Sarah McMahon, Thomas LaFramboise. Carcinogenesis 2014
Times Cited: 46
Times Cited: 46
Times Cited
Times Co-cited
Similarity
Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer.
Young Seok Ju, Ludmil B Alexandrov, Moritz Gerstung, Inigo Martincorena, Serena Nik-Zainal, Manasa Ramakrishna, Helen R Davies, Elli Papaemmanuil, Gunes Gundem, Adam Shlien,[...]. Elife 2014
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Mitochondrial DNA copy number variation across human cancers.
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Spectrum of somatic mitochondrial mutations in five cancers.
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Heteroplasmic mitochondrial DNA mutations in normal and tumour cells.
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ROS-generating mitochondrial DNA mutations can regulate tumor cell metastasis.
Kaori Ishikawa, Keizo Takenaga, Miho Akimoto, Nobuko Koshikawa, Aya Yamaguchi, Hirotake Imanishi, Kazuto Nakada, Yoshio Honma, Jun-Ichi Hayashi. Science 2008
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Mitochondrial DNA mutations and mitochondrial DNA depletion in breast cancer.
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High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection.
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Simultaneous DNA and RNA Mapping of Somatic Mitochondrial Mutations across Diverse Human Cancers.
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Reduced mitochondrial DNA copy number is correlated with tumor progression and prognosis in Chinese breast cancer patients.
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Tumor-specific changes in mtDNA content in human cancer.
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Recurrent tissue-specific mtDNA mutations are common in humans.
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Mitochondrial DNA mutations and breast tumorigenesis.
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Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer.
Katayoon Darvishi, Swarkar Sharma, Audesh K Bhat, Ekta Rai, R N K Bamezai. Cancer Lett 2007
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Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA.
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Mitochondrial DNA mutations regulate metastasis of human breast cancer cells.
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Heteroplasmic shifts in tumor mitochondrial genomes reveal tissue-specific signals of relaxed and positive selection.
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Human mitochondrial DNA: roles of inherited and somatic mutations.
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Mitochondrial genetic background modifies breast cancer risk.
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Universal heteroplasmy of human mitochondrial DNA.
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Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease.
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Extensive tissue-related and allele-related mtDNA heteroplasmy suggests positive selection for somatic mutations.
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Methylation profile of TP53 regulatory pathway and mtDNA alterations in breast cancer patients lacking TP53 mutations.
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Mitochondrial DNA content as a potential marker to predict response to anthracycline in breast cancer patients.
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Enhanced tumorigenicity by mitochondrial DNA mild mutations.
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The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease.
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Somatic mutations throughout the entire mitochondrial genome are associated with elevated PSA levels in prostate cancer patients.
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Automated inference of molecular mechanisms of disease from amino acid substitutions.
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Mitochondrial genome acquisition restores respiratory function and tumorigenic potential of cancer cells without mitochondrial DNA.
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Signatures of mutational processes in human cancer.
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Selected mitochondrial DNA landscapes activate the SIRT3 axis of the UPRmt to promote metastasis.
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mtDNA Variation and Analysis Using Mitomap and Mitomaster.
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A heteroplasmic, not homoplasmic, mitochondrial DNA mutation promotes tumorigenesis via alteration in reactive oxygen species generation and apoptosis.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.