Marie-Lune Simard - Max Planck Institute for Biology of Ageing

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Bio

Marie-Lune Simard currently works at the Department of Mitochondrial Biology, Max Planck Institute for Biology of Ageing. Their most recent publication is 'A novel histochemistry assay to assess and quantify focal cytochrome c oxidase deficiency'.

Research Interests

Papers共 10 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选

Cell Division Can Accelerate the Loss of a Heteroplasmic Mitochondrial DNA Mutation in a Mouse Model of Mitochondrial Disease

Tianhong Su,Tiago M Bernardino Gomes,Anna L M Smith,Julia C Whitehall,Alasdair P Blain,Marie-Lune Simard, Louisa Scholten,James B Stewart,Doug M Turnbull,Conor Lawless,Laura C Greaves

bioRxiv (Cold Spring Harbor Laboratory) (2023)

Cited0Views0Bibtex

Cell lineage-specific mitochondrial resilience during mammalian organogenesis

Stephen P Burr,Florian Klimm,Angelos Glynos,Malwina Prater, Pamella Sendon,Pavel Nash,Christopher A Powell,Marie-Lune Simard,Nina A Bonekamp, Julia Charl,Hector Diaz,Lyuba V Bozhilova,Yu Nie,Haixin Zhang,Michele Frison,Maria Falkenberg,Nick Jones,Michal Minczuk,James B Stewart,Patrick F Chinnery

Cellno. 6 (2023): 1212-1229.e21

Cited4Views0WOSBibtex

Mice Lacking the Mitochondrial Exonuclease MGME1 Develop Inflammatory Kidney Disease with Glomerular Dysfunction

Dusanka Milenkovic,Adrian Sanz-Moreno,Julia Calzada-Wack,Birgit Rathkolb,Oana Veronica Amarie,Raffaele Gerlini,Antonio Aguilar-Pimentel,Jelena Misic,Marie-Lune S. Simard,Eckhard T. Wolf,Helmut S. Fuchs,Valerie T. Gailus-Durner,Martin Hrabe S. de Angelis,Nils-Goeran T. Larsson

PLOS genetics（2022）

Cited7Views0WOSBibtex

Modulation of Mtdna Copy Number Ameliorates the Pathological Consequences of a Heteroplasmic Mtdna Mutation in the Mouse

R. Filograna,C. Koolmeister,M. Upadhyay,A. Pajak,P. Clemente,R. Wibom,M. L. Simard,A. Wredenberg,C. Freyer,J. B. Stewart,N. G. Larsson

Science advances（2019）

Cited85Views0WOSSCIENCEBibtex

Genome Editing in Mitochondria Corrects a Pathogenic Mtdna Mutation in Vivo

Payam A. Gammage,Carlo Viscomi,Marie-Lune Simard,Ana S. H. Costa, Edoardo Gaude,Christopher A. Powell,Lindsey Van Haute,Beverly J. McCann,Pedro Rebelo-Guiomar,Raffaele Cerutti,Lei Zhang,Edward J. Rebar,Massimo Zeviani,Christian Frezza,James B. Stewart,Michal Minczuk

Nature medicine（2018）

Cited212Views0WOSNATUREBibtex

212

Mice Lacking the Mitochondrial Exonuclease MGME1 Accumulate Mtdna Deletions Without Developing Progeria

Stanka Matic,Min Jiang,Thomas J. Nicholls,Jay P. Uhler,Caren Dirksen-Schwanenland,Paola Loguercio Polosa,Marie-Lune Simard, Xinping Li,Ilian Atanassov,Oliver Rackham,Aleksandra Filipovska,James B. Stewart,Maria Falkenberg,Nils-Göran Larsson,Dusanka Milenkovic

Nature communicationsno. 1 (2018)

Cited53Views0WOSNATUREBibtex

A novel histochemistry assay to assess and quantify focal cytochrome c oxidase deficiency

Marie-Lune Simard,Arnaud Mourier,Laura C Greaves,Robert W Taylor,James B Stewart

JOURNAL OF PATHOLOGY（2018）

Cited15Views0WOSBibtex

A Phenotype-Driven Approach to Generate Mouse Models with Pathogenic Mtdna Mutations Causing Mitochondrial Disease

Johanna H K Kauppila, Holly L Baines,Ana Bratic,Marie-Lune Simard,Christoph Freyer,Arnaud Mourier,Craig Stamp,Roberta Filograna,Nils-Göran Larsson,Laura C Greaves,James B Stewart

Cell reportsno. 11 (2016): 2980-2990

Cited93Views0WOSBibtex

NG2 and NG2-positive cells delineate focal cerebral infarct demarcation in rats

Helene L Claus,Maureen Walberer,Marie L Simard,Beata Emig,Sophia M Muesken,Maria A Rueger,Gereon R Fink,Michael Schroeter

NEUROPATHOLOGY（2013）

Cited17Views0WOSBibtex

NG2 and NG2-positive cells delineate focal cerebral infarct demarcation in rats: NG2 constitutes infarct demarcation

Michael Schroeter,Gereon R Fink,Maria A Rueger,Sophia M Muesken,Beata Emig,Marie L Simard,Maureen Walberer,Helene L Claus

Neuropathology（2012）

Cited23Views0Bibtex

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