Proteomic manifestations of genetic defects in autosomal recessive congenital ichthyosis-Reference-Cited by-同舟云学术

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Proteomic manifestations of genetic defects in autosomal recessive congenital ichthyosis

Published:2019-06 Issue: Volume:201 Page:104-109
ISSN:1874-3919
Container-title:Journal of Proteomics
language:en
Short-container-title:Journal of Proteomics

Author:

Karim Noreen,Durbin-Johnson Blythe,Rocke David M.,Salemi Michelle,Phinney Brett S.,Naeem Muhammad^ORCID,Rice Robert H.^ORCID

Funder

International Research Support Initiative Program of the Higher Education Commission of Pakistan

National Center for Advancing Translational Sciences

USDA(NIFA)/University of California Agricultural Experiment Station, USA

Publisher

Elsevier BV

Subject

Biochemistry,Biophysics

Reference29 articles.

1. Inherited ichthyosis: non-syndromic forms;Takeichi;J. Dermatol.,2016

2. Corneocyte lipid envelope (CLE), the key structure for skin barrier function and ichthyosis pathogenesis;Akiyama;J. Dermatol. Sci.,2017

3. Mutations in SULT2B1 cause autosomal-recessive congenital ichthyosis in humans;Heinz;Am. J. Hum. Genet.,2017

4. Abnormal barrier function in the pathogenesis of ichthyosis: therapeutic implications for lipid metabolic disorders;Elias;Clin. Dermatol.,2012

5. Autosomal recessive congenital ichthyosis;Richard,2017

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