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Research 18
- Keratin expression by corneal and limbal stem cells during development
- Keratin disorders: from gene to therapy
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- The human keratins: biology and pathology
- Beyond Expectations
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- The molecular basis of human keratin disorders
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Keratins and disease at a glance
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Protein Kinase C as a Therapeutic Target
- Food Bioactive Compounds and Emerging Techniques for Their Extraction: Polyphenols as a Case Study
- In vitro and in vivo study of dye diffusion into the human skin and hair follicles
- Upper gastrointestinal bleeding during the COVID-19 pandemic; particularities of diagnosis and therapy