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Research 211–240 of 1000+
- Cell death in skin function, inflammation, and disease
- Trichothiodystrophy
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Poster Presentations
- The Mechanisms of Fur Development and Color Formation in American Mink Revealed Using Comparative Transcriptomics
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Oral Presentations
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- 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
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Congenital atrichia with papular lesions
- Topical minoxidil improves congenital hypotrichosis caused by <i>LIPH</i> mutations
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Congenital atrichia with papular lesions
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- Reply
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Alopezien und Hypotrichosen im Kindesalter
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia