Euro L - Search Results

1

Functional analysis of H. sapiens DNA polymerase gamma spacer mutation W748S with and without common variant E1143G.

Palin EJ, Lesonen A, Farr CL, Euro L, Suomalainen A, Kaguni LS. Palin EJ, et al. Among authors: euro l. Biochim Biophys Acta. 2010 Jun;1802(6):545-51. doi: 10.1016/j.bbadis.2010.02.003. Epub 2010 Feb 12. Biochim Biophys Acta. 2010. PMID: 20153822 Free PMC article.

2

Conserved lysine residues of the membrane subunit NuoM are involved in energy conversion by the proton-pumping NADH:ubiquinone oxidoreductase (Complex I).

Euro L, Belevich G, Verkhovsky MI, Wikström M, Verkhovskaya M. Euro L, et al. Biochim Biophys Acta. 2008 Sep;1777(9):1166-72. doi: 10.1016/j.bbabio.2008.06.001. Epub 2008 Jun 9. Biochim Biophys Acta. 2008. PMID: 18590697 Free article.

3

The role of the invariant glutamate 95 in the catalytic site of Complex I from Escherichia coli.

Euro L, Belevich G, Bloch DA, Verkhovsky MI, Wikström M, Verkhovskaya M. Euro L, et al. Biochim Biophys Acta. 2009 Jan;1787(1):68-73. doi: 10.1016/j.bbabio.2008.11.002. Epub 2008 Nov 13. Biochim Biophys Acta. 2009. PMID: 19061856 Free article.

4

POLG1 manifestations in childhood.

Isohanni P, Hakonen AH, Euro L, Paetau I, Linnankivi T, Liukkonen E, Wallden T, Luostarinen L, Valanne L, Paetau A, Uusimaa J, Lönnqvist T, Suomalainen A, Pihko H. Isohanni P, et al. Among authors: euro l. Neurology. 2011 Mar 1;76(9):811-5. doi: 10.1212/WNL.0b013e31820e7b25. Neurology. 2011. PMID: 21357833

5

Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy.

Götz A, Tyynismaa H, Euro L, Ellonen P, Hyötyläinen T, Ojala T, Hämäläinen RH, Tommiska J, Raivio T, Oresic M, Karikoski R, Tammela O, Simola KO, Paetau A, Tyni T, Suomalainen A. Götz A, et al. Among authors: euro l. Am J Hum Genet. 2011 May 13;88(5):635-42. doi: 10.1016/j.ajhg.2011.04.006. Epub 2011 May 5. Am J Hum Genet. 2011. PMID: 21549344 Free PMC article.

6

Clustering of Alpers disease mutations and catalytic defects in biochemical variants reveal new features of molecular mechanism of the human mitochondrial replicase, Pol γ.

Euro L, Farnum GA, Palin E, Suomalainen A, Kaguni LS. Euro L, et al. Nucleic Acids Res. 2011 Nov;39(21):9072-84. doi: 10.1093/nar/gkr618. Epub 2011 Aug 8. Nucleic Acids Res. 2011. PMID: 21824913 Free PMC article. Review.

7

Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy.

Elo JM, Yadavalli SS, Euro L, Isohanni P, Götz A, Carroll CJ, Valanne L, Alkuraya FS, Uusimaa J, Paetau A, Caruso EM, Pihko H, Ibba M, Tyynismaa H, Suomalainen A. Elo JM, et al. Among authors: euro l. Hum Mol Genet. 2012 Oct 15;21(20):4521-9. doi: 10.1093/hmg/dds294. Epub 2012 Jul 23. Hum Mol Genet. 2012. PMID: 22833457

8

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. Carroll CJ, et al. Among authors: euro l. J Med Genet. 2013 Mar;50(3):151-9. doi: 10.1136/jmedgenet-2012-101375. Epub 2013 Jan 12. J Med Genet. 2013. PMID: 23315540

9

Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B3.

Khan NA, Auranen M, Paetau I, Pirinen E, Euro L, Forsström S, Pasila L, Velagapudi V, Carroll CJ, Auwerx J, Suomalainen A. Khan NA, et al. Among authors: euro l. EMBO Mol Med. 2014 Jun;6(6):721-31. doi: 10.1002/emmm.201403943. EMBO Mol Med. 2014. PMID: 24711540 Free PMC article.

10

Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion.

Matilainen S, Isohanni P, Euro L, Lönnqvist T, Pihko H, Kivelä T, Knuutila S, Suomalainen A. Matilainen S, et al. Among authors: euro l. Eur J Hum Genet. 2015 Mar;23(3):325-30. doi: 10.1038/ejhg.2014.128. Epub 2014 Jul 2. Eur J Hum Genet. 2015. PMID: 24986829 Free PMC article. Review.

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