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Journal Abstract Search


461 related items for PubMed ID: 19601998

  • 1. Variation in genes of the epidermal differentiation complex in German atopic dermatitis patients.
    Stemmler S, Nothnagel M, Parwez Q, Petrasch-Parwez E, Epplen JT, Hoffjan S.
    Int J Immunogenet; 2009 Aug; 36(4):217-22. PubMed ID: 19601998
    [Abstract] [Full Text] [Related]

  • 2. On the role of the epidermal differentiation complex in ichthyosis vulgaris, atopic dermatitis and psoriasis.
    Hoffjan S, Stemmler S.
    Br J Dermatol; 2007 Sep; 157(3):441-9. PubMed ID: 17573887
    [Abstract] [Full Text] [Related]

  • 3. Single nucleotide polymorphisms and the haplotype in the DEFB1 gene are associated with atopic dermatitis in a Korean population.
    Kim E, Lee JE, Namkung JH, Kim PS, Kim S, Shin ES, Cho EY, Yang JM.
    J Dermatol Sci; 2009 Apr; 54(1):25-30. PubMed ID: 19135873
    [Abstract] [Full Text] [Related]

  • 4. Association of Filaggrin loss-of-function-mutations with atopic dermatitis and asthma in the Early Treatment of the Atopic Child (ETAC) population.
    Müller S, Marenholz I, Lee YA, Sengler C, Zitnik SE, Griffioen RW, Meglio P, Wahn U, Nickel R.
    Pediatr Allergy Immunol; 2009 Jun; 20(4):358-61. PubMed ID: 19538357
    [Abstract] [Full Text] [Related]

  • 5. Filaggrin null mutations in childhood atopic dermatitis among the Chinese.
    Ching GK, Hon KL, Ng PC, Leung TF.
    Int J Immunogenet; 2009 Aug; 36(4):251-4. PubMed ID: 19602001
    [Abstract] [Full Text] [Related]

  • 6. Filaggrin mutations in children with severe atopic dermatitis.
    Morar N, Cookson WO, Harper JI, Moffatt MF.
    J Invest Dermatol; 2007 Jul; 127(7):1667-72. PubMed ID: 17301831
    [Abstract] [Full Text] [Related]

  • 7. Mutations in the filaggrin gene in Han Chinese patients with atopic dermatitis.
    Zhang H, Guo Y, Wang W, Shi M, Chen X, Yao Z.
    Allergy; 2011 Mar; 66(3):420-7. PubMed ID: 21039602
    [Abstract] [Full Text] [Related]

  • 8. Lack of association between filaggrin gene mutations and onset of psoriasis in childhood.
    Winge MC, Suneson J, Lysell J, Nikamo P, Liedén A, Nordenskjöld M, Wahlgren CF, Bradley M, Ståhle M.
    J Eur Acad Dermatol Venereol; 2013 Jan; 27(1):e124-7. PubMed ID: 22182180
    [Abstract] [Full Text] [Related]

  • 9. Loss-of-function polymorphisms in the filaggrin gene are associated with an increased susceptibility to chronic irritant contact dermatitis: a case-control study.
    de Jongh CM, Khrenova L, Verberk MM, Calkoen F, van Dijk FJ, Voss H, John SM, Kezic S.
    Br J Dermatol; 2008 Sep; 159(3):621-7. PubMed ID: 18637008
    [Abstract] [Full Text] [Related]

  • 10. Association of psoriasis to PGLYRP and SPRR genes at PSORS4 locus on 1q shows heterogeneity between Finnish, Swedish and Irish families.
    Kainu K, Kivinen K, Zucchelli M, Suomela S, Kere J, Inerot A, Baker BS, Powles AV, Fry L, Samuelsson L, Saarialho-Kere U.
    Exp Dermatol; 2009 Feb; 18(2):109-15. PubMed ID: 18643845
    [Abstract] [Full Text] [Related]

  • 11. Filaggrin mutations confer susceptibility to atopic dermatitis but not to asthma.
    Rogers AJ, Celedón JC, Lasky-Su JA, Weiss ST, Raby BA.
    J Allergy Clin Immunol; 2007 Dec; 120(6):1332-7. PubMed ID: 18073125
    [Abstract] [Full Text] [Related]

  • 12. Polymorphisms in human histamine receptor H4 gene are associated with atopic dermatitis.
    Yu B, Shao Y, Zhang J, Dong XL, Liu WL, Yang H, Liu L, Li MH, Yue CF, Fang ZY, Zhang C, Hu XP, Chen BC, Wu Q, Chen YW, Zhang W, Wan J.
    Br J Dermatol; 2010 May; 162(5):1038-43. PubMed ID: 20199554
    [Abstract] [Full Text] [Related]

  • 13. Polymorphisms within the CTLA4 gene are associated with infant atopic dermatitis.
    Jones G, Wu S, Jang N, Fulcher D, Hogan P, Stewart G.
    Br J Dermatol; 2006 Mar; 154(3):467-71. PubMed ID: 16445777
    [Abstract] [Full Text] [Related]

  • 14. A prospective study of filaggrin null mutations in keratoconus patients with or without atopic disorders.
    Droitcourt C, Touboul D, Ged C, Ezzedine K, Cario-André M, de Verneuil H, Colin J, Taïeb A.
    Dermatology; 2011 Mar; 222(4):336-41. PubMed ID: 21701148
    [Abstract] [Full Text] [Related]

  • 15. Association screen for atopic dermatitis candidate gene regions using microsatellite markers in pooled DNA samples.
    Hoffjan S, Parwez Q, Petrasch-Parwez E, Falkenstein D, Nothnagel M, Epplen JT.
    Int J Immunogenet; 2006 Dec; 33(6):401-9. PubMed ID: 17117949
    [Abstract] [Full Text] [Related]

  • 16. Association between a common IL10 distal promoter haplotype and IgE production in individuals with atopic dermatitis.
    Lacy K, Archer C, Wood N, Bidwell J.
    Int J Immunogenet; 2009 Aug; 36(4):213-6. PubMed ID: 19552724
    [Abstract] [Full Text] [Related]

  • 17. Analysis of four prevalent filaggrin mutations (R501X, 2282del4, R2447X and S3247X) in Austrian and German patients with atopic dermatitis.
    Greisenegger E, Novak N, Maintz L, Bieber T, Zimprich F, Haubenberger D, Gleiss A, Stingl G, Kopp T, Zimprich A.
    J Eur Acad Dermatol Venereol; 2010 May; 24(5):607-10. PubMed ID: 19874431
    [Abstract] [Full Text] [Related]

  • 18. Investigation of the eotaxin gene -426C-->T, -384A-->G and 67G-->a single-nucleotide polymorphisms and atopic dermatitis in Italian children using family-based association methods.
    Rigoli L, Caminiti L, Di Bella C, Procopio V, Cuppari C, Vita D, Barberio G, Salpietro C, Pajno GB.
    Clin Exp Dermatol; 2008 May; 33(3):316-21. PubMed ID: 18312459
    [Abstract] [Full Text] [Related]

  • 19. Association of variation in the LAMA3 gene, encoding the alpha-chain of laminin 5, with atopic dermatitis in a German case-control cohort.
    Stemmler S, Parwez Q, Petrasch-Parwez E, Epplen JT, Hoffjan S.
    BMC Dermatol; 2014 Nov 03; 14():17. PubMed ID: 25363238
    [Abstract] [Full Text] [Related]

  • 20. Analysis of SPINK 5, KLK 7 and FLG genotypes in a French atopic dermatitis cohort.
    Hubiche T, Ged C, Benard A, Léauté-Labrèze C, McElreavey K, de Verneuil H, Taïeb A, Boralevi F.
    Acta Derm Venereol; 2007 Nov 03; 87(6):499-505. PubMed ID: 17989887
    [Abstract] [Full Text] [Related]


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