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 *

319 related articles for article (PubMed ID: 15840119)

  • 1. A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a.
    García-Rio I; Peñas PF; García-Díez A; McLean WH; Smith FJ
    Br J Dermatol; 2005 Apr; 152(4):800-2. PubMed ID: 15840119
    [No Abstract]   [Full Text] [Related]  

  • 2. Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2.
    Celebi JT; Tanzi EL; Yao YJ; Michael EJ; Peacocke M
    J Invest Dermatol; 1999 Nov; 113(5):848-50. PubMed ID: 10571744
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocystoma multiplex and Hutchinson-like tooth deformity.
    Oh SW; Kim MY; Lee JS; Kim SC
    J Dermatol; 2006 Mar; 33(3):161-4. PubMed ID: 16620218
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cloning of multiple keratin 16 genes facilitates prenatal diagnosis of pachyonychia congenita type 1.
    Smith FJ; McKusick VA; Nielsen K; Pfendner E; Uitto J; McLean WH
    Prenat Diagn; 1999 Oct; 19(10):941-6. PubMed ID: 10521820
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Type I pachyonychia congenita (Jadarssohn-Lewandowsky)].
    Wimmershoff MB; Stolz W; Schiffner R; Landthaler M
    Klin Padiatr; 1999; 211(3):179-83. PubMed ID: 10412130
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Pachyonychia congenita type 2 due to mutation in the keratin 6b gene].
    Toth GG; Van Goor H; McLean WH; Jonkman MF
    Ned Tijdschr Geneeskd; 2000 Aug; 144(32):1563-4. PubMed ID: 10979817
    [No Abstract]   [Full Text] [Related]  

  • 7. Identification of a recurrent mutation in keratin 6a in a patient with overlapping clinical features of pachyonychia congenita types 1 and 2.
    Ward KM; Cook-Bolden FE; Christiano AM; Celebi JT
    Clin Exp Dermatol; 2003 Jul; 28(4):434-6. PubMed ID: 12823309
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [A de nono I462S mutation in the KRT6A gene is associated with pachyonychia congenita type I].
    Kang XJ; Sun M; Yang W; Yu M; Ju Q; Lo WH; Xia LQ; Zhang X
    Zhonghua Yi Xue Za Zhi; 2004 Aug; 84(16):1344-7. PubMed ID: 15387942
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1.
    Smith FJ; McKenna KE; Irvine AD; Bingham EA; Coleman CM; Uitto J; McLean WH
    Exp Dermatol; 1999 Apr; 8(2):109-14. PubMed ID: 10232400
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Pachyonychia congenita. Keratin gene mutations with pleiotropic effect].
    Swensson O
    Hautarzt; 1999 Jul; 50(7):483-90. PubMed ID: 10464680
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Focal palmoplantar and gingival keratosis: a distinct palmoplantar ectodermal dysplasia with epidermolytic alterations but lack of mutations in known keratins.
    Kolde G; Hennies HC; Bethke G; Reichart PA
    J Am Acad Dermatol; 2005 Mar; 52(3 Pt 1):403-9. PubMed ID: 15761417
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation of a type II keratin gene (K6a) in pachyonychia congenita.
    Bowden PE; Haley JL; Kansky A; Rothnagel JA; Jones DO; Turner RJ
    Nat Genet; 1995 Jul; 10(3):363-5. PubMed ID: 7545493
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The genetic basis of pachyonychia congenita.
    Smith FJ; Liao H; Cassidy AJ; Stewart A; Hamill KJ; Wood P; Joval I; van Steensel MA; Björck E; Callif-Daley F; Pals G; Collins P; Leachman SA; Munro CS; McLean WH
    J Investig Dermatol Symp Proc; 2005 Oct; 10(1):21-30. PubMed ID: 16250206
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mouse models in preclinical studies for pachyonychia congenita.
    Chen J; Roop DR
    J Investig Dermatol Symp Proc; 2005 Oct; 10(1):37-46. PubMed ID: 16250208
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Treatment of pachyonychia congenita.
    Milstone LM; Fleckman P; Leachman SA; Leigh IM; Paller AS; van Steensel MA; Swartling C
    J Investig Dermatol Symp Proc; 2005 Oct; 10(1):18-20. PubMed ID: 16250205
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Keratin 16 and keratin 17 mutations cause pachyonychia congenita.
    McLean WH; Rugg EL; Lunny DP; Morley SM; Lane EB; Swensson O; Dopping-Hepenstal PJ; Griffiths WA; Eady RA; Higgins C
    Nat Genet; 1995 Mar; 9(3):273-8. PubMed ID: 7539673
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Insights into genotype-phenotype correlation in pachyonychia congenita from the human intermediate filament mutation database.
    McLean WH; Smith FJ; Cassidy AJ
    J Investig Dermatol Symp Proc; 2005 Oct; 10(1):31-6. PubMed ID: 16250207
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1.
    Smith FJ; Del Monaco M; Steijlen PM; Munro CS; Morvay M; Coleman CM; Rietveld FJ; Uitto J; McLean WH
    Br J Dermatol; 1999 Dec; 141(6):1010-6. PubMed ID: 10606845
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Novel keratin 17 mutations in pachyonychia congenita type 2.
    Smith FJ; Coleman CM; Bayoumy NM; Tenconi R; Nelson J; David A; McLean WH
    J Invest Dermatol; 2001 May; 116(5):806-8. PubMed ID: 11348474
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.