Search
for
Sort by
Research 271–300 of 1000+
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- TRP Channels in Skin Biology and Pathophysiology
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- 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
- Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
- 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
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Ptosis in childhood
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Keratins of the Human Hair Follicle
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- 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
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Acne Syndromes and Mosaicism
- Systemic Comorbidities in Central Centrifugal Cicatricial Alopecia: A Systematic Review and Meta-analysis
- Madarosis: A marker of many Maladies
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Management OF Patients with Polycystic Ovary Syndrom
- A rare pediatric case of loose anagen hair syndrome
- Polycystic Ovarian Syndrome: The Androgenized Adolescent