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Research 331–360 of 806
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- The Role of Histone Demethylases in Disease
- Adrenal causes of endocrine hypertension in childhood or adolescence
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Genetic Defects of Female Sexual Differentiation
- Australasian Society for Dermatology Research Meeting, May 2006
- Syndromes of Severe Insulin Resistance (SSIRs)
- 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
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary 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
- Cantú syndrome with coexisting familial pituitary adenoma
- 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