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Research 61–90 of 111
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Genetic Hair Disorders: A Review
- Genetically modified laboratory mice with sebaceous glands abnormalities
- New developments in the molecular treatment of ichthyosis: review of the literature
- Skin Barrier Dysfunction in Acne Vulgaris: Pathogenesis and Therapeutic Approaches
- Protease activity, localization and inhibition in the human hair follicle
- Non-invasive human skin transcriptome analysis using mRNA in skin surface lipids
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Facial pore refining by targeting dermal and epidermal functions: Assessment across age and gender
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Sphingolipid metabolism orchestrates establishment of the hair follicle stem cell compartment
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Current Genetics in Hair Diseases
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- 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
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Evaluation of the Safety and Effectiveness of Oral Minoxidil in Children: A Systematic Review
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Molecular Genetics of Human Hair Diseases
- Nanoparticles for Topical Application in the Treatment of Skin Dysfunctions—An Overview of Dermo-Cosmetic and Dermatological Products
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- The genetics of alopecia areata: New approaches, new findings, new treatments