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- Myeloid cell leukemia sequence-i 髓样细胞白血病-1
- Keywords Aminopeptidase N, myelo-specific promoter;multidrug resistance 1 gene;manganese superoxide dismutase gene;retrovirus;hepatoma cell;myeloid cell; 氨肽酶N;骨髓特异性启动子;锰超氧化物歧化酶基因;多药耐药基因;逆转录病毒载体;骨髓细胞;肝癌细胞;
- BclZ mRNA wasdetectable not only in lymphoid cell lines (Raji , CEM)but also in myeloid cell lines(K562 , HL-60 , U937)except for Molt-4 (T-cell leukemia). 6种白血病细胞株中5种bcl－2mRNA阳性（Molt－4例外），它们分别为CEM、Raji、HL－60、U937及K562。
- The stem cell leukemia( SCL) gene is a new oncogene related with leukemogenesis. 干细胞白血病(CL)因是新发现的与白血病发生有关的癌基因。
- Study on expression of IRF?1 gene in human leukemia with RT?PCR and the silver sequence techniques. 逆转录-聚合酶链反应银染分析IRF-1基因在白血病中的表达
- High sense mutation of HVR 1 gene was found. （4）HVR1基因有义突变率相当高。
- Mutations in the ABCA 1 gene cause Tangier disease. ABCA 1基因的突变引起Tangier病 (TD)。
- Over expression of PAI 1 gene leads to mesangial ECM accumulation. 首次建立了系膜细胞PAI 1的过度表达体系 ,证实细胞过度表达PAI 1可以直接导致ECM的积聚。
- Myeloid cell leukelia-1(MCL-1) is the most affluent in BCL-2 family proteins in human cervical cancer tissue. 髓样细胞白血病-1（MCL-1）在人类宫颈癌组织中的表达是BCL-2家族抗凋亡蛋白中最丰富的。
- The carnosinase 1 gene produces an enzyme called carnosinase. 肌肽酶1基因翻译表达肌肽酶。
- Conclusion Blastic NK cell leukemia has an aggressive clinical course with poor response to treatment and unfav... 结论原始NK细胞白血病易发生髓外浸润,且治疗反应差、预后不良。
- AML 1 gene abnormalities, including both chromosome translocation and mutation (point mutation, insertion, deletion mutation, et al), which lead to the lost of transcript activation, are general in acute leukemia. 在急性白血病中常见AML1基因结构异常，包括平衡易位及突变(如点突变、插入或缺失突变等)，导致AML1的转录活性丧失，提示此基因功能缺失在急性白血病的发生及发展中起着重要作用。
- It is approved for the treatment of chronic myelogenous leukemia (CML) and hairy cell leukemia. 它被批准用于慢性髓细胞白血病和毛细胞白血病的治疗。
- Methods The characteristics of blastic NK cell leukemia and its treatment were discussed with review of literatures. 方法报道1例原始NK细胞白血病及其治疗经过,并进行文献复习。
- The goal of the present study was to investigate whether telomere shortening in CHD is restricted to specific peripheral blood lymphocyte and/or myeloid cell subpopulations. 该研究的目的是探究CHD的端粒缩短是否仅限于特殊的外周血白细胞和/或髓样细胞亚群。
- This showed that ETPs give rise to myeloid cells in the normal thymus. 这表明在正常胸腺中，一些早期胸腺细胞成为了髓细胞。
- GCH 1 gene mutation is only one of reasons to the DRD patients onset. GCH-1基因突变只是部分DRD患者的发病原因。
- ETP cells retained the ability to become either T cells or myeloid cells. 早期胸腺祖细胞同时保留成为T细胞或髓细胞能力。
- Adhering spindle-shaped MSCs were also obtained in adherence separation group with domestic FBS cultured in F12-DMEM, but many myeloid cell witch similar to round shape and few spindle-shaped MSCs were obtained in DMEM group. 采用国产血清培养的两组细胞中,给予F12-DMEM培养基可以获得梭形细胞,而给予DMEM培养基后则多为类圆形骨髓样细胞,仅见极少梭形细胞。
- Intact BHRF1, DNase, thymidine kinase (TK) and nuclear antigen?1 gene fragments of EBV were amplified using PCR technique with DNAs from B??95?8? and SUNE?1 cell lines as template. PCR从SUNE?1细胞DNA中扩增出EB病毒的4种（BHRF1、DNA酶、胸苷激酶及核抗原?1）全基因片段；
