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Journal Abstract Search

129 related items for PubMed ID: 10336597

  • 1.
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  • 3. Association between variants of mast cell chymase gene and serum IgE levels in eczema.
    Mao XQ, Shirakawa T, Enomoto T, Shimazu S, Dake Y, Kitano H, Hagihara A, Hopkin JM.
    Hum Hered; 1998; 48(1):38-41. PubMed ID: 9463800
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  • 5. Association study of mast cell chymase polymorphisms with atopy.
    Weidinger S, Rümmler L, Klopp N, Wagenpfeil S, Baurecht HJ, Fischer G, Holle R, Gauger A, Schäfer T, Jakob T, Ollert M, Behrendt H, Wichmann HE, Ring J, Illig T.
    Allergy; 2005 Oct; 60(10):1256-61. PubMed ID: 16134991
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  • 6. Absence of association between a variant of the mast cell chymase gene and atopic dermatitis in an Italian population.
    Pascale E, Tarani L, Meglio P, Businco L, Battiloro E, Cimino-Reale G, Verna R, D'Ambrosio E.
    Hum Hered; 2001 Oct; 51(3):177-9. PubMed ID: 11173969
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  • 7. Extrinsic and intrinsic asthma: influence of classification on family history of asthma and allergic disease.
    Sibbald B.
    Clin Allergy; 1980 May; 10(3):313-8. PubMed ID: 7418189
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  • 9. Loss-of-function variants of the filaggrin gene are associated with atopic eczema and associated phenotypes in Swedish families.
    Ekelund E, Liedén A, Link J, Lee SP, D'Amato M, Palmer CN, Kockum I, Bradley M.
    Acta Derm Venereol; 2008 May; 88(1):15-9. PubMed ID: 18176743
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  • 11. Juvenile diabetes mellitus and atopy.
    Hermansson B, Holmgren G, Samuelson G.
    Hum Hered; 1971 May; 21(5):504-8. PubMed ID: 5147508
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  • 13. Eleven loci with new reproducible genetic associations with allergic disease risk.
    Ferreira MAR, Vonk JM, Baurecht H, Marenholz I, Tian C, Hoffman JD, Helmer Q, Tillander A, Ullemar V, Lu Y, Rüschendorf F, 23andMe Research Team23andMe, Inc, Mountain View, Calif., SHARE study, Hinds DA, Hübner N, Weidinger S, Magnusson PKE, Jorgenson E, Lee YA, Boomsma DI, Karlsson R, Almqvist C, Koppelman GH, Paternoster L.
    J Allergy Clin Immunol; 2019 Feb; 143(2):691-699. PubMed ID: 29679657
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  • 14. Filaggrin loss-of-function mutations as a predictor for atopic eczema, allergic sensitization and eczema-associated asthma in Polish children population.
    Dębińska A, Danielewicz H, Drabik-Chamerska A, Kalita D, Boznański A.
    Adv Clin Exp Med; 2017 Sep; 26(6):991-998. PubMed ID: 29068602
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  • 15. Types of allergic reaction.
    Pepys J.
    Clin Allergy; 1973 Dec; 3 Suppl():491-509. PubMed ID: 4283599
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  • 16. Lack of association between atopic eczema and the genetic variants of interleukin-4 and the interleukin-4 receptor alpha chain gene: heterogeneity of genetic backgrounds on immunoglobulin E production in atopic eczema patients.
    Tanaka K, Sugiura H, Uehara M, Hashimoto Y, Donnelly C, Montgomery DS.
    Clin Exp Allergy; 2001 Oct; 31(10):1522-7. PubMed ID: 11678851
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  • 17. Interleukin-13 receptor A1 gene polymorphism and IL-13 serum level in atopic and non-atopic Egyptian children.
    Hussein YM, El-Tarhouny SA, Shalaby SM, Mohamed RH, Hassan TH, El-Sherbeny HM, Mohamed NA.
    Immunol Invest; 2011 Oct; 40(5):523-34. PubMed ID: 21425907
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  • 18. Prevalence and familial association of atopic disease and its relationship to serum IgE levels in 1,061 school children and their families.
    Turner KJ, Rosman DL, O'Mahony J.
    Int Arch Allergy Appl Immunol; 1974 Oct; 47(5):650-64. PubMed ID: 4430508
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  • 19. Allergy in 7000 twin pairs.
    Edfors-Lubs ML.
    Acta Allergol; 1971 Aug; 26(4):249-85. PubMed ID: 4255830
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  • 20. Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.
    Ferreira MA, Vonk JM, Baurecht H, Marenholz I, Tian C, Hoffman JD, Helmer Q, Tillander A, Ullemar V, van Dongen J, Lu Y, Rüschendorf F, Esparza-Gordillo J, Medway CW, Mountjoy E, Burrows K, Hummel O, Grosche S, Brumpton BM, Witte JS, Hottenga JJ, Willemsen G, Zheng J, Rodríguez E, Hotze M, Franke A, Revez JA, Beesley J, Matheson MC, Dharmage SC, Bain LM, Fritsche LG, Gabrielsen ME, Balliu B, 23andMe Research Team, AAGC collaborators, BIOS consortium, LifeLines Cohort Study, Nielsen JB, Zhou W, Hveem K, Langhammer A, Holmen OL, Løset M, Abecasis GR, Willer CJ, Arnold A, Homuth G, Schmidt CO, Thompson PJ, Martin NG, Duffy DL, Novak N, Schulz H, Karrasch S, Gieger C, Strauch K, Melles RB, Hinds DA, Hübner N, Weidinger S, Magnusson PKE, Jansen R, Jorgenson E, Lee YA, Boomsma DI, Almqvist C, Karlsson R, Koppelman GH, Paternoster L.
    Nat Genet; 2017 Dec; 49(12):1752-1757. PubMed ID: 29083406
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