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Research 361–390 of 866
- Australasian Society for Dermatology Research Meeting, May 2006
- Syndromes of Severe Insulin Resistance (SSIRs)
- Androgen receptors and their biology
- The role of aquaporins in polycystic ovary syndrome – A way towards a novel drug target in PCOS
- A Newborn With Hair Loss
- Clinical-Exome Sequencing Unveils the Genetic Landscape of Polycystic Ovarian Syndrome (PCOS) Focusing on Lean and Obese Phenotypes: Implications for Cost-Effective Diagnosis and Personalized Treatment
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- Genetics
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- FOXN1 deficient nude severe combined immunodeficiency
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Steatocystoma Multiplex
- When whorls collide: the development of hair patterns in frizzled 6 mutant mice
- Human Regulatory T Cells: Understanding the Role of Tregs in Select Autoimmune Skin Diseases and Post-Transplant Nonmelanoma Skin Cancers
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- The resistance mechanisms of bacteria against ciprofloxacin and new approaches for enhancing the efficacy of this antibiotic
- Genetic Disorders and Defects in Vitamin D Action
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Myotonic Dystrophy—A Progeroid Disease?
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells