Diagnosis of Creatine Metabolism Disorders by Determining Creatine and Guanidinoacetate in Plasma and Urine
Author:
Publisher
Humana Press
Link
http://link.springer.com/content/pdf/10.1007/978-1-60761-459-3_17.pdf
Reference26 articles.
1. Monge, C., Beraud, N., Kuznetsov, A.V., Rostovtseva, T., Sackett, D., Schlattner, U., Vendelin, M. and Saks, V.A. (2008) Regulation of respiration in brain mitochondria and synaptosomes: restrictions of ADP diffusion in situ, roles of tubulin, and mitochondrial creatine kinase. Mol Cell Biochem, 318, 147–165.
2. Saks, V., Kaambre, T., Guzun, R., Anmann, T., Sikk, P., Schlattner, U., Wallimann, T., Aliev, M. and Vendelin, M. (2007) The creatine kinase phosphotransfer network: thermodynamic and kinetic considerations, the impact of the mitochondrial outer membrane and modelling approaches. Subcell Biochem, 46, 27–65.
3. Saks, V., Kuznetsov, A., Andrienko, T., Usson, Y., Appaix, F., Guerrero, K., Kaambre, T., Sikk, P., Lemba, M. and Vendelin, M. (2003) Heterogeneity of ADP diffusion and regulation of respiration in cardiac cells. Biophys J, 84, 3436–3456.
4. Braissant, O., Bachmann, C. and Henry, H. (2007) Expression and function of AGAT, GAMT and CT1 in the mammalian brain. Subcell Biochem, 46, 67–81.
5. Ganesan, V., Johnson, A., Connelly, A., Eckhardt, S. and Surtees, R.A. (1997) Guanidinoacetate methyltransferase deficiency: new clinical features. Pediatr Neurol, 17, 155–157.
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Lipid nanoparticle-targeted mRNA therapy as a treatment for the inherited metabolic liver disorder arginase deficiency;Proceedings of the National Academy of Sciences;2019-09-09
2. Human recombinant arginase enzyme reduces plasma arginine in mouse models of arginase deficiency;Human Molecular Genetics;2015-09-10
3. Myocyte-mediated Arginase Expression Controls Hyperargininemia but not Hyperammonemia in Arginase-deficient Mice;Molecular Therapy;2014-10
4. Biochemical, molecular, and clinical diagnoses of patients with cerebral creatine deficiency syndromes;Molecular Genetics and Metabolism;2013-07
5. Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms;Orphanet Journal of Rare Diseases;2012-12
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3