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Research 241–270 of 1000+
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Learning from nudity: lessons from the nude phenotype
- What causes hidradenitis suppurativa ?—15 years after
- Neuronal plasticity of the “brain–skin connection”: stress-triggered up-regulation of neuropeptides in dorsal root ganglia and skin via nerve growth factor-dependent pathways
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Idiopathic Hirsutism*
- The nude gene and the skin
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Diagnostic approach to low‐renin hypertension
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Phospholipase A2 in skin biology: new insights from gene-manipulated mice and lipidomics
- Alopecia Areata
- Relationship between betacoronaviruses and the endocrine system: a new key to understand the COVID-19 pandemic—A comprehensive review
- The dermatological consequences of obesity
- Epigenetic regulation in adult stem cells and cancers
- Characterization of minoxidil/hydroxypropyl-β-cyclodextrin inclusion complex in aqueous alginate gel useful for alopecia management: Efficacy evaluation in male rat
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- The hair shaft: normality, abnormality, and genetics
- Epidermal expression of receptor for advanced glycation end products (RAGE) is related to inflammation and apoptosis in human skin
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Inhibitory effect of tianeptine on catagen induction in alopecia areata-like lesions induced by ultrasonic wave stress in mice
- 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
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Gender-specific alteration of steroid metabolism and its impact on viral replication in a mouse model of hepatitis B virus infection