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Research 31–60 of 1000+
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Hair loss
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Hair in health and disease: an introduction
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Keratin disorders: from gene to therapy
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Disease causing homozygous variants in the human hairless gene
- Review paper The use of reflectance confocal microscopy in selected inflammatory skin diseases
- Skin manifestations of chronic kidney disease
- Cutaneous signals of immune system disease
- A Brief Review on Acne Vulgaris: Chronic Inflammatory Disease
- A curated catalog of canine and equine keratin genes
- Pinnal Diseases
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- Diseases of Periocular Hair
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation