 PAX2 Transcription Factor
"PAX2 Transcription Factor" 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 paired box transcription factor that is essential for ORGANOGENESIS of the CENTRAL NERVOUS SYSTEM and KIDNEY.
| Descriptor ID |
D051762
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| MeSH Number(s) |
D12.776.260.645.750 D12.776.930.700.750
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| Concept/Terms |
PAX2 Transcription Factor- PAX2 Transcription Factor
- Transcription Factor, PAX2
- Paired Box Gene 2 Protein
- Transcription Factor PAX2
- Factor PAX2, Transcription
- PAX2, Transcription Factor
- Paired Box Transcription Factor 2
- Paired Box Protein Pax-2
- Paired Box Protein Pax 2
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Below are MeSH descriptors whose meaning is more general than "PAX2 Transcription Factor".
Below are MeSH descriptors whose meaning is more specific than "PAX2 Transcription Factor".
This graph shows the total number of publications written about "PAX2 Transcription Factor" by people in this website by year, and whether "PAX2 Transcription Factor" 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 |
|---|
| 2011 | 1 | 0 | 1 | | 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "PAX2 Transcription Factor" by people in Profiles.
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Bekheirnia MR, Bekheirnia N, Bainbridge MN, Gu S, Coban Akdemir ZH, Gambin T, Janzen NK, Jhangiani SN, Muzny DM, Michael M, Brewer ED, Elenberg E, Kale AS, Riley AA, Swartz SJ, Scott DA, Yang Y, Srivaths PR, Wenderfer SE, Bodurtha J, Applegate CD, Velinov M, Myers A, Borovik L, Craigen WJ, Hanchard NA, Rosenfeld JA, Lewis RA, Gonzales ET, Gibbs RA, Belmont JW, Roth DR, Eng C, Braun MC, Lupski JR, Lamb DJ. Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene. Genet Med. 2017 04; 19(4):412-420.
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Thomas R, Sanna-Cherchi S, Warady BA, Furth SL, Kaskel FJ, Gharavi AG. HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort. Pediatr Nephrol. 2011 Jun; 26(6):897-903.
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