Risultati della ricerca - Kari Majamaa

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  1. 1
    Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletes

    Mitochondrial DNA and ACTN3 genotypes in Finnish elite endurance and sprint athletes di Anna‐Kaisa Niemi, Kari Majamaa

    Pubblicazione 2005
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  2. 2
    Reduction of collagen production in keloid fibroblast cultures by ethyl-3,4-dihydroxybenzoate. Inhibition of prolyl hydroxylase activity as a mechanism of action.

    Reduction of collagen production in keloid fibroblast cultures by ethyl-3,4-dihydroxybenzoate. Inhibition of prolyl hydroxylase activity as a mechanism of action. di Takaaki Sasaki, Kari Majamaa, Jouni Uitto

    Pubblicazione 1987
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  3. 3
    Phylogenetic Network for European mtDNA

    Phylogenetic Network for European mtDNA di Saara Finnilä, Mervi S. Lehtonen, Kari Majamaa

    Pubblicazione 2001
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  4. 4
    Phylogenetic Network of the mtDNA Haplogroup U in Northern Finland Based on Sequence Analysis of the Complete Coding Region by Conformation-Sensitive Gel Electrophoresis

    Phylogenetic Network of the mtDNA Haplogroup U in Northern Finland Based on Sequence Analysis of the Complete Coding Region by Conformation-Sensitive Gel Electrophoresis di Saara Finnilä, Ilmo E. Hassinen, Leena Ala‐Kokko, Kari Majamaa

    Pubblicazione 2000
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  5. 5
    Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G

    Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G di Kirsi Majamaa‐Voltti, Keijo Peuhkurinen, Marja‐Leena Kortelainen, Ilmo E. Hassinen, Kari Majamaa

    Pubblicazione 2002
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  6. 6
    Partial identity of the 2-oxoglutarate and ascorbate binding sites of prolyl 4-hydroxylase.

    Partial identity of the 2-oxoglutarate and ascorbate binding sites of prolyl 4-hydroxylase. di Kari Majamaa, Volkmar Günzler, Hartmut M. Hanauske‐Abel, Raili Myllylä, Kari I. Kivirikko

    Pubblicazione 1986
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  7. 7
    Treatment for mitochondrial disorders

    Treatment for mitochondrial disorders di Gerald Pfeffer, Kari Majamaa, Douglass M. Turnbull, David R. Thorburn, Patrick F. Chinnery

    Pubblicazione 2012
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  8. 8
    Ascorbate is consumed stoichiometrically in the uncoupled reactions catalyzed by prolyl 4-hydroxylase and lysyl hydroxylase.

    Ascorbate is consumed stoichiometrically in the uncoupled reactions catalyzed by prolyl 4-hydroxylase and lysyl hydroxylase. di Raili Myllylä, Kari Majamaa, Volkmar Günzler, Hartmut M. Hanauske‐Abel, Kari I. Kivirikko

    Pubblicazione 1984
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  9. 9
    APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage

    APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage di Anne Rovelet‐Lecrux, Thierry Frébourg, Hannu Tuominen, Kari Majamaa, Dominique Campion, Anne M. Remes

    Pubblicazione 2007
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  10. 10
    Psychiatric and neurological disorders are associated with bullous pemphigoid – a nationwide Finnish Care Register study

    Psychiatric and neurological disorders are associated with bullous pemphigoid – a nationwide Finnish Care Register study di Anna‐Kaisa Försti, Jari Jokelainen, Hanna Ansakorpi, Allan Seppänen, Kari Majamaa, Markku Timonen, Kaisa Tasanen

    Pubblicazione 2016
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  11. 11
    A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects

    A combination of three common inherited mitochondrial DNA polymorphisms promotes longevity in Finnish and Japanese subjects di Anna-Kaisa Niemi, Jukka S. Moilanen, Masashi Tanaka, Antti Hervonen, Mikko Hurme, Terho Lehtimäki, Yasumichi Arai, Nobuyoshi Hirose, Kari Majamaa

    Pubblicazione 2004
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  12. 12
    Differences between collagen hydroxylases and 2-oxoglutarate dehydrogenase in their inhibition by structural analogues of 2-oxoglutarate

    Differences between collagen hydroxylases and 2-oxoglutarate dehydrogenase in their inhibition by structural analogues of 2-oxoglutarate di Kari Majamaa, Taina Turpeenniemi‐Hujanen, Pirjo M. Latipää, Volkmar Günzler, Hartmut M. Hanauske‐Abel, Ilmo E. Hassinen, K.I. Kivirikko

    Pubblicazione 1985
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  13. 13
    Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study

    Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study di Ari Siitonen, Michael A. Nalls, Dena G. Hernandez, J. Raphael Gibbs, Jinhui Ding, Pauli Ylikotila, Connor Edsall, Andrew Singleton, Kari Majamaa

    Pubblicazione 2017
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  14. 14
    Acute liver failure after valproate exposure in patients with<i>POLG1</i>mutations and the prognosis after liver transplantation

    Acute liver failure after valproate exposure in patients with<i>POLG1</i>mutations and the prognosis after liver transplantation di Johanna Hynynen, Tuomas Komulainen, Eija Tukiainen, Arno Nordin, Johanna Arola, Reetta Kälviäinen, Leena Jutila, Matias Röyttä, Reetta Hinttala, Kari Majamaa, Heikki Mäkisalo, Johanna Uusimaa

    Pubblicazione 2014
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  15. 15
    Homozygous W748S mutation in the <i>POLG1</i> gene in patients with juvenile‐onset Alpers syndrome and status epilepticus

    Homozygous W748S mutation in the <i>POLG1</i> gene in patients with juvenile‐onset Alpers syndrome and status epilepticus di Johanna Uusimaa, Reetta Hinttala, Heikki Rantala, Markku Päivärinta, Riitta Herva, Matias Röyttä, Heidi K. Soini, Jukka S. Moilanen, Anne M. Remes, Ilmo E. Hassinen, Kari Majamaa

    Pubblicazione 2008
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  16. 16
    Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population

    Epidemiology of A3243G, the Mutation for Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes: Prevalence of the Mutation in an Adult Population di Kari Majamaa, Jukka S. Moilanen, Seija Uimonen, Anne M. Remes, Pasi Salmela, Mikko Kärppä, Kirsi Majamaa‐Voltti, Harri Rusanen, Martti Sorri, Keijo Peuhkurinen, Ilmo E. Hassinen

    Pubblicazione 1998
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  17. 17
    Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin

    Mitochondrial DNA Polymerase W748S Mutation: A Common Cause of Autosomal Recessive Ataxia with Ancient European Origin di Anna H. Hakonen, Silja Heiskanen, Vesa Juvonen, Ilse Lappalainen, Petri Luoma, Maria Rantamäki, Gert Van Goethem, A. Löfgren, Peter Hackman, Anders Paetau, Seppo Kaakkola, Kari Majamaa, Teppo Varilo, Bjarne Udd, Helena Kääriäinen, Laurence A. Bindoff, Anu Suomalainen

    Pubblicazione 2005
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  18. 18
    The Matrilineal Ancestry of Ashkenazi Jewry: Portrait of a Recent Founder Event

    The Matrilineal Ancestry of Ashkenazi Jewry: Portrait of a Recent Founder Event di Doron M. Behar, Ene Metspalu, Toomas Kivisild, Alessandro Achilli, Yarin Hadid, Shay Tzur, Luı́sa Pereira, António Amorim, Lluı́s Quintana-Murci, Kari Majamaa, Corinna Herrnstadt, Neil Howell, Oleg Balanovsky, Ildus Kutuev, Andrey Pshenichnov, David Gurwitz, Batsheva Bonné‐Tamir, Antonio Torroni, Richard Villems, Karl Skorecki

    Pubblicazione 2006
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  19. 19
    New treatments for mitochondrial disease—no time to drop our standards

    New treatments for mitochondrial disease—no time to drop our standards di Gerald Pfeffer, Rita Horváth, Thomas Klopstock, Vamsi K. Mootha, Anu Suomalainen, Saskia Koene, Michio Hirano, Massimo Zeviani, Laurence A. Bindoff, Patrick Yu‐Wai‐Man, Michael G. Hanna, Valério Carelli, Robert McFarland, Kari Majamaa, Douglass M. Turnbull, Jan Smeitink, Patrick F. Chinnery

    Pubblicazione 2013
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  20. 20
    Status epilepticus in POLG disease: a large multinational study

    Status epilepticus in POLG disease: a large multinational study di Omar Hikmat, K Naess, Martin Engvall, Claus Klingenberg, Magnhild Rasmussen, Eylert Brodtkorb, Elsebet Østergaard, I.F.M. de Coo, Leticia Pías‐Peleteiro, Pirjo Isohanni, Johanna Uusimaa, Kari Majamaa, Mikko Kärppä, Juan Darío Ortigoza‐Escobar, Trine Tangeraas, Siren Berland, Emma Harrison, Heather Biggs, Rita Horváth, Niklas Darín, Shamima Rahman, Laurence A. Bindoff

    Pubblicazione 2024
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