Zobrazeno 1 - 10
of 68
pro vyhledávání: '"M.R. Ven Murthy"'
Publikováno v:
Central Nervous System Agents in Medicinal Chemistry. 10:238-246
Ayurveda is a Sanskrit word, which means "the scripture for longevity". It represents an ancient system of traditional medicine prevalent in India and in several other south Asian countries. It is based on a holistic view of treatment which is believ
Publikováno v:
Journal of Biological Chemistry. 279:27302-27314
Thioredoxin-2 (Trx2) is a mitochondrial protein-disulfide oxidoreductase essential for control of cell survival during mammalian embryonic development. This suggests that mitochondrial thioredoxin reductase-2 (TrxR2), responsible for reducing oxidize
Publikováno v:
Journal of Biological Chemistry. 278:9698-9705
Lipoprotein lipase (LPL) is a key enzyme involved in the metabolism of lipoproteins, providing tissues like adipose tissue or skeletal muscle with fatty acids. LPL is also expressed in the brain, fulfilling yet unknown functions. Using a neuroblastom
Autor:
François Cadelis, Michael R. Hayden, Paul J. Lupien, Claude Gagné, Georges Lévesque, Sital Moorjani, Pierre Julien, M.R. Ven Murthy
Publikováno v:
Human Mutation. 11:S148-S153
Publikováno v:
Journal of Neuroscience Research. 48:53-62
Glial fibrillary acidic protein (GFAP), an astroglial marker, has been detected in the peripheral nervous system (PNS) in a shorter version and its mRNA in a longer form (beta-type) than the brain alpha-type. To determine the characteristics of the G
Autor:
M.R. Ven Murthy, Kastelein John J P, Bonnie I. Wilson, Saskia Bijvoet, Henk D. Bakker, Michael R. Hayden, Howard E. Henderson, Elizabeth Cramb, John D. Brunzell, Ghislaine Roederer, Pierre Julien, Yuanhong Ma
Publikováno v:
Genomics, 13(3), 649-653. Academic Press Inc.
We have previously reported two common lipoprotein lipase (LPL) gene mutations underlying LPL deficiency in the majority of 37 French Canadians (Monsalve et al. , 1990. J. Clin. Invest. 86: 728–734; Ma et al. , 1991. N. Engl. J. Med. 324: 1761–17
Autor:
M.R. Ven Murthy, Michael R. Hayden, Howard E. Henderson, Paul J. Lupien, Pierre Julien, Ghislaine Roederer, Claude Gagné, Jean Davignon, Lorne A. Clarke, Maria V. Monsalve, John D. Brunzell, Yuanhong Ma, Marie Lambert, Thierry Normand
Publikováno v:
New England Journal of Medicine
New England Journal of Medicine, Massachusetts Medical Society, 1991, 324 (25), pp.1761-1766. ⟨10.1056/NEJM199106203242502⟩
Scopus-Elsevier
New England Journal of Medicine, Massachusetts Medical Society, 1991, 324 (25), pp.1761-1766. ⟨10.1056/NEJM199106203242502⟩
Scopus-Elsevier
Lipoprotein lipase hydrolyzes the triglyceride core of chylomicrons and very-low-density lipoproteins and has a crucial role in regulating plasma lipoprotein levels. Deficiencies of lipoprotein lipase activity lead to aberrations in lipoprotein level
Publikováno v:
Progress in neuro-psychopharmacologybiological psychiatry. 28(5)
Reactive oxygen species (ROS) are produced in the course of normal metabolism and they serve important physiological functions. However, because of their high reactivity, accumulation of ROS beyond the immediate needs of the cell may affect cellular
Publikováno v:
Brain research. Developmental brain research. 149(1)
Lipoprotein lipase (LPL) is well known for its role in the catabolism of plasma triglyceride (Tg)-rich lipoproteins, such as very low density lipoproteins (VLDL) and chylomicrons. The action of LPL on Tg-rich lipoproteins provides free fatty acids to
Autor:
Claude Gagné, Pierre Julien, Sophie Boudriau, L.D. Brun, Peter Rogers, M.R. Ven Murthy, Bernard Cantin, Paul-J. Lupien, Michel Bertrand
Publikováno v:
Metabolism: clinical and experimental. 44(5)
A slight to moderate hemolysis is often present in plasma from patients with primary lipoprotein lipase (LPL) deficiency. To determine the nature of this hemolysis, we measured erythrocyte hypo-osmotic fragility, plasma free hemoglobin, and phospholi