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ret protooncogene mutations and endocrine neoplasia--a story intertwined with neural crest differentiation.

作者信息

Gagel R F

出版信息

Endocrinology. 1996 May;137(5):1509-11. doi: 10.1210/endo.137.5.8612478.

DOI:10.1210/endo.137.5.8612478
PMID:8612478
Abstract
摘要

相似文献

1
ret protooncogene mutations and endocrine neoplasia--a story intertwined with neural crest differentiation.
Endocrinology. 1996 May;137(5):1509-11. doi: 10.1210/endo.137.5.8612478.
2
RET mutations in multiple endocrine neoplasia type 2 and Hirschsprung disease.
Curr Opin Pediatr. 1995 Dec;7(6):702-9. doi: 10.1097/00008480-199512000-00014.
3
Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes and Hirschsprung disease.
J Cell Sci Suppl. 1994;18:43-9. doi: 10.1242/jcs.1994.supplement_18.6.
4
[From gene to disease; from the RET gene to multiple endocrine neoplasia types 2A and 2B, sporadic and familial medullary thyroid carcinoma, Hirschsprung disease and papillary thyroid carcinoma].[从基因到疾病;从RET基因到2A和2B型多发性内分泌腺瘤、散发性和家族性甲状腺髓样癌、先天性巨结肠病及甲状腺乳头状癌]
Ned Tijdschr Geneeskd. 2001 Nov 17;145(46):2217-21.
5
Genetic basis of endocrine disease: multiple endocrine neoplasia type 2.内分泌疾病的遗传基础:2型多发性内分泌腺瘤病
J Clin Endocrinol Metab. 1995 Jul;80(7):1989-95. doi: 10.1210/jcem.80.7.7608246.
6
[One gene--four diseases: on the importance of mutations in the ret gene in MEN 2A, MEN 2B, Hirschsprung disease and medullary thyroid carcinoma].[一个基因——四种疾病:论RET基因中的突变在2A型多发性内分泌腺瘤、2B型多发性内分泌腺瘤、先天性巨结肠症和甲状腺髓样癌中的重要性]
Z Gastroenterol. 1994 Jul;32(7):416-7.
7
RET activation by germline MEN2A and MEN2B mutations.种系MEN2A和MEN2B突变导致的RET激活。
Oncogene. 1995 Dec 7;11(11):2419-27.
8
A mutation in the RET proto-oncogene in Hirschsprung's disease affects the tyrosine kinase activity associated with multiple endocrine neoplasia type 2A and 2B.先天性巨结肠症中RET原癌基因的突变会影响与2A型和2B型多发性内分泌肿瘤相关的酪氨酸激酶活性。
Biochem J. 1996 Mar 1;314 ( Pt 2)(Pt 2):397-400. doi: 10.1042/bj3140397.
9
Molecular mechanisms of development of multiple endocrine neoplasia 2 by RET mutations.RET 突变导致多发性内分泌腺瘤 2 型发生发展的分子机制。
J Intern Med. 1998 Jun;243(6):509-13.
10
Mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2.
Cancer Surv. 1995;25:195-205.

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Hereditary syndromes predisposing to endocrine tumors and their skin manifestations.易患内分泌肿瘤及其皮肤表现的遗传性综合征。
Rev Endocr Metab Disord. 2016 Sep;17(3):381-388. doi: 10.1007/s11154-016-9401-0.
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RET codon 618 mutations in Saudi families with multiple endocrine neoplasia Type 2A and familial medullary thyroid carcinoma.沙特多个患有2A型多发性内分泌腺瘤病和家族性甲状腺髓样癌的家庭中RET密码子618突变
Ann Saudi Med. 2013 Mar-Apr;33(2):155-8. doi: 10.5144/0256-4947.2013.155.
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Concurrent Pheochromocytoma, Paraganglioma, Papillary Thyroid Carcinoma, and Desmoid Tumor: A Case Report with Analyses at the Molecular Level.
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Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes.多发性内分泌肿瘤、卡尼综合征及相关综合征的临床遗传学
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