M. Calvaruso

发表

Glutamine oxidation maintains the TCA cycle and cell survival during impaired mitochondrial pyruvate transport.

R. Deberardinis, J. Rutter, Lei Jiang, 2014, Molecular cell.

Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells

M. Attimonelli, P. Lollini, V. Giorgio, 2013, Cancer & Metabolism.

NOA1 is an essential GTPase required for mitochondrial protein synthesis

S. Mundlos, M. Vingron, M. Schuelke, 2011, Molecular biology of the cell.

Electrophoresis techniques to investigate defects in oxidative phosphorylation.

J. Smeitink, L. Nijtmans, M. Calvaruso, 2008, Methods.

Analysis of the mitochondrial proteome of cybrid cells harbouring a truncative mitochondrial DNA mutation in respiratory complex I.

L. Zolla, A. Porcelli, A. Timperio, 2014, Molecular bioSystems.

Mitochondrial complex III stabilizes complex I in the absence of NDUFS4 to provide partial activity.

R. Palmiter, J. Smeitink, P. Willems, 2012, Human molecular genetics.

Mitochondrial complex I assembly in man and mouse

M. Calvaruso, 2013 .

Genome-wide expression profiling and functional characterization of SCA28 lymphoblastoid cell lines reveal impairment in cell growth and activation of apoptotic pathways

S. Gustincich, A. Durr, S. Forlani, 2013, BMC Medical Genomics.

The Assembly of Human Complex I

L. Nijtmans, M. Calvaruso, J. Nouws, 2012 .

Metabolic plasticity maintains proliferation in pyruvate dehydrogenase deficient cells

Robert A. Egnatchik, R. Deberardinis, P. Scaglioni, 2015, Cancer & metabolism.

Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment.

P. Lollini, V. Giorgio, A. Porcelli, 2014, Human molecular genetics.

Respiratory complex I is essential to induce a Warburg profile in mitochondria-defective tumor cells

M. Attimonelli, P. Lollini, V. Giorgio, 2013, Cancer & metabolism.

Complex I impairment in mitochondrial diseases and cancer: parallel roads leading to different outcomes.

A. Porcelli, M. Calvaruso, G. Gasparre, 2013, The international journal of biochemistry & cell biology.

Chronic innate immune activation of TBK1 suppresses mTORC1 activity and dysregulates cellular metabolism

Nan Yan, R. Deberardinis, N. Dobbs, 2017, Proceedings of the National Academy of Sciences.

Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions

G. Rizzo, A. Torroni, P. Barboni, 2013, Biochimica et biophysica acta.

Metabolic consequences of NDUFS4 gene deletion in immortalized mouse embryonic fibroblasts.

R. Rodenburg, A. de Groof, B. Wieringa, 2012, Biochimica et biophysica acta.

Random point mutations with major effects on protein-coding genes are the driving force behind premature aging in mtDNA mutator mice.

Jan Nedergaard, Barbara Cannon, Daniel Edgar, 2009, Cell metabolism.

The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexes.

F. Daldal, A. Martinuzzi, J. Vissing, 2013, Human molecular genetics.

A unique combination of rare mitochondrial ribosomal RNA variants affects the kinetics of complex I assembly.

A. Porcelli, M. Calvaruso, G. Gasparre, 2016, The international journal of biochemistry & cell biology.

New mitochondrial tRNA HIS mutation in a family with lactic acidosis and stroke-like episodes (MELAS).

R. Rodenburg, J. Smeitink, L. Nijtmans, 2011, Mitochondrion.

Alterations in the supramolecular interactions of respiratory chain complexes and enhanced superoxide production by the cytochrome b Y278C mutation which causes a multisystem disorder

F. Daldal, A. Martinuzzi, J. Vissing, 2012 .

Metabolic consequences of NDUFS4 gene deletion in immortalized mouse embryonic fibroblasts.

R. Rodenburg, A. de Groof, B. Wieringa, 2012, Biochimica et biophysica acta.

Different mtDNA mutations modify tumor progression in dependence of the degree of respiratory complex I impairment.

P. Lollini, V. Giorgio, A. Porcelli, 2014, Human molecular genetics.