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Research 271–300 of 944
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- The Overexpression of Tβ4 in the Hair Follicle Tissue of Alpas Cashmere Goats Increases Cashmere Yield and Promotes Hair Follicle Development
- Effects of ultra violet radiation on the soluble proteins of human hair
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Cosmeceutical Applications of Phlorotannins from Brown Seaweeds
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- A case of loose anagen hair syndrome associated with trichotillomania in a 14-year-old girl
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Nonscarring alopecia in systemic lupus erythematosus: A cross-sectional study with trichoscopic, histopathologic, and immunopathologic analyses
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Epigallocatechin-3 Gallate Inhibits STAT-1/JAK2/IRF-1/HLA-DR/HLA-B and Reduces CD8 MKG2D Lymphocytes of Alopecia Areata Patients
- Polymer- and Lipid-Based Nanostructures for Wound Healing with Barrier-Resolved Design
- Diabetes mellitus remission in a cat with hyperadrenocorticism after cabergoline treatment
- Systems for Mitochondria-Protective Cosmetic Actives: Opportunities in Post-Oncologic Skin Regeneration
- Animals in Dermatology
- Monilethrix – Case report of a rare disease
- The Multi-Faceted Role of Gut Microbiota in Alopecia Areata
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6