(Q28272479)

4

object named as

Massimo Zeviani

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author name string

Maria A Graziewicz

1

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Matthew J Longley

2

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William C Copeland

Nature Structural & Molecular Biology

5

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language of work or name

English

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publication date

August 2004

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published in

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volume

11

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issue

8

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page(s)

770-6

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cites work

Role of adenine nucleotide translocator 1 in mtDNA maintenance

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

20 April 2017

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Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

20 April 2017

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Cloning and characterization of the human mitochondrial DNA polymerase, DNA polymerase gamma

20 April 2017

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Visualizing DNA replication in a catalytically active Bacillus DNA polymerase crystal

20 April 2017

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Crystal structure of a bacteriophage T7 DNA replication complex at 2.2 A resolution

20 April 2017

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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

20 April 2017

1 reference

Protein structure comparison by alignment of distance matrices

20 April 2017

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T-Coffee: A novel method for fast and accurate multiple sequence alignment

20 April 2017

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

20 April 2017

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Mitochondrial diseases in man and mouse

20 April 2017

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Mitochondrial genetics: a paradigm for aging and degenerative diseases?

20 April 2017

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Defects of intergenomic communication: autosomal disorders that cause multiple deletions and depletion of mitochondrial DNA.

21 January 2018

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Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy.

21 January 2018

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Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.

21 January 2018

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

21 January 2018

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Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.

21 January 2018

1 reference

Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)

21 January 2018

1 reference

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

21 January 2018

1 reference

An attempt to unify the structure of polymerases

21 January 2018

1 reference

Yeast mitochondrial DNA polymerase is related to the family A DNA polymerases

21 January 2018

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Compilation and alignment of DNA polymerase sequences

21 January 2018

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Structure of large fragment of Escherichia coli DNA polymerase I complexed with dTMP

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

1 reference

Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia

21 January 2018

1 reference

Deoxynucleoside triphosphate and pyrophosphate binding sites in the catalytically competent ternary complex for the polymerase reaction catalyzed by DNA polymerase I (Klenow fragment).

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region

21 January 2018

1 reference

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

21 January 2018

1 reference

Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domain

31 March 2020

1 reference