3 research outputs found

    Synthesizing a Solution Space for Prescriptive Design Knowledge Codification

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    One of Design Science Research’s (DSR) principal purposes is to generate and codify design knowledge. Codification in DSR is done by providing clear chunks of prescriptive knowledge that guide the design of future solutions, including instructions on how to design (parts of) artifacts. Although various codification mechanisms have emerged over the last years, design principles are among the most prominent mechanisms. Yet, distinguishing between different codification mechanisms is often blurry, hindering designers from making informed decisions regarding appropriate mechanisms for their research aim and leveraging the full potential of the prescriptive knowledge. We seek to bridge the challenge of selecting from the fuzzy array of codification mechanisms by proposing an inductively generated solution space. We provide a taxonomy to organize essential elements of prescriptive knowledge based on an analysis of design-oriented literature in four meta-dimensions (i.e., communication, application, development, and justification). These meta-dimensions make transparent how codified prescriptive design knowledge works. Overall, the taxonomy guides designers in reflecting on and selecting from the set of suitable elements for their statements. Also, providing a synthesis of options for codifying prescriptive design knowledge will simplify the identification and advance the positioning of DSR contributions

    Minimal information for studies of extracellular vesicles 2018 (MISEV2018): a position statement of the International Society for Extracellular Vesicles and update of the MISEV2014 guidelines

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    The last decade has seen a sharp increase in the number of scientific publications describing physiological and pathological functions of extracellular vesicles (EVs), a collective term covering various subtypes of cell-released, membranous structures, called exosomes, microvesicles, microparticles, ectosomes, oncosomes, apoptotic bodies, and many other names. However, specific issues arise when working with these entities, whose size and amount often make them difficult to obtain as relatively pure preparations, and to characterize properly. The International Society for Extracellular Vesicles (ISEV) proposed Minimal Information for Studies of Extracellular Vesicles ("MISEV") guidelines for the field in 2014. We now update these "MISEV2014" guidelines based on evolution of the collective knowledge in the last four years. An important point to consider is that ascribing a specific function to EVs in general, or to subtypes of EVs, requires reporting of specific information beyond mere description of function in a crude, potentially contaminated, and heterogeneous preparation. For example, claims that exosomes are endowed with exquisite and specific activities remain difficult to support experimentally, given our still limited knowledge of their specific molecular machineries of biogenesis and release, as compared with other biophysically similar EVs. The MISEV2018 guidelines include tables and outlines of suggested protocols and steps to follow to document specific EV-associated functional activities. Finally, a checklist is provided with summaries of key points
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