H. Nůsková

发表

Mutant Wars2 gene in spontaneously hypertensive rats impairs brown adipose tissue function and predisposes to visceral obesity.

V. Zídek, M. Pravenec, P. Mlejnek, 2017, Physiological research.

Antioxidant enzymes in cerebral cortex of immature rats following experimentally-induced seizures: upregulation of mitochondrial MnSOD (SOD2)

J. Houštěk, J. Folbergrová, P. Ješina, 2013, International Journal of Developmental Neuroscience.

Wars2 is a determinant of angiogenesis

L. Bottolo, E. Petretto, S. Cook, 2016, Nature Communications.

Wars 2 is a determinant of angiogenesis

L. Bottolo, E. Petretto, S. Cook, 2016 .

Stearic acid blunts growth-factor signaling via oleoylation of GNAI proteins

Aubry K. Miller, A. Teleman, B. Brügger, 2021, Nature Communications.

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

V. Melenovský, M. Macek, J. Zeman, 2020, Journal of clinical medicine.

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

J. Kautzner, V. Melenovský, J. Houštěk, 2017, European journal of heart failure.

Evaluation of basic mitochondrial functions using rat tissue homogenates.

J. Houštěk, P. Pecina, Z. Drahota, 2011, Mitochondrion.

Wars2 is a determinant of angiogenesis this article openly available. Please share how this access benefits you. Your story matters

L. Bottolo, E. Petretto, M. Rotival, 2016 .

Competition for cysteine acylation by C16:0 and C18:0 derived lipids is a global phenomenon in the proteome

Aubry K. Miller, A. Teleman, A. Kopp-Schneider, 2022, bioRxiv.

Alteration of structure and function of ATP synthase and cytochrome c oxidase by lack of Fo-a and Cox3 subunits caused by mitochondrial DNA 9205delTA mutation.

S. Seneca, K. Hejzlarová, V. Kaplanová, 2015, The Biochemical journal.

High Molecular Weight Forms of Mammalian Respiratory Chain Complex II

K. Hejzlarová, M. Vrbacký, J. Houštěk, 2013, PloS one.

Succinimidyl oleate, established inhibitor of CD36/FAT translocase inhibits complex III of mitochondrial respiratory chain.

V. Zídek, M. Pravenec, M. Vrbacký, 2010, Biochemical and biophysical research communications.

Cyanide inhibition and pyruvate-induced recovery of cytochrome c oxidase

M. Vrbacký, J. Houštěk, Z. Drahota, 2010, Journal of bioenergetics and biomembranes.

Mitochondrial ATP synthasome: Expression and structural interaction of its components.

M. Vrbacký, J. Houštěk, T. Mráček, 2015, Biochemical and biophysical research communications.

Data on cytochrome c oxidase assembly in mice and human fibroblasts or tissues induced by SURF1 defect

M. Zeviani, M. Vrbacký, J. Houštěk, 2016, Data in brief.

Role of the mitochondrial ATP synthase central stalk subunits γ and δ in the activity and assembly of the mammalian enzyme.

V. Kaplanová, J. Houštěk, T. Mráček, 2012, Biochimica et biophysica acta. Bioenergetics.

Low level of antioxidant capacity biomarkers but not target overexpression predicts vulnerability to ROS-inducing drugs

Aubry K. Miller, M. Muckenthaler, A. Teleman, 2023, bioRxiv.

Biochemical thresholds for pathological presentation of ATP synthase deficiencies.

J. Houštěk, T. Mráček, P. Pecina, 2019, Biochemical and biophysical research communications.

Tissue- and species-specific differences in cytochrome c oxidase assembly induced by SURF1 defects

M. Zeviani, M. Vrbacký, J. Houštěk, 2016, Biochimica et biophysica acta.

Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1 epsilon subunit.

V. Kaplanová, V. Havlíčková, J. Houštěk, 2010, Human molecular genetics.

Knockout of Tmem70 alters biogenesis of ATP synthase and leads to embryonal lethality in mice.

M. Vrbacký, J. Houštěk, P. Hozák, 2016, Human Molecular Genetics.

Peroxidative damage of mitochondrial respiration is substrate-dependent.

Z. Červinková, H. Rauchová, Z. Drahota, 2008, Physiological research.

Pharmacological inhibition of fatty-acid oxidation synergistically enhances the effect of l-asparaginase in childhood ALL cells

G. Kroemer, I. Heřmanová, D. Kavan, 2016, Leukemia.

Nuclear genetic defects of mitochondrial ATP synthase.

K. Hejzlarová, M. Vrbacký, V. Kaplanová, 2014, Physiological research.

Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry

M. Tesařová, J. Zeman, J. Houštěk, 2014, BBA clinical.

Compensatory upregulation of respiratory chain complexes III and IV in isolated deficiency of ATP synthase due to TMEM70 mutation.

K. Hejzlarová, S. Kmoch, J. Houštěk, 2012, Biochimica et biophysica acta.

Knockout of Tmem70 alters biogenesis of ATP synthase and leads to embryonal lethality in mice.

M. Vrbacký, J. Houštěk, P. Hozák, 2016, Human Molecular Genetics.

Knockdown of F1 epsilon subunit decreases mitochondrial content of ATP synthase and leads to accumulation of subunit c.

V. Kaplanová, V. Havlíčková, J. Houštěk, 2010, Biochimica et biophysica acta.

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

M. Vrbacký, V. Kaplanová, J. Houštěk, 2020, bioRxiv.

L-Asparaginase Causes Metabolic Reprogramming in ALL Cells

I. Heřmanová, D. Kavan, A. Carracedo, 2014 .

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

M. Vrbacký, V. Kaplanová, J. Houštěk, 2019, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.