(Q24547869)

2

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Ling-Ling Liu

3

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Ren-Kui Bai

4

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Yu-Fen Wang

5

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Kun-Tu Yeh

6

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Lee-Jun C Wong

Control region mutations and the 'common deletion' are frequent in the mitochondrial DNA of patients with esophageal squamous cell carcinoma

7

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language of work or name

English

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publication date

2006

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published in

BMC Cancer

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volume

6

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issue

1

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page(s)

93

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cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Prevention of apoptosis by Bcl-2: release of cytochrome c from mitochondria blocked

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Sequence and organization of the human mitochondrial genome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Somatic mutations in the D-loop and decrease in the copy number of mitochondrial DNA in human hepatocellular carcinoma

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Facile detection of mitochondrial DNA mutations in tumors and bodily fluids

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Alteration of the copy number and deletion of mitochondrial DNA in human hepatocellular carcinoma

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Molecular alterations in mitochondrial DNA of hepatocellular carcinomas: is there a correlation with clinicopathological profile?

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Compensatory amplification of mtDNA in a patient with a novel deletion/duplication and high mutant load

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Mitochondrial DNA alterations in cancer.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

High frequency of mitochondrial DNA mutations in glioblastoma multiforme identified by direct sequence comparison to blood samples

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Somatic mutations of the mitochondrial genome in human colorectal tumours

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Mitochondrial DNA mutations in human degenerative diseases and aging

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Biogenesis of mitochondria

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Novel heteroplasmic frameshift and missense somatic mitochondrial DNA mutations in oral cancer of betel quid chewers

27 September 2017

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Alteration of the bioenergetic phenotype of mitochondria is a hallmark of breast, gastric, lung and oesophageal cancer.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

The bioenergetic signature of lung adenocarcinomas is a molecular marker of cancer diagnosis and prognosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Mutations in mitochondrial control region DNA in gastric tumours of Japanese patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Quantitative PCR analysis of mitochondrial DNA content in patients with mitochondrial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Detection of mitochondrial DNA mutations in the tumor and cerebrospinal fluid of medulloblastoma patients

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Comprehensive scanning of the entire mitochondrial genome for mutations.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1459869

Mitochondrial DNA alteration in esophageal cancer

28 November 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Familial aggregation of oesophageal cancer in Yangcheng County, Shanxi Province, China

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Prospective study of serum selenium levels and incident esophageal and gastric cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Frequent somatic mutations of mitochondrial DNA in esophageal squamous cell carcinoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Detection of mitochondrial DNA mutations using temporal temperature gradient gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Detection of CFTR mutations using temporal temperature gradient gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2407-6-93

Somatic mitochondrial DNA mutations in neurofibromatosis type 1-associated tumors

21 January 2018

1 reference

12 December 2020

Nuclear and mitochondrial genome instability in human breast cancer

1 reference

12 December 2020

High incidence of somatic mitochondrial DNA mutations in human ovarian carcinomas

1 reference

12 December 2020

Detection of mitochondrial DNA mutations in primary breast cancer and fine-needle aspirates

1 reference

12 December 2020

Comprehensive scanning of somatic mitochondrial DNA mutations in breast cancer

1 reference

12 December 2020