Associated Papers
Filaggrin-Associated Atopic Skin, Eye, Airways, and Gut Disease, Modifying the Presentation of X-Linked Reticular Pigmentary Disorder (XLPDR).
Li MWY et al.
Journal of Clinical Immunology, 2024
In silico analysis of the profilaggrin sequence indicates alterations in the stability, degradation route, and intracellular protein fate in filaggrin null mutation carriers.
Paul AA et al.
Frontiers in Molecular Biosciences, 2023
Factors associated with persistence of early-onset atopic dermatitis up to the age of 12 years: a prospective cohort study in China.
Zhang Z et al.
European Journal of Dermatology : Ejd, 2021
Filaggrin gene mutations with special reference to atopic dermatitis.
Gupta J et al.
Current Treatment Options in Allergy, 2020
Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants.
Wong XFCC et al.
The Journal of Allergy and Clinical Immunology, 2018
The study of filaggrin gene mutations and copy number variation in atopic dermatitis patients from Volga-Ural region of Russia.
Gimalova GF et al.
Gene, 2016
Novel FLG null mutations in Korean patients with atopic dermatitis and comparison of the mutational spectra in Asian populations.
Park J et al.
The Journal of Dermatology, 2015
Evidence That Loss-of-Function Filaggrin Gene Mutations Evolved in Northern Europeans to Favor Intracutaneous Vitamin D3 Production.
Thyssen JP et al.
Evolutionary Biology, 2014
Ichthyosis vulgaris: the filaggrin mutation disease.
Thyssen JP et al.
The British Journal of Dermatology, 2013
[Association of filaggrin gene polymorphism with atopic dermatitis in southern Chinese Han population].
Li CX et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2011
Associations of FLG mutations between ichthyosis vulgaris and atopic dermatitis in Han Chinese.
Zhang H et al.
Allergy, 2011
Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations.
Chen H et al.
The British Journal of Dermatology, 2011
Full sequencing of the FLG gene in Italian patients with atopic eczema: evidence of new mutations, but lack of an association.
Cascella R et al.
The Journal of Investigative Dermatology, 2011
Mutations in the filaggrin gene in Han Chinese patients with atopic dermatitis.
Zhang H et al.
Allergy, 2011
Filaggrin gene defects and the risk of developing allergic disorders.
Osawa R et al.
Allergology International : Official Journal of the Japanese Society of Allergology, 2011
Novel and recurrent mutations in the filaggrin gene in Chinese patients with ichthyosis vulgaris.
Zhang X et al.
The British Journal of Dermatology, 2010
FLG mutation p.Lys4021X in the C-terminal imperfect filaggrin repeat in Japanese patients with atopic eczema.
Nemoto-Hasebe I et al.
The British Journal of Dermatology, 2009
Analysis of Taiwanese ichthyosis vulgaris families further demonstrates differences in FLG mutations between European and Asian populations.
Hsu CK et al.
The British Journal of Dermatology, 2009
Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup.
Oji V et al.
The British Journal of Dermatology, 2009
Eczema genetics: current state of knowledge and future goals.
Brown SJ et al.
The Journal of Investigative Dermatology, 2009
Unique and recurrent mutations in the filaggrin gene in Singaporean Chinese patients with ichthyosis vulgaris.
Chen H et al.
The Journal of Investigative Dermatology, 2008
Filaggrin and the great epidermal barrier grief.
McGrath JA
The Australasian Journal of Dermatology, 2008
Filaggrin Gene Mutation in Pediatric Patients with Atopic Dermatitis: A Look into Indian Gene Pool, a Pilot Study.
Rajeshwari KA et al.
Indian Journal of Dermatology, 0
Neonatal Filaggrin Genetic Screening and Counseling to Prevent Atopic Dermatitis in High-Risk Infants.
Chen HY et al.
Dermatitis : Contact, Atopic, Occupational, Drug, 0