Filaggrin loss-of-function variant contributes to atopic dermatitis risk in the population of Northern Germany

被引:85
作者
Ruether, A.
Stoll, M.
Schwarz, T.
Schreiber, S. [1 ]
Foelster-Holst, R.
机构
[1] Univ Kiel, Inst Clin Mol Biol, D-24105 Kiel, Germany
[2] Univ Kiel, Dept Dermatol, D-24105 Kiel, Germany
[3] Leibniz Inst Arteriosclerosis Res, Munster, Germany
关键词
PROTEIN; DISEASE;
D O I
10.1111/j.1365-2133.2006.07500.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
引用
收藏
页码:1093 / 1094
页数:2
相关论文
共 11 条
[1]  
DALE BA, 1985, ANN NY ACAD SCI, V455, P330, DOI 10.1111/j.1749-6632.1985.tb50420.x
[2]   Lack of association of SPINK5 polymorphisms with nonsyndromic atopic dermatitis in the population of Northern Germany [J].
Fölster-Holst, R ;
Stoll, M ;
Koch, WA ;
Hampe, J ;
Christophers, E ;
Schreiber, S .
BRITISH JOURNAL OF DERMATOLOGY, 2005, 152 (06) :1365-1367
[3]  
HANIFIN JM, 1980, ACTA DERM-VENEREOL, P44
[4]   PopGen: Population-based recruitment of patients and controls for the analysis of complex genotype-phenotype relationships [J].
Krawczak, M ;
Nikolaus, S ;
von Eberstein, H ;
Croucher, PJP ;
El Mokhtari, NE ;
Schreiber, S .
COMMUNITY GENETICS, 2006, 9 (01) :55-61
[5]  
Kuokkanen K, 1969, Acta Derm Venereol Suppl (Stockh), V62, P1
[6]   Efficient multipoint linkage analysis through reduction of inheritance space [J].
Markianos, K ;
Daly, MJ ;
Kruglyak, L .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (04) :963-977
[7]   Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis [J].
Palmer, CNA ;
Irvine, AD ;
Terron-Kwiatkowski, A ;
Zhao, YW ;
Liao, HH ;
Lee, SP ;
Goudie, DR ;
Sandilands, A ;
Campbell, LE ;
Smith, FJD ;
O'Regan, GM ;
Watson, RM ;
Cecil, JE ;
Bale, SJ ;
Compton, JG ;
DiGiovanna, JJ ;
Fleckman, P ;
Lewis-Jones, S ;
Arseculeratne, G ;
Sergeant, A ;
Munro, CS ;
El Houate, B ;
McElreavey, K ;
Halkjaer, LB ;
Bisgaard, H ;
Mukhopadhyay, S ;
McLean, WHI .
NATURE GENETICS, 2006, 38 (04) :441-446
[8]   Genetics of Crohn disease, an archetypal inflammatory barrier disease [J].
Schreiber, S ;
Rosenstiel, P ;
Albrecht, M ;
Hampe, J ;
Krawczak, M .
NATURE REVIEWS GENETICS, 2005, 6 (05) :376-388
[9]   Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris [J].
Smith, FJD ;
Irvine, AD ;
Terron-Kwiatkowski, A ;
Sandilands, A ;
Campbell, LE ;
Zhao, YW ;
Liao, HH ;
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, WHI .
NATURE GENETICS, 2006, 38 (03) :337-342
[10]   Genetic variation in DLG5 is associated with inflammatory bowel disease [J].
Stoll, M ;
Corneliussen, B ;
Costello, CM ;
Waetzig, GH ;
Mellgard, B ;
Koch, WA ;
Rosenstiel, P ;
Albrecht, M ;
Croucher, PJP ;
Seegert, D ;
Nikolaus, S ;
Hampe, J ;
Lengauer, T ;
Pierrou, S ;
Foelsch, UR ;
Mathew, CG ;
Lagerstrom-Fermer, M ;
Schreiber, S .
NATURE GENETICS, 2004, 36 (05) :476-480