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202 related items for PubMed ID: 23297869

  • 21. Altered stratum corneum barrier and enhanced percutaneous immune responses in filaggrin-null mice.
    Kawasaki H, Nagao K, Kubo A, Hata T, Shimizu A, Mizuno H, Yamada T, Amagai M.
    J Allergy Clin Immunol; 2012 Jun; 129(6):1538-46.e6. PubMed ID: 22409988
    [Abstract] [Full Text] [Related]

  • 22. Mapping of the associated phenotype of an absent granular layer in ichthyosis vulgaris to the epidermal differentiation complex on chromosome 1.
    Compton JG, DiGiovanna JJ, Johnston KA, Fleckman P, Bale SJ.
    Exp Dermatol; 2002 Dec; 11(6):518-26. PubMed ID: 12473059
    [Abstract] [Full Text] [Related]

  • 23. Filaggrin gene mutations in African Americans with both ichthyosis vulgaris and atopic dermatitis.
    Polcari I, Becker L, Stein SL, Smith MS, Paller AS.
    Pediatr Dermatol; 2014 Dec; 31(4):489-92. PubMed ID: 24920311
    [Abstract] [Full Text] [Related]

  • 24. Specific filaggrin mutations cause ichthyosis vulgaris and are significantly associated with atopic dermatitis in Japan.
    Nomura T, Akiyama M, Sandilands A, Nemoto-Hasebe I, Sakai K, Nagasaki A, Ota M, Hata H, Evans AT, Palmer CN, Shimizu H, McLean WH.
    J Invest Dermatol; 2008 Jun; 128(6):1436-41. PubMed ID: 18200065
    [Abstract] [Full Text] [Related]

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  • 26. Loss of normal profilaggrin and filaggrin in flaky tail (ft/ft) mice: an animal model for the filaggrin-deficient skin disease ichthyosis vulgaris.
    Presland RB, Boggess D, Lewis SP, Hull C, Fleckman P, Sundberg JP.
    J Invest Dermatol; 2000 Dec; 115(6):1072-81. PubMed ID: 11121144
    [Abstract] [Full Text] [Related]

  • 27. Filaggrin loss-of-function mutations are associated with early-onset eczema, eczema severity and transepidermal water loss at 3 months of age.
    Flohr C, England K, Radulovic S, McLean WH, Campbel LE, Barker J, Perkin M, Lack G.
    Br J Dermatol; 2010 Dec; 163(6):1333-6. PubMed ID: 21137118
    [Abstract] [Full Text] [Related]

  • 28. Revisiting the Roles of Filaggrin in Atopic Dermatitis.
    Moosbrugger-Martinz V, Leprince C, Méchin MC, Simon M, Blunder S, Gruber R, Dubrac S.
    Int J Mol Sci; 2022 May 10; 23(10):. PubMed ID: 35628125
    [Abstract] [Full Text] [Related]

  • 29. No remarkable differences in rates of sensitization to common type I and IV allergens between FLG loss-of-function mutation carriers and wild-type subjects.
    Landeck L, Visser M, Skudlik C, Brans R, Kezic S, John SM.
    Contact Dermatitis; 2014 Jan 10; 70(1):27-34. PubMed ID: 23848345
    [Abstract] [Full Text] [Related]

  • 30. Unique and recurrent mutations in the filaggrin gene in Singaporean Chinese patients with ichthyosis vulgaris.
    Chen H, Ho JC, Sandilands A, Chan YC, Giam YC, Evans AT, Lane EB, McLean WH.
    J Invest Dermatol; 2008 Jul 10; 128(7):1669-75. PubMed ID: 18239616
    [Abstract] [Full Text] [Related]

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  • 32. Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.
    Smith FJ, Irvine AD, Terron-Kwiatkowski A, Sandilands A, Campbell LE, Zhao Y, Liao H, Evans AT, Goudie DR, Lewis-Jones S, Arseculeratne G, Munro CS, Sergeant A, O'Regan G, Bale SJ, Compton JG, DiGiovanna JJ, Presland RB, Fleckman P, McLean WH.
    Nat Genet; 2006 Mar 10; 38(3):337-42. PubMed ID: 16444271
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  • 34. 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 10; 27(1):e124-7. PubMed ID: 22182180
    [Abstract] [Full Text] [Related]

  • 35. Simultaneous effect of ursolic acid and oleanolic acid on epidermal permeability barrier function and epidermal keratinocyte differentiation via peroxisome proliferator-activated receptor-alpha.
    Lim SW, Hong SP, Jeong SW, Kim B, Bak H, Ryoo HC, Lee SH, Ahn SK.
    J Dermatol; 2007 Sep 10; 34(9):625-34. PubMed ID: 17727365
    [Abstract] [Full Text] [Related]

  • 36. Clinical severity correlates with impaired barrier in filaggrin-related eczema.
    Nemoto-Hasebe I, Akiyama M, Nomura T, Sandilands A, McLean WH, Shimizu H.
    J Invest Dermatol; 2009 Mar 10; 129(3):682-9. PubMed ID: 18818676
    [Abstract] [Full Text] [Related]

  • 37. Novel and recurrent mutations in the filaggrin gene in Chinese patients with ichthyosis vulgaris.
    Zhang X, Liu S, Chen X, Zhou B, Liu D, Lei G, Xiao X, Liu H, Wang H.
    Br J Dermatol; 2010 Jul 10; 163(1):63-9. PubMed ID: 20222934
    [Abstract] [Full Text] [Related]

  • 38. Filaggrin and Skin Barrier Function.
    Kezic S, Jakasa I.
    Curr Probl Dermatol; 2016 Jul 10; 49():1-7. PubMed ID: 26844893
    [Abstract] [Full Text] [Related]

  • 39. [Filaggrin gene mutations are frequent and increase the risk of skin disease].
    Meyer MW, Thyssen JP.
    Ugeskr Laeger; 2011 Oct 24; 173(43):2705-8. PubMed ID: 22027225
    [Abstract] [Full Text] [Related]

  • 40. [Mutation analysis of FLG gene in 10 Chinese families with ichthyosis vulgaris].
    Gu Y, Shao M, Du X, Li M, Shi H, Zhang G.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Jun 24; 30(3):257-60. PubMed ID: 23744309
    [Abstract] [Full Text] [Related]

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