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List of works by Francoise Lespinasse

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

scientific article

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

scientific article published on 15 October 2004

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

scientific article

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

scientific article

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

scientific article published on January 1, 1998

Expression and chromosomal localization of the Requiem gene

scientific journal article

Glutathione and cysteine levels in human tumour biopsies

scientific article published in July 1990

Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice

scientific article

MSH4 acts in conjunction with MLH1 during mammalian meiosis

scientific article (publication date: August 2000)

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

scientific journal article

Partial hypoxia as a cause of radioresistance in a human tumor xenograft: its influence illustrated by the sensitizing effect of misonidazole and hyperbaric oxygen.

scientific article published on August 1986

Radiosensitization by the combination of etanidazole (SR-2508) and pimonidazole (Ro 03-8799) in human tumor xenografts

scientific article published in November 1991

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

scientific article published on 12 February 2015

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

scientific article published on 27 October 2014

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

scientific article published on 8 January 2015

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

scientific article published on 30 December 2015

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

scientific article published on 7 May 2015

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

scientific article published on 26 September 2014

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

scientific article published on 11 August 2014

Ro 03-8799: preferential relative uptake in human tumor xenografts compared to a murine tumor: comparison with SR-2508.

scientific article published in April 1989

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

scientific article

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

scientific article published in April 1998

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

scientific article

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