(Q28119120)

English

ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint-like inclusion body formation, and selective degeneration of dopaminergic neurons

scientific journal article

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scholarly article

1 reference

4 January 2017

ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint-like inclusion body formation, and selective degeneration of dopaminergic neurons (English)

1 reference

4 January 2017

regulation of lysosomal protein catabolic process

2 references

Gene Ontology release 2020-05-02

Gene Ontology ID

GOA release 2020-03-11

ATPase cation transporting 13A2

1 reference

GOA release 2020-03-11

1 reference

based on heuristic

inferred from title

Norihito Uemura

object named as

Norihito Uemura

10

0 references

Manabu Funayama

object named as

Manabu Funayama

7

0 references

object named as

Masato Koike

4

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Shunichi Takeda

object named as

Shunichi Takeda

13

0 references

Nobutaka Hattori

15

object named as

Nobutaka Hattori

1 reference

4 January 2017

author name string

Hideaki Matsui

1

1 reference

4 January 2017

Fumiaki Sato

2

1 reference

4 January 2017

Shigeto Sato

3

1 reference

4 January 2017

Yosuke Taruno

5

1 reference

4 January 2017

Shinji Saiki

6

1 reference

4 January 2017

Hidefumi Ito

8

1 reference

4 January 2017

Yoshihito Taniguchi

9

1 reference

4 January 2017

Atsushi Toyoda

11

1 reference

4 January 2017

Yoshiyuki Sakaki

12

1 reference

4 January 2017

Yasuo Uchiyama

14

1 reference

4 January 2017

Ryosuke Takahashi

16

1 reference

4 January 2017

language of work or name

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publication date

2 May 2013

1 reference

4 January 2017

1 reference

4 January 2017

587

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4 January 2017

9

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4 January 2017

1316–1325

1 reference

4 January 2017

Update on the genetics of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Parkinson's disease: from monogenic forms to genetic susceptibility factors

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Generation of medaka gene knockout models by target-selected mutagenesis

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

A chemical neurotoxin, MPTP induces Parkinson's disease like phenotype, movement disorders and persistent loss of dopamine neurons in medaka fish

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Proteasome inhibition in medaka brain induces the features of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Mutation of the glycosylated asparagine residue 286 in human CLN2 protein results in loss of enzymatic activity.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Alpha-synuclein in Lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

α-Synuclein Is Degraded by Both Autophagy and the Proteasome

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Parkin is recruited selectively to impaired mitochondria and promotes their autophagy

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Novel mutation and the first prenatal screening of cathepsin D deficiency (CLN10).

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Cathepsin D deficiency is associated with a human neurodegenerative disorder

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Fabry's disease without angiokeratomas showing unusual eccrine gland vacuolation

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Loss of PINK1 in medaka fish (Oryzias latipes) causes late-onset decrease in spontaneous movement

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Ammonium chloride and tunicamycin are novel toxins for dopaminergic neurons and induce Parkinson's disease-like phenotypes in medaka fish

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Dopamine induced neurodegeneration in a PINK1 model of Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: contribution to the apoptotic theory in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.FEBSLET.2013.02.046

21 January 2018

Identifiers

10.1016/J.FEBSLET.2013.02.046

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1 reference

4 January 2017

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