312 related articles for article (PubMed ID: 21271994)
41. Genetic approaches to understanding the keratinopathies.
Bale SJ; DiGiovanna JJ
Adv Dermatol; 1997; 12():99-113; discussion 114. PubMed ID: 8973737
[TBL] [Abstract][Full Text] [Related]
42. Two cases of primarily palmoplantar keratoderma associated with novel mutations in keratin 1.
Terron-Kwiatkowski A; Paller AS; Compton J; Atherton DJ; McLean WH; Irvine AD
J Invest Dermatol; 2002 Oct; 119(4):966-71. PubMed ID: 12406346
[TBL] [Abstract][Full Text] [Related]
43. Epidermolytic hyperkeratosis with polycyclic psoriasiform plaques resulting from a mutation in the keratin 1 gene.
Michael EJ; Schneiderman P; Grossman ME; Christiano AM
Exp Dermatol; 1999 Dec; 8(6):501-3. PubMed ID: 10597140
[TBL] [Abstract][Full Text] [Related]
44. A novel mutation of a leucine residue in coil 1A of keratin 9 in epidermolytic palmoplantar keratoderma.
Endo H; Hatamochi A; Shinkai H
J Invest Dermatol; 1997 Jul; 109(1):113-5. PubMed ID: 9204965
[TBL] [Abstract][Full Text] [Related]
45. Epidermolytic hyperkeratosis and epidermolysis bullosa simplex caused by frameshift mutations altering the v2 tail domains of keratin 1 and keratin 5.
Sprecher E; Yosipovitch G; Bergman R; Ciubutaro D; Indelman M; Pfendner E; Goh LC; Miller CJ; Uitto J; Richard G
J Invest Dermatol; 2003 Apr; 120(4):623-6. PubMed ID: 12648226
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. Mutations in the H1 and 1A domains in the keratin 1 gene in epidermolytic hyperkeratosis.
Yang JM; Chipev CC; DiGiovanna JJ; Bale SJ; Marekov LN; Steinert PM; Compton JG
J Invest Dermatol; 1994 Jan; 102(1):17-23. PubMed ID: 7507151
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. Keratin genes and epidermolytic hyperkeratosis.
Burton JL
Lancet; 1994 Oct; 344(8930):1103-4. PubMed ID: 7523811
[No Abstract] [Full Text] [Related]
50. Epidermolytic hyperkeratosis.
Bale SJ; Compton JG; DiGiovanna JJ
Semin Dermatol; 1993 Sep; 12(3):202-9. PubMed ID: 7692917
[TBL] [Abstract][Full Text] [Related]
51. [Keratin diseases].
Jensen PK; Sørensen CB; Andresen BS; Brandrup F; Veien NK; Buus SK; Gregersen N; Bolund L
Ugeskr Laeger; 2000 Mar; 162(13):1867-72. PubMed ID: 10765692
[TBL] [Abstract][Full Text] [Related]
52. How do keratinizing disorders and blistering disorders overlap?
Hamada T; Tsuruta D; Fukuda S; Ishii N; Teye K; Numata S; Dainichi T; Karashima T; Ohata C; Furumura M; Hashimoto T
Exp Dermatol; 2013 Feb; 22(2):83-7. PubMed ID: 23039137
[TBL] [Abstract][Full Text] [Related]
53. Bullous congenital ichthyosiform erythroderma: a sporadic case produced by a new KRT10 gene mutation.
Betlloch I; Lucas Costa A; Mataix J; Pérez-Crespo M; Ballester I
Pediatr Dermatol; 2009; 26(4):489-91. PubMed ID: 19689541
[TBL] [Abstract][Full Text] [Related]
54. A novel keratin 9 gene mutation (Met156Arg) in a Japanese patient with epidermolytic palmoplantar keratoderma.
Shimazu K; Tsunemi Y; Hattori N; Saeki H; Komine M; Adachi M; Tamaki K
Int J Dermatol; 2006 Sep; 45(9):1128-30. PubMed ID: 16961539
[No Abstract] [Full Text] [Related]
55. 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]
56. New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.
Whittock NV; Ashton GH; Griffiths WA; Eady RA; McGrath JA
Br J Dermatol; 2001 Aug; 145(2):330-5. PubMed ID: 11531804
[TBL] [Abstract][Full Text] [Related]
57. Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).
Reis A; Hennies HC; Langbein L; Digweed M; Mischke D; Drechsler M; Schröck E; Royer-Pokora B; Franke WW; Sperling K
Nat Genet; 1994 Feb; 6(2):174-9. PubMed ID: 7512862
[TBL] [Abstract][Full Text] [Related]
58. 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]
59. 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]
60. Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene.
Cserhalmi-Friedman PB; Squeo R; Gordon D; Garzon M; Schneiderman P; Grossman ME; Christiano AM
Clin Exp Dermatol; 2000 May; 25(3):241-3. PubMed ID: 10844506
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
