frameshift

frameshift

1. Fifteen mutations were nonsense, frameshift, or splice-site alterations predicted to result in truncated proteins lacking phosphatase activity.

15个突变是无义突变，移码突变或者剪切位点改变，这些突变被预测导致蛋白缩短而缺失磷酸酶活性。

2. Two novel frameshift mutations of the EBP gene in two unrelated Thai girls with Conradi-Hunermann-Happle syndrome

2例无关的泰国女性Conradi-Hunermann-Happle综合征患者的EBP基因出现两个新的移码突变

3. Ames test showed that both of the base pair transversion and frameshift mutant in DNA was not induced by irradiated starch.

Ames试验也说明辐照淀粉不诱发DNA中碱基对的置换型和移码型突变。

4. No association was observed between TRF length and MSI or frameshift mutation. But LOH at the DCC locus were associated with telomere shortening ( P <0.01).

DCC基因LOH与TRF缩短有关 ,APC和MCC基因亦有随TRF缩短而LOH率增高的倾向。

5. reciprocal frameshift

交互移码

6. A deletion mutation with frameshift of neurofibromatosis type 2 gene was detected by DNA sequencing.

以DNA序列分析出，在第二型纤维细胞瘤基因上发生染色体缺失造成移码突变。

7. Keywords NADP（H）-dependent retinol dehydrogenase/reductase;alternative splicing;frameshift;

依赖的视黄醇脱氢酶;选择性剪接;框移突变;

8. Some simple genome elements previously shown to be important, including the ribosomal gag-pol frameshift stem-loop, are components of larger RNA motifs.

当然该RNA的结构也包括核糖体结合翻译区，聚合酶识别区和环状结构。

9. A point mutation in the napA gene may cause the negative characteristic of nitrate reduction in Mediaevalis and Microus strains. A 122-bp frameshift deletion in the araC gene may lead to the arabinose negative phenotype of Microus strains.

所有脱氮阴性菌株的napA基因发生了突变 ,所有甘油利用阴性菌株的 glpD基因发生了突变 ,所有阿拉伯糖利用阴性菌株的araC基因发生了突变。

10. frameshift mutant

支架转变型突变体

11. ribosomal frameshift

核糖体移码

12. This protein is produced through ribosomal frameshift (F protein).

此蛋白的产生，是核糖体转译时，改变其转译系列所致。

13. However, only three somatic BRCA2 mutations, 1 frameshift and 2 missense variants [6,7,9], were reported in 270 cases of primary sporadic female breast tumors.

然而在270例初期女性散发性乳癌的案件中，只有三例BRCA2体突变，一例移码突变及二例错义突变[6,7,9] 被报告出来。

14. About 129 different HHT-related mutations have been reported so far, 79 in ENG and 50 in ALK-1, including missense, nonsense, frameshift, splice-site.

目前发现与HHT有关的不同的突变有129个,其中有79个与ENG基因突变有关,50个与ALK-1基因突变有关。 ENG基因或ALK-1基因的突变有错义突变、无义突变、剪接点突变。

15. frameshift mutagen

码组错位诱变

16. frameshift window

移格窗

17. frameshift variant

移码变异

18. frameshift type of mutagen

移码型突变剂

19. frameshift suppression

移码抑制

20. frameshift suppressor tRNA

移码抑制tRNA

21. frameshift suppressor

移码抑制因子

22. frameshift fidelity

移码的保真性,移码真实性

23. frameshift mutation

移码突变

24. frameshift mutation phaseshift mutation

移码突变, 相移突变

25. Both frameshift and missense mutations can be suppressed by intragenic suppressors.

移码突变和异义突变都能被基因内抑制基因所抑制。

26. Programmed -1 ribosomal frameshift

程序性-1核糖体移码

27. Keywords schizophrenia;KCNN3 gene;frameshift mutation;haplotype-based hoplotype relative risk;transmission/disequilibruim test;

精神分裂症;KCNN3基因;移码突变;基于单倍型的单倍型相对风险率;传递/不平衡检验;

28. Results A 13389G deletion in exon 6 was characterized in propositus, and this mutation led to frameshift.

结果先证者表现为抗凝血酶基因外显子6区13389G缺失,引起移码突变。

29. Results: We found 4 mutations in 36 schwwannomas, all in acoustic neuroma.Of them, two frameshift mutations and two missense mutations.

结果：我们共发现4例突变，均为听神经瘤，其中移码突变2例、反义突变2例。

30. Results Mutations(point and frameshift mutations)of P53exon 4(6/6)and exon 5(2/6)in fibroblasts derived from keloids...

结论瘢痕疙瘩成纤维细胞存在P53基因突变,这可引起其细胞增殖凋亡异常。

31. translation frameshift

翻译移码

32. Three severe cases of EBS Dowling-Meara caused by missense and frameshift mutations in the keratin 14 gene

角蛋白14基因发生错义和移码突变导致3例严重的Dowling-Meara型单纯型大疱性表皮松解症

33. Among these sequences, only 12 were intact, and others had a frameshift, a stop condon, or both.

这57个序列中，仅有12个为完整的序列，其余的都有移码突变，终止子或二者兼有。

34. These flat-ringed planar compounds intercalate with the cells' nucleic acids .and act as frameshift mutagens and carcinogens.

这些平面扁平环形化合物能插入细胞的核酸中并且充当移码突变剂和致癌剂。

35. Among these sequences, 29 clones had unique nucleotide sequences (intact sequences), and the others had a frameshift, a stop condon, or both.

这些序列中有29条是完整的,其余的有移码突变、终止子或者是二者均有。