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Research 991–1000 of 1000+
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening
- A partially automated method for DNA extraction from marmoset hair follicles to avoid blood chimerism
- Evaluation of Sexual Function With an International Index of Erectile Function in Subjects Taking Finasteride for Androgenetic Alopecia
- Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Conflicting Reports Regarding the Histopathological Features of Androgenic Alopecia: Are Biopsy Location, Hair Diameter Diversity, and Relative Hair Follicle Miniaturization Partly to Blame?
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives