Transcription Factors
"Transcription Factors" 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.
Endogenous substances, usually proteins, which are effective in the initiation, stimulation, or termination of the genetic transcription process.
| Descriptor ID |
D014157
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| MeSH Number(s) |
D12.776.930
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| Concept/Terms |
Transcription Factors- Transcription Factors
- Factors, Transcription
- Transcription Factor
- Factor, Transcription
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Below are MeSH descriptors whose meaning is more general than "Transcription Factors".
Below are MeSH descriptors whose meaning is more specific than "Transcription Factors".
This graph shows the total number of publications written about "Transcription Factors" by people in this website by year, and whether "Transcription Factors" 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 |
|---|
| 1996 | 23 | 7 | 30 | | 1997 | 22 | 12 | 34 | | 1998 | 16 | 14 | 30 | | 1999 | 18 | 10 | 28 | | 2000 | 22 | 13 | 35 | | 2001 | 22 | 19 | 41 | | 2002 | 38 | 21 | 59 | | 2003 | 36 | 19 | 55 | | 2004 | 47 | 24 | 71 | | 2005 | 28 | 33 | 61 | | 2006 | 23 | 23 | 46 | | 2007 | 22 | 11 | 33 | | 2008 | 23 | 22 | 45 | | 2009 | 22 | 22 | 44 | | 2010 | 17 | 25 | 42 | | 2011 | 20 | 21 | 41 | | 2012 | 27 | 32 | 59 | | 2013 | 34 | 23 | 57 | | 2014 | 28 | 24 | 52 | | 2015 | 14 | 23 | 37 | | 2016 | 33 | 25 | 58 | | 2017 | 30 | 21 | 51 | | 2018 | 27 | 19 | 46 | | 2019 | 20 | 18 | 38 | | 2020 | 17 | 25 | 42 | | 2021 | 18 | 19 | 37 | | 2022 | 10 | 39 | 49 | | 2023 | 7 | 33 | 40 | | 2024 | 7 | 18 | 25 | | 2025 | 16 | 6 | 22 | | 2026 | 7 | 8 | 15 |
To return to the timeline, click here.
Below are the most recent publications written about "Transcription Factors" by people in Profiles.
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Kim BJ, Hernández-García A, Curtis DL, Thompson O, Champaigne N, Priolo M, Radio FC, Tartaglia M, Gucsavas-Calikoglu M, Shiloh-Malawsky Y, Perilla-Young Y, Josephi-Taylor S, Bournazos AM, Cooper ST, van Gassen K, van den Boogaard MJ, Ozekin YH, Bates EA, Kongchan N, Hsu CW, Scott DA. SPEN deficiency contributes to the development of orofacial clefts in humans and mice. Hum Mol Genet. 2026 Jul 15; 35(15).
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Sarbaugh D, Oliveira TG, Guney MA, Casey MR, Hoelscher VM, Hill CJ, Michel CR, Wells KL, Benninger RKP, Sussel L. CHD4 and NKX2.2 Cooperate to Regulate ß-Cell Function by Repressing Non-ß-Cell Gene Programs. Diabetes. 2026 07 01; 75(7):1189-1200.
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Hawkins MB, Zdral S, Naranjo S, Juliá M, Sánchez-Martín M, Daane JM, Cumplido N, Jandzik D, Medeiros DM, McMenamin SK, Harris MP, Tena JJ, Ros MA. The origin and evolution of dorsal determination mechanisms in vertebrate paired appendages. Curr Biol. 2026 Jul 06; 36(13):3245-3257.e7.
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Jafree DJ, Russell LG, Stathopoulou A, O'Riordan C, Rowan CJ, White AT, Kolatsi-Joannou M, Price KL, Ivins S, Ridge LA, Roberts C, Rose A, Webb S, Vijayabaskar MS, Chandler JC, Wilson L, Pomeranz G, Moulding D, Davis B, Mitchell H, Siegenthaler J, Haniffa M, Woolf AS, Riley PR, Ruhrberg C, Scambler PJ, Rosenblum ND, Long DA. Osr1-expressing mesoderm contributes to lymphatic vessel assembly and complexity in the mammalian kidney. Cell Rep. 2026 Jul 28; 45(7):117560.
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Chiles JW, Rocco A, Srinivasasainagendra V, Rossiter HB, Casaburi R, Thalacker-Mercer A, Wells JM, Wan ES, Silverman EK, Cho MH, Hersh CP, Psaty BM, Gharib SA, Gao Y, O'Connor GT, Lange LA, Rich SS, Manichaikul AW, Barr RG, Ortega VE, Meyers DA, Smith AV, Tiwari HK, McDonald MN. Whole Genome Sequence Analysis of Weight Loss in 16?972 Participants With COPD Reveals Novel Risk Loci in DRAIC and RFX3. J Cachexia Sarcopenia Muscle. 2026 Jun; 17(3):e70293.
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Balolia A, Arena KA, Shahood A, Russom H, Tran LN, Winkler CC, O'Rourke R, Vue TY, Sagerström CG, Appel BH, Franco SJ. Ascl1 promotes OPC specification across species and central nervous system regions and its gliogenic function is regulated by phosphorylation. Dev Biol. 2026 Aug; 536:184-201.
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Kendirli PK, Erdem S, Kisaarslan AP, Gök V, Kayhan E, Özcan A, Dogan ME, Klein C, Ünal E, Eken A. A novel ELF4 gene variant disrupts T and NK cell function in a patient with immune thrombocytopenia (ITP). Inflamm Res. 2026 May 19; 75(1).
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Bledsoe JR, Ferry JA, Li J, Sassoon A, Stonhill MA, Siegele B, Liang X, Dalton J, Mochel MC, Ivashkevich Y, Johari V, Sadigh S, Selove W, Sood S, Ward N, Woda B, Degar B, Feraco AM, Rowe J, Davies K, Al-Ibraheemi A, Amador C, Kovach AE, Fleming MD, Harris MH, Tsai HK. Recurrent SWI/SNF Deficiency Defines a Subset of Peripheral T-Cell Lymphoma With Distinct Clinicopathologic Features. Mod Pathol. 2026 Jul; 39(7):101015.
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Watts LM, Chang MSM, Lewis-Orr E, Walton IS, Leinhos L, Tooze RS, Pei Y, Calpena E, Vedovato-Dos-Santos JH, Steel D, Reid KM, Kurian MA, Mohammad SS, Cantagrel V, Siquier K, Boddaert N, Rio M, Blyth M, Kraus A, Al Mutairi F, Holder SE, Clowes VE, Cobben JM, Timberlake AT, Elias ER, Stewart H, Johnson D, Cohen JS, Barañano KW, Ceulemans S, Jones MC, Ortega Rico RI, Haug MG, Berland S, Bombei HM, Paulson A, Sidhu A, Gooch CF, da Rocha KM, Passos Bueno MR, Topa A, Muslimovic AZ, Maltese G, Tan TY, McCann E, Lord H, Chin HL, Lin J, Li-Meng Goh D, Keren B, Charles P, Delchev T, Avdjieva-Tzavella D, Alawbathani S, Almeida L, Kdissa A, Al-Ali R, Bertoli-Avella AM, Johnson D, Wilkie AOM, Arkell RM, Shears DJ, Twigg SRF. Expanding the phenotypic spectrum associated with ZIC1 variants: A neurodevelopmental disorder with and without craniosynostosis. Genet Med. 2026 Jun; 28(6):102585.
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Bidany-Mizrahi T, Maroun K, Mancini M, Hidmi O, Ansari I, Monin J, Keidar Haran T, Maly A, Melino G, Candi E, Aqeilan RI. WWOX maintains epidermal identity and suppresses EMT to prevent aggressive cutaneous squamous cell carcinoma. Proc Natl Acad Sci U S A. 2026 Apr 21; 123(16):e2534844123.
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