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Research 961–990 of 1000+
- The Role of Hormonal Imbalances in Amenorrhea
- Grahams Little Piccardi Lausseur Syndrome - A Rare Case Report with Review of Literature
- Assessment of prognostic markers of alopecia areata in pediatric patients
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- 498 Efficacy of photobiomodulation therapy for the off-label treatment of alopecia in skin types V-VI
- Ageratum Conyzoides L. Extract Inhibits 5α-Reductase Gene Expression and Prostaglandin D2 Release in Human Hair Dermal Papilla Cells and Improves Symptoms of Hair Loss in Otherwise Healthy Males and Females in an Open Label Pilot Study
- Encapsulación en ciclodextrinas de compuestos con actividad frente a la alopecia androgénica masculina.
- Pubic Hair Restorative Surgery Using Grafts Harvested by the Nonshaven Follicular Unit Extraction Technique
- 5α- Reductase Inhibitors in Prostate Cancer: An Overview
- 475 Paraoxonase 1 (PON1) L55M and Q192R polymorphisms, lipid profiles and psoriasis
- 476 Development of an intrinsic skin sensor for blood glucose level with CRISPR-mediated genome editing in epidermal stem cells
- Plasmaproteinbindung endogener Glucocorticosteroide und deren Einfluss auf Haar- und Speichelkonzentrationen
- Epidermal Notch1 recruits innate lymphoid cells to orchestrate normal skin repair
- Immunopathogenesis of Primary Cicatricial Alopecia
- Baseline methotrexate does not impact the incidence of infliximab infusion reactions: Results from a Canadian real-world treatment registry
- Australasian Society for Dermatology Research Meeting, May 2006
- Minireview: vitamin D receptor: new assignments for an already busy receptor. - eScholarship
- Dermatological concerns for women and girls with turner syndrome
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Homozygous whole body <i>Cbs</i> knockout in adult mice features minimal pathology during ageing despite severe homocysteinemia
- The TRF1 telomere protein is essential for the generation and maintenance of iPS cells and marks both pluripotent and adult stem cells
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Bicalutamide: A review
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Human tissue kallikreins as promiscuous modulators of homeostatic skin barrier functions
- Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient With Steroid Sulfatase Deficiency
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex