Cellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disorders (Q27003886)

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English	Cellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disorders	scientific article

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scholarly article

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20 March 2020

Cellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disorders (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24904274%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

Parkinson's disease

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based on heuristic

inferred from title

1

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20 March 2020

Danny Mollerup Sørensen

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20 March 2020

Michael Broberg Palmgren

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20 March 2020

Peter Vangheluwe

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20 March 2020

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Tine Holemans

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20 March 2020

Henrik W Holen

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20 March 2020

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27 May 2014

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20 March 2020

Frontiers in Molecular Neuroscience

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20 March 2020

7

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20 March 2020

48

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20 March 2020

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

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21 March 2017

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

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21 March 2017

Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicity

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Syndrome of hepatic cirrhosis, dystonia, polycythemia, and hypermanganesemia caused by mutations in SLC30A10, a manganese transporter in man

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21 March 2017

Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism

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21 March 2017

Alpha-synuclein promotes SNARE-complex assembly in vivo and in vitro

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Membrane Curvature Induction and Tubulation Are Common Features of Synucleins and Apolipoproteins

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21 March 2017

Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy

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21 March 2017

A novel mechanism of P-type ATPase autoinhibition involving both termini of the protein

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21 March 2017

Parkinson's disease: clinical features and diagnosis

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Crystal structure of the sodium–potassium pump

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21 March 2017

Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models

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21 March 2017

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism

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21 March 2017

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

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21 March 2017

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

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21 March 2017

A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network

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21 March 2017

Crystal structure of Na+, K(+)-ATPase in the Na(+)-bound state

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21 March 2017

Mutations in a P-type ATPase gene cause axonal degeneration

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21 March 2017

Crystal structure of a copper-transporting PIB-type ATPase

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21 March 2017

Crystal structure of the sodium-potassium pump at 2.4 A resolution

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21 March 2017

Crystal structure of the calcium pump of sarcoplasmic reticulum at 2.6 A resolution

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21 March 2017

Alpha-synuclein in Lewy bodies

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21 March 2017

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

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21 March 2017

Parkinson's disease-linked human PARK9/ATP13A2 maintains zinc homeostasis and promotes α-Synuclein externalization via exosomes

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21 March 2017

Interaction of divalent cations with peptide fragments from Parkinson's disease genes

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21 March 2017

The nuclear localization of SWI/SNF proteins is subjected to oxygen regulation

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21 March 2017

Shadows of an absent partner: ATP hydrolysis and phosphoenzyme turnover of the Spf1 (sensitivity to Pichia farinosa killer toxin) P5-ATPase

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21 March 2017

Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity

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21 March 2017

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

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21 March 2017

Yeast TAF(II)145 required for transcription of G1/S cyclin genes and regulated by the cellular growth state

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21 March 2017

Dependence of Ypt1 and Sec4 membrane attachment on Bet2.

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21 March 2017

Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove

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21 March 2017

Parkinson's disease-associated human P5B-ATPase ATP13A2 increases spermidine uptake

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21 March 2017

Zn²⁺ dyshomeostasis caused by loss of ATP13A2/PARK9 leads to lysosomal dysfunction and alpha-synuclein accumulation

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21 March 2017

ATP13A2 regulates mitochondrial bioenergetics through macroautophagy

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21 March 2017

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

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21 March 2017

PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity

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21 March 2017

P4 ATPases: flippases in health and disease

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21 March 2017

ATP7A-related copper transport diseases-emerging concepts and future trends

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21 March 2017

Familial basilar migraine associated with a new mutation in the ATP1A2 gene

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21 March 2017

Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation

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Variability of familial hemiplegic migraine with novel A1A2 Na+/K+-ATPase variants

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21 March 2017

Biology, structure and mechanism of P-type ATPases

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21 March 2017

Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase

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21 March 2017

Isolation of a partial candidate gene for Menkes disease by positional cloning

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21 March 2017

Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

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21 March 2017

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

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7 April 2017

Parkinson's disease

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7 April 2017

Impaired degradation of mutant alpha-synuclein by chaperone-mediated autophagy

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7 April 2017

Critical roles of isoleucine-364 and adjacent residues in a hydrophobic gate control of phospholipid transport by the mammalian P4-ATPase ATP8A2.

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28 September 2017

Parkinson's disease-associated human ATP13A2 (PARK9) deficiency causes zinc dyshomeostasis and mitochondrial dysfunction

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28 September 2017

The Sybtraps: control of synaptobrevin traffic by synaptophysin, α-synuclein and AP-180.

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28 September 2017

Genetics in dystonia

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28 September 2017

Manganese and the brain

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28 September 2017

CATP-6, a C. elegans ortholog of ATP13A2 PARK9, positively regulates GEM-1, an SLC16A transporter

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28 September 2017

The function of α-synuclein

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28 September 2017

Auto-inhibition of Drs2p, a yeast phospholipid flippase, by its carboxyl-terminal tail

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28 September 2017

Proteolytic processing of Atg32 by the mitochondrial i-AAA protease Yme1 regulates mitophagy

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28 September 2017

Role of the P-Type ATPases, ATP7A and ATP7B in brain copper homeostasis

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28 September 2017

Genetics of dystonia: what's known? What's new? What's next?

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28 September 2017

Type IV P-type ATPases distinguish mono- versus diacyl phosphatidylserine using a cytofacial exit gate in the membrane domain.

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28 September 2017

Lysosomal impairment in Parkinson's disease

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28 September 2017

Plasma membrane--endoplasmic reticulum contact sites regulate phosphatidylcholine synthesis

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28 September 2017

Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits

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28 September 2017

Advances in the mechanisms of Parkinson's disease.

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28 September 2017

Manganese efflux in Parkinsonism: insights from newly characterized SLC30A10 mutations

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28 September 2017

Two-gate mechanism for phospholipid selection and transport by type IV P-type ATPases

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28 September 2017

Linkage disequilibrium and haplotype analysis of the ATP7B gene in Alzheimer's disease

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28 September 2017

Lysosome-dependent pathways as a unifying theme in Parkinson's disease.

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28 September 2017

Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis

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28 September 2017

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion

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28 September 2017

Characterization of cellular protective effects of ATP13A2/PARK9 expression and alterations resulting from pathogenic mutants

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28 September 2017

Common pathogenic effects of missense mutations in the P-type ATPase ATP13A2 (PARK9) associated with early-onset parkinsonism

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28 September 2017

Ca2+ induces spontaneous dephosphorylation of a novel P5A-type ATPase.

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28 September 2017

Phosphorylation-dependent regulation of cyclin D1 and cyclin A gene transcription by TFIID subunits TAF1 and TAF7

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28 September 2017

Loss of P-type ATPase ATP13A2/PARK9 function induces general lysosomal deficiency and leads to Parkinson disease neurodegeneration.

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28 September 2017

The role of the Parkinson's disease gene PARK9 in essential cellular pathways and the manganese homeostasis network in yeast

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28 September 2017

PINK1- and Parkin-mediated mitophagy at a glance

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28 September 2017

Deficiency of ATP13A2 leads to lysosomal dysfunction, α-synuclein accumulation, and neurotoxicity

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28 September 2017

Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis

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28 September 2017

Mutations in SLC30A10 cause parkinsonism and dystonia with hypermanganesemia, polycythemia, and chronic liver disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Inhibitory effect of dietary lipids on chaperone-mediated autophagy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Critical role of a transmembrane lysine in aminophospholipid transport by mammalian photoreceptor P4-ATPase ATP8A2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Hypoxia regulation of ATP13A2 (PARK9) gene transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Phosphorylation of α-synuclein protein at Ser-129 reduces neuronal dysfunction by lowering its membrane binding property in Caenorhabditis elegans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Inhibition of phosphorylation of na+,k+-ATPase by mutations causing familial hemiplegic migraine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

A one base pair deletion in the canine ATP13A2 gene causes exon skipping and late-onset neuronal ceroid lipofuscinosis in the Tibetan terrier

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Parkinson's disease and cancer: two wars, one front

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Membrane curvature sensing by amphipathic helices: a single liposome study using α-synuclein and annexin B12

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

α-Synuclein and ALPS motifs are membrane curvature sensors whose contrasting chemistry mediates selective vesicle binding.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Regulation of intracellular manganese homeostasis by Kufor-Rakeb syndrome-associated ATP13A2 protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Mutant Atp13a2 proteins involved in parkinsonism are degraded by ER-associated degradation and sensitize cells to ER-stress induced cell death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Autophagic pathways in Parkinson disease and related disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Na+, K+-ATPase: functions in the nervous system and involvement in neurologic disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Effects of curvature and composition on α-synuclein binding to lipid vesicles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Inhibition of mitochondrial fusion by α-synuclein is rescued by PINK1, Parkin and DJ-1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

The sarcoplasmic Ca2+-ATPase: design of a perfect chemi-osmotic pump

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

α-Synuclein: membrane interactions and toxicity in Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Human copper transporters: mechanism, role in human diseases and therapeutic potential

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Lysosomal degradation of alpha-synuclein in vivo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

BLAST-EXPLORER helps you building datasets for phylogenetic analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Structural basis for the high Ca2+ affinity of the ubiquitous SERCA2b Ca2+ pump.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Amphipathic helices and membrane curvature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Zinc in the physiology and pathology of the CNS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Caenorhabditis elegans P5B-type ATPase CATP-5 operates in polyamine transport and is crucial for norspermidine-mediated suppression of RNA interference

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Intracellular Ca2+- and Mn2+-transport ATPases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

How Ca2+-ATPase pumps ions across the sarcoplasmic reticulum membrane

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Flippases: still more questions than answers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

The V-type H+-ATPase in vesicular trafficking: targeting, regulation and function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Protons and how they are transported by proton pumps.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Biochemical aspects of active transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Hypothesis-based RNAi screening identifies neuroprotective genes in a Parkinson's disease model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Crystal structure of the plasma membrane proton pump.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Reduced neuron-specific expression of the TAF1 gene is associated with X-linked dystonia-parkinsonism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

A general amphipathic alpha-helical motif for sensing membrane curvature.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Mitochondrial toxins and neurodegenerative diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Evidence that translation reinitiation leads to a partially functional Menkes protein containing two copper-binding sites.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Function of FXYD proteins, regulators of Na, K-ATPase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Modulating sarco(endo)plasmic reticulum Ca2+ ATPase 2 (SERCA2) activity: cell biological implications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Kufor Rakeb disease: autosomal recessive, levodopa-responsive parkinsonism with pyramidal degeneration, supranuclear gaze palsy, and dementia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

The Na/K-ATPase-mediated signal transduction as a target for new drug development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Flippases and vesicle-mediated protein transport

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

The pathobiology of the septin gene family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

A conditional mutation affecting localization of the Menkes disease copper ATPase. Suppression by copper supplementation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

A primate model of parkinsonism: selective destruction of dopaminergic neurons in the pars compacta of the substantia nigra by N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

Synuclein: a neuron-specific protein localized to the nucleus and presynaptic nerve terminal

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

BET1, BOS1, and SEC22 are members of a group of interacting yeast genes required for transport from the endoplasmic reticulum to the Golgi complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

28 September 2017

CHO cells expressing the human P₅-ATPase ATP13A2 are more sensitive to the toxic effects of herbicide paraquat

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

31 May 2018

Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

31 May 2018

Cd2+, Mn2+, Ni2+ and Se2+ toxicity to Saccharomyces cerevisiae lacking YPK9p the orthologue of human ATP13A2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

31 May 2018

Neurological manifestations in Wilson's disease: Report of 119 cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4033846

31 May 2018

A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

ATP13A2-related neurodegeneration (PARK9) without evidence of brain iron accumulation.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Mitochondrial dysfunctions in Parkinson's disease

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Structural and functional features of the transmembrane domain of the Na,K-ATPase beta subunit revealed by tryptophan scanning.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Patterns of levels of biological metals in CSF differ among neurodegenerative diseases.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

A copper treatable Menkes disease mutation associated with defective trafficking of a functional Menkes copper ATPase

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

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

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Role of magnesium and a phagosomal P-type ATPase in intracellular bacterial killing

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

The zebrafish homologue of Parkinson's disease ATP13A2 is essential for embryonic survival.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

The phosphatidylethanolamine level of yeast mitochondria is affected by the mitochondrial components Oxa1p and Yme1p

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Neurological disease mutations compromise a C-terminal ion pathway in the Na(+)/K(+)-ATPase.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

High levels of Mn²⁺ inhibit secretory pathway Ca²⁺/Mn²⁺-ATPase (SPCA) activity and cause Golgi fragmentation in neurons and glia

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Mitochondrial inhibitor models of Huntington's disease and Parkinson's disease induce zinc accumulation and are attenuated by inhibition of zinc neurotoxicity in vitro or in vivo

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Cys(x)His(y)-Zn2+ interactions: thiol vs. thiolate coordination

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Structural divergence between the two subgroups of P5 ATPases.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

α-Synuclein Is Degraded by Both Autophagy and the Proteasome

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Developmental expression of P5 ATPase mRNA in the mouse.

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

PARK9-LINKED PARKINSONISM IN EASTERN ASIA: MUTATION DETECTION IN ATP13A2 AND CLINICAL PHENOTYPE

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

P-type ATPases at a glance

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Crystal structure of a Na+-bound Na+,K+-ATPase preceding the E1P state

1 reference

https://api.crossref.org/works/10.3389%2FFNMOL.2014.00048

21 January 2018

Three sisters with very-late-onset major depression and parkinsonism

1 reference

https://pubmed.ncbi.nlm.nih.gov/24904274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/24904274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/24904274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ATP1A3 mutations: what is the phenotype?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24904274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Calmodulin and the plasma membrane calcium pump

1 reference

https://pubmed.ncbi.nlm.nih.gov/24904274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parkinson's disease in a chemist working with 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine

1 reference

https://pubmed.ncbi.nlm.nih.gov/24904274

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.3389/FNMOL.2014.00048

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24904274%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24904274%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24904274%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

ResearchGate publication ID

0 references

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