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Research 61–90 of 1000+
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Hair Growth Promoting Effect of 4HGF Encapsulated with PGA Nanoparticles (PGA-4HGF) by β-Catenin Activation and Its Related Cell Cycle Molecules
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Against the Rules: Human Keratin K80
- The Catalog of Human Hair Keratins
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Revealing biological mechanisms of skin pigment recovery during treatment in vitiligo patients: A proteomic analysis
- Identification of key genes and signaling pathways related to Hetian sheep wool density by RNA-seq technology
- The Type I Keratin 19 Possesses Distinct and Context-dependent Assembly Properties
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Cylindroma as Tumor of Hair Follicle Origin
- 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
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Congenital hair loss disorders: Rare, but not too rare
- Structural features and sites of expression of a new murine 65 kD and 48 kD hair-related keratin pair, associated with a special type of parakeratotic epithelial differentiation
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Genetic and biochemical aspects of the synthesis of keratin by hair follicles
- Baicalin inhibits recruitment of GATA1 to the HSD3B2 promoter and reverses hyperandrogenism of PCOS
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Transcriptomic Analysis Provides Molecular Insights into Skin Development in Dezhou Donkey Foals