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Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency

Journal of allergy and clinical immunology, 2012-04, Vol.129 (4), p.1031-1039.e1

2012

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Identification of a novel circ_0018289/miR-183-5p/TMED5 regulatory network in cervical cancer development

World journal of surgical oncology, 2021-08, Vol.19 (1), p.246-246, Article 246

2021

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Raman profiles of the stratum corneum define 3 filaggrin genotype–determined atopic dermatitis endophenotypes

Journal of allergy and clinical immunology, 2010-09, Vol.126 (3), p.574-580.e1

2010

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The effect of growth hormone on the metabolome of follicular fluid in patients with diminished ovarian reserve

Reproductive biology and endocrinology, 2023-02, Vol.21 (1), p.21-21, Article 21

2023

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Second-generation compound for the modulation of utrophin in the therapy of DMD

Human molecular genetics, 2015-08, Vol.24 (15), p.4212-4224

2015

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Cortisol dysregulation in anxiety infertile women and the influence on IVF treatment outcome

Frontiers in endocrinology (Lausanne), 2023-06, Vol.14, p.1107765-1107765

2023

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The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases

Human mutation, 2008-03, Vol.29 (3), p.351-360

2008

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Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations

Journal of dermatological science, 2011-12, Vol.64 (3), p.159-162

2011

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Missing C-terminal filaggrin expression, NFkappaB activation and hyperproliferation identify the dog as a putative model to study epidermal dysfunction in atopic dermatitis

Experimental dermatology, 2010-08, Vol.19 (8), p.e343-e346

2010

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Unique and Recurrent Mutations in the Filaggrin Gene in Singaporean Chinese Patients with Ichthyosis Vulgaris

Journal of investigative dermatology, 2008-07, Vol.128 (7), p.1669-1675

2008

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Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5) , kallikrein-related peptidase 7 (KLK7) , and filaggrin (FLG) polymorphisms to eczema risk

Journal of allergy and clinical immunology, 2008-09, Vol.122 (3), p.560-568.e4

2008

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A new simple fluorescent probe for imaging endogenous hydrogen peroxide in RAW 264.7 cells

Tetrahedron letters, 2023-11, Vol.132, p.154818, Article 154818

2023

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Association of Skin Barrier Genes within the PSORS4 Locus Is Enriched in Singaporean Chinese with Early-Onset Psoriasis

Journal of investigative dermatology, 2009-03, Vol.129 (3), p.606-614

2009

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Filaggrin Null Mutations Are Not a Protective Factor for Acne Vulgaris

Journal of investigative dermatology, 2011-06, Vol.131 (6), p.1378-1380

2011

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Impact of vaginal microecological differences on pregnancy outcomes and endometrial microbiota in frozen embryo transfer cycles

Journal of assisted reproduction and genetics, 2024-04, Vol.41 (4), p.929-938

2024

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Advances in genetic therapeutic strategies for Duchenne muscular dystrophy

Experimental physiology, 2015-12, Vol.100 (12), p.1458-1467

2015

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A rare connexin 26 mutation in a patient with a forme fruste of keratitis-ichthyosis-deafness (KID) syndrome

International journal of dermatology, 2009-10, Vol.48 (10), p.1078-1081

2009

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Methodological Considerations in N-of-1 Trials of Traditional Chinese Medicine

Evidence-based complementary and alternative medicine, 2021-06, Vol.2021, p.1-11

2021

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A Series of N-of-1 Trials for Traditional Chinese Medicine Using a Bayesian Method: Study Rationale and Protocol

Evidence-based complementary and alternative medicine, 2021, Vol.2021, p.9976770-8

2021

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Identification of serum protein biomarkers for utrophin based DMD therapy

Scientific reports, 2017-03, Vol.7 (1), p.43697-43697, Article 43697

2017

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Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants

Journal of allergy and clinical immunology, 2018-02, Vol.141 (2), p.814-816

2018

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Research on the Integration and Development of Internet Economy and Real Economy Represented by Short Video Platform in China

BCP Business & Management, 2022-08, Vol.23, p.476-482

2022

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Skin barrier dysfunction in common genetic disorders

Chen, Huijia

2011

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Validation of GWAS Loci for Atopic Dermatitis in a Singapore Chinese Population

Journal of investigative dermatology, 2012-05, Vol.132 (5), p.1505-1507

2012

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Unique and Recurrent Mutations in the Filaggrin Gene in Singaporean Chinese Patients with Ichthyosis Vulgaris

Journal of investigative dermatology, 2008-07, Vol.128 (7), p.1669-1675

2008

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Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency

Identification of a novel circ_0018289/miR-183-5p/TMED5 regulatory network in cervical cancer development

Raman profiles of the stratum corneum define 3 filaggrin genotype–determined atopic dermatitis endophenotypes

The effect of growth hormone on the metabolome of follicular fluid in patients with diminished ovarian reserve

Second-generation compound for the modulation of utrophin in the therapy of DMD

Cortisol dysregulation in anxiety infertile women and the influence on IVF treatment outcome

The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases

Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations

Missing C-terminal filaggrin expression, NFkappaB activation and hyperproliferation identify the dog as a putative model to study epidermal dysfunction in atopic dermatitis

Unique and Recurrent Mutations in the Filaggrin Gene in Singaporean Chinese Patients with Ichthyosis Vulgaris

Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5) , kallikrein-related peptidase 7 (KLK7) , and filaggrin (FLG) polymorphisms to eczema risk

A new simple fluorescent probe for imaging endogenous hydrogen peroxide in RAW 264.7 cells

Association of Skin Barrier Genes within the PSORS4 Locus Is Enriched in Singaporean Chinese with Early-Onset Psoriasis

Filaggrin Null Mutations Are Not a Protective Factor for Acne Vulgaris

Impact of vaginal microecological differences on pregnancy outcomes and endometrial microbiota in frozen embryo transfer cycles

Advances in genetic therapeutic strategies for Duchenne muscular dystrophy

A rare connexin 26 mutation in a patient with a forme fruste of keratitis-ichthyosis-deafness (KID) syndrome

Methodological Considerations in N-of-1 Trials of Traditional Chinese Medicine

A Series of N-of-1 Trials for Traditional Chinese Medicine Using a Bayesian Method: Study Rationale and Protocol

Identification of serum protein biomarkers for utrophin based DMD therapy

Array-based sequencing of filaggrin gene for comprehensive detection of disease-associated variants

Research on the Integration and Development of Internet Economy and Real Economy Represented by Short Video Platform in China

Skin barrier dysfunction in common genetic disorders

Validation of GWAS Loci for Atopic Dermatitis in a Singapore Chinese Population

Unique and Recurrent Mutations in the Filaggrin Gene in Singaporean Chinese Patients with Ichthyosis Vulgaris

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