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Research 631–660 of 1000+
- Werner's syndrome: incidental finding during pregnancy
- Molecular Mechanisms and Targeted Therapeutics in Androgenetic Alopecia: From Signaling Pathways to Regenerative Approaches
- Carcinogenesis of the Human Scalp. An Immunometabolic Centered View
- Dynamics and Epigenetics of the Epidermal Differentiation Complex
- New frontiers in CRISPR/Cas9 delivery systems delivery for gene editing
- Hair & Cutaneous Development
- Generalised Glucocorticoid Resistance
- Female Androgenetic (?) Alopecia
- Pili trianguli et canaliculi as a phenotypic subtype in patients with central centrifugal cicatricial alopecia: A scanning electron microscopy study
- Using the Mechanisms of Action Involved in the Pathogenesis of Androgenetic Alopecia to Treat Hair Loss
- Androgenic Alopecia: A Comprehensive Literature Review of Epidemiology, Pathophysiology, Diagnosis, and Management
- Therapie der androgenetischen Alopezie der Frau mit Minoxidil-Lösung
- Hair Follicle Pigmentation
- Host-microbiome interactions and recent progress into understanding the biology of acne vulgaris
- Tracking adult stem cells
- Wounding induces dedifferentiation of epidermal Gata6+ cells and acquisition of stem cell properties
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Uncharted waters
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Research Techniques Made Simple: Zebrafish Models for Human Dermatologic Disease
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil