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Research 391–420 of 1000+
- Extracellular Vesicles in Osteogenesis: A Comprehensive Review of Mechanisms and Therapeutic Potential for Bone Regeneration
- Role of FGFR2-signaling in the pathogenesis of acne
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Serum levels of vitamin C, vitamin E, and total antioxidant capacity in premature graying hair
- Lactate dehydrogenase activity drives hair follicle stem cell activation
- Distinct Regulatory Programs Control the Latent Regenerative Potential of Dermal Fibroblasts during Wound Healing
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Clinical application of 5α-reductase inhibitors
- Epidermal keratinocytes initiate wound healing and pro-inflammatory immune responses following percutaneous schistosome infection
- Natural Molecules in the Management of Polycystic Ovary Syndrome (PCOS): An Analytical Review
- Platelet-Rich Plasma in Androgenic Alopecia: Indications, Technique, and Potential Benefits
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Sustained Postnatal Skin Regeneration Upon Prenatal Application of Functionalized Collagen Scaffolds
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Human Epidermal Neural Crest Stem Cells (hEPI-NCSC)—Characterization and Directed Differentiation into Osteocytes and Melanocytes
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Symptomatic zinc deficiency in a full-term breast-fed infant