• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Erythrocytes in muscular dystrophy. Investigation with 31P nuclear magnetic resonance spectroscopy.

作者信息

Sarpel G, Lubansky H J, Danon M J, Omachi A

出版信息

Arch Neurol. 1981 May;38(5):271-4. doi: 10.1001/archneur.1981.00510050037003.

DOI:10.1001/archneur.1981.00510050037003
PMID:7224909
Abstract

Phosphorus 31 nuclear magnetic resonance (31P NMR) signals were recorded from intact human erythrocytes for 16 hours. Total phosphate concentration, which was estimated as the sum of the individual 31P signals, was 25% lower in erythrocytes from men with myotonic dystrophy than in control erythrocytes. The inorganic-phosphate fraction contained the highest average phosphate concentration over the 16-hour period, and made the major contribution to the difference in total phosphate between the two groups. This result was not observed in erythrocytes from either women with myotonic dystrophy or patients with Duchenne's dystrophy and may be due to a change in cell membrane permeability to inorganic phosphate, which leads to lower steady-state concentrations of the intracellular phosphates.

摘要

相似文献

1
Erythrocytes in muscular dystrophy. Investigation with 31P nuclear magnetic resonance spectroscopy.
Arch Neurol. 1981 May;38(5):271-4. doi: 10.1001/archneur.1981.00510050037003.
2
Erythrocyte metabolism in muscular dystrophy.肌肉萎缩症中的红细胞代谢
Arch Neurol. 1978 Sep;35(9):592-5. doi: 10.1001/archneur.1978.00500330040008.
3
1H and 31P nuclear magnetic resonance spectroscopy of erythrocyte extracts in myotonic muscular dystrophy.强直性肌营养不良症红细胞提取物的1H和31P核磁共振波谱分析
Isr J Med Sci. 1984 Aug;20(8):672-6.
4
Lipid composition of erythrocytes. Findings in Duchenne's muscular dystrophy and myotonic atrophy.红细胞的脂质组成。杜兴氏肌营养不良症和强直性肌萎缩症的研究结果。
Arch Neurol. 1979 Jun;36(6):351-4. doi: 10.1001/archneur.1979.00500420061007.
5
Phosphorylation of intact erythrocytes in human muscular dystrophy.人类肌肉萎缩症中完整红细胞的磷酸化作用
Ann Neurol. 1986 Apr;19(4):397-9. doi: 10.1002/ana.410190418.
6
Phosphate compounds in erythrocytes and plasma in Duchenne muscular dystrophy.杜兴氏肌营养不良症患者红细胞和血浆中的磷酸盐化合物
Clin Chem. 1984 Jun;30(6):1101-2.
7
Muscle energy metabolism in Duchenne dystrophy studied by 31P-NMR: controlled trials show no effect of allopurinol or ribose.通过31P-NMR研究杜氏肌营养不良症中的肌肉能量代谢:对照试验表明别嘌呤醇或核糖无作用。
Muscle Nerve. 1985 Nov-Dec;8(9):760-7. doi: 10.1002/mus.880080904.
8
[Influence of ouabain on the electrophoretic mobility of erythrocytes in 7 patients with Duchenne's muscular dystrophy].[哇巴因对7例杜兴氏肌营养不良症患者红细胞电泳迁移率的影响]
Helv Paediatr Acta. 1976 Oct;31(3):249-56.
9
Study on the erythrocytes from myotonic dystrophy with multi-nuclear NMR.利用多核核磁共振技术对强直性肌营养不良症患者红细胞的研究。
Muscle Nerve. 1991 Jan;14(1):57-63. doi: 10.1002/mus.880140110.
10
Spin-label studies of erythrocytes in myotonic dystrophy: no increase in membrane fluidity.强直性肌营养不良症患者红细胞的自旋标记研究:膜流动性未增加。
Neurology. 1980 Mar;30(3):272-6. doi: 10.1212/wnl.30.3.272.

引用本文的文献

1
Scanning electron microscopy studies of erythrocytes in spinocerebellar degeneration.脊髓小脑变性中红细胞的扫描电子显微镜研究。
J Neurol Neurosurg Psychiatry. 1984 Mar;47(3):269-74. doi: 10.1136/jnnp.47.3.269.