(Q24299243)

mitochondrion organization

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

mitochondrion

1 reference

inferred from title

frontotemporal dementia

1 reference

amyotrophic lateral sclerosis and frontotemporal dementia

inferred from title

1 reference

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24934289%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Valérie Serre

9

1 reference

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8 June 2020

David Moore

10

1 reference

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8 June 2020

Francoise Lespinasse

16

1 reference

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8 June 2020

Alexis Brice

19

1 reference

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8 June 2020

20

Patrick Yu-Wai-Man

1 reference

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8 June 2020

author name string

Sylvie Bannwarth

1

1 reference

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8 June 2020

Samira Ait-El-Mkadem

2

1 reference

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8 June 2020

Annabelle Chaussenot

3

1 reference

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8 June 2020

Sandra Lacas-Gervais

5

1 reference

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8 June 2020

Konstantina Fragaki

6

1 reference

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8 June 2020

Laetitia Berg-Alonso

7

1 reference

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8 June 2020

Yusuke Kageyama

8

1 reference

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8 June 2020

Annie Verschueren

11

1 reference

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8 June 2020

Cécile Rouzier

12

1 reference

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8 June 2020

Isabelle Le Ber

13

1 reference

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8 June 2020

Gaëlle Augé

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24934289%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

Charlotte Cochaud

15

1 reference

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8 June 2020

Karine N'Guyen

17

1 reference

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8 June 2020

Anne de Septenville

18

1 reference

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8 June 2020

Hiromi Sesaki

21

1 reference

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8 June 2020

Jean Pouget

22

1 reference

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8 June 2020

Véronique Paquis-Flucklinger

23

1 reference

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8 June 2020

language of work or name

English

0 references

publication date

August 2014

0 references

published in

Brain

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24934289%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

volume

137

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24934289%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

issue

Pt 8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24934289%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

page(s)

2329-2345

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24934289%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

8 June 2020

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4107737/fullTextXML

inferred from PubMed Central ID database lookup

cites work

CHCM1/CHCHD6, novel mitochondrial protein linked to regulation of mitofilin and mitochondrial cristae morphology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

ChChd3, an inner mitochondrial membrane protein, is essential for maintaining crista integrity and mitochondrial function

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Functional annotation of heart enriched mitochondrial genes GBAS and CHCHD10 through guilt by association

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Quantitation of mitochondrial dynamics by photolabeling of individual organelles shows that mitochondrial fusion is blocked during the Bax activation phase of apoptosis

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Structural characterization of CHCHD5 and CHCHD7: two atypical human twin CX9C proteins

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Protein structure prediction on the Web: a case study using the Phyre server

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Systematic analysis of the twin cx(9)c protein family.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Mitochondrial cristae shape determines respiratory chain supercomplexes assembly and respiratory efficiency

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

STED super-resolution microscopy reveals an array of MINOS clusters along human mitochondria

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Targeting and import mechanism of coiled-coil helix coiled-coil helix domain-containing protein 3 (ChChd3) into the mitochondrial intermembrane space.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

The human MSH5 (MutSHomolog 5) protein localizes to mitochondria and protects the mitochondrial genome from oxidative damage

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

The MIA pathway: a tight bond between protein transport and oxidative folding in mitochondria

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Defects in mitochondrial DNA replication and human disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Superresolution fluorescence imaging of mitochondrial nucleoids reveals their spatial range, limits, and membrane interaction

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Mechanisms of mitochondrial diseases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Mechanistic analysis of a DNA damage-induced, PTEN-dependent size checkpoint in human cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Genome-wide analysis of eukaryotic twin CX9C proteins

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Physiological functions of mitochondrial fusion

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Mitochondrial DNA depletion syndromes--many genes, common mechanisms

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Mitofusins and OPA1 mediate sequential steps in mitochondrial membrane fusion

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

The coiled coil-helix-coiled coil-helix proteins may be redox proteins

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Cristae formation-linking ultrastructure and function of mitochondria

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Structural basis of mitochondrial tethering by mitofusin complexes.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

The ratio of oxidative phosphorylation complexes I-V in bovine heart mitochondria and the composition of respiratory chain supercomplexes

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

A technique for ultracryotomy of cell suspensions and tissues

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Mitochondrial fusion intermediates revealed in vitro

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4107737

Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion.

30 May 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU138

Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU138

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU138

Role of MINOS in mitochondrial membrane architecture and biogenesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU138

OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWU138

21 January 2018

Mitochondrial diseases

1 reference

12 December 2020

Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay

1 reference

12 December 2020

Biochemical and molecular investigations in respiratory chain deficiencies

1 reference

12 December 2020

Rapid mapping of mitochondrial dna deletions by large-fragment PCR

1 reference

12 December 2020

Identifiers

DOI

10.1093/BRAIN/AWU138

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24934289%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24934289%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

PubMed publication ID

24934289

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24934289%20AND%20SRC:MED&resulttype=core&format=json