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1)  RET gene mutation
RET基因突变
2)  RET gene
RET基因
1.
PCR and DNA direct sequencing were used to evaluate the mutation of 634RET gene in exon 11.
目的:分析家族性摩擦性黑变病遗传特点,并探讨RET基因突变情况。
2.
Up till now, RET gene, VHL gene, and SDHx gene have been known to get involved in the tumorigenesis of the pheochromocytoma and paraganglioma.
迄今为止,已了解的与嗜铬细胞瘤有关的基因为RET基因、VHL基因和SDHx基因。
3.
RET gene mutation .
RET基因突变类型有一定的规律性,即基因型和表现型之间有非常好的相关性。
3)  RET proto-oncogene
RET基因
1.
The relationship between Hirschsprung disease and single nucleotide polymorphisms of c135 in RET proto-oncogene;
先天性巨结肠与RET基因c135位点单核苷酸多态性相关性分析
2.
Mutations of RET proto-oncogene in Chinese familial Hirschsprung s disease;
中国人先天性巨结肠RET基因突变家系研究
3.
Dominant-activating mutations in the RET proto-oncogene have been identified as the main cause of MTC.
甲状腺髓样癌来源于分泌降钙素的甲状腺滤泡旁细胞(又称C细胞),且多因RET基因突变引发,其发病、诊断和治疗等都独具特点,本文重点综述了近年来甲状腺髓样癌基础研究和临床治疗方面的进展。
4)  RET [英][ret]  [美][rɛt]
RET基因
1.
Mutations of RET proto-oncogene in Hirschsprung s disease and its allied disorders;
先天性巨结肠与其同源病的RET基因突变的研究
2.
Mutation of EDNRB/EDN3 Gnens and Polymorphism Analysis of RET+3 in Chinese with Hirschsprung Disease;
近年来,RET基因已经被证实是HD的主要致病基因。
5)  ret/PTC gene
ret/PTC基因
1.
ret/PTC gene mutation in papillary thyroid carcinoma by sonographically-guided fine-needle;
超声引导下细针穿刺检测甲状腺乳头状癌ret/PTC基因重组突变
6)  RET proto-oncogene
RET原癌基因
1.
Mutation screening of RET proto-oncogene in Chinese sporadic patients with pheochromocytom;
散发性嗜铬细胞瘤患者RET原癌基因突变检测
2.
Investigation of RET proto-oncogene mutation in patients with medullary thyroid carcinoma;
甲状腺髓样癌患者RET原癌基因突变的研究
3.
Report of a family with multiple endocrine neoplasia type Ⅱb induced by a mutation of Met to Thr of RET proto-oncogene;
一个RET原癌基因Met918Thr突变的多发性内分泌腺瘤病Ⅱb家系报道
补充资料:操纵基因突变体
分子式:
CAS号:

性质:因操纵子的操纵基因突变而导致调节蛋白无法与之结合的细菌突变体。其特点是操纵子结构基因所编码的与代谢作用直接有关的酶为组成型表达。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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