Zobrazeno 1 - 10
of 21
pro vyhledávání: '"T J, Rea"'
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 11, Pp 2365-2373 (1997)
We have developed a cDNA-dependent scintillation proximity assay (SPA) for rabbit apolipoprotein A-I that follows a classic radioimmunoassay scheme, in that antiserum and radiolabeled ligand are used in a process to quantify a source containing unlab
Externí odkaz:
https://doaj.org/article/88f5fd37341645f3b78599ec76d8da6e
Publikováno v:
Journal of Lipid Research, Vol 36, Iss 4, Pp 823-838 (1995)
A human cDNA clone (K1) was recently isolated that encodes functional acyl-CoA:cholesterol acyltransferase (ACAT) protein (Chang et al. J. Biol. Chem. 1993. 268: 20747-20755). We used the K1 clone to screen a rabbit liver cDNA library and isolated a
Externí odkaz:
https://doaj.org/article/fe9cbf6c731747dda4882ccbd5cdd106
Publikováno v:
Journal of Lipid Research, Vol 35, Iss 7, Pp 1274-1282 (1994)
Apolipoprotein A-I (apoA-I), the primary protein of high density lipoprotein, originates from intestine and liver of almost all mammalian species. In contrast to most species, intact rabbit liver is only capable of producing minute amounts of apoA-I
Externí odkaz:
https://doaj.org/article/bf7a55451e2044db9d57d5b27eea112c
Autor:
Marsha V. Vartanian, A. D. Essenburg, Benjamin P. Koester, Charles L. Bisgaier, Jeffrey C. Hanselman, Steven A. Gray, T J Rea, MichaelE. Pape
Publikováno v:
Molecular and Cellular Biochemistry. 217:91-97
Two alternatively spliced forms of human PPARα mRNA, PPARα1 and PPARα2, have been identified. PPARα1 mRNA gives rise to an active PPARα protein while PPARα2 mRNA gives rise to a form of PPAR which lacks the ligand-binding domain. PPARα2 is una
Autor:
M E Pape, Jeffrey C. Hanselman, T J Rea, Brian R. Krause, David A. Schwab, Charles L. Bisgaier
Publikováno v:
Life Sciences. 66:1683-1694
Past studies have shown that a high saturated fatty acid diet containing coconut oil elevates plasma HDL cholesterol and apolipoprotein A-I (apoA-1) in rabbits through a mechanism involving increased synthesis. We have extended those studies by inves
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 11, Pp 2365-2373 (1997)
We have developed a cDNA-dependent scintillation proximity assay (SPA) for rabbit apolipoprotein A-I that follows a classic radioimmunoassay scheme, in that antiserum and radiolabeled ligand are used in a process to quantify a source containing unlab
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism. 1299:67-74
A partial rabbit cDNA clone (14b) for ACAT has been characterized and used to demonstrate that hepatic and aortic ACAT mRNA14b abundance increased 2-3-fold in rabbits receiving a high fat/high cholesterol-diet compared to chow fed animals (Pape et al
Autor:
Charles L. Bisgaier, Roger S. Newton, P.A. Schultz, T J Rea, K.A. Kieft, M E Pape, Brian R. Krause, Ronald B. DeMattos
Publikováno v:
Journal of Lipid Research, Vol 36, Iss 4, Pp 823-838 (1995)
A human cDNA clone (K1) was recently isolated that encodes functional acyl-CoA:cholesterol acyltransferase (ACAT) protein (Chang et al. J. Biol. Chem. 1993. 268: 20747-20755). We used the K1 clone to screen a rabbit liver cDNA library and isolated a
Publikováno v:
Journal of Lipid Research, Vol 35, Iss 7, Pp 1274-1282 (1994)
Apolipoprotein A-I (apoA-I), the primary protein of high density lipoprotein, originates from intestine and liver of almost all mammalian species. In contrast to most species, intact rabbit liver is only capable of producing minute amounts of apoA-I
Publikováno v:
Journal of Lipid Research, Vol 34, Iss 11, Pp 1901-1910 (1993)
The liver plays a central role in lipid metabolism and plasma lipoprotein homeostasis. This dynamic process is regulated by a variety of liver-derived proteins. However, the specific liver cells that express these proteins are largely unknown. In the