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Journal Abstract Search

203 related items for PubMed ID: 14962091

  • 1. Molecular consequences of deletion of the cytoplasmic domain of bullous pemphigoid 180 in a patient with predominant features of epidermolysis bullosa simplex.
    Fontao L, Tasanen K, Huber M, Hohl D, Koster J, Bruckner-Tuderman L, Sonnenberg A, Borradori L.
    J Invest Dermatol; 2004 Jan; 122(1):65-72. PubMed ID: 14962091
    [Abstract] [Full Text] [Related]

  • 2. Deletion of the cytoplasmatic domain of BP180/collagen XVII causes a phenotype with predominant features of epidermolysis bullosa simplex.
    Huber M, Floeth M, Borradori L, Schäcke H, Rugg EL, Lane EB, Frenk E, Hohl D, Bruckner-Tuderman L.
    J Invest Dermatol; 2002 Jan; 118(1):185-92. PubMed ID: 11851893
    [Abstract] [Full Text] [Related]

  • 3. Hemidesmosome formation is initiated by the beta4 integrin subunit, requires complex formation of beta4 and HD1/plectin, and involves a direct interaction between beta4 and the bullous pemphigoid antigen 180.
    Schaapveld RQ, Borradori L, Geerts D, van Leusden MR, Kuikman I, Nievers MG, Niessen CM, Steenbergen RD, Snijders PJ, Sonnenberg A.
    J Cell Biol; 1998 Jul 13; 142(1):271-84. PubMed ID: 9660880
    [Abstract] [Full Text] [Related]

  • 4. Role of the bullous pemphigoid antigen 180 (BP180) in the assembly of hemidesmosomes and cell adhesion--reexpression of BP180 in generalized atrophic benign epidermolysis bullosa keratinocytes.
    Borradori L, Chavanas S, Schaapveld RQ, Gagnoux-Palacios L, Calafat J, Meneguzzi G, Sonnenberg A.
    Exp Cell Res; 1998 Mar 15; 239(2):463-76. PubMed ID: 9521865
    [Abstract] [Full Text] [Related]

  • 5. Analysis of the interactions between BP180, BP230, plectin and the integrin alpha6beta4 important for hemidesmosome assembly.
    Koster J, Geerts D, Favre B, Borradori L, Sonnenberg A.
    J Cell Sci; 2003 Jan 15; 116(Pt 2):387-99. PubMed ID: 12482924
    [Abstract] [Full Text] [Related]

  • 6. Deletion of a cytoplasmic domain of integrin beta4 causes epidermolysis bullosa simplex.
    Jonkman MF, Pas HH, Nijenhuis M, Kloosterhuis G, Steege G.
    J Invest Dermatol; 2002 Dec 15; 119(6):1275-81. PubMed ID: 12485428
    [Abstract] [Full Text] [Related]

  • 7. The localization of bullous pemphigoid antigen 180 (BP180) in hemidesmosomes is mediated by its cytoplasmic domain and seems to be regulated by the beta4 integrin subunit.
    Borradori L, Koch PJ, Niessen CM, Erkeland S, van Leusden MR, Sonnenberg A.
    J Cell Biol; 1997 Mar 24; 136(6):1333-47. PubMed ID: 9087447
    [Abstract] [Full Text] [Related]

  • 8. 180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosa.
    Jonkman MF, de Jong MC, Heeres K, Pas HH, van der Meer JB, Owaribe K, Martinez de Velasco AM, Niessen CM, Sonnenberg A.
    J Clin Invest; 1995 Mar 24; 95(3):1345-52. PubMed ID: 7883981
    [Abstract] [Full Text] [Related]

  • 9. The molecular architecture of hemidesmosomes, as revealed with super-resolution microscopy.
    Nahidiazar L, Kreft M, van den Broek B, Secades P, Manders EM, Sonnenberg A, Jalink K.
    J Cell Sci; 2015 Oct 15; 128(20):3714-9. PubMed ID: 26330528
    [Abstract] [Full Text] [Related]

  • 10. Hemidesmosome assembly assessed by expression of a wild-type integrin beta 4 cDNA in junctional epidermolysis bullosa keratinocytes.
    Gagnoux-Palacios L, Gache Y, Ortonne JP, Meneguzzi G.
    Lab Invest; 1997 Nov 15; 77(5):459-68. PubMed ID: 9389789
    [Abstract] [Full Text] [Related]

  • 11. Direct interaction between the intracellular domains of bullous pemphigoid antigen 2 (BP180) and beta 4 integrin, hemidesmosomal components of basal keratinocytes.
    Aho S, Uitto J.
    Biochem Biophys Res Commun; 1998 Feb 24; 243(3):694-9. PubMed ID: 9500991
    [Abstract] [Full Text] [Related]

  • 12. Molecular genetic studies of a human epidermal autoantigen (the 180-kD bullous pemphigoid antigen/BP180): identification of functionally important sequences within the BP180 molecule and evidence for an interaction between BP180 and alpha 6 integrin.
    Hopkinson SB, Baker SE, Jones JC.
    J Cell Biol; 1995 Jul 24; 130(1):117-25. PubMed ID: 7790367
    [Abstract] [Full Text] [Related]

  • 13. 14-3-3 sigma isoform interacts with the cytoplasmic domain of the transmembrane BP180 in keratinocytes.
    Li Y, Lin X, Kilani RT, Jones JC, Ghahary A.
    J Cell Physiol; 2007 Sep 24; 212(3):675-81. PubMed ID: 17443672
    [Abstract] [Full Text] [Related]

  • 14. A homozygous in-frame deletion in the collagenous domain of bullous pemphigoid antigen BP180 (type XVII collagen) causes generalized atrophic benign epidermolysis bullosa.
    Chavanas S, Gache Y, Tadini G, Pulkkinen L, Uitto J, Ortonne JP, Meneguzzi G.
    J Invest Dermatol; 1997 Jul 24; 109(1):74-8. PubMed ID: 9204958
    [Abstract] [Full Text] [Related]

  • 15. Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosa.
    Pulkkinen L, Marinkovich MP, Tran HT, Lin L, Herron GS, Uitto J.
    J Invest Dermatol; 1999 Dec 24; 113(6):1114-8. PubMed ID: 10636730
    [Abstract] [Full Text] [Related]

  • 16. Loss of interaction between plectin and type XVII collagen results in epidermolysis bullosa simplex.
    Natsuga K, Nishie W, Nishimura M, Shinkuma S, Watanabe M, Izumi K, Nakamura H, Hirako Y, Shimizu H.
    Hum Mutat; 2017 Dec 24; 38(12):1666-1670. PubMed ID: 28941359
    [Abstract] [Full Text] [Related]

  • 17. The N terminus of the transmembrane protein BP180 interacts with the N-terminal domain of BP230, thereby mediating keratin cytoskeleton anchorage to the cell surface at the site of the hemidesmosome.
    Hopkinson SB, Jones JC.
    Mol Biol Cell; 2000 Jan 24; 11(1):277-86. PubMed ID: 10637308
    [Abstract] [Full Text] [Related]

  • 18. Generalized atrophic benign epidermolysis bullosa. Either 180-kd bullous pemphigoid antigen or laminin-5 deficiency.
    Jonkman MF, de Jong MC, Heeres K, Steijlen PM, Owaribe K, Küster W, Meurer M, Gedde-Dahl T, Sonnenberg A, Bruckner-Tuderman L.
    Arch Dermatol; 1996 Feb 24; 132(2):145-50. PubMed ID: 8629821
    [Abstract] [Full Text] [Related]

  • 19. A homozygous nonsense mutation within the dystonin gene coding for the coiled-coil domain of the epithelial isoform of BPAG1 underlies a new subtype of autosomal recessive epidermolysis bullosa simplex.
    Groves RW, Liu L, Dopping-Hepenstal PJ, Markus HS, Lovell PA, Ozoemena L, Lai-Cheong JE, Gawler J, Owaribe K, Hashimoto T, Mellerio JE, Mee JB, McGrath JA.
    J Invest Dermatol; 2010 Jun 24; 130(6):1551-7. PubMed ID: 20164846
    [Abstract] [Full Text] [Related]

  • 20. Respective contribution of neutrophil elastase and matrix metalloproteinase 9 in the degradation of BP180 (type XVII collagen) in human bullous pemphigoid.
    Verraes S, Hornebeck W, Polette M, Borradori L, Bernard P.
    J Invest Dermatol; 2001 Nov 24; 117(5):1091-6. PubMed ID: 11710917
    [Abstract] [Full Text] [Related]

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