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A FUNCTIONAL DISORDER OF MUSCLE ASSOCIATED WITH THE ABSENCE OF PHOSPHORYLASE.

作者信息

Mommaerts W F, Illingworth B, Pearson C M, Guillory R J, Seraydarian K

机构信息

DEPARTMENT OF MEDICINE, THE UNIVERSITY OF CALIFORNIA AT LOS ANGELES.

出版信息

Proc Natl Acad Sci U S A. 1959 Jun;45(6):791-7. doi: 10.1073/pnas.45.6.791.

DOI:10.1073/pnas.45.6.791
PMID:16590445
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC222638/
Abstract
摘要

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本文引用的文献

1
Enzymes of glycogen synthesis in glycogen-deposition disease.糖原沉积病中糖原合成的酶。
Biochim Biophys Acta. 1959 Jun;33(2):554-6. doi: 10.1016/0006-3002(59)90149-0.
2
Evidence for direct utilization of fructose in working muscle in man.人体工作肌肉中直接利用果糖的证据。
Proc Soc Exp Biol Med. 1959 Apr;100(4):671-2. doi: 10.3181/00379727-100-24739.
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A uridine coenzyme-linked pathway of glycogen synthesis in muscle.肌肉中糖原合成的尿苷辅酶连接途径。
Biochim Biophys Acta. 1958 Nov;30(2):449. doi: 10.1016/0006-3002(58)90086-6.
4
Histochemical demonstration of branching enzyme (amylo-1,4-1,6-transglucosidase) in animal tissues.动物组织中分支酶（淀粉-1,4-1,6-转葡萄糖苷酶）的组织化学显示
J Histochem Cytochem. 1958 May;6(3):208-16. doi: 10.1177/6.3.208.
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The phosphorylase b to a converting enzyme of rabbit skeletal muscle.兔骨骼肌磷酸化酶b向a的转化酶
Biochim Biophys Acta. 1956 Apr;20(1):150-7. doi: 10.1016/0006-3002(56)90273-6.
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Conversion of phosphorylase b to phosphorylase a in muscle extracts.肌肉提取物中磷酸化酶b向磷酸化酶a的转化。
J Biol Chem. 1955 Sep;216(1):121-32.
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Glycogen structure and enzyme deficiencies in glycogen storage disease.糖原贮积病中的糖原结构与酶缺乏症
Harvey Lect. 1952;48:145-71.
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Spectrophotometric determination of fructose-1:6-diphosphate, hexosemonophosphates, adenosinetriphosphate and adenosinediphosphate.分光光度法测定1:6 - 二磷酸果糖、己糖单磷酸、三磷酸腺苷和二磷酸腺苷。
Biochem J. 1953 Jan;53(1):157-67. doi: 10.1042/bj0530157.
9
Structure of glycogens and amylopectins. III. Normal and abnormal human glycogen.糖原与支链淀粉的结构。III. 正常与异常人体糖原
J Biol Chem. 1952 Dec;199(2):653-60.
10
Structure of glycogens and amylopectins. I. Enzymatic determination of chain length.糖原与支链淀粉的结构。I. 链长的酶法测定
J Biol Chem. 1952 Dec;199(2):631-40.