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First person – Marie Rodinova

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. Marie Vanisova (née Rodinova) is first author on ‘Skeletal muscle in an early manifest tran...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679382/
http://dx.doi.org/10.1242/dmm.041285
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description 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. Marie Vanisova (née Rodinova) is first author on ‘Skeletal muscle in an early manifest transgenic minipig model of Huntington's disease revealed deterioration of mitochondrial bioenergetics and ultrastructure impairment’, published in DMM. Marie is a PhD student in the lab of Hana Hansikova in the Department of Paediatrics and Adolescent Medicine, Charles University and General University Hospital in Prague, Czech Republic, investigating mitochondrial dysfunction in Huntington's disease (HD) and its role in the progress of HD.
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spelling pubmed-66793822019-08-12 First person – Marie Rodinova Dis Model Mech First Person 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. Marie Vanisova (née Rodinova) is first author on ‘Skeletal muscle in an early manifest transgenic minipig model of Huntington's disease revealed deterioration of mitochondrial bioenergetics and ultrastructure impairment’, published in DMM. Marie is a PhD student in the lab of Hana Hansikova in the Department of Paediatrics and Adolescent Medicine, Charles University and General University Hospital in Prague, Czech Republic, investigating mitochondrial dysfunction in Huntington's disease (HD) and its role in the progress of HD. The Company of Biologists Ltd 2019-07-01 2019-07-26 /pmc/articles/PMC6679382/ http://dx.doi.org/10.1242/dmm.041285 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle First Person
First person – Marie Rodinova
title First person – Marie Rodinova
title_full First person – Marie Rodinova
title_fullStr First person – Marie Rodinova
title_full_unstemmed First person – Marie Rodinova
title_short First person – Marie Rodinova
title_sort first person – marie rodinova
topic First Person
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679382/
http://dx.doi.org/10.1242/dmm.041285