Zobrazeno 1 - 10
of 46
pro vyhledávání: '"H. E. Henderson"'
Autor:
S Bijvoet, S E Gagné, S Moorjani, C Gagné, H E Henderson, J C Fruchart, J Dallongeville, P Alaupovic, M Prins, J J Kastelein, M R Hayden
Publikováno v:
Journal of Lipid Research, Vol 37, Iss 3, Pp 640-650 (1996)
We have assessed the expression of heterozygosity for lipoprotein lipase (LPL) deficiency by studying a single large French Canadian family comprising 92 persons including 21 carriers of the catalytically defective P207L mutation. Phenotypic changes
Externí odkaz:
https://doaj.org/article/f6d46694496c48ba8ee491d845205a23
Autor:
Y Ma, H E Henderson, M S Liu, H Zhang, I J Forsythe, I Clarke-Lewis, M R Hayden, J D Brunzell
Publikováno v:
Journal of Lipid Research, Vol 35, Iss 11, Pp 2049-2059 (1994)
Lipoprotein lipase (LPL) interaction with membrane-associated polyanions is a critical component of normal catalytic function. Two strong candidate binding regions, rich in arginine and lysine residues, have been defined in the N-terminal domain (aa2
Externí odkaz:
https://doaj.org/article/74c0221f8d86456f8a289175112f5015
Publikováno v:
Tribology Transactions. 49:490-501
Over the past two decades, the performance requirements for automatic transmission fluids (ATFs) have undergone a significant number of changes in response to mandated legislation by government and regulatory bodies to improve the air quality through
Autor:
John E. Drake, H. E. Henderson, Boris M. Glavinčevski, E. J. Stampf, J. D. Odom, Raymond T. Hemmings
Publikováno v:
Inorganic Syntheses, Volume 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c817e3a35fb21d18ee129748a2aa122
https://doi.org/10.1002/9780470132494.ch28
https://doi.org/10.1002/9780470132494.ch28
Publikováno v:
Clinical genetics. 62(2)
Only one study has reported on the genetic basis of spinal muscular atrophy (SMA) in South African subjects. This was conducted in the Johannesburg region and has suggested that black South Africans only (indigenous Africans) differ from the norm. We
Publikováno v:
SAE Technical Paper Series.
Autor:
S M, Clee, N, Bissada, F, Miao, L, Miao, A D, Marais, H E, Henderson, P, Steures, J, McManus, B, McManus, R C, LeBoeuf, J J, Kastelein, M R, Hayden
Publikováno v:
Journal of lipid research. 41(4)
Lipoprotein lipase (LPL) is a key enzyme in lipoprotein metabolism, and has been hypothesized to exert either pro- or anti-atherogenic effects, depending on its localization. Decreased plasma LPL activity is associated with the high triglyceride (TG)
Autor:
H E, Henderson, J J, Kastelein, A H, Zwinderman, E, Gagné, J W, Jukema, P W, Reymer, B E, Groenemeyer, K I, Lie, A V, Bruschke, M R, Hayden, H, Jansen
Publikováno v:
Journal of lipid research. 40(4)
Lipoprotein lipase (LPL) is crucial in the hydrolysis of triglycerides (TG) in TG-rich lipoproteins in the formation of HDL particles. As both these lipoproteins play an important role in the pathogenesis of atherosclerotic vascular disease, we sough
Autor:
D G, Ginzinger, S M, Clee, J, Dallongeville, M E, Lewis, H E, Henderson, E, Bauje, Q R, Rogers, D R, Jensen, R H, Eckel, R, Dyer, S, Innis, B, Jones, J C, Fruchart, M R, Hayden
Publikováno v:
European journal of clinical investigation. 29(1)
We have previously described a colony of domestic cats with a naturally occurring mutation in the lipoprotein lipase (LPL) gene. We have now further characterized cats homozygous for LPL deficiency (LPL -/-, homozygotes), and have contrasted these wi