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Research 391–420 of 1000+
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- An Update of Congenital Adrenal Hyperplasia
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Congenital Adrenal Hyperplasia
- Significance of the polyglutamine tract polymorphism in the androgen receptor
- Diagnostic approach to low‐renin hypertension
- Genetics of Structural Hair Disorders
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Nano-Enabled CRISPR-Cas Gene Editing for Cancer Therapeutics
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Inherited Epidermolysis Bullosa: A Clinical Case
- Australasian Society for Dermatology Research Meeting, May 2006
- Main Plenary Sessions: Summaries of Papers
- Nonclassic adrenal hyperplasia
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Biology of the Hair Follicle: The Basics
- 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
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Biology and Genetics of Hair