Xeroderma Pigmentosum Group D Protein
"Xeroderma Pigmentosum Group D Protein" 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 DNA helicase that is a component of TRANSCRIPTION FACTOR TFIIH. It plays an essential role in NUCLEOTIDE EXCISION REPAIR, and mutations in this protein are associated with XERODERMA PIGMENTOSUM.
Descriptor ID |
D051759
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MeSH Number(s) |
D08.811.277.040.025.159.500 D08.811.399.340.500 D12.776.260.775.875.875.500 D12.776.930.930.875.875.500
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Concept/Terms |
Xeroderma Pigmentosum Group D Protein- Xeroderma Pigmentosum Group D Protein
- Excision Repair Cross-Complementing Rodent Repair Deficiency, Group 2 Protein
- Excision Repair Cross Complementing Rodent Repair Deficiency, Group 2 Protein
- Xeroderma Pigmentosum Complementation Group D Protein
- ERCC2 Protein
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Below are MeSH descriptors whose meaning is more general than "Xeroderma Pigmentosum Group D Protein".
Below are MeSH descriptors whose meaning is more specific than "Xeroderma Pigmentosum Group D Protein".
This graph shows the total number of publications written about "Xeroderma Pigmentosum Group D Protein" by people in this website by year, and whether "Xeroderma Pigmentosum Group D Protein" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1997 | 0 | 1 | 1 |
2000 | 0 | 2 | 2 |
2001 | 0 | 1 | 1 |
2002 | 0 | 3 | 3 |
2004 | 0 | 2 | 2 |
2005 | 1 | 2 | 3 |
2006 | 1 | 1 | 2 |
2007 | 0 | 1 | 1 |
2008 | 2 | 1 | 3 |
2009 | 0 | 2 | 2 |
2010 | 0 | 1 | 1 |
2011 | 2 | 0 | 2 |
2012 | 2 | 1 | 3 |
2013 | 1 | 2 | 3 |
2016 | 1 | 0 | 1 |
2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Xeroderma Pigmentosum Group D Protein" by people in Profiles.
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Envisioning how the prototypic molecular machine TFIIH functions in transcription initiation and DNA repair. DNA Repair (Amst). 2020 12; 96:102972.
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Exploratory analysis of ERCC2 DNA methylation in survival among pediatric medulloblastoma patients. Cancer Epidemiol. 2016 10; 44:161-166.
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ERCC1 and ERCC2 variants predict survival in gastric cancer patients. PLoS One. 2013; 8(9):e71994.
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Variants in nucleotide excision repair core genes and susceptibility to recurrence of squamous cell carcinoma of the oropharynx. Int J Cancer. 2013 Aug 01; 133(3):695-704.
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Polymorphisms of nucleotide excision repair genes predict melanoma survival. J Invest Dermatol. 2013 Jul; 133(7):1813-21.
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Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells. Proc Natl Acad Sci U S A. 2013 Jan 15; 110(3):E212-20.
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A Turkish trichothiodystrophy patient with homozygous XPD mutation and genotype-phenotype relationship. J Dermatol. 2012 Dec; 39(12):1016-21.
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DNA charge transport as a first step in coordinating the detection of lesions by repair proteins. Proc Natl Acad Sci U S A. 2012 Feb 07; 109(6):1856-61.
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ATP-stimulated, DNA-mediated redox signaling by XPD, a DNA repair and transcription helicase. J Am Chem Soc. 2011 Oct 19; 133(41):16378-81.
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XPB and XPD helicases in TFIIH orchestrate DNA duplex opening and damage verification to coordinate repair with transcription and cell cycle via CAK kinase. DNA Repair (Amst). 2011 Jul 15; 10(7):697-713.