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RNA Editing in Pathogenesis of Cancer

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (14), p.3733-3739

2017

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Revisiting the TCA cycle: signaling to tumor formation

Trends in molecular medicine, 2011-11, Vol.17 (11), p.641-649

2011

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APOBEC3A cytidine deaminase induces RNA editing in monocytes and macrophages

Nature communications, 2015-04, Vol.6 (1), p.6881-6881, Article 6881

2015

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Stem-loop structure preference for site-specific RNA editing by APOBEC3A and APOBEC3G

PeerJ (San Francisco, CA), 2017-12, Vol.5, p.e4136, Article e4136

2017

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Mitochondrial hypoxic stress induces widespread RNA editing by APOBEC3G in natural killer cells

Genome Biology, 2019-02, Vol.20 (1), p.37-37, Article 37

2019

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The double-domain cytidine deaminase APOBEC3G is a cellular site-specific RNA editing enzyme

Scientific reports, 2016-12, Vol.6 (1), p.39100-39100, Article 39100

2016

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A recurrent stop-codon mutation in succinate dehydrogenase subunit B gene in normal peripheral blood and childhood T-cell acute leukemia

PloS one, 2007-05, Vol.2 (5), p.e436-e436

2007

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The implications of APOBEC3-mediated C-to-U RNA editing for human disease

Communications biology, 2024-05, Vol.7 (1), p.529-10, Article 529

2024

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RNA editing enzyme APOBEC3A promotes pro-inflammatory M1 macrophage polarization

Communications biology, 2021-01, Vol.4 (1), p.102-102, Article 102

2021

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Succinate dehydrogenase inversely regulates red cell distribution width and healthy life span in chronically hypoxic mice

JCI insight, 2022-09, Vol.7 (17)

2022

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Relationship Between ERCC1 Polymorphisms, Disease Progression, and Survival in the Gynecologic Oncology Group Phase III Trial of Intraperitoneal Versus Intravenous Cisplatin and Paclitaxel for Stage III Epithelial Ovarian Cancer

Journal of clinical oncology, 2008-07, Vol.26 (21), p.3598-3606

2008

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Transient overexpression of exogenous APOBEC3A causes C-to-U RNA editing of thousands of genes

RNA biology, 2017-05, Vol.14 (5), p.603-610

2017

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Genotype and Tumor Locus Determine Expression Profile of Pseudohypoxic Pheochromocytomas and Paragangliomas

Neoplasia (New York, N.Y.), 2013-04, Vol.15 (4), p.435-IN22

2013

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Genomic imprinting and environment in hereditary paraganglioma

American journal of medical genetics. Part C, Seminars in medical genetics, 2004-08, Vol.129C (1), p.85-90

Baysal, Bora E.

2004

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Coordinate up-regulation of TMEM97 and cholesterol biosynthesis genes in normal ovarian surface epithelial cells treated with progesterone: implications for pathogenesis of ovarian cancer

BMC cancer, 2007-12, Vol.7 (1), p.223-223, Article 223

2007

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Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA

BMC biology, 2007-03, Vol.5 (1), p.12-12, Article 12

2007

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Hypoxia-inducible C-to-U coding RNA editing downregulates SDHB in monocytes

PeerJ (San Francisco, CA), 2013-09, Vol.1, p.e152-e152

2013

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Mitochondrial complex II regulates a distinct oxygen sensing mechanism in monocytes

Human molecular genetics, 2017-04, Vol.26 (7), p.1328-1339

2017

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On the association of succinate dehydrogenase mutations with hereditary paraganglioma

Trends in endocrinology and metabolism, 2003-12, Vol.14 (10), p.453-459

Baysal, Bora E.

2003

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Mutations in SDHD, A Mitochondrial Complex II Gene, in Hereditary Paraganglioma

Science (American Association for the Advancement of Science), 2000-02, Vol.287 (5454), p.848-851

2000

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Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene

JAMA : the journal of the American Medical Association, 2005-10, Vol.294 (16), p.2057

2005

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Biochemically Silent Abdominal Paragangliomas in Patients with Mutations in the Succinate Dehydrogenase Subunit B Gene

The journal of clinical endocrinology and metabolism, 2008-12, Vol.93 (12), p.4826-4832

2008

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Genetics of Carney Triad: Recurrent Losses at Chromosome 1 but Lack of Germline Mutations in Genes Associated with Paragangliomas and Gastrointestinal Stromal Tumors

The journal of clinical endocrinology and metabolism, 2007-08, Vol.92 (8), p.2938-2943

2007

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A Phenotypic Perspective on Mammalian Oxygen Sensor Candidates

Annals of the New York Academy of Sciences, 2006-08, Vol.1073 (1), p.221-233

BAYSAL, BORA E.

2006

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Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria

Journal of human genetics, 2010-03, Vol.55 (3), p.182-185

2010

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RNA Editing in Pathogenesis of Cancer

Revisiting the TCA cycle: signaling to tumor formation

APOBEC3A cytidine deaminase induces RNA editing in monocytes and macrophages

Stem-loop structure preference for site-specific RNA editing by APOBEC3A and APOBEC3G

Mitochondrial hypoxic stress induces widespread RNA editing by APOBEC3G in natural killer cells

The double-domain cytidine deaminase APOBEC3G is a cellular site-specific RNA editing enzyme

A recurrent stop-codon mutation in succinate dehydrogenase subunit B gene in normal peripheral blood and childhood T-cell acute leukemia

The implications of APOBEC3-mediated C-to-U RNA editing for human disease

RNA editing enzyme APOBEC3A promotes pro-inflammatory M1 macrophage polarization

Succinate dehydrogenase inversely regulates red cell distribution width and healthy life span in chronically hypoxic mice

Relationship Between ERCC1 Polymorphisms, Disease Progression, and Survival in the Gynecologic Oncology Group Phase III Trial of Intraperitoneal Versus Intravenous Cisplatin and Paclitaxel for Stage III Epithelial Ovarian Cancer

Transient overexpression of exogenous APOBEC3A causes C-to-U RNA editing of thousands of genes

Genotype and Tumor Locus Determine Expression Profile of Pseudohypoxic Pheochromocytomas and Paragangliomas

Genomic imprinting and environment in hereditary paraganglioma

Coordinate up-regulation of TMEM97 and cholesterol biosynthesis genes in normal ovarian surface epithelial cells treated with progesterone: implications for pathogenesis of ovarian cancer

Sequence variation in human succinate dehydrogenase genes: evidence for long-term balancing selection on SDHA

Hypoxia-inducible C-to-U coding RNA editing downregulates SDHB in monocytes

Mitochondrial complex II regulates a distinct oxygen sensing mechanism in monocytes

On the association of succinate dehydrogenase mutations with hereditary paraganglioma

Mutations in SDHD, A Mitochondrial Complex II Gene, in Hereditary Paraganglioma

Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene

Biochemically Silent Abdominal Paragangliomas in Patients with Mutations in the Succinate Dehydrogenase Subunit B Gene

Genetics of Carney Triad: Recurrent Losses at Chromosome 1 but Lack of Germline Mutations in Genes Associated with Paragangliomas and Gastrointestinal Stromal Tumors

A Phenotypic Perspective on Mammalian Oxygen Sensor Candidates

Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria

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