152 related articles for article (PubMed ID: 25808222)
1. A KRT1 gene mutation related to epidermolytic ichthyosis in a Chinese family.
Ji YZ; Bai Y; Wang S; Li FQ
Clin Exp Dermatol; 2015 Dec; 40(8):879-82. PubMed ID: 25808222
[TBL] [Abstract][Full Text] [Related]
2. Two cases of KRT1 mutation-associated epidermolytic ichthyosis without typical epidermolytic hyperkeratosis in the neonatal skin lesions.
Kim T; Kim SC; Lee SE
Pediatr Dermatol; 2023; 40(6):1149-1151. PubMed ID: 37170713
[TBL] [Abstract][Full Text] [Related]
3. Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma.
Smith FJD; Kreuser-Genis IM; Jury CS; Wilson NJ; Terron-Kwiatowski A; Zamiri M
Clin Exp Dermatol; 2019 Jul; 44(5):528-534. PubMed ID: 30288772
[TBL] [Abstract][Full Text] [Related]
4. Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis.
Hotz A; Oji V; Bourrat E; Jonca N; Mazereeuw-Hautier J; Betz RC; Blume-Peytavi U; Stieler K; Morice-Picard F; Schönbuchner I; Markus S; Schlipf N; Fischer J
Acta Derm Venereol; 2016 May; 96(4):473-8. PubMed ID: 26581228
[TBL] [Abstract][Full Text] [Related]
5. A recurrent missense mutation of keratin 1 gene in a Chinese family with epidermolytic hyperkeratosis (severe palmoplantar hyperkeratosis, type 1).
Zeng YP; Chai WX; Fang K; Sun QN; Zuo YG
Int J Dermatol; 2012 Feb; 51(2):182-5. PubMed ID: 22250628
[TBL] [Abstract][Full Text] [Related]
6. Epidermolytic ichthyosis in a child and systematized epidermolytic nevi in the mosaic parent associated with a KRT1 variant.
Chia SY; Tan EC; Wei H; Zhao Y; Koh MJA
Eur J Med Genet; 2021 Nov; 64(11):104324. PubMed ID: 34461324
[TBL] [Abstract][Full Text] [Related]
7. A de novo mutation of KRT1 in a baby girl causing epidermolytic ichthyosis with impressive epidermolytic palmoplantar keratoderma.
Calì F; Failla P; Vinci M; Siragusa M; Schepis C
Dermatol Online J; 2020 Jul; 26(7):. PubMed ID: 32898404
[TBL] [Abstract][Full Text] [Related]
8. A de novo variant in the keratin 1 gene (KRT1) in a Chinese shar-pei dog with severe congenital cornification disorder and non-epidermolytic ichthyosis.
Affolter VK; Kiener S; Jagannathan V; Nagle T; Leeb T
PLoS One; 2022; 17(10):e0275367. PubMed ID: 36251712
[TBL] [Abstract][Full Text] [Related]
9. Epidermolytic Ichthyosis Sine Epidermolysis.
Eskin-Schwartz M; Drozhdina M; Sarig O; Gat A; Jackman T; Isakov O; Shomron N; Samuelov L; Malchin N; Peled A; Vodo D; Hovnanian A; Ruzicka T; Koshkin S; Harmon RM; Koetsier JL; Green KJ; Paller AS; Sprecher E
Am J Dermatopathol; 2017 Jun; 39(6):440-444. PubMed ID: 28121638
[TBL] [Abstract][Full Text] [Related]
10. A novel mutation in the L12 domain of keratin 1 is associated with mild epidermolytic ichthyosis.
Bolling MC; Bladergroen RS; van Steensel MA; Willemsen M; Jonkman MF; van Geel M
Br J Dermatol; 2010 Apr; 162(4):875-9. PubMed ID: 20500210
[TBL] [Abstract][Full Text] [Related]
11. Splice site and deletion mutations in keratin (KRT1 and KRT10) genes: unusual phenotypic alterations in Scandinavian patients with epidermolytic hyperkeratosis.
Virtanen M; Smith SK; Gedde-Dahl T; Vahlquist A; Bowden PE
J Invest Dermatol; 2003 Nov; 121(5):1013-20. PubMed ID: 14708600
[TBL] [Abstract][Full Text] [Related]
12. A p.478I>T KRT1 mutation in a case of annular epidermolytic ichthyosis.
Zaki TD; Yoo KY; Kassardjian M; Choate KA
Pediatr Dermatol; 2018 Nov; 35(6):e414-e415. PubMed ID: 30152556
[TBL] [Abstract][Full Text] [Related]
13. Phenotypic variation in epidermolytic ichthyosis: clinical and functional evaluation of the novel p.(Met339Lys) mutation in the L12 domain of KRT1.
Nellen RG; Nagtzaam IF; Hoogeboom AJ; Bladergroen RS; Jonkman MF; Steijlen PM; van Steensel MA; van Geel M
Exp Dermatol; 2015 Nov; 24(11):883-5. PubMed ID: 26120802
[No Abstract] [Full Text] [Related]
14. Intrafamilial phenotypic heterogeneity of epidermolytic ichthyosis associated with a new missense mutation in keratin 10.
Abdul-Wahab A; Takeichi T; Liu L; Stephens C; Akiyama M; McGrath JA
Clin Exp Dermatol; 2016 Apr; 41(3):290-3. PubMed ID: 26338057
[TBL] [Abstract][Full Text] [Related]
15. Extensive Post-zygotic Mosaicism of KRT1 or KRT10 Mutation Mimicking Classical Epider-molytic Ichthyosis.
Severino-Freire M; Jonca N; Pichery M; Tournier E; Chassaing N; Mazereeuw-Hautier J
Acta Derm Venereol; 2017 Mar; 97(3):387-388. PubMed ID: 27722766
[No Abstract] [Full Text] [Related]
16. Nonsense mutations in KRT1 caused recessive epidermolytic palmoplantar keratoderma with knuckle pads.
Mo R; Lin M; Lee M; Yan W; Wang H; Lin Z
J Eur Acad Dermatol Venereol; 2022 Oct; 36(10):1857-1862. PubMed ID: 35490383
[TBL] [Abstract][Full Text] [Related]
17. Infantile epidermolytic ichthyosis with prominent maternal palmoplantar keratoderma.
Austin Smith W; Cope A; Fernandez M; Parekh P
Dermatol Online J; 2016 Apr; 22(4):. PubMed ID: 27617465
[TBL] [Abstract][Full Text] [Related]
18. Expanding the keratin mutation database: novel and recurrent mutations and genotype-phenotype correlations in 28 patients with epidermolytic ichthyosis.
Arin MJ; Oji V; Emmert S; Hausser I; Traupe H; Krieg T; Grimberg G
Br J Dermatol; 2011 Feb; 164(2):442-7. PubMed ID: 21271994
[TBL] [Abstract][Full Text] [Related]
19. Mild phenotype of epidermolytic hyperkeratosis mimicking ichthyosis bullosa of Siemens is related to specific mutation in 2B domain of KRT1.
Sung JY; Oh SW; Kim SE; Kim SC
J Dermatol Sci; 2013 Jun; 70(3):220-2. PubMed ID: 23623204
[No Abstract] [Full Text] [Related]
20. Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation location.
Vodo D; Sarig O; Peled A; Samuelov L; Malchin N; Grafi-Cohen M; Sprecher E
Clin Exp Dermatol; 2018 Mar; 43(2):187-190. PubMed ID: 29277919
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
