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Said was diagnosed with chronic lymphocytic leukemia in 1991, a malignant cancer of the bone marrow and blood.

说，被确诊为慢性淋巴细胞白血病於1991年，一种恶性肿瘤的骨髓和血液。

Chronic lymphocytic leukemia is a blood and bone marrow cancer that affects 10,000 new patients each year in the United States.

慢性淋巴细胞性白血病是一种血液和骨髓肿瘤，在美国每年有10，000新患者。

The results suggest that REV viral determination is same in both the group;REV viral antigen could be detected in the bursa of Fabricius, bone marrow, and glandularis venticuli, spleen, thymus, liver, lung, kidney and heart;viruses located maily in the immature lymphotaxis and reticular cell.

REV抗原阳性细胞的分布及形态特征基本相同，阳性细胞主要是正在发育成熟的淋巴细胞和上皮性网状细胞。

Methods Nested polymerase chain reaction was used to detect HPV B19-DNA on stock bone marrow smears from 84 children with ITP. Twenty-four cases of macrocytic anemia were chosen as controls.

应用巢式聚合酶链反应技术检测84例ITP患儿存档骨髓涂片标本中HPV B19-DNA，并以24例巨幼细胞性贫血患儿为对照。

LH_750, an automatic complete blood corpuscle analyzer was used to screening 96 patients, admitted in pediatric department of our hospital with Macrocytic anemia in 3 years period (from January 1, 2005 to July 30, 2008), The medical case history of macrocytic anemia was investigated by physical examinations as well as reticulomacroerthroycyte count, peripheral blood and bone marrow morphology, l...

利用LH-750全自动血细胞分析仪，从我院近3年(2005年1月1日至2008年7月30日)儿科住院贫血患儿中共发现大红细胞贫血患儿96例，上述大红细胞贫血患儿进行了详细的病史采集和体查、网织大红细胞计数、外周血及骨髓形态学、肝功能测定，甲状腺功能测定等，依据上述资料确定病因诊断。

Objective: The genes were connected basing on obtain gene of MCP and DAF of liver and fetal marrow of Chinese adult and then design mammiferous vector of the hMCP-DAF fusion gene. Finally transfer hMCP-DAF fusion gene to the early embryo of jinhua''s pig.

目的 在获得中国成人肝脏、胎儿骨髓MCP、DAF基因克隆的基础上，进一步将两个基因串接，并构建hMCP-DAF融合基因的哺乳动物表达载体，筛选出具表达活性的hMCP-DAF并导入金华猪早期胚胎。

Defects implanted with TGF-β/BMP in animals killed at 16 weeks showed histologically new lamellar and woven bone which was formed in continuity with the cut ends of the cortex. Medullar canal was recanalized and contained marrow elements with normal appearance.

术后第12～16周3组缺损区完全性修复，其密度近正常骨，可见皮质骨和骨髓腔结构。16周时TGF-β和TGF-β/BMP组骨缺损区周围外骨痂少，而BMP组中仍可见较多尚未完全吸收的外骨痂。

Objective: To discuss the significance of characteristics of morphological change of bone marrow cell in differential diagnosis of myelodysplastic syndromerefractory anemia and megaloblastic anemia.

目的：探讨骨髓细胞形态学变化特征在鉴别诊断骨髓增生异常综合征及巨幼红细胞性贫血中的意义。

Results Erythrocyte count, hemoglobin concentration and hematocrit of all the patients with malignant digestive tumor decreased, mean corpuscular volume and mean corpuscular hemoglobin increased, arid there was inconspicuous change in total leukocyte count. The indications of megaloblastic anemia and proliferative anemia in bone marrow hemogram were found in the patients. It was common that the percentage of neutrophils was higher and that of lymphocytes was lower than that of the normal controls.

结果 消化道恶性肿瘤患者的红细胞计数、血红蛋白、红细胞压积均减少，平均红细胞体积、平均红细胞血红蛋白量增高，均表现为巨幼细胞性贫血，骨髓象呈增生性贫血改变，而白细胞总数的变化较小，白细胞分类，中性粒细胞百分比超过正常范围与淋巴细胞百分比低于正常范围者多见，血小板数异常远较血红蛋白与白细胞为少，但36例肝癌患者中28例出现血小板减少。

Yelodysplastic syndromes,as a disease of dyspoiestichematopoietic stem cell,have a disturbance of DNA synthesis,cellsdifferentiation and some leudemic characterization.It's marrow cell displaylike megaloblastic change,so we postulated that folate receptor have adifference of both quantitative and quanlititive in megalolbastic anemia,MDSand lenkemia.

DS作为异常干细胞克隆性增生疾病，在DNA的合成及细胞分化异常，表现出白血病的某些特征和骨髓细胞具有不同程度的巨幼变，因而我们推测巨幼贫、白血病和MDS的叶酸受体不但有量的改变，而且有质的变化。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。