Haemoglobin Volga, beta27, (B9) Ala leads to Asp, a new highly unstable haemoglobin with a suppressed charge. - Suppr | 超能文献

Haemoglobin Volga, beta27, (B9) Ala leads to Asp, a new highly unstable haemoglobin with a suppressed charge.

作者信息

Idelson L I, Didkovsky N A, Filippova A V, Casey R, Kynoch P A, Leyman N

出版信息

FEBS Lett. 1975 Oct 15;58(1):122-5. doi: 10.1016/0014-5793(75)80239-0.

DOI:10.1016/0014-5793(75)80239-0

Abstract

摘要

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Haemoglobin Volga, beta27, (B9) Ala leads to Asp, a new highly unstable haemoglobin with a suppressed charge.

FEBS Lett. 1975 Oct 15;58(1):122-5. doi: 10.1016/0014-5793(75)80239-0.

2

Severe hemolytic anemia associated with Hb Volga [beta27(B9)Ala-->Asp]: GCC-->GAC at codon 27 in a Turkish family.

Am J Hematol. 2004 Aug;76(4):378-82. doi: 10.1002/ajh.20128.

3

Enzymatic antioxidative defence of erythrocytes in an Italian family with Hb Volga or alpha 2 beta 2 27 (B9) Ala----Asp.一个患有伏尔加血红蛋白病或α2β2 27（B9）丙氨酸→天冬氨酸突变的意大利家族中红细胞的酶促抗氧化防御

Clin Chim Acta. 1988 Dec 30;178(3):345-7. doi: 10.1016/0009-8981(88)90243-4.

4

[Hemoglobin Volga beta 27 (B9) alanine substituted for aspartic acid (new anomalous hemoglobin with expressed instability)].[血红蛋白伏尔加β27（B9）丙氨酸取代天冬氨酸（具有明显不稳定性的新型异常血红蛋白）]

Probl Gematol Pereliv Krovi. 1977 Apr;22(4):30-4.

5

A new unstable hemoglobin, Hb Yokohama beta 31 (B13)Leu substituting for Pro, causing hemolytic anemia.

Hemoglobin. 1981;5(7-8):667-78. doi: 10.3109/03630268108991834.

6

Hb-Volga or alpha 2 beta 2 27(B9)Ala replaced by Asp. An unstable hemoglobin variant in three generations of a Dutch family.血红蛋白-伏尔加型或α2β2 27（B9）位的丙氨酸被天冬氨酸取代。一个荷兰家族三代人中的一种不稳定血红蛋白变异体。

Biochim Biophys Acta. 1976 Jul 19;439(1):63-9. doi: 10.1016/0005-2795(76)90161-6.

7

Structure of haemoglobin Wien beta 130 (H8) tyrosine-aspartic acid: an unstable haemoglobin variant.血红蛋白维也纳β130（H8）酪氨酸-天冬氨酸的结构：一种不稳定的血红蛋白变体

Acta Haematol. 1974;51(6):351-61. doi: 10.1159/000208318.

8

Hb Volga [beta 27(B9)Ala-->Asp]: detection of a de novo mutation by Ava II digestion of PCR-amplified DNA.血红蛋白伏尔加型[β27（B9）丙氨酸→天冬氨酸]：通过对聚合酶链反应扩增的DNA进行Ava II酶切检测到一种新发突变。

Hemoglobin. 1993 Jun;17(3):209-15. doi: 10.3109/03630269308998895.

9

[Congenital hemolytic anemia caused by the carriage of hemoglobin Bristol beta 67 Bal-->Asp].

Ter Arkh. 1992;64(7):78-81.

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[Hereditary Heinz body hemolytic anemia and unstable hemoglobin].[遗传性 Heinz 小体溶血性贫血与不稳定血红蛋白]

Ned Tijdschr Geneeskd. 1976 Mar 27;120(13):565-8.

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De novo mutations producing unstable hemoglobins or hemoglobins M : I. Establishment of a Depository and use of data to test for an association of de novo mutation with advanced parental age.产生不稳定血红蛋白或血红蛋白 M 的新突变：I. 建立一个储存库，并利用数据来检验新突变与高龄父母的关联性。

Hum Genet. 1981 Oct;58(4):396-404. doi: 10.1007/BF00282822.

2

The diagnostic dilemma of congenital unstable hemoglobinopathies.先天性不稳定血红蛋白病的诊断困境。

Pediatr Blood Cancer. 2010 Dec 15;55(7):1393-5. doi: 10.1002/pbc.22702.

3

Thalassemic hemoglobinopathies.地中海贫血血红蛋白病

Am J Pathol. 1983 Dec;113(3):396-409.