(Q47740183)

5 February 2018

title

Homoplasmic MELAS A3243G mtDNA mutation in a colon cancer sample (English)

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5 February 2018

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2

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5 February 2018

Paweł Golik

3

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5 February 2018

Jerzy Ostrowski

5

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5 February 2018

Anna Lorenc

Anna Lorenc

1

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Maciej Pronicki

Maciej Pronicki

6

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Ewa Bartnik

9

Ewa Bartnik

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5 February 2018

Małgorzata Szołkowska

8

Małgorzata Szołkowska

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5 February 2018

Jolanta Kupryjanczyk

4

Jolanta Kupryjańczyk

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5 February 2018

Andrzej Semczuk

7

Andrzej Semczuk

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5 February 2018

publication date

1 October 2003

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5 February 2018

published in

Mitochondrion

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5 February 2018

volume

3

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5 February 2018

issue

2

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5 February 2018

page(s)

119-124

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5 February 2018

Sequence and organization of the human mitochondrial genome

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Genetic instability and darwinian selection in tumours

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Mitochondrial defects in cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

In situ and slot hybridization analysis of RNA in colorectal tumours and normal colon shows distinct distributions of mitochondrial sequences

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

VACTERL with the mitochondrial np 3243 point mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

A tRNA suppressor mutation in human mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Mitochondrial tRNALeu isoforms in lung carcinoma cybrid cells containing the np 3243 mtDNA mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Facile detection of mitochondrial DNA mutations in tumors and bodily fluids

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

A novel point mutation in the mitochondrial tRNA(Leu)(UUR) gene in a family with mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

The hypoxic core: a possible answer to the cancer paradox

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Recovery of the missing tumorigenicity in mitochondrial DNA-less HeLa cells by introduction of mitochondrial DNA from normal human cells

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Increased steady-state levels of several mitochondrial and nuclear gene transcripts in rat hepatoma with a low content of mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Mitochondrial diabetes: investigation and identification of a novel mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

The emerging tree of West Eurasian mtDNAs: a synthesis of control-region sequences and RFLPs

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Defective respiratory capacity and mitochondrial protein synthesis in transformant cybrids harboring the tRNA(Leu(UUR)) mutation associated with maternally inherited myopathy and cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Level of heteroplasmy for the mitochondrial mutation A3243G correlates with age at onset of diabetes and deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Enhanced oxidative damage in human cells harboring A3243G mutation of mitochondrial DNA: implication of oxidative stress in the pathogenesis of mitochondrial diabetes

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

The pathogenic A3243G mutation in human mitochondrial tRNALeu(UUR) decreases the efficiency of aminoacylation

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Mitochondrial DNA in human malignancy.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Somatic mutations of the mitochondrial genome in human colorectal tumours

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Defective mitochondrial ATP synthesis in oxyphilic thyroid tumors.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Differential expression of the mitochondrial gene cytochrome oxidase II in benign and malignant breast tissue

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation)

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNA(Trp) gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Low mitochondrial respiratory chain content correlates with tumor aggressiveness in renal cell carcinoma.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Mitochondrial DNA determines the cellular response to cancer therapeutic agents

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Mitochondrial NP 3243 point mutation is not a common cause of VACTERL association

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

On the Origin of Cancer Cells

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1567-7249%2803%2900106-5

7 January 2021

10.1016/S1567-7249(03)00106-5

Identifiers

DOI

1 reference

5 February 2018

1 reference

5 February 2018