SEPT5_v2 is a parkin-binding protein (Q28209755)

ORCID Public Data File 2021

author name string

P Choi

1

0 references

H Snyder

2

0 references

L Petrucelli

3

0 references

C Theisler

4

0 references

M Chong

5

0 references

Y Zhang

6

0 references

K Lim

7

0 references

K K K Chung

8

0 references

K Kehoe

9

0 references

L D'Adamio

10

0 references

J M Lee

11

0 references

E Cochran

12

0 references

R Bowser

13

0 references

T M Dawson

14

0 references

B Wolozin

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

15

0 references

language of work or name

English

0 references

publication date

7 October 2003

0 references

published in

Molecular Brain Research

0 references

volume

117

0 references

issue

2

0 references

page(s)

179-89

0 references

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

The septin CDCrel-1 binds syntaxin and inhibits exocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Co-association of parkin and alpha-synuclein

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

1 reference

7 January 2021

Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusions

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Lewy bodies and parkinsonism in families with parkin mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Septins: cytoskeletal polymers or signalling GTPases?

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Role of cytochrome c as a stimulator of alpha-synuclein aggregation in Lewy body disease

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Association of the cytoskeletal GTP-binding protein Sept4/H5 with cytoplasmic inclusions found in Parkinson's disease and other synucleinopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

CHIP is associated with Parkin, a gene responsible for familial Parkinson's disease, and enhances its ubiquitin ligase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

An unfolded putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress, is a substrate of Parkin

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Parkin suppresses unfolded protein stress-induced cell death through its E3 ubiquitin-protein ligase activity

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Identification of septins in neurofibrillary tangles in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Parkinson's disease. First of two parts

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Mutations in NR4A2 associated with familial Parkinson disease

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

The ubiquitin pathway in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Association between early-onset Parkinson's disease and mutations in the parkin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Mammalian septins nomenclature

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Parkin protects against the toxicity associated with mutant alpha-synuclein: proteasome dysfunction selectively affects catecholaminergic neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Parkin localizes to the Lewy bodies of Parkinson disease and dementia with Lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Ubiquitination of a new form of alpha-synuclein by parkin from human brain: implications for Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Structural studies of the interaction between ubiquitin family proteins and proteasome subunit S5a

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Parkin suppresses dopaminergic neuron-selective neurotoxicity induced by Pael-R in Drosophila

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Mutation of the conserved N-terminal cysteine (Cys92) of human presenilin 1 causes increased A beta42 secretion in mammalian cells but impaired Notch/lin-12 signalling in C. elegans

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1

1 reference

https://api.crossref.org/works/10.1016%2FS0169-328X%2803%2900318-8

7 January 2021

10.1016/S0169-328X(03)00318-8

Identifiers

DOI

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/3pvf5lqrvjcxrk3a6uf72une7q

30 July 2022

mapped directly with Wikidata item

Fatcat ID

release_3pvf5lqrvjcxrk3a6uf72une7q

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/3pvf5lqrvjcxrk3a6uf72une7q

30 July 2022

mapped directly with Wikidata item

1 reference

https://api.fatcat.wiki/v0/release/3pvf5lqrvjcxrk3a6uf72une7q

30 July 2022