Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 2
1990 1
1992 2
1993 1
1995 1
2000 1
2001 1
2002 2
2004 2
2005 1
2006 1
2008 1
2009 3
2010 2
2011 2
2012 2
2013 4
2014 1
2015 4
2016 3
2017 3
2018 2
2019 3
2020 2
2021 1
2022 2
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

42 results

Results by year

Filters applied: . Clear all
Your search was processed without automatic term mapping because it retrieved zero results.
Page 1
Xeroderma pigmentosum group C sensor: unprecedented recognition strategy and tight spatiotemporal regulation.
Puumalainen MR, Rüthemann P, Min JH, Naegeli H. Puumalainen MR, et al. Cell Mol Life Sci. 2016 Feb;73(3):547-66. doi: 10.1007/s00018-015-2075-z. Epub 2015 Oct 31. Cell Mol Life Sci. 2016. PMID: 26521083 Free PMC article. Review.
The cellular defense system known as global-genome nucleotide excision repair (GG-NER) safeguards genome stability by eliminating a plethora of structurally unrelated DNA adducts inflicted by chemical carcinogens, ultraviolet (UV) radiation or endogenous metabolic by-products. …
The cellular defense system known as global-genome nucleotide excision repair (GG-NER) safeguards genome stability by eliminating a plethora …
Xeroderma pigmentosum complementation group F: Report of a case and review of Japanese patients.
Tofuku Y, Nobeyama Y, Kamide R, Moriwaki S, Nakagawa H. Tofuku Y, et al. J Dermatol. 2015 Sep;42(9):897-9. doi: 10.1111/1346-8138.12942. Epub 2015 May 25. J Dermatol. 2015. PMID: 26010807 Review.
Xeroderma pigmentosum (XP) is an autosomal recessive genetic disorder characterized by extraordinary sensitivity to sunlight, resulting in cutaneous malignant tumors. Among XP, XP-F presents relatively uniquely in Japanese. To clarify the characteristics of this
Xeroderma pigmentosum (XP) is an autosomal recessive genetic disorder characterized by extraordinary sensitivity to sunlight,
Identification of a novel DDB2 mutation in a Chinese Han family with Xeroderma pigmentosum group E:a case report and literature review.
Yang R, Kong Q, Duan Y, Li W, Sang H. Yang R, et al. BMC Med Genet. 2020 Mar 30;21(1):67. doi: 10.1186/s12881-020-00997-0. BMC Med Genet. 2020. PMID: 32228487 Free PMC article. Review.
BACKGROUND: Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis. ...CASE PRESENTATION: We report a case of a 28-year-old Chinese woman with freckle-like hyperpigmented macules in a sun-exposed area who is prone to develop basal cell carcinomas. A …
BACKGROUND: Xeroderma pigmentosum (XP) is a rare autosomal recessive genodermatosis. ...CASE PRESENTATION: We report a case of …
XPC beyond nucleotide excision repair and skin cancers.
Zebian A, Shaito A, Mazurier F, Rezvani HR, Zibara K. Zebian A, et al. Mutat Res Rev Mutat Res. 2019 Oct-Dec;782:108286. doi: 10.1016/j.mrrev.2019.108286. Epub 2019 Jul 8. Mutat Res Rev Mutat Res. 2019. PMID: 31843141 Review.
Xeroderma pigmentosum group C (XPC) has been known as a DNA damage recognition factor of bulky adducts and as an initiator of global genome nucleotide excision repair (GG-NER). XP-C patients have been shown to have a predisposition to develop sk
Xeroderma pigmentosum group C (XPC) has been known as a DNA damage recognition factor of bulky adducts and as an
Characteristics of Xeroderma Pigmentosum in Japan: Lessons From Two Clinical Surveys and Measures for Patient Care.
Nishigori C, Nakano E, Masaki T, Ono R, Takeuchi S, Tsujimoto M, Ueda T. Nishigori C, et al. Photochem Photobiol. 2019 Jan;95(1):140-153. doi: 10.1111/php.13052. Epub 2018 Dec 28. Photochem Photobiol. 2019. PMID: 30565713 Review.
Xeroderma pigmentosum (XP) is a rare autosomal recessive hereditary disease caused by deficiency in repair of DNA lesions generated by ultraviolet radiation and other compounds. ...We conducted a nationwide survey for XP since 1980. In Japan, the frequency of the XP
Xeroderma pigmentosum (XP) is a rare autosomal recessive hereditary disease caused by deficiency in repair of DNA lesions gene
Molecular analysis directs the prognosis, management and treatment of patients with xeroderma pigmentosum.
Lehmann AR, Fassihi H. Lehmann AR, et al. DNA Repair (Amst). 2020 Sep;93:102907. doi: 10.1016/j.dnarep.2020.102907. DNA Repair (Amst). 2020. PMID: 33087273 Review.
Xeroderma pigmentosum (XP) is a well-studied disorder of (in most cases) nucleotide excision repair. ...Splicing mutations in XPA and XPD and a specific amino acid change in XPD are associated with mild phenotypes, and individuals assigned to the XP-F group a
Xeroderma pigmentosum (XP) is a well-studied disorder of (in most cases) nucleotide excision repair. ...Splicing mutations in
The association between XPG polymorphisms and cancer susceptibility: Evidence from observational studies.
Han C, Huang X, Hua R, Song S, Lyu L, Ta N, Zhu J, Zhang P. Han C, et al. Medicine (Baltimore). 2017 Aug;96(32):e7467. doi: 10.1097/MD.0000000000007467. Medicine (Baltimore). 2017. PMID: 28796034 Free PMC article. Review.
If not properly repaired, the DNA damages may increase the risk of carcinogenesis. Xeroderma pigmentosum group G (XPG) gene is an essential gene in the nucleotide excision repair (NER) pathway. ...However, we observed strong correlation between rs751402 polym …
If not properly repaired, the DNA damages may increase the risk of carcinogenesis. Xeroderma pigmentosum group G (XPG) …
Xeroderma pigmentosum: from symptoms and genetics to gene-based skin therapy.
Magnaldo T, Sarasin A. Magnaldo T, et al. Cells Tissues Organs. 2004;177(3):189-98. doi: 10.1159/000079993. Cells Tissues Organs. 2004. PMID: 15388993 Review.
Xeroderma pigmentosum (XP) is a rare, recessively inherited genodermatosis prone to ultraviolet (UV)-induced skin neoplasms from keratinocyte origin, i.e. basal and squamous cell carcinoma. ...Encouraging results of retrovirus-based genetic correction of XP keratino
Xeroderma pigmentosum (XP) is a rare, recessively inherited genodermatosis prone to ultraviolet (UV)-induced skin neoplasms fr
DNA repair as an emerging target for COPD-lung cancer overlap.
Sears CR. Sears CR. Respir Investig. 2019 Mar;57(2):111-121. doi: 10.1016/j.resinv.2018.11.005. Epub 2019 Jan 7. Respir Investig. 2019. PMID: 30630751 Free article. Review.
We discuss emerging data supporting a key role for the DNA repair protein, xeroderma pigmentosum group C (XPC), in cigarette smoke-induced COPD and early lung cancer development. ...
We discuss emerging data supporting a key role for the DNA repair protein, xeroderma pigmentosum group C (XPC), …
The role of UV-DDB in processing 8-oxoguanine during base excision repair.
Nagpal A, Raja S, Van Houten B. Nagpal A, et al. Biochem Soc Trans. 2022 Oct 31;50(5):1481-1488. doi: 10.1042/BST20220748. Biochem Soc Trans. 2022. PMID: 36305644 Free PMC article. Review.
Recent data from our laboratory has shown that the nucleotide excision repair (NER) proteins UV-damaged DNA-binding protein (UV-DDB), xeroderma pigmentosum group C (XPC), and xeroderma pigmentosum group A (XPA) play important roles …
Recent data from our laboratory has shown that the nucleotide excision repair (NER) proteins UV-damaged DNA-binding protein (UV-DDB), xer
42 results