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Research 571–600 of 1000+
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Hair Anomalies in a 6-Year-Old Girl
- Potential Use of Human Periapical Cyst-Mesenchymal Stem Cells (hPCy-MSCs) as a Novel Stem Cell Source for Regenerative Medicine Applications
- The Biological Actions of Dehydroepiandrosterone Involves Multiple Receptors
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- The Vitamin D Receptor Is a Wnt Effector that Controls Hair Follicle Differentiation and Specifies Tumor Type in Adult Epidermis
- Vitamin D and the skin
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- The vitamin D receptor, the skin and stem cells
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- New and Consolidated Therapeutic Options for Pubertal Induction in Hypogonadism: In-depth Review of the Literature
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- Protective Efficacy of Vitamin F against Acrylamide Induced Toxicity: Studies on Oxidative Stress Biomarkers
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Regulatory mechanisms of LGR4 on cancer and cancer stem cell properties
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Efficacy and Safety of Baricitinib in Patients With Alopecia Areata: A Real‐World Cohort Study
- An overview of animal models induced by glucocorticoids
- TONGUE, RED
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Zebrafish Model of Hereditary Pigmentary Disorders
- Cellular and molecular mechanisms of repair in acute and chronic wound healing
- Regulation of adult stem cell quiescence and its functions in the maintenance of tissue integrity
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Bone morphogenetic protein (BMP) signaling controls hair pigmentation by means of cross-talk with the melanocortin receptor-1 pathway
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation