Skip to main page content
U.S. flag

An official website of the United States government

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Results by year

1990
2025

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

Year Number of Results
1990 2
1993 1
1994 1
1995 1
1996 2
1997 1
1999 1
2000 2
2001 3
2003 3
2005 1
2006 4
2008 5
2009 8
2010 4
2011 1
2013 1
2014 2
2015 7
2016 7
2017 2
2018 2
2019 3
2020 2
2023 1
2025 0

Publication date

Text availability

Article attribute

Article type

Additional filters

Search Results

63 results

Results by year

Filters applied: . Clear all
Page 1
DNA damage, aging, and cancer.
Hoeijmakers JH. Hoeijmakers JH. N Engl J Med. 2009 Oct 8;361(15):1475-85. doi: 10.1056/NEJMra0804615. N Engl J Med. 2009. PMID: 19812404 Review. No abstract available.
Ethnic hair disorders.
Lindsey SF, Tosti A. Lindsey SF, et al. Curr Probl Dermatol. 2015;47:139-49. doi: 10.1159/000369414. Epub 2015 Feb 20. Curr Probl Dermatol. 2015. PMID: 26370652 Review.
TFIIH central activity in nucleotide excision repair to prevent disease.
Theil AF, Häckes D, Lans H. Theil AF, et al. DNA Repair (Amst). 2023 Dec;132:103568. doi: 10.1016/j.dnarep.2023.103568. Epub 2023 Sep 7. DNA Repair (Amst). 2023. PMID: 37977600 Free article. Review.
TFIIH is essential for life and hereditary mutations in TFIIH cause the devastating human syndromes xeroderma pigmentosum, Cockayne syndrome or trichothiodystrophy, or combinations of these. ...
TFIIH is essential for life and hereditary mutations in TFIIH cause the devastating human syndromes xeroderma pigmentosum, Cockayne s …
Trichothiodystrophy, a transcription syndrome.
Bergmann E, Egly JM. Bergmann E, et al. Trends Genet. 2001 May;17(5):279-86. doi: 10.1016/s0168-9525(01)02280-6. Trends Genet. 2001. PMID: 11335038 Review.
Trichothiodystrophy (TTD) is a rare genetic disorder characterized by a hair dysplasia and associated with numerous symptoms affecting mainly organs derived from the neuroectoderm. ...
Trichothiodystrophy (TTD) is a rare genetic disorder characterized by a hair dysplasia and associated with numerous symptoms affectin
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.
Differential diagnosis must distinguish xeroderma pigmentosum from other so-called DNA-repair-deficiency syndromes like the Cockayne Syndrome and trichothiodystrophy. Currently, there are reports of successful application of a topical DNA Repair Enzyme. ...
Differential diagnosis must distinguish xeroderma pigmentosum from other so-called DNA-repair-deficiency syndromes like the Cockayne …
Male fertility and skin diseases.
Abdel-Naser MB, Zouboulis CC. Abdel-Naser MB, et al. Rev Endocr Metab Disord. 2016 Sep;17(3):353-365. doi: 10.1007/s11154-016-9368-x. Rev Endocr Metab Disord. 2016. PMID: 27342409 Review.
Several genodermatoses affect the skin and several other organs including the male reproductive system, commonly in the form of cryptorchidism and hypogonadism. The most relevant syndromes are associated with dyschromias, such as deSanctis-Cacchione, poikiloderma congenita …
Several genodermatoses affect the skin and several other organs including the male reproductive system, commonly in the form of cryptorchidi …
[Chromosome instability syndromes].
Tomaszewska A, Srebniak M, Gnyś A. Tomaszewska A, et al. Pol Merkur Lekarski. 2006 May;20(119):577-81. Pol Merkur Lekarski. 2006. PMID: 16875167 Review. Polish.
Defects of DNA repair underlie genetic syndromes. Chromosomal aberrations and mutations might cause specific inborn defects. There are several syndromes with characteristic clinical features, which appear to be caused by chromosome instability which is a consequence …
Defects of DNA repair underlie genetic syndromes. Chromosomal aberrations and mutations might cause specific inborn defects. There ar …
Trichothiodystrophy: Photosensitive, TTD-P, TTD, Tay syndrome.
Lambert WC, Gagna CE, Lambert MW. Lambert WC, et al. Adv Exp Med Biol. 2010;685:106-10. doi: 10.1007/978-1-4419-6448-9_10. Adv Exp Med Biol. 2010. PMID: 20687499 Review.
Although the term, "trichothiodystrophy" (TTD) refers to the hair anomalies in this group of patients, this is a heterogeneous, multisystem disease in which any or every organ in the body may be affected. ...These patients are designated as having trichothiodystrophy
Although the term, "trichothiodystrophy" (TTD) refers to the hair anomalies in this group of patients, this is a heterogeneous, multi …
Nucleotide excision repair genes shaping embryonic development.
Araújo SJ, Kuraoka I. Araújo SJ, et al. Open Biol. 2019 Oct 31;9(10):190166. doi: 10.1098/rsob.190166. Epub 2019 Oct 30. Open Biol. 2019. PMID: 31662099 Free PMC article. Review.
Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy are three human disorders caused by inherited defects in NER. The symptoms and severity of these diseases vary dramatically, ranging from profound developmental delay to cancer predisposition and accelerated …
Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy are three human disorders caused by inherited defects in NER. The sy …
Hair loss in children.
Alves R, Grimalt R. Alves R, et al. Curr Probl Dermatol. 2015;47:55-66. doi: 10.1159/000369405. Epub 2015 Feb 20. Curr Probl Dermatol. 2015. PMID: 26370644 Review.
63 results