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Enzymes of the glycogen cycle and glycolysis in various human neuromuscular disorders.

作者信息

Di Mauro S, Angelini C, Catani C

出版信息

J Neurol Neurosurg Psychiatry. 1967 Oct;30(5):411-5. doi: 10.1136/jnnp.30.5.411.

DOI:10.1136/jnnp.30.5.411
PMID:4228900
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC496216/
Abstract
摘要

相似文献

1
Enzymes of the glycogen cycle and glycolysis in various human neuromuscular disorders.各种人类神经肌肉疾病中糖原循环和糖酵解的酶。
J Neurol Neurosurg Psychiatry. 1967 Oct;30(5):411-5. doi: 10.1136/jnnp.30.5.411.
2
[Histochemical study of the skeletal muscle--histochemical findings of the normal and hypofunctional muscles].骨骼肌的组织化学研究——正常及功能减退肌肉的组织化学发现
Seikei Geka. 1969 Jul;20(9):943-55.
3
Changes in muscle chemistry associated with stiffness and pain.与僵硬和疼痛相关的肌肉化学变化。
Neurology. 1972 Nov;22(11):1172-5. doi: 10.1212/wnl.22.11.1172.
4
[On progressive myopathy with muscle phosphorylase deficiency and giant mitochondria].[关于伴有肌肉磷酸化酶缺乏和巨大线粒体的进行性肌病]
Wien Klin Wochenschr. 1967 Dec 8;79(49):917-21.
5
Glycogen metabolism and glycolytic enzymes.
Annu Rev Biochem. 1970;39:639-72. doi: 10.1146/annurev.bi.39.070170.003231.
6
Mitochondria-lipid-glycogen (MLG) disease of muscle. A morphologically regressive congenital myopathy.肌肉线粒体-脂质-糖原(MLG)病。一种形态学上进行性发展的先天性肌病。
Arch Neurol. 1973 Sep;29(3):162-9. doi: 10.1001/archneur.1973.00490270044007.
7
Distribution of some enzymes concerning carbohydrate metabolism in sea urchin eggs.海胆卵中一些与碳水化合物代谢相关的酶的分布
Exp Cell Res. 1975 May;92(2):444-50. doi: 10.1016/0014-4827(75)90400-0.
8
Enzymatic characteristics of human basal cell epithelioma.人类基底细胞上皮瘤的酶学特征
Arch Dermatol. 1968 Jul;98(1):80-4.
9
[Thyrotoxic and hypothyroid myopathy. Biochemical and histopathological study].
Riv Patol Nerv Ment. 1970 Jun;91(3):123-38.
10
[Action of thyroxin on glucose-6-phosphatase of the liver, ineffectiveness on phosphofructokinase of the kidney, on phosphoglycerate kinase of the liver and muscle, on aldolase of the kidney, on phosphorylase of the liver, on lactate dehydrogenae of the liver and on glucose-6-phosphatase of the kidney].[甲状腺素对肝脏葡萄糖-6-磷酸酶的作用,对肾脏磷酸果糖激酶、肝脏和肌肉磷酸甘油酸激酶、肾脏醛缩酶、肝脏磷酸化酶、肝脏乳酸脱氢酶以及肾脏葡萄糖-6-磷酸酶无作用]
Boll Soc Ital Biol Sper. 1968 Oct 15;44(19):1639-40.

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The Role of Autophagy in Skeletal Muscle Diseases.自噬在骨骼肌疾病中的作用。
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The Dystrophin Node as Integrator of Cytoskeletal Organization, Lateral Force Transmission, Fiber Stability and Cellular Signaling in Skeletal Muscle.肌营养不良蛋白节点作为骨骼肌细胞骨架组织、侧向力传递、纤维稳定性和细胞信号整合者
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Adenylosuccinic acid therapy ameliorates murine Duchenne Muscular Dystrophy.腺嘌呤琥珀酸治疗改善小鼠杜氏肌营养不良症。
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Nutrients. 2015 Nov 26;7(12):9734-67. doi: 10.3390/nu7125498.
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Deficiency of phosphofructo-1-kinase/muscle subtype in humans impairs insulin secretion and causes insulin resistance.人类中磷酸果糖-1-激酶/肌肉亚型的缺乏会损害胰岛素分泌并导致胰岛素抵抗。
J Clin Invest. 1997 Dec 1;100(11):2833-41. doi: 10.1172/JCI119831.
6
Acid maltase levels in muscle in heterozygous acid maltase deficiency and in non-weak and neuromuscular disease controls.杂合性酸性麦芽糖酶缺乏症患者肌肉中的酸性麦芽糖酶水平以及非虚弱型和神经肌肉疾病对照者肌肉中的酸性麦芽糖酶水平。
J Neurol Neurosurg Psychiatry. 1970 Dec;33(6):801-4. doi: 10.1136/jnnp.33.6.801.
7
[Muscle energy metabolism in children with progressive muscular dystrophy type Duchenne. Metabolites of the Embden-Meyerhof pathway, the citric acid cycle and high energy phosphates and enzyme activity of alpha-glycerol-oxidase, succinate-dehydrogenase and 6-phospho-gluconate-dehydrogenase (author's transl)].杜兴氏进行性肌营养不良症患儿的肌肉能量代谢。糖酵解途径、柠檬酸循环的代谢产物及高能磷酸盐,以及α-甘油氧化酶、琥珀酸脱氢酶和6-磷酸葡萄糖酸脱氢酶的酶活性(作者译)
Klin Wochenschr. 1973 Oct 1;51(19):957-68. doi: 10.1007/BF01468251.
8
Peroneal muscular atrophy. A histochemical study.
Acta Neuropathol. 1968 Nov 1;11(4):301-10. doi: 10.1007/BF00686727.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Synthesis of glycogen from uridine diphosphate glucose in liver.肝脏中由尿苷二磷酸葡萄糖合成糖原。
J Biol Chem. 1960 Apr;235:919-23.
3
MCARDLE'S DISEASE. HEREDITARY MYOPATHY DUE TO ABSENCE OF MUSCLE PHOSPHORYLASE.
Arch Neurol. 1963 Oct;9:325-42. doi: 10.1001/archneur.1963.00460100013001.
4
Sources of error in the biochemical diagnosis of muscular dystrophy.肌营养不良生化诊断中的误差来源。
J Neurol Neurosurg Psychiatry. 1962 Aug;25(3):191-202. doi: 10.1136/jnnp.25.3.191.
5
Progressive muscular dystrophy: a review.进行性肌营养不良症:综述
Rev Can Biol. 1962 Sep-Dec;21:337-51.
6
Some applications of histochemistry to the study of skeletal muscle.
Rev Can Biol. 1962 Sep-Dec;21:391-407.
7
[Muscle lactic dehydrogenase in myopathy: apparent persistence of the fetal type].[肌病中的肌肉乳酸脱氢酶:胎儿型的明显持续存在]
C R Hebd Seances Acad Sci. 1962 Jun 18;254:4384-6.
8
Regulatory mechanisms in carbohydrate metabolism. III. Limiting factors in glycolysis of ascites tumor cells.碳水化合物代谢中的调节机制。III. 腹水肿瘤细胞糖酵解中的限制因素。
J Biol Chem. 1959 May;234(5):1029-35.
9
Determination of organic phosphorus compounds by phosphate analysis.通过磷酸盐分析测定有机磷化合物
Methods Biochem Anal. 1956;3:1-22. doi: 10.1002/9780470110195.ch1.
10
On the classification, natural history and treatment of the myopathies.关于肌病的分类、自然史及治疗
Brain. 1954;77(2):169-231. doi: 10.1093/brain/77.2.169.