BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

577 related articles for article (PubMed ID: 18194361)

  • 1. Genetic analysis of autoimmune regulator haplotypes in alopecia areata.
    Wengraf DA; McDonagh AJ; Lovewell TR; Vasilopoulos Y; Macdonald-Hull SP; Cork MJ; Messenger AG; Tazi-Ahnini R
    Tissue Antigens; 2008 Mar; 71(3):206-12. PubMed ID: 18194361
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The autoimmune regulator gene (AIRE) is strongly associated with vitiligo.
    Tazi-Ahnini R; McDonagh AJ; Wengraf DA; Lovewell TR; Vasilopoulos Y; Messenger AG; Cork MJ; Gawkrodger DJ
    Br J Dermatol; 2008 Sep; 159(3):591-6. PubMed ID: 18616774
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dermatological manifestations of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome.
    Collins SM; Dominguez M; Ilmarinen T; Costigan C; Irvine AD
    Br J Dermatol; 2006 Jun; 154(6):1088-93. PubMed ID: 16704638
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Role of the autoimmune regulator (AIRE) gene in alopecia areata: strong association of a potentially functional AIRE polymorphism with alopecia universalis.
    Tazi-Ahnini R; Cork MJ; Gawkrodger DJ; Birch MP; Wengraf D; McDonagh AJ; Messenger AG
    Tissue Antigens; 2002 Dec; 60(6):489-95. PubMed ID: 12542742
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Polymorphisms at +49A/G and CT60 sites in the 3' UTR of the CTLA-4 gene and APECED-related AIRE gene mutations analysis in sporadic idiopathic hypoparathyroidism.
    Goswami R; Gupta N; Ray D; Rani R; Tomar N; Sarin R; Vupputuri MR
    Int J Immunogenet; 2005 Dec; 32(6):393-400. PubMed ID: 16313305
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Evaluation of the autoimmune regulator (AIRE) gene mutations in a cohort of Italian patients with autoimmune-polyendocrinopathy-candidiasis-ectodermal-dystrophy (APECED) and in their relatives.
    Cervato S; Mariniello B; Lazzarotto F; Morlin L; Zanchetta R; Radetti G; De Luca F; Valenzise M; Giordano R; Rizzo D; Giordano C; Betterle C
    Clin Endocrinol (Oxf); 2009 Mar; 70(3):421-8. PubMed ID: 18616706
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of the autoimmune regulator gene in patients with autoimmune non-APECED polyendocrinopathies.
    Palma A; Gianchecchi E; Palombi M; Luciano R; Di Carlo P; Crinò A; Cappa M; Fierabracci A
    Genomics; 2013 Sep; 102(3):163-8. PubMed ID: 23643663
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel AIRE mutations and P450 cytochrome autoantibodies in Central and Eastern European patients with APECED.
    Cihakova D; Trebusak K; Heino M; Fadeyev V; Tiulpakov A; Battelino T; Tar A; Halász Z; Blümel P; Tawfik S; Krohn K; Lebl J; Peterson P
    Hum Mutat; 2001 Sep; 18(3):225-32. PubMed ID: 11524733
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The genetic background of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy and its autoimmune disease components.
    Vogel A; Strassburg CP; Obermayer-Straub P; Brabant G; Manns MP
    J Mol Med (Berl); 2002 Apr; 80(4):201-11. PubMed ID: 11976729
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel and recurrent mutations in the AIRE gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients.
    Faiyaz-Ul-Haque M; Bin-Abbas B; Al-Abdullatif A; Abdullah Abalkhail H; Toulimat M; Al-Gazlan S; Almutawa AM; Al-Sagheir A; Peltekova I; Al-Dayel F; Zaidi SH
    Clin Genet; 2009 Nov; 76(5):431-40. PubMed ID: 19758376
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Association of Autoimmune Regulator Gene Rs2075876 Variant, but Not Gene Expression with Alopecia Areata in Males: A Case-control Study.
    Toraih EA; Ameen HM; Hussein MH; Youssef Elabd AA; Mohamed AM; Abdel-Gawad AR; Fawzy MS
    Immunol Invest; 2020 Feb; 49(1-2):146-165. PubMed ID: 31601134
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Positional cloning of the APECED gene.
    Nagamine K; Peterson P; Scott HS; Kudoh J; Minoshima S; Heino M; Krohn KJ; Lalioti MD; Mullis PE; Antonarakis SE; Kawasaki K; Asakawa S; Ito F; Shimizu N
    Nat Genet; 1997 Dec; 17(4):393-8. PubMed ID: 9398839
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel heterozygous mutation of the AIRE gene in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED).
    Fierabracci A; Bizzarri C; Palma A; Milillo A; Bellacchio E; Cappa M
    Gene; 2012 Dec; 511(1):113-7. PubMed ID: 23000069
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The TRAF1/C5 locus confers risk for familial and severe alopecia areata.
    Redler S; Brockschmidt FF; Forstbauer L; Giehl KA; Herold C; Eigelshoven S; Hanneken S; De Weert J; Lutz G; Wolff H; Kruse R; Blaumeiser B; Böhm M; Becker T; Nöthen MM; Betz RC
    Br J Dermatol; 2010 Apr; 162(4):866-9. PubMed ID: 20030635
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Lupus-like panniculitis in a patient with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED).
    Füchtenbusch M; Vogel A; Achenbach P; Gummer M; Ziegler AG; Albert E; Standl E; Manns MP
    Exp Clin Endocrinol Diabetes; 2003 Aug; 111(5):288-93. PubMed ID: 12951636
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The non-synonymous C1858T substitution in the PTPN22 gene is associated with susceptibility to the severe forms of alopecia areata.
    Kemp EH; McDonagh AJ; Wengraf DA; Messenger AG; Gawkrodger DJ; Cork MJ; Tazi-Ahnini R
    Hum Immunol; 2006 Jul; 67(7):535-9. PubMed ID: 16829308
    [TBL] [Abstract][Full Text] [Related]  

  • 17. APECED mutations in the autoimmune regulator (AIRE) gene.
    Heino M; Peterson P; Kudoh J; Shimizu N; Antonarakis SE; Scott HS; Krohn K
    Hum Mutat; 2001 Sep; 18(3):205-11. PubMed ID: 11524731
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HLA-D locus associations in alopecia areata. DRw52a may confer disease resistance.
    Duvic M; Hordinsky MK; Fiedler VC; O'Brien WR; Young R; Reveille JD
    Arch Dermatol; 1991 Jan; 127(1):64-8. PubMed ID: 1670917
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular background of polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome in a Polish population: novel AIRE mutations and an estimate of disease prevalence.
    Stolarski B; Pronicka E; Korniszewski L; Pollak A; Kostrzewa G; Rowińska E; Włodarski P; Skórka A; Gremida M; Krajewski P; Ploski R
    Clin Genet; 2006 Oct; 70(4):348-54. PubMed ID: 16965330
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Aire-deficient C57BL/6 mice mimicking the common human 13-base pair deletion mutation present with only a mild autoimmune phenotype.
    Hubert FX; Kinkel SA; Crewther PE; Cannon PZ; Webster KE; Link M; Uibo R; O'Bryan MK; Meager A; Forehan SP; Smyth GK; Mittaz L; Antonarakis SE; Peterson P; Heath WR; Scott HS
    J Immunol; 2009 Mar; 182(6):3902-18. PubMed ID: 19265170
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 29.