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Phosphorylase kinase deficiency in mice.

作者信息

Huijing F

机构信息

Department of Biochemistry, University of Miami School of Medicine, 33152, Miami, Florida, USA

出版信息

FEBS Lett. 1970 Oct;10(5):328-332. doi: 10.1016/0014-5793(70)80465-3.

DOI:10.1016/0014-5793(70)80465-3
PMID:11945425
Abstract
摘要

相似文献

1
Phosphorylase kinase deficiency in mice.小鼠中的磷酸化酶激酶缺乏症。
FEBS Lett. 1970 Oct;10(5):328-332. doi: 10.1016/0014-5793(70)80465-3.
2
The molecular basis of skeletal muscle phosphorylase kinase deficiency.
Eur J Biochem. 1976 Jul 1;66(2):347-56. doi: 10.1111/j.1432-1033.1976.tb10524.x.
3
Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency.正常人及Ⅵ型糖原贮积病患者溶血产物中的糖原磷酸化酶及其转换酶。磷酸化酶激酶缺乏症的研究。
Biochem J. 1975 Apr;147(1):23-35. doi: 10.1042/bj1470023.
4
Stimulation of glycogenolysis by beta adrenergic agonists in skeletal muscle of mice with the phosphorylase kinase deficiency mutation (I strain).在具有磷酸化酶激酶缺陷突变的小鼠（I 品系）骨骼肌中，β肾上腺素能激动剂对糖原分解的刺激作用。
J Pharmacol Exp Ther. 1976 Sep;198(3):526-38.
5
Metabolic adaptation in phosphorylase kinase deficiency. Changes in metabolite concentrations during tetanic stimulation of mouse leg muscles.磷酸化酶激酶缺乏症中的代谢适应。小鼠腿部肌肉强直刺激期间代谢物浓度的变化。
Biochem J. 1980 Jan 15;186(1):331-41. doi: 10.1042/bj1860331.
6
Comparison of the mechanism of isoproterenol-stimulated glycogenolysis in skeletal muscle of normal and phosphorylase kinase-deficient mice (I strain).
J Pharmacol Exp Ther. 1978 Jun;205(3):732-42.
7
Adult phosphorylase b kinase deficiency.
Ann Neurol. 1990 Oct;28(4):529-38. doi: 10.1002/ana.410280410.
8
Phosphorylase kinase of the liver: deficiency in a girl with increased hepatic glycogen.肝脏磷酸化酶激酶：一名肝糖原增加女童的缺乏症
Science. 1966 Sep 23;153(3743):1534-5. doi: 10.1126/science.153.3743.1534.
9
Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB).由于磷酸化酶激酶缺乏导致的肝脏和肌肉常染色体糖原贮积病是由磷酸化酶激酶β亚基（PHKB）的突变引起的。
Hum Mol Genet. 1997 Jul;6(7):1109-15. doi: 10.1093/hmg/6.7.1109.
10
A new type of glycogen storage disease caused by deficiency of cardiac phosphorylase kinase.一种由心脏磷酸化酶激酶缺乏引起的新型糖原贮积病。
Biochem Biophys Res Commun. 1984 Mar 15;119(2):582-7. doi: 10.1016/s0006-291x(84)80288-0.

引用本文的文献

1
X-linked dominant inheritance of partial phosphorylase kinase deficiency in mice.小鼠部分磷酸化酶激酶缺乏症的X连锁显性遗传
Biochem Genet. 1980 Apr;18(3-4):247-61. doi: 10.1007/BF00484240.
2
Inherited metabolic disease in laboratory animals: a review.实验动物中的遗传性代谢疾病：综述
J Inherit Metab Dis. 1980;3(4):133-43. doi: 10.1007/BF02312547.
3
Glycogen storage diseases in animals and their potential value as models of human disease.动物中的糖原贮积病及其作为人类疾病模型的潜在价值。
J Inherit Metab Dis. 1983;6(1):3-16. doi: 10.1007/BF02391186.
4
Location of phosphorylase kinase (Phk) in the mouse X chromosome.磷酸化酶激酶（Phk）在小鼠X染色体中的定位。
Biochem Genet. 1973 Jun;9(2):193-6. doi: 10.1007/BF00487449.
5
Glycogen-storage disease associated with phosphorylase kinase deficiency: evidence for X inactivation.与磷酸化酶激酶缺乏相关的糖原贮积病：X染色体失活的证据。
Am J Hum Genet. 1974 May;26(3):360-8.
6
The phosphorylase kinase deficiency (Phk) locus in the mouse: evidence that the mutant allele codes for an enzyme with an abnormal structure.
Biochem Genet. 1975 Oct;13(9-10):567-84. doi: 10.1007/BF00484916.
7
Glycogen phosphorylase and its converter enzymes in haemolysates of normal human subjects and of patients with type VI glycogen-storage disease. A study of phosphorylase kinase deficiency.正常人及Ⅵ型糖原贮积病患者溶血产物中的糖原磷酸化酶及其转换酶。磷酸化酶激酶缺乏症的研究。
Biochem J. 1975 Apr;147(1):23-35. doi: 10.1042/bj1470023.