Search Results - "Rodinova, Marie"
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Loss of Mitochondrial AAA Proteases AFG3L2 and YME1L Impairs Mitochondrial Structure and Respiratory Chain Biogenesis
Published in International journal of molecular sciences (07-12-2018)“…Mitochondrial protein quality control is crucial for the maintenance of correct mitochondrial homeostasis. It is ensured by several specific mitochondrial…”
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Increased nuclear DNA damage precedes mitochondrial dysfunction in peripheral blood mononuclear cells from Huntington’s disease patients
Published in Scientific reports (29-06-2018)“…Huntington’s disease (HD) is a progressive neurodegenerative disorder primarily affecting the basal ganglia and is caused by expanded CAG repeats in the…”
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Deterioration of mitochondrial bioenergetics and ultrastructure impairment in skeletal muscle of a transgenic minipig model in the early stages of Huntington's disease
Published in Disease models & mechanisms (01-07-2019)“…Skeletal muscle wasting and atrophy is one of the more severe clinical impairments resulting from the progression of Huntington's disease (HD). Mitochondrial…”
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Isolation and Characterization of Small Extracellular Vesicles from Porcine Blood Plasma, Cerebrospinal Fluid, and Seminal Plasma
Published in Proteomes (25-04-2019)“…Extracellular vesicles (EVs) are a highly attractive subject of biomedical research as possible carriers of nucleic acid and protein biomarkers. EVs released…”
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A transgenic minipig model of Huntington's disease shows early signs of behavioral and molecular pathologies
Published in Disease models & mechanisms (01-10-2018)“…Huntington's disease (HD) is a monogenic, progressive, neurodegenerative disorder with currently no available treatment. The Libechov transgenic minipig model…”
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First person – Marie Rodinova
Published in Disease models & mechanisms (01-07-2019)“…First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms, helping early-career…”
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The mammalian homologue of yeast Afg1 ATPase (lactation elevated 1) mediates degradation of nuclear-encoded complex IV subunits
Published in Biochemical journal (15-03-2016)“…Mitochondrial protein homeostasis is crucial for cellular function and integrity and is therefore maintained by several classes of proteins possessing…”
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A37 Buccal respiratory chain complexes I and IV quantities in huntington’s disease patients
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2018)“…Alterations in mitochondrial parameteres are an important hallmark of Huntington’s disease (HD). Given the ubiquitous expression of mutant huntingtin raises…”
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C17 Increased mitochondrial number, cellular stress and glycogen accumulation in heart of minipig model transgenic for N-terminal part of human mutated huntingtin
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2016)“…BackgroundMinipig model transgenic for N-terminal part of human mutated huntingtin (TgHD) created in Libechov allows us to study the development of…”
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B12 Longitudinal view of mitochondrial bioenergetics in skeletal muscle of premanifest transgenic minipig model for huntington’s disease
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2018)“…BackgroundSkeletal muscle wasting and atrophy is one of the severe clinical impairment connected with progression of Huntington’s disease (HD). Mitochondrial…”
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C18 The hunt for biomarkers in presymptomatic large animal model: mitochondrial metabolism in spermatozoa of transgenic minipigs modelling huntington’s disease
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2016)“…BackgroundLarge-animal minipig transgenic model of Huntington’s disease (HD), carrying N-terminal part of human mutated huntingtin, was developed in Libechov…”
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Mitochondrial Metabolism in a Large-Animal Model of Huntington Disease: The Hunt for Biomarkers in the Spermatozoa of Presymptomatic Minipigs
Published in Neuro-degenerative diseases (01-01-2017)“…Huntington disease (HD) is a fatal neurodegenerative disorder involving reduced muscle coordination, mental and behavioral changes, and testicular…”
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A17 Targeting mitophagy in huntington’s disease patients’ fibroblasts
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2021)“…Huntington’s disease (HD) belongs to a group of neurodegenerative diseases characterized by features, such as the accumulation of aggregates of misfolded…”
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PP100 - Changes in hydrogen sulfide production in cystathionine beta-synthase deficiency
Published in Nitric oxide (01-05-2015)Get full text
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Changes in hydrogen sulfide production in cystathionine beta-synthase deficiency
Published in Nitric oxide (01-05-2015)Get full text
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