globin

Expression of PEG 3 and Plakoglobin in Human Gliomas.

PEG3和plakoglobin在人脑胶质瘤中的表达.

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globin chain electrophoresis showed that the fast and slow moving components were α-and β-chain variants.

肽链解离电泳结果表明快速成分为α-链变异体，慢速成分为β-链变异体。

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the sdspage bands of of glutelin and globin had sore differences among different rape varieties.

谷蛋白和球蛋白的SDS-PAGE谱带在不同油菜品种间存在差异。

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However, naturally occurring deletion or point mutations within the β-globin gene cluster may interfere with the fetal-to-adult switching and result in the expression of the y-globin genes persisting at high levels in adults.

然而，天然发生的β-珠蛋白基因簇内的缺失突变或γ-珠蛋白基因启动子点突变可能影响胎儿到成人的开关，导致γ-珠蛋白基因在成人期持续活跃表达。

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The Study of the Mechanisms of γ-globin Gene Reactivation in Non-deletion HPFH and Yunnanese ( A γδβ)~ 0-thalassemia in Transgenic Mice

利用转基因小鼠研究启动子突变HPFH及Yunnanese（Aγδβ）～0-地贫中γ-珠蛋白基因再活化的机制

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Identification of β-globin Gene in Peking Duck's Genomic DNA

北京鸭核DNA中β-珠蛋白基因的初步鉴定

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Cloning and sequencing analysis of Chinese yak β-globin gene

中国牦牛β-珠蛋白基因的克隆和序列分析

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Use of probe α globin 3' HVR in fingerprinting in laboratory mice

应用α-珠蛋白3'-HVR探针进行小鼠的DNA指纹分析

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Appearance of some novel proteins binding enhancer element of globin gene ( hs_2) during erythroid terminal differentiation

红细胞终末分化期出现与珠蛋白基因表达增强子HS2序列特异结合的蛋白质因子

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α-Thalassemia major is a hereditary disease with a syndrome of hemolytic anemia, often caused bv the complete or partial deletion of a-globin genes.

α-地中海贫血是由于α-珠蛋白基因全部和部分缺失所致的一种遗传性溶血性贫血综合征。

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Microsatellite Polymorphism of β-globin locus ( HBB) in Four Altitude Chinese Yak Populations

中国四个海拔牦牛群体血红蛋白β链微卫星多态性分析

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Reactivation of Fetal Globin Gene in Adult Bone Marrow Erythroid Cells in Culture Conditions

成人骨髓红细胞中胎儿珠蛋白基因在培养条件下重新活化

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The α-globin gene of yak was amplified and cloned by using the primers based on the conserved region of the upstream from the initiation codon and the downstream from the termination codon.

根据α-珠蛋白基因起始密码子上游及终止密码子下游的保守序列设计引物，以牦牛基因组DNA为模板克隆并测定了α-珠蛋白基因序列。

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Results By PCR-RDB, nine people were proven to have typical phenotypes of β-thalassemia, which were not categorized into the sixteen known genotypes though. The β-globin gene mutations were characterized by PCR-reverse dot blot ( RDB).

结果运用PCR-反向点杂交技术进行基因筛查，发现9例具有典型β-地中海贫血表型特征，但不属于已知的16种β-地中海贫血突变类型。

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Quantitative Analysis of Human Globin Gene Expression in β-thalassemia Using Real-Time RT-PCR

应用实时定量RT-PCR技术检测β地中海贫血珠蛋白基因的表达

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The primary structure of globin moiety is determined by the plant genome.

球蛋白一半的最初构造决定于植物的染色体组.

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Repair of thalassemic human β globin mRNA in cultured erythroid cells by antisense RNA

反义RNA对地中海贫血红系细胞β-珠蛋白mRNA异常剪接的纠正作用

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effects of preparations of different deer fetus and placenta on the immune organs index, the content of serum globin, the phagocytosis ratio of macrophage and phagocytosis index in aged male rats were investigated.

研究了鹿胎及胎盘制剂对老年雄性大鼠免疫器官指数、血清球蛋白含量和巨噬细胞吞噬率及吞噬指数的影响。

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However, MyoD 1, myosin , myoglobin, S 100, desmin , CK, EMA, CD 68 and CD 117 were negative.

而MyoD1 、 myosin 、 myoglobin 、 S-100 、 Des 、 CK 、 EMA 、 CD68以及CD117均(-).

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Analysis of mRNA Expression in Human β~ ( 654) Globin Gene Transgenic Mice by Fluorescent Quantitive RT-PCR

荧光定量RT-PCR技术分析人地中海贫血β~（654）珠蛋白基因转基因小鼠mRNA的表达

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The Transcriptional Regulation Study on Human δ Globin Gene with CAAT Box C → T Point Mutation in Its Promoter

人δ珠蛋白基因启动子区CAAT盒C→T突变对其转录的影响

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