Zobrazeno 1 - 10
of 15
pro vyhledávání: '"B L, Vaisman"'
Autor:
M E Brousseau, S Santamarina-Fojo, B L Vaisman, D Applebaum-Bowden, A M Bérard, G D Talley, H B Brewer, Jr, J M Hoeg
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 12, Pp 2537-2547 (1997)
Lecithin:cholesterol acyltransferase (LCAT) is an enzyme well known for its involvement in the intravascular metabolism of high density lipoproteins; however, its role in the regulation of apolipoprotein (apo) B-containing lipoproteins remains elusiv
Externí odkaz:
https://doaj.org/article/b352b7ce0aec4d8b8c8838cdea68e5bb
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 9, Pp 1822-1832 (1997)
In order to evaluate the coordinate role that hepatic lipase (HL) and lecithin:cholesterol acyltransferase (LCAT) play in modulating HDL particle heterogeneity and function in vivo we utilized recombinant adenovirus to express HL in control and LCAT
Externí odkaz:
https://doaj.org/article/056c9c361c5c4141b003f30aefc40f69
Autor:
A. P. Dyban, B. L. Vaisman
Publikováno v:
Biopolymers and Cell. 6:3-12
Autor:
M E, Brousseau, J, Wang, S J, Demosky, B L, Vaisman, G D, Talley, S, Santamarina-Fojo, H B, Brewer, J M, Hoeg
Publikováno v:
Journal of lipid research. 39(8)
Familial hypercholesterolemia (FH), a disease caused by a variety of mutations in the low density lipoprotein receptor (LDLr) gene, leads not only to elevated LDL-cholesterol (C) concentrations but to reduced high density lipoprotein (HDL)-C and apol
Autor:
M E, Brousseau, S, Santamarina-Fojo, B L, Vaisman, D, Applebaum-Bowden, A M, Bérard, G D, Talley, H B, Brewer, J M, Hoeg
Publikováno v:
Journal of lipid research. 38(12)
Lecithin:cholesterol acyltransferase (LCAT) is an enzyme well known for its involvement in the intravascular metabolism of high density lipoproteins; however, its role in the regulation of apolipoprotein (apo) B-containing lipoproteins remains elusiv
Autor:
N, Sakai, B L, Vaisman, C A, Koch, R F, Hoyt, S M, Meyn, G D, Talley, J A, Paiz, H B, Brewer, S, Santamarina-Fojo
Publikováno v:
The Journal of biological chemistry. 272(11)
We have established a mouse model for human LCAT deficiency by performing targeted disruption of the LCAT gene in mouse embryonic stem cells. Homozygous LCAT-deficient mice were healthy at birth and fertile. Compared with age-matched wild-type litter
Publikováno v:
Bulletin of Experimental Biology and Medicine. 91:682-685
Publikováno v:
Bulletin of Experimental Biology and Medicine. 96:910-913
Publikováno v:
Bulletin of Experimental Biology and Medicine. 92:1707-1710
Publikováno v:
Bulletin of Experimental Biology and Medicine. 91:664-666