Business Goal – Transition all systems to use the new AML process over the next year. 业务战略目标&明年把所有系统转换为使用新的AML过程。
The information for the mapping is retrieved from AML as shown in Table 1. 映射的信息可从AML获取,如表1所示。
For the AML case, it is expected that this assessment is based on new account information gathered around the new customers 'specific checks, and on transaction activities. 对于AML的情况,人们希望这个评估是基于从新客户特定支票和交易活动中所收集的新帐户信息。
In this case, the duplication within the MLL gene contributes to an aggressive form of AML. 这种情况下,MLL基因中的复制导致AML的的侵略性。
MA9 is commonly found in acute myeloid leukemia ( AML) and occasionally in acute lymphoid leukemia and is associated with intermediate to poor outcome. MA9常见于急性髓性白血病,偶尔也在急性淋巴白血病中发现,并且会导致较差的预后。
In other words, has there been a silent conclusion that the FATF Recommendations do not actually solve the AML/ CFT problem? 换言之。我们是否下了这样的一个沉默结论,就是:FATF建议实际上并没有解决AML/CFT问题?
Effects of hematopoietic growth factor receptors on proliferation of AML cells 造血生长因子受体对急性髓性白血病细胞增殖的调控作用
Expressions of SHP-1 and JAKs Genes in AML Patients and Their Correlation SHP-1和JAKs基因在成人急性髓系白血病患者中的异常表达及其相关性
Objective To investigate the expression of AML1/ ETO fusion gene mRNA in acute myeloid leukemia ( AML) and its clinical significance. 目的了解急性髓系白血病中AML1/ETO融合基因表达情况及相关临床意义。
The management of microbial infection is one of the important issues for patients with acute myeloid leukemia ( AML). 微生物感染的治疗是急性髓样白血病(AML)患者面临的重要问题之一。
We conducted a trial to analyze the efficacy and safety of voriconazole in the prevention of lung infiltrates during induction chemotherapy for acute myelogenous leukaemia ( AML). 我们进行了一项临床试验旨在分析伏立康唑在急性髓细胞白血病化疗诱导阶段预防肺部浸润的有效性和安全性。
Conclusion: DCIK can induce specific immunoreaction in the immune system and has satisfactory clinical anticancer efficacy in treatment of AML. 结论:DCIK能诱导机体产生特异性的免疫反应,对急性髓细胞性白血病的治疗有较好的临床疗效。
PCR-capillary electrophoresis is convenient to screen NPM1 mutations of AML in clinical practice. AML的NPM1基因突变临床检测采用PCR-毛细管电泳法更方便。
The expression of plasmin associated proteins in bone marrow and plasma in AML 纤溶酶相关蛋白在急性髓性白血病血浆和骨髓中的表达
Antiangiogenic treatment with endostatin inhibits progression of AML in vivo. 标题血管内皮抑素的抗血管生成治疗可抑制体内急性单核性白血病癌细胞的进展。
Outcomes and survival analysis of patients with AML and high risk MDS treated by CAG regimen CAG方案治疗AML和高危MDS患者的疗效及生存分析
Conclusions: There is gene rearrangement in the leukemiacells of AML in children. 结论:急性粒细胞白血病患儿的白血病细胞存在基因重排;
Patients with NR of AML, neutropenia or agranulocytosis, and long-term broad-spectrum anti-biotics usage are susceptible to IPFI. AML未缓解、粒细胞缺乏或减少和长时间广谱抗生素应用时易发生IPFI。
This study was to explore the clinical significance of FLT3 internal tandem duplication ( FLT3/ ITD) in acute myeloid leukemia ( AML) with chromosome abnormality. 本研究旨在探讨伴有染色体异常急性髓系白血病患者FLT3跨膜区内部串联重复突变检测的临床意义。
Renal angiomyolipoma ( AML) is a benign tumor composed of vascular, smooth muscle and adipose tissue. 肾肌脂肪血管瘤是由血管、平滑肌、与脂肪组织所构成的良性肿瘤。
This study was aimed to explore the relationship of6; 9 chromosome translocation with DEK-CAN fusion gene expression in patients with acute myeloid leukemia ( AML) and its clinical significance. 本研究旨在探讨急性髓系白血病(AML)患者6;9染色体易位与DEK-CAN融合基因表达之间的关系及临床意义。
This study was aimed to explore prognostic significance of minimal residual disease ( MRD) detection in patients with acute myeloid leukemia ( AML) by multiparameter flow cytometry ( MCF). 本研究探讨多参数流式细胞术检测急性髓系白血病(AML)微量残留病(MRD)的方法和预后意义。
Background and objective: Relapse AML, refractory AML, AML in the old and secondary AML are all AML subtypes hard to cure. 背景和目的:难治性急性髓系白血病(AML)包括复发性AML、原发耐药AML、老年AML及继发AML,是目前白血病治疗困难的类型。
Conclusions Genotypes defined by the mutational status of NPM1, FLT3, CEBPA, and MLL are associated with the outcome of treatment for patients with cytogenetically normal AML. 结论:由NPM1,FLT3,CEBPA,和MLL基因的突变状态所界定的基因型与细胞遗传学正常的急性髓细胞白血病患者的临床治疗结局之间存在相关性。
They then received supportive care such as blood transfusions and AML treatments that included relatively harsh chemotherapy. 然后,他们接受支持性的照顾,例如输血和急性髓系白血病的治疗,其中包括比较苛刻的化疗。
Methods: Mononuclear cells were isolated from bone marrow ( BM) of CML ( 14 cases), AML ( 12 cases) and normal individuals ( 20 cases). 方法收集12例AML、14例CML和20例正常对照骨髓标本,分离单个核细胞。
Objective To study the immunophenotype and P-glycoprotein expression in CD7 positive adult acute myeloid leukemia ( CD7+ AML). 目的研究CD7阳性急性髓系白血病(CD7+AML)的临床生物学特征。
We previously reported the feasibility of clofarabine and cytarabine combinations in AML. 我们此前报道了氯法拉滨与阿糖胞苷联合使用治疗AML的可行性。
The new mouse model should help leukemia researchers to learn how this mutation contributes to AML development, and it may lead to new ways to treat, diagnose and perhaps prevent the disease. 新的小鼠模型将有助于白血病研究人员了解上述突变是怎样导致AML发展的,并且该模型可能为新的治疗、诊断或许新的预防AML方法指出方向。