chromosome deletion

美 [ˈkroʊməsoʊm dɪˈliʃən]英 [ˈkrəʊməsəʊm dɪˈliːʃən]
  • 染色体缺失
chromosome deletionchromosome deletion
  1. 2 cases of Y chromosome deletion ;

    缺失Y染色体12例;

  2. Chromosome deletion was observed in some cells of haploid or double haploid plants .

    观察到再生株中个别细胞染色体的丢失现象。

  3. The derivative chromosomes resulted from unbalanced translocations , most of which were missed as chromosome deletion , additional material of unknown origin , monosomy and marker chromosome .

    后者均系不平衡易位所致,其中不少被CC误认为染色体部分缺失、不明来源的额外物质、染色体单体和标记染色体等。

  4. Objective : To investigate the relation between Y chromosome deletion and idiopathic azoospermia , severe oligozoospermia ; and investigate variability of Y chromosome deletion situs and rate in the nations .

    目的:研究Y染色体基因微缺失与特发性无精子症和严重少精子症的关系,及探讨Y染色体基因微缺失的位点、缺失率有无民族间的差异性。

  5. Chromosome deletion was triggered by Cre / loxP-mediated inverse sister chromatid recombination in the G2 / M phase of the cell cycle , leading to the generation of daughter cells missing part of or the entire recombinant chromosome .

    在细胞有丝分裂的G2/M期,Cre/loxP介导的反向染色单体重组可以导致染色体删除,分裂后产生的子细胞将丢失全部或者部分的重组染色体。

  6. Detecting chromosome 13 deletion in multiple myeloma with fluorescence in situ hybridization

    荧光原位杂交技术检测多发性骨髓瘤13号染色体缺失

  7. Clinical and Experimental Studies of Derivative Chromosome 9 Deletion in Patients with Ph-positive Leukemia

    Ph+染色体白血病患者中衍生9号染色体部分序列缺失的临床和实验研究

  8. Establishment large chromosome fragment deletion on the basis of genomic library constructed with novel cosmid vector .

    3利用新型载体构建基因组文库以进行DNA大片段的敲除。

  9. Microsatellite instability and allele-specific chromosome 3p deletion in breast cancer and precancerous lesions

    乳腺癌与癌前病变的微卫星不稳定性与3p杂合性缺失

  10. This study was aimed to investigate the cytogenetic changes of MDS cell line ( MUTZ-1 ) with chromosome 5q deletion .

    本研究的目的是观察伴有5号染色体缺失的MDS细胞株MUTZ-1细胞的遗传学变化。

  11. NBCCS secondary to an interstitial chromosome 9q deletion

    继发于裂隙染色体9q缺失的痣样基底细胞癌综合征

  12. Some researches revealed that the chromosome 3p deletion in clear cell renal cell carcinoma is widely existed , and the deletion showed little relationship with stage of the tumor .

    研究发现肾透明细胞癌中普遍存在着3号染色体短臂的缺失,且缺失的发生与肿瘤的分期、分级无关。

  13. PCR-LOH of Chromosome 1p Deletion in Neuroblastoma

    PCR-LOH检测神经母细胞瘤1号染色体短臂缺失

  14. Conclusion : Chromosome 3p deletion are existed in most of multifocal clear cell renal cell carcinomas , and most of primary tumors and satellite tumors have the same 3p deletion .

    结论:本实验中多数肾透明细胞癌都发现有3号染色体短臂的缺失,且大部分的原发灶和多中心灶有着相同的缺失类型。