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Research 31–60 of 1000+
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Congenital hair loss disorders: Rare, but not too rare
- Molecular Genetics of Alopecias
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Hair keratin pattern in human hair follicles grown <i>in vitro</i>
- The Catalog of Human Hair Keratins
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Type II Keratins Are Phosphorylated on a Unique Motif during Stress and Mitosis in Tissues and Cultured Cells
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- Adsorption of Diclofenac and PFBS on a Hair Keratin Dimer
- Biology and Genetics of Hair
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- The molecular basis of human keratin disorders
- Transcription Regulation and Protein Subcellular Localization of the Truncated Basic Hair Keratin hHb1-ΔN in Human Breast Cancer Cells
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- [Studies on monilethrix].
- Hair Anomalies in a 6-Year-Old Girl
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Alopezien und Hypotrichosen im Kindesalter
- Current Genetics in Hair Diseases
- Transglutaminase-3 Enzyme: A Putative Actor in Human Hair Shaft Scaffolding?
- Monilethrix