(Q24308200)

GOA release 2020-03-11

mitochondrial DNA repair

1 reference

GOA release 2020-03-11

mitochondrion

1 reference

based on heuristic

inferred from title

mitochondrial disease

1 reference

22

0 references

Holger Prokisch

25

0 references

Thomas J Nicholls

Thomas J Nicholls

2

0 references

Joanna Rorbach

Joanna Rorbach

9

0 references

Michał Mińczuk

Michal Minczuk

23

0 references

Gábor Zsurka

Gábor Zsurka

8

0 references

Dario Ronchi

Dario Ronchi

13

0 references

Wolfram S. Kunz

Wolfram S Kunz

24

0 references

Giacomo P Comi

Giacomo P Comi

14

0 references

Salvatore DiMauro

17

Salvatore DiMauro

0 references

Maurizio Moggio

15

Maurizio Moggio

0 references

Monica Sciacco

12

Monica Sciacco

0 references

Cornelia Kornblum

1

Cornelia Kornblum

0 references

Tobias B Haack

3

Tobias B Haack

0 references

Katharina Danhauser

6

Katharina Danhauser

0 references

Arcangela Iuso

10

Arcangela Iuso

0 references

Thomas Wieland

11

Thomas Wieland

0 references

Sarah E Calvo

18

Sarah E Calvo

0 references

Vamsi Mootha

19

Vamsi K Mootha

0 references

Thomas Klopstock

20

Thomas Klopstock

0 references

Tim M Strom

21

Tim M Strom

0 references

author name string

Susanne Schöler

4

0 references

Viktoriya Peeva

5

0 references

Kerstin Hallmann

7

0 references

Catarina M Quinzii

Human Dna2 is a nuclear and mitochondrial DNA maintenance protein

16

0 references

language of work or name

English

0 references

publication date

February 2013

0 references

published in

Nature Genetics

0 references

volume

45

0 references

issue

2

0 references

page(s)

214-9

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Human DNA2 is a mitochondrial nuclease/helicase for efficient processing of DNA replication and repair intermediates

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

A mitochondrial protein compendium elucidates complex I disease biology

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Role of adenine nucleotide translocator 1 in mtDNA maintenance

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Crystal structure of RecBCD enzyme reveals a machine for processing DNA breaks

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Sequence, structure and functional diversity of PD-(D/E)XK phosphodiesterase superfamily

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Apoptosis induced by persistent single-strand breaks in mitochondrial genome: critical role of EXOG (5'-EXO/endonuclease) in their repair

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

PDE12 removes mitochondrial RNA poly(A) tails and controls translation in 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=3678843

Mammalian mitochondrial DNA replication intermediates are essentially duplex but contain extensive tracts of RNA/DNA hybrid

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

DNA2 resolves expanding flap in mitochondrial base excision repair

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

MitoP2: an integrative tool for the analysis of the mitochondrial proteome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Removal of oxidative DNA damage via FEN1-dependent long-patch base excision repair in human cell 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=3678843

Expression of catalytic mutants of the mtDNA helicase Twinkle and polymerase POLG causes distinct replication stalling phenotypes.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Release of replication termination controls mitochondrial DNA copy number after depletion with 2',3'-dideoxycytidine

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA 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=3678843

SURVEY AND SUMMARY: holliday junction resolvases and related nucleases: identification of new families, phyletic distribution and evolutionary trajectories

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

Coupled leading- and lagging-strand synthesis of mammalian mitochondrial DNA.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3678843

POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts.

27 September 2017

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2501

Clonally expanded mitochondrial DNA mutations in epileptic individuals with mutated DNA polymerase gamma

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2501

Cellular rescue-assay aids verification of causative DNA-variants in mitochondrial complex I deficiency

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.2501

Analysis of replicating mitochondrial DNA by two-dimensional agarose gel electrophoresis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23313956

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.2501

1 reference

Dimensions Publication ID

1008201705

0 references

1 reference

1 reference

PubMed publication ID

23313956

1 reference