| P50 | author | Wenting Wang | Q60331741 |
| | Sheng-Xi Wu | Q81472605 |
| | Baolin Guo | Q92093871 |
| | Marie-Sophie van der Goes | Q96096679 |
| P2093 | author name string | Guoping Feng | |
| | Qian Chen | |
| | Chenchen Li | |
| | Ying Zang | |
| | Annie Y Yao | |
| | Charles R Gerfen | |
| | Congyi Lu | |
| | Dongqing Wang | |
| | James Hawrot | |
| | Katherine Lyman | |
| | Qiangge Zhang | |
| | Xian Gao | |
| | Zhanyan Fu | |
| P2860 | cites work | Subunit composition, kinetic, and permeation properties of AMPA receptors in single neocortical nonpyramidal cells. | Q48633429 |
| | Striatal volume on magnetic resonance imaging and repetitive behaviors in autism | Q48866759 |
| | Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype | Q50313091 |
| | Behavior and the basal ganglia | Q72582225 |
| | Validation of a new system for the automatic registration of behaviour in mice and rats | Q73630996 |
| | Transcriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant mice | Q21198691 |
| | Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication | Q21198697 |
| | Shank, a novel family of postsynaptic density proteins that binds to the NMDA receptor/PSD-95/GKAP complex and cortactin | Q22010466 |
| | Advances in autism genetics: on the threshold of a new neurobiology | Q22251023 |
| | Neuroligins and neurexins link synaptic function to cognitive disease | Q22251092 |
| | Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders | Q24337114 |
| | Identification of a novel cortactin SH3 domain-binding protein and its localization to growth cones of cultured neurons | Q24522731 |
| | Altered synaptic plasticity in a mouse model of fragile X mental retardation | Q24530695 |
| | Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q13.3 deletion syndrome | Q24535749 |
| | Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3 | Q24596677 |
| | Shank3 mutant mice display autistic-like behaviours and striatal dysfunction | Q24597501 |
| | Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry | Q24630976 |
| | Glutamate abnormalities in obsessive compulsive disorder: neurobiology, pathophysiology, and treatment | Q24633004 |
| | The postsynaptic density proteins Homer and Shank form a polymeric network structure | Q24645689 |
| | Contribution of SHANK3 mutations to autism spectrum disorder | Q24648672 |
| | Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome | Q24656220 |
| | Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms | Q24676539 |
| | Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand | Q24676976 |
| | Sequential super-stereotypy of an instinctive fixed action pattern in hyper-dopaminergic mutant mice: a model of obsessive compulsive disorder and Tourette's | Q24797858 |
| | Autism-associated neuroligin-3 mutations commonly impair striatal circuits to boost repetitive behaviors | Q26269833 |
| | Early hyperactivity and precocious maturation of corticostriatal circuits in Shank3B(-/-) mice | Q27311527 |
| | Proline-rich synapse-associated protein-1/cortactin binding protein 1 (ProSAP1/CortBP1) is a PDZ-domain protein highly enriched in the postsynaptic density | Q28140303 |
| | Coupling of mGluR/Homer and PSD-95 complexes by the Shank family of postsynaptic density proteins | Q28141190 |
| | The Shank family of scaffold proteins | Q28144084 |
| | Proline-rich synapse-associated proteins ProSAP1 and ProSAP2 interact with synaptic proteins of the SAPAP/GKAP family | Q28145992 |
| | 22q13 deletion syndrome | Q28200653 |
| | Projection subtypes of rat neostriatal matrix cells revealed by intracellular injection of biocytin | Q28264640 |
| | Molecular and phenotypic characterization of ring chromosome 22 | Q28264937 |
| | Mice with Shank3 Mutations Associated with ASD and Schizophrenia Display Both Shared and Distinct Defects | Q28271310 |
| | Adult restoration of Shank3 expression rescues selective autistic-like phenotypes | Q28273413 |
| | L-type calcium channels: the low down | Q28288051 |
| | An architectural framework that may lie at the core of the postsynaptic density | Q28293971 |
| | Clinical utility gene card for: deletion 22q13 syndrome | Q28300606 |
| | Smaller dendritic spines, weaker synaptic transmission, but enhanced spatial learning in mice lacking Shank1. | Q28512788 |
| | Neuronal Ca(V)1.3alpha(1) L-type channels activate at relatively hyperpolarized membrane potentials and are incompletely inhibited by dihydropyridines | Q28582608 |
| | Parallel Organization of Functionally Segregated Circuits Linking Basal Ganglia and Cortex | Q29391304 |
| | The mGluR theory of fragile X mental retardation | Q29615060 |
| | A translational profiling approach for the molecular characterization of CNS cell types | Q29615252 |
| | D1 and D2 dopamine receptor-regulated gene expression of striatonigral and striatopallidal neurons | Q29615480 |
| | PDZ domain proteins of synapses | Q29616399 |
| | A gene expression atlas of the central nervous system based on bacterial artificial chromosomes | Q29617753 |
| | A synaptic trek to autism | Q29622832 |
| | Regulation of dendritic spine morphology and synaptic function by Shank and Homer | Q30014842 |
| | Altered Striatal Synaptic Function and Abnormal Behaviour in Shank3 Exon4-9 Deletion Mouse Model of Autism | Q30362074 |
| | Impaired Dendritic Development and Memory in Sorbs2 Knock-Out Mice. | Q30376404 |
| | SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism. | Q30428959 |
| | Balanced activity in basal ganglia projection pathways is critical for contraversive movements | Q30434712 |
| | Loss of predominant Shank3 isoforms results in hippocampus-dependent impairments in behavior and synaptic transmission | Q30438299 |
| | SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties | Q30438816 |
| | Reduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant mice | Q30461096 |
| | Repeated cortico-striatal stimulation generates persistent OCD-like behavior | Q30574071 |
| | Concurrent activation of striatal direct and indirect pathways during action initiation. | Q30579307 |
| | Functional neuroimaging and the neuroanatomy of obsessive-compulsive disorder | Q33181070 |
| | Ca(2+) permeable AMPA receptor induced long-term potentiation requires PI3/MAP kinases but not Ca/CaM-dependent kinase II. | Q33405238 |
| | Generation of designer receptors exclusively activated by designer drugs (DREADDs) using directed molecular evolution | Q33523314 |
| | Distinct roles of GABAergic interneurons in the regulation of striatal output pathways | Q33720464 |
| | Inhibitory control of neostriatal projection neurons by GABAergic interneurons | Q33861738 |
| | Activation of group I mGluRs is necessary for induction of long-term depression at striatal synapses | Q34100802 |
| | Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci | Q34495555 |
| | Dopaminergic control of corticostriatal long-term synaptic depression in medium spiny neurons is mediated by cholinergic interneurons. | Q34521936 |
| | Retro-orbital injections in mice. | Q35171751 |
| | Mutations causing syndromic autism define an axis of synaptic pathophysiology | Q35587150 |
| | Dynamic aspects of CNS synapse formation. | Q35652924 |
| | Metabotropic glutamate receptor-dependent long-term depression is impaired due to elevated ERK signaling in the ΔRG mouse model of tuberous sclerosis complex | Q35748464 |
| | MAGUKs in synapse assembly and function: an emerging view | Q35750293 |
| | Neuroligin 1 modulates striatal glutamatergic neurotransmission in a pathway and NMDAR subunit-specific manner | Q35898012 |
| | Decreased probability of neurotransmitter release underlies striatal long-term depression and postnatal development of corticostriatal synapses | Q36054269 |
| | Learning From Animal Models of Obsessive-Compulsive Disorder | Q36249163 |
| | Identification and differential subcellular localization of the neuronal class C and class D L-type calcium channel alpha 1 subunits | Q36383289 |
| | The role of the GluR2 subunit in AMPA receptor function and synaptic plasticity. | Q36854587 |
| | Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency | Q37001013 |
| | Direct-pathway striatal neurons regulate the retention of decision-making strategies | Q37048139 |
| | Scaffolding proteins at the postsynaptic density: shank as the architectural framework | Q37168233 |
| | Habits, rituals, and the evaluative brain | Q37193050 |
| | Neurotransmitter roles in synaptic modulation, plasticity and learning in the dorsal striatum | Q37680104 |
| | Modeling autism by SHANK gene mutations in mice | Q38098737 |
| | Striatal circuits, habits, and implications for obsessive-compulsive disorder. | Q38252883 |
| | Striatal direct and indirect pathways control decision-making behavior. | Q38271951 |
| | Distinct roles for direct and indirect pathway striatal neurons in reinforcement. | Q41894840 |
| | Autism-like Deficits in Shank3-Deficient Mice Are Rescued by Targeting Actin Regulators | Q42018247 |
| | Long-term synaptic depression in the striatum: physiological and pharmacological characterization | Q42453585 |
| | Coordinated Regulation of Synaptic Plasticity at Striatopallidal and Striatonigral Neurons Orchestrates Motor Control | Q42484851 |
| | Endocannabinoid-mediated rescue of striatal LTD and motor deficits in Parkinson's disease models | Q42508054 |
| | Drd1a-tdTomato BAC transgenic mice for simultaneous visualization of medium spiny neurons in the direct and indirect pathways of the basal ganglia. | Q42525723 |
| | Application of a translational profiling approach for the comparative analysis of CNS cell types | Q42585641 |
| | The pathophysiology of restricted repetitive behavior | Q42729995 |
| | Novel de novo SHANK3 mutation in autistic patients | Q43768017 |
| | Postsynaptic endocannabinoid release is critical to long-term depression in the striatum | Q43971441 |
| | Selective alleviation of compulsive lever-pressing in rats by D1, but not D2, blockade: possible implications for the involvement of D1 receptors in obsessive-compulsive disorder | Q44259226 |
| | Selective blockade of spontaneous motor stereotypy via intrastriatal pharmacological manipulation | Q44384952 |
| | G-protein-coupled receptor modulation of striatal CaV1.3 L-type Ca2+ channels is dependent on a Shank-binding domain. | Q45249950 |
| | Functional state of corticostriatal synapses determines their expression of short- and long-term plasticity | Q46255311 |
| | Dopamine modulation of state-dependent endocannabinoid release and long-term depression in the striatum. | Q46279749 |
| | Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons. | Q46425942 |
| | Combined activation of L-type Ca2+ channels and synaptic transmission is sufficient to induce striatal long-term depression. | Q48130770 |
| | An MRI study of the basal ganglia in autism | Q48173058 |
| | OCD-Like behaviors caused by a neuropotentiating transgene targeted to cortical and limbic D1+ neurons | Q48188537 |
| | A functional magnetic resonance imaging study of tic suppression in Tourette syndrome | Q48485554 |
| P433 | issue | 5 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | autism | Q38404 |
| P304 | page(s) | 1978-1990 | |
| P577 | publication date | 2017-04-17 | |
| P1433 | published in | Journal of Clinical Investigation | Q3186904 |
| P1476 | title | Striatopallidal dysfunction underlies repetitive behavior in Shank3-deficient model of autism | |
| P478 | volume | 127 | |