Aromatic L-acid decarboxylase (AADC) deficiency causes severe motor disturbances in affected children. A putamen-targeted gene therapy improves the motor function of patients. The present study investigated the electrical properties of dopaminergic (DA) neurons in the substantia nigra compacta (SNc) of mice with an AADC deficiency (DdcKI). The basal firing of DA neurons, which determines DA release in the putamen, was abnormal in the DdcKI mice, including a low frequency and irregular firing pattern, because of a decrease in the after-hyperpolarization (AHP) amplitude of action potentials (APs). The frequency of spontaneous excitatory postsynaptic currents (sEPSCs) increased and that of spontaneous inhibitory PSCs (sIPSCs) decreased in the ...
Niemann-Pick disease type A (NPDA) is a fatal disease due to mutations in the acid sphingomyelinase ...
The Phelan-McDermid syndrome (PMD) is a genetic disorder caused by deletion or rearrangements of the...
Fulltext embargoed for: 12 months post date of publicationEpileptic encephalopathies, including Drav...
Aromatic L-acid decarboxylase (AADC) deficiency causes severe motor disturbances in affected childre...
Aromatic L-amino acid decarboxylase (AADC) is responsible for the syntheses of dopamine and serotoni...
The Niemann-Pick type C1 (NPC1) is a rare genetic disease characterized by the accumulation of endoc...
The Niemann-Pick type C1 (NPC1) is a rare genetic disease characterized by the accumulation of endoc...
Aromatic L-amino acid decarboxylase (AADC) deficiency is a complex inherited neurological disorder o...
Aim: Missense mutations of dynactin subunit p150Glued have been associated with multiple neurodegene...
Copyright: 2014 The PLOS ONE Staff. This is an open-access article distributed under the terms of ...
Introduction: Aromatic L-amino acid decarboxylase deficiency (AADC) is a rare autosomal recessive pe...
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-linked neurodevelopme...
Huntington’s disease (HD) is a heritable neurological disorder that affects cognitive and motor perf...
Dyslexia is a phenotypically complex developmental disorder that involves significant impairment in ...
Genomic analysis has revealed that the genes for various chromatin regulators are mutated in many in...
Niemann-Pick disease type A (NPDA) is a fatal disease due to mutations in the acid sphingomyelinase ...
The Phelan-McDermid syndrome (PMD) is a genetic disorder caused by deletion or rearrangements of the...
Fulltext embargoed for: 12 months post date of publicationEpileptic encephalopathies, including Drav...
Aromatic L-acid decarboxylase (AADC) deficiency causes severe motor disturbances in affected childre...
Aromatic L-amino acid decarboxylase (AADC) is responsible for the syntheses of dopamine and serotoni...
The Niemann-Pick type C1 (NPC1) is a rare genetic disease characterized by the accumulation of endoc...
The Niemann-Pick type C1 (NPC1) is a rare genetic disease characterized by the accumulation of endoc...
Aromatic L-amino acid decarboxylase (AADC) deficiency is a complex inherited neurological disorder o...
Aim: Missense mutations of dynactin subunit p150Glued have been associated with multiple neurodegene...
Copyright: 2014 The PLOS ONE Staff. This is an open-access article distributed under the terms of ...
Introduction: Aromatic L-amino acid decarboxylase deficiency (AADC) is a rare autosomal recessive pe...
Cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder (CDD) is a severe X-linked neurodevelopme...
Huntington’s disease (HD) is a heritable neurological disorder that affects cognitive and motor perf...
Dyslexia is a phenotypically complex developmental disorder that involves significant impairment in ...
Genomic analysis has revealed that the genes for various chromatin regulators are mutated in many in...
Niemann-Pick disease type A (NPDA) is a fatal disease due to mutations in the acid sphingomyelinase ...
The Phelan-McDermid syndrome (PMD) is a genetic disorder caused by deletion or rearrangements of the...
Fulltext embargoed for: 12 months post date of publicationEpileptic encephalopathies, including Drav...