Filaggrin loss-of-function mutation R501X and 2282del4 carrier status is associated with fissured skin on the hands: results from a cross-sectional population study-Reference-Cited by-同舟云学术

Filaggrin loss-of-function mutation R501X and 2282del4 carrier status is associated with fissured skin on the hands: results from a cross-sectional population study

Published:2011-11-02 Issue:1 Volume:166 Page:46-53
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:

Author:

Thyssen J.P.,Ross-Hansen K.,Johansen J.D.,Zachariae C.,Carlsen B.C.,Linneberg A.,Bisgaard H.,Carson C.G.,Nielsen N.H.,Meldgaard M.,Szecsi P.B.,Stender S.,Menné T.

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2011.10530.x/fullpdf

Reference43 articles.

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3. Histidine-rich proteins (filaggrins): structural and functional heterogeneity during epidermal differentiation;Harding;J Mol Biol,1983

4. The characterization of human epidermal filaggrin. A histidine-rich, keratin filament-aggregating protein;Lynley;Biochim Biophys Acta,1983

5. The filaggrin story: novel insights into skin-barrier function and disease;McGrath;Trends Mol Med,2008

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