Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Inflammation and SAA1[original query] |
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An allele of serum amyloid A1 associated with amyloidosis in both Japanese and Caucasians. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2003 Mar 10 (1): 7-11. Yamada Toshiyuki, Okuda Yasuaki, Takasugi Kiyoshi, Wang Lishan, Marks Duane, Benson Merrill D, Kluve-Beckerman Barba |
Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in Hyper-IgD syndrome. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2005 Jun 12 (2): 115-9. van der Hilst J C H, Drenth J P H, Bodar E J, Bijzet J, van der Meer J W M, Simon A, |
Association of genetic variation in serum amyloid-A with cardiovascular disease and interactions with IL6, IL1RN, IL1beta and TNF genes in the Cardiovascular Health Study. Journal of atherosclerosis and thrombosis 2009 Aug 16 (4): 419-30. Carty Cara L, Heagerty Patrick, Heckbert Susan R, Enquobahrie Daniel A, Jarvik Gail P, Davis Scott, Tracy Russell P, Reiner Alexander |
Serum uric acid levels are associated with polymorphism in the SAA1 gene in Chinese subjects. PloS one 2012 7 (6): e40263. Xie Xiang, Ma Yi-Tong, Yang Yi-Ning, Li Xiao-Mei, Fu Zhen-Yan, Zheng Ying-Ying, Ma Xiang, Chen Bang-Dang, Liu Fen, Huang Ying, Yu Zi-Xiang, Chen Y |
Bcii--RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis. Renal failure 2015 Mar 37 (2): 292-6. Ozdemir Ozturk, Kayatas Mansur, Cetinkaya Selma, Yildirim Malik Ejder, Silan Fatma, Kurtulgan Hande Kucuk, Koksal Binnur, Urfali Mine, Candan Ferh |
Serum amyloid a gene polymorphism and its association with lipid profile in Saudi females with osteoporosis. Pakistan journal of medical sciences 0 31 (5): 1124-9. Abdu-Allah Azza M, Tarhouny Shereen A El, Baghdadi Hussam Husse |
Serum Amyloid A Type 1 Gene Polymorphism in Egyptian Children with Familial Mediterranean Fever. Pathobiology : journal of immunopathology, molecular and cellular biology 2016 83 (6): 295-300. Wilson Manal, Abou-Elalla Amany A, Zakaria Mervat Talaat, Marzouk Huda, Fayed Hala Lotfy, Hanna Mariam Onsy |
Murine MTHFD1-synthetase deficiency, a model for the human MTHFD1 R653Q polymorphism, decreases growth of colorectal tumors. Molecular carcinogenesis 2016 Sep . Lévesque Nancy, Christensen Karen E, Van Der Kraak Lauren, Best Ana F, Deng Liyuan, Caldwell Don, MacFarlane Amanda J, Beauchemin Nicole, Rozen Ri |
AA amyloidosis - Benefits and prospects of IL-6 inhibitors. Modern rheumatology 2018 8 29 (2): 268-274. Okuda Yasua |
Mild Methylenetetrahydrofolate Reductase Deficiency Alters Inflammatory and Lipid Pathways in Liver. Molecular nutrition & food research 2018 Nov e1801001. Leclerc Daniel, Christensen Karen E, Cauvi Olivia, Yang Ethan, Fournelle Frédéric, Bahous Renata H, Malysheva Olga V, Deng Liyuan, Wu Qing, Zhou Zili, Gao Zu-Hua, Chaurand Pierre, Caudill Marie A, Rozen Ri |
Serum amyloid A levels are associated with polymorphic variants in the serum amyloid A 1 and 2 genes. Irish journal of medical science 2019 3 188 (4): 1175-1183. Griffiths Kayleigh, Maxwell Alexander P, McCarter Rachel V, Nicol Patrick, Hogg Ruth E, Harbinson Mark, McKay Gareth |
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