(Q47071097)

5 January 2018

title

Vitamin K2 is a mitochondrial electron carrier that rescues pink1 deficiency (English)

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5 January 2018

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Heixuedian Dmel_CG5876

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GOA release 2020-03-11

author

Patrik Verstreken

12

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5 January 2018

Bart De Strooper

9

object named as

Bart De Strooper

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5 January 2018

Melissa Vos

1

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5 January 2018

Giovanni Esposito

2

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5 January 2018

Janaka N Edirisinghe

3

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5 January 2018

Sven Vilain

4

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5 January 2018

Dominik M Haddad

5

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5 January 2018

Jan R Slabbaert

6

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5 January 2018

Stefanie Van Meensel

7

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5 January 2018

Onno Schaap

8

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5 January 2018

R Meganathan

10

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5 January 2018

Vanessa A Morais

11

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5 January 2018

language of work or name

English

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publication date

10 May 2012

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5 January 2018

published in

Science

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5 January 2018

volume

336

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5 January 2018

issue

6086

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5 January 2018

page(s)

1306-1310

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5 January 2018

Genetic clues to the pathogenesis of Parkinson's disease

cites work

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https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

A cell biological perspective on mitochondrial dysfunction in Parkinson disease and other neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Drosophila pink1 is required for mitochondrial function and interacts genetically with parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Mitochondrial dysfunction in Drosophila PINK1 mutants is complemented by parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Tweek, an evolutionarily conserved protein, is required for synaptic vesicle recycling

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

The v-ATPase V0 subunit a1 is required for a late step in synaptic vesicle exocytosis in Drosophila.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Loss of skywalker reveals synaptic endosomes as sorting stations for synaptic vesicle proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

The yeast complex I equivalent NADH dehydrogenase rescues pink1 mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Identification of UBIAD1 as a novel human menaquinone-4 biosynthetic enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

The Parkinson's disease genes pink1 and parkin promote mitochondrial fission and/or inhibit fusion in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

UBIAD1 mutation alters a mitochondrial prenyltransferase to cause Schnyder corneal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Vitamin K distribution in rat tissues: dietary phylloquinone is a source of tissue menaquinone-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Diagnostic value of immunostaining in cultured skin fibroblasts from patients with oxidative phosphorylation defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Mitochondrial DNA alterations and reduced mitochondrial function in aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Hereditary crystalline stromal dystrophy of Schnyder. II. Histopathology and ultrastructure

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Parkin negatively regulates JNK pathway in the dopaminergic neurons of Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Drosophila parkin mutants have decreased mass and cell size and increased sensitivity to oxygen radical stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Drosophila sbo regulates lifespan through its function in the synthesis of coenzyme Q in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

A genome-wide transgenic RNAi library for conditional gene inactivation in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Systematic generation of high-resolution deletion coverage of the Drosophila melanogaster genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

The DrosDel deletion collection: a Drosophila genomewide chromosomal deficiency resource

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Searching for pattern and mutation in the Drosophila genome with a P-lacZ vector

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

A Deficiency Screen for Dominant Suppressors of Telomeric Silencing in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

The Drosophila gene collection: identification of putative full-length cDNAs for 70% of D. melanogaster genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

P[acman]: a BAC transgenic platform for targeted insertion of large DNA fragments in D. melanogaster.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Synaptic mitochondria are critical for mobilization of reserve pool vesicles at Drosophila neuromuscular junctions

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Hypersensitivity to oxygen and shortened lifespan in a Drosophila mitochondrial complex II mutant

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

Anaerobic Growth of Escherichia coli K12 with Fumarate as Terminal Electron Acceptor. Genetic Studies with Menaquinone and Fluoroacetate-resistant Mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1218632

21 January 2018

Identifiers

DOI

10.1126/SCIENCE.1218632

1 reference

5 January 2018

release_j2izeqs35fd6vo7fbpnt3egif4

ADS bibcode

2012Sci...336.1306V

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Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/j2izeqs35fd6vo7fbpnt3egif4

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

5 January 2018