articles/67305; https://doaj.org/toc/2050-084X

URL الوصول: https://doaj.org/article/db3925eccb7d4d0082a7c6bf78d0e797

المؤلفون: Lee Davidson, Laura Francis, Ross A. Cordiner, Joshua D. Eaton, Chris Estell, Sara Macias, Javier F. Cáceres, Steven West

المصدر: Cell Reports, Vol 26, Iss 10, Pp 2779-2791.e5 (2019)

مصطلحات موضوعية: Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2211124719301743; https://doaj.org/toc/2211-1247

URL الوصول: https://doaj.org/article/d371ae4c1a99434ea1385794f47c8f8f

المؤلفون: Lee Davidson, Adam Monier, Pieter C. Steketee, Steven West, Chris Estell

مصطلحات موضوعية: Transcription (software), Biology, Coding (social sciences), Cell biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0a3b1d20a9826d6d98a5d8301901ccfa
https://doi.org/10.7554/elife.67305.sa2

المؤلفون: Pieter C. Steketee, Chris Estell, Lee Davidson, Adam Monier, Steven West

المصدر: Estell, C, Davidson, L, Steketee, P C, Monier, A & West, S 2021, ' ZC3H4 restricts non-coding transcription in human cells ', eLIFE, vol. 10, 2021;10:e67305 . https://doi.org/10.7554/eLife.67305
eLife, Vol 10 (2021)
eLife

مصطلحات موضوعية: RNA, Untranslated, Transcription, Genetic, QH301-705.5, Science, RNA polymerase II, non-coding transcription, Biology, Exosome, General Biochemistry, Genetics and Molecular Biology, Cell Line, 03 medical and health sciences, 0302 clinical medicine, Downregulation and upregulation, Transcription (biology), Gene expression, Humans, exosome, Biology (General), Promoter Regions, Genetic, Enhancer, Gene, Cell Proliferation, transcription termination, 030304 developmental biology, 0303 health sciences, General Immunology and Microbiology, General Neuroscience, 030302 biochemistry & molecular biology, RNA-Binding Proteins, RNA, General Medicine, Chromosomes and Gene Expression, Cell biology, Multicellular organism, Gene Expression Regulation, integrator, biology.protein, Medicine, Human genome, enhancer, 030217 neurology & neurosurgery, Research Article, Human

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c57a9a647ed1ac578f15e8e7e965131
https://doi.org/10.1101/2021.02.10.430684

المؤلفون: Lee Davidson, Laura Francis, Ross A. Cordiner, Joshua D. Eaton, Chris Estell, Sara Macias, Javier F. Cáceres, Steven West

المصدر: Cell Reports
Davidson, L, Francis, L, Cordiner, R A, Eaton, J D, Estell, C, Macias, S, Cáceres, J F & West, S 2019, ' Rapid Depletion of DIS3, EXOSC10, or XRN2 Reveals the Immediate Impact of Exoribonucleolysis on Nuclear RNA Metabolism and Transcriptional Control ', Cell Reports, vol. 26, no. 10, pp. 2779-2791.e5 . https://doi.org/10.1016/j.celrep.2019.02.012
Cell Reports, Vol 26, Iss 10, Pp 2779-2791.e5 (2019)

مصطلحات موضوعية: EXOSC10/Rrp6, Exosome Multienzyme Ribonuclease Complex, Transcription, Genetic, non-coding RNA, HCT116 Cells, Article, HEK293 Cells, lcsh:Biology (General), Gene Expression Regulation, Exoribonucleases, Humans, RNA, exosome, DIS3, transcription, XRN2, lcsh:QH301-705.5, RNA, Nuclear, degradation

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::c01f194d3be95421f55758a6baa3aa55
https://pubmed.ncbi.nlm.nih.gov/30840897