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Research 601–630 of 1000+
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Cylindroma as Tumor of Hair Follicle Origin
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Significance of stress keratin expression in normal and diseased epithelia
- Dynamic expression of Runx1 in skin affects hair structure
- A clinical study of cutaneous changes in pregnancy
- Thyroid hormone action on skin
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Avaliação dos efeitos adversos clínicos e alterações laboratoriais em pacientes com acne vulgar tratados com isotretinoína oral
- The Role of Nutrition in Immune-Mediated, Inflammatory Skin Disease: A Narrative Review
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Reconstitution of full-thickness skin by microcolumn grafting
- Ichthyosis with confetti: clinics, molecular genetics and management
- The extraction and characterization of human nail keratin
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Neutralization of IL-8 Prevents the Induction of Dermatologic Adverse Events Associated with the Inhibition of Epidermal Growth Factor Receptor
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Genetic Hair Disorders: A Review
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review