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Research 661–690 of 1000+
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Skin Development and Disease: A Molecular Perspective
- Epidermal stem cell fate: what can we learn from embryonic stem cells?
- TRPV Channels in Osteoarthritis: A Comprehensive Review
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Hair shaft disorders in children – An update
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Reduced SMAD2/3 activation independently predicts increased depth of human cutaneous squamous cell carcinoma
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Non-classical congenital adrenal hyperplasia: current insights into clinical implications, diagnosis and treatment
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Update on polycystic ovary syndrome
- Identification of Beta-Sitosterol and Stigmasterol as Possible Inhibitors of 5 Alpha-Reductase 1: An In-Silico Study
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- TRPV3 Ion Channel: From Gene to Pharmacology
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Dermatologic care of patients with differences of sex development