Full name : Martinat Cecile
First name : Cecile
Mail : INSERM UMR 861, I-Stem AFM, Evry Cedex 91030
Zip Code :
City :
Country : France
Email : cmartinat@istem.fr
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Comment
Title : Molecular Analysis of a Congenital Myasthenic Syndrome Due to a Pathogenic Variant Affecting the C-Terminus of ColQ - Barbeau_2023_Int.J.Mol.Sci_24_ |
Author(s) : Barbeau S , Semprez F , Dobbertin A , Merriadec L , Roussange F , Eymard B , Sternberg D , Fournier E , Karasoy H , Martinat C , Legay C |
Ref : Int J Mol Sci , 24 : , 2023 |
Abstract : |
PubMedSearch : Barbeau_2023_Int.J.Mol.Sci_24_ |
PubMedID: 38003406 |
Title : Building neuromuscular junctions in vitro - Barbeau_2020_Development_147_ |
Author(s) : Barbeau S , Tahraoui-Bories J , Legay C , Martinat C |
Ref : Development , 147 : , 2020 |
Abstract : |
PubMedSearch : Barbeau_2020_Development_147_ |
PubMedID: 33199350 |
Title : Generation of a human induced pluripotent stem cell line (iPSC) from peripheral blood mononuclear cells of a patient with a myasthenic syndrome due to mutation in COLQ - Barbeau_2020_Stem.Cell.Res_49_102106 |
Author(s) : Barbeau S , Desprat R , Eymard B , Martinat C , Lemaitre JM , Legay C |
Ref : Stem Cell Res , 49 :102106 , 2020 |
Abstract : |
PubMedSearch : Barbeau_2020_Stem.Cell.Res_49_102106 |
PubMedID: 33370874 |
Title : Combinatorial analysis of developmental cues efficiently converts human pluripotent stem cells into multiple neuronal subtypes - Maury_2015_Nat.Biotechnol_33_89 |
Author(s) : Maury Y , Come J , Piskorowski RA , Salah-Mohellibi N , Chevaleyre V , Peschanski M , Martinat C , Nedelec S |
Ref : Nat Biotechnol , 33 :89 , 2015 |
Abstract : |
PubMedSearch : Maury_2015_Nat.Biotechnol_33_89 |
PubMedID: 25383599 |
Title : Genetically-modified human pluripotent stem cells: new hopes for the understanding and the treatment of neurological diseases? - Nedelec_2013_Curr.Gene.Ther_13_111 |
Author(s) : Nedelec S , Onteniente B , Peschanski M , Martinat C |
Ref : Curr Gene Therapy , 13 :111 , 2013 |
Abstract : |
PubMedSearch : Nedelec_2013_Curr.Gene.Ther_13_111 |
PubMedID: 23444870 |
Title : A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1 - Gauthier_2013_Hum.Mol.Genet_22_5188 |
Author(s) : Gauthier M , Marteyn A , Denis JA , Cailleret M , Giraud-Triboult K , Aubert S , Lecuyer C , Marie J , Furling D , Vernet R , Yanguas C , Baldeschi C , Pietu G , Peschanski M , Martinat C |
Ref : Hum Mol Genet , 22 :5188 , 2013 |
Abstract : |
PubMedSearch : Gauthier_2013_Hum.Mol.Genet_22_5188 |
PubMedID: 23922231 |
Title : Human pluripotent stem cells for disease modelling and drug screening - Maury_2012_Bioessays_34_61 |
Author(s) : Maury Y , Gauthier M , Peschanski M , Martinat C |
Ref : Bioessays , 34 :61 , 2012 |
Abstract : |
PubMedSearch : Maury_2012_Bioessays_34_61 |
PubMedID: 22038777 |
Title : Mutant human embryonic stem cells reveal neurite and synapse formation defects in type 1 myotonic dystrophy - Marteyn_2011_Cell.Stem.Cell_8_434 |
Author(s) : Marteyn A , Maury Y , Gauthier MM , Lecuyer C , Vernet R , Denis JA , Pietu G , Peschanski M , Martinat C |
Ref : Cell Stem Cell , 8 :434 , 2011 |
Abstract : |
PubMedSearch : Marteyn_2011_Cell.Stem.Cell_8_434 |
PubMedID: 21458401 |