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A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvementThe DNA mismatch-repair MLH3 protein interacts with MSH4 in meiotic cells, supporting a role for this MutL homolog in mammalian meiotic recombinationMSH4 acts in conjunction with MLH1 during mammalian meiosisExpression and chromosomal localization of the Requiem geneMutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe EncephalopathyInactivation of Pif1 helicase causes a mitochondrial myopathy in micehMSH5 is a nucleocytoplasmic shuttling protein whose stability depends on its subcellular localization.CRM1-dependent nuclear export and dimerization with hMSH5 contribute to the regulation of hMSH4 subcellular localization.CHCHD10 mutations promote loss of mitochondrial cristae junctions with impaired mitochondrial genome maintenance and inhibition of apoptosis.Partial hypoxia as a cause of radioresistance in a human tumor xenograft: its influence illustrated by the sensitizing effect of misonidazole and hyperbaric oxygen.Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisReply: High prevalence of CHCHD10 mutations in patients with frontotemporal dementia from ChinaReply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis.Reply: Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.Reply: Are CHCHD10 mutations indeed associated with familial amyotrophic lateral sclerosis?Radiosensitization by the combination of etanidazole (SR-2508) and pimonidazole (Ro 03-8799) in human tumor xenografts.Ro 03-8799: preferential relative uptake in human tumor xenografts compared to a murine tumor: comparison with SR-2508.Reply: Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?Association between MSH4 (MutS homologue 4) and the DNA strand-exchange RAD51 and DMC1 proteins during mammalian meiosis.The mouse homologs of human GIF, DDB1, and CFL1 genes are located on Chromosome 19Glutathione and cysteine levels in human tumour biopsies
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description
hulumtuese
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researcher
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wetenschapper
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հետազոտող
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name
Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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Francoise Lespinasse
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0000-0001-7710-0649