Ahola S - Search Results

1

Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.

Horvath R, Hudson G, Ferrari G, Fütterer N, Ahola S, Lamantea E, Prokisch H, Lochmüller H, McFarland R, Ramesh V, Klopstock T, Freisinger P, Salvi F, Mayr JA, Santer R, Tesarova M, Zeman J, Udd B, Taylor RW, Turnbull D, Hanna M, Fialho D, Suomalainen A, Zeviani M, Chinnery PF. Horvath R, et al. Among authors: ahola s. Brain. 2006 Jul;129(Pt 7):1674-84. doi: 10.1093/brain/awl088. Epub 2006 Apr 18. Brain. 2006. PMID: 16621917

2

Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease.

Luoma PT, Eerola J, Ahola S, Hakonen AH, Hellström O, Kivistö KT, Tienari PJ, Suomalainen A. Luoma PT, et al. Among authors: ahola s. Neurology. 2007 Sep 11;69(11):1152-9. doi: 10.1212/01.wnl.0000276955.23735.eb. Neurology. 2007. PMID: 17846414

3

Mitochondrial EFTs defects in juvenile-onset Leigh disease, ataxia, neuropathy, and optic atrophy.

Ahola S, Isohanni P, Euro L, Brilhante V, Palotie A, Pihko H, Lönnqvist T, Lehtonen T, Laine J, Tyynismaa H, Suomalainen A. Ahola S, et al. Neurology. 2014 Aug 19;83(8):743-51. doi: 10.1212/WNL.0000000000000716. Epub 2014 Jul 18. Neurology. 2014. PMID: 25037205 Free PMC article.

4

MtDNA mutagenesis impairs elimination of mitochondria during erythroid maturation leading to enhanced erythrocyte destruction.

Ahlqvist KJ, Leoncini S, Pecorelli A, Wortmann SB, Ahola S, Forsström S, Guerranti R, De Felice C, Smeitink J, Ciccoli L, Hämäläinen RH, Suomalainen A. Ahlqvist KJ, et al. Among authors: ahola s. Nat Commun. 2015 Mar 9;6:6494. doi: 10.1038/ncomms7494. Nat Commun. 2015. PMID: 25751021 Free article.

5

Metabolomes of mitochondrial diseases and inclusion body myositis patients: treatment targets and biomarkers.

Buzkova J, Nikkanen J, Ahola S, Hakonen AH, Sevastianova K, Hovinen T, Yki-Järvinen H, Pietiläinen KH, Lönnqvist T, Velagapudi V, Carroll CJ, Suomalainen A. Buzkova J, et al. Among authors: ahola s. EMBO Mol Med. 2018 Dec;10(12):e9091. doi: 10.15252/emmm.201809091. EMBO Mol Med. 2018. PMID: 30373890 Free PMC article.

6

Modified Atkins diet induces subacute selective ragged-red-fiber lysis in mitochondrial myopathy patients.

Ahola S, Auranen M, Isohanni P, Niemisalo S, Urho N, Buzkova J, Velagapudi V, Lundbom N, Hakkarainen A, Muurinen T, Piirilä P, Pietiläinen KH, Suomalainen A. Ahola S, et al. EMBO Mol Med. 2016 Nov 2;8(11):1234-1247. doi: 10.15252/emmm.201606592. Print 2016 Nov. EMBO Mol Med. 2016. PMID: 27647878 Free PMC article.

7

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. Nikkanen J, et al. Among authors: ahola s. Cell Metab. 2016 Apr 12;23(4):635-48. doi: 10.1016/j.cmet.2016.01.019. Epub 2016 Feb 25. Cell Metab. 2016. PMID: 26924217 Free article.

8

Mitochondrial Proteolysis and Metabolic Control.

Ahola S, Langer T, MacVicar T. Ahola S, et al. Cold Spring Harb Perspect Biol. 2019 Jul 1;11(7):a033936. doi: 10.1101/cshperspect.a033936. Cold Spring Harb Perspect Biol. 2019. PMID: 30670467 Free PMC article. Review.

9

Loss of the mitochondrial i-AAA protease YME1L leads to ocular dysfunction and spinal axonopathy.

Sprenger HG, Wani G, Hesseling A, König T, Patron M, MacVicar T, Ahola S, Wai T, Barth E, Rugarli EI, Bergami M, Langer T. Sprenger HG, et al. Among authors: ahola s. EMBO Mol Med. 2019 Jan;11(1):e9288. doi: 10.15252/emmm.201809288. EMBO Mol Med. 2019. PMID: 30389680 Free PMC article.

10

OMA1-mediated integrated stress response protects against ferroptosis in mitochondrial cardiomyopathy.

Ahola S, Rivera Mejías P, Hermans S, Chandragiri S, Giavalisco P, Nolte H, Langer T. Ahola S, et al. Cell Metab. 2022 Nov 1;34(11):1875-1891.e7. doi: 10.1016/j.cmet.2022.08.017. Epub 2022 Sep 15. Cell Metab. 2022. PMID: 36113464 Free article.

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