Search
for
Sort by
Research 31–60 of 1000+
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Keratins: Dynamic, flexible structural proteins of epithelial cells
- Transcriptome sequencing reveals the expression profiles of lncRNAs and mRNAs in goat skin tissues with different types of wool coats
- Ectopic Expression of a Truncated Isoform of Hair Keratin 81 in Breast Cancer Alters Biophysical Characteristics to Promote Metastatic Propensity
- Studies on the Proteome of Human Hair - Identification of Histones and Deamidated Keratins
- Assembly of Hair Keratins in Transfected Epithelial Cells
- Keratins and disease at a glance
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Against the Rules: Human Keratin K80
- Isolation and Characterization of a Novel Hair Follicle–Specific Gene, Hacl-1
- The swelling behaviour of hair studied through the structural change of keratin protein during the permanent waving treatment
- Identification of the C-terminal tail domain of AHF/trichohyalin as the critical site for modulation of the keratin filamentous meshwork in the keratinocyte
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- The keratins and their disorders
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Keratins and skin disease
- Nucleation and growth of macrofibrils in trichocyte (hard-α) keratins
- Rational design of keratin nanoparticles utilizing diverse hair protein fractions for controlled drug release
- Type II Keratins Are Phosphorylated on a Unique Motif during Stress and Mitosis in Tissues and Cultured Cells
- 1301 STIM1, but not STIM2, is the calcium sensor critical for sweat secretion
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Bidirectional binding property of high glycine–tyrosine keratin-associated protein contributes to the mechanical strength and shape of hair
- Mapping the accessibility of the disulfide crosslink network in the wool fiber cortex
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions