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...

(RTS), Cockayne syndrome (CS), xeroderma pigmentosum (XP), trichothiodystrophy (TTD), combined xeroderma pigmentosum-Cockayne syndrome (XP-CS), restrictive...

allergens such as fragrances, parabens, and lanolin. Eczema Ichthyosis Xeroderma pigmentosum Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007)...

known as XPV, because loss of this gene results in the disease xeroderma pigmentosum. Polymerase eta is particularly important for allowing accurate...

MUTYH-associated polyposis, Rothmund–Thomson syndrome, Werner syndrome and Xeroderma pigmentosum. Although cancer syndromes exhibit an increased risk of cancer,...

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...

diseases that result from in-born genetic mutations of NER proteins. Xeroderma pigmentosum and Cockayne's syndrome are two examples of NER associated diseases...

will live into adulthood. Xeroderma pigmentosum-Cockayne syndrome (XP-CS) occurs when an individual also has xeroderma pigmentosum, another DNA repair disease...

conformation across guanine, which it flips to the syn conformation. Xeroderma pigmentosum variant (XPV) cells lack DNA polymerase eta (η). Instead these cells...

result in three different disorders: the cancer-prone syndrome xeroderma pigmentosum complementation group D, photosensitive trichothiodystrophy, and...

genetic disorder characterized by the skin and eye symptoms of xeroderma pigmentosum (XP) occurring in association with microcephaly, progressive intellectual...

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...

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...

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...

absent, these mutations can lead to human syndromes, including xeroderma pigmentosum, Cockayne syndrome and Fanconi anemia. ERCC1 and ERCC4 are the human...

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...

autosomal recessive gene causing degrees of the variant form of xeroderma pigmentosum, an inherited condition causing decreased ability to repair DNA...

Xpa mutant individuals often show the severe clinical symptoms of xeroderma pigmentosum, a condition involving extreme sensitivity to sunlight and a high...

the consequence of otherwise rare genetic diseases, for example xeroderma pigmentosum, stemming from recessive genes achieving greater dominance. An alternative...

porphyria are aggravated by sunlight. A rare hereditary condition xeroderma pigmentosum (a defect in DNA repair) is thought to increase the risk of...

The amino acid linking the N- and I-regions are not conserved. Xeroderma pigmentosum (XP) is a human autosomal recessive disease, characterised by a...

significant source of UV radiation. Genetic predispositions, such as xeroderma pigmentosum and certain forms of epidermolysis bullosa, also increase susceptibility...

sensitive to sunlight. Certain genetic conditions, for example, xeroderma pigmentosum, increase a person's susceptibility to sunburn and subsequent skin...

Atypical fibroxanthoma has also been associated with P53 mutations, xeroderma pigmentosum, radiation therapy, trauma, and immunosuppression. Because atypical...

genetic defects that cause disorders such as sickle cell disease, xeroderma pigmentosum, and epidermolysis bullosa. Recently, it was shown that TALEN can...

of cancers. An example of such a hereditary cancer syndrome is xeroderma pigmentosum, which causes the development of skin cancers in response to even...

defects can result in other rare autosomal recessive diseases like xeroderma pigmentosum and Cockayne syndrome. Currently, mutations in four genes are recognized...

Camp Sundown is a summer camp for children with xeroderma pigmentosum. All activities are held after sundown, to ensure that the children are not injured...

ataxia–telangiectasia, Nijmegen breakage syndrome, some subgroups of xeroderma pigmentosum, trichothiodystrophy, Fanconi anemia, Bloom syndrome and Rothmund–Thomson...

excinuclease occurs in a rare autosomal recessive disease called xeroderma pigmentosum. This disease can cause light-skin, extreme freckling and facial...