Two new pathological haemoglobins: Olmsted beta 141 (H19) Leu leads to Arg and Malmö beta 97 (FG4) His leads to Gln.
作者信息
Lorkin P A, Lehmann H
出版信息
Biochem J. 1970 Oct;119(5):68P. doi: 10.1042/bj1190068pa.
Abstract
摘要
相似文献
1
Two new pathological haemoglobins: Olmsted beta 141 (H19) Leu leads to Arg and Malmö beta 97 (FG4) His leads to Gln.两种新的病理性血红蛋白：奥姆斯特德β141（H19）亮氨酸突变为精氨酸和马尔默β97（FG4）组氨酸突变为谷氨酰胺。
Biochem J. 1970 Oct;119(5):68P. doi: 10.1042/bj1190068pa.
2
Hemoglobin Wood beta97(FG4) His replaced by Leu. A new high-oxygen-affinity hemoglobin associated with familial erythrocytosis.血红蛋白伍德β97（FG4）处的组氨酸被亮氨酸取代。一种与家族性红细胞增多症相关的新型高氧亲和力血红蛋白。
Biochim Biophys Acta. 1975 Aug 19;400(2):348-53.
3
Double heterozygosity for hemoglobin Malmö [beta 97 (FG 4) His----Gln] and beta-thalassemia traits.血红蛋白马尔默[β97（FG4）组氨酸→谷氨酰胺]与β地中海贫血性状的双重杂合性。
Haematologica. 1989 Mar-Apr;74(2):187-90.
4
Functional studies of Hb Malmö beta97 (FG4) His leads to Gln.血红蛋白马尔默β97（FG4）中组氨酸突变为谷氨酰胺的功能研究。
FEBS Lett. 1977 Dec 1;84(1):71-3. doi: 10.1016/0014-5793(77)81059-4.
5
Comparison of hemoglobins Wood (alpha 2 beta 2 97 leu) and Malmö (alpha 2 beta 2 97 gln). Diagnostic value of citrate agar electrophoresis.
Am J Clin Pathol. 1979 Jun;71(6):668-71. doi: 10.1093/ajcp/71.6.668.
6
Two different mutations in codon 97 of the beta-globin gene cause Hb Malmö in Sweden.β-珠蛋白基因第97密码子的两种不同突变导致了瑞典的马尔默血红蛋白（Hb Malmö）。
Am J Hematol. 1996 Jan;51(1):32-6. doi: 10.1002/(SICI)1096-8652(199601)51:1<32::AID-AJH6>3.0.CO;2-8.
7
[Polycythemia resulting from abnormal hemoglobin with increased affinity for oxygen. Two cases (author's transl)].因血红蛋白异常对氧亲和力增加所致的红细胞增多症。两例（作者译）
Nouv Presse Med. 1980 Jan 26;9(5):285-9.
8
Hemoglobin Barcelona beta 94 (FG1) Asp leads to His : a new hemoglobin Variant with increased oxygen affinity.血红蛋白巴塞罗那β94（FG1）天冬氨酸突变为组氨酸：一种具有增加氧亲和力的新型血红蛋白变体。
Nouv Rev Fr Hematol (1978). 1981;23(5):267-73.
9
Letter: A new kindred with hemoglobin Malmö (beta97 leads to Gln).信函：一个新的血红蛋白马尔默家系（β97位突变为谷氨酰胺）。
J Pediatr. 1976 Jun;88(6):1061-3. doi: 10.1016/s0022-3476(76)81083-9.
10
Screening methods for haemoglobins with high oxygen affinity.
New Istanbul Contrib Clin Sci. 1978 Dec;12(3-4):182-4.
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At high altitude in the Netherlands: secondary erythrocytosis due to HB-Malmö.在荷兰的高海拔地区：由HB-马尔默引起的继发性红细胞增多症。
BMJ Case Rep. 2014 Mar 5;2014:bcr2014203701. doi: 10.1136/bcr-2014-203701.
本文引用的文献
1
Variations in the structure of human haemoglobin. With particular reference to the unstable haemoglobins.人类血红蛋白结构的变异。特别涉及不稳定血红蛋白。
Br Med Bull. 1969 Jan;25(1):14-23. doi: 10.1093/oxfordjournals.bmb.a070664.
2
Three families with unstable hemoglobinopathies (Köln, Olmsted and Santa Ana) causing hemolytic anemia with inclusion bodies and pigmenturia.三个患有不稳定血红蛋白病（科隆型、奥姆斯特德型和圣安娜型）的家族，这些疾病导致溶血性贫血，并伴有包涵体和色素尿。
Am J Med. 1969 Mar;46(3):344-59. doi: 10.1016/0002-9343(69)90037-0.
3
Molecular pathology of human haemoglobin.人类血红蛋白的分子病理学
Nature. 1968 Aug 31;219(5157):902-9. doi: 10.1038/219902a0.
4
Three-dimensional Fourier synthesis of horse oxyhaemoglobin at 2.8 A resolution: the atomic model.分辨率为2.8埃的马氧合血红蛋白的三维傅里叶合成：原子模型
Nature. 1968 Jul 13;219(5150):131-9. doi: 10.1038/219131a0.
5
Three-dimensional Fourier synthesis of horse oxyhaemoglobin at 2.8 A resolution: (1) x-ray analysis.
Nature. 1968 Jul 6;219(5149):29-32. doi: 10.1038/219029a0.
6
Hemoglobin-Bibba or alpha-2-136Pro-beta 2, an unstable alpha chain abnormal hemoglobin.血红蛋白 Bibba 或α-2-136Pro-β2，一种不稳定的α链异常血红蛋白。
Biochim Biophys Acta. 1968 Jan 22;154(1):220-2. doi: 10.1016/0005-2795(68)90274-2.
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