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Research 211–240 of 1000+
- Physiological Insights from the Vitamin D Receptor Knockout Mouse
- Inflammatory bowel disease: pathogenesis, diagnosis and current therapeutic approach
- Men’s health in the United States: a national health paradox
- Topical and Systemic Therapies in Melasma: A Systematic Review
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- Tissue Repair Mechanisms of Dental Pulp Stem Cells: A Comprehensive Review from Cutaneous Regeneration to Mucosal Healing
- Trends in the global organoid technology and industry: from organogenesis in a dish to the commercialization of organoids
- The Role of Paracellular Transport in the Intestinal Absorption and Biopharmaceutical Characterization of Minoxidil
- Alopecia areata
- Food of Eyebrow: Local Knowledge and Mechanism of Hair Growth Promotion of Isatis tinctoria L. Along the Silk Road
- Cedrol restricts the growth of colorectal cancer <i>in vitro</i> and<i> in vivo</i> by inducing cell cycle arrest and caspase-dependent apoptotic cell death
- Plasma rico en plaquetas en pacientes con trasplante capilar. Revisión de la literatura
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- SHISA6 Confers Resistance to Differentiation-Promoting Wnt/β-Catenin Signaling in Mouse Spermatogenic Stem Cells
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Efficient In Vivo Targeting of Epidermal Stem Cells by Early Gestational Intraamniotic Injection of Lentiviral Vector Driven by the Keratin 5 Promoter
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Gene variants associated with acne vulgaris presentation and severity: a systematic review and meta-analysis
- Ornithine decarboxylase is upregulated by the androgen receptor in skeletal muscle and regulates myoblast proliferation
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Distinct Fibroblast Lineages Give Rise to NG2+ Pericyte Populations in Mouse Skin Development and Repair
- An Autophagy-Related Kinase Is Essential for the Symbiotic Relationship between <i>Phaseolus vulgaris</i> and Both Rhizobia and Arbuscular Mycorrhizal Fungi
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- Monitoring of clinical signs in goats with transmissible spongiform encephalopathies
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- 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