 Genes, Reporter
"Genes, Reporter" 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.
Genes whose expression is easily detectable and therefore used to study promoter activity at many positions in a target genome. In recombinant DNA technology, these genes may be attached to a promoter region of interest.
| Descriptor ID |
D017930
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| MeSH Number(s) |
G05.360.340.024.340.435
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Genes, Reporter".
Below are MeSH descriptors whose meaning is more specific than "Genes, Reporter".
This graph shows the total number of publications written about "Genes, Reporter" by people in this website by year, and whether "Genes, Reporter" 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 |
|---|
| 1994 | 0 | 2 | 2 | | 1995 | 0 | 2 | 2 | | 1996 | 0 | 3 | 3 | | 1997 | 0 | 1 | 1 | | 1998 | 0 | 7 | 7 | | 1999 | 0 | 10 | 10 | | 2000 | 0 | 6 | 6 | | 2001 | 0 | 9 | 9 | | 2002 | 0 | 9 | 9 | | 2003 | 0 | 11 | 11 | | 2004 | 0 | 14 | 14 | | 2005 | 1 | 10 | 11 | | 2006 | 1 | 9 | 10 | | 2007 | 1 | 9 | 10 | | 2008 | 0 | 6 | 6 | | 2009 | 1 | 10 | 11 | | 2010 | 0 | 7 | 7 | | 2011 | 0 | 10 | 10 | | 2012 | 0 | 5 | 5 | | 2013 | 0 | 4 | 4 | | 2014 | 0 | 5 | 5 | | 2015 | 0 | 7 | 7 | | 2016 | 0 | 5 | 5 | | 2017 | 0 | 3 | 3 | | 2018 | 1 | 3 | 4 | | 2019 | 0 | 4 | 4 | | 2020 | 0 | 2 | 2 | | 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genes, Reporter" by people in Profiles.
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Poddar A, Azam MS, Kayikcioglu T, Bobrovskyy M, Zhang J, Ma X, Labhsetwar P, Fei J, Singh D, Luthey-Schulten Z, Vanderpool CK, Ha T. Effects of individual base-pairs on in vivo target search and destruction kinetics of bacterial small RNA. Nat Commun. 2021 02 08; 12(1):874.
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Hsiao CJ, Tung P, Blischak JD, Burnett JE, Barr KA, Dey KK, Stephens M, Gilad Y. Characterizing and inferring quantitative cell cycle phase in single-cell RNA-seq data analysis. Genome Res. 2020 04; 30(4):611-621.
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Shalaby S, Khater M, Laknaur A, Arbab A, Al-Hendy A. Molecular Bio-Imaging Probe for Non-Invasive Differentiation Between Human Leiomyoma Versus Leiomyosarcoma. Reprod Sci. 2020 02; 27(2):644-654.
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Miller ML, McIntosh CM, Wang Y, Chen L, Wang P, Lei YM, Daniels MD, Watkins E, Mora Solano C, Chong AS, Alegre ML. Resilience of T cell-intrinsic dysfunction in transplantation tolerance. Proc Natl Acad Sci U S A. 2019 11 19; 116(47):23682-23690.
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Liu L, Alizadeh K, Donnelly SC, Dassanayake P, Hou TT, McGirr R, Thompson RT, Prato FS, Gelman N, Hoffman L, Goldhawk DE. MagA expression attenuates iron export activity in undifferentiated multipotent P19 cells. PLoS One. 2019; 14(6):e0217842.
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Kim KX, Payne S, Yang-Hood A, Li SZ, Davis B, Carlquist J, V-Ghaffari B, Gantz JA, Kallogjeri D, Fitzpatrick JAJ, Ohlemiller KK, Hirose K, Rutherford MA. Vesicular Glutamatergic Transmission in Noise-Induced Loss and Repair of Cochlear Ribbon Synapses. J Neurosci. 2019 06 05; 39(23):4434-4447.
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Dan K, Veetil AT, Chakraborty K, Krishnan Y. DNA nanodevices map enzymatic activity in organelles. Nat Nanotechnol. 2019 03; 14(3):252-259.
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Szczaluba K, Chmielewska JJ, Sokolowska O, Rydzanicz M, Szymanska K, Feleszko W, Wlodarski P, Biernacka A, Murcia Pienkowski V, Walczak A, Bargel E, Królewczyk K, Nowacka A, Stawinski P, Nowis D, Dziembowska M, Ploski R. Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines. Clin Genet. 2018 12; 94(6):581-585.
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Dettinger P, Frank T, Etzrodt M, Ahmed N, Reimann A, Trenzinger C, Loeffler D, Kokkaliaris KD, Schroeder T, Tay S. Automated Microfluidic System for Dynamic Stimulation and Tracking of Single Cells. Anal Chem. 2018 09 18; 90(18):10695-10700.
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Wang XP, Liu YL, Mei LY, He CF, Niu ZJ, Sun J, Zhao YL, Feng Y, Zhang H. Wnt signaling pathway involvement in genotypic and phenotypic variations in Waardenburg syndrome type 2 with MITF mutations. J Hum Genet. 2018 May; 63(5):639-646.
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