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Nature Genetics|August 19, 2003
Mitochondrial DNA modifies cognition in interaction with the nuclear genome and age in micePierre L Roubertoux, Frans Sluyter, Michèle Carlier, et al.Behavior Genetics|May 5, 2011
From molecules to behavior: lessons from the study of rare genetic disordersPierre L Roubertoux, Petrus J de VriesTwin Research : the Official Journal of the International Society for Twin Studies|April 1, 2004
Failure to obtain reliable retrospective determination of chorion type using parent information: confirmation with French dataMichèle Carlier, Elisabeth SpitzTranslational Psychiatry|March 16, 2022
Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviorsXavier Caubit, Paolo Gubellini, Pierre L Roubertoux, et al.BMC Neuroscience|May 26, 2011
Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brainNicolas Panayotis, Adeline Ghata, Laurent Villard, et al.Laterality|October 30, 2004
Measuring handedness: a validation study of Bishop's reaching card testAnne-Lise Doyen, Michèle CarlierBehavior Genetics|March 9, 2006
Mouse models of cognitive disorders in trisomy 21: a reviewZohra Sérégaza, Pierre L Roubertoux, Marc Jamon, et al.Behavioural Brain Research|August 18, 2010
Progressive motor and respiratory metabolism deficits in post-weaning Mecp2-null male miceMichel Pratte, Nicolas Panayotis, Adeline Ghata, et al.Brain : a Journal of Neurology|October 31, 2022
Imbalance of NRG1-ERBB2/3 signalling underlies altered myelination in Charcot-Marie-Tooth disease 4HLara El-Bazzal, Adeline Ghata, Clothilde Estève, et al.Plos One|April 13, 2012
Tracking subtle stereotypes of children with trisomy 21: from facial-feature-based to implicit stereotypingClaire Enea-Drapeau, Michèle Carlier, Pascal HuguetPageof 5