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Research 331–360 of 1000+
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Keratinization of sheath and calamus cells in developing and regenerating feathers
- Natural polymers for natural hair: the smart use of an innovative nanocarrier
- Chemical bonds and hair behaviour—A review
- Structure–property relationships of meta-kerateine biomaterials derived from human hair
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- Characters of KRT80 and its roles in neoplasms diseases
- Current Genetics in Hair Diseases
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Comparative proteomic analyses using iTRAQ-labeling provides insights into fiber diversity in sheep and goats
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Identification of novel glucocorticoid receptor-regulated genes involved in epidermal homeostasis and hair follicle differentiation
- Novel Compounds for Hair Repair: Chemical Characterization and In Vitro Analysis of Thiol Cross-Linking Agents
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Growth of wool follicles in culture
- Steatocystoma Multiplex
- Reply to: The ends of a conundrum?
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Fundamental hair follicle biology and fine fibre production in animals
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Porosity at Different Structural Levels in Human and Yak Belly Hair and Its Effect on Hair Dyeing
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- A Raman spectroscopy investigation of the resilience of hair cuticular scales under uniaxial stress
- Nascent blood vessels in the skin arise from nestin-expressing hair-follicle cells
- The structure of people’s hair
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules