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Research 601–630 of 1000+
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer
- Genetic Basis of Alopecia Areata
- Regeneration Genetics
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Alopecia Universalis Successfully Treated With Adalimumab
- The Effects of Androgens on T Cells: Clues to Female Predominance in Autoimmune Liver Diseases?
- Polymorphisms of FST gene and their association with wool quality traits in Chinese Merino sheep
- Testosterone in COVID-19: An Adversary Bane or Comrade Boon
- British Association of Dermatologists guidelines for the management of people with cutaneous lupus erythematosus 2021
- Evaluation of the Relationship between Alopecia Areata and Viral Antigen Exposure
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- The Role of Nrf2 in Hearing Loss
- Systemic Comorbidities in Korean Patients with Rosacea: Results from a Multi-Institutional Case-Control Study
- Adverse Events Associated with Azathioprine Treatment in Korean Pediatric Inflammatory Bowel Disease Patients
- Genomic Inbreeding and Runs of Homozygosity Analysis of Cashmere Goat
- Research Relevant Conditions and Pathology in Nonhuman Primates
- Third International Research Workshop on Alopecia Areata
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Autoantigen Discovery in the Hair Loss Disorder, Alopecia Areata: Implication of Post-Translational Modifications
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Genetically predicted levels of circulating cytokines and the risk of six immune skin diseases: a two-sample Mendelian randomization study
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review