Showing 61 - 64 results of 64 for search '"G20"', query time: 0.04s Refine Results
  1. 61

    Comparative Evaluation of Intra-articular Ozone and Steroid Treatments in Patients with Coxarthrosis under Ultrasound Guidance: A Retrospective Study by Yilmaz Karaduman, Arzu Muz, Azize Serçe, Servi Yildirim, Ismail Eren Durmus, Suna Akin Takmaz

    Published 2025-02-01
    “…Patients unresponsive to conventional treatments were divided into two groups: Group A (n=30) received intra-articular steroid (triamcinolone acetonide), and Group B (n=23) received three weekly ozone sessions (200 μg/20 mL), both under USG. Clinical outcomes were assessed using the Visual Analog Scale (VAS) for pain and the Harris Hip Score (HHS) for functional status, both pre- and post-treatment. …”
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  2. 62

    ارزیابی تنوع فنوتیپی، ژنتیکی و مقدار نسبی DNA هسته در فستوکای پا بلند (Festuca arundinacea) by سهیلا افکار, قاسم کریم زاده, علی اشرف جعفری

    Published 2020-08-01
    “…نتایج مقایسه میانگین نشان داد ژنوتیپ‌ها در 7 گروه قرار می‌گیرند که بالاترین و کمترین مقدار نسبی DNA هسته به ترتیب در ژنوتیپ‌های G13, G20, G21 وG22, G16 بود. با توجه به مطالعات گذشته، تغییر در مقدار نسبی DNA هسته را در این ژنوتیپ‌ها را می‌توان به وجود کروموزوم B و تغییر در طول کروموزوم نسبت داد. …”
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  3. 63

    Massively parallel variant-to-function mapping determines functional regulatory variants of non-small cell lung cancer by Congcong Chen, Yang Li, Yayun Gu, Qiqi Zhai, Songwei Guo, Jun Xiang, Yuan Xie, Mingxing An, Chenmeijie Li, Na Qin, Yanan Shi, Liu Yang, Jun Zhou, Xianfeng Xu, Ziye Xu, Kai Wang, Meng Zhu, Yue Jiang, Yuanlin He, Jing Xu, Rong Yin, Liang Chen, Lin Xu, Juncheng Dai, Guangfu Jin, Zhibin Hu, Cheng Wang, Hongxia Ma, Hongbing Shen

    Published 2025-02-01
    “…Accordingly, we proposed three genetic architectures underlying NSCLC susceptibility: multiple causal variants in a single haplotype block (e.g. 4q22.1), multiple causal variants in multiple haplotype blocks (e.g. 5p15.33), and a single causal variant (e.g. 20q11.23). We developed a modified polygenic risk score using the potential causal variants from Chinese populations, improving the performance of risk prediction in 450,821 Europeans from the UK Biobank. …”
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  4. 64