血色素
- Hemoglobin;hemochrome;hemachrome
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吡啶血色素光谱显示了酶分子以原卟啉Ⅸ(protohemeⅨ)作为辅基。
The pyridine hemochrome spectrum indicated the presence of protoheme ⅸ as the prosthetic group .
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贫血:香蕉铁质含量高,能刺激血液内的血色素。
Anaemia : The content of banana iron is high , can stimulate the hemochrome in the blood .
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结果对色相和血色素的影响不大;PH值逐渐上升;
Results revealed that colorphase and haematochrome were not quite affected , PH value gradually rose ;
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结果:灌流前后血细胞计数和血色素值、血浆电解质及蛋白质浓度没有统计学差异(P0.05)。
Results : Blood cell not damaged , concentration of hemoglobin , electrolytes and protein in plasma not altered ( P0.05 ) .
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小结节型肝硬化也可见于Wilson病、原发性胆汁硬化和血色素沉着症。
Micronodular cirrhosis may also be seen with Wilson 's disease , primary biliary cirrhosis , and hemochromatosis .
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早产儿换血过程中更易发生内环境紊乱,早产组血钾、白细胞、血色素、血小板下降明显,其变化与足月组比较差异有显著性(P0.01或0.05)。
Preterm infants were more likely to develop disturbance of internal milieu ( P0 . 01 or 0 . 05 ) .
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结果发现韩国男女运动员的血色素(Hb)平均值高于我省运动员;
It showed that the average of KOREA athlete was higher than our athletes ' in Hemoglobin ( HB );
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新型核苷逆转录酶抑制剂、越高的平均红细胞体积和血色素,越低的HIV核糖核酸和血红蛋白与A1C和血糖的差距有关。
Current nucleoside reverse transcriptase inhibitors ( NRTIs ), higher MCV and hemoglobin , and lower HIV RNA and haptoglobin were associated with greater A1C-glucose discordance .
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HFE基因与遗传性血色素沉着症
Relationship between HFE gene and hereditary hemochromatosis
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目的:探讨肾损伤程度、ISS、损伤原因、损伤机制、休克、血色素等因素对肾损伤治疗方式选择及预后的影响。
Obejectine : To evaluate factors such as mechanism and cause of renal injury , ISS values , hemochrome , shock , renal injury grade affecting management and prognosis in renal injury .
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血铅、血锌卟啉、血色素、红细胞总数和尿中HVA、VMA等指标两组差别有非常显著性(P<0.01)。
The lead and ZPP in blood , Hb , RBC count and HVA , VMA in urine of both groups showed significant difference ( P < 0.01 ) .
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被调查儿童,血色素平均值为12.4g,离均差为0.92;血色素低于11g的占8.7%;
Among the investigated children , the average hemoglobin is 12.4g , the discrepancy from the standard is 0.92.The percentage of the children hemoglobin , below 11g is 8.7 % .
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HFE基因发现于1996年,属于HLA类样基因,是遗传性血色素沉着症候选基因。HFE分子的功能可能是参与调节转铁蛋白与转铁蛋白受体间的相互作用。
HFE gene is a major histocompatibility complex class ⅰ - like gene , which was identified as a candidate gene for hemochromatosis in 1996 . The proposed role for HFE is its part in the regulation of the interaction of the transferrin receptor with transferrin .
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血球或血色素浓度增加。
Anemia characterized by an increase in the concentration of corpuscular hemoglobin .
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对你这个年龄的人来说,你的血色素不算太低。
Your hemoglobin isn 't too low for people of your age .
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从血色素中除去亚铁血红素而获得的一种无色蛋白质。
A colorless protein obtained by removing heme from hemoglobin .
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内镜下血色素指数色图测定对上消化道病变的诊断价值
Usefulness of IHb map in the diagnosis of upper gastrointestinal tract lesions
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由于血色素合成有误引起的遗传性贫血症。
An inherited form of anemia caused by faulty synthesis of hemoglobin .
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当发生器官功能障碍时,则用血色素沉着症表示。
The term " hemochromatosis " is used when organ dysfunction occurs .
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青铜色的色素沉着见于血色素沉着症和砷中毒。
Bronze hyperpigmentation is seen in hemochromatosis and arsenic intoxication .
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用于快速检测血色素的生物传感器研究
Research on Biosensor for the Fast Determination of Hemoglobin
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98例幼儿血色素及微量元素检测结果分析
Analysis on Hemoglobin and Trace Elements in 98 Children
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优秀赛艇运动员血色素的分析
A Analysis of the Hemoglobin of the Excellence Rowers
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血色素催化鲁米诺化学发光法检测过氧化苯甲酰的研究
Luminol chemiluminescence detection of benzoyl peroxide catalyzed with hematin
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胃血色素指数的测定对幽门螺杆菌的诊断价值
Efficacy of index of haemoglobin on diagnosis of helicobacter pylori with chronic gastritis
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可有带有试管的血色素测量机构或卡。
There may be a hemoglobin measurement mechanism or card with a cuvette .
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继发性肝血色素沉积症一例
One case report of secondary hemosiderosis in liver
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运动性低血色素大鼠脾脏T淋巴细胞亚群变化的研究
Study on Changes of Spleen T Homeocyte Subgroup When Sports Hypochrosis Happens in Rats
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暗红色的污点是红细胞坏死后漏出的血色素造成的。
The faint reddish staining is from hemoglobin that leaked from RBC 's following death .
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具有挑战性的是调整血色素,以使它用于血液替代品。
The challenge is to modify hemoglobin to allow it for use as blood substitutes .