F. Lespinasse

发表

MSH4 acts in conjunction with MLH1 during mammalian meiosis

D. Walpita, C. Desnuelle, V. Paquis‐Flucklinger, 2000, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice.

J. Kolesar, B. Kaufman, J. Ricci, 2016, Mitochondrion.

Association between MSH4 (MutS homologue 4) and the DNA strand-exchange RAD51 and DMC1 proteins during mammalian meiosis.

V. Paquis‐Flucklinger, P. Moens, S. Santucci-Darmanin, 2004, Molecular human reproduction.

CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis

E. Génin, P. Yu-Wai-Man, J. Ricci, 2015, EMBO molecular medicine.

NeuroKit2: A Python toolbox for neurophysiological signal processing.

Jan C. Brammer, D. Makowski, S. H. A. Chen, 2021, Behavior research methods.

The DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombination.

S. Santucci-Darmanin, F. Lespinasse, P. Gaudray, 2002, Human molecular genetics.

CRM1-dependent nuclear export and dimerization with hMSH5 contribute to the regulation of hMSH4 subcellular localization.

S. Santucci-Darmanin, F. Lespinasse, S. Neyton, 2007, Experimental cell research.

Mitochondrial defect in muscle precedes neuromuscular junction degeneration and motor neuron death in CHCHD10S59L/+ mouse

E. Génin, D. Bohl, J. Ricci, 2019, Acta Neuropathologica.

hMSH5 is a nucleocytoplasmic shuttling protein whose stability depends on its subcellular localization

S. Santucci-Darmanin, F. Lespinasse, P. Staccini, 2010, Nucleic acids research.

Expression and chromosomal localization of the Requiem gene

C. Larsson, B. Teh, N. Copeland, 1998, Mammalian Genome.

Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

Comparative mapping of two adjacent regions of MMU19 with their human counterpart on HSA11q13

J. Guénet, G. Carle, C. Poirier, 1998, Cytogenetic and Genome Research.

Loss of MICOS complex integrity and mitochondrial damage, but not TDP-43 mitochondrial localisation, are likely associated with severity of CHCHD10-related diseases

E. Génin, J. Ricci, B. Udd, 2018, Neurobiology of Disease.

Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

A. Brice, P. Yu-Wai-Man, J. Pouget, 2015, Brain : a journal of neurology.

Burning characteristics of aluminum-air flames

F. Halter, C. Chauveau, V. Lago, 2017 .

Reply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from China.

E. Génin, A. Brice, P. Yu-Wai-Man, 2016, Brain : a journal of neurology.

SLP2/prohibitins aggregates and instability of the PHB complex are key elements in CHCHD10S59L-related disease

S. Bannwarth, F. Lespinasse, S. Lacas‐Gervais, 2021, bioRxiv.

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement.

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

The human MSH5 (MutSHomolog 5) protein localizes to mitochondria and protects the mitochondrial genome from oxidative damage.

A. Rötig, J. Ricci, S. Bannwarth, 2012, Mitochondrion.

NeuroKit2: A Python toolbox for neurophysiological signal processing

Jan C. Brammer, D. Makowski, Christopher Schölzel, 2020, Behavior Research Methods.

Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy

Robert W. Taylor, J. Gagneur, E. Génin, 2016, American journal of human genetics.

Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?

E. Génin, A. Brice, P. Yu-Wai-Man, 2015, Brain : a journal of neurology.

Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.

E. Génin, A. Brice, P. Yu-Wai-Man, 2015, Brain : a journal of neurology.

Reply : CHCHD 10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis

E. Génin, A. Brice, P. Yu-Wai-Man, 2015 .

Reply : Is CHCHD 10 Pro 34 Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis ?

E. Génin, A. Brice, P. Yu-Wai-Man, 2015 .

Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

Reply : Are CHCHD 10 mutations indeed associated with familial amyotrophic lateral sclerosis ?

E. Génin, A. Brice, P. Yu-Wai-Man, 2014 .

The mouse homologs of human GIF, DDB1, and CFL1 genes are located on Chromosome 19

G. Carle, C. Poirier, F. Lespinasse, 1998, Mammalian Genome.

CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability.

T. Wai, S. Bannwarth, F. Lespinasse, 2022, Brain : a journal of neurology.

The human MSH5 (MutSHomolog 5) protein localizes to mitochondria and protects the mitochondrial genome from oxidative damage.

A. Rötig, J. Ricci, S. Bannwarth, 2012, Mitochondrion.

CHCHD10S59L/+ mouse model: Behavioral and neuropathological features of frontotemporal dementia

F. Lespinasse, V. Paquis-Flucklinger, Alessandra Mauri-Crouzet, 2024, Neurobiology of Disease.

Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?

E. Génin, A. Brice, P. Yu-Wai-Man, 2014, Brain : a journal of neurology.

Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

P. Yu-Wai-Man, J. Pouget, I. Le Ber, 2015, Brain : a journal of neurology.