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
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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 |
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1999 | 0 | 1 | 1 |
2002 | 0 | 1 | 1 |
2003 | 0 | 1 | 1 |
2004 | 0 | 2 | 2 |
2007 | 0 | 1 | 1 |
2010 | 1 | 1 | 2 |
2011 | 1 | 0 | 1 |
2014 | 3 | 0 | 3 |
2016 | 0 | 1 | 1 |
2017 | 0 | 1 | 1 |
2020 | 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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Pigmented PRRX1::NCOA1-rearranged fibroblastic tumor: A rare morphologic variant of an emerging mesenchymal tumor. J Cutan Pathol. 2022 Sep; 49(9):802-807.
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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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Three Types of Nodal Melanocytic Nevi in Sentinel Lymph Nodes of Patients With Melanoma: Pitfalls, Immunohistochemistry, and a Review of the Literature. Am J Dermatopathol. 2020 Oct; 42(10):739-744.
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Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies. Hum Mol Genet. 2018 04 01; 27(7):1228-1240.
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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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Decrease in newly generated oligodendrocytes leads to motor dysfunctions and changed myelin structures that can be rescued by transplanted cells. Glia. 2016 12; 64(12):2201-2218.
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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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Reliability of immunostaining using pan-melanoma cocktail, SOX10, and microphthalmia transcription factor in confirming a diagnosis of melanoma on fine-needle aspiration smears. Cancer Cytopathol. 2014 Oct; 122(10):779-85.
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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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Sox10-positive sustentacular cells in neuroendocrine carcinoma of the lung. Histopathology. 2011 Jan; 58(2):276-85.