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Research 30 of 801
- The keratins and their disorders
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Keratin gene mutations in disorders of human skin and its appendages
- Keratin disorders: from gene to therapy
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Ichthyosis
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Beyond Expectations
- Secondary cicatricial and other permanent alopecias
- Hair and Nail Relationship
- The human keratins: biology and pathology
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Establishment of keratinocyte cell lines from human hair follicles
- Dermatomyositis Disease in Dogs
- Congenital atrichia and hypotrichosis
- The epidermis: rising to the surface
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- The molecular basis of human keratin disorders
- Vitamin D and the Skin: A Review for Dermatologists
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- 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
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis