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Items: 1 to 20 of 50

1.
Osteocytes/Osteoblasts Produce SAA3 to Regulate Hepatic Metabolism of Cholesterol
Shijiang Huang, Yuanjun Jiang, Jing Li, Linlin Mao, Zeyou Qiu, Sheng Zhang, Yuhui Jiang, Yong Liu, Wen Liu, Zhi Xiong, Wuju Zhang, Xiaolin Liu, Yue Zhang, Xiaochun Bai, Bin Guo
Adv Sci (Weinh) 2024 Jun; 11(24): 2307818. Published online 2024 Apr 13. doi: 10.1002/advs.202307818
PMCID:
PMC11199997
AbstractArticlePDF–18M
2.
Genetic determinants of micronucleus formation in vivo
D. J. Adams, B. Barlas, R. E. McIntyre, I. Salguero, L. van der Weyden, A. Barros, J. R. Vicente, N. Karimpour, A. Haider, M. Ranzani, G. Turner, N. A. Thompson, V. Harle, R. Olvera-León, C. D. Robles-Espinoza, A. O. Speak, N. Geisler, W. J. Weninger, S. H. Geyer, J. Hewinson, N. A. Karp, The Sanger Mouse Genetics Project, B. Fu, F. Yang, Z. Kozik, J. Choudhary, L. Yu, M. S. van Ruiten, B. D. Rowland, C. J. Lelliott, M. del Castillo Velasco-Herrera, R. Verstraten, L. Bruckner, A. G. Henssen, M. A. Rooimans, J. de Lange, T. J. Mohun, M. J. Arends, K. A. Kentistou, P. A. Coelho, Y. Zhao, H. Zecchini, J. R. B. Perry, S. P. Jackson, G. Balmus
Nature. 2024; 627(8002): 130–136. Published online 2024 Feb 14. doi: 10.1038/s41586-023-07009-0
PMCID:
PMC10917660
AbstractArticlePDF–4.8M
3.
Deficiency of Acute-Phase Serum Amyloid A Exacerbates Sepsis-Induced Mortality and Lung Injury in Mice
Ailing Ji, Andrea C. Trumbauer, Victoria P. Noffsinger, Luke W. Meredith, Brittany Dong, Qian Wang, Ling Guo, Xiangan Li, Frederick C. De Beer, Nancy R. Webb, Lisa R. Tannock, Marlene E. Starr, Christopher M. Waters, Preetha Shridas
Int J Mol Sci. 2023 Dec; 24(24): 17501. Published online 2023 Dec 15. doi: 10.3390/ijms242417501
PMCID:
PMC10744229
AbstractArticlePDF–2.6M
4.
Effects of Ozone on Sickness and Depressive-like Behavioral and Biochemical Phenotypes and Their Regulation by Serum Amyloid A in Mice
Kristen K. Baumann, W. Sandy Liang, Daniel V. Quaranta, Miranda L. Wilson, Helina S. Asrat, Jarl A. Thysell, Angelo V. Sarchi, William A. Banks, Michelle A. Erickson
Int J Mol Sci. 2023 Jan; 24(2): 1612. Published online 2023 Jan 13. doi: 10.3390/ijms24021612
PMCID:
PMC9860713
AbstractArticlePDF–4.5M
5.
Maternal siRNA silencing of placental SAA2 mitigates preterm birth following intrauterine inflammation
Yang Liu, Jin Liu, Anguo Liu, Hillary Yin, Irina Burd, Jun Lei
Front Immunol. 2022; 13: 902096. Published online 2022 Sep 23. doi: 10.3389/fimmu.2022.902096
PMCID:
PMC9539923
AbstractArticlePDF–5.2M
6.
Serum Amyloid A is not obligatory for high-fat, high-sucrose, cholesterol-fed diet-induced obesity and its metabolic and inflammatory complications
Ailing Ji, Andrea C. Trumbauer, Victoria P. Noffsinger, Hayce Jeon, Avery C. Patrick, Frederick C. De Beer, Nancy R. Webb, Lisa R. Tannock, Preetha Shridas
PLoS One. 2022; 17(4): e0266688. Published online 2022 Apr 18. doi: 10.1371/journal.pone.0266688
PMCID:
PMC9015120
AbstractArticlePDF–2.6M
7.
Sexually dimorphic relationships among serum amyloid A3, inflammation, and cholesterol metabolism modulate atherosclerosis in mice
A Chait, S Wang, L Goodspeed, D Gomes, KE Turk, T Wietecha, J Tang, C Storey, KD O’Brien, KB Rubinow, C Tang, T Vaisar, SA Gharib, AJ Lusis, LJ den Hartigh
Arterioscler Thromb Vasc Biol. Author manuscript; available in PMC 2022 Jun 1.
Published in final edited form as: Arterioscler Thromb Vasc Biol. 2021 Jun; 41(6): e299–e313. Published online 2021 Mar 25. doi: 10.1161/ATVBAHA.121.316066
PMCID:
PMC8159856
AbstractArticlePDF–2.3M
8.
Serum amyloid A3 deficiency impairs in vitro and in vivo adipocyte differentiation
Ellen Vercalsteren, Christine Vranckx, Ines Vermeire, Max Gooijen, Roger Lijnen, Ilse Scroyen
Adipocyte. 2021; 10(1): 242–250. Published online 2021 Apr 25. doi: 10.1080/21623945.2021.1916220
PMCID:
PMC8078753
AbstractArticlePDF–4.4M
9.
Serum amyloid A inhibits astrocyte migration via activating p38 MAPK
Aihua Lin, Jin Liu, Ping Gong, Yanqing Chen, Haibo Zhang, Yan Zhang, Yang Yu
J Neuroinflammation. 2020; 17: 254. Published online 2020 Aug 29. doi: 10.1186/s12974-020-01924-z
PMCID:
PMC7456509
AbstractArticlePDF–5.1M
10.
Presence of serum amyloid A3 in mouse plasma is dependent on the nature and extent of the inflammatory stimulus
Alan Chait, Laura J. den Hartigh, Shari Wang, Leela Goodspeed, Ilona Babenko, William A. Altemeier, Tomas Vaisar
Sci Rep. 2020; 10: 10397. Published online 2020 Jun 25. doi: 10.1038/s41598-020-66898-7
PMCID:
PMC7316782
AbstractArticlePDF–2.0M
11.
Serum Amyloid A Proteins Induce Pathogenic TH17 Cells and Promote Inflammatory Disease
June-Yong Lee, Jason A. Hall, Lina Kroehling, Lin Wu, Tariq Najar, Henry H. Nguyen, Woan-Yu Lin, Stephen T. Yeung, Hernandez Moura Silva, Dayi Li, Ashley Hine, P’ng Loke, David Hudesman, Jerome C. Martin, Ephraim Kenigsberg, Miriam Merad, Kamal M. Khanna, Dan R. Littman
Cell. Author manuscript; available in PMC 2021 Jan 9.
Published in final edited form as: Cell. 2020 Jan 9; 180(1): 79–91.e16. Published online 2019 Dec 19. doi: 10.1016/j.cell.2019.11.026
Correction in:
Cell. 2020 Dec 23; 183(7): 2036–2039.
PMCID:
PMC7039443
AbstractArticlePDF–2.1M
12.
The serum amyloid A3 promoter-driven luciferase reporter mice is a valuable tool to image early renal fibrosis development and shows the therapeutic effect of glucosyl-hesperidin treatment
Thanutchaporn Kumrungsee, Taishi Kariya, Kotaro Hashimoto, Takayuki Koyano, Nao Yazawa, Takao Hashimoto, Yohei Sanada, Makoto Matsuyama, Yusuke Sotomaru, Hiroaki Sakurai, Fons A. J. van de Loo, Noriyuki Yanaka
Sci Rep. 2019; 9: 14101. Published online 2019 Oct 1. doi: 10.1038/s41598-019-50685-0
PMCID:
PMC6773767
AbstractArticlePDF–5.4M
13.
Continuous PTH in Male Mice Causes Bone Loss Because It Induces Serum Amyloid A
Shilpa Choudhary, Elizabeth Santone, Sui-Pok Yee, Joseph Lorenzo, Douglas J Adams, Alexandra Goetjen, Mary Beth McCarthy, Augustus D Mazzocca, Carol Pilbeam
Endocrinology. 2018 Jul; 159(7): 2759–2776. Published online 2018 May 10. doi: 10.1210/en.2018-00265
PMCID:
PMC6692876
AbstractArticle
14.
Serum Amyloid A3 is required for normal lung development and survival following influenza infection
Jennifer L. Ather, Oliver Dienz, Jonathan E. Boyson, Vikas Anathy, Eyal Amiel, Matthew E. Poynter
Sci Rep. 2018; 8: 16571. Published online 2018 Nov 8. doi: 10.1038/s41598-018-34901-x
PMCID:
PMC6224415
AbstractArticlePDF–2.3M
15.
Serum amyloid A3 is pro-atherogenic
Joel C Thompson, Patricia G Wilson, Preetha Shridas, Ailing Ji, Maria de Beer, Frederick C de Beer, Nancy R Webb, Lisa R Tannock
Atherosclerosis. Author manuscript; available in PMC 2019 Jan 1.
Published in final edited form as: Atherosclerosis. 2018 Jan; 268: 32–35. Published online 2017 Nov 17. doi: 10.1016/j.atherosclerosis.2017.11.011
PMCID:
PMC5839639
AbstractArticlePDF–683K
16.
Saa3 is a key mediator of the protumorigenic properties of cancer-associated fibroblasts in pancreatic tumors
Magdolna Djurec, Osvaldo Graña, Albert Lee, Kevin Troulé, Elisa Espinet, Lavinia Cabras, Carolina Navas, María Teresa Blasco, Laura Martín-Díaz, Miranda Burdiel, Jing Li, Zhaoqi Liu, Mireia Vallespinós, Francisco Sanchez-Bueno, Martin R. Sprick, Andreas Trumpp, Bruno Sainz, Jr., Fátima Al-Shahrour, Raul Rabadan, Carmen Guerra, Mariano Barbacid
Proc Natl Acad Sci U S A. 2018 Feb 6; 115(6): E1147–E1156. Published online 2018 Jan 19. doi: 10.1073/pnas.1717802115
PMCID:
PMC5819438
AbstractArticlePDF–1.9M
17.
Serum amyloid A3 is a high density lipoprotein-associated acute-phase protein
Lisa R. Tannock, Maria C. De Beer, Ailing Ji, Preetha Shridas, Victoria P. Noffsinger, Laura den Hartigh, Alan Chait, Frederick C. De Beer, Nancy R. Webb
J Lipid Res. 2018 Feb; 59(2): 339–347. Published online 2017 Dec 15. doi: 10.1194/jlr.M080887
PMCID:
PMC5794427
AbstractArticlePDF–1.1M
18.
Serum amyloid A3 is required for normal weight and immunometabolic function in mice
Jennifer L. Ather, Matthew E. Poynter
PLoS One. 2018; 13(2): e0192352. Published online 2018 Feb 1. doi: 10.1371/journal.pone.0192352
PMCID:
PMC5794179
AbstractArticlePDF–3.1M
19.
High-throughput discovery of novel developmental phenotypes
Mary E. Dickinson, Ann M. Flenniken, Xiao Ji, Lydia Teboul, Michael D. Wong, Jacqueline K. White, Terrence F. Meehan, Wolfgang J. Weninger, Henrik Westerberg, Hibret Adissu, Candice N. Baker, Lynette Bower, James M. Brown, L. Brianna Caddle, Francesco Chiani, Dave Clary, James Cleak, Mark J. Daly, James M. Denegre, Brendan Doe, Mary E. Dolan, Sarah M. Edie, Helmut Fuchs, Valerie Gailus-Durner, Antonella Galli, Alessia Gambadoro, Juan Gallegos, Shiying Guo, Neil R. Horner, Chih-wei Hsu, Sara J. Johnson, Sowmya Kalaga, Lance C. Keith, Louise Lanoue, Thomas N. Lawson, Monkol Lek, Manuel Mark, Susan Marschall, Jeremy Mason, Melissa L. McElwee, Susan Newbigging, Lauryl M.J. Nutter, Kevin A. Peterson, Ramiro Ramirez-Solis, Douglas J. Rowland, Edward Ryder, Kaitlin E. Samocha, John R. Seavitt, Mohammed Selloum, Zsombor Szoke-Kovacs, Masaru Tamura, Amanda G Trainor, Ilinca Tudose, Shigeharu Wakana, Jonathan Warren, Olivia Wendling, David B. West, Leeyean Wong, Atsushi Yoshiki, The International Mouse Phenotyping Consortium, Daniel G. MacArthur, Glauco P. Tocchini-Valentini, Xiang Gao, Paul Flicek, Allan Bradley, William C. Skarnes, Monica J. Justice, Helen E. Parkinson, Mark Moore, Sara Wells, Robert E. Braun, Karen L. Svenson, Martin Hrabe de Angelis, Yann Herault, Tim Mohun, Ann-Marie Mallon, R. Mark Henkelman, Steve D.M. Brown, David J. Adams, K.C. Kent Lloyd, Colin McKerlie, Arthur L. Beaudet, Maja Bucan, Stephen A. Murray
Nature. Author manuscript; available in PMC 2017 Mar 14.
Published in final edited form as: Nature. 2016 Sep 22; 537(7621): 508–514. Published online 2016 Sep 14. doi: 10.1038/nature19356
Correction in:
Nature. 2017 Nov 16; 551(7680): 398.
PMCID:
PMC5295821
AbstractArticlePDF–3.0M
20.
Serum Amyloid A3 Gene Expression in Adipocytes is an Indicator of the Interaction with Macrophages
Yohei Sanada, Takafumi Yamamoto, Rika Satake, Akiko Yamashita, Sumire Kanai, Norihisa Kato, Fons AJ van de Loo, Fusanori Nishimura, Philipp E. Scherer, Noriyuki Yanaka
Sci Rep. 2016; 6: 38697. Published online 2016 Dec 8. doi: 10.1038/srep38697
PMCID:
PMC5144138
AbstractArticlePDF–1.6M

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