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 |
|---|
| 1995 | 0 | 1 | 1 |
| 1997 | 0 | 3 | 3 |
| 1998 | 0 | 1 | 1 |
| 1999 | 0 | 3 | 3 |
| 2000 | 0 | 2 | 2 |
| 2001 | 0 | 6 | 6 |
| 2002 | 0 | 3 | 3 |
| 2003 | 0 | 8 | 8 |
| 2004 | 0 | 6 | 6 |
| 2005 | 3 | 6 | 9 |
| 2006 | 7 | 7 | 14 |
| 2007 | 22 | 8 | 30 |
| 2008 | 23 | 11 | 34 |
| 2009 | 18 | 11 | 29 |
| 2010 | 20 | 13 | 33 |
| 2011 | 18 | 13 | 31 |
| 2012 | 23 | 13 | 36 |
| 2013 | 27 | 17 | 44 |
| 2014 | 22 | 12 | 34 |
| 2015 | 21 | 6 | 27 |
| 2016 | 11 | 7 | 18 |
| 2017 | 8 | 7 | 15 |
| 2018 | 5 | 1 | 6 |
| 2019 | 6 | 6 | 12 |
| 2020 | 4 | 3 | 7 |
| 2021 | 3 | 6 | 9 |
| 2022 | 3 | 11 | 14 |
| 2023 | 1 | 8 | 9 |
| 2024 | 1 | 2 | 3 |
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Below are the most recent publications written about "Forkhead Transcription Factors" by people in Profiles.
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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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Differential Upregulation of Th1/Th17-Associated Proteins and PD-L1 in Granulomatous Mycosis Fungoides. Cells. 2024 Feb 27; 13(5).
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Reduced FOXF1 links unrepaired DNA damage to pulmonary arterial hypertension. Nat Commun. 2023 Nov 21; 14(1):7578.
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FoxO1 as a tissue-specific therapeutic target for type 2 diabetes. Front Endocrinol (Lausanne). 2023; 14:1286838.
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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.
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Foxi3GFP and Foxi3CreER mice allow identification and lineage labeling of pharyngeal arch ectoderm and endoderm, and tooth and hair placodes. Dev Dyn. 2023 Dec; 252(12):1462-1470.
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Histologic features and decreased lung FOXF1 gene expression in severe bronchopulmonary dysplasia without a genetic diagnosis of alveolar capillary dysplasia. Pediatr Pulmonol. 2023 10; 58(10):2746-2749.