一般常见的说法是“纯合缺失”(homozygous deletion),指一个个体的两条等位基因(alleles)都缺失了;“杂合突变”(heterozygous mutation)指两条等位基因一条为野生型,另一条发...
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...s of heterozygosity; Homozygous deletion; Pancreatic cancer [gap=520]关键词: 单核苷酸多态性芯片; 杂合性缺失; 纯合性缺失; 胰腺癌 ...
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... homozygous deletion 纯合性缺失 ; 纯合缺失 ; 纯合型缺失 ; 的纯合性缺失 methionine homozygous 甲硫胺酸合子 homozygous dominants 纯合子显性 ...
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homozygous deletion polymorphism 缺失多态
p gene homozygous deletion p16基因缺失
homozygous deletion of gene 基因纯合缺失
homozygous deletion of p gene p16基因纯合性缺失
There was distinct correlation between homozygous deletion of exon 5 and exon 8 in DTC tissue (χ2= 23.212,P<0.01).
DTC组织中,FHIT基因E5、E8纯合性缺失的发生相关(χ2=23.212,P<0.01)。
参考来源 - 分化型甲状腺癌组织中脆性组氨酸三联体基因外显子5、8纯合性缺失及突变检测·2,447,543篇论文数据,部分数据来源于NoteExpress
Results:In ALL, the incidence of P16 hypermethylation or homozygous deletion is 80%, there is no abnormal in control.
结果:AL L P16基因高度甲基化或纯合缺失发生率为80 % ,而对照组无一例P16基因失活;
The rate of homozygous deletion of Exon8 was 29.3%(12/41), and it was related to the tumor pathological grade, TNM stage and lymph node metastasis (P<0.05).
第8外显子纯合性缺失率为29.3%(12/41),且与患者TNM分期、病理分级及淋巴结转移有关(P<0.05);
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