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Research 181–210 of 1000+
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Sic Transit Gloria: Farewell to the Epidermal Transit Amplifying Cell?
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Adult polycystic ovary syndrome begins in childhood
- Changes in Expression and Function of Extrasynaptic GABA<sub>A</sub>Receptors in the Rat Hippocampus during Pregnancy and after Delivery
- Extracellular vesicle-based drug overview: research landscape, quality control and nonclinical evaluation strategies
- Hair Follicle: A Novel Source of Multipotent Stem Cells for Tissue Engineering and Regenerative Medicine
- Delivery of Tissue-Targeted Scalpels: Opportunities and Challenges for <i>In Vivo</i> CRISPR/Cas-Based Genome Editing
- The role of lymphocytes in the development and treatment of alopecia areata
- How to diagnose a lipodystrophy syndrome
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- Skin and hair: models for exploring organ regeneration
- Skin organoids: A new human model for developmental and translational research
- Hidradenitis Suppurativa
- Androgen antagonists in androgen target tissues
- Lifestyle and Physiological Factors Associated with Facial Wrinkling in Men and Women
- Peripheral blood gene expression in alopecia areata reveals molecular pathways distinguishing heritability, disease and severity
- The quality of European dermatological guidelines: critical appraisal of the quality of EDF guidelines using the AGREE II instrument
- Promoting axonal regeneration through exosomes: An update of recent findings on exosomal PTEN and mTOR modifiers
- Inhibition of 5α Reductase Impairs Cognitive Performance, Alters Dendritic Morphology and Increases Tau Phosphorylation in the Hippocampus of Male 3xTg-AD Mice
- The Potential Relevance of the Microbiome to Hair Physiology and Regeneration: The Emerging Role of Metagenomics
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- The hair shaft: normality, abnormality, and genetics
- Androgens in Women – Critical Evaluation of the Methods for Their Determination in Diagnostics of Endocrine Disorders
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Targeted elimination of the follicular label-retaining cells by photo-induced cell killing caused a defect on follicular renewal on mice
- Fractional Laser-assisted Hair Regrowth and Microneedling for the Treatment of Alopecia Areata: A Review
- Biomaterials and Stem Cells: Promising Tools in Tissue Engineering and Biomedical Applications