HuGE Literature Finder
Records 1-9
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Association between the rs9131 and rs3806792 polymorphisms of the CXCL2 gene and the risk of HBV-related hepatocellular carcinoma in a Guangxi population.
Journal of clinical laboratory analysis 2020 Apr e23310. Lu Yu, Zeng Jie, Yang Shi, Hu Zuojian, Li Limin, Yu Hongli, Qin X |
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Impact of DARC, GSDMA and CXCL2 polymorphisms on induction toxicity in children with acute lymphoblastic leukemia: A complementary study.
Leukemia research 2019 Sep 86 106228. Gatineau-Sailliant S, Glisovic S, Gagné V, Laverdière C, Leclerc J M, Silverman L B, Sinnett D, Krajinovic M, Pastore |
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Impact of genetic polymorphisms determining leukocyte/neutrophil count on chemotherapy toxicity.
The pharmacogenomics journal 2018 04 18 (2): 270-274. Glisovic S J, Pastore Y D, Gagne V, Plesa M, Laverdière C, Leclerc J M, Sinnett D, Krajinovic |
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Association of CXCL1 promoter polymorphism with ischaemic stroke in Korean population.
International journal of immunogenetics 2012 Nov . Park HJ, Yun DH, Kim SK, Chung JH, Lee JS, Park HK, Chon J, Kim DH, Yoo SD, Kim HS |
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Expression and Regulation of Interferon-Related Development Regulator 1 (IFRD1) in Cystic Fibrosis Neutrophils.
American journal of respiratory cell and molecular biology 2012 Oct . Hector A, Kormann M, Kammermeier J, Burdi S, Marcos V, Rieber N, Mays L, Illig T, Klopp N, Falkenstein F, Kappler M, Riethmueller J, Graepler-Mainka U, Stern M, Eickmeier O, Serve F, Zielen S, Döring G, Griese M, Hartl D |
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).
PLoS genetics 2011 Jun 7 (6): e1002108. Reiner Alexander P, Lettre Guillaume, Nalls Michael A, Ganesh Santhi K, Mathias Rasika, Austin Melissa A, Dean Eric, Arepalli Sampath, Britton Angela, Chen Zhao, Couper David, Curb J David, Eaton Charles B, Fornage Myriam, Grant Struan F A, Harris Tamara B, Hernandez Dena, Kamatini Naoyuki, Keating Brendan J, Kubo Michiaki, LaCroix Andrea, Lange Leslie A, Liu Simin, Lohman Kurt, Meng Yan, Mohler Emile R, Musani Solomon, Nakamura Yusuke, O'Donnell Christopher J, Okada Yukinori, Palmer Cameron D, Papanicolaou George J, Patel Kushang V, Singleton Andrew B, Takahashi Atsushi, Tang Hua, Taylor Herman A, Taylor Kent, Thomson Cynthia, Yanek Lisa R, Yang Lingyao, Ziv Elad, Zonderman Alan B, Folsom Aaron R, Evans Michele K, Liu Yongmei, Becker Diane M, Snively Beverly M, Wilson James |
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A CXCL2 polymorphism is associated with better outcomes in patients with severe sepsis.
Critical care medicine 2007 Oct 35 (10): 2292-7. Villar Jesús, Pérez-Méndez Lina, Flores Carlos, Maca-Meyer Nicole, Espinosa Elena, Muriel Arturo, Sangüesa Rubén, Blanco Jesús, Muros Mercedes, Kacmarek Robert |
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A CXCL2 tandem repeat promoter polymorphism is associated with susceptibility to severe sepsis in the Spanish population.
Genes and immunity 2006 Mar 7 (2): 141-9. Flores C, Maca-Meyer N, Pérez-Méndez L, Sangüesa R, Espinosa E, Muriel A, Blanco J, Villar J, , |
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Polymorphisms in the promoter regions of the CXCL1 and CXCL2 genes contribute to increased risk of alopecia areata in the Korean population.
Genetics and molecular research : GMR 0 14 (3): 9667-9674. Kim S K, Chung J-H, Park H J, Kang S W, Lim D-J, Byun S H, Baek D G, Ko H Y, Lew B-L, Baik2 And W-Y Sim H |
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- Page last updated:Feb 24, 2021
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