RAD52 polymorphisms contribute to the development of papillary thyroid cancer susceptibility in Middle Eastern population (Q83014197)

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18 January 2020

title

RAD52 polymorphisms contribute to the development of papillary thyroid cancer susceptibility in Middle Eastern population (English)

1 reference

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18 January 2020

main subject

papillary thyroid cancer

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7

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18 January 2020

author name string

A K Siraj

1

1 reference

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18 January 2020

M Al-Rasheed

2

1 reference

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18 January 2020

M Ibrahim

3

1 reference

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18 January 2020

K Siddiqui

4

1 reference

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18 January 2020

F Al-Dayel

5

1 reference

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18 January 2020

O Al-Sanea

6

1 reference

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18 January 2020

K Al-Kuraya

8

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18 January 2020

publication date

1 October 2008

1 reference

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Journal of Endocrinological Investigation

18 January 2020

published in

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18 January 2020

volume

31

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18 January 2020

issue

10

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18 January 2020

page(s)

893-899

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Polymorphisms in exon 13 and intron 14 of the RET protooncogene: genetic modifiers of medullary thyroid carcinoma?

18 January 2020

cites work

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Rapid assessment of repair of ultraviolet DNA damage with a modified host-cell reactivation assay using a luciferase reporter gene and correlation with polymorphisms of DNA repair genes in normal human lymphocytes.

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No association between a stop codon polymorphism in RAD52 and breast cancer risk

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Incidence of thyroid cancer in Scandinavia following fallout from atomic bomb testing: an analysis of birth cohorts

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DNA repair gene polymorphisms, bulky DNA adducts in white blood cells and bladder cancer in a case-control study

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Common nonsense mutations in RAD52

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Variants in DNA double-strand break repair genes and breast cancer susceptibility

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A variant within the DNA repair gene XRCC3 is associated with the development of melanoma skin cancer.

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XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages

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Correction of chromosomal instability and sensitivity to diverse mutagens by a cloned cDNA of the XRCC3 DNA repair gene

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Radiation response genotype and risk of differentiated thyroid cancer: a case-control analysis

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Germline polymorphism of codon 727 of human thyroid-stimulating hormone receptor is associated with toxic multinodular goiter

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Mechanisms of mutagenesis in mammalian cells. Application to human thyroid tumours

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Polymorphisms of XRCC1 and XRCC3 genes and susceptibility to breast cancer

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12 December 2020

Association of Polymorphisms in ERCC2 Gene with Non-Familial Thyroid Cancer Risk

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12 December 2020

Intronic single nucleotide polymorphisms in the RET protooncogene are associated with a subset of apparently sporadic pheochromocytoma and may modulate age of onset

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12 December 2020

A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers

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12 December 2020

Thyrotropin receptor polymorphisms and thyroid diseases

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12 December 2020

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

1 reference

12 December 2020