Ohcanbohtosat - Anu Suomalainen

Aiddostahte ozu
  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 Dahkki Anu Suomalainen

    Almmustuhtton 2013
    Viečča ollesdeavstta Viečča ollesdeavstta
    Editorial
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  2. 2
    Mechanisms of mitochondrial diseases

    Mechanisms of mitochondrial diseases Dahkki Emil Ylikallio, Anu Suomalainen

    Almmustuhtton 2011
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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 Dahkki Shuichi Yatsuga, Anu Suomalainen

    Almmustuhtton 2011
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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 Dahkki Henna Tyynismaa, Anu Suomalainen

    Almmustuhtton 2009
    Viečča ollesdeavstta
    Revisão
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  5. 5
    Mitochondria: In Sickness and in Health

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

    Almmustuhtton 2012
    Viečča ollesdeavstta
    Revisão
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  6. 6
    Mitochondria at the crossroads of health and disease

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

    Almmustuhtton 2024
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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 Dahkki Thomas G. McWilliams, Anu Suomalainen

    Almmustuhtton 2019
    Viečča ollesdeavstta Viečča ollesdeavstta
    Carta
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  8. 8
    Next‐generation sequencing for mitochondrial disorders

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

    Almmustuhtton 2013
    Viečča ollesdeavstta Viečča ollesdeavstta
    Revisão
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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 Dahkki Sofia Rahman, Joanna Poulton, Jackie Marchington, Anu Suomalainen

    Almmustuhtton 2001
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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  10. 10
    Stem cells, mitochondria and aging

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

    Almmustuhtton 2015
    Viečča ollesdeavstta
    Revisão
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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 Dahkki Sofia Khan, Gulayse Ince-Dunn, Anu Suomalainen, Laura L. Elo

    Almmustuhtton 2020
    Viečča ollesdeavstta Viečča ollesdeavstta
    Revisão
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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 Dahkki Anu Suomalainen, L. Peltonen, Anders Paetau, Hannu Leinonen, Anna Majander, Hannu Somer

    Almmustuhtton 1992
    Viečča ollesdeavstta
    Artigo
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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 Dahkki Riikka H. Hämäläinen, Tuula Manninen, Hanna Koivumäki, Mikhail Kislin, Timo Otonkoski, Anu Suomalainen

    Almmustuhtton 2013
    Viečča ollesdeavstta
    Artigo
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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 Dahkki Anna H. Hakonen, Pirjo Isohanni, Anders Paetau, Riitta Herva, Anu Suomalainen, Tuula Lönnqvist

    Almmustuhtton 2007
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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 Dahkki Steffi Goffart, Helen Cooper, Henna Tyynismaa, Sjoerd Wanrooij, Anu Suomalainen, Johannes N. Spelbrink

    Almmustuhtton 2008
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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 Dahkki Anna Majander, Anu Suomalainen, Kim Vettenranta, Hannu Sariola, Mikko Perkio, Christer Holmberg, Helena Pihko

    Almmustuhtton 1991
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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 Dahkki Henna Tyynismaa, Emil Ylikallio, Mehul D. Patel, Mária Judit Molnár, Ronald G. Haller, Anu Suomalainen

    Almmustuhtton 2009
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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. Dahkki Anu Suomalainen, Anna Majander, Matti Haltia, Hannu Somer, Jouko Lönnqvist, M L Savontaus, Leena Peltonen

    Almmustuhtton 1992
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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 Dahkki Päivi Mäkelä‐Bengs, Anu Suomalainen, Anna Majander, Juhani Rapola, Hannu Kalimo, Auli Nuutila, Helena Pihko

    Almmustuhtton 1995
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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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 Dahkki Kaisu Nikali, Anu Suomalainen, Juha Saharinen, Mikko Kuokkanen, Johannes N. Spelbrink, Tuula Lönnqvist, Leena Peltonen

    Almmustuhtton 2005
    Viečča ollesdeavstta Viečča ollesdeavstta
    Artigo
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