about
Enhanced hippocampal long-term potentiation and fear memory in Btbd9 mutant miceWhisker-related neuronal patterns fail to develop in the trigeminal brainstem nuclei of NMDAR1 knockout miceBeta1-integrins are critical for cerebellar granule cell precursor proliferationDisrupted motor learning and long-term synaptic plasticity in mice lacking NMDAR1 in the striatumIncreased c-fos expression in the central nucleus of the amygdala and enhancement of cued fear memory in Dyt1 DeltaGAG knock-in miceForebrain glutamatergic neurons mediate leptin action on depression-like behaviors and synaptic depressionNeuronal targets for reducing mutant huntingtin expression to ameliorate disease in a mouse model of Huntington's diseaseExclusive paternal expression and novel alternatively spliced variants of epsilon-sarcoglycan mRNA in mouse brain.Cholinergic dysregulation produced by selective inactivation of the dystonia-associated protein torsinA.Chemical enhancement of torsinA function in cell and animal models of torsion dystonia.Postnatal NMDA receptor ablation in corticolimbic interneurons confers schizophrenia-like phenotypes.N-methyl-D-aspartic acid receptors on striatal neurons are essential for cocaine cue reactivity in miceAltered dendritic morphology of Purkinje cells in Dyt1 ΔGAG knock-in and purkinje cell-specific Dyt1 conditional knockout mice.Alteration of striatal dopaminergic neurotransmission in a mouse model of DYT11 myoclonus-dystonia.Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.Decreased dopamine receptor 1 activity and impaired motor-skill transfer in Dyt1 ΔGAG heterozygous knock-in mice.Pre-synaptic release deficits in a DYT1 dystonia mouse model.Behavioral and electrophysiological characterization of Dyt1 heterozygous knockout mice.An anticholinergic reverses motor control and corticostriatal LTD deficits in Dyt1 ΔGAG knock-in mice.Motor deficits and hyperactivity in Dyt1 knockdown mice.Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse modelsThe pathophysiological basis of dystonias.Engineering animal models of dystoniaNucleic acid-binding specificities of tobacco chloroplast ribonucleoproteins.Striatopallidal Neuron NMDA Receptors Control Synaptic Connectivity, Locomotor, and Goal-Directed Behaviors.Lhx2 selector activity specifies cortical identity and suppresses hippocampal organizer fate.Reduced anxiety-- and depression-like behaviors in Emx1 homozygous mutant mice.Collybistin is required for both the formation and maintenance of GABAergic postsynapses in the hippocampus.Increased seizure susceptibility and cortical malformation in beta-catenin mutant mice.cDNA cloning and sequencing of tobacco chloroplast ribosomal protein L12.Normal corpus callosum in Emx1 mutant mice with C57BL/6 backgroundCre-mediated cerebellum- and hippocampus-restricted gene mutation in mouse brainEmx1-specific expression of foreign genes using "knock-in" approachSpecificity and efficiency of Cre-mediated recombination in Emx1-Cre knock-in miceThe Role of BTBD9 in Striatum and Restless Legs Syndrome
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Yuqing Li
@ast
Yuqing Li
@en
Yuqing Li
@es
Yuqing Li
@nl
Yuqing Li
@sl
type
label
Yuqing Li
@ast
Yuqing Li
@en
Yuqing Li
@es
Yuqing Li
@nl
Yuqing Li
@sl
prefLabel
Yuqing Li
@ast
Yuqing Li
@en
Yuqing Li
@es
Yuqing Li
@nl
Yuqing Li
@sl
P1053
G-1596-2011
P106
P31
P3829
P496
0000-0003-1211-5529
P569
2000-01-01T00:00:00Z