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Neurobiology of Disease, ISSN 0969-9961, 03/2018, Volume 111, pp. 91 - 101
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2011, Volume 88, Issue 4, pp. 422 - 432
Journal Article
Cell Stem Cell, ISSN 1934-5909, 2011, Volume 9, Issue 5, pp. 447 - 462
Journal Article
Brain, ISSN 0006-8950, 06/2015, Volume 138, Issue 6, pp. 1613 - 1628
Malformations of cortical development containing dysplastic neuronal and glial elements, including hemimegalencephaly and focal cortical dysplasia, are common... 
Childhood epilepsy | Molecular genetics | Malformations of cortical development | Brain development | molecular genetics | brain development | MAMMALIAN TARGET | LHERMITTE-DUCLOS-DISEASE | RILEY-RUVALCABA-SYNDROME | NEUROSCIENCES | CLINICAL NEUROLOGY | DOMINANT SKIN DISORDERS | PTEN GENE | EPIDERMAL NEVI | malformations of cortical development | childhood epilepsy | COWDEN SYNDROME | INTRACTABLE EPILEPSY | ACTIVATING MUTATIONS | HAMARTOMA TUMOR SYNDROME | Neuroimaging | Megalencephaly - pathology | Ribosomal Protein S6 Kinases - metabolism | Humans | Child, Preschool | Hemimegalencephaly - metabolism | Infant | Male | Brain - abnormalities | Proto-Oncogene Proteins c-akt - genetics | Brain - metabolism | Female | Malformations of Cortical Development - pathology | Proto-Oncogene Proteins c-akt - metabolism | Child | Infant, Newborn | Megalencephaly - genetics | PTEN Phosphohydrolase - genetics | Genetic Predisposition to Disease - genetics | Malformations of Cortical Development - metabolism | Hemimegalencephaly - pathology | Megalencephaly - metabolism | Signal Transduction - genetics | Malformations of Cortical Development - genetics | Phosphatidylinositol 3-Kinases - genetics | Magnetic Resonance Imaging | Class I Phosphatidylinositol 3-Kinases | Adolescent | Mutation | Hemimegalencephaly - genetics | Index Medicus | Abridged Index Medicus | Original
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 10/2014, Volume 111, Issue 42, pp. E4468 - E4477
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2012, Volume 7, Issue 8, pp. e42504 - e42504
Etiology of aberrant social behavior consistently points to a strong polygenetic component involved in fundamental developmental pathways, with the potential... 
C-OXIDASE DEFICIENCY | LHERMITTE-DUCLOS-DISEASE | ALZHEIMERS-DISEASE | COPY NUMBER | DNA-DAMAGE | BIOLOGY | TUMOR-SUPPRESSOR GENE | FRAGILE-X-SYNDROME | RILEY-RUVALCABA-SYNDROME | AUTISM SPECTRUM DISORDERS | TRANSCRIPTION FACTOR | Megalencephaly - genetics | Haploinsufficiency - genetics | PTEN Phosphohydrolase - genetics | Social Behavior Disorders - genetics | Cerebellar Cortex - metabolism | Cerebellum - metabolism | HCT116 Cells | Humans | Tumor Suppressor Protein p53 - metabolism | PTEN Phosphohydrolase - metabolism | Male | Mitochondria - metabolism | Social Behavior Disorders - metabolism | Tumor Suppressor Protein p53 - genetics | Electron Transport Complex IV - metabolism | Mice, Knockout | Behavior, Animal | Hippocampus - metabolism | Animals | Mitochondria - genetics | Female | Mice | Neurons - metabolism | Autism | Phosphatases | Neurons | Genetic aspects | Behavior | Social aspects | Tumor proteins | Cerebellum | Cytochrome | Oxidative stress | Veterinary colleges | GTP-binding protein | p53 Protein | Cytochrome-c oxidase | Disabilities | Homology | AKT protein | Mitochondrial DNA | Defects | Proteins | Signal transduction | Mitochondria | Social behavior | Pathways | Bioenergetics | Etiology | Rodents | Animal tissues | Neostriatum | Alzheimer's disease | Tensin | Gene dosage | Neurodegenerative diseases | Abnormalities | 1-Phosphatidylinositol 3-kinase | Signaling | Grooming | Avoidance behavior | Dogs | Mutation | Aberration | PTEN protein | Index Medicus
Journal Article
DMM Disease Models and Mechanisms, ISSN 1754-8403, 09/2013, Volume 6, Issue 5, pp. 1185 - 1197
Journal Article
Journal Article
Journal Article
Journal Article
Cell, ISSN 0092-8674, 07/2014, Volume 158, Issue 2, pp. 263 - 276
Journal Article