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Research 691–720 of 1000+
- Targeted Overexpression of the Angiogenesis Inhibitor Thrombospondin-1 in the Epidermis of Transgenic Mice Prevents Ultraviolet-B-Induced Angiogenesis and Cutaneous Photo-Damage
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Existence of trichohyalin-keratohyalin hybrid granules: Co-localization of two major intermediate filament-associated proteins in non-follicular epithelia
- Thrombospondin-1 Plays a Critical Role in the Induction of Hair Follicle Involution and Vascular Regression During the Catagen Phase
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Characterization of Mouse Profilaggrin: Evidence for Nuclear Engulfment and Translocation of the Profilaggrin B-Domain during Epidermal Differentiation
- Recombinant human hepatitis B vaccine initiating alopecia areata: testing the hypothesis using the C3H/HeJ mouse model
- μ-Crystallin, Thyroid Hormone-binding Protein, is Expressed Abundantly in the Murine Inner Root Sheath Cells
- A Soy-Derived Immunostimulating Peptide Inhibits Etoposide-Induced Alopecia in Neonatal Rats
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis
- Third International Research Workshop on Alopecia Areata
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- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- Matrix Metalloproteinase-19 Expression in Normal and Diseased Skin: Dysregulation by Epidermal Proliferation
- Transport of Biotin in Human Keratinocytes
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Expression Profiles of Tyrosine Kinases in Cultured Follicular Papilla Cells Versus Dermal Fibroblasts
- An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice
- GSDMA deficiency impairs cutaneous squamous cell carcinoma growth
- Effects of FGF5-mediated LncRNA on the skin fibroblast growth of Liaoning Cashmere goats
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Birt–Hogg–Dubé syndrome
- Androgens/Androgen Receptor in the Management of Skin Diseases