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Research 61–90 of 516
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- The role of disulfide bond formation in the structural transition observed in the intermediate filaments of developing hair
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Structural changes in trichocyte keratin intermediate filaments during keratinization
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- The location of the thioglycolic acid molecules in intrafibrillar unordered areas of the human hair keratin structure
- Intramembrane Proteolysis of Astrotactins
- Chemical bonds and hair behaviour—A review
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Resurgent Clinical Science (and it's all about Health)
- Hair Strengthening Evaluation of Anisotropic Osmolite Solutions (Inositol + Arginine): Cross-Talk between Dermal Papilla Fibroblast and Keratinocytes of the Outer Root Sheath Using a µHair Follicle 3D Model
- Worldwide diversity of hair curliness: a new method of assessment
- Syntaxin 9 is Enriched in Skin Hair Follicle Epithelium and Interacts With the Epidermal Growth Factor Receptor
- Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Primary Hypothyroidism and Thyroid Goiter in an Adult Cat
- Self-consistent field theory for the interactions between keratin intermediate filaments
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- Structural Transition of Trichocyte Keratin Intermediate Filaments During Development in the Hair Follicle
- A general mathematical model for the in vitro assembly dynamics of intermediate filament proteins
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Recent Advances in Genome-Editing Technology with CRISPR/Cas9 Variants and Stimuli-Responsive Targeting Approaches within Tumor Cells: A Future Perspective of Cancer Management
- Chirality Effect on Physical and Biological Properties of Peptide-Based Hydrogels
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies