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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2015 | 1 | 1 | 2 |
| 2022 | 0 | 2 | 2 |
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Below are the most recent publications written about "Forkhead Transcription Factors" by people in Profiles.
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Genome-wide association study of actinic keratosis identifies new susceptibility loci implicated in pigmentation and immune regulation pathways. Commun Biol. 2022 04 21; 5(1):386.
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Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1. Genes (Basel). 2022 02 24; 13(3).
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Stromal immune infiltration in HIV-related diffuse large B-cell lymphoma is associated with HIV disease history and patient survival. AIDS. 2015 Sep 24; 29(15):1943-51.
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A newly identified susceptibility locus near FOXP1 modifies the association of gastroesophageal reflux with Barrett's esophagus. Cancer Epidemiol Biomarkers Prev. 2015 Nov; 24(11):1739-47.
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Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. Am J Hum Genet. 2011 Oct 07; 89(4):529-42.