Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome (Q40365390)

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scientific article published on February 2006

Language	Label	Description	Also known as
English	Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome	scientific article published on February 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

mitochondrial DNA

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author name string

Abu-Amero KK

1

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Alzahrani AS

2

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Zou M

3

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Shi Y

4

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

language of work or name

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publication date

1 February 2006

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

25

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

677-684

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines.

1 reference

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Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas

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Enzymology of mitochondrial base excision repair

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

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Oxidative DNA damage: mechanisms, mutation, and disease

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RET exon 11 (G691S) polymorphism is significantly more frequent in sporadic medullary thyroid carcinoma than in the general population

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Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age.

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A role for mitochondrial enzymes in inherited neoplasia and beyond

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Genetics of follicular thyroid cancer.

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Facile detection of mitochondrial DNA mutations in tumors and bodily fluids

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Medullary thyroid carcinoma: clinical features and long-term follow-up of seventy-eight patients treated between 1969 and 1986.

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Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis

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Hypoxia--a key regulatory factor in tumour growth

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Mitochondrial oxidative stress can lead to nuclear hypermutability

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A National Cancer Data Base report on 53,856 cases of thyroid carcinoma treated in the U.S., 1985-1995 [see commetns]

1 reference

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Mitochondrial Oxidative Stress and Mitochondrial DNA

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Ultraviolet light induces redox reaction-mediated dimerization and superactivation of oncogenic Ret tyrosine kinases

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Possible cause of G-C-->C-G transversion mutation by guanine oxidation product, imidazolone

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UVR-induced G-C to C-G transversions from oxidative DNA damage

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Hereditary leiomyomatosis and renal cell cancer (HLRCC).

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The role of oxidative stress in carcinogenesis

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Cell signalling and gene expression mediated by RET tyrosine kinase

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Base excision repair of mitochondrial DNA damage in mammalian cells

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Mitochondrial DNA repair and aging

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RET proto-oncogene mutations in multiple endocrine neoplasia type 2 and medullary thyroid carcinoma

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Diagnosis and management of medullary thyroid carcinoma

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Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hürthle cell tumors

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Management of a solitary thyroid nodule

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The RET receptor is linked to stress response pathways

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Somatic mutations of the mitochondrial genome in human colorectal tumours

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RET codon 634 mutations in multiple endocrine neoplasia type 2: variable clinical features and clinical outcome

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Human non-synonymous SNPs: server and survey

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Transforming ability of MEN2A-RET requires activation of the phosphatidylinositol 3-kinase/AKT signaling pathway.

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Mitochondrial repair of 8-oxoguanine and changes with aging.

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Identifiers

10.1038/SJ.ONC.1209094

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

ResearchGate publication ID

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