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Items: 1 to 20 of 31

1.
Amyloidogenesis. One serum amyloid A isotype is selectively removed from the circulation
J Exp Med. 1986 Mar 1; 163(3): 499–510. doi: 10.1084/jem.163.3.499
PMCID:
PMC2188051
SummaryPDF–1.0M
2.
Polymorphisms in the SAA1/2 Gene Are Associated with Carotid Intima Media Thickness in Healthy Han Chinese Subjects: The Cardiovascular Risk Survey
Xiang Xie, Yi-Tong Ma, Yi-Ning Yang, Zhen-Yan Fu, Xiao-Mei Li, Ding Huang, Xiang Ma, Bang-Dang Chen, Fen Liu
PLoS One. 2010; 5(11): e13997. Published online 2010 Nov 16. doi: 10.1371/journal.pone.0013997
PMCID:
PMC2982816
AbstractArticlePDF–99K
3.
Association of genetic variation in serum amyloid-A with cardiovascular disease and interactions with the IL6, IL1RN, IL1β and TNF genes in the Cardiovascular Health Study
Cara L. Carty, Patrick Heagerty, Susan R. Heckbert, Daniel A. Enquobahrie, Gail P. Jarvik, Scott Davis, Russell P. Tracy, Alexander P. Reiner
J Atheroscler Thromb. Author manuscript; available in PMC 2010 Sep 3.
Published in final edited form as: J Atheroscler Thromb. 2009 Aug; 16(4): 419–430. Published online 2009 Sep 3. doi: 10.5551/jat.no968
PMCID:
PMC2890297
AbstractArticlePDF–787K
4.
A Seven-transmembrane, G Protein–coupled Receptor, FPRL1, Mediates the Chemotactic Activity of Serum Amyloid A for Human Phagocytic Cells
Shao Bo Su, Wanghua Gong, Ji-Liang Gao, Weiping Shen, Philip M. Murphy, Joost J. Oppenheim, Ji Ming Wang
J Exp Med. 1999 Jan 18; 189(2): 395–402. doi: 10.1084/jem.189.2.395
PMCID:
PMC2192984
AbstractArticlePDF–205K
5.
Serum amyloid A is a chemoattractant: induction of migration, adhesion, and tissue infiltration of monocytes and polymorphonuclear leukocytes
J Exp Med. 1994 Jul 1; 180(1): 203–209. doi: 10.1084/jem.180.1.203
PMCID:
PMC2191543
SummaryPDF–2.1M
6.
Acute-Phase Serum Amyloid A: An Inflammatory Adipokine and Potential Link between Obesity and Its Metabolic Complications
Rong-Ze Yang, Mi-Jeong Lee, Hong Hu, Toni I Pollin, Alice S Ryan, Barbara J Nicklas, Soren Snitker, Richard B Horenstein, Kristen Hull, Nelson H Goldberg, Andrew P Goldberg, Alan R Shuldiner, Susan K Fried, Da-Wei Gong
PLoS Med. 2006 Jun; 3(6): e287. Published online 2006 Jun 6. doi: 10.1371/journal.pmed.0030287
PMCID:
PMC1472697
AbstractArticlePDF–706K
7.
Heterogeneity of human serum amyloid A protein. Five different variants from one individual demonstrated by cDNA sequence analysis.
A Steinkasserer, E H Weiss, W Schwaeble, R P Linke
Biochem J. 1990 May 15; 268(1): 187–193. doi: 10.1042/bj2680187
PMCID:
PMC1131410
SummaryPage BrowsePDF–1.7M
8.
Human serum amyloid A. Three hepatic mRNAs and the corresponding proteins in one person.
B Kluve-Beckerman, F E Dwulet, M D Benson
J Clin Invest. 1988 Nov; 82(5): 1670–1675. doi: 10.1172/JCI113779
PMCID:
PMC442736
SummaryPage BrowsePDF–1.2M
9.
Expression of apolipoprotein serum amyloid A mRNA in human atherosclerotic lesions and cultured vascular cells: implications for serum amyloid A function.
R L Meek, S Urieli-Shoval, E P Benditt
Proc Natl Acad Sci U S A. 1994 Apr 12; 91(8): 3186–3190. doi: 10.1073/pnas.91.8.3186
PMCID:
PMC43540
SummaryPage BrowsePDF–1.5M
10.
Serum Amyloid A is a Soluble Pattern Recognition Receptor that Drives Type 2 Immunity
Ursula Smole, Naina Gour, Jordan Phelan, Gerhard Hofer, Cordula Köhler, Bernhard Kratzer, Peter A. Tauber, Xiao Xiao, Nu Yao, Jan Dvorak, Luis Caraballo, Leonardo Puerta, Sandra Rosskopf, Jamila Chakir, Ernst Malle, Andrew P. Lane, Winfried F. Pickl, Stephane Lajoie, Marsha Wills-Karp
Nat Immunol. Author manuscript; available in PMC 2022 Jul 18.
Published in final edited form as: Nat Immunol. 2020 Jul; 21(7): 756–765. Published online 2020 Jun 22. doi: 10.1038/s41590-020-0698-1
PMCID:
PMC9291269
AbstractArticlePDF–3.7M
11.
Serum amyloid A exhibits pH dependent antibacterial action and contributes to host defense against Staphylococcus aureus cutaneous infection
Han Zheng, Haifeng Li, Jingyuan Zhang, Hanlu Fan, Lina Jia, Wenqiang Ma, Shuoqian Ma, Shenghong Wang, Hua You, Zhinan Yin, Xiangdong Li
J Biol Chem. 2020 Feb 28; 295(9): 2570–2581. Published online 2019 Dec 9. doi: 10.1074/jbc.RA119.010626
PMCID:
PMC7049966
AbstractArticlePDF–4.0M
12.
Expression of SAA1, SAA2 and SAA4 genes in human primary monocytes and monocyte-derived macrophages
Claire Jumeau, Fawaz Awad, Eman Assrawi, Laetitia Cobret, Philippe Duquesnoy, Irina Giurgea, Dominique Valeyre, Gilles Grateau, Serge Amselem, Jean-François Bernaudin, Sonia-Athina Karabina
PLoS One. 2019; 14(5): e0217005. Published online 2019 May 17. doi: 10.1371/journal.pone.0217005
PMCID:
PMC6524798
AbstractArticlePDF–1.4M
13.
Comparison of C-Reactive Protein and Serum Amyloid A Protein in Septic Shock Patients
Domingos Dias Cicarelli, Joaquim Edson Vieira, Fábio Ely Martins Benseñor
Mediators Inflamm. 2008; 2008: 631414. Published online 2008 Mar 12. doi: 10.1155/2008/631414
PMCID:
PMC2277077
AbstractArticlePDF–523K
14.
mRNA expression and release of interleukin-8 induced by serum amyloid A in neutrophils and monocytes.
Fernanda Pereira Ribeiro, Cristiane Jaciara Furlaneto, Elaine Hatanaka, Wesley Bueno Ribeiro, Glaucia Mendes Souza, Marco A Cassatella, Ana Campa
Mediators Inflamm. 2003 Jun; 12(3): 173–178. doi: 10.1080/0962935031000134897
PMCID:
PMC1781605
SummaryPDF–213K
15.
Murine apolipoprotein serum amyloid A in solution forms a hexamer containing a central channel
Limin Wang, Hilal A. Lashuel, Thomas Walz, Wilfredo Colón
Proc Natl Acad Sci U S A. 2002 Dec 10; 99(25): 15947–15952. Published online 2002 Nov 27. doi: 10.1073/pnas.252508399
PMCID:
PMC138545
AbstractArticlePDF–417K
16.
Pathogenic Serum Amyloid A 1.1 Shows a Long Oligomer-rich Fibrillation Lag Phase Contrary to the Highly Amyloidogenic Non-pathogenic SAA2.2
Saipraveen Srinivasan, Sanket Patke, Yun Wang, Zhuqiu Ye, Jeffrey Litt, Sunit K. Srivastava, Maria M. Lopez, Dmitry Kurouski, Igor K. Lednev, Ravi S. Kane, Wilfredo Colón
J Biol Chem. 2013 Jan 25; 288(4): 2744–2755. Published online 2012 Dec 5. doi: 10.1074/jbc.M112.394155
PMCID:
PMC3554940
AbstractArticlePDF–2.4M
17.
Proteolysis of AA Amyloid Fibril Proteins by Matrix Metalloproteinases-1, -2, and -3
Barbara Stix, Thilo Kähne, Knut Sletten, John Raynes, Albert Roessner, Christoph Röcken
Am J Pathol. 2001 Aug; 159(2): 561–570. doi: 10.1016/S0002-9440(10)61727-0
PMCID:
PMC1850551
AbstractArticlePDF–336K
18.
Cross-Linking Mass Spectrometry Uncovers Interactions Between High-Density Lipoproteins and the SARS-CoV-2 Spike Glycoprotein
Sean A. Burnap, Ana Maria Ortega-Prieto, Jose M. Jimenez-Guardeño, Hashim Ali, Kaloyan Takov, Matthew Fish, Manu Shankar-Hari, Mauro Giacca, Michael H. Malim, Manuel Mayr
Mol Cell Proteomics. 2023 Aug; 22(8): 100600. Published online 2023 Jun 19. doi: 10.1016/j.mcpro.2023.100600
PMCID:
PMC10279469
AbstractArticlePDF–3.2M
19.
A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition
Sarah E Harris, Helen Fox, Alan F Wright, Caroline Hayward, John M Starr, Lawrence J Whalley, Ian J Deary
BMC Genet. 2007; 8: 43. Published online 2007 Jul 2. doi: 10.1186/1471-2156-8-43
PMCID:
PMC1933580
AbstractArticlePDF–397K
20.
Expression of Conjoined Genes: Another Mechanism for Gene Regulation in Eukaryotes
Tulika Prakash, Vineet K. Sharma, Naoki Adati, Ritsuko Ozawa, Naveen Kumar, Yuichiro Nishida, Takayoshi Fujikake, Tadayuki Takeda, Todd D. Taylor
PLoS One. 2010; 5(10): e13284. Published online 2010 Oct 12. doi: 10.1371/journal.pone.0013284
PMCID:
PMC2953495
AbstractArticlePDF–1.0M

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