First person – Amy Findlay

First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms, helping early-career researchers promote themselves alongside their papers. Amy Findlay is first author on ‘Mouse Idh3a mutations cause retinal degeneration and reduce...

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Published inDisease models & mechanisms Vol. 11; no. 12
Format Journal Article
LanguageEnglish
Published Cambridge The Company of Biologists Ltd 01.12.2018
The Company of Biologists
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Abstract First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms, helping early-career researchers promote themselves alongside their papers. Amy Findlay is first author on ‘Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function’, published in DMM. Amy is a postdoc in the lab of Ian Jackson at MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK. The focus of her research is using mouse models of human disease to investigate the genetic causes of retinal degeneration.
AbstractList First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms, helping early-career researchers promote themselves alongside their papers. Amy Findlay is first author on ‘ Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function ’, published in DMM. Amy is a postdoc in the lab of Ian Jackson at MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK. The focus of her research is using mouse models of human disease to investigate the genetic causes of retinal degeneration.
First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms, helping early-career researchers promote themselves alongside their papers. Amy Findlay is first author on ‘Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function’, published in DMM. Amy is a postdoc in the lab of Ian Jackson at MRC Human Genetics Unit, University of Edinburgh, Edinburgh, UK. The focus of her research is using mouse models of human disease to investigate the genetic causes of retinal degeneration.
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Cites_doi 10.1242/dmm.036426
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Copyright 2018. This work is licensed under http://creativecommons.org/licenses/by/4.0 (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2018. Published by The Company of Biologists Ltd 2018
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  article-title: Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function
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