The Ncoa7 locus regulates V-ATPase formation and function, neurodevelopment and behaviour
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Title
The Ncoa7 locus regulates V-ATPase formation and function, neurodevelopment and behaviour
Authors
Keywords
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Journal
CELLULAR AND MOLECULAR LIFE SCIENCES
Volume -, Issue -, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-12-19
DOI
10.1007/s00018-020-03721-6
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Note: Only part of the references are listed.- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
- (2020) F. Kyle Satterstrom et al. CELL
- Neuropathophysiology of Lysosomal Storage Diseases: Synaptic Dysfunction as a Starting Point for Disease Progression
- (2020) Camila Pará et al. Journal of Clinical Medicine
- Nuclear Receptor Coactivators (NCOAs) and Corepressors (NCORs) in the Brain
- (2020) Zheng Sun et al. ENDOCRINOLOGY
- OXR1A, a Coactivator of PRMT5 Regulating Histone Arginine Methylation
- (2020) Mingyi Yang et al. Cell Reports
- The emerging roles of vacuolar-type ATPase-dependent Lysosomal acidification in neurodegenerative diseases
- (2020) Qiaoyun Song et al. Translational Neurodegeneration
- Reciprocal Regulation of V-ATPase and Glycolytic Pathway Elements in Health and Disease
- (2019) Summer R. Hayek et al. Frontiers in Physiology
- The rare mutation in the endosome-associated recycling protein gene VPS50 is associated with human neural tube defects
- (2019) Zhiwen Shi et al. Molecular Cytogenetics
- Ubiquilins regulate autophagic flux through mTOR signalling and lysosomal acidification
- (2019) Mümine Şentürk et al. NATURE CELL BIOLOGY
- The phenotypic landscape of a Tbc1d24 mutant mouse includes convulsive seizures resembling human early infantile epileptic encephalopathy
- (2019) Risa Tona et al. HUMAN MOLECULAR GENETICS
- Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities
- (2019) Michelle Stewart et al. Disease Models & Mechanisms
- TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neurons
- (2019) Davide Aprile et al. CELL DEATH AND DIFFERENTIATION
- Interaction of the late endo-lysosomal lipid PI(3,5)P2 with the Vph1 isoform of yeast V-ATPase increases its activity and cellular stress tolerance
- (2019) Subhrajit Banerjee et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration
- (2019) Takuo Hirose et al. JOURNAL OF CLINICAL INVESTIGATION
- Distal renal tubular acidosis: genetic causes and management
- (2019) Sílvia Bouissou Morais Soares et al. World Journal of Pediatrics
- TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model
- (2019) Kevin Lüthy et al. BRAIN
- Refinement of 16p13.3 microdeletion syndrome from a case presentation of a girl with epilepsy and intellectual disability
- (2019) Yukiko Kuroda et al. CONGENITAL ANOMALIES
- Recessive gene disruptions in autism spectrum disorder
- (2019) Ryan N. Doan et al. NATURE GENETICS
- Neuronal Soma-Derived Degradative Lysosomes Are Continuously Delivered to Distal Axons to Maintain Local Degradation Capacity
- (2019) Tamar Farfel-Becker et al. Cell Reports
- The Altered Somatic Brain Network in State Anxiety
- (2019) Xianrui Li et al. Frontiers in Psychiatry
- Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course
- (2019) Alessandro Esposito et al. BRAIN
- Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction
- (2019) Julia Wang et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Lysosomes and Brain Health
- (2018) Jaiprakash Sharma et al. Annual Review of Neuroscience
- De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy
- (2018) Anna Fassio et al. BRAIN
- The curious case of vacuolar ATPase: regulation of signaling pathways
- (2018) Sahithi Pamarthy et al. Molecular Cancer
- Oxidation Resistance 1 Modulates Glycolytic Pathways in the Cerebellum via an Interaction with Glucose-6-Phosphate Isomerase
- (2018) Mattéa J. Finelli et al. MOLECULAR NEUROBIOLOGY
- Sociability and synapse subtype-specific defects in mice lacking SRPX2, a language-associated gene
- (2018) Breeanne M. Soteros et al. PLoS One
- A mouse model of autism implicates endosome pH in the regulation of presynaptic calcium entry
- (2018) Julie C. Ullman et al. Nature Communications
- GRAM domain proteins specialize functionally distinct ER-PM contact sites in human cells
- (2018) Marina Besprozvannaya et al. eLife
- A new microdeletion syndrome involving TBC1D24, ATP6V0C, and PDPK1 causes epilepsy, microcephaly, and developmental delay
- (2018) Bettina E. Mucha et al. GENETICS IN MEDICINE
- Chromophore-Assisted Light Inactivation of the V-ATPase V0c Subunit Inhibits Neurotransmitter Release Downstream of Synaptic Vesicle Acidification
- (2018) Sylvain Rama et al. MOLECULAR NEUROBIOLOGY
- 5-HT release in nucleus accumbens rescues social deficits in mouse autism model
- (2018) Jessica J. Walsh et al. NATURE
- Activation of autophagy rescues synaptic and cognitive deficits in fragile X mice
- (2018) Jingqi Yan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- TBC1d24-ephrinB2 interaction regulates contact inhibition of locomotion in neural crest cell migration
- (2018) Jaeho Yoon et al. Nature Communications
- Oxidation resistance 1 regulates post-translational modifications of peroxiredoxin 2 in the cerebellum
- (2018) Daria M. Svistunova et al. FREE RADICAL BIOLOGY AND MEDICINE
- The epilepsy-associated protein TBC1D24 is required for normal development, survival and vesicle trafficking in mammalian neurons
- (2018) Mattéa J Finelli et al. HUMAN MOLECULAR GENETICS
- The lysosome as a cellular centre for signalling, metabolism and quality control
- (2018) Rosalie E. Lawrence et al. NATURE CELL BIOLOGY
- Synaptopathology Involved in Autism Spectrum Disorder
- (2018) Shiqi Guang et al. Frontiers in Cellular Neuroscience
- The interferon-inducible isoform of NCOA7 inhibits endosome-mediated viral entry
- (2018) Tomas Doyle et al. Nature Microbiology
- TLDc proteins: new players in the oxidative stress response and neurological disease
- (2017) Mattéa J. Finelli et al. MAMMALIAN GENOME
- Fundamental Elements in Autism: From Neurogenesis and Neurite Growth to Synaptic Plasticity
- (2017) James Gilbert et al. Frontiers in Cellular Neuroscience
- Misrouting of v-ATPase subunit V0a1 dysregulates lysosomal acidification in a neurodegenerative lysosomal storage disease model
- (2017) Maria B. Bagh et al. Nature Communications
- Disorders of lysosomal acidification—The emerging role of v-ATPase in aging and neurodegenerative disease
- (2016) Daniel J. Colacurcio et al. AGEING RESEARCH REVIEWS
- Regulation of V-ATPase assembly and function of V-ATPases in tumor cell invasiveness
- (2016) Christina McGuire et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- The Number of Parvalbumin-Expressing Interneurons Is Decreased in the Medial Prefrontal Cortex in Autism
- (2016) Ezzat Hashemi et al. CEREBRAL CORTEX
- Comparative efficacy and tolerability of antidepressants for major depressive disorder in children and adolescents: a network meta-analysis
- (2016) Andrea Cipriani et al. LANCET
- Skywalker-TBC1D24 has a lipid-binding pocket mutated in epilepsy and required for synaptic function
- (2016) Baptiste Fischer et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- TBC1D24genotype–phenotype correlation
- (2016) Simona Balestrini et al. NEUROLOGY
- Lack of Cdkl5 Disrupts the Organization of Excitatory and Inhibitory Synapses and Parvalbumin Interneurons in the Primary Visual Cortex
- (2016) Riccardo Pizzo et al. Frontiers in Cellular Neuroscience
- Skywalker-TBC1D24 has a lipid-binding pocket mutated in epilepsy and required for synaptic function
- (2016) Baptiste Fischer et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- PRRT2 Is a Key Component of the Ca 2+ -Dependent Neurotransmitter Release Machinery
- (2016) Pierluigi Valente et al. Cell Reports
- Autophagy linked FYVE (Alfy/WDFY3) is required for establishing neuronal connectivity in the mammalian brain
- (2016) Joanna M Dragich et al. eLife
- The Evolutionarily Conserved Tre2/Bub2/Cdc16 (TBC), Lysin Motif (LysM), Domain Catalytic (TLDc) Domain Is Neuroprotective against Oxidative Stress
- (2015) Mattéa J. Finelli et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Induction of a Unique Isoform of theNCOA7Oxidation Resistance Gene by Interferon β-1b
- (2015) Lijian Yu et al. JOURNAL OF INTERFERON AND CYTOKINE RESEARCH
- Shared Pathways Among Autism Candidate Genes Determined by Co-expression Network Analysis of the Developing Human Brain Transcriptome
- (2015) Ahmed Mahfouz et al. JOURNAL OF MOLECULAR NEUROSCIENCE
- Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome
- (2015) Fanny Kortüm et al. NATURE GENETICS
- Anxiety as a neurodevelopmental disorder in a neuronal subpopulation: Evidence from gene expression data
- (2015) Adela Viggiano et al. PSYCHIATRY RESEARCH
- Mapping the H+ (V)-ATPase interactome: identification of proteins involved in trafficking, folding, assembly and phosphorylation
- (2015) Maria Merkulova et al. Scientific Reports
- Neurodegenerative lysosomal disorders: A continuum from development to late age
- (2014) Ralph A. Nixon et al. Autophagy
- Human OXR1 maintains mitochondrial DNA integrity and counteracts hydrogen peroxide-induced oxidative stress by regulating antioxidant pathways involving p21
- (2014) Mingyi Yang et al. FREE RADICAL BIOLOGY AND MEDICINE
- The signaling lipid PI(3,5)P2 stabilizes V1–Vo sector interactions and activates the V-ATPase
- (2014) Sheena Claire Li et al. MOLECULAR BIOLOGY OF THE CELL
- The role of de novo mutations in the genetics of autism spectrum disorders
- (2014) Michael Ronemus et al. NATURE REVIEWS GENETICS
- Dendritic Inhibition in the Hippocampus Supports Fear Learning
- (2014) M. Lovett-Barron et al. SCIENCE
- V-ATPase inhibition by archazolid leads to lysosomal dysfunction resulting in impaired cathepsin B activationin vivo
- (2013) Rebekka Kubisch et al. INTERNATIONAL JOURNAL OF CANCER
- Inhibition of inhibition in visual cortex: the logic of connections between molecularly distinct interneurons
- (2013) Carsten K Pfeffer et al. NATURE NEUROSCIENCE
- Synaptic PI(3,4,5)P3 Is Required for Syntaxin1A Clustering and Neurotransmitter Release
- (2013) Thang Manh Khuong et al. NEURON
- At the end of the autophagic road: an emerging understanding of lysosomal functions in autophagy
- (2013) Han-Ming Shen et al. TRENDS IN BIOCHEMICAL SCIENCES
- The GABA system in anxiety and depression and its therapeutic potential
- (2011) Hanns Möhler NEUROPHARMACOLOGY
- Oxr1 Is Essential for Protection against Oxidative Stress-Induced Neurodegeneration
- (2011) Peter L. Oliver et al. PLoS Genetics
- Long noncoding RNA genes: conservation of sequence and brain expression among diverse amniotes
- (2010) Rebecca A Chodroff et al. GENOME BIOLOGY
- Lysosomal disorders: From storage to cellular damage
- (2008) Andrea Ballabio et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
- The vacuolar-ATPase B1 subunit in distal tubular acidosis: novel mutations and mechanisms for dysfunction
- (2008) D.G. Fuster et al. KIDNEY INTERNATIONAL
- Regulation of the V-ATPase along the Endocytic Pathway Occurs through Reversible Subunit Association and Membrane Localization
- (2008) Céline Lafourcade et al. PLoS One
- Molecular characterization and bioinformatics analysis of Ncoa7B, a novel ovulation-associated and reproduction system-specific Ncoa7 isoform
- (2008) Ketty Shkolnik et al. REPRODUCTION
- Dendritic-targeting GABA neurons in monkey prefrontal cortex: Comparison of somatostatin- and calretinin-immunoreactive axon terminals
- (2008) Darlene S. Melchitzky et al. SYNAPSE
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