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Research 18
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- A genomic approach to susceptibility and pathogenesis leads to identifying potential novel therapeutic targets in androgenetic alopecia
- Genome-wide association study of skin complex diseases
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Genetic Basis of Alopecia Areata
- ANALYSIS OF CTLA 4 GENE +49A/G AND CT60 A/G POLYMORPHISMS IN ALOPECIA AREATA PATIENTS
- Surgical approach of ectropion in lamellar ichthyosis
- Ischemic onycholysis of the hands
- The Changing Landscape of Alopecia Areata: The Translational Landscape
- Alopecia in general medicine
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Ethanol extract of asiasari radix preferentially induces apoptosis in G361 human melanoma cells by differential regulation of p53
- Current and future pharmacotherapy for alopecia areata
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- The Genetic Architecture of Alopecia Areata
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System