Report for Chelly J

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References (7)

Title : Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment - Quartier_2019_Hum.Mutat_40_2021
Author(s) : Quartier A , Courraud J , Thi Ha T , McGillivray G , Isidor B , Rose K , Drouot N , Savidan MA , Feger C , Jagline H , Chelly J , Shaw M , Laumonnier F , Gecz J , Mandel JL , Piton A
Ref : Hum Mutat , 40 :2021 , 2019
Abstract : Quartier_2019_Hum.Mutat_40_2021
ESTHER : Quartier_2019_Hum.Mutat_40_2021
PubMedSearch : Quartier_2019_Hum.Mutat_40_2021
PubMedID: 31184401
Gene_locus related to this paper: human-NLGN3

Title : X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family - Laumonnier_2004_Am.J.Hum.Genet_74_552
Author(s) : Laumonnier F , Bonnet-Brilhault F , Gomot M , Blanc R , David A , Moizard MP , Raynaud M , Ronce N , Lemonnier E , Calvas P , Laudier B , Chelly J , Fryns JP , Ropers HH , Hamel BC , Andres C , Barthelemy C , Moraine C , Briault S
Ref : American Journal of Human Genetics , 74 :552 , 2004
Abstract : Laumonnier_2004_Am.J.Hum.Genet_74_552
ESTHER : Laumonnier_2004_Am.J.Hum.Genet_74_552
PubMedSearch : Laumonnier_2004_Am.J.Hum.Genet_74_552
PubMedID: 14963808
Gene_locus related to this paper: human-NLGN4X

Title : In vitro follicular growth affects oocyte imprinting establishment in mice - Kerjean_2003_Eur.J.Hum.Genet_11_493
Author(s) : Kerjean A , Couvert P , Heams T , Chalas C , Poirier K , Chelly J , Jouannet P , Paldi A , Poirot C
Ref : Eur J Hum Genet , 11 :493 , 2003
Abstract : Kerjean_2003_Eur.J.Hum.Genet_11_493
ESTHER : Kerjean_2003_Eur.J.Hum.Genet_11_493
PubMedSearch : Kerjean_2003_Eur.J.Hum.Genet_11_493
PubMedID: 12825069

Title : Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons - Francis_1999_Neuron_23_247
Author(s) : Francis F , Koulakoff A , Boucher D , Chafey P , Schaar B , Vinet MC , Friocourt G , McDonnell N , Reiner O , Kahn A , McConnell SK , Berwald-Netter Y , Denoulet P , Chelly J
Ref : Neuron , 23 :247 , 1999
Abstract : Francis_1999_Neuron_23_247
ESTHER : Francis_1999_Neuron_23_247
PubMedSearch : Francis_1999_Neuron_23_247
PubMedID: 10399932

Title : A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome - des Portes_1998_Cell_92_51
Author(s) : des Portes V , Pinard JM , Billuart P , Vinet MC , Koulakoff A , Carrie A , Gelot A , Dupuis E , Motte J , Berwald-Netter Y , Catala M , Kahn A , Beldjord C , Chelly J
Ref : Cell , 92 :51 , 1998
Abstract : des Portes_1998_Cell_92_51
ESTHER : des Portes_1998_Cell_92_51
PubMedSearch : des Portes_1998_Cell_92_51
PubMedID: 9489699

Title : Dystrophin gene transcribed from different promoters in neuronal and glial cells - Chelly_1990_Nature_344_64
Author(s) : Chelly J , Hamard G , Koulakoff A , Kaplan JC , Kahn A , Berwald-Netter Y
Ref : Nature , 344 :64 , 1990
Abstract : Chelly_1990_Nature_344_64
ESTHER : Chelly_1990_Nature_344_64
PubMedSearch : Chelly_1990_Nature_344_64
PubMedID: 2406613

Title : Quantitative estimation of minor mRNAs by cDNA-polymerase chain reaction. Application to dystrophin mRNA in cultured myogenic and brain cells - Chelly_1990_Eur.J.Biochem_187_691
Author(s) : Chelly J , Montarras D , Pinset C , Berwald-Netter Y , Kaplan JC , Kahn A
Ref : European Journal of Biochemistry , 187 :691 , 1990
Abstract : Chelly_1990_Eur.J.Biochem_187_691
ESTHER : Chelly_1990_Eur.J.Biochem_187_691
PubMedSearch : Chelly_1990_Eur.J.Biochem_187_691
PubMedID: 2406139