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2
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Blood. 1996 Mar 1;87(5):1900-11.
3
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Expression of the NF-kappaB targets BCL2 and BIRC5/Survivin characterizes small B-cell and aggressive B-cell lymphomas, respectively.核因子-κB靶标BCL2和BIRC5/生存素的表达分别是小B细胞淋巴瘤和侵袭性B细胞淋巴瘤的特征。
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本文引用的文献

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Global conformational rearrangements during the activation of the GDP/GTP exchange factor Vav3.GDP / GTP交换因子Vav3激活过程中的全局构象重排。
EMBO J. 2005 Apr 6;24(7):1330-40. doi: 10.1038/sj.emboj.7600617. Epub 2005 Mar 10.
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Ectopic expression of VAV1 reveals an unexpected role in pancreatic cancer tumorigenesis.VAV1的异位表达揭示了其在胰腺癌肿瘤发生中的意外作用。
Cancer Cell. 2005 Jan;7(1):39-49. doi: 10.1016/j.ccr.2004.11.024.
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Vav mediates Ras stimulation by direct activation of the GDP/GTP exchange factor Ras GRP1.Vav通过直接激活GDP/GTP交换因子Ras GRP1来介导Ras刺激。
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Rho GTPases in cell biology.细胞生物学中的Rho GTP酶
Nature. 2002 Dec 12;420(6916):629-35. doi: 10.1038/nature01148.
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Detection of inv(16) and t(16;16) by fluorescence in situ hybridization in acute myeloid leukemia M4Eo.荧光原位杂交技术检测急性髓系白血病M4Eo中的inv(16)和t(16;16)
Haematologica. 2000 May;85(5):481-5.
6
Tyrosine phosphorylation mediates both activation and downmodulation of the biological activity of Vav.酪氨酸磷酸化介导Vav生物活性的激活和下调。
Mol Cell Biol. 2000 Mar;20(5):1678-91. doi: 10.1128/MCB.20.5.1678-1691.2000.
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Regulatory and signaling properties of the Vav family.Vav家族的调控与信号传导特性。
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8
A functional T-cell receptor signaling pathway is required for p95vav activity.p95vav活性需要功能性T细胞受体信号通路。
Mol Cell Biol. 1995 Aug;15(8):4337-46. doi: 10.1128/MCB.15.8.4337.

VAV原癌基因产物的过表达与13q缺失的B细胞慢性淋巴细胞白血病相关。

Overexpression of the VAV proto-oncogene product is associated with B-cell chronic lymphocytic leukaemia displaying loss on 13q.

作者信息

Prieto-Sánchez Rosario M, Hernández José A, García Juan L, Gutiérrez Norma C, San Miguel Jesús, Bustelo Xosé R, Hernández Jesús M

机构信息

Centro de Investigación del Cáncer, Hospital Clínico Universitario de Salamanca, Salamanca, Spain.

出版信息

Br J Haematol. 2006 Jun;133(6):642-5. doi: 10.1111/j.1365-2141.2006.06094.x.

DOI:10.1111/j.1365-2141.2006.06094.x
PMID:16704440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1950221/
Abstract

The expression of the VAV proto-oncogene in 57 patients with chronic myeloproliferative disease (CMD), B-cell acute lymphoblastic leukaemia (B-ALL) and B-cell non-Hodgkin Lymphoma (B-NHL), and 61 with B-cell chronic lymphocytic leukaemia (B-CLL) was analysed. VAV overexpression was observed in 19.5% of cases and 81% of VAV-positive tumours also displayed VAV phosphorylation. Overexpression was not observed in B-ALL or CMD, but 13% of B-NHL and 34.4% of B-CLL patients (P = 0.002) overexpressed VAV. The overexpression and phosphorylation of VAV was detected more frequently in 13q- chronic lymphocytic leukaemias (71.4%) versus other B-CLLs (23.4%, P = 0.001). Overexpression of VAV protein is a frequent event in patients with B-CLL displaying loss of 13q sequences.

摘要

分析了57例慢性骨髓增殖性疾病(CMD)、B细胞急性淋巴细胞白血病(B-ALL)和B细胞非霍奇金淋巴瘤(B-NHL)患者以及61例B细胞慢性淋巴细胞白血病(B-CLL)患者中VAV原癌基因的表达情况。在19.5%的病例中观察到VAV过表达,并且81%的VAV阳性肿瘤也显示出VAV磷酸化。在B-ALL或CMD中未观察到过表达,但13%的B-NHL患者和34.4%的B-CLL患者(P = 0.002)VAV过表达。与其他B-CLL相比,13q-慢性淋巴细胞白血病中VAV的过表达和磷酸化检测更为频繁(71.4% 对23.4%,P = 0.001)。VAV蛋白过表达在显示13q序列缺失的B-CLL患者中是常见事件。