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Research 541–570 of 1000+
- Rat hair-follicle-associated pluripotent (HAP) stem cells can differentiate into atrial or ventricular cardiomyocytes in culture controlled by specific supplementation
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- Expression of the Orphan Protein Plet-1 during Trichilemmal Differentiation of Anagen Hair Follicles
- Carbonylation of hair proteins: A robust biomarker of molecular and structural oxidative damage in hair fibres
- In vivo transcriptional governance of hair follicle stem cells by canonical Wnt regulators
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- Stable isotope analyses of carbon and nitrogen in hair keratin of suspected man-eating wolves from 1880s
- Application of PCR Technique to Detect Polymorphism of the KRTAP1.1 Gene in Three Sheep Breeds - A Review
- Exploring the neural mechanisms of finasteride: a proteomic analysis in the nucleus accumbens
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Regulation of somatic cell reprogramming through inducible mir-302 expression
- Mechanical Stretch Upregulates SDF-1α in Skin Tissue and Induces Migration of Circulating Bone Marrow-Derived Stem Cells into the Expanded Skin
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Cutaneous Lesions in Systemic Lupus Erythematosus
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Emerging 3D bioprinting applications in plastic surgery
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- Assessment of the quality of the healing process in experimentally induced skin lesions treated with autologous platelet concentrate associated or unassociated with allogeneic mesenchymal stem cells: preliminary results in a large animal model
- Mechanically Robust MXene‐Metal Polyphenol Network Hybrid Interfaces for Multifunctional Protection of Keratin Fibers
- Effectiveness and Adverse Drug Reaction Mechanisms Associated with Valproic Acid Use: A Cross-Sectional Prospective Study in Indonesia
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- β-catenin-mediated hair growth induction effect of 3,4,5-tri-O-caffeoylquinic acid
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Characterizing Wool Keratin
- Comparative analysis of 3D and 2D cell-culturing methods in hair follicle spheroid morphogenesis and drug responsiveness