The E646D-ATP13A4 mutation associated with autism reveals a defect in calcium regulation (Q28506199)

Crossref

https://api.crossref.org/works/10.1007%2FS10571-009-9445-8

PMR1/SPCA Ca2+ pumps and the role of the Golgi apparatus as a Ca2+ store

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10571-009-9445-8

Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland

21 January 2018

1 reference

12 December 2020

Cdc50p, a protein required for polarized growth, associates with the Drs2p P-type ATPase implicated in phospholipid translocation in Saccharomyces cerevisiae

1 reference

12 December 2020

Cod1p/Spf1p is a P-type ATPase involved in ER function and Ca2+ homeostasis

1 reference

12 December 2020

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

1 reference

12 December 2020

Yeast genes controlling responses to topogenic signals in a model transmembrane protein

1 reference

12 December 2020

ATP8B1 requires an accessory protein for endoplasmic reticulum exit and plasma membrane lipid flippase activity

1 reference

12 December 2020

SERCA pump level is a critical determinant of Ca(2+)homeostasis and cardiac contractility

1 reference

12 December 2020

The plasma membrane calcium pump--a physiological perspective on its regulation

1 reference

12 December 2020

The developmentally regulated expression of Menkes protein ATP7A suggests a role in axon extension and synaptogenesis.

1 reference

12 December 2020

Physical link and functional coupling of presynaptic calcium channels and the synaptic vesicle docking/fusion machinery.

1 reference

12 December 2020

Calcium pumps in the central nervous system

1 reference

12 December 2020

Calcium stores and synaptic plasticity

1 reference

12 December 2020

Validation of internal control genes for expression studies: effects of the neurotrophin BDNF on hippocampal neurons

1 reference

12 December 2020

Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT

1 reference

12 December 2020

Characterization of the P5 subfamily of P-type transport ATPases in mice

1 reference

12 December 2020

CACNA1H mutations in autism spectrum disorders.

1 reference

12 December 2020

A novel isoform of the secretory pathway Ca2+,Mn(2+)-ATPase, hSPCA2, has unusual properties and is expressed in the brain

1 reference

12 December 2020

Cell migration and subplate loss in explant cultures of murine cerebral cortex.

1 reference

12 December 2020

Identification and functional expression of four isoforms of ATPase II, the putative aminophospholipid translocase. Effect of isoform variation on the ATPase activity and phospholipid specificity

1 reference

12 December 2020

Mitochondria and neuronal activity.

1 reference

12 December 2020

Plasma membrane Ca2+ ATPase 2 contributes to short-term synapse plasticity at the parallel fiber to Purkinje neuron synapse

1 reference

12 December 2020

Reduction of GluR2 RNA editing, a molecular change that increases calcium influx through AMPA receptors, selective in the spinal ventral gray of patients with amyotrophic lateral sclerosis

1 reference

12 December 2020

The fates of cells in the developing cerebral cortex of normal and methylazoxymethanol acetate-lesioned mice.

1 reference

12 December 2020

The calcium channel and the organization of the presynaptic transmitter release face

1 reference

12 December 2020

Mutational analysis of the Lem3p-Dnf1p putative phospholipid-translocating P-type ATPase reveals novel regulatory roles for Lem3p and a carboxyl-terminal region of Dnf1p independent of the phospholipid-translocating activity of Dnf1p in yeast

1 reference

12 December 2020

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27

1 reference

12 December 2020

1 reference

12 December 2020

Structure and mechanism of Na,K-ATPase: functional sites and their interactions

1 reference

12 December 2020

Regulation of HMG-CoA reductase degradation requires the P-type ATPase Cod1p/Spf1p

1 reference

12 December 2020

The fates of cells generated at the end of neurogenesis in developing mouse cortex

1 reference

12 December 2020

Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay.

1 reference

12 December 2020

Linkage and association of the glutamate receptor 6 gene with autism

1 reference

12 December 2020

The role of the endoplasmic reticulum Ca2+ store in the plasticity of central neurons

1 reference

12 December 2020

Immunochemical and mutational analyses of P-type ATPase Spf1p involved in the yeast secretory pathway.

1 reference

12 December 2020

Tissue subcellular fractionation and protein extraction for use in mass-spectrometry-based proteomics

1 reference

12 December 2020

Presynaptic plasma membrane Ca2+ ATPase isoform 2a regulates excitatory synaptic transmission in rat hippocampal CA3

1 reference

12 December 2020

Chilling tolerance in Arabidopsis involves ALA1, a member of a new family of putative aminophospholipid translocases

1 reference

12 December 2020

Isoform-specific distribution of the plasma membrane Ca2+ ATPase in the rat brain

1 reference

12 December 2020

Activity and localization of the secretory pathway Ca2+-ATPase isoform 1 (SPCA1) in different areas of the mouse brain during postnatal development.

1 reference

12 December 2020

A new generation of Ca2+ indicators with greatly improved fluorescence properties

1 reference

12 December 2020

Structural complexity and functional diversity of endoplasmic reticulum Ca(2+) stores

1 reference

12 December 2020

Calcium as a versatile second messenger in the control of gene expression

1 reference

12 December 2020

Evolution of substrate specificities in the P-type ATPase superfamily.

1 reference

12 December 2020

Deranged neuronal calcium signaling and Huntington disease.

1 reference

12 December 2020

A model for beta-amyloid aggregation and neurotoxicity based on free radical generation by the peptide: relevance to Alzheimer disease

1 reference

12 December 2020

Phylogenetic analysis of P5 P-type ATPases, a eukaryotic lineage of secretory pathway pumps

1 reference

12 December 2020

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

1 reference

12 December 2020

Calcium, ageing, and neuronal vulnerability in Parkinson's disease

1 reference

12 December 2020

Glutamate potentiates the toxicity of mutant Cu/Zn-superoxide dismutase in motor neurons by postsynaptic calcium-dependent mechanisms

1 reference

12 December 2020

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism

1 reference

12 December 2020

The metabotropic glutamate receptor 8 gene at 7q31: partial duplication and possible association with autism

1 reference

12 December 2020

How does calcium trigger neurotransmitter release?

1 reference

12 December 2020

Calcium signaling and the control of dendritic development

1 reference

12 December 2020

Two distinctly localized p-type ATPases collaborate to maintain organelle homeostasis required for glycoprotein processing and quality control

1 reference

12 December 2020

P-type ATPase spf1 mutants show a novel resistance mechanism for the killer toxin SMKT.

1 reference

12 December 2020

The network of calcium regulation in muscle

1 reference

12 December 2020