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Journal Abstract Search

269 related items for PubMed ID: 16197419

  • 1. Inherited disorders of desmosomes.
    McGrath JA.
    Australas J Dermatol; 2005 Nov; 46(4):221-9. PubMed ID: 16197419
    [Abstract] [Full Text] [Related]

  • 2. Desmosomal genodermatoses.
    Petrof G, Mellerio JE, McGrath JA.
    Br J Dermatol; 2012 Jan; 166(1):36-45. PubMed ID: 21929534
    [Abstract] [Full Text] [Related]

  • 3. Molecular abnormalities of the desmosomal protein desmoplakin in human disease.
    Lai Cheong JE, Wessagowit V, McGrath JA.
    Clin Exp Dermatol; 2005 May; 30(3):261-6. PubMed ID: 15807686
    [Abstract] [Full Text] [Related]

  • 4. Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome.
    McGrath JA, McMillan JR, Shemanko CS, Runswick SK, Leigh IM, Lane EB, Garrod DR, Eady RA.
    Nat Genet; 1997 Oct; 17(2):240-4. PubMed ID: 9326952
    [Abstract] [Full Text] [Related]

  • 5. Human hair abnormalities resulting from inherited desmosome gene mutations.
    McGrath JA, Wessagowit V.
    Keio J Med; 2005 Jun; 54(2):72-9. PubMed ID: 16077256
    [Abstract] [Full Text] [Related]

  • 6. Ectodermal dysplasia-skin fragility syndrome.
    McGrath JA, Mellerio JE.
    Dermatol Clin; 2010 Jan; 28(1):125-9. PubMed ID: 19945625
    [Abstract] [Full Text] [Related]

  • 7. Novel truncating mutations in PKP1 and DSP cause similar skin phenotypes in two Brazilian families.
    Tanaka A, Lai-Cheong JE, Café ME, Gontijo B, Salomão PR, Pereira L, McGrath JA.
    Br J Dermatol; 2009 Mar; 160(3):692-7. PubMed ID: 19016709
    [Abstract] [Full Text] [Related]

  • 8. Desmosomal gene evaluation in Boxers with arrhythmogenic right ventricular cardiomyopathy.
    Meurs KM, Ederer MM, Stern JA.
    Am J Vet Res; 2007 Dec; 68(12):1338-41. PubMed ID: 18052738
    [Abstract] [Full Text] [Related]

  • 9. A novel genodermatosis caused by mutations in plakophilin 1, a structural component of desmosomes.
    McGrath JA.
    J Dermatol; 1999 Nov; 26(11):764-9. PubMed ID: 10635620
    [Abstract] [Full Text] [Related]

  • 10. De novo formation of desmosomes in cultured cells upon transfection of genes encoding specific desmosomal components.
    Koeser J, Troyanovsky SM, Grund C, Franke WW.
    Exp Cell Res; 2003 Apr 15; 285(1):114-30. PubMed ID: 12681292
    [Abstract] [Full Text] [Related]

  • 11. Ectodermal dysplasia-skin fragility syndrome resulting from a new homozygous mutation, 888delC, in the desmosomal protein plakophilin 1.
    Ersoy-Evans S, Erkin G, Fassihi H, Chan I, Paller AS, Sürücü S, McGrath JA.
    J Am Acad Dermatol; 2006 Jul 15; 55(1):157-61. PubMed ID: 16781314
    [Abstract] [Full Text] [Related]

  • 12. Hereditary diseases of desmosomes.
    McGrath JA.
    J Dermatol Sci; 1999 Jun 15; 20(2):85-91. PubMed ID: 10379701
    [Abstract] [Full Text] [Related]

  • 13. Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network.
    Wan H, Dopping-Hepenstal PJ, Gratian MJ, Stone MG, Zhu G, Purkis PE, South AP, Keane F, Armstrong DK, Buxton RS, McGrath JA, Eady RA.
    Br J Dermatol; 2004 May 15; 150(5):878-91. PubMed ID: 15149499
    [Abstract] [Full Text] [Related]

  • 14. Lack of plakophilin 1 increases keratinocyte migration and reduces desmosome stability.
    South AP, Wan H, Stone MG, Dopping-Hepenstal PJ, Purkis PE, Marshall JF, Leigh IM, Eady RA, Hart IR, McGrath JA.
    J Cell Sci; 2003 Aug 15; 116(Pt 16):3303-14. PubMed ID: 12840072
    [Abstract] [Full Text] [Related]

  • 15. Lack of plakoglobin leads to lethal congenital epidermolysis bullosa: a novel clinico-genetic entity.
    Pigors M, Kiritsi D, Krümpelmann S, Wagner N, He Y, Podda M, Kohlhase J, Hausser I, Bruckner-Tuderman L, Has C.
    Hum Mol Genet; 2011 May 01; 20(9):1811-9. PubMed ID: 21320868
    [Abstract] [Full Text] [Related]

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  • 18. A unique and specific interaction between alphaT-catenin and plakophilin-2 in the area composita, the mixed-type junctional structure of cardiac intercalated discs.
    Goossens S, Janssens B, Bonné S, De Rycke R, Braet F, van Hengel J, van Roy F.
    J Cell Sci; 2007 Jun 15; 120(Pt 12):2126-36. PubMed ID: 17535849
    [Abstract] [Full Text] [Related]

  • 19. Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.
    Antoniades L, Tsatsopoulou A, Anastasakis A, Syrris P, Asimaki A, Panagiotakos D, Zambartas C, Stefanadis C, McKenna WJ, Protonotarios N.
    Eur Heart J; 2006 Sep 15; 27(18):2208-16. PubMed ID: 16893920
    [Abstract] [Full Text] [Related]

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