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Research 811–840 of 1000+
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- The Pathogenesis of Primary Cicatricial Alopecias
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Fundamental Concepts and Novel Aspects of Polycystic Ovarian Syndrome: Expert Consensus Resolutions
- Regulatory T Cells: the Many Faces of Foxp3
- Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Cytochrome P450: A Target for Drug Development for Skin Diseases
- Overview of Alopecia Areata
- The structure of people’s hair
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Wool Keratin-Associated Protein Genes in Sheep—A Review
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- The Lipid Profiles in Different Characteristics of Women with PCOS and the Interaction Between Dyslipidemia and Metabolic Disorder States: A Retrospective Study in Chinese Population
- Female Pattern Hair Loss: a clinical and pathophysiological review
- Hidradenitis suppurativa: A practical review of possible medical treatments based on over 350 hidradenitis patients
- American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for the Diagnosis and Treatment of Hyperandrogenic Disorders
- Androgenetic alopecia: An update
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Breast implant illness: a topic in review
- Partial biotinidase deficiency: Clinical and biochemical features
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possible pathophysiologic mechanisms
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Molecular mechanisms of asymmetric divisions in mammary stem cells