217 related articles for article (PubMed ID: 10536990)
1. R162W mutation of keratin 9 in a family with autosomal dominant palmoplantar keratoderma with unique histologic features.
Mayuzumi N; Shigihara T; Ikeda S; Ogawa H
J Investig Dermatol Symp Proc; 1999 Sep; 4(2):150-2. PubMed ID: 10536990
[TBL] [Abstract][Full Text] [Related]
2. Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma.
Navsaria HA; Swensson O; Ratnavel RC; Shamsher M; McLean WH; Lane EB; Griffiths D; Eady RA; Leigh IM
J Invest Dermatol; 1995 Mar; 104(3):425-9. PubMed ID: 7532198
[TBL] [Abstract][Full Text] [Related]
3. Identification of the keratin K9 R162W mutation in patients of Italian origin with epidermolytic palmoplantar keratoderma.
Terrinoni A; Cocuroccia B; Gubinelli E; Zambruno G; Candi E; Melino G; Girolomoni G
Eur J Dermatol; 2004; 14(6):375-8. PubMed ID: 15564199
[TBL] [Abstract][Full Text] [Related]
4. Keratin 9 mutations in the coil 1A region in epidermolytic palmoplantar keratoderma.
Szalai S; Szalai C; Becker K; Török E
Pediatr Dermatol; 1999; 16(6):430-5. PubMed ID: 10632938
[TBL] [Abstract][Full Text] [Related]
5. De novo mutation of keratin 9 gene in two Taiwanese patients with epidermolytic palmoplantar keratoderma.
Yang MH; Lee JY; Lin JH; Chao SC
J Formos Med Assoc; 2003 Jul; 102(7):492-6. PubMed ID: 14517588
[TBL] [Abstract][Full Text] [Related]
6. Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families.
Shamsher MK; Navsaria HA; Stevens HP; Ratnavel RC; Purkis PE; Kelsell DP; McLean WH; Cook LJ; Griffiths WA; Gschmeissner S
Hum Mol Genet; 1995 Oct; 4(10):1875-81. PubMed ID: 8595410
[TBL] [Abstract][Full Text] [Related]
7. A novel mutation of keratin 9 gene (R162P) in a Japanese family with epidermolytic palmoplantar keratoderma.
Kon A; Itagaki K; Yoneda K; Takagaki K
Arch Dermatol Res; 2005 Feb; 296(8):375-8. PubMed ID: 15605275
[TBL] [Abstract][Full Text] [Related]
8. Keratin-9 gene mutation in a family with epidermolytic palmoplantar keratoderma.
Amichai B; Karpati M; Goldman B; Peleg L
J Eur Acad Dermatol Venereol; 2002 Mar; 16(2):134-6. PubMed ID: 12046815
[TBL] [Abstract][Full Text] [Related]
9. A novel nonepidermolytic palmoplantar keratoderma: a clinical and histopathologic study of six cases.
Magro CM; Baden LA; Crowson AN; Bowden PE; Baden HP
J Am Acad Dermatol; 1997 Jul; 37(1):27-33. PubMed ID: 9216520
[TBL] [Abstract][Full Text] [Related]
10. Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene.
Terron-Kwiatkowski A; Terrinoni A; Didona B; Melino G; Atherton DJ; Irvine AD; McLean WH
Br J Dermatol; 2004 Jun; 150(6):1096-103. PubMed ID: 15214894
[TBL] [Abstract][Full Text] [Related]
11. Mutations in the 1A domain of keratin 9 in patients with epidermolytic palmoplantar keratoderma.
Rothnagel JA; Wojcik S; Liefer KM; Dominey AM; Huber M; Hohl D; Roop DR
J Invest Dermatol; 1995 Mar; 104(3):430-3. PubMed ID: 7532199
[TBL] [Abstract][Full Text] [Related]
12. Keratin 9 gene mutations in five Korean families with epidermolytic palmoplantar keratoderma.
Lee JH; Ahn KS; Lee CH; Youn SJ; Kim JW; Lee DY; Lee ES; Steinert PM; Yang JM
Exp Dermatol; 2003 Dec; 12(6):876-81. PubMed ID: 14675368
[TBL] [Abstract][Full Text] [Related]
13. Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratoderma.
Yang JM; Lee S; Kang HJ; Lee JH; Yeo UC; Son IY; Park KB; Steinert PM; Lee ES
Acta Derm Venereol; 1998 Nov; 78(6):412-6. PubMed ID: 9833037
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A unique pattern of dyskeratosis characterizes epidermolytic hyperkeratosis and epidermolytic palmoplantar keratoderma.
Bergman R; Khamaysi Z; Sprecher E
Am J Dermatopathol; 2008 Apr; 30(2):101-5. PubMed ID: 18360110
[TBL] [Abstract][Full Text] [Related]
16. A novel keratin 9 gene mutation (Asn160His) in a Taiwanese family with epidermolytic palmoplantar keratoderma.
Lin JH; Lin MH; Yang MH; Chao SC
Clin Exp Dermatol; 2004 May; 29(3):308-10. PubMed ID: 15115518
[TBL] [Abstract][Full Text] [Related]
17. Epidermolytic palmoplantar keratoderma due to a novel type of keratin mutation, a 3-bp insertion in the keratin 9 helix termination motif.
Coleman CM; Munro CS; Smith FJ; Uitto J; McLean WH
Br J Dermatol; 1999 Mar; 140(3):486-90. PubMed ID: 10233272
[TBL] [Abstract][Full Text] [Related]
18. Mutation S233L in the 1B domain of keratin 1 causes epidermolytic palmoplantar keratoderma with "tonotubular" keratin.
Terron-Kwiatkowski A; van Steensel MA; van Geel M; Lane EB; McLean WH; Steijlen PM
J Invest Dermatol; 2006 Mar; 126(3):607-13. PubMed ID: 16439967
[TBL] [Abstract][Full Text] [Related]
19. Identification of a de novo keratin 1 mutation in epidermolytic hyperkeratosis with palmoplantar involvement.
Math A; Frank J; Handisurya A; Poblete-Gutiérrez P; Slupetzky K; Födinger D; Winter D; Stingl G; Kirnbauer R
Eur J Dermatol; 2006; 16(5):507-10. PubMed ID: 17101470
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
