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Editorial

Editorial Alternatives to Laboratory Animals 2020, Vol. 48(3) 95–96 ª The Author(s) 2020 Article reuse guidelines: sagepub.com/journals-permissions DOI: 10.1177/0261192920953233 journals.sagepub.com/home/atl Welcome to this issue of ATLA, my first as the new editor- based ‘models’ for psychiatric disorders, as well as the in-chief. I would like to take this opportunity to thank limitations of translation of preclinical studies based on these models to humans, in what is clearly one of the most Michael Balls for all of his hard work and dedication to challenging areas of medicine in which to develop the journal for over 30 years. This demonstrates his true models. commitment, and I can state from the outset my tenure King et al. describe a proof-of-concept study, in which will not match his record! I would like to thank Susan modified human erythrocytes were shown to be a suitable Trigwell and Rita Seabra for their work in ensuring the alternative to animal-derived erythrocytes for the evalua- continuity and quality of the journal. I also appreciate the tion of complement activity, under optimised pre- effort of both current and former associate editors, edi- treatment conditions. The overall method, being a partial torial board members, contributors and SAGE Publishing replacement of http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Alternatives to Laboratory Animals SAGE

Editorial

Madden, Judith C.
Alternatives to Laboratory Animals , Volume 48 (3): 2 – May 1, 2020
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References (4)

Publisher
SAGE
Copyright
© The Author(s) 2020
ISSN
0261-1929
eISSN
2632-3559
DOI
10.1177/0261192920953233
Publisher site
See Article on Publisher Site

Abstract

Alternatives to Laboratory Animals 2020, Vol. 48(3) 95–96 ª The Author(s) 2020 Article reuse guidelines: sagepub.com/journals-permissions DOI: 10.1177/0261192920953233 journals.sagepub.com/home/atl Welcome to this issue of ATLA, my first as the new editor- based ‘models’ for psychiatric disorders, as well as the in-chief. I would like to take this opportunity to thank limitations of translation of preclinical studies based on these models to humans, in what is clearly one of the most Michael Balls for all of his hard work and dedication to challenging areas of medicine in which to develop the journal for over 30 years. This demonstrates his true models. commitment, and I can state from the outset my tenure King et al. describe a proof-of-concept study, in which will not match his record! I would like to thank Susan modified human erythrocytes were shown to be a suitable Trigwell and Rita Seabra for their work in ensuring the alternative to animal-derived erythrocytes for the evalua- continuity and quality of the journal. I also appreciate the tion of complement activity, under optimised pre- effort of both current and former associate editors, edi- treatment conditions. The overall method, being a partial torial board members, contributors and SAGE Publishing replacement of

Journal

Alternatives to Laboratory Animals – SAGE

Published: May 1, 2020

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