BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

251 related articles for article (PubMed ID: 7509838)

  • 21. Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.
    Sybert VP; Francis JS; Corden LD; Smith LT; Weaver M; Stephens K; McLean WH
    Am J Hum Genet; 1999 Mar; 64(3):732-8. PubMed ID: 10053007
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical heterogeneity in epidermolytic hyperkeratosis.
    DiGiovanna JJ; Bale SJ
    Arch Dermatol; 1994 Aug; 130(8):1026-35. PubMed ID: 8053700
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. A novel Y160C mutation of Keratin 10 gene in a Chinese male infant with epidermolytic hyperkeratosis.
    Zhao C; Li Y; Shi G; Shi X; Zhang G
    Turk J Pediatr; 2018; 60(4):426-428. PubMed ID: 30859768
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutations in the genes for epidermal keratins in epidermolysis bullosa and epidermolytic hyperkeratosis.
    Leigh IM; Lane EB
    Arch Dermatol; 1993 Dec; 129(12):1571-7. PubMed ID: 7504434
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel H1 mutation in the keratin 1 chain in epidermolytic hyperkeratosis.
    Yang JM; Nam K; Park KB; Kim WS; Moon KC; Koh JK; Steinert PM; Lee ES
    J Invest Dermatol; 1996 Sep; 107(3):439-41. PubMed ID: 8751983
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A transgenic mouse model that recapitulates the clinical features of both neonatal and adult forms of the skin disease epidermolytic hyperkeratosis.
    Bickenbach JR; Longley MA; Bundman DS; Dominey AM; Bowden PE; Rothnagel JA; Roop DR
    Differentiation; 1996 Dec; 61(2):129-39. PubMed ID: 8983179
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Epidermolytic hyperkeratosis type PS-1 caused by aberrant splicing of KRT1.
    Tal O; Bergman R; Alcalay J; Indelman M; Sprecher E
    Clin Exp Dermatol; 2005 Jan; 30(1):64-7. PubMed ID: 15663507
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis.
    Rothnagel JA; Fisher MP; Axtell SM; Pittelkow MR; Anton-Lamprecht I; Huber M; Hohl D; Roop DR
    Hum Mol Genet; 1993 Dec; 2(12):2147-50. PubMed ID: 7509230
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Keratin 1 and keratin 10 mutations causing epidermolytic hyperkeratosis in Chinese patients.
    Sun XK; Ma LL; Xie YQ; Zhu XJ
    J Dermatol Sci; 2002 Sep; 29(3):195-200. PubMed ID: 12234709
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A mouse keratin 1 mutation causes dark skin and epidermolytic hyperkeratosis.
    McGowan KA; Aradhya S; Fuchs H; de Angelis MH; Barsh GS
    J Invest Dermatol; 2006 May; 126(5):1013-6. PubMed ID: 16528356
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene.
    Moraru R; Cserhalmi-Friedman PB; Grossman ME; Schneiderman P; Christiano AM
    Clin Exp Dermatol; 1999 Sep; 24(5):412-5. PubMed ID: 10564334
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A novel substitution in keratin 10 in epidermolytic hyperkeratosis.
    Arin MJ; Longley MA; Anton-Lamprecht I; Kurze G; Huber M; Hohl D; Rothnagel JA; Roop DR
    J Invest Dermatol; 1999 Apr; 112(4):506-8. PubMed ID: 10201536
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Preferential sites in keratin 10 that are mutated in epidermolytic hyperkeratosis.
    Chipev CC; Yang JM; DiGiovanna JJ; Steinert PM; Marekov L; Compton JG; Bale SJ
    Am J Hum Genet; 1994 Feb; 54(2):179-90. PubMed ID: 7508181
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis.
    Rothnagel JA; Lin MT; Longley MA; Holder RA; Hazen PG; Levy ML; Roop DR
    Prenat Diagn; 1998 Aug; 18(8):826-30. PubMed ID: 9742571
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Epidermolytic hyperkeratosis.
    Kwak J; Maverakis E
    Dermatol Online J; 2006 Sep; 12(5):6. PubMed ID: 16962021
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Systematized linear epidermolytic hyperkeratosis.
    Kumar P; Kumar R; Mandal RK; Hassan S
    Dermatol Online J; 2014 Jan; 20(1):21248. PubMed ID: 24456951
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type II keratin gene cluster on chromosome 12.
    Bonifas JM; Bare JW; Chen MA; Lee MK; Slater CA; Goldsmith LA; Epstein EH
    J Invest Dermatol; 1992 Nov; 99(5):524-7. PubMed ID: 1385543
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.