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Translating cell biology of ageing? On the importance of choreographing knowledge 翻译衰老的细胞生物学?论编舞知识的重要性
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-09-26 DOI: 10.1080/14636778.2020.1825932
Tiago Moreira
This paper describes and explores how translational research models, embedded in institutions and standards, interact with the epistemic and material practices of cell biologists of ageing, a field re-energized by emergent technoscientific promises that hinge on the possibility of eliminating or manipulating senescent cells to tackle age-related diseases. Drawing on a 3-year long lab ethnography, the paper suggests that knowledge making in cell biology of ageing relies on two different epistemic and material cultures, to then argue that these cultures combine in four different types of experimental systems, only one of which can properly be seen as pertaining to translation as usually conceived. The paper further analyses how cell biologists articulate the linear temporality of translational research with the unfolding experimental chains where, by shifting between types of experimental system, cell biologists are able to generatively reconfigure their epistemic objects, and the consequences of this fragile arrangements for the field.
本文描述并探讨了嵌入机构和标准中的转化研究模型如何与衰老细胞生物学家的认知和材料实践相互作用,这是一个由新兴技术科学承诺重新激活的领域,这些承诺取决于消除或操纵衰老细胞以解决与年龄相关的疾病的可能性。根据一项长达3年的实验室人种志研究,本文认为,衰老细胞生物学中的知识制造依赖于两种不同的认知和物质文化,然后认为这些文化结合在四种不同类型的实验系统中,其中只有一种可以被视为与通常设想的翻译有关。本文进一步分析了细胞生物学家如何通过展开实验链来阐明转化研究的线性暂时性,其中,通过在不同类型的实验系统之间转换,细胞生物学家能够生成地重新配置他们的认知对象,以及这种脆弱安排对该领域的后果。
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引用次数: 1
Genetic ancestry testing, whiteness and the limits of anti-racism 基因血统测试,白人和反种族主义的局限性
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-08-24 DOI: 10.1080/14636778.2020.1811656
K. Tyler
This article explores how a branch of genomic science that embraces and advocates anti-racism, public participation, consultation and inclusion unintentionally supports everyday discourses of race and racism. It focuses on the reproduction of racism and exposes the limits of anti-racist discourses that are embedded in public engagements with the science and technology of genetic ancestry testing. I deploy a case study which is centerd on the analysis of commentaries posted on the internet which were written in response to a newspaper article that criticized the science of genetic ancestry testing. This article was published in The Daily Telegraph, a broadsheet “quality” newspaper in the UK. I analyse the ways in which ideas and images of British indigeneity and shared human descent that support white Western racial hierarchies, power and privileges emerge in the posts that responded to the newspaper article.
这篇文章探讨了基因组科学的一个分支是如何拥抱和倡导反种族主义、公众参与、协商和包容的,无意中支持了种族和种族主义的日常话语。它侧重于种族主义的再现,并揭示了反种族主义话语的局限性,这些话语嵌入了公众与基因血统检测科学和技术的接触中。我采用了一个案例研究,其核心是对互联网上发表的评论进行分析,这些评论是针对一篇批评基因血统测试科学的报纸文章而写的。这篇文章发表在《每日电讯报》上,这是英国的一份“优质”大报。我分析了支持西方白人种族等级制度、权力和特权的英国本土和共同人类血统的思想和形象是如何出现在回应报纸文章的帖子中。
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引用次数: 5
Decision-making about non-invasive prenatal testing: women’s moral reasoning in the absence of a risk of miscarriage in Germany 关于非侵入性产前检查的决策:德国妇女在没有流产风险的情况下的道德推理
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-08-16 DOI: 10.1080/14636778.2020.1805305
S. Reinsch, Anika König, C. Rehmann-Sutter
This paper examines women’s experiences with decision-making about non-invasive prenatal testing (NIPT). Such tests offer knowledge about chromosomal disorders early in pregnancy, without the risk of miscarriage associated with invasive procedures such as amniocentesis. Based on qualitative interviews with women in Germany who used, or declined, NIPT, we show how some women, who would not consider amniocentesis due to the risk of miscarriage, welcome the knowledge provided by, and the additional agency resulting from, NIPT. For others, declining the offer to “know more” becomes increasingly difficult to articulate. The absence of risk strips women of a “good reason” to justify their decision not to test, thus implicitly challenging their “right not to know.” Moreover, NIPT heightens moral dilemmas within relationships with partners, existing children, and sometimes other close relatives. While clinically “non-invasive,” we argue that NIPT changes decision-making in an ethically and socially highly significant way.
本文探讨了妇女在非侵入性产前检测(NIPT)决策方面的经验。这类检查提供了关于妊娠早期染色体疾病的知识,没有与羊膜穿刺术等侵入性手术相关的流产风险。基于对使用或拒绝NIPT的德国妇女的定性访谈,我们展示了一些由于流产风险而不考虑羊膜穿刺术的妇女是如何欢迎NIPT提供的知识和由NIPT产生的额外代理的。对其他人来说,拒绝“了解更多”的提议变得越来越难以表达。风险的缺失剥夺了女性决定不做检测的“好理由”,从而含蓄地挑战了她们的“不知道的权利”。此外,NIPT加剧了与伴侣、现有子女,有时甚至是其他近亲之间关系中的道德困境。虽然临床上“非侵入性”,但我们认为NIPT在道德和社会方面改变了决策。
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引用次数: 8
Biotechnologies in pest wasp control: taking the sting out of pest management for Māori businesses? 害虫黄蜂控制中的生物技术:为Māori企业消除害虫管理中的刺痛?
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-07-31 DOI: 10.1080/14636778.2020.1799344
Symon Palmer, O. Mercier
In Aotearoa New Zealand, the government’s ambitious target of becoming “predator-free” by 2050 has reignited public discussion on biotechnologies. The disproportionate abundance of German and common wasps in New Zealand disrupts native biodiversity and costs $133 million annually to the economy, making exotic wasps an expedient trial pest species for novel biotechnological controls. Māori businesses occupy primary industries said to benefit from wasp control. A Māori-centered mixed-method study gauged the perceptions of eight Māori businesses about the potential use of five specific new biotechnological controls in pest management. Participants raised concerns about risk and side effects; called for further information and a reconfiguring of how information is presented; reflected on previous pest challenges; and took positions in reference to Māori customary concepts. While all agree that doing nothing is not an option, careful, informed deliberation is required on whether and how best to move forward with these new biotechnological controls.
在新西兰奥特罗阿,政府雄心勃勃的目标是到2050年实现“无捕食者”,这再次引发了公众对生物技术的讨论。在新西兰,大量的德国黄蜂和普通黄蜂破坏了当地的生物多样性,每年给经济造成1.33亿美元的损失,使外来黄蜂成为新型生物技术控制的权宜之计。Māori企业占据了据说从黄蜂控制中受益的第一产业。一项Māori-centered混合方法研究衡量了8家Māori企业对五种特定的新生物技术控制在有害生物管理中的潜在用途的看法。与会者提出了对风险和副作用的担忧;要求提供进一步的信息并重新配置信息的呈现方式;反思以往的虫害挑战;并就Māori习惯概念采取了立场。虽然所有人都同意什么都不做不是一种选择,但对于是否以及如何最好地推进这些新的生物技术控制,需要进行仔细的、知情的审议。
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引用次数: 1
Non-humans in the making of nations 非人类参与国家的建立
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-07-29 DOI: 10.1080/14636778.2020.1799346
Annika Lonkila
How does non-human agency factor in nation-building? Sakari Tamminen explores this question through several in-depth and rich empirical cases, weaving together ethnographic fieldwork on multiple si...
非人类机构在国家建设中是如何发挥作用的?Sakari Tamminen通过几个深入而丰富的实证案例探讨了这个问题,将多个民族志领域的田野调查编织在一起。
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引用次数: 0
The somatic mode: doing good in targeted cancer therapy 体细胞模式:在肿瘤靶向治疗中大有作为
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-07-28 DOI: 10.1080/14636778.2020.1799345
Ivana Bogicevic, K. Rohrberg, E. Høgdall, M. Svendsen
This article explores the ethical challenges following the use of genetic information in experimental cancer treatment. In Danish healthcare, current ethical debates on the wider use of genetic information are highly focused on the heredity of genetic information. This focus accords with the international bioethical literature and the established practices of assessing inherited risks for cancer. Drawing on Pols’ (2003. “Enforcing Rights or Improving Care? The Interference of two Modes of Doing Good in Mental Health Care.” Sociology of Health & Illness 25 (4): 320–347. doi:10.1111/1467-9566.00349) concept of modes of doing good, we show that this has led to a certain understanding of the ethical challenges regarding genetic information – an understanding we term the germline mode. We argue that the germline mode overlooks crucial dilemmas facing healthcare professionals who use genetic information to target treatment directly at patients’ somatic mutations, i.e. alterations in the DNA occurring only in the tumor. In this article, we develop the concept of the somatic mode and explore the ethical challenges that emerge when genetic information takes a somatic turn.
这篇文章探讨了在实验性癌症治疗中使用遗传信息所带来的伦理挑战。在丹麦的医疗保健中,目前关于更广泛地使用遗传信息的伦理辩论高度集中在遗传信息的遗传上。这一重点符合国际生物伦理文献和评估癌症遗传风险的既定做法。借鉴波尔斯(2003)。“加强权利还是改善医疗?”两种行善模式在精神卫生保健中的干扰健康与疾病社会学,25(4):320-347。Doi:10.1111/1467-9566.00349)行善模式的概念,我们表明这已经导致了对遗传信息的伦理挑战的一定理解-我们称之为种系模式的理解。我们认为,生殖系模式忽略了医疗保健专业人员面临的关键困境,他们使用遗传信息直接针对患者的体细胞突变进行治疗,即仅在肿瘤中发生的DNA改变。在这篇文章中,我们发展了体细胞模式的概念,并探讨了当遗传信息发生体细胞转变时出现的伦理挑战。
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引用次数: 7
Frozen: social and bioethical aspects of cryopreservation 冷冻:冷冻保存的社会和生物伦理方面
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-07-02 DOI: 10.1080/14636778.2020.1802823
O. Katz, Yael Hashiloni-Dolev, C. Kroløkke, Aviad E. Raz
This foreword is written during the high time of the COVID-19 world epidemic. We are presently reminded that our advanced medical technologies are moving fast forward to realms unimaginable a few d...
本前言是在2019冠状病毒病(COVID-19)全球流行最严重的时候写成的。我们现在被提醒,我们先进的医疗技术正在快速向前发展到几个世纪以前无法想象的领域。
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引用次数: 3
Afterword: freezing technologies and melting distinctions 后记:冷冻技术与融化技术的区别
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-07-02 DOI: 10.1080/14636778.2020.1802822
K. Hoeyer
Frozen – it is rare to find an introduction to an academic collection that shares a title with a popular Disney movie. For this particular volume, it is strangely fitting. It is a special issue edi...
《冰雪奇缘》——很少能找到一本学术文集的介绍与一部热门迪士尼电影同名。对于这本书来说,这是非常合适的。这是一个特别的问题……
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引用次数: 0
A genetic unraveling: book review of Making Sense of Genes by Kostas Kampourakis 基因的解开:Kostas Kampourakis对《基因的意义》的书评
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-06-16 DOI: 10.1080/14636778.2020.1775565
D. Moore
Despite the growing consensus among molecular biologists that individual genes cannot determine traits (i.e., phenotypes) such as intelligence, shyness, or affinity for addictive substances – or ev...
尽管分子生物学家之间越来越多的共识是,个体基因不能决定智力、害羞或对成瘾物质的亲和力等特征(即表型)。
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引用次数: 0
Paternity: the elusive quest for the father 亲子关系:对父亲的难以捉摸的追求
IF 1.8 4区 医学 Q2 Social Sciences Pub Date : 2020-06-16 DOI: 10.1080/14636778.2020.1778460
Chase Ledin
Modern paternity is not simply a question for empirical analysis: “Who is the father?” Instead, as Nara Milanich argues, paternity must also be understood through normative inquiry: “What do we wan...
现代亲子关系不仅仅是一个实证分析的问题:“谁是父亲?”相反,正如奈良·米拉尼奇(Nara Milanich)所主张的那样,亲子关系也必须通过规范性探究来理解:“我们想要什么……
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New Genetics and Society
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