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Research 301–330 of 1000+
- Dutasteride reduces alcohol’s sedative effects in men in a human laboratory setting and reduces drinking in the natural environment
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Thiopurines: Recent Topics and Their Role in the Treatment of Inflammatory Bowel Diseases
- Enriching Proteolysis Targeting Chimeras with a Second Modality: When Two Are Better Than One
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Frontiers in Topical Photoprotection
- An update of polycystic ovary syndrome: causes and therapeutics options
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review
- The effects of low-dose radiation therapy in patients with mild-to-moderate Alzheimer's dementia: an interim analysis of a pilot study
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Zebrafish Model of Hereditary Pigmentary Disorders
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Design of Liposome Formulations for CRISPR/Cas9 Enzyme Immobilization: Evaluation of 5-Alpha-Reductase Enzyme Knockout for Androgenic Disorders
- Analysis of 72,469 UK Biobank exomes links rare variants to male-pattern hair loss
- TRANSMEDCON 2022: E-Poster Abstracts
- Congenital Adrenal Hyperplasia
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Editor's evaluation: Plant Trans-Golgi Network/Early Endosome pH regulation requires Cation Chloride Cotransporter (CCC1)
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.