相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Behavioral encoding across timescales by region-specific dopamine dynamics
Søren H. Jørgensen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2023)
Isradipine therapy in Cacna1dIle772Met/+ mice ameliorates primary aldosteronism and neurologic abnormalities
Gabriel Stoelting et al.
JCI INSIGHT (2023)
Genotype-phenotype correlation of CACNA1A variants in children with epilepsy
Xueyang Niu et al.
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY (2022)
Cav1.3 calcium channels are full-range linear amplifiers of firing frequencies in lateral DA SN neurons
Josef Shin et al.
SCIENCE ADVANCES (2022)
Voltage-Gated Ca2+-Channel α1-Subunit de novo Missense Mutations: Gain or Loss of Function - Implications for Potential Therapies
Joerg Striessnig
FRONTIERS IN SYNAPTIC NEUROSCIENCE (2021)
Infantile-Onset Syndromic Cerebellar Ataxia and CACNA1G Mutations
Sabina Barresi et al.
PEDIATRIC NEUROLOGY (2020)
Early Restoration of Shank3 Expression in Shank3 Knock-Out Mice Prevents Core ASD-Like Behavioral Phenotypes
Thomas C. Jaramillo et al.
eNeuro (2020)
De novo CACAN1D Ca2+channelopathies: clinical phenotypes and molecular mechanism
Nadine J. Ortner et al.
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY (2020)
A de novo CACNA1D missense mutation in a patient with congenital hyperinsulinism, primary hyperaldosteronism and hypotonia
Maria Carmen De Mingo Alemany et al.
CHANNELS (2020)
What, If, and When to Move: Basal Ganglia Circuits and Self-Paced Action Initiation
Andreas Klaus et al.
Annual Review of Neuroscience (2019)
Autism-linked dopamine transporter mutation alters striatal dopamine neurotransmission and dopamine-dependent behaviors
Gabriella E. DiCarlo et al.
JOURNAL OF CLINICAL INVESTIGATION (2019)
In vivo functional diversity of midbrain dopamine neurons within identified axonal projections
Navid Farassat et al.
ELIFE (2019)
Impaired chromaffin cell excitability and exocytosis in autistic Timothy syndrome TS2-neo mouse rescued by L-type calcium channel blockers
Chiara Calorio et al.
JOURNAL OF PHYSIOLOGY-LONDON (2019)
Chromaffin Cells of the Adrenal Medulla: Physiology, Pharmacology, and Disease
Emilio Carbone et al.
COMPREHENSIVE PHYSIOLOGY (2019)
Genomic diagnostics within a medically underserved population: efficacy and implications
Kevin A. Strauss et al.
GENETICS IN MEDICINE (2018)
De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene
Jean Chemin et al.
BRAIN (2018)
Brain region-specific disruption of Shank3 in mice reveals a dissociation for cortical and striatal circuits in autism-related behaviors
Alexandra L. Bey et al.
TRANSLATIONAL PSYCHIATRY (2018)
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias
Katherine L. Helbig et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2018)
Gating defects of disease-causing de novo mutations in Ca(v)1.3 Ca2+ channels
Alexandra Pinggera et al.
CHANNELS (2018)
Lower Affinity of Isradipine for L-Type Ca2+ Channels during Substantia Nigra Dopamine Neuron-Like Activity: Implications for Neuroprotection in Parkinson's Disease
Nadine J. Ortner et al.
JOURNAL OF NEUROSCIENCE (2017)
A CACNA1D mutation in a patient with persistent hyperinsulinaemic hypoglycaemia, heart defects, and severe hypotonia
S. E. Flanagan et al.
PEDIATRIC DIABETES (2017)
Loss of α2δ-1 Calcium Channel Subunit Function Increases the Susceptibility for Diabetes
Vincenzo Mastrolia et al.
DIABETES (2017)
Neurobiology of rodent self-grooming and its value for translational neuroscience
Allan V. Kalueff et al.
NATURE REVIEWS NEUROSCIENCE (2016)
Direct and indirect dorsolateral striatum pathways reinforce different action strategies
Ana M. Vicente et al.
CURRENT BIOLOGY (2016)
Role of voltage-gated calcium channels in the regulation of aldosterone production from zona glomerulosa cells of the adrenal cortex
Paula Q. Barrett et al.
JOURNAL OF PHYSIOLOGY-LONDON (2016)
Adult restoration of Shank3 expression rescues selective autistic-like phenotypes
Yuan Mei et al.
NATURE (2016)
Advancing the understanding of autism disease mechanisms through genetics
Luis de la Torre-Ubieta et al.
NATURE MEDICINE (2016)
Splice variants of the CaV1.3 L-type calcium channel regulate dendritic spine morphology
Ruslan Stanika et al.
SCIENTIFIC REPORTS (2016)
An autism-associated mutation in CaV1.3 channels has opposing effects on voltage- and Ca2+-dependent regulation
Worawan B. Limpitikul et al.
SCIENTIFIC REPORTS (2016)
CACNA1D De Novo Mutations in Autism Spectrum Disorders Activate Cav1.3 L-Type Calcium Channels
Alexandra Pinggera et al.
BIOLOGICAL PSYCHIATRY (2015)
The L-type calcium channel Cav1.3 is required for proper hippocampal neurogenesis and cognitive functions
Julia Marschallinger et al.
CELL CALCIUM (2015)
FoxP1 orchestration of ASD-relevant signaling pathways in the striatum
Daniel J. Araujo et al.
GENES & DEVELOPMENT (2015)
Treatment during a vulnerable developmental period rescues a genetic epilepsy
Stephan Lawrence Marguet et al.
NATURE MEDICINE (2015)
Cell-type-specific tuning of Cav1.3 Ca2+-channels by a C-terminal automodulatory domain
Anja Scharinger et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2015)
Compensatory T-type Ca2+ channel activity alters D2-autoreceptor responses of Substantia nigra dopamine neurons from Cav1.3 L-type Ca2+ channel KO mice
Christina Poetschke et al.
SCIENTIFIC REPORTS (2015)
The Physiology, Pathology, and Pharmacology of Voltage-Gated Calcium Channels and Their Future Therapeutic Potential
Gerald W. Zamponi et al.
PHARMACOLOGICAL REVIEWS (2015)
Repetitive behavior profile and supersensitivity to amphetamine in the C58/J mouse model of autism
Sheryl S. Moy et al.
BEHAVIOURAL BRAIN RESEARCH (2014)
The role of L-type voltage-gated calcium channels Cav1.2 and Cav1.3 in normal and pathological brain function
Stefan M. Berger et al.
CELL AND TISSUE RESEARCH (2014)
Genetic targeting of the amphetamine and methylphenidate-sensitive dopamine transporter: On the path to an animal model of attention-deficit hyperactivity disorder
Marc A. Mergy et al.
NEUROCHEMISTRY INTERNATIONAL (2014)
The rare DAT coding variant Val559 perturbs DA neuron function, changes behavior, and alters in vivo responses to psychostimulants
Marc A. Mergy et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Modest CaV1.342-selective inhibition by compound 8 is β-subunit dependent
Hua Huang et al.
NATURE COMMUNICATIONS (2014)
Pyrimidine-2,4,6-triones are a new class of voltage-gated L-type Ca2+ channel activators
Nadine J. Ortner et al.
NATURE COMMUNICATIONS (2014)
Exploring the dominant role of Cav1 channels in signalling to the nucleus
Huan Ma et al.
BIOSCIENCE REPORTS (2013)
The human L-type calcium channel Cav1.3 regulates insulin release and polymorphisms in CACNA1D associate with type 2 diabetes
T. M. Reinbothe et al.
DIABETOLOGIA (2013)
Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism
Ute I. Scholl et al.
NATURE GENETICS (2013)
Mutant mouse models of autism spectrum disorders
Giovanni Provenzano et al.
DISEASE MARKERS (2012)
Differential regulation of motor control and response to dopaminergic drugs by D1R and D2R neurons in distinct dorsal striatum subregions
Pierre F. Durieux et al.
EMBO JOURNAL (2012)
CaV1.3-Driven SK Channel Activation Regulates Pacemaking and Spike Frequency Adaptation in Mouse Chromaffin Cells
David H. F. Vandael et al.
JOURNAL OF NEUROSCIENCE (2012)
Synaptic Refinement of an Inhibitory Topographic Map in the Auditory Brainstem Requires Functional CaV1.3 Calcium Channels
Jan J. Hirtz et al.
JOURNAL OF NEUROSCIENCE (2012)
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
Brian J. O'Roak et al.
NATURE (2012)
CaV1.3-selective L-type calcium channel antagonists as potential new therapeutics for Parkinson's disease
Soosung Kang et al.
NATURE COMMUNICATIONS (2012)
Evidence-Based Behavioral Interventions for Repetitive Behaviors in Autism
Brian A. Boyd et al.
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS (2012)
Cav1.3 Calcium Channels Are Required for Normal Development of the Auditory Brainstem
Jan J. Hirtz et al.
JOURNAL OF NEUROSCIENCE (2011)
Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness
Shahid M. Baig et al.
NATURE NEUROSCIENCE (2011)
Voltage-Gated Calcium Channels
William A. Catterall
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY (2011)
Cav1.3 L-type Ca2+ channels modulate depression-like behaviour in mice independent of deaf phenotype
Perrine Busquet et al.
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY (2010)
Loss of Cav1.3 Channels Reveals the Critical Role of L-Type and BK Channel Coupling in Pacemaking Mouse Adrenal Chromaffin Cells
Andrea Marcantoni et al.
JOURNAL OF NEUROSCIENCE (2010)
Molecular Switch from L-Type Cav1.3 to Cav1.2 Ca2+ Channel Signaling Underlies Long-Term Psychostimulant-Induced Behavioral and Molecular Plasticity
Thomas P. Giordano et al.
JOURNAL OF NEUROSCIENCE (2010)
Robust Pacemaking in Substantia Nigra Dopaminergic Neurons
Jaime N. Guzman et al.
JOURNAL OF NEUROSCIENCE (2009)
Expression and 1,4-Dihydropyridine-Binding Properties of Brain L-Type Calcium Channel Isoforms
Martina J. Sinnegger-Brauns et al.
MOLECULAR PHARMACOLOGY (2009)
Impaired long-term potentiation and enhanced neuronal excitability in the amygdala of CaV1.3 knockout mice
Brandon C. McKinney et al.
NEUROBIOLOGY OF LEARNING AND MEMORY (2009)
L-type calcium channels in adrenal chromaffin cells: Role in pace-making and secretion
A. Marcantoni et al.
CELL CALCIUM (2007)
'Rejuvenation' protects neurons in mouse models of Parkinson's disease
C. Savio Chan et al.
NATURE (2007)
Up-regulation of dopamine D2L mRNA levels in the ventral tegmental area and dorsal striatum of amphetamine-sensitized C57BL/6 mice:: role of Cav1.3 L-type Ca2+ channels
T. P. Giordano et al.
JOURNAL OF NEUROCHEMISTRY (2006)
The L-type voltage-gated calcium channel CaV1.3 mediates consolidation, but not extinction, of contextually conditioned fear in mice
Brandon C. McKinney et al.
LEARNING & MEMORY (2006)
Investigating the structure of the restricted, repetitive behaviours and interests domain of autism
Peter Szatmari et al.
JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY (2006)
Novelty seeking and stereotypic activation of behavior in mice with disruption of the Dat1 gene
VM Pogorelov et al.
NEUROPSYCHOPHARMACOLOGY (2005)
G-protein-coupled receptor modulation of striatal CaV1.3 L-type Ca2+ channels is dependent on a Shank-binding domain
PA Olson et al.
JOURNAL OF NEUROSCIENCE (2005)
Kinetic and cardiovascular comparison of immediate-release isradipine and sustained-release isradipine among non-treatment-seeking, cocaine-dependent individuals
BA Johnson et al.
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY (2005)
Spontaneous voltage oscillations in striatal projection neurons in a rat corticostriatal slice
R Vergara et al.
JOURNAL OF PHYSIOLOGY-LONDON (2003)
α1D (Cav1.3) subunits can form L-type Ca2+ channels activating at negative voltages
A Koschak et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels
J Platzer et al.
CELL (2000)