C. Pujol

发表

The CoQH2/CoQ Ratio Serves as a Sensor of Respiratory Chain Efficiency.

P. Navas, J. Enríquez, E. Calvo, 2016, Cell reports.

Import of tRNAs and aminoacyl-tRNA synthetases into mitochondria

L. Marechal-Drouard, A. Duchêne, C. Pujol, 2009, Current Genetics.

Dual-targeted tRNA-dependent amidotransferase ensures both mitochondrial and chloroplastic Gln-tRNAGln synthesis in plants

M. Bailly, H. Becker, D. Kern, 2008, Proceedings of the National Academy of Sciences.

Hereditary spastic paraplegia type 56: what a mouse can tell – a narrative review

C. Pujol, L. Parodi, 2022, Journal of Bio-X Research.

Characterization of Arabidopsis thaliana genes encoding functional homologues of the yeast metal chaperone Cox19p, involved in cytochrome c oxidase biogenesis

D. Gonzalez, G. Bonnard, E. Welchen, 2007, Plant Molecular Biology.

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.

Simon C. Potter, Miguel Ángel Martínez, C. Spencer, 2016, American journal of human genetics.

How can organellar protein N-terminal sequences be dual targeting signals? In silico analysis and mutagenesis approach.

L. Marechal-Drouard, A. Duchêne, C. Pujol, 2007, Journal of molecular biology.

MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy

T. Wai, A. Slama, P. Gaignard, 2022, Brain : a journal of neurology.

The Genetics of Rhizobium Host Range Control: Allelic and Non-Allelic Variation

G. Truchet, J. Dénarié, F. Debellé, 1995 .

Inhibition of Lysosome Membrane Recycling Causes Accumulation of Gangliosides that Contribute to Neurodegeneration

A. Durr, B. Colsch, A. Brice, 2003, Cell reports.

FGF21 modulates mitochondrial stress response in cardiomyocytes only under mild mitochondrial dysfunction

A. Trifunovic, Karolina Szczepanowska, Harshita Kaul, 2022, Science advances.

Defining the determinants for dual targeting of amino acyl-tRNA synthetases to mitochondria and chloroplasts.

A. Duchêne, E. Glaser, A. Berglund, 2009, Journal of molecular biology.

Tissue-specific loss of DARS2 activates stress responses independently of respiratory chain deficiency in the heart.

E. Rugarli, R. Wibom, A. Trifunovic, 2014, Cell metabolism.

The mitochondrial seryl-tRNA synthetase SARS2 modifies onset in spastic paraplegia type 4.

A. Durr, C. Depienne, A. Brice, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Implication of folate deficiency in CYP2U1 loss of function

A. Durr, F. Lamari, S. Picaud, 2021, The Journal of experimental medicine.

Succinate Dehydrogenase Upregulation Destabilize Complex I and Limits the Lifespan of gas-1 Mutant

Jürgen Hench, J. Hench, L. Baumann, 2013, PloS one.

CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56

A. Durr, F. Rivier, G. Stevanin, 2018, Human mutation.

Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56

A. Durr, C. Orssaud, G. Stevanin, 2020, Journal of internal medicine.

A Tissue-Specific Approach to the Analysis of Metabolic Changes in Caenorhabditis elegans

S. Frank, M. Tolnay, S. Brodesser, 2011, PloS one.

Tissue-specific loss of DARS2 activates stress responses independently of respiratory chain deficiency in the heart.

E. Rugarli, R. Wibom, A. Trifunovic, 2014, Cell metabolism.