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Behavioral and Electrophysiological Characterization of Dyt1 Heterozygous Knockout Mice

https://doi.org/10.1371/journal.pone.0120916

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ana.10358openalex-snapshot

ε‐sarcoglycan mutations found in combination with other dystonia gene mutations

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Mutant torsinA, which causes early‐onset primary torsion dystonia, is redistributed to membranous structures enriched in vesicular monoamine transporter in cultured human SH‐SY5Y cells

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Phenomenology and classification of dystonia: A consensus update

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Engineering animal models of dystonia

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Anticholinergic drugs rescue synaptic plasticity in DYT1 dystonia: Role of M1 muscarinic receptors

inferredcites →https://doi.org/10.1002/syn.21571openalex-snapshot

Miniature release events of glutamate from hippocampal neurons are influenced by the dystonia‐associated protein torsinA

inferredcites →https://doi.org/10.1006/abio.1976.9999openalex-snapshot

A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding

inferredcites →https://doi.org/10.1007/s100480100111openalex-snapshot

Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism

inferredcites →https://doi.org/10.1016/j.bbr.2010.09.009openalex-snapshot

Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism

inferredcites →https://doi.org/10.1016/j.bbr.2011.10.002openalex-snapshot

An anticholinergic reverses motor control and corticostriatal LTD deficits in Dyt1 ΔGAG knock-in mice

inferredcites →https://doi.org/10.1016/j.bbr.2011.10.024openalex-snapshot

Abnormal nuclear envelope in the cerebellar Purkinje cells and impaired motor learning in DYT11 myoclonus-dystonia mouse models

inferredcites →https://doi.org/10.1016/j.bbr.2012.02.029openalex-snapshot

Improved motor performance in Dyt1 ΔGAG heterozygous knock-in mice by cerebellar Purkinje-cell specific Dyt1 conditional knocking-out

inferredcites →https://doi.org/10.1016/j.conb.2011.01.007openalex-snapshot

Differential regulation of spontaneous and evoked neurotransmitter release at central synapses

inferredcites →https://doi.org/10.1016/j.expneurol.2005.08.025openalex-snapshot

Generation and characterization of Dyt1 ΔGAG knock-in mouse as a model for early-onset dystonia

inferredcites →https://doi.org/10.1016/j.expneurol.2007.12.027openalex-snapshot

Abnormal motor function and dopamine neurotransmission in DYT1 ΔGAG transgenic mice

inferredcites →https://doi.org/10.1016/j.nbd.2010.04.016openalex-snapshot

Cell-autonomous alteration of dopaminergic transmission by wild type and mutant (ΔE) TorsinA in transgenic mice

inferredcites →https://doi.org/10.1016/j.nbd.2012.03.024openalex-snapshot

Generation of a novel rodent model for DYT1 dystonia

inferredcites →https://doi.org/10.1016/j.nbd.2014.01.016openalex-snapshot

Regional specificity of synaptic plasticity deficits in a knock-in mouse model of DYT1 dystonia

inferredcites →https://doi.org/10.1016/j.neures.2006.09.005openalex-snapshot

Motor deficits and hyperactivity in Dyt1 knockdown mice

inferredcites →https://doi.org/10.1016/j.neures.2009.07.004openalex-snapshot

Increased c-fos expression in the central nucleus of the amygdala and enhancement of cued fear memory in Dyt1 ΔGAG knock-in mice

inferredcites →https://doi.org/10.1016/j.neuron.2005.11.010openalex-snapshot

Loss of the Dystonia-Associated Protein TorsinA Selectively Disrupts the Neuronal Nuclear Envelope

inferredcites →https://doi.org/10.1016/j.neuron.2005.12.006openalex-snapshot

Dystonia and the Nuclear Envelope

inferredcites →https://doi.org/10.1016/j.neuron.2008.12.029openalex-snapshot

Snapin Facilitates the Synchronization of Synaptic Vesicle Fusion

inferredcites →https://doi.org/10.1016/j.neuroscience.2008.09.028openalex-snapshot

Consequences of the DYT1 mutation on torsinA oligomerization and degradation

inferredcites →https://doi.org/10.1016/j.neuroscience.2009.09.017openalex-snapshot

Mutant torsinA interacts with tyrosine hydroxylase in cultured cells

inferredcites →https://doi.org/10.1016/s0306-4522(02)00205-1openalex-snapshot

Subacute systemic 3-nitropropionic acid intoxication induces a distinct motor disorder in adult C57Bl/6 mice: behavioural and histopathological characterisation

inferredcites →https://doi.org/10.1021/bi0349569openalex-snapshot

Recombinant Expression, Purification, and Comparative Characterization of TorsinA and Its Torsion Dystonia-Associated Variant ΔE-TorsinA

inferredcites →https://doi.org/10.1034/j.1600-0404.2003.01362.xopenalex-snapshot

Focal and segmental primary dystonia in north-western Germany - a clinico-genetic study

inferredcites →https://doi.org/10.1038/5673openalex-snapshot

Snapin: a SNARE–associated protein implicated in synaptic transmission

inferredcites →https://doi.org/10.1038/emboj.2010.285openalex-snapshot

CSN complex controls the stability of selected synaptic proteins via a torsinA‐dependent process

inferredcites →https://doi.org/10.1038/ng0997-40openalex-snapshot

The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein

inferredcites →https://doi.org/10.1038/nrn2337openalex-snapshot

The pathophysiological basis of dystonias

inferredcites →https://doi.org/10.1073/pnas.0304375101openalex-snapshot

Mislocalization to the nuclear envelope: An effect of the dystonia-causing torsinA mutation

inferredcites →https://doi.org/10.1073/pnas.0308088101openalex-snapshot

Effect of torsinA on membrane proteins reveals a loss of function and a dominant-negative phenotype of the dystonia-associated ΔE-torsinA mutant

inferredcites →https://doi.org/10.1073/pnas.0308760101openalex-snapshot

TorsinA in the nuclear envelope

inferredcites →https://doi.org/10.1074/jbc.m407206200openalex-snapshot

Regulation of Type VI Adenylyl Cyclase by Snapin, a SNAP25-binding Protein

inferredcites →https://doi.org/10.1074/jbc.m704097200openalex-snapshot

The Dystonia-associated Protein TorsinA Modulates Synaptic Vesicle Recycling

inferredcites →https://doi.org/10.1074/jbc.m910025199openalex-snapshot

Torsin A and Its Torsion Dystonia-associated Mutant Forms Are Lumenal Glycoproteins That Exhibit Distinct Subcellular Localizations

inferredcites →https://doi.org/10.1093/hmg/9.9.1403openalex-snapshot

Mutant torsinA, responsible for early-onset torsion dystonia, forms membrane inclusions in cultured neural cells

inferredcites →https://doi.org/10.1093/hmg/ddh208openalex-snapshot

A Drosophila model of early onset torsion dystonia suggests impairment in TGF-β signaling

inferredcites →https://doi.org/10.1093/hmg/ddn173openalex-snapshot

Dystonia-associated mutations cause premature degradation of torsinA protein and cell-type-specific mislocalization to the nuclear envelope

inferredcites →https://doi.org/10.1093/hmg/ddr528openalex-snapshot

Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models

inferredcites →https://doi.org/10.1093/jb/mvj138openalex-snapshot

Myoclonus, Motor Deficits, Alterations in Emotional Responses and Monoamine Metabolism in ε-Sarcoglycan Deficient Mice

inferredcites →https://doi.org/10.1093/jb/mvm191openalex-snapshot

Motor Deficits and Hyperactivity in Cerebral Cortex-specific Dyt1 Conditional Knockout Mice

inferredcites →https://doi.org/10.1093/jb/mvq078openalex-snapshot

Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce

inferredcites →https://doi.org/10.1111/j.1468-1331.2010.03057.xopenalex-snapshot

The role of torsinA in dystonia

inferredcites →https://doi.org/10.1111/j.1471-4159.2009.06095.xopenalex-snapshot

TorsinA and dystonia: from nuclear envelope to synapse

inferredcites →https://doi.org/10.1113/jphysiol.1996.sp021204openalex-snapshot

Paired‐pulse facilitation and depression at unitary synapses in rat hippocampus: quantal fluctuation affects subsequent release.

inferredcites →https://doi.org/10.1136/jmg.27.7.409openalex-snapshot

The genetics of idiopathic torsion dystonia.

inferredcites →https://doi.org/10.1136/jnnp.2008.148270openalex-snapshot

Novel TOR1A mutation p.Arg288Gln in early-onset dystonia (DYT1)

inferredcites →https://doi.org/10.1136/jnnp.2008.162099openalex-snapshot

Myoclonus-dystonia: clinical and genetic evaluation of a large cohort

inferredcites →https://doi.org/10.1212/01.wnl.0000090560.20641.abopenalex-snapshot

Candidate gene studies in focal dystonia

inferredcites →https://doi.org/10.1212/wnl.59.8.1244openalex-snapshot

Clinical findings of a myoclonus-dystonia family with two distinct mutations

inferredcites →https://doi.org/10.1371/journal.pone.0024539openalex-snapshot

Motor Deficits and Decreased Striatal Dopamine Receptor 2 Binding Activity in the Striatum-Specific Dyt1 Conditional Knockout Mice

inferredcites →https://doi.org/10.1371/journal.pone.0035518openalex-snapshot

Enhanced Hippocampal Long-Term Potentiation and Fear Memory in Btbd9 Mutant Mice

inferredcites →https://doi.org/10.1371/journal.pone.0072491openalex-snapshot

Pre-Synaptic Release Deficits in a DYT1 Dystonia Mouse Model

inferredcites →https://doi.org/10.1371/journal.pone.0110086openalex-snapshot

4-Phenylbutyrate Attenuates the ER Stress Response and Cyclic AMP Accumulation in DYT1 Dystonia Cell Models

inferredcites →https://doi.org/10.1385/jmn:25:1:105openalex-snapshot

Dystonia-Associated Forms of TorsinA Are Deficient in ATPase Activity

inferredcites →https://doi.org/10.1523/jneurosci.3016-05.2005openalex-snapshot

Silencing Primary Dystonia: Lentiviral-Mediated RNA Interference Therapy for DYT1 Dystonia

inferredcites →https://doi.org/10.1523/jneurosci.4461-03.2004openalex-snapshot

Aberrant Cellular Behavior of Mutant TorsinA Implicates Nuclear Envelope Dysfunction in DYT1 Dystonia

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Cortically Dependent Motor Training Does Not Induce Abnormal Movements in DYT1‐Knock In Mice

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Electromyographic evidence in support of a knock‐in mouse model of DYT1 Dystonia

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Characterization of the direct pathway in Dyt1 ΔGAG heterozygous knock-in mice and dopamine receptor 1-expressing-cell-specific Dyt1 conditional knockout mice

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Optogenetic Activation of Striatopallidal Neurons Reveals Altered HCN Gating in DYT1 Dystonia

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Reversal of motor-skill transfer impairment by trihexyphenidyl and reduction of dorsolateral striatal cholinergic interneurons in Dyt1 ΔGAG knock-in mice

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inferred← citeshttps://doi.org/10.1016/j.nbd.2019.104529openalex-snapshot

Perturbed Ca2+-dependent signaling of DYT2 hippocalcin mutant as mechanism of autosomal recessive dystonia

inferred← citeshttps://doi.org/10.1016/j.nbd.2019.104638openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.nbd.2021.105342openalex-snapshot

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Ultrastructural analysis of nigrostriatal dopaminergic terminals in a knockin mouse model of DYT1 dystonia

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Reconsideration of the firing loop models for dystonia and Parkinson's disease

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Dysfunctional Hippocampal-Prefrontal Network Underlies a Multidimensional Neuropsychiatric Phenotype following Early-Life Seizure

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Dysfunctional hippocampal-prefrontal network underlies a multidimensional neuropsychiatric phenotype following early-life seizure

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