Leigh syndrome in Drosophila melanogaster: morphological and biochemical characterization of Surf1 post-transcriptional silencing (Q38962266)

8 September 2017

Leigh syndrome in Drosophila melanogaster: morphological and biochemical characterization of Surf1 post-transcriptional silencing (English)

1 reference

8 September 2017

Drosophila melanogaster

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Surfeit 1 Dmel_CG9943

1 reference

GOA release 2020-03-11

author

Paolo Bernardi

8

1 reference

8 September 2017

Alberto Biscontin

3

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Massimo Zeviani

7

object named as

Massimo Zeviani

1 reference

8 September 2017

2

Sophia von Stockum

1 reference

8 September 2017

Caterina Da-Rè

1

1 reference

8 September 2017

Caterina Millino

4

1 reference

8 September 2017

Paola Cisotto

5

1 reference

8 September 2017

Mauro A Zordan

6

1 reference

8 September 2017

Cristiano De Pittà

9

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8 September 2017

Rodolfo Costa

10

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8 September 2017

language of work or name

English

0 references

publication date

27 August 2014

1 reference

Journal of Biological Chemistry

8 September 2017

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8 September 2017

289

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8 September 2017

29235-29246

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8 September 2017

42

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describes a project that uses

8 September 2017

limma

object named as

LIMMA

2 references

22 June 2022

https://europepmc.org/article/PMC/4200275

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

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Decreased in vitro mitochondrial function is associated with enhanced brain metabolism, blood flow, and memory in Surf1-deficient mice

9 September 2017

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9 September 2017

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Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies

9 September 2017

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9 September 2017

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Analysis of Leigh syndrome mutations in the yeast SURF1 homolog reveals a new member of the cytochrome oxidase assembly factor family

9 September 2017

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Regulation of mitochondrial respiratory chain biogenesis by estrogens/estrogen receptors and physiological, pathological and pharmacological implications

9 September 2017

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9 September 2017

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Evidence that the assembly of the yeast cytochrome bc1 complex involves the formation of a large core structure in the inner mitochondrial membrane

9 September 2017

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Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects

9 September 2017

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Shy1 couples Cox1 translational regulation to cytochrome c oxidase assembly

9 September 2017

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Biochemical assays of respiratory chain complex activity

9 September 2017

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Identification of mitochondrial complex I assembly intermediates by tracing tagged NDUFS3 demonstrates the entry point of mitochondrial subunits

9 September 2017

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Linear models and empirical bayes methods for assessing differential expression in microarray experiments

9 September 2017

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Post-transcriptional silencing and functional characterization of the Drosophila melanogaster homolog of human Surf1.

9 September 2017

1 reference

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Biogenesis of cytochrome oxidase-sophisticated assembly lines in the mitochondrial inner membrane

9 September 2017

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9 September 2017

Mitochondrial disorders

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Subacute necrotizing encephalomyelopathy in an infant

9 September 2017

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Differences in assembly or stability of complex I and other mitochondrial OXPHOS complexes in inherited complex I deficiency

9 September 2017

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Mitochondrial respiratory-chain diseases

9 September 2017

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Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in mice

9 September 2017

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A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

9 September 2017

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MR findings in Leigh syndrome with COX deficiency and SURF-1 mutations

9 September 2017

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

9 September 2017

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Shy1p occurs in a high molecular weight complex and is required for efficient assembly of cytochrome c oxidase in yeast

9 September 2017

1 reference

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Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome C oxidase deficiency

9 September 2017

1 reference

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Nuclear gene defects in mitochondrial disorders

9 September 2017

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Expression and functional analysis of SURF1 in Leigh syndrome patients with cytochrome c oxidase deficiency

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

9 September 2017

1 reference

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Proton pump coupled to cytochrome c oxidase in mitochondria

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Molecular defects in cytochrome oxidase in mitochondrial diseases

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Mimicking a SURF1 allele reveals uncoupling of cytochrome c oxidase assembly from translational regulation in yeast

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Shy1p is necessary for full expression of mitochondrial COX1 in the yeast model of Leigh's syndrome

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Respiratory active mitochondrial supercomplexes.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Subunits of mitochondrial complex I exist as part of matrix- and membrane-associated subcomplexes in living cells

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

L-glutamate as an excitatory transmitter at the Drosophila larval neuromuscular junction

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Mutations in mitochondrial complex III uniquely affect complex I in Caenorhabditis elegans

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Regulation of the permeability transition pore in skeletal muscle mitochondria. Modulation By electron flow through the respiratory chain complex i.

17 June 2018

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Human cytochrome c oxidase: structure, function, and deficiency.

17 June 2018

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Neural specificity of elav expression: defining a Drosophila promoter for directing expression to the nervous system.

17 June 2018

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Staging the metamorphosis of Drosophila melanogaster.

17 June 2018

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Cell lines derived from late embryonic stages of Drosophila melanogaster

17 June 2018

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UCP4C mediates uncoupled respiration in larvae of Drosophila melanogaster

17 June 2018

1 reference

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Expression of the Ciona intestinalis alternative oxidase (AOX) in Drosophila complements defects in mitochondrial oxidative phosphorylation.

21 August 2018

1 reference

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Quantification of mitochondrial DNA copy number: pre-analytical factors

21 August 2018

1 reference

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Quantification of mitochondrial DNA deletion, depletion, and overreplication: application to diagnosis.

21 August 2018

1 reference

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Sequence conservation from human to prokaryotes of Surf1, a protein involved in cytochrome c oxidase assembly, deficient in Leigh syndrome.

21 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200275

Supercomplexes and subcomplexes of mitochondrial oxidative phosphorylation

21 August 2018

1 reference

12 December 2020

Loss-of-function mutations of SURF-1 are specifically associated with Leigh syndrome with cytochromec oxidase deficiency

1 reference

12 December 2020

Improved insulin sensitivity associated with reduced mitochondrial complex IV assembly and activity

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12 December 2020

Assembly of nuclear DNA-encoded subunits into mitochondrial complex IV, and their preferential integration into supercomplex forms in patient mitochondria

1 reference

12 December 2020

Increased longevity and refractoriness to Ca(2+)-dependent neurodegeneration in Surf1 knockout mice

1 reference

12 December 2020

Improved stability of Drosophila larval neuromuscular preparations in haemolymph-like physiological solutions

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12 December 2020

Identifiers

DOI

10.1074/JBC.M114.602938

1 reference

8 September 2017

1 reference

8 September 2017

1 reference