首页 > 最新文献

Journal of biomedical discovery and collaboration最新文献

英文 中文
Collaboration and distances between German immunological institutes--a trend analysis. 德国免疫学研究所之间的合作与距离——趋势分析。
Pub Date : 2006-06-14 DOI: 10.1186/1747-5333-1-6
Frank Havemann, Michael Heinz, Hildrun Kretschmer

Background: The hypothesis that distance matters but that in recent years geographical proximity has become less important for research collaboration was tested. We have chosen a sample--authors at German immunological institutes--that is relatively homogeneous with regard to research field, language and culture, which beside distance are other possible factors influencing the willingness to co-operate. We analyse yearly distributions of co-authorship links between institutes and compare them with the yearly distributions of distances of all institutes producing papers in journals indexed in the Science Citation Index, editions 1992 till 2002. We weight both types of distributions properly with paper numbers.

Results: One interesting result is that place matters but if a researcher has to leave the home town to find a collaborator distance does not matter any longer. This result holds for all years considered, but is statistically most significant in 2002. The tendency to leave the own town for collaborators has slightly increased in the sample. In addition, yearly productivity distributions of institutes have been found to be lognormal.

Conclusion: The Internet did not change much the collaboration patterns between German immunological institutes.

背景:距离很重要的假设,但近年来地理邻近对研究合作的重要性已经降低,这一假设得到了检验。我们选择了一个样本——德国免疫学研究所的作者——他们在研究领域、语言和文化方面相对同质,除了距离之外,这些因素也是影响合作意愿的其他可能因素。我们分析了机构之间合作关系的年度分布,并将其与所有在科学引文索引(1992年至2002年版)索引的期刊上发表论文的机构的年度距离分布进行了比较。我们用纸面数字适当地衡量这两种分布。结果:一个有趣的结果是,地点很重要,但如果研究人员不得不离开家乡寻找合作者,距离就不再重要了。这一结果适用于所有年份,但在2002年统计上最为显著。在样本中,离开自己的城市寻找合作者的趋势略有增加。此外,各研究所的年度生产率分布也符合对数正态分布。结论:互联网并没有改变德国免疫学研究所之间的合作模式。
{"title":"Collaboration and distances between German immunological institutes--a trend analysis.","authors":"Frank Havemann,&nbsp;Michael Heinz,&nbsp;Hildrun Kretschmer","doi":"10.1186/1747-5333-1-6","DOIUrl":"https://doi.org/10.1186/1747-5333-1-6","url":null,"abstract":"<p><strong>Background: </strong>The hypothesis that distance matters but that in recent years geographical proximity has become less important for research collaboration was tested. We have chosen a sample--authors at German immunological institutes--that is relatively homogeneous with regard to research field, language and culture, which beside distance are other possible factors influencing the willingness to co-operate. We analyse yearly distributions of co-authorship links between institutes and compare them with the yearly distributions of distances of all institutes producing papers in journals indexed in the Science Citation Index, editions 1992 till 2002. We weight both types of distributions properly with paper numbers.</p><p><strong>Results: </strong>One interesting result is that place matters but if a researcher has to leave the home town to find a collaborator distance does not matter any longer. This result holds for all years considered, but is statistically most significant in 2002. The tendency to leave the own town for collaborators has slightly increased in the sample. In addition, yearly productivity distributions of institutes have been found to be lognormal.</p><p><strong>Conclusion: </strong>The Internet did not change much the collaboration patterns between German immunological institutes.</p>","PeriodicalId":87404,"journal":{"name":"Journal of biomedical discovery and collaboration","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1747-5333-1-6","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"26089242","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 44
Nomen est Omen: do antidepressants increase p11 or S100A10? 女性:抗抑郁药会增加p11或S100A10吗?
Pub Date : 2006-04-13 DOI: 10.1186/1747-5333-1-5
Hari Manev, Radmila Manev

Occasionally, multiple names are given to the same gene/protein. When this happens, different names can be used in subsequent publications, for example in different research areas, sometimes with little or no awareness that the same entity known under a different name may have a major role in another field of science. Recent reports about the protein p11 presented findings that this protein, commonly known as S100A10, may play a crucial role in depression and antidepressant treatment mechanisms. One set of data showed an increased expression of this protein in the brain of mice treated with antidepressants. P11/S100A10 is only one of several S100 proteins expressed in the brain. Interestingly, it has been previously noted that antidepressant treatment increases the brain content of another S100 protein, S100B. It appears that up-regulating the brain content of various S100 proteins might be a common feature of antidepressants. In cells coexpressing S100A10 and S100B, these proteins may interact and exert opposite regulatory roles. Nevertheless, S100A10 is predominantly expressed in certain types of neurons whereas S100B is more abundant in glia. Thus, an interplay among multiple members of the S100 proteins might be important in determining the region and cell specificity of antidepressant mechanisms. Calling the p11 protein by its other name, S100A10, may prompt more investigators from different fields to participate in this new direction of neurobiological research.

有时,同一基因/蛋白质会有多个名称。当这种情况发生时,在随后的出版物中可以使用不同的名称,例如在不同的研究领域,有时很少或根本没有意识到以不同名称已知的同一实体可能在另一个科学领域发挥重要作用。最近关于p11蛋白的报道发现,这种通常被称为S100A10的蛋白可能在抑郁症和抗抑郁药物治疗机制中发挥关键作用。一组数据显示,在服用抗抑郁药的老鼠大脑中,这种蛋白质的表达有所增加。P11/S100A10只是大脑中表达的几种S100蛋白之一。有趣的是,之前已经注意到抗抑郁治疗增加了大脑中另一种S100蛋白S100B的含量。看来,上调大脑中各种S100蛋白的含量可能是抗抑郁药的一个共同特征。在共表达S100A10和S100B的细胞中,这些蛋白可能相互作用并发挥相反的调节作用。然而,S100A10主要在某些类型的神经元中表达,而S100B在胶质细胞中表达更为丰富。因此,在确定抗抑郁机制的区域和细胞特异性方面,S100蛋白多个成员之间的相互作用可能是重要的。将p11蛋白命名为S100A10,可能会促使更多来自不同领域的研究人员参与到这一神经生物学研究的新方向。
{"title":"Nomen est Omen: do antidepressants increase p11 or S100A10?","authors":"Hari Manev,&nbsp;Radmila Manev","doi":"10.1186/1747-5333-1-5","DOIUrl":"https://doi.org/10.1186/1747-5333-1-5","url":null,"abstract":"<p><p> Occasionally, multiple names are given to the same gene/protein. When this happens, different names can be used in subsequent publications, for example in different research areas, sometimes with little or no awareness that the same entity known under a different name may have a major role in another field of science. Recent reports about the protein p11 presented findings that this protein, commonly known as S100A10, may play a crucial role in depression and antidepressant treatment mechanisms. One set of data showed an increased expression of this protein in the brain of mice treated with antidepressants. P11/S100A10 is only one of several S100 proteins expressed in the brain. Interestingly, it has been previously noted that antidepressant treatment increases the brain content of another S100 protein, S100B. It appears that up-regulating the brain content of various S100 proteins might be a common feature of antidepressants. In cells coexpressing S100A10 and S100B, these proteins may interact and exert opposite regulatory roles. Nevertheless, S100A10 is predominantly expressed in certain types of neurons whereas S100B is more abundant in glia. Thus, an interplay among multiple members of the S100 proteins might be important in determining the region and cell specificity of antidepressant mechanisms. Calling the p11 protein by its other name, S100A10, may prompt more investigators from different fields to participate in this new direction of neurobiological research.</p>","PeriodicalId":87404,"journal":{"name":"Journal of biomedical discovery and collaboration","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-04-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1747-5333-1-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"26042116","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
The TREC 2004 genomics track categorization task: classifying full text biomedical documents. TREC 2004基因组跟踪分类任务:分类全文生物医学文献。
Pub Date : 2006-03-14 DOI: 10.1186/1747-5333-1-4
Aaron M Cohen, William R Hersh

Background: The TREC 2004 Genomics Track focused on applying information retrieval and text mining techniques to improve the use of genomic information in biomedicine. The Genomics Track consisted of two main tasks, ad hoc retrieval and document categorization. In this paper, we describe the categorization task, which focused on the classification of full-text documents, simulating the task of curators of the Mouse Genome Informatics (MGI) system and consisting of three subtasks. One subtask of the categorization task required the triage of articles likely to have experimental evidence warranting the assignment of GO terms, while the other two subtasks were concerned with the assignment of the three top-level GO categories to each paper containing evidence for these categories.

Results: The track had 33 participating groups. The mean and maximum utility measure for the triage subtask was 0.3303, with a top score of 0.6512. No system was able to substantially improve results over simply using the MeSH term Mice. Analysis of significant feature overlap between the training and test sets was found to be less than expected. Sample coverage of GO terms assigned to papers in the collection was very sparse. Determining papers containing GO term evidence will likely need to be treated as separate tasks for each concept represented in GO, and therefore require much denser sampling than was available in the data sets. The annotation subtask had a mean F-measure of 0.3824, with a top score of 0.5611. The mean F-measure for the annotation plus evidence codes subtask was 0.3676, with a top score of 0.4224. Gene name recognition was found to be of benefit for this task.

Conclusion: Automated classification of documents for GO annotation is a challenging task, as was the automated extraction of GO code hierarchies and evidence codes. However, automating these tasks would provide substantial benefit to biomedical curation, and therefore work in this area must continue. Additional experience will allow comparison and further analysis about which algorithmic features are most useful in biomedical document classification, and better understanding of the task characteristics that make automated classification feasible and useful for biomedical document curation. The TREC Genomics Track will be continuing in 2005 focusing on a wider range of triage tasks and improving results from 2004.

背景:TREC 2004基因组学专题会议的重点是应用信息检索和文本挖掘技术来提高基因组信息在生物医学中的应用。基因组学轨道包括两个主要任务,特别检索和文档分类。在本文中,我们描述了以全文文档分类为重点的分类任务,该任务模拟了小鼠基因组信息学(MGI)系统管理员的任务,由三个子任务组成。分类任务的一个子任务要求对可能有实验证据支持GO术语分配的文章进行分类,而其他两个子任务涉及将三个顶级GO类别分配给包含这些类别证据的每篇论文。结果:该赛道共有33个参与组。分诊子任务的均值和最大效用测度为0.3303,最高得分为0.6512。没有一种系统能够比简单地使用MeSH术语小鼠显著改善结果。对训练集和测试集之间显著特征重叠的分析发现比预期的要少。在收集中,分配给论文的GO术语的样本覆盖率非常少。确定包含GO术语证据的论文可能需要被视为GO中表示的每个概念的单独任务,因此需要比数据集中可用的更密集的采样。注释子任务的平均f值为0.3824,最高f值为0.5611。注释加证据码子任务的平均f值为0.3676,最高得分为0.4224。基因名称识别被发现对这项任务有好处。结论:GO注释文档的自动分类是一项具有挑战性的任务,GO代码层次和证据代码的自动提取也是一项具有挑战性的任务。然而,自动化这些任务将为生物医学管理提供实质性的好处,因此这一领域的工作必须继续下去。额外的经验将允许比较和进一步分析哪些算法特征在生物医学文档分类中最有用,并更好地理解使自动分类对生物医学文档管理可行和有用的任务特征。TREC基因组学跟踪将在2005年继续,重点放在更广泛的分类任务上,并从2004年开始改进结果。
{"title":"The TREC 2004 genomics track categorization task: classifying full text biomedical documents.","authors":"Aaron M Cohen,&nbsp;William R Hersh","doi":"10.1186/1747-5333-1-4","DOIUrl":"https://doi.org/10.1186/1747-5333-1-4","url":null,"abstract":"<p><strong>Background: </strong>The TREC 2004 Genomics Track focused on applying information retrieval and text mining techniques to improve the use of genomic information in biomedicine. The Genomics Track consisted of two main tasks, ad hoc retrieval and document categorization. In this paper, we describe the categorization task, which focused on the classification of full-text documents, simulating the task of curators of the Mouse Genome Informatics (MGI) system and consisting of three subtasks. One subtask of the categorization task required the triage of articles likely to have experimental evidence warranting the assignment of GO terms, while the other two subtasks were concerned with the assignment of the three top-level GO categories to each paper containing evidence for these categories.</p><p><strong>Results: </strong>The track had 33 participating groups. The mean and maximum utility measure for the triage subtask was 0.3303, with a top score of 0.6512. No system was able to substantially improve results over simply using the MeSH term Mice. Analysis of significant feature overlap between the training and test sets was found to be less than expected. Sample coverage of GO terms assigned to papers in the collection was very sparse. Determining papers containing GO term evidence will likely need to be treated as separate tasks for each concept represented in GO, and therefore require much denser sampling than was available in the data sets. The annotation subtask had a mean F-measure of 0.3824, with a top score of 0.5611. The mean F-measure for the annotation plus evidence codes subtask was 0.3676, with a top score of 0.4224. Gene name recognition was found to be of benefit for this task.</p><p><strong>Conclusion: </strong>Automated classification of documents for GO annotation is a challenging task, as was the automated extraction of GO code hierarchies and evidence codes. However, automating these tasks would provide substantial benefit to biomedical curation, and therefore work in this area must continue. Additional experience will allow comparison and further analysis about which algorithmic features are most useful in biomedical document classification, and better understanding of the task characteristics that make automated classification feasible and useful for biomedical document curation. The TREC Genomics Track will be continuing in 2005 focusing on a wider range of triage tasks and improving results from 2004.</p>","PeriodicalId":87404,"journal":{"name":"Journal of biomedical discovery and collaboration","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-03-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1747-5333-1-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"26043295","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 51
Launching the "Journal of Biomedical Discovery and Collaboration" 创办《生物医学发现与合作杂志》
Pub Date : 2006-03-13 DOI: 10.1186/1747-5333-1-1
Neil R Smalheiser
{"title":"Launching the \"Journal of Biomedical Discovery and Collaboration\"","authors":"Neil R Smalheiser","doi":"10.1186/1747-5333-1-1","DOIUrl":"https://doi.org/10.1186/1747-5333-1-1","url":null,"abstract":"","PeriodicalId":87404,"journal":{"name":"Journal of biomedical discovery and collaboration","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1747-5333-1-1","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"65689532","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 13
Enhancing access to the Bibliome: the TREC 2004 Genomics Track. 加强对书目的访问:TREC2004基因组学轨道。
Pub Date : 2006-03-13 DOI: 10.1186/1747-5333-1-3
William R Hersh, Ravi Teja Bhupatiraju, Laura Ross, Phoebe Roberts, Aaron M Cohen, Dale F Kraemer

Background: The goal of the TREC Genomics Track is to improve information retrieval in the area of genomics by creating test collections that will allow researchers to improve and better understand failures of their systems. The 2004 track included an ad hoc retrieval task, simulating use of a search engine to obtain documents about biomedical topics. This paper describes the Genomics Track of the Text Retrieval Conference (TREC) 2004, a forum for evaluation of IR research systems, where retrieval in the genomics domain has recently begun to be assessed.

Results: A total of 27 research groups submitted 47 different runs. The most effective runs, as measured by the primary evaluation measure of mean average precision (MAP), used a combination of domain-specific and general techniques. The best MAP obtained by any run was 0.4075. Techniques that expanded queries with gene name lists as well as words from related articles had the best efficacy. However, many runs performed more poorly than a simple baseline run, indicating that careful selection of system features is essential.

Conclusion: Various approaches to ad hoc retrieval provide a diversity of efficacy. The TREC Genomics Track and its test collection resources provide tools that allow improvement in information retrieval systems.

背景:TREC基因组学跟踪的目标是通过创建测试集合来改进基因组学领域的信息检索,使研究人员能够改进和更好地了解其系统的故障。2004年的曲目包括一个特别的检索任务,模拟使用搜索引擎获取有关生物医学主题的文档。本文介绍了2004年文本检索会议(TREC)的基因组学轨道,这是一个评估IR研究系统的论坛,最近开始评估基因组学领域的检索。结果:共有27个研究小组提交了47份不同的报告。通过平均精度(MAP)的主要评估测量来衡量最有效的运行,使用了特定领域和通用技术的组合。通过任何运行获得的最佳MAP为0.4075。利用基因名称列表以及相关文章中的单词扩展查询的技术效果最好。然而,许多运行的性能比简单的基线运行差,这表明仔细选择系统功能是至关重要的。结论:各种方法的特设检索提供了多样的疗效。TREC基因组学跟踪及其测试收集资源提供了改进信息检索系统的工具。
{"title":"Enhancing access to the Bibliome: the TREC 2004 Genomics Track.","authors":"William R Hersh,&nbsp;Ravi Teja Bhupatiraju,&nbsp;Laura Ross,&nbsp;Phoebe Roberts,&nbsp;Aaron M Cohen,&nbsp;Dale F Kraemer","doi":"10.1186/1747-5333-1-3","DOIUrl":"10.1186/1747-5333-1-3","url":null,"abstract":"<p><strong>Background: </strong>The goal of the TREC Genomics Track is to improve information retrieval in the area of genomics by creating test collections that will allow researchers to improve and better understand failures of their systems. The 2004 track included an ad hoc retrieval task, simulating use of a search engine to obtain documents about biomedical topics. This paper describes the Genomics Track of the Text Retrieval Conference (TREC) 2004, a forum for evaluation of IR research systems, where retrieval in the genomics domain has recently begun to be assessed.</p><p><strong>Results: </strong>A total of 27 research groups submitted 47 different runs. The most effective runs, as measured by the primary evaluation measure of mean average precision (MAP), used a combination of domain-specific and general techniques. The best MAP obtained by any run was 0.4075. Techniques that expanded queries with gene name lists as well as words from related articles had the best efficacy. However, many runs performed more poorly than a simple baseline run, indicating that careful selection of system features is essential.</p><p><strong>Conclusion: </strong>Various approaches to ad hoc retrieval provide a diversity of efficacy. The TREC Genomics Track and its test collection resources provide tools that allow improvement in information retrieval systems.</p>","PeriodicalId":87404,"journal":{"name":"Journal of biomedical discovery and collaboration","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1747-5333-1-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"26043349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 38
A tutorial on information retrieval: basic terms and concepts. 关于信息检索的教程:基本术语和概念。
Pub Date : 2006-03-13 DOI: 10.1186/1747-5333-1-2
Wei Zhou, Neil R Smalheiser, Clement Yu

This informal tutorial is intended for investigators and students who would like to understand the workings of information retrieval systems, including the most frequently used search engines: PubMed and Google. Having a basic knowledge of the terms and concepts of information retrieval should improve the efficiency and productivity of searches. As well, this knowledge is needed in order to follow current research efforts in biomedical information retrieval and text mining that are developing new systems not only for finding documents on a given topic, but extracting and integrating knowledge across documents.

这个非正式的教程是为那些想要了解信息检索系统的工作原理的研究者和学生准备的,包括最常用的搜索引擎:PubMed和Google。掌握信息检索的术语和概念的基本知识可以提高搜索的效率和生产力。此外,为了跟上当前在生物医学信息检索和文本挖掘方面的研究工作,这些研究工作正在开发新的系统,不仅用于查找给定主题的文档,而且还用于提取和集成文档中的知识。
{"title":"A tutorial on information retrieval: basic terms and concepts.","authors":"Wei Zhou,&nbsp;Neil R Smalheiser,&nbsp;Clement Yu","doi":"10.1186/1747-5333-1-2","DOIUrl":"https://doi.org/10.1186/1747-5333-1-2","url":null,"abstract":"<p><p>This informal tutorial is intended for investigators and students who would like to understand the workings of information retrieval systems, including the most frequently used search engines: PubMed and Google. Having a basic knowledge of the terms and concepts of information retrieval should improve the efficiency and productivity of searches. As well, this knowledge is needed in order to follow current research efforts in biomedical information retrieval and text mining that are developing new systems not only for finding documents on a given topic, but extracting and integrating knowledge across documents.</p>","PeriodicalId":87404,"journal":{"name":"Journal of biomedical discovery and collaboration","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2006-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1747-5333-1-2","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"26042581","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 35
期刊
Journal of biomedical discovery and collaboration
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1