Two new hemoglobin variants with deletion. Hemoglobin tours: Thr 8 7 (F 3 ) deleted and hemoglobin St Antoine: Gly-Leu 74-75 (E 18-19 deleted. Consequences for oxygen affinity and protein stability.
作者信息
Wajcman H, Labie D, Schapira G
出版信息
Biochim Biophys Acta. 1973 Feb 21;295(2):495-504.
PMID:4699574
Abstract
摘要
相似文献
1
Two new hemoglobin variants with deletion. Hemoglobin tours: Thr 8 7 (F 3 ) deleted and hemoglobin St Antoine: Gly-Leu 74-75 (E 18-19 deleted. Consequences for oxygen affinity and protein stability.两种新的缺失型血红蛋白变体。图尔血红蛋白：第87位苏氨酸（F3）缺失；圣安托万血红蛋白：第74 - 75位甘氨酸 - 亮氨酸（E18 - 19）缺失。对氧亲和力和蛋白质稳定性的影响。
Biochim Biophys Acta. 1973 Feb 21;295(2):495-504.
2
Hemoglobin Ta-Li: 83 Gly leads to Cys.
Biochim Biophys Acta. 1971 Sep 28;243(3):467-74.
3
[Hemolytic anaemia due to unstable hemoglobin with deletion, study of two new cases: Hb Tours (Thr beta87 (F3) deleted) and Hb St.-Antoine (Gly-Leu beta74-75 (E18-19) deleted) (author's transl)].因不稳定血红蛋白缺失导致的溶血性贫血：两例新病例研究：Hb Tours（β87（F3）位苏氨酸缺失）和Hb圣安托万（β74 - 75（E18 - 19）位甘氨酸 - 亮氨酸缺失）（作者译）
Nouv Rev Fr Hematol. 1973 Nov-Dec;13(6):803-16.
4
Hb-Genova ( 2 2 28(B10)Leu leads to Pro ); methods for detection and analysis of unstable hemoglobins.血红蛋白热那亚（2 2 28（B10）位亮氨酸突变为脯氨酸）；不稳定血红蛋白的检测与分析方法
Clin Chim Acta. 1973 Mar 14;44(2):217-27. doi: 10.1016/0009-8981(73)90384-7.
5
A new case of hemoglobin Genova 2 2 28(B10) Leu leads to Pro. Further studies on the mechanism of instability and defective synthesis.血红蛋白热那亚2 2 28（B10）亮氨酸突变为脯氨酸的一例新病例。关于不稳定性和合成缺陷机制的进一步研究。
Biochim Biophys Acta. 1973 Jan 25;295(1):67-76. doi: 10.1016/0005-2795(73)90074-3.
6
Haemoglobin Buccureşti 42(CD1) Phe-Leu, a cause of unstable haemoglobin haemolytic anaemia.血红蛋白布加勒斯特42（CD1）苯丙氨酸-亮氨酸，一种不稳定血红蛋白溶血性贫血的病因。
Biochim Biophys Acta. 1971 Oct;251(1):1-6. doi: 10.1016/0005-2795(71)90051-1.
7
Hemoglobins A 2 -Sphakiá and A 2 -NYU in Canada.
Can J Biochem. 1972 Jul;50(7):841-3. doi: 10.1139/o72-117.
8
Hemoglobin Abruzzo: beta 143 (H 21) His leads to Arg.血红蛋白阿布鲁佐：β143（H21）位组氨酸突变为精氨酸。
Clin Chim Acta. 1972 Apr;38(1):258-62. doi: 10.1016/0009-8981(72)90241-0.
9
Hb Ft. Worth: a27Glu changed to Gly(B8). A variant present in unusually low concentration.
Biochim Biophys Acta. 1971 Aug 27;243(2):164-9. doi: 10.1016/0005-2795(71)90072-9.
10
Hemoglobin M Saskatoon: further data on biophysics and oxygen equilibrium.血红蛋白M萨斯卡通：生物物理学和氧平衡的更多数据。
Biochim Biophys Acta. 1971 Jul 25;243(1):117-25. doi: 10.1016/0005-2795(71)90045-6.
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Thalassemic hemoglobinopathies.地中海贫血血红蛋白病
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2
beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0].与一种新的β链结构变异体Hb Vicksburg [β75 (E19)Leu导致0]顺式存在的β地中海贫血。
Proc Natl Acad Sci U S A. 1981 Jan;78(1):469-73. doi: 10.1073/pnas.78.1.469.
3
Are human hemoglobin variants distributed randomly among the positions?人类血红蛋白变体在各个位置上是随机分布的吗？
J Mol Evol. 1973;2(2-3):181-6. doi: 10.1007/BF01653998.
4
Hemoglobin Grady: the first example of a variant with elongated chains due to an insertion of residues.血红蛋白格雷迪：由于残基插入导致链延长的变体的首个实例。
Proc Natl Acad Sci U S A. 1974 Aug;71(8):3270-3. doi: 10.1073/pnas.71.8.3270.
5
Molecular analysis of the gene of the alpha 1-antitrypsin deficiency variant, Mnichinan.α1-抗胰蛋白酶缺乏变异体Mnichinan基因的分子分析。
Am J Hum Genet. 1990 Mar;46(3):602-12.
6
Hemoglobin Vancouver [alpha2beta2(73)(E17) Asp replaced by Tyr]: its structure and function.
J Mol Evol. 1976 Dec 31;9(1):37-44. doi: 10.1007/BF01796121.
7
Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine replaced by threonine at position 75 )E 19) of the gamma chain.γ链第75位（E19）由异亮氨酸替换为苏氨酸的新型人类胎儿血红蛋白的意义。
Hum Genet. 1976 Jun 29;32(3):305-13. doi: 10.1007/BF00295821.
8
Hemoglobin Lincoln Park: a betadelta fusion (anti-Lepore) variant with an amino acid deletion in the delta chain-derived segment.血红蛋白林肯公园：一种βδ融合（抗Lepore）变体，在δ链衍生片段中有一个氨基酸缺失。
Proc Natl Acad Sci U S A. 1978 Mar;75(3):1475-9. doi: 10.1073/pnas.75.3.1475.
9
Characterization of hemoglobin Burke [beta 107 (G9) Gly replaced by Arg].血红蛋白伯克的特征[β107（G9）位的甘氨酸被精氨酸取代]
Biochem Genet. 1976 Aug;14(7-8):577-85. doi: 10.1007/BF00485836.
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