Bilaketaren emaitzak - 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 nork Anu Suomalainen

    Argitaratua 2013
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  2. 2
    Mechanisms of mitochondrial diseases

    Mechanisms of mitochondrial diseases nork Emil Ylikallio, Anu Suomalainen

    Argitaratua 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 nork Shuichi Yatsuga, Anu Suomalainen

    Argitaratua 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 nork Henna Tyynismaa, Anu Suomalainen

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

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

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

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

    Argitaratua 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 nork Thomas G. McWilliams, Anu Suomalainen

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

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

    Argitaratua 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 nork Sofia Rahman, Joanna Poulton, Jackie Marchington, Anu Suomalainen

    Argitaratua 2001
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  10. 10
    Stem cells, mitochondria and aging

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

    Argitaratua 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 nork Sofia Khan, Gulayse Ince-Dunn, Anu Suomalainen, Laura L. Elo

    Argitaratua 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 nork Anu Suomalainen, L. Peltonen, Anders Paetau, Hannu Leinonen, Anna Majander, Hannu Somer

    Argitaratua 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 nork Riikka H. Hämäläinen, Tuula Manninen, Hanna Koivumäki, Mikhail Kislin, Timo Otonkoski, Anu Suomalainen

    Argitaratua 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 nork Anna H. Hakonen, Pirjo Isohanni, Anders Paetau, Riitta Herva, Anu Suomalainen, Tuula Lönnqvist

    Argitaratua 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 nork Steffi Goffart, Helen Cooper, Henna Tyynismaa, Sjoerd Wanrooij, Anu Suomalainen, Johannes N. Spelbrink

    Argitaratua 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 nork Anna Majander, Anu Suomalainen, Kim Vettenranta, Hannu Sariola, Mikko Perkio, Christer Holmberg, Helena Pihko

    Argitaratua 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 nork Henna Tyynismaa, Emil Ylikallio, Mehul D. Patel, Mária Judit Molnár, Ronald G. Haller, Anu Suomalainen

    Argitaratua 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. nork Anu Suomalainen, Anna Majander, Matti Haltia, Hannu Somer, Jouko Lönnqvist, M L Savontaus, Leena Peltonen

    Argitaratua 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 nork Päivi Mäkelä‐Bengs, Anu Suomalainen, Anna Majander, Juhani Rapola, Hannu Kalimo, Auli Nuutila, Helena Pihko

    Argitaratua 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 nork Kaisu Nikali, Anu Suomalainen, Juha Saharinen, Mikko Kuokkanen, Johannes N. Spelbrink, Tuula Lönnqvist, Leena Peltonen

    Argitaratua 2005
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