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ras基因突变在骨髓增殖性疾病中的作用。

The role of ras gene mutations in myeloproliferative disorders.

作者信息

Liu E T

机构信息

Department of Medicine, University of North Carolina, Chapel Hill.

出版信息

Clin Lab Med. 1990 Dec;10(4):797-807.

PMID:2272174
Abstract

Mutations in the ras genes frequently are found in myeloproliferative disorders. These abnormalities have prognostic significance in the myelodysplastic syndromes, but their clinical importance in other hematopathic states remains unclear. The study of this gene in leukemic conditions is providing insights into the genetic pathways leading to leukemic progression.

摘要

ras基因的突变在骨髓增殖性疾病中经常被发现。这些异常在骨髓增生异常综合征中具有预后意义,但它们在其他血液病状态中的临床重要性仍不清楚。在白血病情况下对该基因的研究正在为导致白血病进展的遗传途径提供见解。

相似文献

1
The role of ras gene mutations in myeloproliferative disorders.ras基因突变在骨髓增殖性疾病中的作用。
Clin Lab Med. 1990 Dec;10(4):797-807.
2
N-ras and p53 gene mutations in Japanese patients with myeloproliferative disorders.日本骨髓增殖性疾病患者的N-ras和p53基因突变
Am J Hematol. 2002 Oct;71(2):131-3. doi: 10.1002/ajh.10188.
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Mutations in ras genes in myelocytic leukemias and myelodysplastic syndromes.
Blood Cells. 1988;14(2-3):533-8.
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Analysis of ras gene mutations and methylation state in human leukemias.
Oncogene. 1989 Aug;4(8):1029-36.
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N-RAS activation in the terminal stage of undifferentiated chronic myeloproliferative disease.
Int J Hematol. 1992 Aug;56(1):9-15.
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Rapid mutational analysis of N-ras proto-oncogene in hematologic malignancies: study of 77 Greek patient.
Haematologica. 2001 Sep;86(9):918-27.
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Hypereosinophilic syndrome with evolution to myeloproliferative disorder: temporal relationship to loss of Y chromosome and c-N-ras activation.
Hematol Pathol. 1990;4(3):149-55.
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RAS gene mutations in acute and chronic myelocytic leukemias, chronic myeloproliferative disorders, and myelodysplastic syndromes.急性和慢性粒细胞白血病、慢性骨髓增殖性疾病及骨髓增生异常综合征中的RAS基因突变
Proc Natl Acad Sci U S A. 1987 Dec;84(24):9228-32. doi: 10.1073/pnas.84.24.9228.
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Ras gene mutations in patients with acute myeloid leukaemia and exposure to chemical agents.急性髓系白血病患者的Ras基因突变与化学物质暴露
Carcinogenesis. 2004 May;25(5):749-55. doi: 10.1093/carcin/bgh057. Epub 2003 Dec 19.
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Mutant molecules of interest in myeloproliferative neoplasms: introduction.骨髓增殖性肿瘤中感兴趣的突变分子:引言
Acta Haematol. 2008;119(4):192-3. doi: 10.1159/000140629. Epub 2008 Jun 20.

引用本文的文献

1
The PEBP2betaMYH11 fusion created by Inv(16)(p13;q22) in myeloid leukemia impairs neutrophil maturation and contributes to granulocytic dysplasia.在髓系白血病中,由inv(16)(p13;q22)产生的PEBP2β-MYH11融合蛋白会损害中性粒细胞成熟,并导致粒细胞发育异常。
Proc Natl Acad Sci U S A. 1998 Sep 29;95(20):11863-8. doi: 10.1073/pnas.95.20.11863.
2
The process of leukemogenesis.白血病发生的过程。
Environ Health Perspect. 1996 Dec;104 Suppl 6(Suppl 6):1239-46. doi: 10.1289/ehp.961041239.