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Research 181–210 of 1000+
- Diseases of Periocular Hair
- General Dermatology
- Immunological control of skin development: from homeostasis to developmental pathologies
- Therapeutic approach and management of Marz-e-Shayb (Premature greying of hair) in the perspective of Unani medicine: A case study
- Normal Hair Growth in Children
- The involvement of androgens in human hair growth
- The first 20 years of skin of color dermatology: An era of advancements in skin, hair, and nail disorders
- 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
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Editors' Picks
- Folliculin: A surprising molecular brake in the human hair follicle
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Loose anagen hair syndrome: Treatment with systemic minoxidil characterised by marked hair colour change
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- The Nutrient–Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Immunostaining study of cytokeratins in human hair follicle development
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Skin Sceneries of Thyroid Disorders and Impact of Thyroid on Different Skin Diseases: A Scoping Review Focused on Pediatric Patients
- Keratins of the Human Hair Follicle
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Skin Manifestations in Primary Immunodeficient Children
- A rare pediatric case of loose anagen hair syndrome