179 related articles for article (PubMed ID: 29277919)
1. 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]
2. Lethal autosomal recessive epidermolytic ichthyosis due to a novel donor splice-site mutation in KRT10.
Covaciu C; Castori M; De Luca N; Ghirri P; Nannipieri A; Ragone G; Zambruno G; Castiglia D
Br J Dermatol; 2010 Jun; 162(6):1384-7. PubMed ID: 20302579
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs.
Credille KM; Barnhart KF; Minor JS; Dunstan RW
Br J Dermatol; 2005 Jul; 153(1):51-8. PubMed ID: 16029326
[TBL] [Abstract][Full Text] [Related]
5. A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.
Müller FB; Huber M; Kinaciyan T; Hausser I; Schaffrath C; Krieg T; Hohl D; Korge BP; Arin MJ
Hum Mol Genet; 2006 Apr; 15(7):1133-41. PubMed ID: 16505000
[TBL] [Abstract][Full Text] [Related]
6. Gene Editing-Mediated Disruption of Epidermolytic Ichthyosis-Associated KRT10 Alleles Restores Filament Stability in Keratinocytes.
March OP; Lettner T; Klausegger A; Ablinger M; Kocher T; Hainzl S; Peking P; Lackner N; Rajan N; Hofbauer JP; Guttmann-Gruber C; Bygum A; Koller U; Reichelt J
J Invest Dermatol; 2019 Aug; 139(8):1699-1710.e6. PubMed ID: 30998984
[TBL] [Abstract][Full Text] [Related]
7. Mild recessive bullous congenital ichthyosiform erythroderma due to a previously unidentified homozygous keratin 10 nonsense mutation.
Tsubota A; Akiyama M; Kanitakis J; Sakai K; Nomura T; Claudy A; Shimizu H
J Invest Dermatol; 2008 Jul; 128(7):1648-52. PubMed ID: 18219278
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Epidermolytic Acanthoma of the Genitalia Does Not Show Mutations in KRT1 or KRT10.
Egozi-Reinman E; Avitan-Hersh E; Barzilai A; Indelman M; Bergman R
Am J Dermatopathol; 2016 Feb; 38(2):164-5. PubMed ID: 26825163
[No Abstract] [Full Text] [Related]
12. 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]
13. R156C mutation of keratin 10 causes mild form of epidermolytic hyperkeratosis.
Haruna K; Suga Y; Mizuno Y; Hasegawa T; Kourou K; Matsuba S; Muramatsu S; Ikeda S
J Dermatol; 2007 Aug; 34(8):545-8. PubMed ID: 17683385
[TBL] [Abstract][Full Text] [Related]
14. Mutations in KRT10 in epidermolytic acanthoma.
Cheraghlou S; Atzmony L; Roy SF; McNiff JM; Choate KA
J Cutan Pathol; 2020 Jun; 47(6):524-529. PubMed ID: 32045015
[TBL] [Abstract][Full Text] [Related]
15. Extensive postzygotic mosaicism for a novel keratin 10 mutation in epidermolytic ichthyosis.
Kiritsi D; Nanda A; Kohlhase J; Bernhard C; Bruckner-Tuderman L; Happle R; Has C
Acta Derm Venereol; 2014 May; 94(3):346-8. PubMed ID: 24096702
[No Abstract] [Full Text] [Related]
16. [Mutation analysis of KRT10 gene in a patient with bullous congenital ichthyosiform erythroderma].
Zhang SD; Liu JJ; Tian W; Zhao ZJ; Zhao JJ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):421-3. PubMed ID: 21811984
[TBL] [Abstract][Full Text] [Related]
17. 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]
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. 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]
20. Mutations Affecting Keratin 10 Surface-Exposed Residues Highlight the Structural Basis of Phenotypic Variation in Epidermolytic Ichthyosis.
Mirza H; Kumar A; Craiglow BG; Zhou J; Saraceni C; Torbeck R; Ragsdale B; Rehder P; Ranki A; Choate KA
J Invest Dermatol; 2015 Dec; 135(12):3041-3050. PubMed ID: 26176760
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
