Zobrazeno 1 - 10
of 117
pro vyhledávání: '"F. C. De Beer"'
Autor:
F C de Beer, M C de Beer, D R van der Westhuyzen, L W Castellani, A J Lusis, M E Swanson, D S Grass
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 11, Pp 2232-2239 (1997)
Lipoprotein metabolism is markedly altered during inflammation. The concentration of human secretory phospholipase A2 (sPLA2) can increase hundreds of fold in inflammatory fluids and in the circulation. It was detected in atherosclerotic lesions wher
Externí odkaz:
https://doaj.org/article/b0b04a3bec634fc89029e625b6727249
Autor:
N R Webb, M C de Beer, D R van der Westhuyzen, M S Kindy, C L Banka, K Tsukamoto, D L Rader, F C de Beer
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 8, Pp 1583-1590 (1997)
Serum amyloid A (SAA) is an acute phase reactant that can become the predominant apolipoprotein of high density lipoprotein (HDL) during severe inflammatory states. However, the function of SAA is unknown. To study the ability of SAA to form HDL in t
Externí odkaz:
https://doaj.org/article/4f4602b97430432e9f1f07491d7d753e
Publikováno v:
Journal of Lipid Research, Vol 38, Iss 7, Pp 1490-1495 (1997)
The class B, type I scavenger receptor has been implicated as a receptor for high density lipoprotein (HDL). We have isolated a murine cDNA clone encoding an alternative form of SR-BI that differs in the putative cytoplasmic domain of the receptor. T
Externí odkaz:
https://doaj.org/article/7e27528ca9314ccfa3e283d176cc4d50
Publikováno v:
Journal of Lipid Research, Vol 37, Iss 10, Pp 2109-2116 (1996)
The human apoSAA proteins comprise both acute phase (apoSAA1, apoSAA2) and constitutive (apoSAA4) isoforms; all are expressed in human atherosclerotic lesions as well as in liver. Recombinant acute phase apoSAA binds cholesterol with an affinity of a
Externí odkaz:
https://doaj.org/article/bb5ac42240424f85ac9a7e9a364b7a43
Publikováno v:
Journal of Lipid Research, Vol 36, Iss 5, Pp 1058-1065 (1995)
Normal high density lipoprotein (N-HDL) is remodeled during acute phase (AP) reactions by the association of serum amyloid A (SAA) and the depletion of apolipoprotein (apo) A-I. To determine the impact of this remodeling on HDL function, the capaciti
Externí odkaz:
https://doaj.org/article/e3d24020503749678c2e5a129c25d82f
Publikováno v:
Journal of Lipid Research, Vol 36, Iss 3, Pp 526-534 (1995)
Serum amyloid A proteins (SAAs), a family of homologous molecules, are apolipoproteins of high density lipoprotein (HDL). They can be divided into two groups. The first group comprises the well-characterized acute phase SAAs that associate with HDL d
Externí odkaz:
https://doaj.org/article/078ea6cb5fc5462884abd0d1f86544f9
Publikováno v:
Atherosclerosis. 275:e2
Publikováno v:
Journal of Lipid Research, Vol 42, Iss 2, Pp 309-313 (2001)
Apolipoprotein A-I (apoA-I) is an important ligand for the high density lipoprotein (HDL) scavenger re- ceptor class B type I (SR-BI). SR-BI binds both free and lipoprotein-associated apoA-I, but the effects of particle size, composition, and apolipo
Publikováno v:
Biochemical Journal. 332:721-728
the SAA # protein was capable of forming amyloid fibrils, whereas the CE}J SAA was incapable. Radiolabelled SAAs were associated with normal or acute-phase high-density lipoproteins (HDLs); we examined them for their clearance from the circulation. I
Autor:
F C de Beer, W. J. S. De Villiers, Aldon J. Lusis, M C de Beer, Diana M. Shih, Yu-Rong Xia, Zhiming Jiang, D.R. van der Westhuyzen
Publikováno v:
Genomics. 50:199-205
Murine macrosialin and its human homologue CD68 are heavily glycosylated transmembrane proteins expressed specifically in macrophages and macrophage-related cells. Macrosialin is predominantly a late endosomal protein but is also found on the cell su