Report for Martinat C

General

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

Phone :

Fax :

Website :

Directory :

References (8)

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 : Barbeau_2023_Int.J.Mol.Sci_24_
ESTHER : Barbeau_2023_Int.J.Mol.Sci_24_
PubMedSearch : Barbeau_2023_Int.J.Mol.Sci_24_
PubMedID: 38003406

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 : Barbeau_2020_Stem.Cell.Res_49_102106
ESTHER : Barbeau_2020_Stem.Cell.Res_49_102106
PubMedSearch : Barbeau_2020_Stem.Cell.Res_49_102106
PubMedID: 33370874

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 : Barbeau_2020_Development_147_
ESTHER : Barbeau_2020_Development_147_
PubMedSearch : Barbeau_2020_Development_147_
PubMedID: 33199350

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 : Maury_2015_Nat.Biotechnol_33_89
ESTHER : Maury_2015_Nat.Biotechnol_33_89
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 : Nedelec_2013_Curr.Gene.Ther_13_111
ESTHER : Nedelec_2013_Curr.Gene.Ther_13_111
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 : Gauthier_2013_Hum.Mol.Genet_22_5188
ESTHER : Gauthier_2013_Hum.Mol.Genet_22_5188
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 : Maury_2012_Bioessays_34_61
ESTHER : Maury_2012_Bioessays_34_61
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 : Marteyn_2011_Cell.Stem.Cell_8_434
ESTHER : Marteyn_2011_Cell.Stem.Cell_8_434
PubMedSearch : Marteyn_2011_Cell.Stem.Cell_8_434
PubMedID: 21458401