查询词典 enzyme

Methods The subjects were divided into two groups: PIH group (n= 15) and normotensive control group (n=15). Peripheral lymphocytes of the subjucts were separated by Ficoll-Hypaque density centrifugation. The lymphocytes were cultured in RPMI-1640 medium with or without pokeweed mitogen for ten days.Then the supernatant was collected and the IgG and IgM were measured by enzyme linked immunosorbent assay.

采用密度梯度离心法分离妊高征组(15例)和正常妊娠组(15例)的外周血B淋巴细胞，并在有或无美洲商陆有丝分裂原存在的情况下培养10天后，收集上清液，采用酶联免疫吸附试验测定每1×106个B淋巴细胞所分泌的IgG和IgM的量。

Methods: This study was approved by the Department of Nephrology, the second hospital of Hebei Medical University. We choose 36 cases of IgA nephropathy(25 males and 11 fema- les).The mean age of them was 35.0±12.6 years.They were defi- nited by renal biopsy from July 2008 to Feb.2009.Patients with hypertension, diabetes mellitus, Lupus Nephritis, HBV-GN associated glomerulonephritis,thyropathy,renal damage induced by polyarthritis destruens,neoplasms associated nephropathy and those on glucocorticoid,immunosuppressive agents,enoxa- parin sodium and angiotensin converting enzyme inhibitor be- fore renal biopsy were excluded from this study.

河北医科大学第二临床医学院肾内科于2008年07月到2009年02月间经肾活检确诊的IgA肾病患者36例(其中男性25例，女性11例，年龄35.0±12.6岁)，临床上除外高血压肾损害、紫癜性肾炎、乙肝病毒相关性肾炎、狼疮性肾炎、甲状腺病相关性肾损害、类风湿性关节炎肾损害、肿瘤相关性肾病等继发性肾脏病患者，并除外肥胖、妊娠、糖尿病、肝脏疾病、药物等导致的肾损伤及急性间质性肾炎等患者。

When the substrate by the enzyme polyphenol oxidation, it will make the color difference.

当由多酚氧化酶的底物，它将使色差。

The third part concerned the degradability of apple pomace in rumen enzyme's influence on it.

同时对苹果渣的瘤胃降解品质及其与其它物质混合青贮料的品质进行研究和评定，为苹果渣在生产实践中的应用提供理论依据。

My child was picked up by neonatal screening for Pompe disease because of low enzyme activity.

我的小孩因为接受庞贝氏症新生儿筛检，发现其酵素活性偏低。

Enzymatic diagnosis of Pompe disease is hampered by the presence of several isoenzymes in whole blood, of which the neutrophil enzyme maltase-glucoamylase is of particular concern due to its low pH optimum.

酶法诊断庞佩病是受到在场的几个同工酶全血，而中性酶麦芽糖-糖化酶是特别关注，由於其低ph最优。

Background: Pompe disease is due to a deficiency of lysosomal acid alpha glucosidase, and currently an enzyme replacement therapy has been developed.

中文摘要背景：庞贝氏症是一种因为溶小体缺乏酸性醣苷酶无法分解肝醣所引起之疾病。

Background Pompe''s disease is a metabolic myopathy caused by a deficiency of acid alpha glucosidase, an enzyme that degrades lysosomal glycogen.

配景 蓬佩病是一种由酸性α葡萄糖苷酶（GAA，一种降解溶酶体肝糖的酶）缺乏引起的代谢性肌病。

Pompe's disease is a rare hereditary condition that causes an enzyme deficiency, which in turn leads to the buildup of glycogen, a stored form of sugar used for energy. The glycogen buildup causes progressive muscle weakness throughout the body, particularly in the heart, skeletal muscles, liver, and nervous system. In extreme cases, children can also die of heart failure.

庞贝氏症是一种遗传的罕见疾病，因为缺乏体内的酵素，导致肝醣无法分解堆积，因肝醣无法分解堆积造成心脏肥大、肌肉无力，肝脏和神经系统衰弱，在ㄧ些更极端的病例中，最后就因为心脏衰竭死亡。

On June 18, the FDA granted orphan drug designation to 1-deoxynojirimycin hydrochloride for the treatment of Pompe disease, an inherited lysosomal storage disorder caused by a mutation that alters the structure and stability of α-glucosidase, an enzyme responsible for the breakdown of glycogen.

6月18日，FDA批准孤儿药盐酸1-脱氧野尻霉素（Amicus Therapeutics， Inc）治疗蓬佩病。该疾病是一种遗传性溶体缺陷症，因突变导致破坏糖原的α糖苷酶的结构和稳定性改变。

According to the clear water experiment, aeration performance of the new equipment is good with high total oxygen transfer coefficient and oxygen utilization ratio.

曝气设备的动力效率在叶轮转速为120rpm～150rpm时取得最大值，此时氧利用率和充氧能力也具有较高值。

The environmental stability of that world - including its crushing pressures and icy darkness - means that some of its most famous inhabitants have survived for eons as evolutionary throwbacks, their bodies undergoing little change.

稳定的海底环境─包括能把人压扁的压力和冰冷的黑暗─意谓海底某些最知名的栖居生物已以演化返祖的样态活了万世，形体几无变化。