Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 20 of 33

1.

Mitochondrial stress response triggered by defects in protein synthesis quality control.

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, Lombès A, Taylor RW, Battersby BJ.

Life Sci Alliance. 2019 Jan 25;2(1). pii: e201800219. doi: 10.26508/lsa.201800219. Print 2019 Feb.

2.

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

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, Donetti E, Giorgio E, Cavalieri S, Di Gregorio E, Pozzi E, Ferrero M, Riberi E, Casari G, Altruda F, Turco E, Gasparre G, Battersby BJ, Porcelli AM, Ferrero E, Brusco A, Tempia F.

Neurobiol Dis. 2019 Apr;124:14-28. doi: 10.1016/j.nbd.2018.10.018. Epub 2018 Oct 30.

PMID:
30389403
3.

A variant in MRPS14 (uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement.

Jackson CB, Huemer M, Bolognini R, Martin F, Szinnai G, Donner BC, Richter U, Battersby BJ, Nuoffer JM, Suomalainen A, Schaller A.

Hum Mol Genet. 2019 Feb 15;28(4):639-649. doi: 10.1093/hmg/ddy374.

PMID:
30358850
4.

RNA modification landscape of the human mitochondrial tRNALys regulates protein synthesis.

Richter U, Evans ME, Clark WC, Marttinen P, Shoubridge EA, Suomalainen A, Wredenberg A, Wedell A, Pan T, Battersby BJ.

Nat Commun. 2018 Sep 27;9(1):3966. doi: 10.1038/s41467-018-06471-z.

5.

OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect.

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, Brown GK, Marttinen P, McFarland R, Sanz A, Battersby BJ, Bonnen PE, Ryan MT, Chrzanowska-Lightowlers ZM, Lightowlers RN, Taylor RW.

EMBO Mol Med. 2018 Nov;10(11). pii: e9060. doi: 10.15252/emmm.201809060.

6.

Mitochondrial diseases: the contribution of organelle stress responses to pathology.

Suomalainen A, Battersby BJ.

Nat Rev Mol Cell Biol. 2018 Feb;19(2):77-92. doi: 10.1038/nrm.2017.66. Epub 2017 Aug 9. Review.

PMID:
28792006
7.

A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy.

Jackson CB, Hahn D, Schröter B, Richter U, Battersby BJ, Schmitt-Mechelke T, Marttinen P, Nuoffer JM, Schaller A.

Eur J Med Genet. 2017 Jun;60(6):345-351. doi: 10.1016/j.ejmg.2017.04.006. Epub 2017 Apr 13.

PMID:
28412374
8.

Mitochondrial DNA Replication Defects Disturb Cellular dNTP Pools and Remodel One-Carbon Metabolism.

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, Pirnes-Karhu S, Paetau A, Lönnqvist T, Sajantila A, Isohanni P, Tyynismaa H, Nomura DK, Battersby BJ, Velagapudi V, Carroll CJ, Suomalainen A.

Cell Metab. 2016 Apr 12;23(4):635-48. doi: 10.1016/j.cmet.2016.01.019. Epub 2016 Feb 25.

9.

Tissue-specific modulation of mitochondrial DNA segregation by a defect in mitochondrial division.

Jokinen R, Marttinen P, Stewart JB, Neil Dear T, Battersby BJ.

Hum Mol Genet. 2016 Feb 15;25(4):706-14. doi: 10.1093/hmg/ddv508. Epub 2015 Dec 17.

PMID:
26681804
10.

Quality control of mitochondrial protein synthesis is required for membrane integrity and cell fitness.

Richter U, Lahtinen T, Marttinen P, Suomi F, Battersby BJ.

J Cell Biol. 2015 Oct 26;211(2):373-89. doi: 10.1083/jcb.201504062.

11.

Quantitative changes in Gimap3 and Gimap5 expression modify mitochondrial DNA segregation in mice.

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.

Genetics. 2015 May;200(1):221-35. doi: 10.1534/genetics.115.175596. Epub 2015 Mar 25.

12.

No recombination of mtDNA after heteroplasmy for 50 generations in the mouse maternal germline.

Hagström E, Freyer C, Battersby BJ, Stewart JB, Larsson NG.

Nucleic Acids Res. 2014 Jan;42(2):1111-6. doi: 10.1093/nar/gkt969. Epub 2013 Oct 25.

13.

Why translation counts for mitochondria - retrograde signalling links mitochondrial protein synthesis to mitochondrial biogenesis and cell proliferation.

Battersby BJ, Richter U.

J Cell Sci. 2013 Oct 1;126(Pt 19):4331-8. doi: 10.1242/jcs.131888. Epub 2013 Sep 6.

14.

A mitochondrial ribosomal and RNA decay pathway blocks cell proliferation.

Richter U, Lahtinen T, Marttinen P, Myöhänen M, Greco D, Cannino G, Jacobs HT, Lietzén N, Nyman TA, Battersby BJ.

Curr Biol. 2013 Mar 18;23(6):535-41. doi: 10.1016/j.cub.2013.02.019. Epub 2013 Feb 28.

15.

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

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.

J Med Genet. 2013 Mar;50(3):151-9. doi: 10.1136/jmedgenet-2012-101375. Epub 2013 Jan 12.

PMID:
23315540
16.

Insight into mammalian mitochondrial DNA segregation.

Jokinen R, Battersby BJ.

Ann Med. 2013 Mar;45(2):149-55. doi: 10.3109/07853890.2012.693190. Epub 2012 Jul 9. Review.

PMID:
22775146
17.

The production and verification of pristine semi-fluorinated thiol monolayers on gold.

Ford K, Battersby BJ, Wood BJ, Gentle IR.

J Colloid Interface Sci. 2012 Mar 15;370(1):162-9. doi: 10.1016/j.jcis.2011.10.081. Epub 2011 Dec 6.

PMID:
22257960
18.

Gimap3: A foot-in-the-door to tissue-specific regulation of mitochondrial DNA genetics.

Jokinen R, Junnila H, Battersby BJ.

Small GTPases. 2011 Jan;2(1):31-35.

19.

Gimap3 regulates tissue-specific mitochondrial DNA segregation.

Jokinen R, Marttinen P, Sandell HK, Manninen T, Teerenhovi H, Wai T, Teoli D, Loredo-Osti JC, Shoubridge EA, Battersby BJ.

PLoS Genet. 2010 Oct 14;6(10):e1001161. doi: 10.1371/journal.pgen.1001161.

20.

Reactive oxygen species and the segregation of mtDNA sequence variants.

Battersby BJ, Shoubridge EA.

Nat Genet. 2007 May;39(5):571-2; author reply 572. No abstract available.

PMID:
17460678

Supplemental Content

Loading ...
Support Center