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Research 301–330 of 503
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- 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
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- 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 Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Beta-caryophyllene enhances wound healing through multiple routes
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Biomarkers of alopecia areata disease activity and response to corticosteroid treatment
- Divergent roles of HDAC1 and HDAC2 in the regulation of epidermal development and tumorigenesis
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- Involvement of Wnt, Eda and Shh at defined stages of sweat gland development
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Structure and Mechanical Properties of Human Trichocyte Keratin Intermediate Filament Protein
- Integrative analysis reveals ncRNA-mediated molecular regulatory network driving secondary hair follicle regression in cashmere goats
- Sprayable biomimetic double mask with rapid autophasing and hierarchical programming for scarless wound healing
- Bone Morphogenetic Protein Antagonist Noggin Promotes Skin Tumorigenesis via Stimulation of the Wnt and Shh Signaling Pathways
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Development of Hair Fibres
- Coactivator MED1 Ablation in Keratinocytes Results in Hair-Cycling Defects and Epidermal Alterations
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats