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Research 901–930 of 1000+
- Acidic and basic hair/nail ("hard") keratins: their colocalization in upper cortical and cuticle cells of the human hair follicle and their relationship to "soft" keratins.
- Dermal β-catenin activity in response to epidermal Wnt ligands is required for fibroblast proliferation and hair follicle initiation
- Quiescent Tissue Stem Cells Evade Immune Surveillance
- Genetic Disorders and Defects in Vitamin D Action
- Cell death in the skin
- Effects of Melatonin Supplementation on Hormonal, Inflammatory, Genetic, and Oxidative Stress Parameters in Women With Polycystic Ovary Syndrome
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- Ceramide Synthase 4 Regulates Stem Cell Homeostasis and Hair Follicle Cycling
- Clinical biochemistry of dihydrotestosterone
- Involvement of the Edar Signaling in the Control of Hair Follicle Involution (Catagen)
- Lipid-Based Drug Delivery Systems in Regenerative Medicine
- Hair regrowth following fecal microbiota transplantation in an elderly patient with alopecia areata: A case report and review of the literature
- A Review of the Evidence for and against a Role for Mast Cells in Cutaneous Scarring and Fibrosis
- Interleukin-25-Mediated-IL-17RB Upregulation Promotes Cutaneous Wound Healing in Diabetic Mice by Improving Endothelial Cell Functions
- Melatonin Exerts Prominent, Differential Epidermal and Dermal Anti-Aging Properties in Aged Human Eyelid Skin Ex Vivo
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Alleviation of Mechanical Allodynia by 14,15-Epoxyeicosatrienoic Acid in a Central Poststroke Pain Model: Possible Role of Allopregnanolone and δ-Subunit-Containing Gamma-Aminobutyric Acid A Receptors
- COVID-19 and hypopituitarism
- Stress-sensing in the human greying hair follicle: Ataxia Telangiectasia Mutated (ATM) depletion in hair bulb melanocytes in canities-prone scalp
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Factors regulating quiescent stem cells: insights from the intestine and other self-renewing tissues
- Highly Upregulated Lhx2 in the Foxn1−/− Nude Mouse Phenotype Reflects a Dysregulated and Expanded Epidermal Stem Cell Niche
- Prediction of the Mechanism of Shaoyao Gancao Decoction in the Treatment of Alopecia Areata by Network Pharmacology and Its Preliminary Verification Study
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Orchestration of tissue‐scale mechanics and fate decisions by polarity signalling
- Bone Metabolism in Patients with Hidradenitis Suppurativa: A Case-control Study
- Intracellular protons accelerate aging and switch on aging hallmarks in mice
- Paxillin regulates androgen receptor expression associated with granulosa cell focal adhesions
- Clinical Translation of Microbiome Research in Alopecia Areata: A New Perspective?
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle