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Research 391–420 of 1000+
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Depletion of <i>Gsdma1/2/3</i> alleviates PMA-induced epidermal hyperplasia by inhibiting the EGFR–Stat3/Akt pathway
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Deep phenotyping of skin tissue remodeling in patients with systemic sclerosis treated with CD19-CAR T cells
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Histological and immunohistochemical examination of the effect of the nonsteroidal antiandrogen {flutamide} on some organs of the male reproductive system in albino rats
- Australasian Society for Dermatology Research Meeting, May 2006
- Main Plenary Sessions: Summaries of Papers
- Nonclassic adrenal hyperplasia
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- An Update of Congenital Adrenal Hyperplasia
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Learning from nudity: lessons from the nude phenotype
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- The nude gene and the skin
- Morphological Approach to Hair Disorders
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Diagnostic approach to low‐renin hypertension
- Interaction between stem cell factor and endothelin-1: effects on melanogenesis in human skin xenografts