Jianwen Han

ORCID: 0000-0001-5440-6290
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About
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Research Areas
  • Psoriasis: Treatment and Pathogenesis
  • Dermatology and Skin Diseases
  • Systemic Lupus Erythematosus Research
  • Asthma and respiratory diseases
  • Cytokine Signaling Pathways and Interactions
  • Cell Adhesion Molecules Research
  • Diabetes and associated disorders
  • Skin and Cellular Biology Research
  • Connexins and lens biology
  • Dermatologic Treatments and Research
  • Hedgehog Signaling Pathway Studies
  • Atherosclerosis and Cardiovascular Diseases
  • Cancer and Skin Lesions
  • Immune Response and Inflammation
  • Acne and Rosacea Treatments and Effects
  • NF-κB Signaling Pathways
  • Genetic and rare skin diseases.
  • Arsenic contamination and mitigation
  • T-cell and B-cell Immunology

Inner Mongolia Medical University
2013-2025

Anhui Medical University
2010

Summary The polymorphisms of tumour necrosis factor alpha‐induced protein 3 ( TNFAIP ) have been found to associate with several autoimmune diseases. This study aimed explore the association single nucleotide SNP s) gene systemic lupus erythematosus SLE in Han Chinese. Thirty‐two s were genotyped 284 patients and 630 controls using ligation detection reaction LDR method. quality control steps statistical analyses performed plink 1.07 package haploview software. We that 13 showed significant...

10.1111/iji.12250 article EN International Journal of Immunogenetics 2016-02-05

ABSTRACT Background This study aimed to investigate the association between genetic variants of ERAP1 (OMIM: 606832) and psoriasis vulgaris (PsV) susceptibility in Inner Mongolia Han nationality. Methods For primary screening, subjects included 142 PsV cases 100 healthy controls without psoriasis. The 27 exons gene were sequenced screen significant variants. validation study, 1030 965 controls. A total 18 mutations detected for significance screening previously reported Results In stage, 13...

10.1002/mgg3.70021 article EN cc-by Molecular Genetics & Genomic Medicine 2024-11-01

Rationale: Nevoid basal cell carcinoma syndrome (NBCCS) is a rare clinical disease characterized by disproportionate number of to sun exposure and skin types. Patched 1 (PTCH1) gene proposed be implicated in the pathogenesis NBCCS. This study aimed investigate whether PTCH1 causative Chinese patients with Patient concerns: Here we detected first nonsense mutation Sanger sequencing blood samples from mother her second daughter (NM000264: exon14: c.2080C>T: p.Q694X). Diagnoses: Both had...

10.1097/md.0000000000040471 article EN cc-by-nc Medicine 2024-11-29

Generalized pustular psoriasis (GPP) is a rare and severe type of psoriasis. Previous studies have reported that metabolic syndrome its components been associated with psoriasis.To investigate the association syndrome-related single-nucleotide polymorphisms (SNPs) GPP in Chinese Han population.One hundred thirty-six (136) patients 965 healthy controls were recruited study. Approximately, 4 ml peripheral venous blood was collected from each participant. After collection, second-generation...

10.1002/ski2.18 article EN Skin Health and Disease 2021-05-02

Objective To investigate skin manifestations and comorbidities of chronic arsenicosis due to conta-minated drinking water, explore their possible risk factors. Methods Data about demographic characteristics, were collected from 95 patients with contaminated water in Inner Mongolia, retrospectively analyzed. A logistic regression model was established analyze associations patients' gender, age, age at onset arsenic-contaminated arsenic concentrations duration...

10.3760/cma.j.issn.0412-4030.2016.10.004 article EN Chinese Journal of Dermatology 2016-10-15
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