1 - 25 of 34 results for author:"Suomalainen A." in Literature citations
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| Effect of bezafibrate treatment on late-onset mitochondrial myopathy in mice. Yatsuga S., Suomalainen A. Hum. Mol. Genet. 21:526-535(2012) · Mapped (2) |
| FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study. Suomalainen A., Elo J.M., Pietilainen K.H., Hakonen A.H., Sevastianova K., Korpela M., Isohanni P., Marjavaara S.K., Tyni T., Kiuru-Enari S. et al. Lancet Neurol 10:806-818(2011) · Mapped (1) |
| Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy. Gotz A., Tyynismaa H., Euro L., Ellonen P., Hyotylainen T., Ojala T., Hamalainen R.H., Tommiska J., Raivio T., Oresic M. et al. Am. J. Hum. Genet. 88:635-642(2011) · UniProtKB (1) · Mapped (2) |
| POLG1 manifestations in childhood. Isohanni P., Hakonen A.H., Euro L., Paetau I., Linnankivi T., Liukkonen E., Wallden T., Luostarinen L., Valanne L., Paetau A. et al. Neurology 76:811-815(2011) · Mapped (7) |
| Liver fat but not other adiposity measures influence circulating FGF21 levels in healthy young adult twins. Tyynismaa H., Raivio T., Hakkarainen A., Ortega-Alonso A., Lundbom N., Kaprio J., Rissanen A., Suomalainen A., Pietilainen K.H. J. Clin. Endocrinol. Metab. 96:E351-5(2011) · Mapped (1) |
| Ribonucleotide reductase is not limiting for mitochondrial DNA copy number in mice. Ylikallio E., Page J.L., Xu X., Lampinen M., Bepler G., Ide T., Tyynismaa H., Weiss R.S., Suomalainen A. Nucleic Acids Res. 38:8208-8218(2010) · Mapped (7) |
| Mitochondrial myopathy induces a starvation-like response. Tyynismaa H., Carroll C.J., Raimundo N., Ahola-Erkkila S., Wenz T., Ruhanen H., Guse K., Hemminki A., Peltola-Mjosund K.E., Tulkki V. et al. Hum. Mol. Genet. 19:3948-3958(2010) · Mapped (5) |
| CIP2A increases self-renewal and is linked to Myc in neural progenitor cells. Kerosuo L., Fox H., Perala N., Ahlqvist K., Suomalainen A., Westermarck J., Sariola H., Wartiovaara K. Differentiation 80:68-77(2010) · Mapped (5) |
| POLG1 polyglutamine tract variants associated with Parkinson's disease. Eerola J., Luoma P.T., Peuralinna T., Scholz S., Paisan-Ruiz C., Suomalainen A., Singleton A.B., Tienari P.J. Neurosci. Lett. 477:1-5(2010) · Mapped (7) |
| Functional analysis of H. sapiens DNA polymerase gamma spacer mutation W748S with and without common variant E1143G. Palin E.J., Lesonen A., Farr C.L., Euro L., Suomalainen A., Kaguni L.S. Biochim. Biophys. Acta 1802:545-551(2010) · Mapped (7) |
| A heterozygous truncating mutation in RRM2B causes autosomal-dominant progressive external ophthalmoplegia with multiple mtDNA deletions. Tyynismaa H., Ylikallio E., Patel M., Molnar M.J., Haller R.G., Suomalainen A. Am. J. Hum. Genet. 85:290-295(2009) · UniProtKB (1) · Mapped (2) |
| DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis. Isohanni P., Linnankivi T., Buzkova J., Lonnqvist T., Pihko H., Valanne L., Tienari P.J., Elovaara I., Pirttila T., Reunanen M. et al. J. Med. Genet. 47:66-70(2010) · Mapped (4) |
| Do mitochondrial mutations cause recurrent miscarriage? Kaare M., Gotz A., Ulander V.M., Ariansen S., Kaaja R., Suomalainen A., Aittomaki K. Mol. Hum. Reprod. 15:295-300(2009) · Mapped (7) |
| Downregulation of SRF-FOS-JUNB pathway in fumarate hydratase deficiency and in uterine leiomyomas. Raimundo N., Vanharanta S., Aaltonen L.A., Hovatta I., Suomalainen A. Oncogene 28:1261-1273(2009) · Mapped (11) |
| Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling. Goffart S., Cooper H.M., Tyynismaa H., Wanrooij S., Suomalainen A., Spelbrink J.N. Hum. Mol. Genet. 18:328-340(2009) · Mapped (6) |
| Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism. Lyly A., Marjavaara S.K., Kyttala A., Uusi-Rauva K., Luiro K., Kopra O., Martinez L.O., Tanhuanpaa K., Kalkkinen N., Suomalainen A. et al. Hum. Mol. Genet. 17:1406-1417(2008) · Mapped (11) |
| Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance. Hudson G., Amati-Bonneau P., Blakely E.L., Stewart J.D., He L., Schaefer A.M., Griffiths P.G., Ahlqvist K., Suomalainen A., Reynier P. et al. Brain 131:329-337(2008) · Mapped (10) |
| Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion. Hakonen A.H., Isohanni P., Paetau A., Herva R., Suomalainen A., Lonnqvist T. |
| Do carriers of POLG mutation W748S have disease manifestations? Rantamaki M., Luoma P., Virta J.J., Rinne J.O., Paetau A., Suomalainen A., Udd B. Clin. Genet. 72:532-537(2007) · Mapped (7) |
| Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease. Luoma P.T., Eerola J., Ahola S., Hakonen A.H., Hellstrom O., Kivisto K.T., Tienari P.J., Suomalainen A. Neurology 69:1152-1159(2007) · Mapped (7) |
| Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the United States explained by single ancient European founders. Hakonen A.H., Davidzon G., Salemi R., Bindoff L.A., Van Goethem G., Dimauro S., Thorburn D.R., Suomalainen A. Eur. J. Hum. Genet. 15:779-783(2007) · Mapped (7) |
| Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. Horvath R., Hudson G., Ferrari G., Fuetterer N., Ahola S., Lamantea E., Prokisch H., Lochmueller H., McFarland R., Ramesh V. et al. Brain 129:1674-1684(2006) · UniProtKB (1) |
| Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky. Nikali K., Suomalainen A., Saharinen J., Kuokkanen M., Spelbrink J.N., Loennqvist T., Peltonen L. Hum. Mol. Genet. 14:2981-2990(2005) · UniProtKB (1) · Mapped (3) |
| Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin. Hakonen A.H., Heiskanen S., Juvonen V., Lappalainen I., Luoma P.T., Rantamaeki M., Van Goethem G., Loefgren A., Hackman P., Paetau A. et al. Am. J. Hum. Genet. 77:430-441(2005) · UniProtKB (1) · Mapped (6) |
| Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4: premature ageing or just coincidence? Melberg A., Nennesmo I., Moslemi A.R., Kollberg G., Luoma P., Suomalainen A., Holme E., Oldfors A. Acta Neuropathol. 110:315-316(2005) · Mapped (7) |