These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

332 related articles for article (PubMed ID: 16505000)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex.
    Corden LD; Mellerio JE; Gratian MJ; Eady RA; Harper JI; Lacour M; Magee G; Lane EB; McGrath JA; McLean WH
    Hum Mutat; 1998; 11(4):279-85. PubMed ID: 9554744
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A keratin K10 gene mutation in a Japanese patient with epidermolytic hyperkeratosis.
    Nomura K; Meng X; Umeki K; Tamai K; Sawamura D; Hashimoto I; Kikuchi T
    Jpn J Hum Genet; 1997 Mar; 42(1):217-23. PubMed ID: 9184002
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Epidermolytic hyperkeratosis.
    Bale SJ; Compton JG; DiGiovanna JJ
    Semin Dermatol; 1993 Sep; 12(3):202-9. PubMed ID: 7692917
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis.
    Arin MJ; Longley MA; Epstein EH; Rothnagel JA; Roop DR
    Exp Dermatol; 2000 Feb; 9(1):16-9. PubMed ID: 10688370
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q.
    Compton JG; DiGiovanna JJ; Santucci SK; Kearns KS; Amos CI; Abangan DL; Korge BP; McBride OW; Steinert PM; Bale SJ
    Nat Genet; 1992 Jul; 1(4):301-5. PubMed ID: 1284546
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens.
    Rothnagel JA; Traupe H; Wojcik S; Huber M; Hohl D; Pittelkow MR; Saeki H; Ishibashi Y; Roop DR
    Nat Genet; 1994 Aug; 7(4):485-90. PubMed ID: 7524919
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Recessive epidermolysis bullosa simplex phenotype reproduced in vitro: ablation of keratin 14 is partially compensated by keratin 17.
    El Ghalbzouri A; Jonkman M; Kempenaar J; Ponec M
    Am J Pathol; 2003 Nov; 163(5):1771-9. PubMed ID: 14578178
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Disruption of the suprabasal keratin network by mutation M150T in the helix initiation motif of keratin 10 does not affect cornified cell envelope formation in human epidermis.
    Akiyama M; Takizawa Y; Sawamura D; Matsuo I; Shimizu H
    Exp Dermatol; 2003 Oct; 12(5):638-45. PubMed ID: 14705805
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Epidermolytic hyperkeratosis: a keratin 1 or 10 mutational event.
    Lacz NL; Schwartz RA; Kihiczak G
    Int J Dermatol; 2005 Jan; 44(1):1-6. PubMed ID: 15663649
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 17.