Zobrazeno 1 - 6
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pro vyhledávání: '"Jessica G. Hardy"'
Publikováno v:
BMC Research Notes, Vol 12, Iss 1, Pp 1-4 (2019)
Abstract Objectives Transcription of eukaryotic protein-coding genes by RNA polymerase II (pol II) is highly regulated at initiation, elongation and termination. Transcription is also coordinated with co-transcriptional processing of the emerging pre
Externí odkaz:
https://doaj.org/article/d9265bd783834153bf022bb010c24c42
Publikováno v:
BMC Research Notes, Vol 11, Iss 1, Pp 1-3 (2018)
Abstract Objectives Transcription of eukaryotic protein-coding genes by RNA polymerase II (pol II) is a highly regulated process. Most human genes have multiple poly(A) sites, which define different possible mRNA ends, suggesting the existence of mec
Externí odkaz:
https://doaj.org/article/f461c8a805c14d7891edd6ce2d0a2087
Autor:
Jessica G. Hardy, Chris J. Norbury
Publikováno v:
Biochemical Society Transactions. 44:1051-1057
Most mammalian protein coding genes are subject to alternative cleavage and polyadenylation (APA), which can generate distinct mRNA 3′UTRs with differing regulatory potential. Although this process has been intensely studied in recent years, it rem
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 11, Iss 1, Pp 1-3 (2018)
BMC Research Notes, Vol 11, Iss 1, Pp 1-3 (2018)
Objectives Transcription of eukaryotic protein-coding genes by RNA polymerase II (pol II) is a highly regulated process. Most human genes have multiple poly(A) sites, which define different possible mRNA ends, suggesting the existence of mechanisms t
Autor:
Jessica G. Hardy
Publikováno v:
The Biochemist. 38:38-40
Cancer. It's an emotive word, and a dreaded diagnosis. We all know someone affected by this horrible disease, and quite understandably, we all want to know: what causes cancer, and is there anything we can do to stop ourselves from getting it?
Many eukaryotic protein-coding genes give rise to alternative mRNA isoforms with identical protein-coding capacities but which differ in the extents of their 3´ untranslated regions (3´UTRs), due to the usage of alternative sites of pre-mRNA cleava
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc0c2f766fac002e45da36874a4a2183