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Research 121–150 of 1000+
- Pathway enrichment and network analysis of differentially expressed genes in pashmina goat
- Intermolecular disulfide cross-linked structural change induced by permanent wave treatment of human hair with thioglycolic acid.
- Tumores "borderline" de músculo liso del útero
- Heterozygous <i>KRT32</i> variant is responsible for autosomal dominant loose anagen hair syndrome
- QS8: Analysis of the Whole Transcriptome in Breast Cancer Patients Undergoing Radiotherapy and Breast Reconstruction
- Faculty Opinions recommendation of The keratins of the human beard hair medulla: the riddle in the middle.
- Trichohyalin Mechanically Strengthens the Hair Follicle
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Keratins: Dynamic, flexible structural proteins of epithelial cells
- A detailed mapping of the readily accessible disulphide bonds in the cortex of wool fibres
- Formation and Structure of Human Hair
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Proteome Analysis of Human Hair Shaft
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Human Hair Keratin-Associated Proteins
- Keratins and skin disease
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- The keratins and their disorders
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Organization and Expression of Hair Follicle Genes.
- Effect of varied hair protein fractions on the gel properties of keratin/chitosan hydrogels for the use in tissue engineering
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Proteopedia entry: Coiled‐coil structure of keratins
- Morphological analyses in fragility of pili torti with Björnstad syndrome
- An in vitro analysis of the hemostatic efficacy of fibrinogen precipitation with varied keratin fraction compositions
- Rational design of keratin nanoparticles utilizing diverse hair protein fractions for controlled drug release