Intragenic mutations in thyroid cancer.

Abstract:

:The close genotype-phenotype relationship that characterizes thyroid oncology stimulated the authors to address this article by using a mixed, genetic and phenotypic approach. As such, this article addresses the following aspects of intragenic mutations in thyroid cancer: thyroid stimulating hormone receptor and guanine-nucleotide-binding proteins of the stimulatory family mutations in hyperfunctioning tumors; mutations in RAS and other genes and aneuploidy; PAX8-PPARgamma rearrangements; BRAF mutations; mutations in oxidative phosphorylation and Krebs cycle genes in Hürthle cell tumors; mutations in succinate dehydrogenase genes in medullary carcinoma and C-cell hyperplasia; and mutations in TP53 and other genes in poorly differentiated and anaplastic carcinomas.

authors

Sobrinho-Simões M,Máximo V,Rocha AS,Trovisco V,Castro P,Preto A,Lima J,Soares P

doi

10.1016/j.ecl.2008.02.004

subject

Has Abstract

pub_date

2008-06-01 00:00:00

pages

333-62, viii

issue

2

eissn

0889-8529

issn

1558-4410

pii

S0889-8529(08)00008-X

journal_volume

37

pub_type

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