单细胞中蛋白质的免疫化学定量分析。I. 一些正常和异常红细胞中的碳酸酐酶B、β-链血红蛋白和γ-链血红蛋白。 - Suppr

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超能文献

Immunochemical quantitation of proteins in single cells. I. Carbon anhydrase B, beta-chain hemoglobin and gamma-chain hemoglobin in some normal and abnormal erythrocytes.

作者信息

Gitlin D, Sasaki T, Vuopio P

出版信息

Blood. 1968 Nov;32(5):796-810.

PMID:4176912

Abstract

摘要

相似文献

Immunochemical quantitation of proteins in single cells. I. Carbon anhydrase B, beta-chain hemoglobin and gamma-chain hemoglobin in some normal and abnormal erythrocytes.单细胞中蛋白质的免疫化学定量分析。I. 一些正常和异常红细胞中的碳酸酐酶B、β-链血红蛋白和γ-链血红蛋白。

Blood. 1968 Nov;32(5):796-810.

The distribution of hemoglobin A2.血红蛋白A2的分布

Ann N Y Acad Sci. 1969 Nov 20;165(1):54-9. doi: 10.1111/j.1749-6632.1969.tb27776.x.

[Abnormal hemoglobins and elevation of A2 hemoglobin and erythrocyte carbonic anhydrase isoenzymes in a hospital population of Puebla].[普埃布拉医院人群中的异常血红蛋白、A2血红蛋白升高及红细胞碳酸酐酶同工酶]

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Studies on abnormal hemoglobins. XI. Sickle cell-thalassemia disease in the Negro; the significance of the S+A+F and S+A patterns obtained by hemoglobin analysis.异常血红蛋白的研究。十一、黑人中的镰状细胞-地中海贫血病；血红蛋白分析得出的S+A+F和S+A模式的意义。

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THE FIRST OBSERVATION OF HOMOZYGOUS HEMOGLOBIN S-ALPHA THALASSEMIA DISEASE AND TWO TYPES OF SICKLE CELL THALASSEMIA DISEASE: (A) SICKLE CELL-ALPHA THALASSEMIA DISEASE, (B) SICKLE CELL-BETA THALASSEMIA DISEASE.纯合子血红蛋白S-α地中海贫血病及两种镰状细胞贫血病的首次观察：(A) 镰状细胞-α地中海贫血病，(B) 镰状细胞-β地中海贫血病。

Blood. 1963 Dec;22:757-69.

[STUDY OF ERYTHROCYTE RESISTANCE IN THE NEWBORN, THE INFANT AND THE CHILD DURING CERTAIN PATHOLOGICAL CONDITIONS].

Ann Biol Clin (Paris). 1963 Jul-Sep;21:609-18.

Clinical manifestations of inherited abnormal hemoglobins. I. The interaction of hemoglobin-S with hemoglobin-D.遗传性异常血红蛋白的临床表现。I. 血红蛋白S与血红蛋白D的相互作用。

Blood. 1955 May;10(5):389-404.

[Isoenzymes B and C of carbonic anhydrase, (HCAB), (HCAC), studied in relation to hemoglobin content in red blood cells of maternal and umbilical cord blood. (Checking of the maternal and infant blood at one week after labor)].碳酸酐酶同工酶B和C，（HCAB），（HCAC），与母血和脐带血红细胞中的血红蛋白含量相关研究。（产后一周对母婴血液进行检查）

Riv Clin Pediatr. 1970 Nov-Dec;83(4):145-54.

Homozygous beta thalassemia in American Blacks: the problem of mild thalassemia.美国黑人中的纯合子β地中海贫血：轻度地中海贫血问题

J Lab Clin Med. 1973 Jun;81(6):857-66.

Studies on abnormal hemoglobins. VI. Electrophoretic demonstration of type S (sickle cell) hemoglobin in erythrocytes incapable of showing the sickle cell phenomenon.异常血红蛋白的研究。VI. 无法表现出镰状细胞现象的红细胞中S型（镰状细胞）血红蛋白的电泳显示

Blood. 1953 Mar;8(3):270-5.

引用本文的文献

ERYTHROPOIESIS DURING AMPHIBIAN METAMORPHOSIS : III. Immunochemical Detection of Tadpole and Frog Hemoglobins (Rana catesbeiana) in Single Erythrocytes.两栖动物变态过程中的红细胞生成：III. 在单个红细胞中检测蝌蚪和成蛙血红蛋白（牛蛙）的免疫化学方法。

J Cell Biol. 1971 May 1;49(2):390-404. doi: 10.1083/jcb.49.2.390.

ERYTHROPOIESIS DURING AMPHIBIAN METAMORPHOSIS : II. Immunochemical Study of Larval and Adult Hemoglobins of Rana catesbeiana.两栖动物变态过程中的红细胞生成：二、牛蛙幼体和成体血红蛋白的免疫化学研究。

J Cell Biol. 1971 May 1;49(2):380-9. doi: 10.1083/jcb.49.2.380.

A radioimmunoassay for quantifying carbonic anhydrase isozymes in crude lysates.一种用于定量粗裂解物中碳酸酐酶同工酶的放射免疫测定法。

Biochem Genet. 1970 Apr;4(2):285-95. doi: 10.1007/BF00485779.

[Nature and ontogenetic development of carboanhydrase isoenzymes in human erythrocytes].[人红细胞中碳酸酐酶同工酶的性质与个体发生发育]

Blut. 1973 Sep;27(3):172-85. doi: 10.1007/BF01634032.

Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.

Am J Hum Genet. 1977 May;29(3):256-71.

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