Xeroderma pigmentosum (XP) is a genetic disorder in which there is a decreased ability to repair DNA damage such as that caused by ultraviolet (UV) light...
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allergens such as fragrances, parabens, and lanolin. Eczema Ichthyosis Xeroderma pigmentosum Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007)...
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Progeroid syndromes (section Xeroderma pigmentosum)
(RTS), Cockayne syndrome (CS), xeroderma pigmentosum (XP), trichothiodystrophy (TTD), combined xeroderma pigmentosum-Cockayne syndrome (XP-CS), restrictive...
74 KB (8,726 words) - 06:14, 3 June 2024
ERCC2 (section Xeroderma pigmentosum)
result in three different disorders: the cancer-prone syndrome xeroderma pigmentosum complementation group D, photosensitive trichothiodystrophy, and...
15 KB (1,846 words) - 03:56, 27 June 2024
XPB (xeroderma pigmentosum type B) is an ATP-dependent DNA helicase in humans that is a part of the TFIIH transcription factor complex. The 3D-structure...
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DNA ligase (section Xeroderma pigmentosum)
caused by lack of or malfunctioning of DNA ligase is as follows. Xeroderma pigmentosum, which is commonly known as XP, is an inherited condition characterized...
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15-year-old boy diagnosed with an incurable skin disease called XP (Xeroderma Pigmentosum). "ドラマ「大奥」医療編に高嶋政伸、木村了、中川翼、味方良介、高木渉、津田健次郎". Natalie. Retrieved October...
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XPA (redirect from Xeroderma pigmentosum group a protein)
Xpa mutant individuals often show the severe clinical symptoms of xeroderma pigmentosum, a condition involving extreme sensitivity to sunlight and a high...
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Schwarzenegger, and Rob Riggle. The story is about a teenaged girl with xeroderma pigmentosum (XP), a medical condition which prevents her from going out into...
22 KB (1,698 words) - 02:51, 16 August 2024
Xeroderma pigmentosum, complementation group C, also known as XPC, is a protein which in humans is encoded by the XPC gene. XPC is involved in the recognition...
16 KB (1,923 words) - 21:51, 26 November 2023
known as XPV, because loss of this gene results in the disease xeroderma pigmentosum. Polymerase eta is particularly important for allowing accurate...
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MUTYH-associated polyposis, Rothmund–Thomson syndrome, Werner syndrome and Xeroderma pigmentosum. Although cancer syndromes exhibit an increased risk of cancer,...
51 KB (5,582 words) - 14:19, 15 July 2024
hereditary Xeroderma Xeroderma pigmentosum Xeroderma pigmentosum, type 1 Xeroderma pigmentosum, type 2 Xeroderma pigmentosum, type 3 Xeroderma pigmentosum, type...
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genetic disorder characterized by the skin and eye symptoms of xeroderma pigmentosum (XP) occurring in association with microcephaly, progressive intellectual...
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Atypical fibroxanthoma has also been associated with P53 mutations, xeroderma pigmentosum, radiation therapy, trauma, and immunosuppression. Because atypical...
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significant source of UV radiation. Genetic predispositions, such as xeroderma pigmentosum and certain forms of epidermolysis bullosa, also increase susceptibility...
52 KB (5,304 words) - 14:34, 29 May 2024
diseases that result from in-born genetic mutations of NER proteins. Xeroderma pigmentosum and Cockayne's syndrome are two examples of NER associated diseases...
33 KB (3,623 words) - 09:45, 28 July 2024
XPG N terminus (section Xeroderma pigmentosum)
The amino acid linking the N- and I-regions are not conserved. Xeroderma pigmentosum (XP) is a human autosomal recessive disease, characterised by a...
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aging diseases" (such as Werner syndrome, Cockayne syndrome or xeroderma pigmentosum), progeria may not be directly caused by defective DNA repair. These...
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polymerase can cause various diseases, such as skin cancer and Xeroderma Pigmentosum Variant (XPS). The importance of these polymerases is evidenced...
59 KB (7,090 words) - 06:49, 30 June 2024
UVRAG gene. This gene complements the ultraviolet sensitivity of xeroderma pigmentosum group C cells and encodes a protein with a C2 domain. The protein...
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are at greater risk. A number of rare genetic conditions, such as xeroderma pigmentosum, also increase the risk. Diagnosis is by biopsy and analysis of...
154 KB (16,076 words) - 04:50, 7 August 2024
type of change in appearance, but pointed to the skin condition xeroderma pigmentosum as an example of a mutation which makes marks on the skin upon exposure...
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ERCC4 (section Xeroderma pigmentosum (XP))
absent, these mutations can lead to human syndromes, including xeroderma pigmentosum, Cockayne syndrome and Fanconi anemia. ERCC1 and ERCC4 are the human...
27 KB (3,315 words) - 00:33, 27 January 2024
will live into adulthood. Xeroderma pigmentosum-Cockayne syndrome (XP-CS) occurs when an individual also has xeroderma pigmentosum, another DNA repair disease...
30 KB (3,089 words) - 22:40, 1 January 2024
of cancers. An example of such a hereditary cancer syndrome is xeroderma pigmentosum, which causes the development of skin cancers in response to even...
96 KB (9,819 words) - 12:03, 26 July 2024
character Christopher Snow, who suffers from the genetic disorder Xeroderma pigmentosum. Only the first two books have been released; no release date is...
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young man who suffers from the rare (but real) disease called XP (xeroderma pigmentosum). Book one, Fear Nothing, was released in 1998, and book two, Seize...
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excinuclease occurs in a rare autosomal recessive disease called xeroderma pigmentosum. This disease can cause light-skin, extreme freckling and facial...
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POLI (section Xeroderma pigmentosum variant)
conformation across guanine, which it flips to the syn conformation. Xeroderma pigmentosum variant (XPV) cells lack DNA polymerase eta (η). Instead these cells...
8 KB (1,030 words) - 01:05, 31 May 2024