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A rapid method for the isolation of large quantities of rat liver parenchymal cells with high anabolic rates.

作者信息

Ingebretsen W R, Wagle S R

出版信息

Biochem Biophys Res Commun. 1972 Apr 28;47(2):403-10. doi: 10.1016/0006-291x(72)90728-0.

DOI:10.1016/0006-291x(72)90728-0
PMID:4350995
Abstract
摘要

相似文献

1
A rapid method for the isolation of large quantities of rat liver parenchymal cells with high anabolic rates.一种快速分离大量具有高合成代谢率的大鼠肝实质细胞的方法。
Biochem Biophys Res Commun. 1972 Apr 28;47(2):403-10. doi: 10.1016/0006-291x(72)90728-0.
2
Characterization of gluconeogenesis in enzymatically isolated parenchymal cells of rat liver.大鼠肝脏酶分离实质细胞中糖异生的特性研究
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3
Studies on gluconeogenesis, protein synthesis and cyclic AMP levels in isolated parenchymal cells following insulin withdrawal from alloxan diabetic rats.
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Gluconeogenesis in the isolated rat liver. Studies with bicarbonate-14C.大鼠离体肝脏中的糖异生作用。用碳酸氢盐-14C进行的研究。
Biochemistry. 1971 Jul 6;10(14):2793-8. doi: 10.1021/bi00790a022.
5
Studies on the perfused rat liver. II. Effect of glucagon on gluconeogenesis.灌注大鼠肝脏的研究。II. 胰高血糖素对糖异生的影响。
Diabetes. 1966 Mar;15(3):188-93. doi: 10.2337/diab.15.3.188.
6
Studies on the in vitro effects of insulin on glycogen synthesis and ultrastructure in isolated rat liver hepatocytes.胰岛素对离体大鼠肝脏肝细胞糖原合成及超微结构的体外作用研究。
Biochem Biophys Res Commun. 1973 Aug 6;53(3):937-43. doi: 10.1016/0006-291x(73)90182-4.
7
Gluconeogenesis in rat liver parenchymal cells in primary culture: permissive effect of the glucocorticoids on glucagon stimulation of gluconeogenesis.原代培养大鼠肝实质细胞中的糖异生作用:糖皮质激素对胰高血糖素刺激糖异生的允许作用
J Cell Physiol. 1981 Apr;107(1):11-9. doi: 10.1002/jcp.1041070103.
8
[Isolation of intact liver parenchymal cells by a modified enzymatic method].[采用改良酶法分离完整肝实质细胞]
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Paths of carbon in gluconeogenesis and lipogenesis: the role of mitochondria in supplying precursors of phosphoenolpyruvate.糖异生和脂肪生成过程中的碳代谢途径:线粒体在提供磷酸烯醇式丙酮酸前体中的作用。
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Parenchymal cells from adult rat liver in nonproliferating monolayer culture. I. Functional studies.来自成年大鼠肝脏的实质细胞的非增殖单层培养。I. 功能研究。
J Cell Biol. 1973 Dec;59(3):722-34. doi: 10.1083/jcb.59.3.722.

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Agglutination kinetics of normal and diabetic adult rat hepatocytes.正常和糖尿病成年大鼠肝细胞的凝集动力学
Pflugers Arch. 1980 Aug;386(3):245-50. doi: 10.1007/BF00587475.
2
Fructose-2,6-P2, chemistry and biological function.果糖-2,6-二磷酸,化学性质与生物学功能
Mol Cell Biochem. 1982 Oct 18;48(2):97-120. doi: 10.1007/BF00227610.
3
Induction of fatty acid synthetase and acetyl-CoA carboxylase by isolated rat liver cells.分离的大鼠肝细胞对脂肪酸合成酶和乙酰辅酶A羧化酶的诱导作用。
Mol Cell Biochem. 1983;53-54(1-2):307-25. doi: 10.1007/BF00225262.
4
The fine structure, potassium content, and respiratory activity of isolated rat liver parenchymal cells prepared by improved enzymatic techniques.采用改良酶法技术制备的离体大鼠肝实质细胞的精细结构、钾含量及呼吸活性。
J Cell Biol. 1973 Jun;57(3):642-58. doi: 10.1083/jcb.57.3.642.
5
Parenchymal cells from adult rat liver in nonproliferating monolayer culture. I. Functional studies.来自成年大鼠肝脏的实质细胞的非增殖单层培养。I. 功能研究。
J Cell Biol. 1973 Dec;59(3):722-34. doi: 10.1083/jcb.59.3.722.
6
Adult liver parenchymal cells in primary culture characteristics and cell recognition standards.原代培养成人肝实质细胞的特性及细胞识别标准。
In Vitro. 1974 Jul-Aug;10:130-42. doi: 10.1007/BF02615346.
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Isoenzyme patterns in parenchymal and non-parenchymal cells isolated from regenerating and regenerated rat liver.从再生和已再生的大鼠肝脏中分离出的实质细胞和非实质细胞中的同工酶模式。
Biochem J. 1973 Dec;136(4):947-54. doi: 10.1042/bj1360947.
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The use of two populations of hepatocytes with different triacylglycerol contents as a model to study the accumulation of liver lipid in the laying hen.使用具有不同三酰甘油含量的两组肝细胞作为模型来研究蛋鸡肝脏脂质的积累。
Biochem J. 1988 Oct 1;255(1):259-65.
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Studies on gluconeogenesis and stimulation of glycogen and protein synthesis in isolated hepatocytes in alloxan diabetic, normal fed and fasted animals.关于四氧嘧啶糖尿病动物、正常进食动物和禁食动物分离肝细胞中糖异生以及糖原和蛋白质合成刺激作用的研究。
Acta Diabetol Lat. 1975 May-Aug;12(3-4):185-98. doi: 10.1007/BF02581299.
10
Conditions affecting primary cell cultures of functional adult rat hepatocytes. 1. The effect of insulin.影响成年大鼠功能性原代肝细胞培养的条件。1. 胰岛素的作用。
In Vitro. 1976 Jul;12(7):521-32. doi: 10.1007/BF02796495.