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
1946 2
1948 1
1953 1
1962 1
1964 2
1965 1
1967 1
1969 2
1970 4
1971 8
1972 5
1973 5
1974 8
1975 12
1976 6
1977 9
1978 20
1979 18
1980 19
1981 28
1982 23
1983 15
1984 21
1985 22
1986 38
1987 22
1988 20
1989 22
1990 18
1991 21
1992 36
1993 28
1994 33
1995 20
1996 32
1997 23
1998 21
1999 28
2000 38
2001 33
2002 37
2003 22
2004 34
2005 41
2006 33
2007 34
2008 43
2009 42
2010 44
2011 56
2012 50
2013 41
2014 52
2015 50
2016 54
2017 40
2018 42
2019 36
2020 34
2021 38
2022 35
2023 34
2024 15

Text availability

Article attribute

Article type

Publication date

Search Results

1,463 results

Results by year

Filters applied: . Clear all
Page 1
Xeroderma pigmentosum.
Norgauer J, Idzko M, Panther E, Hellstern O, Herouy Y. Norgauer J, et al. Eur J Dermatol. 2003 Jan-Feb;13(1):4-9. Eur J Dermatol. 2003. PMID: 12609773 Review.
Xeroderma pigmentosum is a rare disorder transmitted in an autosomal recessive manner. Xeroderma pigmentosum is based on a genetic defect in the DNA repair system. ...
Xeroderma pigmentosum is a rare disorder transmitted in an autosomal recessive manner. Xeroderma pigmentosum is based on a gen …
Xeroderma pigmentosum.
Lehmann AR, McGibbon D, Stefanini M. Lehmann AR, et al. Orphanet J Rare Dis. 2011 Nov 1;6:70. doi: 10.1186/1750-1172-6-70. Orphanet J Rare Dis. 2011. PMID: 22044607 Free PMC article. Review.
Xeroderma pigmentosum (XP) is defined by extreme sensitivity to sunlight, resulting in sunburn, pigment changes in the skin and a greatly elevated incidence of skin cancers. ...
Xeroderma pigmentosum (XP) is defined by extreme sensitivity to sunlight, resulting in sunburn, pigment changes in the skin and a gre …
Xeroderma Pigmentosum - Facts and Perspectives.
Lehmann J, Seebode C, Martens MC, Emmert S. Lehmann J, et al. Anticancer Res. 2018 Feb;38(2):1159-1164. doi: 10.21873/anticanres.12335. Anticancer Res. 2018. PMID: 29374753 Review.
Ultraviolet (UV)-induced DNA lesions are almost exclusively removed by the nucleotide excision repair (NER) pathway, which is essential for prevention of skin cancer development. Patients with xeroderma pigmentosum (XP) are extremely sun sensitive due to a genetic defect i …
Ultraviolet (UV)-induced DNA lesions are almost exclusively removed by the nucleotide excision repair (NER) pathway, which is essential for …
Xeroderma pigmentosum-Cockayne syndrome complex.
Natale V, Raquer H. Natale V, et al. Orphanet J Rare Dis. 2017 Apr 4;12(1):65. doi: 10.1186/s13023-017-0616-2. Orphanet J Rare Dis. 2017. PMID: 28376890 Free PMC article. Review.
Xeroderma pigmentosum-Cockayne syndrome complex is a very rare multisystem degenerative disorder (Orpha: 220295; OMIM: 278730, 278760, 278780, 610651). ...
Xeroderma pigmentosum-Cockayne syndrome complex is a very rare multisystem degenerative disorder (Orpha: 220295; OMIM: 278730, 278760 …
Xeroderma Pigmentosum: Gene Variants and Splice Variants.
Martens MC, Emmert S, Boeckmann L. Martens MC, et al. Genes (Basel). 2021 Jul 29;12(8):1173. doi: 10.3390/genes12081173. Genes (Basel). 2021. PMID: 34440347 Free PMC article. Review.
Alterations in genes of the NER can lead to DNA damage repair disorders such as Xeroderma pigmentosum (XP). XP is a rare autosomal recessive genetic disorder associated with UV-sensitivity and early onset of skin cancer. ...
Alterations in genes of the NER can lead to DNA damage repair disorders such as Xeroderma pigmentosum (XP). XP is a rare autosomal re …
Heterogeneity and overlaps in nucleotide excision repair disorders.
Ferri D, Orioli D, Botta E. Ferri D, et al. Clin Genet. 2020 Jan;97(1):12-24. doi: 10.1111/cge.13545. Epub 2019 Apr 22. Clin Genet. 2020. PMID: 30919937 Review.
Deficiencies in NER typically result in a group of heterogeneous distinct disorders ranging from the mild UV sensitive syndrome to the cancer-prone xeroderma pigmentosum and the neurodevelopmental/progeroid conditions trichothiodystrophy, Cockayne syndrome and cerebro-ocul …
Deficiencies in NER typically result in a group of heterogeneous distinct disorders ranging from the mild UV sensitive syndrome to the cance …
Xeroderma pigmentosum.
Webb S. Webb S. BMJ. 2008 Feb 23;336(7641):444-6. doi: 10.1136/bmj.39485.698356.AD. BMJ. 2008. PMID: 18292171 Free PMC article. Review.
Alex Webb was 4 years old when he was diagnosed with xeroderma pigmentosum nine years ago. This is his story as told by his mother. ...
Alex Webb was 4 years old when he was diagnosed with xeroderma pigmentosum nine years ago. This is his story as told by his mother. . …
Xeroderma pigmentosum and other diseases of human premature aging and DNA repair: molecules to patients.
Niedernhofer LJ, Bohr VA, Sander M, Kraemer KH. Niedernhofer LJ, et al. Mech Ageing Dev. 2011 Jun-Jul;132(6-7):340-7. doi: 10.1016/j.mad.2011.06.004. Epub 2011 Jun 25. Mech Ageing Dev. 2011. PMID: 21708183 Free PMC article. Review.
A workshop(1) to share, consider and discuss the latest developments in understanding xeroderma pigmentosum and other human diseases caused by defects in nucleotide excision repair (NER) of DNA damage was held on September 21-24, 2010 in Virginia. ...
A workshop(1) to share, consider and discuss the latest developments in understanding xeroderma pigmentosum and other human diseases …
Xeroderma pigmentosum.
Der Kaloustian VM, Kurban AK. Der Kaloustian VM, et al. Br J Dermatol. 1973 May;88(5):513-5. doi: 10.1111/j.1365-2133.1973.tb15461.x. Br J Dermatol. 1973. PMID: 4577062 Review. No abstract available.
Xeroderma pigmentosum.
Jan SN, Khan FA, Khan BA. Jan SN, et al. J Coll Physicians Surg Pak. 2011 Feb;21(2):93-6. J Coll Physicians Surg Pak. 2011. PMID: 21333240 Free article.
OBJECTIVE: To describe the features of Xeroderma pigmentosum observed in the stage 3 of the disease. STUDY DESIGN: Case series. PLACE AND DURATION OF STUDY: Mayo Hospital Lahore, from December 2001 to September 2008. METHODOLOGY: All patients diagnosed with Xeroderma …
OBJECTIVE: To describe the features of Xeroderma pigmentosum observed in the stage 3 of the disease. STUDY DESIGN: Case series. PLACE …
1,463 results