The l-arginine/NO pathway and homoarginine are altered in Duchenne muscular dystrophy and improved by glucocorticoids-Reference-Cited by-同舟云学术

The l-arginine/NO pathway and homoarginine are altered in Duchenne muscular dystrophy and improved by glucocorticoids

Published:2015-06-12 Issue:9 Volume:47 Page:1853-1863
ISSN:0939-4451
Container-title:Amino Acids
language:en
Short-container-title:Amino Acids

Author:

Hörster Irina,Weigt-Usinger Katharina,Carmann Christina,Chobanyan-Jürgens Kristine,Köhler Cornelia,Schara Ulrike,Kayacelebi Arslan Arinc,Beckmann Bibiana,Tsikas Dimitrios,Lücke Thomas

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Clinical Biochemistry,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s00726-015-2018-x.pdf

Reference84 articles.

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2. Achan V, Broadhead M, Malaki M, Whitley G, Leiper J, MacAllister R, Vallance P (2003) Asymmetric dimethylarginine causes hypertension and cardiac dysfunction in humans and is actively metabolized by dimethylarginine dimethylaminohydrolase. Arterioscler Thromb Vasc Biol 23:1455–1459

3. Annexstad EJ, Lund-Petersen I, Rasmussen M (2014) Duchenne muscular dystrophy. Tidsskr Nor Laegeforen 134:1361–1364

4. Arahata K, Ishiura S, Ishiguro T, Tsukahara T, Suhara Y, Eguchi C, Ishihara T, Nonaka I, Ozawa E, Sugita H (1988) Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide. Nature 333(6176):861–863

5. Banerjee B, Sharma U, Balasubramanian K, Kalaivani M, Kalra V, Jagannathan NR (2010) Effect of creatine monohydrate in improving cellular energetics and muscle strength in ambulatory Duchenne muscular dystrophy patients: a randomized, placebo-controlled 31P MRS study. Magn Reson Imaging 28(5):698–707

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