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G-6PD Bangkok: a new variant found in congenital nonspherocytic hemolytic disease (CNHD).

作者信息

Talalak P, Beutler E

出版信息

Blood. 1969 May;33(5):772-6.

PMID:5779160
Abstract
摘要

相似文献

1
G-6PD Bangkok: a new variant found in congenital nonspherocytic hemolytic disease (CNHD).葡萄糖-6-磷酸脱氢酶曼谷型:先天性非球形红细胞溶血性贫血(CNHD)中发现的一种新变体。
Blood. 1969 May;33(5):772-6.
2
[Variant Gd(-) "Strasbourg" of glucose-6-phosphate-dehydrogenase].[葡萄糖-6-磷酸脱氢酶的“斯特拉斯堡”变异型Gd(-)]
Nouv Rev Fr Hematol. 1970 Mar-Apr;10(2):312-4.
3
Congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase East Harlem: a new deficient variant.因葡萄糖-6-磷酸脱氢酶东哈莱姆型导致的先天性非球形细胞溶血性贫血:一种新的缺陷变异型
J Pediatr. 1977 Jan;90(1):89-91. doi: 10.1016/s0022-3476(77)80774-9.
4
Glucose-6-phosphate dehydrogenase Beaumont: a new variant with severe enzyme deficiency and chronic nonspherocytic hemolytic anemia.葡萄糖-6-磷酸脱氢酶博蒙特型:一种伴有严重酶缺乏和慢性非球形红细胞溶血性贫血的新变体。
Enzyme. 1985;34(1):15-21. doi: 10.1159/000469354.
5
Two new variants of glucose-6-phosphate dehydrogenase associated with hereditary non-spherocytic hemolytic anemia: G6PD Wayne and G6PD Huron.与遗传性非球形细胞溶血性贫血相关的两种新的葡萄糖-6-磷酸脱氢酶变体:G6PD韦恩和G6PD休伦。
Am J Hematol. 1987 Apr;24(4):357-63. doi: 10.1002/ajh.2830240405.
6
Nonspherocytic congenital hemolytic anemia due to a new G-6-pd variant: g-6-pd alhambra.由一种新的葡萄糖-6-磷酸脱氢酶(G-6-pd)变异体引起的非球形细胞先天性溶血性贫血:G-6-pd阿罕布拉变异体
Pediatrics. 1970 Feb;45(2):230-5.
7
Human glucose-6-phosphate dehydrogenase variants: a supplementary tabulation.人类葡萄糖-6-磷酸脱氢酶变体:补充表格
Ann Hum Genet. 1973 Oct;37(2):151-5. doi: 10.1111/j.1469-1809.1973.tb01823.x.
8
Hereditary hemolytic anemia due to glucose-6-phosphate dehydrogenase Torrance: a new variant.葡萄糖-6-磷酸脱氢酶托伦斯所致的遗传性溶血性贫血:一种新变体。
J Lab Clin Med. 1969 Apr;73(4):657-67.
9
[Glucose-6-phosphate dehydrogenase type Schwaben. A new enzyme variant with spontaneous hemolytic anemia].施瓦本型葡萄糖-6-磷酸脱氢酶。一种伴有自发性溶血性贫血的新型酶变体
Dtsch Med Wochenschr. 1971 Jun 11;96(24):1029-33. doi: 10.1055/s-0028-1108377.
10
Congenital nonspherocytic hemolytic disease (CNHD) due to a G-6-PD variant: G-6-PD Kyoto.由葡萄糖-6-磷酸脱氢酶(G-6-PD)变异引起的先天性非球形红细胞溶血性贫血(CNHD):G-6-PD京都型
Nihon Ketsueki Gakkai Zasshi. 1972 Feb;35(1):32-8.

引用本文的文献

1
Systematic review of the clinical manifestations of glucose-6-phosphate dehydrogenase deficiency in the Greater Mekong Subregion: implications for malaria elimination and beyond.大湄公河次区域葡萄糖-6-磷酸脱氢酶缺乏症临床表现的系统评价:对疟疾消除及其他方面的启示
BMJ Glob Health. 2017 Aug 19;2(3):e000415. doi: 10.1136/bmjgh-2017-000415. eCollection 2017.
2
A trade off between catalytic activity and protein stability determines the clinical manifestations of glucose-6-phosphate dehydrogenase (G6PD) deficiency.催化活性与蛋白质稳定性之间的权衡决定了葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症的临床表现。
Int J Biol Macromol. 2017 Nov;104(Pt A):145-156. doi: 10.1016/j.ijbiomac.2017.06.002. Epub 2017 Jun 3.
3
Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.
对于因葡萄糖-6-磷酸脱氢酶突变导致严重酶缺乏的杂合子,体细胞选择是血细胞表型的主要决定因素。
Am J Hum Genet. 1996 Oct;59(4):887-95.
4
Glucose-6-phosphate dehydrogenase in Thailand. The occurrence of three electrophoretic variants among 1157 nondeficient males.泰国的葡萄糖-6-磷酸脱氢酶。1157名非缺陷男性中三种电泳变体的出现情况。
Hum Genet. 1980 Feb;53(2):227-8. doi: 10.1007/BF00273501.
5
Glucose 6-phosphate dehydrogenase variants of Bali island (Indonesia).印度尼西亚巴厘岛的葡萄糖-6-磷酸脱氢酶变体
Hum Genet. 1982;60(1):60-2. doi: 10.1007/BF00281265.
6
[Glucose-6-P-dehydrogenase type bodensee (a new enzyme variant)].博登湖型葡萄糖-6-磷酸脱氢酶(一种新的酶变体)
Klin Wochenschr. 1971 Oct 1;49(19):1058-62. doi: 10.1007/BF01732914.
7
Glucose-6-phosphate dehydrogenase Boston. A new variant associated with congenital nonspherocytic hemolytic disease.葡萄糖-6-磷酸脱氢酶波士顿型。一种与先天性非球形细胞溶血性疾病相关的新变异型。
Humangenetik. 1971;13(3):218-21. doi: 10.1007/BF00326945.
8
Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita.在日本发现三种与先天性非球形红细胞溶血性贫血相关的新的电泳正常的葡萄糖-6-磷酸脱氢酶变异体:G6PD 荻洼型、横滨型和秋田型。
Hum Genet. 1978 Nov 24;45(1):11-7. doi: 10.1007/BF00277568.