DJ-1 is a redox-dependent molecular chaperone that inhibits alpha-synuclein aggregate formationA defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1Cooperative transcription activation by Nurr1 and Pitx3 induces embryonic stem cell maturation to the midbrain dopamine neuron phenotype.Systemic restoration of UBA1 ameliorates disease in spinal muscular atrophyTheiler's virus infection of primary cultures of bone marrow-derived monocytes/macrophagesHigh throughput screening for inhibitors of REST in neural derivatives of human embryonic stem cells reveals a chemical compound that promotes expression of neuronal genes.In vitro modeling of hyperpigmentation associated to neurofibromatosis type 1 using melanocytes derived from human embryonic stem cellsIn Vitro and In Vivo Modulation of Alternative Splicing by the Biguanide MetforminTranslation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.Induced pluripotent stem cells reveal functional differences between drugs currently investigated in patients with hutchinson-gilford progeria syndrome.Human pluripotent stem cells for genetic disease modeling and drug screening.Genetically-modified human pluripotent stem cells: new hopes for the understanding and the treatment of neurological diseases?Erosion of X Chromosome Inactivation in Human Pluripotent Cells Initiates with XACT Coating and Depends on a Specific Heterochromatin Landscape.mTOR-dependent proliferation defect in human ES-derived neural stem cells affected by myotonic dystrophy type 1.Moving towards treatments for spinal muscular atrophy: hopes and limits.Differentiation of nonhuman primate pluripotent stem cells into functional keratinocytes.Combinatorial analysis of developmental cues efficiently converts human pluripotent stem cells into multiple neuronal subtypes.Mutant human embryonic stem cells reveal neurite and synapse formation defects in type 1 myotonic dystrophy.[Human pluripotent stem cells: opening key for pathological modeling].Unique Preservation of Neural Cells in Hutchinson- Gilford Progeria Syndrome Is Due to the Expression of the Neural-Specific miR-9 MicroRNANovel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriersPluripotent Stem Cell-Based Drug Screening Reveals Cardiac Glycosides as Modulators of Myotonic Dystrophy Type 1[The time has come of a therapeutic (re)positioning of the ultra-rare diseases]Influence of parathyroidectomy on mortality in hemodialysis patients: a prospective observational studyExpression of miRNAs from the Imprinted DLK1/DIO3 Locus Signals the Osteogenic Potential of Human Pluripotent Stem Cells
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P50
description
Frans onderzoekster
@nl
chercheuse française et présidente de la FSSCR
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researcher ORCID ID = 0000-0002-5234-1064
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name
Cécile Martinat
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Cécile Martinat
@en
Cécile Martinat
@es
Cécile Martinat
@fr
Cécile Martinat
@nl
Cécile Martinat
@sl
type
label
Cécile Martinat
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Cécile Martinat
@en
Cécile Martinat
@es
Cécile Martinat
@fr
Cécile Martinat
@nl
Cécile Martinat
@sl
prefLabel
Cécile Martinat
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Cécile Martinat
@en
Cécile Martinat
@es
Cécile Martinat
@fr
Cécile Martinat
@nl
Cécile Martinat
@sl
P214
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P4285
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0000 0003 5808 4860
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P269
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P4285
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0000-0002-5234-1064
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1973-09-24T00:00:00Z
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viaf-203173039