Year |
Citation |
Score |
2023 |
Gorski K, Jackson CB, Nyman TA, Rezov V, Battersby BJ, Lehesjoki AE. Progressive mitochondrial dysfunction in cerebellar synaptosomes of cystatin B-deficient mice. Frontiers in Molecular Neuroscience. 16: 1175851. PMID 37251643 DOI: 10.3389/fnmol.2023.1175851 |
0.535 |
|
2023 |
Ng KY, Battersby BJ. Sucrose Gradient Analysis of Human Mitochondrial Ribosomes and RNA. Methods in Molecular Biology (Clifton, N.J.). 2661: 101-117. PMID 37166634 DOI: 10.1007/978-1-0716-3171-3_7 |
0.519 |
|
2023 |
Tomoda E, Nagao A, Shirai Y, Asano K, Suzuki T, Battersby BJ, Suzuki T. Restoration of mitochondrial function through activation of hypomodified tRNAs with pathogenic mutations associated with mitochondrial diseases. Nucleic Acids Research. PMID 36928678 DOI: 10.1093/nar/gkad139 |
0.562 |
|
2022 |
Ng KY, Lutfullahoglu Bal G, Richter U, Safronov O, Paulin L, Dunn CD, Paavilainen VO, Richer J, Newman WG, Taylor RW, Battersby BJ. Nonstop mRNAs generate a ground state of mitochondrial gene expression noise. Science Advances. 8: eabq5234. PMID 36399564 DOI: 10.1126/sciadv.abq5234 |
0.423 |
|
2022 |
Jett KA, Baker ZN, Hossain A, Boulet A, Cobine PA, Ghosh S, Ng P, Yilmaz O, Barreto K, DeCoteau J, Mochoruk K, Ioannou GN, Savard C, Yuan S, Abdalla OH, ... ... Battersby BJ, et al. Mitochondrial dysfunction reactivates α-fetoprotein expression that drives copper-dependent immunosuppression in mitochondrial disease models. The Journal of Clinical Investigation. PMID 36301669 DOI: 10.1172/JCI154684 |
0.442 |
|
2021 |
Ng KY, Richter U, Jackson CB, Seneca S, Battersby BJ. Translation of MT-ATP6 pathogenic variants reveals distinct regulatory consequences from the co-translational quality control of mitochondrial protein synthesis. Human Molecular Genetics. PMID 34718584 DOI: 10.1093/hmg/ddab314 |
0.521 |
|
2021 |
Hochberg I, Demain LAM, Richer J, Thompson K, Urquhart JE, Rea A, Pagarkar W, Rodríguez-Palmero A, Schlüter A, Verdura E, Pujol A, Quijada-Fraile P, Amberger A, Deutschmann AJ, Demetz S, ... ... Battersby BJ, et al. Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations. American Journal of Human Genetics. 108: 2195-2204. PMID 34715011 DOI: 10.1016/j.ajhg.2021.10.002 |
0.52 |
|
2021 |
Itoh Y, Andréll J, Choi A, Richter U, Maiti P, Best RB, Barrientos A, Battersby BJ, Amunts A. Mechanism of membrane-tethered mitochondrial protein synthesis. Science (New York, N.Y.). 371: 846-849. PMID 33602856 DOI: 10.1126/science.abe0763 |
0.31 |
|
2020 |
Gorski K, Spoljaric A, Nyman TA, Kaila K, Battersby BJ, Lehesjoki AE. Quantitative Changes in the Mitochondrial Proteome of Cerebellar Synaptosomes From Preclinical Cystatin B-Deficient Mice. Frontiers in Molecular Neuroscience. 13: 570640. PMID 33281550 DOI: 10.3389/fnmol.2020.570640 |
0.336 |
|
2019 |
Forsström S, Jackson CB, Carroll CJ, Kuronen M, Pirinen E, Pradhan S, Marmyleva A, Auranen M, Kleine IM, Khan NA, Roivainen A, Marjamäki P, Liljenbäck H, Wang L, Battersby BJ, et al. Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA Deletions. Cell Metabolism. PMID 31523008 DOI: 10.1016/J.Cmet.2019.08.019 |
0.552 |
|
2019 |
Battersby BJ, Richter U, Safronov O. Mitochondrial nascent chain quality control determines organelle form and function. Acs Chemical Biology. PMID 31498990 DOI: 10.1021/Acschembio.9B00518 |
0.531 |
|
2019 |
Richter U, Ng KY, Suomi F, Marttinen P, Turunen T, Jackson C, Suomalainen A, Vihinen H, Jokitalo E, Nyman TA, Isokallio MA, Stewart JB, Mancini C, Brusco A, Seneca S, ... ... Battersby BJ, et al. Mitochondrial stress response triggered by defects in protein synthesis quality control. Life Science Alliance. 2. PMID 30683687 DOI: 10.26508/lsa.201800219 |
0.502 |
|
2018 |
Mancini C, Hoxha E, Iommarini L, Brussino A, Richter U, Montarolo F, Cagnoli C, Parolisi R, Gondor Morosini DI, Nicolò V, Maltecca F, Muratori L, Ronchi G, Geuna S, Arnaboldi F, ... ... Battersby BJ, et al. Mice harbouring a SCA28 patient mutation in AFG3L2 develop late-onset ataxia associated with enhanced mitochondrial proteotoxicity. Neurobiology of Disease. 124: 14-28. PMID 30389403 DOI: 10.1016/J.Nbd.2018.10.018 |
0.604 |
|
2018 |
Jackson CB, Huemer M, Bolognini R, Martin F, Szinnai G, Donner BC, Richter U, Battersby BJ, Nuoffer JM, Suomalainen A, Schaller A. A variant in MRPS14 (uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement. Human Molecular Genetics. PMID 30358850 DOI: 10.1093/Hmg/Ddy374 |
0.608 |
|
2018 |
Richter U, Evans ME, Clark WC, Marttinen P, Shoubridge EA, Suomalainen A, Wredenberg A, Wedell A, Pan T, Battersby BJ. RNA modification landscape of the human mitochondrial tRNA regulates protein synthesis. Nature Communications. 9: 3966. PMID 30262910 DOI: 10.1038/S41467-018-06471-Z |
0.707 |
|
2018 |
Thompson K, Mai N, Oláhová M, Scialó F, Formosa LE, Stroud DA, Garrett M, Lax NZ, Robertson FM, Jou C, Nascimento A, Ortez C, Jimenez-Mallebrera C, Hardy SA, He L, ... ... Battersby BJ, et al. mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect. Embo Molecular Medicine. PMID 30201738 DOI: 10.15252/Emmm.201809060 |
0.42 |
|
2018 |
Thompson K, Mai N, Olahova M, Scialo F, Formosa LE, Stroud DA, Garett M, Lax NZ, Jou C, Nascimento A, Ortez C, Jimenez-Mallabrera C, Hardy SA, He L, Brown GK, ... ... Battersby BJ, et al. Biallelic mutations in Oxa1l cause a mitochondrial encephalopathy and combined oxidative phosphorylation dysfunction Neuromuscular Disorders. 28. DOI: 10.1016/S0960-8966(18)30392-4 |
0.521 |
|
2017 |
Suomalainen A, Battersby BJ. Mitochondrial diseases: the contribution of organelle stress responses to pathology. Nature Reviews. Molecular Cell Biology. PMID 28792006 DOI: 10.1038/Nrm.2017.66 |
0.583 |
|
2017 |
Jackson CB, Hahn D, Schröter B, Richter U, Battersby B, Schmitt-Mechelke T, Martinen P, Nuoffer JM, Schaller A. A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy. European Journal of Medical Genetics. PMID 28412374 DOI: 10.1016/J.Ejmg.2017.04.006 |
0.54 |
|
2016 |
Nikkanen J, Forsström S, Euro L, Paetau I, Kohnz RA, Wang L, Chilov D, Viinamäki J, Roivainen A, Marjamäki P, Liljenbäck H, Ahola S, Buzkova J, Terzioglu M, Khan NA, ... ... Battersby BJ, et al. Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism. Cell Metabolism. PMID 26924217 DOI: 10.1016/J.Cmet.2016.01.019 |
0.554 |
|
2015 |
Jokinen R, Marttinen P, Stewart JB, Neil Dear T, Battersby BJ. Tissue-specific modulation of mitochondrial DNA segregation by a defect in mitochondrial division. Human Molecular Genetics. PMID 26681804 DOI: 10.1093/Hmg/Ddv508 |
0.668 |
|
2015 |
Richter U, Lahtinen T, Marttinen P, Suomi F, Battersby BJ. Quality control of mitochondrial protein synthesis is required for membrane integrity and cell fitness. The Journal of Cell Biology. 211: 373-89. PMID 26504172 DOI: 10.1083/Jcb.201504062 |
0.572 |
|
2015 |
Jokinen R, Lahtinen T, Marttinen P, Myöhänen M, Ruotsalainen P, Yeung N, Shvetsova A, Kastaniotis AJ, Hiltunen JK, Öhman T, Nyman TA, Weiler H, Battersby BJ. Quantitative changes in Gimap3 and Gimap5 expression modify mitochondrial DNA segregation in mice. Genetics. 200: 221-35. PMID 25808953 DOI: 10.1534/Genetics.115.175596 |
0.625 |
|
2014 |
Hagström E, Freyer C, Battersby BJ, Stewart JB, Larsson NG. No recombination of mtDNA after heteroplasmy for 50 generations in the mouse maternal germline. Nucleic Acids Research. 42: 1111-6. PMID 24163253 DOI: 10.1093/Nar/Gkt969 |
0.539 |
|
2013 |
Battersby BJ, Richter U. Why translation counts for mitochondria - retrograde signalling links mitochondrial protein synthesis to mitochondrial biogenesis and cell proliferation. Journal of Cell Science. 126: 4331-8. PMID 24013545 DOI: 10.1242/Jcs.131888 |
0.599 |
|
2013 |
Richter U, Lahtinen T, Marttinen P, Myöhänen M, Greco D, Cannino G, Jacobs HT, Lietzén N, Nyman TA, Battersby BJ. A mitochondrial ribosomal and RNA decay pathway blocks cell proliferation. Current Biology : Cb. 23: 535-41. PMID 23453957 DOI: 10.1016/J.Cub.2013.02.019 |
0.582 |
|
2013 |
Carroll CJ, Isohanni P, Pöyhönen R, Euro L, Richter U, Brilhante V, Götz A, Lahtinen T, Paetau A, Pihko H, Battersby BJ, Tyynismaa H, Suomalainen A. Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy. Journal of Medical Genetics. 50: 151-9. PMID 23315540 DOI: 10.1136/Jmedgenet-2012-101375 |
0.615 |
|
2013 |
Jokinen R, Battersby BJ. Insight into mammalian mitochondrial DNA segregation. Annals of Medicine. 45: 149-55. PMID 22775146 DOI: 10.3109/07853890.2012.693190 |
0.595 |
|
2011 |
Jokinen R, Junnila H, Battersby BJ. Gimap3: A foot-in-the-door to tissue-specific regulation of mitochondrial DNA genetics. Small Gtpases. 2: 31-35. PMID 21686279 DOI: 10.4161/Sgtp.2.1.14937 |
0.604 |
|
2011 |
Jokinen⁎ R, Marttinen P, Sandell K, Manninen T, Teerenhovi H, Wai T, Teoli D, Loredo-Osti J, Shoubridge EA, Battersby BJ. Cloning a novel mitochondrial protein which regulates tissue-specific mtDNA segregation Mitochondrion. 11: 641-642. DOI: 10.1016/J.Mito.2011.03.023 |
0.689 |
|
2010 |
Jokinen R, Marttinen P, Sandell HK, Manninen T, Teerenhovi H, Wai T, Teoli D, Loredo-Osti JC, Shoubridge EA, Battersby BJ. Gimap3 regulates tissue-specific mitochondrial DNA segregation. Plos Genetics. 6: e1001161. PMID 20976251 DOI: 10.1371/Journal.Pgen.1001161 |
0.723 |
|
2010 |
Battersby BJ. 86 Tissue-specific control of mitochondrial DNA genetics Mitochondrion. 10: 224. DOI: 10.1016/J.Mito.2009.12.080 |
0.543 |
|
2007 |
Battersby BJ, Shoubridge EA. Reactive oxygen species and the segregation of mtDNA sequence variants. Nature Genetics. 39: 571-2; author reply . PMID 17460678 DOI: 10.1038/Ng0507-571 |
0.528 |
|
2006 |
Bacman SR, Williams SL, Hernandez D, Battersby BJ, Shoubridge EA, Moraes CT. Manipulating heteroplasmy by delivering restriction endonuclease to mitochondria in a “differential multiple cleavage-site” model Mitochondrion. 6: 15. DOI: 10.1016/J.Mito.2006.08.036 |
0.611 |
|
2005 |
Bayona-Bafaluy MP, Blits B, Battersby BJ, Shoubridge EA, Moraes CT. Rapid directional shift of mitochondrial DNA heteroplasmy in animal tissues by a mitochondrially targeted restriction endonuclease. Proceedings of the National Academy of Sciences of the United States of America. 102: 14392-7. PMID 16179392 DOI: 10.1073/Pnas.0502896102 |
0.717 |
|
2005 |
Battersby BJ, Redpath ME, Shoubridge EA. Mitochondrial DNA segregation in hematopoietic lineages does not depend on MHC presentation of mitochondrially encoded peptides. Human Molecular Genetics. 14: 2587-94. PMID 16049030 DOI: 10.1093/Hmg/Ddi293 |
0.679 |
|
2003 |
Dean NL, Battersby BJ, Ao A, Gosden RG, Tan SL, Shoubridge EA, Molnar MJ. Prospect of preimplantation genetic diagnosis for heritable mitochondrial DNA diseases. Molecular Human Reproduction. 9: 631-8. PMID 12970401 DOI: 10.1093/Molehr/Gag077 |
0.625 |
|
2003 |
Battersby BJ, Loredo-Osti JC, Shoubridge EA. Nuclear genetic control of mitochondrial DNA segregation. Nature Genetics. 33: 183-6. PMID 12539044 DOI: 10.1038/Ng1073 |
0.699 |
|
2001 |
Battersby BJ, Shoubridge EA. Selection of a mtDNA sequence variant in hepatocytes of heteroplasmic mice is not due to differences in respiratory chain function or efficiency of replication. Human Molecular Genetics. 10: 2469-79. PMID 11709534 DOI: 10.1093/Hmg/10.22.2469 |
0.64 |
|
1998 |
Battersby BJ, Moyes CD. Influence of acclimation temperature on mitochondrial DNA, RNA, and enzymes in skeletal muscle. American Journal of Physiology-Regulatory Integrative and Comparative Physiology. 275. PMID 9728090 DOI: 10.1152/Ajpregu.1998.275.3.R905 |
0.412 |
|
1998 |
Leary SC, Battersby BJ, Hansford RG, Moyes CD. Interactions between bioenergetics and mitochondrial biogenesis Biochimica Et Biophysica Acta - Bioenergetics. 1365: 522-530. PMID 9711303 DOI: 10.1016/S0005-2728(98)00105-4 |
0.548 |
|
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