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Research 301–330 of 1000+
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- 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
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- The molecular basis of human keratin disorders
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Fundamental research on the action mechanism of the 800 nm semiconductor laser on skin blackheads and coarse pores
- Granular Parakeratosis of the Eccrine Ostium: A Case Report
- Madarosis and facial keratinaceous spines
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Autophagy-Mediated Cellular Remodeling during Terminal Differentiation of Keratinocytes in the Epidermis and Skin Appendages
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Identification of the C-terminal tail domain of AHF/trichohyalin as the critical site for modulation of the keratin filamentous meshwork in the keratinocyte
- Ultrastructure of the contrasting types of keratinization seen in the tail epidermis of the laboratory mouseMus musculus
- Hair Keratin
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis