(Q40365390)

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

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

19 September 2017

mitochondrial DNA

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author name string

Abu-Amero KK

1

1 reference

Europe PubMed Central

19 September 2017

Alzahrani AS

2

1 reference

Europe PubMed Central

19 September 2017

Zou M

3

1 reference

Europe PubMed Central

19 September 2017

Shi Y

4

1 reference

Europe PubMed Central

19 September 2017

language of work or name

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publication date

1 February 2006

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Europe PubMed Central

19 September 2017

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Europe PubMed Central

19 September 2017

25

1 reference

Europe PubMed Central

19 September 2017

5

1 reference

Europe PubMed Central

19 September 2017

677-684

1 reference

Europe PubMed Central

19 September 2017

https://scigraph.springernature.com/pub.10.1038/sj.onc.1209094

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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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Germline SDHD mutation in familial phaeochromocytoma

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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

1 reference

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Enzymology of mitochondrial base excision repair

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Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency

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

1 reference

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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

1 reference

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

1 reference

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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

1 reference

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

1 reference

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

1 reference

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Hypoxia--a key regulatory factor in tumour growth

1 reference

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Mitochondrial oxidative stress can lead to nuclear hypermutability

1 reference

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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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7 January 2021

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Mitochondrial Oxidative Stress and Mitochondrial DNA

1 reference

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

1 reference

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

1 reference

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

1 reference

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Hereditary leiomyomatosis and renal cell cancer (HLRCC).

1 reference

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The role of oxidative stress in carcinogenesis

1 reference

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Cell signalling and gene expression mediated by RET tyrosine kinase

1 reference

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7 January 2021

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Base excision repair of mitochondrial DNA damage in mammalian cells

1 reference

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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

1 reference

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7 January 2021

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Diagnosis and management of medullary thyroid carcinoma

1 reference

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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

1 reference

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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

1 reference

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Human non-synonymous SNPs: server and survey

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Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

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Minireview: RET: normal and abnormal functions

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

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Tissue inhibitor of metalloproteinases-1 (TIMP-1) mRNA is elevated in advanced stages of thyroid carcinoma

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Positive contribution of pathogenic mutations in the mitochondrial genome to the promotion of cancer by prevention from apoptosis.

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

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The interacting pathways for prevention and repair of oxidative DNA damage

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Mitochondrial repair of 8-oxoguanine and changes with aging.

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

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Mitochondrial diseases in man and mouse

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Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours.

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Identifiers

10.1038/SJ.ONC.1209094

1 reference

Europe PubMed Central

19 September 2017

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1 reference

Europe PubMed Central

19 September 2017

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