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Quoted phrase not found in phrase index: "Trichothiodystrophy 1, photosensitive"
Page 1
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.
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.
Molecular regulation of UV-induced DNA repair.
Shah P, He YY. Shah P, et al. Photochem Photobiol. 2015 Mar-Apr;91(2):254-64. doi: 10.1111/php.12406. Epub 2015 Jan 14. Photochem Photobiol. 2015. PMID: 25534312 Free PMC article. Review.
Genetic loss of nucleotide excision repair leads to severe disorders, namely, xeroderma pigmentosum (XP), trichothiodystrophy (TTD) and Cockayne syndrome (CS), which are associated with predisposition to skin carcinogenesis at a young age as well as developmental and neuro …
Genetic loss of nucleotide excision repair leads to severe disorders, namely, xeroderma pigmentosum (XP), trichothiodystrophy (TTD) a …
Progeroid syndromes and UV-induced oxidative DNA damage.
Kamenisch Y, Berneburg M. Kamenisch Y, et al. J Investig Dermatol Symp Proc. 2009 Aug;14(1):8-14. doi: 10.1038/jidsymp.2009.6. J Investig Dermatol Symp Proc. 2009. PMID: 19675546 Free article. Review.
These syndromes comprise diseases such as Werner syndrome, Bloom syndrome, Rothmund-Thomson syndrome, Hutchinson-Gilford syndrome, Fanconi anemia, and ataxia-telangiectasia, as well as xeroderma pigmentosum, trichothiodystrophy, and Cockayne syndrome. ...The clin …
These syndromes comprise diseases such as Werner syndrome, Bloom syndrome, Rothmund-Thomson syndrome, Hutchinson-Gilford syndrome, Fa …
Understanding photodermatoses associated with defective DNA repair: Photosensitive syndromes without associated cancer predisposition.
Yew YW, Giordano CN, Spivak G, Lim HW. Yew YW, et al. J Am Acad Dermatol. 2016 Nov;75(5):873-882. doi: 10.1016/j.jaad.2016.03.044. J Am Acad Dermatol. 2016. PMID: 27745642 Review.
Photodermatoses associated with defective DNA repair are a group of photosensitive hereditary skin disorders. In this review, we focus on diseases and syndromes with defective nucleotide excision repair that are not accompanied by an increased risk of cutaneous malignancie …
Photodermatoses associated with defective DNA repair are a group of photosensitive hereditary skin disorders. In this review, we focus on di …
Signaling Pathways, Chemical and Biological Modulators of Nucleotide Excision Repair: The Faithful Shield against UV Genotoxicity.
Kobaisi F, Fayyad N, Rezvani HR, Fayyad-Kazan M, Sulpice E, Badran B, Fayyad-Kazan H, Gidrol X, Rachidi W. Kobaisi F, et al. Oxid Med Cell Longev. 2019 Aug 7;2019:4654206. doi: 10.1155/2019/4654206. eCollection 2019. Oxid Med Cell Longev. 2019. PMID: 31485292 Free PMC article. Review.
Deficiencies in the NER pathway underlie the development of several DNA repair diseases, such as xeroderma pigmentosum (XP), Cockayne syndrome (CS), and trichothiodystrophy (TTD). Deficiencies in GG-NER and TC-NER render individuals to become prone to cancer and neurologic …
Deficiencies in the NER pathway underlie the development of several DNA repair diseases, such as xeroderma pigmentosum (XP), Cockayne syndro …
Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.
Itin PH, Sarasin A, Pittelkow MR. Itin PH, et al. J Am Acad Dermatol. 2001 Jun;44(6):891-920; quiz 921-4. doi: 10.1067/mjd.2001.114294. J Am Acad Dermatol. 2001. PMID: 11369901 Review.
Trichothiodystrophy (TTD) refers to a heterogeneous group of autosomal recessive disorders that share the distinctive features of short, brittle hair and an abnormally low sulfur content. Within the spectrum of the TTD syndromes are numerous interrelated neuroectode …
Trichothiodystrophy (TTD) refers to a heterogeneous group of autosomal recessive disorders that share the distinctive features of sho …
Successful treatment of trichothiodystrophy with dupilumab.
Gruber R, Zschocke A, Zellner H, Schmuth M. Gruber R, et al. Clin Exp Dermatol. 2021 Oct;46(7):1381-1383. doi: 10.1111/ced.14642. Epub 2021 May 6. Clin Exp Dermatol. 2021. PMID: 33955026 Free PMC article.
Oxidative and energy metabolism as potential clues for clinical heterogeneity in nucleotide excision repair disorders.
Hosseini M, Ezzedine K, Taieb A, Rezvani HR. Hosseini M, et al. J Invest Dermatol. 2015 Feb;135(2):341-351. doi: 10.1038/jid.2014.365. Epub 2014 Oct 9. J Invest Dermatol. 2015. PMID: 25296907 Free article. Review.
The absence or dysfunction of NER results in the following distinct disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS), cerebro-oculo-facio-skeletal (COFS) syndrome, UV-sensitive syndrome (UVSS), trichothiodystrophy (TTD), or combined syndromes including …
The absence or dysfunction of NER results in the following distinct disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS), cerebro-o …
19 results