scholarly article | Q13442814 |
P356 | DOI | 10.1038/S41380-019-0498-X |
P698 | PubMed publication ID | 31455858 |
P50 | author | Zhen Yan | Q88033022 |
P2093 | author name string | Wei Wang | |
Ping Zhong | |||
Xue Wang | |||
Jun Qu | |||
Kaijie Ma | |||
Luye Qin | |||
Maximiliano Rapanelli | |||
Tao Tan | |||
Zi-Jun Wang | |||
Luciana Frick | |||
P2860 | cites work | Cullin-3 targets cyclin E for ubiquitination and controls S phase in mammalian cells | Q22010574 |
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Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function | Q24338263 | ||
Shank3 mutant mice display autistic-like behaviours and striatal dysfunction | Q24597501 | ||
Rate of de novo mutations and the importance of father's age to disease risk | Q24632353 | ||
Microduplications of 16p11.2 are associated with schizophrenia | Q24634151 | ||
Cul3-KLHL20 ubiquitin ligase: physiological functions, stress responses, and disease implications | Q26752753 | ||
Striatal Circuits as a Common Node for Autism Pathophysiology | Q26768226 | ||
Characteristics of Brains in Autism Spectrum Disorder: Structure, Function and Connectivity across the Lifespan | Q26771768 | ||
Molecular underpinnings of prefrontal cortex development in rodents provide insights into the etiology of neurodevelopmental disorders | Q26853035 | ||
Advancing the understanding of autism disease mechanisms through genetics | Q28069757 | ||
Synaptic, transcriptional and chromatin genes disrupted in autism | Q28250800 | ||
Association between microdeletion and microduplication at 16p11.2 and autism | Q28264205 | ||
Constitutive turnover of cyclin E by Cul3 maintains quiescence | Q28506695 | ||
Regulation of the CUL3 Ubiquitin Ligase by a Calcium-Dependent Co-adaptor | Q28975781 | ||
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations | Q29030218 | ||
Meeting of minds: the medial frontal cortex and social cognition | Q29614739 | ||
The PAR-6 polarity protein regulates dendritic spine morphogenesis through p190 RhoGAP and the Rho GTPase | Q30438135 | ||
Neural signatures of autism spectrum disorders: insights into brain network dynamics | Q30835950 | ||
Patches of disorganization in the neocortex of children with autism | Q34040334 | ||
Epigenetic signatures of autism: trimethylated H3K4 landscapes in prefrontal neurons | Q34230735 | ||
Recurrent 16p11.2 microdeletions in autism | Q34729775 | ||
The emerging family of CULLIN3-RING ubiquitin ligases (CRL3s): cellular functions and disease implications. | Q37163747 | ||
A SMYD3 Small-Molecule Inhibitor Impairing Cancer Cell Growth | Q37183416 | ||
Synaptic Actin Dysregulation, a Convergent Mechanism of Mental Disorders? | Q37444933 | ||
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism | Q37716254 | ||
Corticostriatal connectivity and its role in disease | Q38091300 | ||
Striatal circuits, habits, and implications for obsessive-compulsive disorder. | Q38252883 | ||
Shifting brain inhibitory balance and connectivity of the prefrontal cortex of adults with autism spectrum disorder. | Q41173126 | ||
Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators | Q42018247 | ||
Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases | Q42164701 | ||
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases | Q42175057 | ||
Endocannabinoid-mediated rescue of striatal LTD and motor deficits in Parkinson's disease models | Q42508054 | ||
Cortical excitatory neurons and glia, but not GABAergic neurons, are produced in the Emx1-expressing lineage. | Q42524386 | ||
Structural complexity in the KCTD family of Cullin3-dependent E3 ubiquitin ligases | Q42694183 | ||
Differential electrophysiological properties of dopamine D1 and D2 receptor-containing striatal medium-sized spiny neurons | Q44463501 | ||
Disturbed cingulate glutamate metabolism in adults with high-functioning autism spectrum disorder: evidence in support of the excitatory/inhibitory imbalance hypothesis. | Q45902314 | ||
Identifying specific prefrontal neurons that contribute to autism-associated abnormalities in physiology and social behavior. | Q46407810 | ||
Sensorimotor gating deficits in adults with autism | Q46422161 | ||
Kctd13 deletion reduces synaptic transmission via increased RhoA. | Q47035966 | ||
Cullin 3-Based Ubiquitin Ligases as Master Regulators of Mammalian Cell Differentiation. | Q47284253 | ||
A RhoA Signaling Pathway Regulates Dendritic Golgi Outpost Formation. | Q48265883 | ||
Changes in the development of striatum are involved in repetitive behavior in autism | Q48959458 | ||
Emx1 and Emx2 show different patterns of expression during proliferation and differentiation of the developing cerebral cortex in the mouse. | Q52201737 | ||
Social deficits in Shank3-deficient mouse models of autism are rescued by histone deacetylase (HDAC) inhibition | Q60357933 | ||
Chemogenetic Activation of Prefrontal Cortex Rescues Synaptic and Behavioral Deficits in a Mouse Model of 16p11.2 Deletion Syndrome. | Q64948646 | ||
Regulation of dendritic spine morphology by the rho family of small GTPases: antagonistic roles of Rac and Rho | Q73010224 | ||
P577 | publication date | 2019-08-27 | |
P1433 | published in | Molecular Psychiatry | Q6895973 |
P1476 | title | Behavioral, circuitry, and molecular aberrations by region-specific deficiency of the high-risk autism gene Cul3 |
Q99207743 | A standardized social preference protocol for measuring social deficits in mouse models of autism |
Q100311434 | Control of craniofacial and brain development by Cullin3-RING ubiquitin ligases: Lessons from human disease genetics |
Q89882718 | Reversal of synaptic and behavioral deficits in a 16p11.2 duplication mouse model via restoration of the GABA synapse regulator Npas4 |
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