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The Role of the Environmental Risk Factors in the Pathogenesis and Clinical Outcome of Atopic Dermatitis

BioMed research international, 2019-01, Vol.2019 (2019), p.1-11

2019

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Tumor-Suppressive Function of lncRNA-MEG3 in Glioma Cells by Regulating miR-6088/SMARCB1 Axis

BioMed research international, 2020, Vol.2020 (2020), p.1-15

2020

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The Adenosine A2A Receptor Agonist Accelerates Bone Healing and Adjusts Treg/Th17 Cell Balance through Interleukin 6

BioMed research international, 2020, Vol.2020 (2020), p.1-13

2020

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Exploration of the Potential Mechanism of the Common Differentially Expressed Genes in Psoriasis and Atopic Dermatitis

BioMed research international, 2022, Vol.2022, p.1177299-16

2022

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Associations between ERAP1 Gene Polymorphisms and Psoriasis Susceptibility: A Meta-Analysis of Case-Control Studies

BioMed research international, 2021, Vol.2021, p.1-9

2021

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Long Noncoding RNASBF2-AS1 Promotes Gastric Cancer Progression via Regulating miR-545/EMS1 Axis

BioMed research international, 2020, Vol.2020 (2020), p.1-9

2020

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Whole-Exome Sequencing Reveals a Rare Missense Variant in SLC16A9 in a Pedigree with Early-Onset Gout

BioMed research international, 2020, Vol.2020 (2020), p.1-6

2020

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Association Study of the Caspase Gene Family and Psoriasis Vulgaris Susceptibility in Northeastern China

BioMed research international, 2019-01, Vol.2019 (2019), p.1-11

2019

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Characterisation of APS-1 Experimental Models Is Crucial for Development of Novel Therapies

BioMed research international, 2023, Vol.2023 (1), p.7960443-7960443

2023

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Alopecia areata patients show deficiency of FOXP3+CD39+ T regulatory cells and clonotypic restriction of Treg TCRβ-chain, which highlights the immunopathological aspect of the disease

PloS one, 2019-07, Vol.14 (7), p.e0210308-e0210308

2019

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The 3′-UTR AACCins5874 in the stratum corneum chymotryptic enzyme gene ( SCCE / KLK7 ), associated with atopic dermatitis; causes an increased mRNA expression without altering its stability

Journal of dermatological science, 2011-02, Vol.61 (2), p.131-133

2011

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New perspectives on epidermal barrier dysfunction in atopic dermatitis: Gene–environment interactions

Journal of allergy and clinical immunology, 2006-07, Vol.118 (1), p.3-21

2006

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HLA-C, CSTA and DS12346 susceptibility alleles confer over 100-fold increased risk of developing psoriasis: evidence of gene interaction

Journal of human genetics, 2011-06, Vol.56 (6), p.423-427

2011

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AAV9‐mediated AIRE gene delivery clears circulating antibodies and tissue T‐cell infiltration in a mouse model of autoimmune polyglandular syndrome type‐1

Clinical & translational immunology, 2020, Vol.9 (9), p.e1166-n/a

2020

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First report of SLC39A4 mutation in acrodermatitis enteropathica family from the Middle East

International journal of dermatology, 2017-05, Vol.56 (5), p.e97-e100

2017

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Correction: Alopecia areata patients show deficiency of FOXP3+CD39+ T regulatory cells and clonotypic restriction of Treg TCRβ-chain, which highlights the immunopathological aspect of the disease

PloS one, 2019, Vol.14 (9), p.e0222473-e0222473

2019

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Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2

PloS one, 2019-12, Vol.14 (12), p.e0225943-e0225943

2019

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The AIRE -230Y Polymorphism Affects AIRE Transcriptional Activity: Potential Influence on AIRE Function in the Thymus

PloS one, 2015-05, Vol.10 (5), p.e0127476-e0127476

2015

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Meta-Analysis of Autoimmune Regulator-Regulated Genes in Human and Murine Models: A Novel Human Model Provides Insights on the Role of Autoimmune Regulator in Regulating STAT1 and STAT1-Regulated Genes

Frontiers in immunology, 2018-06, Vol.9, p.1380-1380

2018

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Prevalence and Clinical Features of Atopic Dermatitis in China

BioMed research international, 2016-01, Vol.2016 (2016), p.1-6

2016

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Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified

Experimental dermatology, 2012-05, Vol.21 (5), p.390-393

2012

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Properties of Skin in Chinese Infants: Developmental Changes in Ceramides and in Protein Secondary Structure of the Stratum Corneum

BioMed research international, 2017-01, Vol.2017 (2017), p.1-6

2017

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Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle East

Dermatology research and practice, 2018-01, Vol.2018 (2018), p.1-9

2018

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Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss

Journal of dermatological science, 2013-11, Vol.72 (2), p.186-188

2013

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Novel Genetic Association Between the Corneodesmosin (MHC S) Gene and Susceptibility to Psoriasis

Human molecular genetics, 1999-06, Vol.8 (6), p.1135-1140

1999

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The Role of the Environmental Risk Factors in the Pathogenesis and Clinical Outcome of Atopic Dermatitis

Tumor-Suppressive Function of lncRNA-MEG3 in Glioma Cells by Regulating miR-6088/SMARCB1 Axis

The Adenosine A2A Receptor Agonist Accelerates Bone Healing and Adjusts Treg/Th17 Cell Balance through Interleukin 6

Exploration of the Potential Mechanism of the Common Differentially Expressed Genes in Psoriasis and Atopic Dermatitis

Associations between ERAP1 Gene Polymorphisms and Psoriasis Susceptibility: A Meta-Analysis of Case-Control Studies

Long Noncoding RNASBF2-AS1 Promotes Gastric Cancer Progression via Regulating miR-545/EMS1 Axis

Whole-Exome Sequencing Reveals a Rare Missense Variant in SLC16A9 in a Pedigree with Early-Onset Gout

Association Study of the Caspase Gene Family and Psoriasis Vulgaris Susceptibility in Northeastern China

Characterisation of APS-1 Experimental Models Is Crucial for Development of Novel Therapies

Alopecia areata patients show deficiency of FOXP3+CD39+ T regulatory cells and clonotypic restriction of Treg TCRβ-chain, which highlights the immunopathological aspect of the disease

The 3′-UTR AACCins5874 in the stratum corneum chymotryptic enzyme gene ( SCCE / KLK7 ), associated with atopic dermatitis; causes an increased mRNA expression without altering its stability

New perspectives on epidermal barrier dysfunction in atopic dermatitis: Gene–environment interactions

HLA-C, CSTA and DS12346 susceptibility alleles confer over 100-fold increased risk of developing psoriasis: evidence of gene interaction

AAV9‐mediated AIRE gene delivery clears circulating antibodies and tissue T‐cell infiltration in a mouse model of autoimmune polyglandular syndrome type‐1

First report of SLC39A4 mutation in acrodermatitis enteropathica family from the Middle East

Correction: Alopecia areata patients show deficiency of FOXP3+CD39+ T regulatory cells and clonotypic restriction of Treg TCRβ-chain, which highlights the immunopathological aspect of the disease

Autosomal-dominant hypotrichosis with woolly hair: Novel gene locus on chromosome 4q35.1-q35.2

The AIRE -230Y Polymorphism Affects AIRE Transcriptional Activity: Potential Influence on AIRE Function in the Thymus

Meta-Analysis of Autoimmune Regulator-Regulated Genes in Human and Murine Models: A Novel Human Model Provides Insights on the Role of Autoimmune Regulator in Regulating STAT1 and STAT1-Regulated Genes

Prevalence and Clinical Features of Atopic Dermatitis in China

Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: No association with female pattern hair loss identified

Properties of Skin in Chinese Infants: Developmental Changes in Ceramides and in Protein Secondary Structure of the Stratum Corneum

Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle East

Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss

Novel Genetic Association Between the Corneodesmosin (MHC S) Gene and Susceptibility to Psoriasis

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