杜氏肌营养不良症胎儿的肌肉组织学和肌酸激酶水平 - Suppr

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Muscle histology and creatine kinase levels in the foetus in Duchenne muscular dystrophy.

作者信息

Emery A E

出版信息

Nature. 1977 Mar 31;266(5601):472-3. doi: 10.1038/266472a0.

DOI:10.1038/266472a0

PMID:859617

Abstract

摘要

相似文献

Muscle histology and creatine kinase levels in the foetus in Duchenne muscular dystrophy.杜氏肌营养不良症胎儿的肌肉组织学和肌酸激酶水平

Nature. 1977 Mar 31;266(5601):472-3. doi: 10.1038/266472a0.

Muscle histology in fetuses at risk for Duchenne muscular dystrophy.

Clin Genet. 1974;5(3):230-3. doi: 10.1111/j.1399-0004.1974.tb01687.x.

False elevation of amniotic fluid enzymes of relevance for prenatal diagnosis: creatine kinase measurement in relation to Duchenne muscular dystrophy.

Prenat Diagn. 1984 Jan-Feb;4(1):35-42. doi: 10.1002/pd.1970040106.

The manifesting carrier in Duchenne muscular dystrophy.杜氏肌营养不良症的显性携带者。

Clin Genet. 1974;5(4):271-84. doi: 10.1111/j.1399-0004.1974.tb01694.x.

Pathologic diagnosis of Duchenne muscular dystrophy in an aborted fetus.

Clin Genet. 1978 Apr;13(4):335-8. doi: 10.1111/j.1399-0004.1978.tb01189.x.

[Human embryonal muscles in Duchenne muscular dystrophy].

Vopr Med Khim. 1990 Jan-Feb;36(1):37-9.

The neurogenic and myogenic hypotheses in human (Duchenne) muscular dystrophy.人类（杜兴氏）肌营养不良症中的神经源性和肌源性假说。

Nature. 1974 May 10;249(453):151-2. doi: 10.1038/249151a0.

The foetus in Duchenne muscular dystrophy: muscle growth in tissue culture.

Clin Genet. 1977 Sep;12(3):183-7. doi: 10.1111/j.1399-0004.1977.tb00922.x.

The carrier problem in progressive muscular dystrophy.

Proc Aust Assoc Neurol. 1970;7:85-8.

Muscle nuclear changes in fetuses at risk for Duchenne muscular dystrophy.杜氏肌营养不良症高危胎儿的肌肉细胞核变化。

J Med Genet. 1977 Feb;14(1):13-5. doi: 10.1136/jmg.14.1.13.

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Deficient Astrocyte Homeostatic Support Contributes to Brain Impairment in Duchenne Muscular Dystrophy.星形胶质细胞稳态支持不足导致杜氏肌营养不良症的脑损伤。

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Is dystrophin immunogenicity a barrier to advancing gene therapy for Duchenne muscular dystrophy?抗肌萎缩蛋白的免疫原性是否会阻碍杜氏肌营养不良症基因治疗的进展？

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Uncovering the Embryonic Origins of Duchenne Muscular Dystrophy.揭示杜氏肌营养不良症的胚胎起源。

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Dystrophin deficiency impairs cell junction formation during embryonic myogenesis from pluripotent stem cells.肌营养不良蛋白缺乏会损害多能干细胞在胚胎肌生成过程中的细胞连接形成。

iScience. 2024 Jun 11;27(7):110242. doi: 10.1016/j.isci.2024.110242. eCollection 2024 Jul 19.

Personalized and muscle-specific OXPHOS measurement with integrated CrCEST MRI and proton MR spectroscopy.利用集成的 CrCEST MRI 和质子 MR 波谱进行个性化和肌肉特异性 OXPHOS 测量。

Nat Commun. 2024 Jun 25;15(1):5387. doi: 10.1038/s41467-024-49253-6.

Dystrophin deficiency impairs cell junction formation during embryonic myogenesis.肌营养不良蛋白缺乏会损害胚胎期肌肉生成过程中的细胞连接形成。

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Downregulation of Dystrophin Expression Occurs across Diverse Tumors, Correlates with the Age of Onset, Staging and Reduced Survival of Patients.肌营养不良蛋白表达下调在多种肿瘤中均有发生，与发病年龄、分期及患者生存率降低相关。

Cancers (Basel). 2023 Feb 21;15(5):1378. doi: 10.3390/cancers15051378.

Loss of full-length dystrophin expression results in major cell-autonomous abnormalities in proliferating myoblasts.缺失全长肌营养不良蛋白的表达会导致增殖性成肌细胞发生主要的细胞自主性异常。

Elife. 2022 Sep 27;11:e75521. doi: 10.7554/eLife.75521.

P2X7 Purinoceptor Affects Ectopic Calcification of Dystrophic Muscles.P2X7嘌呤受体影响营养不良性肌肉的异位钙化。

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Disrupted Calcium Homeostasis in Duchenne Muscular Dystrophy: A Common Mechanism behind Diverse Consequences.杜氏肌营养不良症中钙稳态的紊乱：多种后果背后的共同机制。

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