Výsledky vyhledávání - "E. M. Chambers"

Akademický článek

A generative co-design framework for healthcare innovation: development and application of an end-user engagement framework

Autor: M. Bird, M. McGillion, E. M. Chambers, J. Dix, C. J. Fajardo, M. Gilmour, K. Levesque, A. Lim, S. Mierdel, C. Ouellette, A. N. Polanski, S. V. Reaume, C. Whitmore, N. Carter

Publikováno v: Research Involvement and Engagement, Vol 7, Iss 1, Pp 1-12 (2021)

Plain English summary Background Continual improvements to health systems, products, and services are necessary for improvements in health. However, many of these improvements are not incorporated into everyday practice. When designing new health sys

Externí odkaz: https://doaj.org/article/2fd1284839fc482a84fd0823e75ee449

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A generative co-design framework for healthcare innovation: development and application of an end-user engagement framework

Autor: A. N. Polanski, Nancy Carter, M. Gilmour, Carley Ouellette, Marissa Bird, A. Lim, E. M. Chambers, K. Levesque, S. V. Reaume, J. Dix, Carly Whitmore, S. Mierdel, C. J. Fajardo, Michael McGillion

Publikováno v: Research Involvement and Engagement
Research Involvement and Engagement, Vol 7, Iss 1, Pp 1-12 (2021)

Plain English summaryBackgroundContinual improvements to health systems, products, and services are necessary for improvements in health. However, many of these improvements are not incorporated into everyday practice. When designing new health syste

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15db21164d830fe3ead2c11c59549a3f
https://doi.org/10.1186/s40900-021-00252-7

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Microbiological hydroxylation. Part XIV. Hydroxylation in the terminal rings of dioxygenated 5α-androstanes with the fungi Wojnowicia graminis and Ophiobolus herpotrichus

Autor: G. Denis Meakins, Ewart R. H. Jones, John O. Miners, Virginia E. M. Chambers, Alistair L. Wilkins

Publikováno v: J. Chem. Soc., Perkin Trans. 1. :55-58

Dioxo-5α-androstanes having one keto-group in a terminal ring (at position 3 or 2, or at position 17) and the second at a middle ring position (7 or 11) are hydroxylated in the other terminal ring (at 17 or 16, or at 3 or 2) by the fungi Wojnowicia

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1ea3233a4e968cf7bb4775471fb9c2f2
https://doi.org/10.1039/p19750000055

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Microbiological hydroxylation. Part XVII. C-19 hydroxylation of 17-oxo-5α-androstanes and 17-oxo-3α,5-cyclo-5α-androstanes by the fungus Calonectria decora

Autor: John T. Pinhey, G. Denis Meakins, John O. Miners, Alistair L. Wilkins, William A. Denny, Virginia E. M. Chambers, Ewart R. H. Jones

Publikováno v: J. Chem. Soc., Perkin Trans. 1. :1359-1363

The sequence of microbiological reactions involved in the 19-hydroxylation of 5α-androstan-17-one has been established. When a solution of 5α-androstan-17-one in dimethyl sulphoxide is incubated with Calonectria decora, the initial 1β,6α-dihydrox

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::aaf98215ea79b036caa4936d65dde1cd
https://doi.org/10.1039/p19750001359

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