Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders (Q35606895)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17088268%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

title

Modulation of the W748S mutation in DNA polymerase gamma by the E1143G polymorphismin mitochondrial disorders (English)

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21 December 2019

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21 December 2019

Sherine S L Chan

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21 December 2019

Matthew J Longley

series ordinal

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21 December 2019

publication date

6 November 2006

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21 December 2019

published in

Human Molecular Genetics

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21 December 2019

volume

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21 December 2019

issue

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21 December 2019

page(s)

3473-3483

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POLG1 mutations associated with progressive encephalopathy in childhood

21 December 2019

cites work

1 reference

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

12 July 2018

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DNA polymerase gamma in mitochondrial DNA replication and repair.

12 July 2018

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Functional human mitochondrial DNA polymerase gamma forms a heterotrimer

12 July 2018

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Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin

12 July 2018

1 reference

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The common A467T mutation in the human mitochondrial DNA polymerase (POLG) compromises catalytic efficiency and interaction with the accessory subunit.

12 July 2018

1 reference

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Mitochondrial DNA and disease

12 July 2018

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Mutations in the spacer region of Drosophila mitochondrial DNA polymerase affect DNA binding, processivity, and the balance between Pol and Exo function

12 July 2018

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Structure-function defects of human mitochondrial DNA polymerase in autosomal dominant progressive external ophthalmoplegia

12 July 2018

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Structural determinants in human DNA polymerase gamma account for mitochondrial toxicity from nucleoside analogs.

12 July 2018

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The mitochondrial DNA polymerase as a target of oxidative damage

12 July 2018

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Active site mutation in DNA polymerase gamma associated with progressive external ophthalmoplegia causes error-prone DNA synthesis

12 July 2018

1 reference

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The mitochondrial p55 accessory subunit of human DNA polymerase gamma enhances DNA binding, promotes processive DNA synthesis, and confers N-ethylmaleimide resistance

12 July 2018

1 reference

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Neurophysiological and mitochondrial abnormalities in MuSK antibody seropositive myasthenia gravis compared to other immunological subtypes

12 July 2018

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The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases

25 September 2018

1 reference

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Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene

25 September 2018

1 reference

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Molecular diagnosis of Alpers syndrome.

25 September 2018

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Mono-allelic POLG expression resulting from nonsense-mediated decay and alternative splicing in a patient with Alpers syndrome.

25 September 2018

1 reference

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POLG mutations in Alpers syndrome

25 September 2018

1 reference

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Molecular insights into NRTI inhibition and mitochondrial toxicity revealed from a structural model of the human mitochondrial DNA polymerase.

25 September 2018

1 reference

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Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations

25 September 2018

1 reference

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Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.

25 September 2018

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POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement

25 September 2018

1 reference

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Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma

25 September 2018

1 reference

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Rapid segmental and subdomain motions of DNA polymerase beta.

25 September 2018

1 reference

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Differential incorporation and removal of antiviral deoxynucleotides by human DNA polymerase gamma

25 September 2018

1 reference

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Characterization of the native and recombinant catalytic subunit of human DNA polymerase gamma: identification of residues critical for exonuclease activity and dideoxynucleotide sensitivity

25 September 2018

1 reference

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Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population

25 September 2018

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12 December 2020

The fidelity of human DNA polymerase gamma with and without exonucleolytic proofreading and the p55 accessory subunit

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12 December 2020

POLG mutations and Alpers syndrome

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12 December 2020

POLG1, C10ORF2, and ANT1 mutations are uncommon in sporadic progressive external ophthalmoplegia with multiple mitochondrial DNA deletions

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12 December 2020

POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions

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12 December 2020

Progressive external ophthalmoplegia: a new family with tremor and peripheral neuropathy

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12 December 2020

Phage like it HOT: solution structure of the bacteriophage P1-encoded HOT protein, a homolog of the theta subunit of E. coli DNA polymerase III

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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

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12 December 2020

Identifiers

DOI

10.1093/HMG/DDL424

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17088268%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

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21 December 2019

PubMed publication ID

17088268

1 reference

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