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Mitochondrial diseases: the contribution of organelle stress responses to pathology
Author / Creator:Suomalainen, Anu ; Battersby, Brendan J.
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews. Molecular cell biology, 2018-02, Vol.19 (2), p.77-92
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Progressive mitochondrial dysfunction in cerebellar synaptosomes of cystatin B-deficient mice
Author / Creator:Gorski, Katarin ; Jackson, Christopher B. ; Nyman, Tuula A. ; Rezov, Veronika ; Battersby, Brendan J. ; Lehesjoki, Anna-Elina
Publisher:Switzerland: Frontiers Research Foundation
Journal title:Frontiers in molecular neuroscience, 2023-05, Vol.16, p.1175851-1175851
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OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect
Author / Creator:Thompson, Kyle ; Mai, Nicole ; Oláhová, Monika ; Scialó, Filippo ; Formosa, Luke E ; Stroud, David A ; Garrett, Madeleine ; Lax, Nichola Z ; Robertson, Fiona M ; Jou, Cristina ; Nascimento, Andres ; Ortez, Carlos ; Jimenez‐Mallebrera, Cecilia ; Hardy, Steven A ; He, Langping ; Brown, Garry K ; Marttinen, Paula ; McFarland, Robert ; Sanz, Alberto ; Battersby, Brendan J ; Bonnen, Penelope E ; Ryan, Michael T ; Chrzanowska‐Lightowlers, Zofia MA ; Lightowlers, Robert N ; Taylor, Robert W
Publisher:London: Nature Publishing Group UK
Journal title:EMBO molecular medicine, 2018-11, Vol.10 (11), p.1-n/a
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Mitochondrial dysfunction reactivates α-fetoprotein expression that drives copper-dependent immunosuppression in mitochondrial disease models
Author / Creator:Jett, Kimberly A. ; Baker, Zakery N. ; Hossain, Amzad ; Boulet, Aren ; Cobine, Paul A. ; Ghosh, Sagnika ; Ng, Philip ; Yilmaz, Orhan ; Barreto, Kris ; DeCoteau, John ; Mochoruk, Karen ; Ioannou, George N. ; Savard, Christopher ; Yuan, Sai ; Abdalla, Osama H.M.H. ; Lowden, Christopher ; Kim, Byung-Eun ; Cheng, Hai-Ying Mary ; Battersby, Brendan J. ; Gohil, Vishal M. ; Leary, Scot C.
Publisher:United States: American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2023-01, Vol.133 (1), p.1-13
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Quantitative Changes in the Mitochondrial Proteome of Cerebellar Synaptosomes From Preclinical Cystatin B-Deficient Mice
Author / Creator:Gorski, Katarin ; Spoljaric, Albert ; Nyman, Tuula A. ; Kaila, Kai ; Battersby, Brendan J. ; Lehesjoki, Anna-Elina
Publisher:Lausanne: Frontiers Research Foundation
Journal title:Frontiers in molecular neuroscience, 2020-11, Vol.13, p.570640-570640
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RNA modification landscape of the human mitochondrial tRNALys regulates protein synthesis
Author / Creator:Richter, Uwe ; Evans, Molly E. ; Clark, Wesley C. ; Marttinen, Paula ; Shoubridge, Eric A. ; Suomalainen, Anu ; Wredenberg, Anna ; Wedell, Anna ; Pan, Tao ; Battersby, Brendan J.
Publisher:London: Nature Publishing Group UK
Journal title:Nature communications, 2018-09, Vol.9 (1), p.1-11, Article 3966
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Rapid Directional Shift of Mitochondrial DNA Heteroplasmy in Animal Tissues by a Mitochondrially Targeted Restriction Endonuclease
Author / Creator:Bayona-Bafaluy, Maria Pilar ; Blits, Bas ; Battersby, Brendan J. ; Shoubridge, Eric A. ; Moraes, Carlos T. ; Caskey, C. Thomas
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2005-10, Vol.102 (40), p.14392-14397
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Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation
Author / Creator:Jokinen, Riikka ; Marttinen, Paula ; Sandell, Helen Katarin ; Manninen, Tuula ; Teerenhovi, Heli ; Wai, Timothy ; Teoli, Daniella ; Loredo-Osti, J. C. ; Shoubridge, Eric A. ; Battersby, Brendan J.
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2010-10, Vol.6 (10), p.e1001161-e1001161
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Mitochondrial dysfunction reactivates a-fetoprotein expression that drives copper-dependent immunosuppression in mitochondrial disease models
Author / Creator:Jett, Kimberly A ; Baker, Zakery N ; Hossain, Amzad ; Boulet, Aren ; Cobine, Paul A ; Ghosh, Sagnika ; Ng, Philip ; Yilmaz, Orhan ; Barreto, Kris ; DeCoteau, John ; Mochoruk, Karen ; Ioannou, George N ; Savard, Christopher ; Yuan, Sai ; Abdalla, Osama H.M.H ; Lowden, Christopher ; Kim, Byung-Eun ; Cheng, Hai-Ying Mary ; Battersby, Brendan J ; Gohil, Vishal M ; Leary, Scot C
Publisher:American Society for Clinical Investigation
Journal title:The Journal of clinical investigation, 2023-01, Vol.133 (1)
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Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy
Author / Creator:Carroll, Christopher J ; Isohanni, Pirjo ; Pöyhönen, Rosanna ; Euro, Liliya ; Richter, Uwe ; Brilhante, Virginia ; Götz, Alexandra ; Lahtinen, Taina ; Paetau, Anders ; Pihko, Helena ; Battersby, Brendan J ; Tyynismaa, Henna ; Suomalainen, Anu
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2013-03, Vol.50 (3), p.151-159
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ArticlesPeer ReviewedFull Text
Quantitative Changes in Gimap3 and Gimap5 Expression Modify Mitochondrial DNA Segregation in Mice
Author / Creator:Jokinen, Riikka ; Lahtinen, Taina ; Marttinen, Paula ; Myöhänen, Maarit ; Ruotsalainen, Pilvi ; Yeung, Nicolas ; Shvetsova, Antonina ; Kastaniotis, Alexander J ; Hiltunen, J Kalervo ; Öhman, Tiina ; Nyman, Tuula A ; Weiler, Hartmut ; Battersby, Brendan J
Publisher:United States: Genetics Society of America
Journal title:Genetics (Austin), 2015-05, Vol.200 (1), p.221-235
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ArticlesPeer ReviewedFull Text
Nuclear genetic control of mitochondrial DNA segregation
Author / Creator:Battersby, Brendan J. ; Loredo-Osti, J.C. ; Shoubridge, Eric A.
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2003-02, Vol.33 (2), p.183-186
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Reactive oxygen species and the segregation of mtDNA sequence variants
Author / Creator:Battersby, Brendan J ; Shoubridge, Eric A
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2007-05, Vol.39 (5), p.571-572
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Lactation during Hibernation in Wild Black Bears: Effects on Plasma Amino Acids and Nitrogen Metabolites
Author / Creator:Wright, Patricia A. ; Obbard, Martyn E. ; Battersby, Brendan J. ; Felskie, Andrew K. ; LeBlanc, Paul J. ; Ballantyne, James S.
Publisher:United States: The University of Chicago Press
Journal title:Physiological and biochemical zoology, 1999-09, Vol.72 (5), p.597-604
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ArticlesFull Text
Mitochondrial dysfunction triggers secretion of the immunosuppressive factor α-fetoprotein
Author / Creator:Jett, Kimberly A ; Baker, Zakery N ; Hossain, Amzad ; Boulet, Aren ; Cobine, Paul A ; Ghosh, Sagnika ; Ng, Philip ; Yilmaz, Orhan ; Barretto, Kris ; Decoteau, John ; Mochoruk, Karen ; Ioannou, George ; Savard, Christopher ; Yuan, Sai ; Lowden, Christopher ; Byung-Eun, Kim ; Hai-Ying, Mary Cheng ; Battersby, Brendan J ; Gohil, Vishal M M ; Leary, Scot C
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2021-07
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ArticlesPeer ReviewedFull Text
RNA modification landscape of the human mitochondrial tRNA Lys regulates protein synthesis
Author / Creator:Richter, Uwe ; Evans, Molly E ; Clark, Wesley C ; Marttinen, Paula ; Shoubridge, Eric A ; Suomalainen, Anu ; Wredenberg, Anna ; Wedell, Anna ; Pan, Tao ; Battersby, Brendan J
Publisher:England
Journal title:Nature communications, 2018-09, Vol.9 (1), p.3966
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ArticlesPeer ReviewedFull Text
OXA 1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect
Author / Creator:Thompson, Kyle ; Mai, Nicole ; Oláhová, Monika ; Scialó, Filippo ; Formosa, Luke E ; Stroud, David A ; Garrett, Madeleine ; Lax, Nichola Z ; Robertson, Fiona M ; Jou, Cristina ; Nascimento, Andres ; Ortez, Carlos ; Jimenez‐Mallebrera, Cecilia ; Hardy, Steven A ; He, Langping ; Brown, Garry K ; Marttinen, Paula ; McFarland, Robert ; Sanz, Alberto ; Battersby, Brendan J ; Bonnen, Penelope E ; Ryan, Michael T ; Chrzanowska‐Lightowlers, Zofia MA ; Lightowlers, Robert N ; Taylor, Robert W
Publisher:Frankfurt: EMBO Press
Journal title:EMBO molecular medicine, 2018-11, Vol.10 (11)
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Mice harboring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity
Author / Creator:Mancini, Cecilia ; Hoxha, Eriola ; Iommarini, Luisa ; Brussino, Alessandro ; Richter, Uwe ; Montarolo, Francesca ; Cagnoli, Claudia ; Parolisi, Roberta ; Diana Iulia Gondor Morosini ; Nicolo, Valentina ; Maltecca, Francesca ; Muratori, Luisa ; Ronchi, Giulia ; Geuna, Stefano ; Arnaboldi, Francesca ; Donetti, Elena ; Giorgio, Elisa ; Cavalieri, Simona ; Eleonora Di Gregorio ; Pozzi, Elisa ; Ferrero, Marta ; Riberi, Evelise ; Casari, Giorgio ; Altruda, Fiorella ; Turco, Emilia ; Gasparre, Giuseppe ; Battersby, Brendan J ; Porcelli, Anna Maria ; Ferrero, Enza ; Brusco, Alfredo ; Tempia, Filippo
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2018-04
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ArticlesPeer ReviewedFull Text
Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation: e1001161
Author / Creator:Jokinen, Riikka ; Marttinen, Paula ; Sandell, Helen Katarin ; Manninen, Tuula ; Teerenhovi, Heli ; Wai, Timothy ; Teoli, Daniella ; Loredo-Osti, J C ; Shoubridge, Eric A ; Battersby, Brendan J
Publisher:San Francisco: Public Library of Science
Journal title:PLoS genetics, 2010-10, Vol.6 (10)
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DDHD2 provides a critical flux of saturated fatty acids to support neuronal energy demands
Author / Creator:Saber, Saber H ; Yak, Nyakuoy ; Xuan Ling Hilary Yong ; Binder, Tobias ; Lu, Siyuan ; Koludarova, Liidia ; Purushothaman, Reshinthine ; Er, Safak ; Hlushchuk, Irena ; Gaudin, Arnaud ; Nyman, Tuula ; Harmer, Jeffrey ; Gert Hoy Talbo ; Airavaara, Mikko ; Battersby, Brendan ; Van Waardenberg, Ashley J ; Anggono, Victor ; Balistreri, Giuseppe ; Joensuu, Merja
Publisher:Cold Spring Harbor: Cold Spring Harbor Laboratory Press
Journal title:bioRxiv, 2024-02
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Showing 1 to 20 of 21 results

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Mitochondrial diseases: the contribution of organelle stress responses to pathology

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Progressive mitochondrial dysfunction in cerebellar synaptosomes of cystatin B-deficient mice

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OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

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Mitochondrial dysfunction reactivates α-fetoprotein expression that drives copper-dependent immunosuppression in mitochondrial disease models

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Quantitative Changes in the Mitochondrial Proteome of Cerebellar Synaptosomes From Preclinical Cystatin B-Deficient Mice

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RNA modification landscape of the human mitochondrial tRNALys regulates protein synthesis

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Rapid Directional Shift of Mitochondrial DNA Heteroplasmy in Animal Tissues by a Mitochondrially Targeted Restriction Endonuclease

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Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation

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Mitochondrial dysfunction reactivates a-fetoprotein expression that drives copper-dependent immunosuppression in mitochondrial disease models

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Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy

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Quantitative Changes in Gimap3 and Gimap5 Expression Modify Mitochondrial DNA Segregation in Mice

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Nuclear genetic control of mitochondrial DNA segregation

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Reactive oxygen species and the segregation of mtDNA sequence variants

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Lactation during Hibernation in Wild Black Bears: Effects on Plasma Amino Acids and Nitrogen Metabolites

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Mitochondrial dysfunction triggers secretion of the immunosuppressive factor α-fetoprotein

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RNA modification landscape of the human mitochondrial tRNA Lys regulates protein synthesis

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OXA 1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

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Mice harboring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity

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Gimap3 Regulates Tissue-Specific Mitochondrial DNA Segregation: e1001161

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DDHD2 provides a critical flux of saturated fatty acids to support neuronal energy demands

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