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白血病的分子生物学

Molecular biology of leukemia.

作者信息

Wujcik Debra

机构信息

Vanderbilt-Ingram Cancer Center, 691 Preston Research Bldg, Nashville, TN 37232-6868, USA.

出版信息

Semin Oncol Nurs. 2003 May;19(2):83-9. doi: 10.1016/s0749-2081(03)00004-4.

Abstract

OBJECTIVE

To review the current tests for diagnosis and the implications of cytogenetic analysis in leukemia.

DATA SOURCES

Professional journals, books.

CONCLUSION

Leukemia is a genetic disorder with more than 500 recurring translocations. Recurrent chromosomal changes occur in more than one half of all cases of leukemia. Testing includes bone marrow biopsy and aspirate, histochemical staining, immunophenotyping, cytogenetics, and molecular markers. Characterization of specific chromosome changes provides information in determining initial therapy and post-remission therapy.

IMPLICATIONS FOR NURSING PRACTICE

Nurses must continually educate themselves to stay current with developing technology and the results of continuing research. This professional education must then be translated to the bedside throughout the continuum of care.

摘要

目的

回顾当前白血病的诊断检测方法以及细胞遗传学分析的意义。

资料来源

专业期刊、书籍。

结论

白血病是一种具有500多种复发性易位的遗传性疾病。超过一半的白血病病例存在复发性染色体改变。检测包括骨髓活检和抽吸、组织化学染色、免疫表型分析、细胞遗传学和分子标志物。特定染色体改变的特征为确定初始治疗和缓解后治疗提供信息。

对护理实践的启示

护士必须不断自我教育,以跟上技术发展和持续研究的结果。然后,这种专业教育必须在整个护理过程中应用到床边护理中。

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