Inosine triphosphate pyrophosphohydrolase (ITPA) polymorphic sequence variants in adult hematological malignancy patients and possible association with mitochondrial DNA defects (Q37152683)

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scientific article published on 29 March 2013

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English	Inosine triphosphate pyrophosphohydrolase (ITPA) polymorphic sequence variants in adult hematological malignancy patients and possible association with mitochondrial DNA defects	scientific article published on 29 March 2013

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scholarly article

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27 February 2020

Inosine triphosphate pyrophosphohydrolase (ITPA) polymorphic sequence variants in adult hematological malignancy patients and possible association with mitochondrial DNA defects (English)

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27 February 2020

mitochondrial DNA

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3

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27 February 2020

Robert William Taylor

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Robert W Taylor

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27 February 2020

Francis Bowling

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Francis Bowling

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27 February 2020

author name string

Mazin A Zamzami

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27 February 2020

John A Duley

2

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27 February 2020

Deon J Venter

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27 February 2020

John W Yarham

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27 February 2020

Laurence P Catley

7

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27 February 2020

Timothy H J Florin

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27 February 2020

Anthony M Marinaki

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27 February 2020

publication date

29 March 2013

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27 February 2020

Journal of Hematology & Oncology

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27 February 2020

6

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27 February 2020

24

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27 February 2020

describes a project that uses

mitochondrial DNA

1 reference

based on heuristic

inferred from title

Pivotal role of inosine triphosphate pyrophosphatase in maintaining genome stability and the prevention of apoptosis in human cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Insights into N-calls of mitochondrial DNA sequencing using MitoChip v2.0.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Mitochondrial transfection for studying organellar DNA repair, genome maintenance and aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

DNA damage and base excision repair in mitochondria and their role in aging.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Oxidation in the nucleotide pool, the DNA damage response and cellular senescence: Defective bricks build a defective house

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

High-throughput detection of mutations responsible for childhood hearing loss using resequencing microarrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

NUDT16 and ITPA play a dual protective role in maintaining chromosome stability and cell growth by eliminating dIDP/IDP and dITP/ITP from nucleotide pools in mammals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

ReseqChip: automated integration of multiple local context probe data from the MitoChip array in mitochondrial DNA sequence assembly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Mitochondrial DNA mutations and human disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Genetic causes of mitochondrial DNA depletion in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Chromosomal abnormalities in cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Pharmacogenetic significance of inosine triphosphatase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

The ITPA c.94C>A and g.IVS2+21A>C sequence variants contribute to missplicing of the ITPA gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

An oligonucleotide microarray for high-throughput sequencing of the mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

House cleaning, a part of good housekeeping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Mitochondrial DNA mutations in human disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Xanthine, xanthosine and its nucleotides: solution structures of neutral and ionic forms, and relevance to substrate properties in various enzyme systems and metabolic pathways

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Alteration of nucleotide metabolism: a new mechanism for mitochondrial disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Mutagenic potentials of damaged nucleic acids produced by reactive oxygen/nitrogen species: approaches using synthetic oligonucleotides and nucleotides: survey and summary

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Mitochondrial defects in cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Mitochondrial threshold effects.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Genetic basis of hemolytic anemia caused by pyrimidine 5' nucleotidase deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Mitochondrial DNA in human malignancy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Cloning, expression, and characterization of a human inosine triphosphate pyrophosphatase encoded by the itpa gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

Human inosine triphosphatase: Catalytic properties and population studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

6 September 2017

ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

14 September 2017

The Human MitoChip: a high-throughput sequencing microarray for mitochondrial mutation detection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

14 September 2017

Expression analyses identify MLL as a prominent target of 11q23 amplification and support an etiologic role for MLL gain of function in myeloid malignancies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

14 September 2017

Efficient random mutagenesis method with adjustable mutation frequency by use of PCR and dITP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

14 September 2017

Therapy-related myelodysplastic syndrome and acute myeloid leukemia following fludarabine combination chemotherapy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

27 June 2018

Nucleotides function as endogenous chemical sensors for oxidative stress signaling.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

3 September 2018

HaploGrep: a fast and reliable algorithm for automatic classification of mitochondrial DNA haplogroups.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

3 September 2018

ITPase-deficient mice show growth retardation and die before weaning.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

3 September 2018

Distribution of ITPA P32T alleles in multiple world populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

3 September 2018

A Japanese case with inosine triphosphate pyrophosphohydrolase deficiency attributable to an enzymatic defect in white blood cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

3 September 2018

Adverse drug reactions to azathioprine therapy are associated with polymorphism in the gene encoding inosine triphosphate pyrophosphatase (ITPase).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3765497

3 September 2018

Mitochondrial DNA mutations in primary leukemia cells after chemotherapy: clinical significance and therapeutic implications.

1 reference

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3 September 2018

Deoxyuridine accumulation in urine in thymidine phosphorylase deficiency (MNGIE).

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3 September 2018

Somatic mitochondrial DNA mutations in adult-onset leukaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/23547827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased risk of acute myeloid leukaemia due to polymorphisms in detoxification and DNA repair enzymes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23547827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of mitochondrial DNA in 104 patients with myelodysplastic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23547827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms of detoxification and DNA repair enzymes in myelodyplastic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23547827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

6-Thioguanine damages mitochondrial DNA and causes mitochondrial dysfunction in human cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/23547827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation induced by deoxyxanthosine in codon 12 of a synthetic c-Ha-ras gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/23547827

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1756-8722-6-24

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27 February 2020

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27 February 2020

PubMed publication ID

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27 February 2020

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