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Research 271–300 of 1000+
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Folliculin: A surprising molecular brake in the human hair follicle
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Genetic Basis of Male Pattern Baldness
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Hypotrichosis in a child with olmsted syndrome
- Recently Identified Forms of Epidermolysis Bullosa
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- TRP Channels in Skin Biology and Pathophysiology
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- <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
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- 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
- Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
- Keratins of the Human Hair Follicle
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Comparative Anatomy of Mouse and Human Nail Units
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Skin Development and Disease: A Molecular Perspective
- Ptosis in childhood
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle