Zobrazeno 1 - 10
of 43
pro vyhledávání: '"M 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 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
Autor:
Ricardo A. Battaglino, T. E. Van Dyke, Philip Stashenko, M C de Beer, Shuang Xu, Hajime Sasaki, Nobuyuki Kawashima, Kimito Hirai, Hisako Furusho
Publikováno v:
Journal of Dental Research. 98:117-125
In the current concept of bacterial infections, pathogen-associated molecular patterns (PAMPs) derived from pathogens and damage-associated molecular patterns (DAMPs) released from damaged/necrotic host cells are crucial factors in induction of innat
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
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
Autor:
A J Lusis, M C de Beer, L W Castellani, D.R. van der Westhuyzen, D S Grass, M E Swanson, F C de Beer
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
Autor:
M C de Beer, Nancy R. Webb, Mark S. Kindy, F C de Beer, K Tsukamoto, C L Banka, D L Rader, D.R. van der Westhuyzen
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
Publikováno v:
Biochemical Journal. 318:1041-1049
Site-directed mutagenesis of the acute-phase human serum amyloid A (SAA1 alpha) protein was used to evaluate the importance of the N-terminal amino acid residues, namely RSFFSFLGEAF The full-length cDNA clone of SAA1 alpha (pA1.mod.) was used to crea