vu0422288 and Disease-Models--Animal

vu0422288 has been researched along with Disease-Models--Animal* in 1 studies

Other Studies

1 other study(ies) available for vu0422288 and Disease-Models--Animal

Article	Year
mGlu Science translational medicine, 2017, 08-16, Volume: 9, Issue:403 Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the Topics: Animals; Apnea; Autopsy; CA1 Region, Hippocampal; Cognition; Disease Models, Animal; Dose-Response Relationship, Drug; Female; Humans; Long-Term Potentiation; Male; Memory; Methyl-CpG-Binding Protein 2; Mice; Motor Cortex; Neuronal Plasticity; Phenotype; Picolinic Acids; Rats, Sprague-Dawley; Receptors, Metabotropic Glutamate; Respiration; Rett Syndrome; RNA, Messenger; Social Behavior; Transcription, Genetic	2017

Article

Year

Science translational medicine, 2017, 08-16, Volume: 9, Issue:403

Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in the

Topics: Animals; Apnea; Autopsy; CA1 Region, Hippocampal; Cognition; Disease Models, Animal; Dose-Response Relationship, Drug; Female; Humans; Long-Term Potentiation; Male; Memory; Methyl-CpG-Binding Protein 2; Mice; Motor Cortex; Neuronal Plasticity; Phenotype; Picolinic Acids; Rats, Sprague-Dawley; Receptors, Metabotropic Glutamate; Respiration; Rett Syndrome; RNA, Messenger; Social Behavior; Transcription, Genetic

2017