Helen Cooper

Forskningsspecialist, Research services
Email: helen.cooper@abo.fi
Mobile: +358-505679286
Phone: +358-2-2153222


Peer-reviewed publications

A1 Journal article (refereed)
ATPase-deficient mitochondrial inner membrane protein ATAD3A disturbs mitochondrial dynamics in dominant hereditary spastic paraplegia. (2017)
Helen M. Cooper, Yang Yang, Emil Ylikallio, Rafil Khairullin, Rosa Woldegebriel, Kai-Lan Lin, Liliya Euro, Eino Palin, Alexander Wolf, Ras Trokovic, Pirjo Isohanni, Seppo Kaakkola, Mari Auranen, Tuula Lönnqvist, Sjoerd Wanrooij, Henna Tyynismaa
Human Molecular Genetics
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A1 Journal article (refereed)
Mitochondrial ROS produced via reverse electron transport extend animal lifespan (2016)
Filippo Scialò, Ashwin Sriram, Daniel Fernández-Ayala, Nina Gubina, Madis Lõhmus, Glyn Nelson, Angela Logan, Helen M. Cooper, Plácido Navas, Jose Antonio Enríquez, Michael P. Murphy, Alberto Sanz
Cell Metabolism
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A1 Journal article (refereed)
Human Mitochondrial DNA-Protein Complexes Attach to a Cholesterol-Rich Membrane Structure
(2015)
Joachim M Gerhold, Şirin Cansiz-Arda, Madis Lõhmus, Oskar Engberg, Aurelio Reyes, Helga van Rennes, Alberto Sanz, Ian J Holt, Helen M Cooper, Johannes N
Spelbrink

Scientific Reports
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A1 Journal article (refereed)
Human C4orf14 interacts with the mitochondrial nucleoid and is involved in the biogenesis of the small mitochondrial ribosomal subunit. (2012)
He J, Cooper HM, Reyes A, Di Re M, Kazak L, Wood SR, Mao CC, Fearnley IM, Walker JE, Holt IJ
Nucleic Acids Research
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A1 Journal article (refereed)
Mitochondrial nucleoid interacting proteins support mitochondrial protein synthesis. (2012)
He J, Cooper HM, Reyes A, Di Re M, Sembongi H, Litwin TR, Gao J, Neuman KC, Fearnley IM, Spinazzola A, Walker JE, Holt IJ
Nucleic Acids Research
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A1 Journal article (refereed)
A new splice variant of the mouse SIRT3 gene encodes the mitochondrial precursor protein. (2009)
Cooper HM, Huang JY, Verdin E, Spelbrink JN
PLoS ONE
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A1 Journal article (refereed)
Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling (2009)
Goffart S, Cooper HM, Tyynismaa H, Wanrooij S, Suomalainen A, Spelbrink JN
Human Molecular Genetics
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A1 Journal article (refereed)
Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion. (2008)
Hakonen AH, Goffart S, Marjavaara S, Paetau A, Cooper H, Mattila K, Lampinen M, Sajantila A, Lönnqvist T, Spelbrink JN, Suomalainen A.
Human Molecular Genetics
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A1 Journal article (refereed)
The human SIRT3 protein deacetylase is exclusively mitochondrial. (2008)
Cooper HM, Spelbrink JN.
Biochemical Journal
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A1 Journal article (refereed)
In vivo functional analysis of the human mitochondrial DNA polymerase POLG expressed in cultured human cells. (2000)
Spelbrink JN, Toivonen JM, Hakkaart GA, Kurkela JM, Cooper HM, Lehtinen SK, Lecrenier N, Back JW, Speijer D, Foury F, Jacobs HT.
Journal of Biological Chemistry
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Last updated on 2019-27-02 at 17:27