Case of Netherton syndrome with an elevated serum thymus and activation-regulated chemokine level

被引：10

作者：

Akagi, Arisa ^{[1
]}

Kitoh, Akihiko ^{[1
]}

Moniaga, Catharina S. ^{[1
]}

Fujimoto, Atsushi ^{[2
]}

Fujikawa, Hiroki ^{[2
]}

Shimomura, Yutaka ^{[2
]}

Miyachi, Yoshiki ^{[1
]}

Kabashima, Kenji ^{[1
]}

机构：

[1] Kyoto Univ Grad Sch Med, Dept Dermatol, Kyoto 6068507, Japan

[2] Niigata Univ Grad Sch Med & Dent Sci, Lab Genet Skin Dis, Niigata, Japan

来源：

JOURNAL OF DERMATOLOGY | 2013年 / 40卷 / 09期

关键词：

EXPRESSION;

D O I：

10.1111/1346-8138.12209

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

引用

页码：752 / 753

页数：2

共 4 条

[1] Kallikrein 5 induces atopic dermatitis-like lesions through PAR2-mediated thymic stromal lymphopoietin expression in Netherton syndrome [J].

Briot, Anais ;

Deraison, Celine ;

Lacroix, Matthieu ;

Bonnart, Chrystelle ;

Robin, Aurelie ;

Besson, Celine ;

Dubus, Pierre ;

Hovnanian, Alain .

JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (05) :1135-1147

[2] Serum measurement of thymus and activation-regulated chemokine/CCL17 in children with atopic dermatitis: elevated normal levels in infancy and age-specific analysis in atopic dermatitis [J].

Fujisawa, Takao ;

Nagao, Mizuho ;

Hiraguchi, Yukiko ;

Katsumata, Hajime ;

Nishimori, Hisashi ;

Iguchi, Kosei ;

Kato, Yoshiko ;

Higashiura, Masahito ;

Ogawauchi, Izumi ;

Tamaki, Kunihiko .

PEDIATRIC ALLERGY AND IMMUNOLOGY, 2009, 20 (07) :633-641

[3] Serine protease activity and residual LEKTI expression determine phenotype in Netherton syndrome [J].

Hachem, Jean-Pierre ;

Wagberg, Fredrik ;

Schmuth, Matthias ;

Crumrine, Debra ;

Lissens, Willy ;

Jayakumar, Arumugam ;

Houben, Evi ;

Mauro, Theodora M. ;

Leonardsson, Goeran ;

Brattsand, Maria ;

Egelrud, Torbjorn ;

Roseeuw, Diane ;

Clayman, Gary L. ;

Feingold, Kenneth R. ;

Williams, Mary L. ;

Elias, Peter M. .

JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (07) :1609-1621

[4] The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: Implications for mutation detection and first case of prenatal diagnosis [J].

Sprecher, E ;

Chavanas, S ;

DiGiovanna, JJ ;

Amin, S ;

Nielsen, K ;

Prendiville, JS ;

Silverman, R ;

Esterly, NB ;

Spraker, MK ;

Guelig, E ;

de Luna, ML ;

Williams, ML ;

Buehler, B ;

Siegfried, EC ;

Van Maldergem, L ;

Pfendner, E ;

Bale, SJ ;

Uitto, J ;

Hovnanian, A ;

Richard, G .

JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 117 (02) :179-187

← 1 →