Bicc1,Bicc1,在线英语词典,英文翻译,专业英语

1) Bicc1

Bicc1

Cloning of the Mouse Bicaudual-C-1 Gene、Preparation and Application of Anti-Bicc1 Polyclonal Antibody;

小鼠双尾C基因克隆、Bicc1蛋白多克隆抗体制备及初步应用

2) ABCC1

ABCC1

Advance in mechanism study of multi-drug resistance mediated by ABCC1 and its reverse;

ABCC1介导多药耐药机制及其逆转的研究进展

3) NICCD

NICCD

The Clinical Value of the Galactitol Concentration in Urine Filter Paper Analyzed by GC/MS in Screening NICCD Patients;

滤纸尿半乳糖醇GC/MS分析在筛查NICCD中的应用研究

Objective To establish a method of molecular diagnosis of the disease by analyzing the gene mutations in 19 suspected patient of NICCD.

目的建立SLC25A13基因突变分析方法,分析19例临床疑似新生儿肝内胆汁淤积症(NICCD)患儿SLC25A13基因突变情况。

In 2001,SLC25A13 gene mutations were found in Japanese neonatal abnormal metabolism screening intrahepatic cholestasis children,and thus Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency(NICCD) was named.

2001年,Ohura等在日本新生儿代谢筛查异常的肝内胆汁淤积症患儿中发现存在SLC25A13基因突变,并将其命名为Citrin缺乏引起的新生儿肝内胆汁淤积症(Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency,NICCD)。

4) aacC1

aacC1

Antibiotic resistance-related genes(aacC1,aacC2,aacA4,OXA-23,PER-1,AmpC,Int1 and Int2) were detected by PCR.

结果:18株不动杆菌呈现多重耐药;aacC1,aacA4,PER-1,AmpC和Int1阳性率分别为58。

5) HIC-1

肿瘤高甲基化基因-1

6) NKCC1

NKCC1

Effects of Local Mild Hypothermia on the mRNA Level of NKCC1 in Focal Brain Ischemia-Reperfusion Injury Rats;

局部亚低温对大鼠局灶性脑缺血-再灌注模型NKCC1 mRNA水平的影响

The Role of NKCC1 in Auditory Function of Transgenic Mice Detected by ABR and DPOAE;

ABR和DPOAE检测研究NKCC1在不同基因型小鼠耳蜗听觉中的作用

AIM:We generated transgenic mice of NKCC1-/-(homozygous mutant),NKCC1+/-(heterozygous)and NKCC1+/+(wild-type)that have a targeted disruption in the NKCC1 gene to investigate the role of Na-K-2Cl(NKCC1)channel in auditory function of the inner ear.

目的:培育突变型纯合子NKCC1-/-、杂合子NKCC1+/-及野生型NKCC1+/+小鼠,将这3种基因型小鼠作为实验平台,研究NKCC1离子通道(Na-K-2Cl,co-transporter)在耳蜗听觉平衡功能中的作用,并观察不同基因型小鼠的内耳形态特征。

参考词条

PiCCO PICK1 PICK1 PICK1 PICK1 Sicca XRCC1 XRCC1 XRCC1 XRCC1 ERCC1 ERCC1 ERCC1 ERCC1 夏洛特·勃朗蒂己二酸与1,4-丁二醇、1,6-二异氰酸己烷和1,6-己二醇的聚合物

补充资料：肿瘤抑制基因

分子式：
CAS号：

性质：是一类肿瘤抑制基因的总称。第一个分离到的抑癌基因是Rb基因(retinoblastoma gene)或称视网膜母细胞瘤基因。现已证明：结肠癌等多种癌症也检出Rb基因的缺陷。已被证实的抑癌基因有10多种，都是通过缺失或失活而致细胞恶性转化的一类基因。这类基因的作用机制涉及基因表达调控、细胞分裂、分化过程，也可能与生长因子、激酶、信息在胞内的传递密切相关。

说明：补充资料仅用于学习参考，请勿用于其它任何用途。

首页 \| 翻译 \| 影视 \| 论坛 \| 索引 NKCC1 MIC-1 MICCG CICCS PiCCO PiCCO

1) Bicc1 Bicc1 1. Cloning of the Mouse Bicaudual-C-1 Gene、Preparation and Application of Anti-Bicc1 Polyclonal Antibody; 小鼠双尾C基因克隆、Bicc1蛋白多克隆抗体制备及初步应用 2) ABCC1 ABCC1 1. Advance in mechanism study of multi-drug resistance mediated by ABCC1 and its reverse; ABCC1介导多药耐药机制及其逆转的研究进展 3) NICCD NICCD 1. The Clinical Value of the Galactitol Concentration in Urine Filter Paper Analyzed by GC/MS in Screening NICCD Patients; 滤纸尿半乳糖醇GC/MS分析在筛查NICCD中的应用研究 2. Objective To establish a method of molecular diagnosis of the disease by analyzing the gene mutations in 19 suspected patient of NICCD. 目的建立SLC25A13基因突变分析方法,分析19例临床疑似新生儿肝内胆汁淤积症(NICCD)患儿SLC25A13基因突变情况。 3. In 2001,SLC25A13 gene mutations were found in Japanese neonatal abnormal metabolism screening intrahepatic cholestasis children,and thus Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency(NICCD) was named. 2001年,Ohura等在日本新生儿代谢筛查异常的肝内胆汁淤积症患儿中发现存在SLC25A13基因突变,并将其命名为Citrin缺乏引起的新生儿肝内胆汁淤积症(Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency,NICCD)。 4) aacC1 aacC1 1. Antibiotic resistance-related genes(aacC1,aacC2,aacA4,OXA-23,PER-1,AmpC,Int1 and Int2) were detected by PCR. 结果:18株不动杆菌呈现多重耐药;aacC1,aacA4,PER-1,AmpC和Int1阳性率分别为58。 5) HIC-1 肿瘤高甲基化基因-1 6) NKCC1 NKCC1 1. Effects of Local Mild Hypothermia on the mRNA Level of NKCC1 in Focal Brain Ischemia-Reperfusion Injury Rats; 局部亚低温对大鼠局灶性脑缺血-再灌注模型NKCC1 mRNA水平的影响 2. The Role of NKCC1 in Auditory Function of Transgenic Mice Detected by ABR and DPOAE; ABR和DPOAE检测研究NKCC1在不同基因型小鼠耳蜗听觉中的作用 3. AIM:We generated transgenic mice of NKCC1-/-(homozygous mutant),NKCC1+/-(heterozygous)and NKCC1+/+(wild-type)that have a targeted disruption in the NKCC1 gene to investigate the role of Na-K-2Cl(NKCC1)channel in auditory function of the inner ear. 目的:培育突变型纯合子NKCC1-/-、杂合子NKCC1+/-及野生型NKCC1+/+小鼠,将这3种基因型小鼠作为实验平台,研究NKCC1离子通道(Na-K-2Cl,co-transporter)在耳蜗听觉平衡功能中的作用,并观察不同基因型小鼠的内耳形态特征。参考词条 PiCCO PICK1 PICK1 PICK1 PICK1 Sicca XRCC1 XRCC1 XRCC1 XRCC1 ERCC1 ERCC1 ERCC1 ERCC1 夏洛特·勃朗蒂己二酸与1,4-丁二醇、1,6-二异氰酸己烷和1,6-己二醇的聚合物补充资料：肿瘤抑制基因分子式： CAS号：性质：是一类肿瘤抑制基因的总称。第一个分离到的抑癌基因是Rb基因(retinoblastoma gene)或称视网膜母细胞瘤基因。现已证明：结肠癌等多种癌症也检出Rb基因的缺陷。已被证实的抑癌基因有10多种，都是通过缺失或失活而致细胞恶性转化的一类基因。这类基因的作用机制涉及基因表达调控、细胞分裂、分化过程，也可能与生长因子、激酶、信息在胞内的传递密切相关。说明：补充资料仅用于学习参考，请勿用于其它任何用途。
©2008 dictall.com