SOXE Transcription Factors
"SOXE 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 closely-related SOX transcription factors. Members of this subfamily have been implicated in regulating the differentiation of OLIGODENDROCYTES during neural crest formation and in CHONDROGENESIS.
| Descriptor ID |
D055757
|
| MeSH Number(s) |
D12.776.260.719.500 D12.776.660.235.400.750.500 D12.776.664.235.400.750.500 D12.776.930.823.500
|
| Concept/Terms |
SOX8 Transcription Factor- SOX8 Transcription Factor
- Transcription Factor, SOX8
- SOX8 Transcription Factors
- Transcription Factors, SOX8
- SOX-8 Transcription Factor
- SOX 8 Transcription Factor
- Transcription Factor, SOX-8
SOX10 Transcription Factor- SOX10 Transcription Factor
- Transcription Factor, SOX10
- SOX-10 Transcription Factor
- SOX 10 Transcription Factor
- Transcription Factor, SOX-10
|
Below are MeSH descriptors whose meaning is more general than "SOXE Transcription Factors".
Below are MeSH descriptors whose meaning is more specific than "SOXE Transcription Factors".
This graph shows the total number of publications written about "SOXE Transcription Factors" by people in this website by year, and whether "SOXE Transcription Factors" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
| 2003 | 0 | 1 | 1 |
| 2004 | 0 | 1 | 1 |
| 2007 | 0 | 1 | 1 |
| 2010 | 1 | 1 | 2 |
| 2014 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2022 | 1 | 1 | 2 |
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Below are the most recent publications written about "SOXE Transcription Factors" by people in Profiles.
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Diagnostic utility of SOX10 immunostaining in benign lichenoid keratosis: A study of 21 cases. J Cutan Pathol. 2023 Jan; 50(1):51-55.
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TRPS1, GATA3, and SOX10 expression in triple-negative breast carcinoma. Hum Pathol. 2022 07; 125:97-107.
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22q11.2q13 duplication including SOX10 causes sex-reversal and peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, and Hirschsprung disease. Am J Med Genet A. 2017 Apr; 173(4):1066-1070.
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Mutual antagonism between Sox10 and NFIA regulates diversification of glial lineages and glioma subtypes. Nat Neurosci. 2014 Oct; 17(10):1322-9.
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Diagnostic utility and comparative immunohistochemical analysis of MITF-1 and SOX10 to distinguish melanoma in situ and actinic keratosis: a clinicopathological and immunohistochemical study of 70 cases. Am J Dermatopathol. 2014 Feb; 36(2):124-30.
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A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivo. PLoS One. 2010 Dec 16; 5(12):e14346.
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Interruption of SOX10 function in myelinopathies. Ann Neurol. 2010 Aug; 68(2):121-3.
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Translation of SOX10 3' untranslated region causes a complex severe neurocristopathy by generation of a deleterious functional domain. Hum Mol Genet. 2007 Dec 15; 16(24):3037-46.
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Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations. Nat Genet. 2004 Apr; 36(4):361-9.
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Intestinal aganglionosis associated with the Waardenburg syndrome: report of two cases and review of the literature. Pediatr Surg Int. 2003 Dec; 19(11):725-8.