Resultados de búsqueda - Anu Suomalainen

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  1. 1
    Fibroblast growth factor 21: a novel biomarker for human muscle-manifesting mitochondrial disorders

    Fibroblast growth factor 21: a novel biomarker for human muscle-manifesting mitochondrial disorders por Anu Suomalainen

    Publicado 2013
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  2. 2
    Mechanisms of mitochondrial diseases

    Mechanisms of mitochondrial diseases por Emil Ylikallio, Anu Suomalainen

    Publicado 2011
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  3. 3
    Effect of bezafibrate treatment on late-onset mitochondrial myopathy in mice

    Effect of bezafibrate treatment on late-onset mitochondrial myopathy in mice por Shuichi Yatsuga, Anu Suomalainen

    Publicado 2011
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  4. 4
    Mouse models of mitochondrial DNA defects and their relevance for human disease

    Mouse models of mitochondrial DNA defects and their relevance for human disease por Henna Tyynismaa, Anu Suomalainen

    Publicado 2009
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  5. 5
    Mitochondria: In Sickness and in Health

    Mitochondria: In Sickness and in Health por Jodi Nunnari, Anu Suomalainen

    Publicado 2012
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  6. 6
    Mitochondria at the crossroads of health and disease

    Mitochondria at the crossroads of health and disease por Anu Suomalainen, Jodi Nunnari

    Publicado 2024
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  7. 7
    Mitochondrial DNA can be inherited from fathers, not just mothers

    Mitochondrial DNA can be inherited from fathers, not just mothers por Thomas G. McWilliams, Anu Suomalainen

    Publicado 2019
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  8. 8
    Next‐generation sequencing for mitochondrial disorders

    Next‐generation sequencing for mitochondrial disorders por Christopher J. Carroll, Virginia Brilhante, Anu Suomalainen

    Publicado 2013
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  9. 9
    Decrease of 3243 A→G mtDNA Mutation from Blood in MELAS Syndrome: A Longitudinal Study

    Decrease of 3243 A→G mtDNA Mutation from Blood in MELAS Syndrome: A Longitudinal Study por Sofia Rahman, Joanna Poulton, Jackie Marchington, Anu Suomalainen

    Publicado 2001
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  10. 10
    Stem cells, mitochondria and aging

    Stem cells, mitochondria and aging por Kati J. Ahlqvist, Anu Suomalainen, Riikka H. Hämäläinen

    Publicado 2015
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  11. 11
    Integrative omics approaches provide biological and clinical insights: examples from mitochondrial diseases

    Integrative omics approaches provide biological and clinical insights: examples from mitochondrial diseases por Sofia Khan, Gulayse Ince-Dunn, Anu Suomalainen, Laura L. Elo

    Publicado 2020
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  12. 12
    Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA

    Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA por Anu Suomalainen, L. Peltonen, Anders Paetau, Hannu Leinonen, Anna Majander, Hannu Somer

    Publicado 1992
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  13. 13
    Tissue- and cell-type–specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model

    Tissue- and cell-type–specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model por Riikka H. Hämäläinen, Tuula Manninen, Hanna Koivumäki, Mikhail Kislin, Timo Otonkoski, Anu Suomalainen

    Publicado 2013
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  14. 14
    Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion

    Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion por Anna H. Hakonen, Pirjo Isohanni, Anders Paetau, Riitta Herva, Anu Suomalainen, Tuula Lönnqvist

    Publicado 2007
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  15. 15
    Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling

    Twinkle mutations associated with autosomal dominant progressive external ophthalmoplegia lead to impaired helicase function and in vivo mtDNA replication stalling por Steffi Goffart, Helen Cooper, Henna Tyynismaa, Sjoerd Wanrooij, Anu Suomalainen, Johannes N. Spelbrink

    Publicado 2008
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  16. 16
    Congenital Hypoplastic Anemia, Diabetes, and Severe Renal Tubular Dysfunction Associated with a Mitochondrial DNA Deletion

    Congenital Hypoplastic Anemia, Diabetes, and Severe Renal Tubular Dysfunction Associated with a Mitochondrial DNA Deletion por Anna Majander, Anu Suomalainen, Kim Vettenranta, Hannu Sariola, Mikko Perkio, Christer Holmberg, Helena Pihko

    Publicado 1991
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  17. 17
    A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions

    A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions por Henna Tyynismaa, Emil Ylikallio, Mehul D. Patel, Mária Judit Molnár, Ronald G. Haller, Anu Suomalainen

    Publicado 2009
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  18. 18
    Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

    Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia. por Anu Suomalainen, Anna Majander, Matti Haltia, Hannu Somer, Jouko Lönnqvist, M L Savontaus, Leena Peltonen

    Publicado 1992
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  19. 19
    Correlation between the Clinical Symptoms and the Proportion of Mitochondrial DNA Carrying the 8993 Point Mutation in the NARP Syndrome

    Correlation between the Clinical Symptoms and the Proportion of Mitochondrial DNA Carrying the 8993 Point Mutation in the NARP Syndrome por Päivi Mäkelä‐Bengs, Anu Suomalainen, Anna Majander, Juhani Rapola, Hannu Kalimo, Auli Nuutila, Helena Pihko

    Publicado 1995
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  20. 20
    Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky

    Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky por Kaisu Nikali, Anu Suomalainen, Juha Saharinen, Mikko Kuokkanen, Johannes N. Spelbrink, Tuula Lönnqvist, Leena Peltonen

    Publicado 2005
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