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Hana Nůsková

Academy of Sciences of the Czech Republic

41

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537

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MLQ is responsible for stabilisation of subunit a in the holoenzyme of mammalian ATP synthase

2020 bioRxiv
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Desminopathy: Novel Desmin Variants, a New Cardiac Phenotype, and Further Evidence for Secondary Mitochondrial Dysfunction.

2020 Journal of Clinical Medicine
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TMEM70 facilitates biogenesis of mammalian ATP synthase by promoting subunit c incorporation into the rotor structure of the enzyme

2019 The FASEB Journal
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ATP synthase assembly defect and liver damage are major pathology hallmarks of inducible Tmem70 knockout in adult mice

2018 Biochimica et Biophysica Acta
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Knockout of DAPIT protein disrupts ATP synthase oligomerisation and has a profound role in regulation of glucose homeostasis

2018 Biochimica et Biophysica Acta
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mTORC1 inhibition affects mitochondrial morphology

2018 Biochimica et Biophysica Acta
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Mutant Wars2 Gene in Spontaneously Hypertensive Rats Impairs Brown Adipose Tissue Function and Predisposes to Visceral Obesity

2017 Physiological Research
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Myocardial iron content and mitochondrial function in human heart failure: a direct tissue analysis

2017 European Journal of Heart Failure
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Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects

2016 Biochimica et Biophysica Acta
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MLQ protein regulates association of mitochondrially encoded subunits Fo-a and A6L with ATP synthase complex

2016 Journal of World Mitochondria Society
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