印度甲状腺髓样癌患者及“高危”携带者中RET原癌基因的突变分析。 - Suppr

Mutational analysis of RET proto-oncogene among patients with medullary thyroid carcinoma and 'at risk' carriers from India.

作者信息

Pai Rekha, Nehru G Arun, Samuel Prasanna, Paul M J, Thomas Nihal, Premkumar Jennifer Anne, Hephzibah Julie, Shanthly Nylla, Oommen Regi, Nair Aravindan, Seshadri M S, Rajaratnam Simon

出版信息

Clin Endocrinol (Oxf). 2011 Oct;75(4):571-2. doi: 10.1111/j.1365-2265.2011.04069.x.

DOI:10.1111/j.1365-2265.2011.04069.x

PMID:21521337

Abstract

摘要

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Mutational analysis of RET proto-oncogene among patients with medullary thyroid carcinoma and 'at risk' carriers from India.印度甲状腺髓样癌患者及“高危”携带者中RET原癌基因的突变分析。

Clin Endocrinol (Oxf). 2011 Oct;75(4):571-2. doi: 10.1111/j.1365-2265.2011.04069.x.

New presentation of familial medullary thyroid carcinoma in 87-year-old patient with high-risk RET proto-oncogene codon 620 mutation.87岁伴有高危RET原癌基因密码子620突变的家族性甲状腺髓样癌新病例报告

J Laryngol Otol. 2009 Jul;123(7):796-800. doi: 10.1017/S0022215108003472. Epub 2008 Sep 4.

RET polymorphisms in codons 769 and 836 are not associated with predisposition to medullary thyroid carcinoma.

Cancer Detect Prev. 2004;28(4):231-6. doi: 10.1016/j.cdp.2004.04.002.

Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2.MEN2家族儿童的遗传性髓样癌预防、风险评估及RET基因

J Pediatr Surg. 2007 Feb;42(2):326-32. doi: 10.1016/j.jpedsurg.2006.10.005.

Mutation analysis of the RET proto-oncogene and early thyroidectomy: results of a Portuguese cancer centre.RET原癌基因的突变分析与早期甲状腺切除术：一家葡萄牙癌症中心的结果

Surgery. 2007 Jan;141(1):90-5. doi: 10.1016/j.surg.2006.03.025. Epub 2006 Jul 31.

Invited commentary: medullary thyroid cancer: the importance of RET testing.特邀评论：甲状腺髓样癌：RET检测的重要性。

Surgery. 2007 Jan;141(1):96-9. doi: 10.1016/j.surg.2006.08.016.

Occurrence of the Cys611Tyr mutation and a novel Arg886Trp substitution in the RET proto-oncogene in multiple endocrine neoplasia type 2 families and sporadic medullary thyroid carcinoma cases originating from the central region of Portugal.在源自葡萄牙中部地区的2型多发性内分泌腺瘤病家族及散发性甲状腺髓样癌病例中，RET原癌基因出现Cys611Tyr突变及一种新型的Arg886Trp替代。

Clin Endocrinol (Oxf). 2006 Jun;64(6):659-66. doi: 10.1111/j.1365-2265.2006.02524.x.

Chromosome 10 and RET gene copy number alterations in hereditary and sporadic Medullary Thyroid Carcinoma.遗传性和散发性甲状腺髓样癌中 10 号染色体和 RET 基因拷贝数改变。

Mol Cell Endocrinol. 2012 Jan 2;348(1):176-82. doi: 10.1016/j.mce.2011.08.004. Epub 2011 Aug 16.

A rare RET gene exon 8 mutation is found in two Greek kindreds with familial medullary thyroid carcinoma: implications for screening.在两个患有家族性甲状腺髓样癌的希腊家族中发现一种罕见的RET基因外显子8突变：对筛查的意义。

Clin Endocrinol (Oxf). 2006 May;64(5):561-6. doi: 10.1111/j.1365-2265.2006.02509.x.

A novel Czech kindred with familial medullary thyroid carcinoma and Hirschsprung's disease.一个患有家族性甲状腺髓样癌和先天性巨结肠症的新型捷克家族。

J Pediatr Surg. 2005 Jun;40(6):e1-6. doi: 10.1016/j.jpedsurg.2005.03.031.

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Outcome of Treatment for Medullary Thyroid Carcinoma-a Single Centre Experience.甲状腺髓样癌的治疗结果——单中心经验

Indian J Surg Oncol. 2018 Mar;9(1):52-58. doi: 10.1007/s13193-017-0718-2. Epub 2017 Dec 8.

RET mutations in a large indian family with medullary thyroid carcinoma.一个患有甲状腺髓样癌的印度大家族中的RET基因突变

Indian J Endocrinol Metab. 2014 Jul;18(4):516-20. doi: 10.4103/2230-8210.137508.

A complex endocrine conundrum.一个复杂的内分泌难题。

Fam Cancer. 2013 Sep;12(3):577-80. doi: 10.1007/s10689-012-9594-7.

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Mutational analysis of RET proto-oncogene among patients with medullary thyroid carcinoma and 'at risk' carriers from India.

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