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Research 781–810 of 1000+
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- Australasian Society for Dermatology Research Meeting, May 2007
- Alopecia
- Pilosebaceous Unit (PSU)
- Epidermal Polarity Genes in Health and Disease
- Hair Loss in Children
- Liquid Protein Diets and Telogen Effluvium: A Case Report
- Dutasteride Micro-Injections in Androgenetic Alopecia
- A case of hidradenitis suppurativa with treatment effective by finasteride
- Polycystic Ovarian Syndrome: The Androgenized Adolescent
- Hypothalamic DNA methylation in rats with dihydrotestosterone‐induced polycystic ovary syndrome: effects of low‐frequency electro‐acupuncture
- Supplementary material from "Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair"
- Analysis of familial factors using the basic and specific (BASP) classification in Korean patients with androgenetic alopecia
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Effects of platelet-rich plasma application on hair follicle count, telogen/anagen ratio, and miniaturized hair ratio in patients with androgenic alopecia: alone or in combination with other treatments
- Frontal fibrosing alopecia: a review of eleven patients
- Effectiveness of Exosome Treatment in Androgenetic Alopecia: Outcomes of a Prospective Study
- Finasteride induced gynecomastia: Case report and review of the literature
- Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- Androgenetic Alopecia: Clinical Treatment
- Future Directions: Gene Polymorphism Diagnostics Relevant to Hair
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Transposon control as a checkpoint for tissue regeneration
- HSP90 Inhibition and Cellular Stress Elicits Phenotypic Plasticity in Hematopoietic Differentiation
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Werner′s syndrome
- Efficacy and safety of glucocorticoids in the treatment of progressive muscular dystrophy in children: a systematic review and meta-analysis
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings