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Research 721–750 of 1000+
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Plastic surgery : indications, operations, and outcomes
- Topically Applied Minoxidil in Baldness
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- The Genetics of Human Skin Disease
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Diversity of Trichocyte Keratins and Keratin Associated Proteins
- Converging physiological roles of the anthrax toxin receptors
- Lentiviral Arrays for Live-cell Dynamic Monitoring of Gene and Pathway Activity During Stem Cell Differentiation
- Pathogenicity of<i>Ureaplasma urealyticum</i>and<i>Ureaplasma parvum</i>in the lower genital tract of female BALB/c mice
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- Interleukin 6 and STAT3 regulate p63 isoform expression in keratinocytes during regeneration
- SOX9 in organogenesis: shared and unique transcriptional functions
- Testosterone therapy for women with low sexual desire: a position statement from the Brazilian Society of Endocrinology and Metabolism
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Extracellular vesicles in age-related diseases: disease pathogenesis, intervention, and biomarker
- Small molecules facilitate single factor-mediated sweat gland cell reprogramming
- Genome-wide p63-Target Gene Analyses Reveal TAp63/NRF2-Dependent Oxidative Stress Responses
- Making the head: Caspases in life and death
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Runx Family Genes in Tissue Stem Cell Dynamics
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Association between Mesenchymal Stem Cells and COVID-19 Therapy: Systematic Review and Current Trends
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita