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ASPET Journals Support the National Institutes of Health Principles and Guidelines for Reporting Preclinical Research

机译:ASPET 期刊支持美国国立卫生研究院临床前研究报告原则和指南

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Over the last several years there has been growing concern within the biomedical research community regarding a common perception that the level of scientific reproducibility and self-correction in preclinical research is not adequate (Collins and Tabak, 2014). In one initiative to address this situation, the National Institutes of Health (NIH) in collaboration with Nature and Science/American Association for the Advancement of Science held a workshop on June 14, 2014, for biomedical journal editors (including The Journal of Pharmacology and Experimental Therapeutics) that addressed the reproducibility and rigor of published research findings. Workshop attendees provided input to a draft set of methodological guidelines for published research. The ASPET Board of Publications Trustees reviewed the draft guidelines and submitted a response to the NIH on August 19, 2014. On November 5, 2014, the National Institutes of Health announced "Principles and Guidelines for Reporting Preclinical Research" (http://www.nih.gov/about/reporting-pre-clinical-research.htm). The guidelines address five principle areas of concern for the publication of preclinical biological research: rigorous statistical analysis, transparency in reporting, data and material sharing, consideration of refutations, and the establishment of best practice guidelines in the areas of image-based data and the description of biological materials with enough information to uniquely identify the reagents (in particular, antibodies, cell lines, and animals). ASPET publishes three primary research journals: The Journal of Pharmacology and Experimental Therapeutics (JPET; founded in 1909), Molecular Pharmacology (1965), and Drug Metabolism and Disposition (DMD; 1973). ASPET also publishes a review journal, Pharmacological Reviews, established in 1949. It is the intent and mission of ASPET's journals to hold to high standards of scientific rigor.
机译:在过去的几年里,生物医学研究界越来越关注一种普遍的看法,即临床前研究中的科学可重复性和自我纠正水平不足(Collins和Tabak,2014)。2014年6月14日,美国国立卫生研究院(NIH)与《自然与科学》(Nature and Science)/美国科学促进会(American Association for the Advancement of Science)合作,为生物医学期刊编辑(包括《药理学与实验治疗学杂志》(The Journal of Pharmacology and Experimental Therapeutics)举办了一次研讨会,讨论已发表研究结果的可重复性和严谨性。讲习班与会者为已发表研究的一套方法指南草案提供了意见。ASPET 出版理事会审查了指南草案,并于 2014 年 8 月 19 日向 NIH 提交了回复。2014年11月5日,美国国立卫生研究院(National Institutes of Health)公布了《临床前研究报告原则和指南》(http://www.nih.gov/about/reporting-pre-clinical-research.htm)。该指南涉及临床前生物学研究发表的五个主要关注领域:严格的统计分析、报告的透明度、数据和材料共享、反驳的考虑,以及在基于图像的数据和生物材料描述领域建立最佳实践指南,并具有足够的信息来唯一识别试剂(特别是 抗体、细胞系和动物)。ASPET出版了三本主要研究期刊:The Journal of Pharmacology and Experimental Therapeutics(JPET;创刊于1909年)、Molecular Pharmacology(1965年)和Drug Metabolism and Disposition(DMD;1973年)。ASPET 还出版了一本评论期刊《药理学评论》,该杂志创刊于 1949 年。ASPET期刊的宗旨和使命是坚持高标准的科学严谨性。

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