Forkhead Transcription Factors
"Forkhead 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.
A subclass of winged helix DNA-binding proteins that share homology with their founding member fork head protein, Drosophila.
| Descriptor ID |
D051858
|
| MeSH Number(s) |
D12.776.260.950.249 D12.776.930.977.249
|
| Concept/Terms |
Forkhead Transcription Factors- Forkhead Transcription Factors
- Transcription Factors, Forkhead
- Fox Transcription Factors
- Transcription Factors, Fox
- Forkhead Proteins
- Forkhead Box Proteins
- Forkhead Box Transcription Factors
|
Below are MeSH descriptors whose meaning is more general than "Forkhead Transcription Factors".
Below are MeSH descriptors whose meaning is more specific than "Forkhead Transcription Factors".
This graph shows the total number of publications written about "Forkhead Transcription Factors" by people in this website by year, and whether "Forkhead 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 |
|---|
| 1997 | 0 | 3 | 3 |
| 1998 | 0 | 1 | 1 |
| 1999 | 0 | 2 | 2 |
| 2000 | 0 | 2 | 2 |
| 2001 | 0 | 4 | 4 |
| 2002 | 0 | 2 | 2 |
| 2003 | 0 | 4 | 4 |
| 2004 | 0 | 5 | 5 |
| 2005 | 2 | 4 | 6 |
| 2006 | 4 | 3 | 7 |
| 2007 | 9 | 2 | 11 |
| 2008 | 9 | 4 | 13 |
| 2009 | 5 | 9 | 14 |
| 2010 | 6 | 7 | 13 |
| 2011 | 2 | 5 | 7 |
| 2012 | 6 | 9 | 15 |
| 2013 | 12 | 9 | 21 |
| 2014 | 6 | 9 | 15 |
| 2015 | 9 | 4 | 13 |
| 2016 | 9 | 8 | 17 |
| 2017 | 4 | 4 | 8 |
| 2018 | 1 | 1 | 2 |
| 2019 | 6 | 3 | 9 |
| 2020 | 4 | 2 | 6 |
| 2021 | 4 | 6 | 10 |
| 2022 | 2 | 10 | 12 |
| 2023 | 1 | 9 | 10 |
| 2024 | 2 | 1 | 3 |
| 2025 | 0 | 1 | 1 |
| 2026 | 1 | 0 | 1 |
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Below are the most recent publications written about "Forkhead Transcription Factors" by people in Profiles.
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MiR-200c restoration inhibits FOXP3 and metastatic spread in breast cancer: evidence from in vitro and in vivo models. BMC Cancer. 2026 Feb 14; 26(1).
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HLA matching or CRISPR editing of HLA class I/II enables engraftment and effective function of allogeneic human regulatory T cell therapy in a humanized mouse transplantation model. Nat Commun. 2025 Oct 13; 16(1):9090.
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Identification of functional non-coding variants associated with orofacial cleft. Nat Commun. 2025 Jul 16; 16(1):6545.
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Joint contractures is a recurrent clinical feature of individuals with neurodevelopmental disorder due to FOXP1 likely gene disruptive variants. Am J Med Genet A. 2024 Nov; 194(11):e63713.
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Deep sequencing of candidate genes identified 14 variants associated with smoking abstinence in an ethnically diverse sample. Sci Rep. 2024 03 16; 14(1):6385.
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The MiR-200c/FOXP3 Network: A Promising Biomarker for Predicting Trastuzumab Response in HER2-Positive Breast Cancer. Technol Cancer Res Treat. 2024 Jan-Dec; 23:15330338241292226.
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Reduced FOXF1 links unrepaired DNA damage to pulmonary arterial hypertension. Nat Commun. 2023 11 21; 14(1):7578.
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Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasia. Clin Epigenetics. 2023 10 21; 15(1):169.
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The Foxi3 transcription factor is necessary for the fate restriction of placodal lineages at the neural plate border. Development. 2023 10 01; 150(19).
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Single Cell Multiomics Identifies Cells and Genetic Networks Underlying Alveolar Capillary Dysplasia. Am J Respir Crit Care Med. 2023 09 15; 208(6):709-725.