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Research 181–210 of 1000+
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- TONGUE, RED
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- The molecular basis of human keratin disorders
- The developmental basis of fingerprint pattern formation and variation
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Toxic and Metabolic Disorders of the Nervous System
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Eruptive vellus hair cysts: An underdiagnosed entity
- Game Changers: Blockbuster Small-Molecule Drugs Approved by the FDA in 2024
- Familial Dyskeratotic Comedones: A Case Report and Literature Review
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Diseases of Hair
- Diseases of Hair
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Eyebrow and Eyelash Alopecia: A Clinical Review
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
- Madarosis: A marker of many Maladies
- Hair shaft disorders in children – An update
- Off-label uses of retinoids in dermatology