3' Flanking Region
"3' Flanking Region" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
The region of DNA which borders the 3' end of a transcription unit and where a variety of regulatory sequences are located.
Descriptor ID |
D024509
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MeSH Number(s) |
G05.360.340.024.220.280 G05.360.340.024.340.137.290
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Concept/Terms |
3' Flanking Region- 3' Flanking Region
- 3' Flanking Regions
- Flanking Regions, 3'
- Region, 3' Flanking
- Regions, 3' Flanking
- 3' Flanking Sequence
- 3' Flanking Sequences
- Flanking Sequence, 3'
- Flanking Sequences, 3'
- Sequence, 3' Flanking
- Sequences, 3' Flanking
- Flanking Region, 3'
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Below are MeSH descriptors whose meaning is more general than "3' Flanking Region".
Below are MeSH descriptors whose meaning is more specific than "3' Flanking Region".
This graph shows the total number of publications written about "3' Flanking Region" by people in this website by year, and whether "3' Flanking Region" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
Year | Major Topic | Minor Topic | Total |
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2006 | 0 | 1 | 1 | 2008 | 0 | 1 | 1 | 2009 | 1 | 0 | 1 | 2011 | 0 | 1 | 1 | 2018 | 0 | 1 | 1 |
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Below are the most recent publications written about "3' Flanking Region" by people in Profiles.
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Sheridan RM, Fong N, D'Alessandro A, Bentley DL. Widespread Backtracking by RNA Pol II Is a Major Effector of Gene Activation, 5' Pause Release, Termination, and Transcription Elongation Rate. Mol Cell. 2019 01 03; 73(1):107-118.e4.
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Orioli A, Pascali C, Quartararo J, Diebel KW, Praz V, Romascano D, Percudani R, van Dyk LF, Hernandez N, Teichmann M, Dieci G. Widespread occurrence of non-canonical transcription termination by human RNA polymerase III. Nucleic Acids Res. 2011 Jul; 39(13):5499-512.
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Blackledge NP, Ott CJ, Gillen AE, Harris A. An insulator element 3' to the CFTR gene binds CTCF and reveals an active chromatin hub in primary cells. Nucleic Acids Res. 2009 Mar; 37(4):1086-94.
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Han K, Lee J, Meyer TJ, Remedios P, Goodwin L, Batzer MA. L1 recombination-associated deletions generate human genomic variation. Proc Natl Acad Sci U S A. 2008 Dec 09; 105(49):19366-71.
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Kumar TR, Schuff KG, Nusser KD, Low MJ. Gonadotroph-specific expression of the human follicle stimulating hormone beta gene in transgenic mice. Mol Cell Endocrinol. 2006 Mar 09; 247(1-2):103-15.
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