Response Elements
"Response Elements" 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.
Nucleotide sequences, usually upstream, which are recognized by specific regulatory transcription factors, thereby causing gene response to various regulatory agents. These elements may be found in both promoter and enhancer regions.
Descriptor ID |
D020218
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MeSH Number(s) |
G02.111.570.080.689.330.700 G02.111.570.080.689.675.700 G05.360.080.689.330.700 G05.360.080.689.675.700 G05.360.340.024.340.137.750.249.765 G05.360.340.024.340.137.750.680.765
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Concept/Terms |
Response Elements- Response Elements
- Element, Response
- Elements, Response
- Response Element
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Below are MeSH descriptors whose meaning is more general than "Response Elements".
Below are MeSH descriptors whose meaning is more specific than "Response Elements".
This graph shows the total number of publications written about "Response Elements" by people in this website by year, and whether "Response Elements" 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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1998 | 1 | 0 | 1 | 1999 | 0 | 1 | 1 | 2000 | 1 | 3 | 4 | 2002 | 0 | 4 | 4 | 2003 | 0 | 4 | 4 | 2004 | 2 | 1 | 3 | 2005 | 3 | 0 | 3 | 2006 | 0 | 1 | 1 | 2007 | 0 | 2 | 2 | 2009 | 0 | 1 | 1 | 2010 | 0 | 3 | 3 | 2011 | 0 | 2 | 2 | 2012 | 0 | 3 | 3 | 2013 | 0 | 2 | 2 | 2014 | 1 | 1 | 2 | 2015 | 3 | 1 | 4 | 2016 | 1 | 3 | 4 | 2017 | 0 | 2 | 2 | 2018 | 1 | 1 | 2 | 2019 | 1 | 0 | 1 | 2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Response Elements" by people in Profiles.
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Simonett SP, Shin S, Herring JA, Bacher R, Smith LA, Dong C, Rabaglia ME, Stapleton DS, Schueler KL, Choi J, Bernstein MN, Turkewitz DR, Perez-Cervantes C, Spaeth J, Stein R, Tessem JS, Kendziorski C, Keles S, Moskowitz IP, Keller MP, Attie AD. Identification of direct transcriptional targets of NFATC2 that promote ß cell proliferation. J Clin Invest. 2021 11 01; 131(21).
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Calderon D, Nguyen MLT, Mezger A, Kathiria A, Müller F, Nguyen V, Lescano N, Wu B, Trombetta J, Ribado JV, Knowles DA, Gao Z, Blaeschke F, Parent AV, Burt TD, Anderson MS, Criswell LA, Greenleaf WJ, Marson A, Pritchard JK. Landscape of stimulation-responsive chromatin across diverse human immune cells. Nat Genet. 2019 10; 51(10):1494-1505.
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Liu P, Rojo de la Vega M, Sammani S, Mascarenhas JB, Kerins M, Dodson M, Sun X, Wang T, Ooi A, Garcia JGN, Zhang DD. RPA1 binding to NRF2 switches ARE-dependent transcriptional activation to ARE-NRE-dependent repression. Proc Natl Acad Sci U S A. 2018 10 30; 115(44):E10352-E10361.
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Vazquez JM, Sulak M, Chigurupati S, Lynch VJ. A Zombie LIF Gene in Elephants Is Upregulated by TP53 to Induce Apoptosis in Response to DNA Damage. Cell Rep. 2018 08 14; 24(7):1765-1776.
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Mohácsik P, Erdélyi F, Baranyi M, Botz B, Szabó G, Tóth M, Haltrich I, Helyes Z, Sperlágh B, Tóth Z, Sinkó R, Lechan RM, Bianco AC, Fekete C, Gereben B. A Transgenic Mouse Model for Detection of Tissue-Specific Thyroid Hormone Action. Endocrinology. 2018 02 01; 159(2):1159-1171.
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Samant SA, Kanwal A, Pillai VB, Bao R, Gupta MP. The histone deacetylase SIRT6 blocks myostatin expression and development of muscle atrophy. Sci Rep. 2017 09 19; 7(1):11877.
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Starr TN, Picton LK, Thornton JW. Alternative evolutionary histories in the sequence space of an ancient protein. Nature. 2017 09 21; 549(7672):409-413.
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Willett JW, Crosson S. Atypical modes of bacterial histidine kinase signaling. Mol Microbiol. 2017 01; 103(2):197-202.
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Rickels R, Hu D, Collings CK, Woodfin AR, Piunti A, Mohan M, Herz HM, Kvon E, Shilatifard A. An Evolutionary Conserved Epigenetic Mark of Polycomb Response Elements Implemented by Trx/MLL/COMPASS. Mol Cell. 2016 07 21; 63(2):318-328.
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Wang X, Wang H, Shen B, Overholser BR, Cooper BR, Lu Y, Tang H, Zhou C, Sun X, Zhong L, Favus MJ, Decker BS, Liu W, Peng Z. 1-Alpha, 25-dihydroxyvitamin D3 alters the pharmacokinetics of mycophenolic acid in renal transplant recipients by regulating two extrahepatic UDP-glucuronosyltransferases 1A8 and 1A10. Transl Res. 2016 12; 178:54-62.e6.
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