1) homozygous mutant gene
基因纯合缺失
2) homozygous deletion
纯合缺失
1.
RESULTS: No homozygous deletion of p16 gene exon 1, 2 and 3 was observed in any of the 33 cases and no point mutation of p16 gene exon 2 was detected in 10 specimens.
结果:所有标本均未检出纯合缺失,10例标本进行了外显子2的序列测定,也未发现点突变。
2.
Methods: Polymerase chain reaction (PCR) and sequencing analysis were used to detect the homozygous deletion and point mutation of p16 gene in 84 cases of primary hepatocellular carcinomas and their adjacent liver tissues.
方法采用聚合酶链反应(PCR)和全自动序列分析的方法,研究84例肝癌和癌旁肝组织中pl6基因第1、2外显子纯合缺失和点突变的情况。
3.
The frequency of homozygous deletion was 8.
结果发现２例弥漫型胃癌有 ｐ１６基因的纯合缺失，缺失频率为８。
3) Homozygous deletion
纯合性缺失
1.
Detection of homozygous deletion and mutation of exon 5 and exon 8 of FHIT gene in differentiated thyroid carcinoma tissue;
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.
The homozygous deletion was detectyed by multiple PCR analysis and mutation by PCR-SSCP and DNA sequencing followed.
方法采用多重PCR、PCR-SSCP和DNA测序对62例胃癌、癌旁组织及10例正常胃黏膜标本中p16INK4a基因纯合性缺失和突变进行检测。
3.
Aim: To investigate the frequencies of homozygous deletion of entire coding exons of fragile histidine triad (FHIT) gene in laryngeal squamous cell carcinoma (LSCC) tissue and its clinical significance.
目的:探讨喉鳞癌(LSCC)组织中脆性组氨酸三联体(FHIT)基因编码外显子纯合性缺失及其临床意义。
4) deletion
[英][di'li:ʃən] [美][dɪ'liʃən]
基因缺失
1.
Study on p16 gene deletion and promoter 5 CpG island hypomethylation in coal-burning arsenism patients;
燃煤型砷中毒患者p16基因缺失及启动区CpG岛甲基化的观察
2.
Gene clone and deletion of ApxIICA of Actinobacillus pleuropneumoniaeserotype 7 strain 25-4;
猪传染性胸膜肺炎放线杆菌血清型7型25-4株ApxIICA基因的克隆和基因缺失
5) Gene deletion
基因缺失
1.
Detection of p16 gene deletion and methylation in esophageal squamous cell carcinoma tissue;
食管鳞癌组织中p16基因缺失及甲基化检测
2.
Detection of muscular dystrophy gene deletions by 9 pairs of primers;
采用9对引物检测假肥大型肌营养不良症的基因缺失
3.
Investigation on p16 gene deletion in tissues of primary squamous cell carcinoma of esophagus;
原发性食管鳞癌组织p16基因缺失的检测
6) missing gene
缺失基因
补充资料：嵌合基因
分子式：
CAS号：
性质：不同基因组成一个顺反子，也可能是不同基因部分组成一个顺反子。
CAS号：
性质：不同基因组成一个顺反子，也可能是不同基因部分组成一个顺反子。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条