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Research 91–120 of 119
- Dermatoses of pregnancy
- The Genetics of Human Skin Disease
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Crosslinking Between Trichocyte Keratins and Keratin Associated Proteins
- Developmental signals in skin morphogenesis
- Desmogleins: Hair perspective
- Pemphigus Vulgaris IgG and Methylprednisolone Exhibit Reciprocal Effects on Keratinocytes
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Znaczenie chorób pęcherzycowych w diagnostyce różnicowej estetycznych problemów twarzy
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Viewpoint 4
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- In This Issue
- Current Genetics in Hair Diseases
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Cell death by cornification
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- Development of Hair Fibres
- Desmosomes in Developing Human Epidermis
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- 010 Development of a Desmocollin-3 Active Mouse Model Recapitulating Human Atypical Pemphigus