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Research 301–330 of 1000+
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Molecular Genetics of Human Hair Diseases
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Targeting Superficial or Nodular Basal Cell Carcinoma with Topically Formulated Small Molecule Inhibitor of Smoothened
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Management of Colorectal Cancer Using Nanocarriers-based Drug Delivery for Herbal Bioactives: Current and Emerging Approaches
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Role of the ABCA4 Gene Expression in the Clearance of Toxic Vitamin A Derivatives in Human Hair Follicle Stem Cells and Keratinocytes
- Anti-Graying Effects of External and Internal Treatments with Luteolin on Hair in Model Mice
- Aging of the hair follicle pigmentation system
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- Health improvement of human hair and their reshaping using recombinant keratin K31
- Current application of tissue-engineered dermal scaffolds mimicking the extracellular matrix microenvironment in wound healing
- Unlocking the therapeutic potential of TRPV3: Insights into thermosensation, channel modulation, and skin homeostasis involving TRPV3
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Functional characterization and unraveling the structural determinants of novel steroid hydroxylase CYP154C7 from Streptomyces sp. PAMC26508
- Enterococcus faecium secreted the NlpC/P60 family protein to enhance host immunity and indirectly increases Akkermansia muciniphila for slowing aging
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Genetic Disorders and Defects in Vitamin D Action
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- The molecular basis of human keratin disorders
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Dermatoscopy of hair shaft disorders
- Divergent roles of HDAC1 and HDAC2 in the regulation of epidermal development and tumorigenesis
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting