One remarkable molecule: filaggrin.
One remarkable molecule: filaggrin.
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DOI:
10.1038/jid.2011.393
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发表时间:
2012-03
影响因子:
6.5
通讯作者:
McLean, W. H. Irwin
中科院分区:
文献类型:
--
作者:
Brown, Sara J.;McLean, W. H. Irwin
The discovery, in 2006, that loss-of-function mutations in the filaggrin gene (FLG) are the cause of ichthyosis vulgaris – the most common disorder of keratinization – and also a strong genetic risk factor for atopic eczema, marked a significant breakthrough in the understanding of eczema pathogenesis. Subsequent investigations of the role of FLG null mutations have identified a series of significant associations with atopic disease phenotypes, including atopic asthma, allergic rhinitis and peanut allergy. However, many questions remain to be answered in relation to the precise mechanisms by which deficiency of an intracellular protein expressed primarily in the differentiating epidermis may contribute to the development of cutaneous and systemic pathology. This review aims to highlight the key milestones in filaggrin research over the past 25 years, to discuss the mechanistic, clinical and therapeutic implications and to consider possible future directions for ongoing investigation.
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DOI:
10.1016/j.jaci.2011.01.031
发表时间:
2011-03
期刊:
The Journal of allergy and clinical immunology
影响因子:
--
作者:
Brown SJ;Asai Y;Cordell HJ;Campbell LE;Zhao Y;Liao H;Northstone K;Henderson J;Alizadehfar R;Ben-Shoshan M;Morgan K;Roberts G;Masthoff LJ;Pasmans SG;van den Akker PC;Wijmenga C;Hourihane JO;Palmer CN;Lack G;Clarke A;Hull PR;Irvine AD;McLean WH
通讯作者:
McLean WH
影响因子:
6.5
作者:
Betz, Regina C.;Pforr, Jana;Noethen, Markus M.
通讯作者:
Noethen, Markus M.
影响因子:
3.5
作者:
Bowcock, AM;Shannon, W;Menter, A
通讯作者:
Menter, A
影响因子:
14.2
作者:
Cramer, Claudia;Link, Elke;Kraemer, Ursula
通讯作者:
Kraemer, Ursula
影响因子:
30.8
作者:
Cookson, WOCM;Ubhi, B;Harper, JI
通讯作者:
Harper, JI