Evidence of a Low Prevalence ofRASMutations in a Large Medullary Thyroid Cancer Series-Reference-Cited by-同舟云学术

Evidence of a Low Prevalence ofRASMutations in a Large Medullary Thyroid Cancer Series

Published:2013-01 Issue:1 Volume:23 Page:50-57
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Ciampi Raffaele¹,Mian Caterina²,Fugazzola Laura³⁴,Cosci Barbara¹,Romei Cristina¹,Barollo Susi²,Cirello Valentina³⁴,Bottici Valeria¹,Marconcini Giulia¹,Rosa Pelizzo Maria⁵,Borrello Maria Grazia⁶,Basolo Fulvio⁷,Ugolini Clara⁷,Materazzi Gabriele⁷,Pinchera Aldo¹,Elisei Rossella¹

Affiliation:

1. Department of Endocrinology and Metabolism, University Hospital of Pisa, Italy.

2. Operative Unit of Endocrinology, Department of Medicine (DIMED), University of Padua, Padua, Italy.

3. Department of Medical Sciences, University of Milan, Milan, Italy.

4. Endocrine Unit, IRCCS Foundation, Cá Granda, Milan, Italy.

5. Special Surgery Unit, Department of Surgical, Oncological and Gastroenterological Sciences (DISCOG), University of Padua, Padua, Italy.

6. Molecular Mechanisms Unit, Experimental Oncology Department, IRCCS Foundation, Istituto Nazionale dei Tumori, Milan, Italy.

7. Department of Surgery, University Hospital of Pisa, Italy.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2012.0207

Reference46 articles.

1. RETProto-Oncogene: A Review and Update of Genotype–Phenotype Correlations in Hereditary Medullary Thyroid Cancer and Associated Endocrine Tumors

2. Molecular genetics of medullary thyroid carcinoma: the quest for novel therapeutic targets

3. RETGenetic Screening in Patients with Medullary Thyroid Cancer and Their Relatives: Experience with 807 Individuals at One Center

4. Mechanisms of Disease: cancer targeting and the impact of oncogenic RET for medullary thyroid carcinoma therapy

5. Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours

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