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Journal Abstract Search

185 related items for PubMed ID: 24467288

  • 1. Comprehensive screening for a complete set of Japanese-population-specific filaggrin gene mutations.
    Kono M, Nomura T, Ohguchi Y, Mizuno O, Suzuki S, Tsujiuchi H, Hamajima N, McLean WH, Shimizu H, Akiyama M.
    Allergy; 2014 Apr; 69(4):537-40. PubMed ID: 24467288
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  • 5. Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations.
    Chen H, Common JE, Haines RL, Balakrishnan A, Brown SJ, Goh CS, Cordell HJ, Sandilands A, Campbell LE, Kroboth K, Irvine AD, Goh DL, Tang MB, van Bever HP, Giam YC, McLean WH, Lane EB.
    Br J Dermatol; 2011 Jul; 165(1):106-14. PubMed ID: 21428977
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  • 6. FLG mutation p.Lys4021X in the C-terminal imperfect filaggrin repeat in Japanese patients with atopic eczema.
    Nemoto-Hasebe I, Akiyama M, Nomura T, Sandilands A, McLean WH, Shimizu H.
    Br J Dermatol; 2009 Dec; 161(6):1387-90. PubMed ID: 19663875
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  • 8. Analysis of Taiwanese ichthyosis vulgaris families further demonstrates differences in FLG mutations between European and Asian populations.
    Hsu CK, Akiyama M, Nemoto-Hasebe I, Nomura T, Sandilands A, Chao SC, Lee JY, Sheu HM, McLean WH, Shimizu H.
    Br J Dermatol; 2009 Aug; 161(2):448-51. PubMed ID: 19416262
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  • 10. Filaggrin haploinsufficiency is highly penetrant and is associated with increased severity of eczema: further delineation of the skin phenotype in a prospective epidemiological study of 792 school children.
    Brown SJ, Relton CL, Liao H, Zhao Y, Sandilands A, McLean WH, Cordell HJ, Reynolds NJ.
    Br J Dermatol; 2009 Oct; 161(4):884-9. PubMed ID: 19681860
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  • 12. Palmar hyperlinearity in early childhood atopic dermatitis is associated with filaggrin mutation and sensitization to egg.
    Fukuie T, Yasuoka R, Fujiyama T, Sakabe JI, Taguchi T, Tokura Y.
    Pediatr Dermatol; 2019 Mar; 36(2):213-218. PubMed ID: 30810250
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  • 13. Filaggrin gene polymorphisms in Iranian ichthyosis vulgaris and atopic dermatitis patients.
    Hassani B, Isaian A, Shariat M, Mollanoori H, Sotoudeh S, Babaei V, Ziaali A, Teimourian S.
    Int J Dermatol; 2018 Dec; 57(12):1485-1491. PubMed ID: 30246302
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  • 17. Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup.
    Oji V, Seller N, Sandilands A, Gruber R, Gerss J, Hüffmeier U, Hamm H, Emmert S, Aufenvenne K, Metze D, Luger T, Loser K, Hausser I, Traupe H, McLean WH.
    Br J Dermatol; 2009 Apr; 160(4):771-81. PubMed ID: 19183181
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  • 18. Filaggrin loss-of-function mutations as risk factors for ischemic stroke in the general population.
    Varbo A, Nordestgaard BG, Benn M.
    J Thromb Haemost; 2017 Apr; 15(4):624-635. PubMed ID: 28164424
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  • 19. Exacerbation of ichthyosis vulgaris phenotype by co-inheritance of STS and FLG mutations in a Chinese family with ichthyosis: a case report.
    Wang X, Tan L, Shen N, Lu Y, Zhang Y.
    BMC Med Genet; 2018 Jul 18; 19(1):120. PubMed ID: 30021537
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  • 20. 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 18; 26(6):991-998. PubMed ID: 29068602
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