HuGE Literature Finder
Records 1-30
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Endothelial Nitric Oxide Synthase (eNOS) Gene Polymorphisms and Markers of Hemolysis, Inflammation and Endothelial Dysfunction in Brazilian Sickle Cell Anemia Patients.
Biochemical genetics 2020 Apr . Chenou F, Albuquerque D M, Leonardo D P, Domingos I F, Bezerra M A C, Araújo A S, Blotta M H S L, Costa F F, Sonati M F, Paula E V, Santos M N |
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Reticulocyte count is the most important predictor of acute cerebral ischemia and high-risk transcranial Doppler in a newborn cohort of 395 children with sickle cell anemia.
Annals of hematology 2016 Aug . Belisário André Rolim, Sales Rahyssa Rodrigues, Toledo Nayara Evelin, Muniz Maristela Braga de Sousa Rodrigues, Velloso-Rodrigues Cibele, Silva Célia Maria, Viana Marcos Bora |
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Clinical events and their relation to the tumor necrosis factor-alpha and interleukin-10 genotypes in Sickle-Cell-Anemia patients.
Hematology/oncology and stem cell therapy 2015 Dec . Cavalcante J E A, Machado R P G, Laurentino M R, Santos T E J, Bandeira I C J, Filho P A Maia, Figueiredo M F, Martins A M C, Lemes R P |
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Depleted iron stores and iron deficiency anemia associated with reduced ferritin and hepcidin and elevated soluble transferrin receptors in a multiethnic group of preschool-age children.
Applied physiology, nutrition, and metabolism = Physiologie appliquée, nutrition et métabolisme 2015 Sep 40 (9): 887-94. Weiler Hope A, Jean-Philippe Sonia, Cohen Tamara R, Vanstone Catherine A, Agellon Sher |
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The association of cytokine genes polymorphisms and susceptibility to aplastic anemia in Egyptian patients.
Hematology (Amsterdam, Netherlands) 2015 Jul . Zayed Rania A, Abdel-Hamid Samah M, El-Lithy He |
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TNF-? -308 G>A polymorphism and risk of bone marrow failure syndrome: A meta-analysis.
Gene 2015 Jul 565 (1): 1-8. Chen Wancheng, Zhu Haili, Yu Lili, Lu Ziyuan, Yao Zhuoxin, Xiao Ya |
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Polymorphisms in TNF and IFNG are associated with clinical characteristics of aplastic anemia in Argentinean population.
Leukemia & lymphoma 2015 Jun 56 (6): 1793-8. Bestach Yesica, Sieza Yamila, Attie Myriam, Riccheri Cecilia, Verri Verónica, Bolesina Moira, Bengió Raquel, Larripa Irene, Belli Caroli |
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Genetic disposition and modifiable factors independently associated with anemia in patients with type 2 diabetes mellitus.
Diabetes research and clinical practice 2015 Apr 108 (1): 164-9. Chiou Terry Ting-Yu, Lee Jong-Jer, Wang Ming-Chung, Chung Min-Shien, Pan Lin-Lin, Hsieh Ching-Jung, Huang Siang-Ting, Chang Hsueh-Wen, Yang Kuender D, Lee Chien-Te, Liu Rue-Tsu |
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Association of alpha-thalassemia, TNF-alpha (-308G>A) and VCAM-1 (c.1238G>C) gene polymorphisms with cerebrovascular disease in a newborn cohort of 411 children with sickle cell anemia.
Blood cells, molecules & diseases 2015 Jan 54 (1): 44-50. Belisário André Rolim, Nogueira Frederico Lisboa, Rodrigues Rahyssa Sales, Toledo Nayara Evelin, Cattabriga Ana Luiza Moreira, Velloso-Rodrigues Cibele, Duarte Filipe Otávio Chaves, Silva Célia Maria, Viana Marcos Bora |
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Immunoregulatory cytokines gene polymorphisms in Egyptian patients affected with acquired aplastic anemia.
Annals of hematology 2014 Jun 93 (6): 923-9. El Mahgoub Iman R, Afify Reham A Aleem, Botros Shahira K A, Fawzy Ran |
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Chronic inflammatory state in sickle cell anemia patients is associated with HBB(*)S haplotype.
Cytokine 2014 Feb 65 (2): 217-21. Bandeira Izabel C J, Rocha Lillianne B S, Barbosa Maritza C, Elias Darcielle B D, Querioz José A N, Freitas Max Vitor Carioca, Gonçalves Romélia |
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Frequencies of -308G/A (TNFA) and -509C/T (TGFB1) polymorphisms in sickle cell anemia patients from Brazil.
Genetics and molecular research : GMR 2013 12 (4): 6762-6. Torres L S, Belini Júnior E, Silva D G, Lobo C L, Ruiz M A, Bonini-Domingos C |
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Association analysis of cytokine polymorphisms and plasma level in Northern Chinese Han patients with paroxysmal nocturnal hemoglobinuria.
Chinese medical journal 2012 May 125 (9): 1576-80. Wang Shu-Ye, Yang Xi-Jing, Yang Shan-Shan, Wang Wei, Tian Yao-Yao, Cao Feng-Lin, Zhou J |
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Pharmacogenetics of efficacy and safety of HCV treatment in HCV-HIV coinfected patients: significant associations with IL28B and SOCS3 gene variants.
PloS one 2012 7 (11): e47725. Vidal Francesc, López-Dupla Miguel, Laguno Montserrat, Veloso Sergi, Mallolas Josep, Murillas Javier, Cifuentes Carmen, Gallart Lluis, Auguet Teresa, Sampériz Gloria, Payeras Antoni, Hernandez Pilar, Arnedo Mireia, Gatell Josep Ma, Richart Cristób |
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The presence of -308A TNF? is associated with anemia and thrombocytopenia in patients with myelodysplastic syndromes.
Blood cells, molecules & diseases 2011 Dec 47 (4): 255-8. Belli Carolina B, Bestach Yesica, Sieza Yamila, Gelemur Marta, Giunta Mario, Flores María G, Watman Nora, Bengió Raquel, Larripa Ire |
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TNF-alpha and IL-8: serum levels and gene polymorphisms (-308G>A and -251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia.
Cytokine 2011 Nov 56 (2): 312-7. Cajado C, Cerqueira B A V, Couto F D, Moura-Neto J P, Vilas-Boas W, Dorea M J, Lyra I M, Barbosa C G, Reis M G, Goncalves M |
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Impact of immunogenetic polymorphisms in bone marrow failure syndromes.
Mini reviews in medicinal chemistry 2011 Jun 11 (6): 544-52. Serio B, Selleri C, Maciejewski J |
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Impact of cytokine gene polymorphisms on risk and treatment outcomes of aplastic anemia.
Annals of hematology 2011 May 90 (5): 515-21. Lee Yun-Gyoo, Kim Inho, Kim Jin Hee, Bae Ji-Yeon, Kwon Ji-Hyun, Shin Dong-Yeop, Lee Jong-Eun, Song Eun Young, Kim Hyun Kyoung, Yoon Sung-Soo, Park Sung Sup, Lee Dong Soon, Han Kyou-Sup, Park Myoung Hee, Hong Yun-Chul, Park Seonyang, Kim Byoung Ko |
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Absence of Association between TNF-? Polymorphism and Cerebral Large-Vessel Abnormalities in Adults with Sickle Cell Anemia.
Acta haematologica 2010 Dec 125 (3): 3. Vicari P, Silva GS, Nogutti MA, Neto FM, Dos Santos NJ, Massaro AR, Figueiredo MS |
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Ferroportin (SLC40A1) Q248H mutation is associated with lower circulating plasma tumor necrosis factor-alpha and macrophage migration inhibitory factor concentrations in African children.
Clinica chimica acta; international journal of clinical chemistry 2010 Sep 411 (17-18): 1248-52. Kasvosve Ishmael, Debebe Zufan, Nekhai Sergei, Gordeuk Victor |
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Haplotypes of IL-10 promoter variants are associated with susceptibility to severe malarial anemia and functional changes in IL-10 production.
Human genetics 2008 Dec 124 (5): 515-24. Ouma Collins, Davenport Gregory C, Were Tom, Otieno Michael F, Hittner James B, Vulule John M, Martinson Jeremy, Ong'echa John M, Ferrell Robert E, Perkins Douglas |
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Tumor necrosis factor SNP haplotypes are associated with iron deficiency anemia in West African children.
Blood 2008 Nov 112 (10): 4276-83. Atkinson Sarah H, Rockett Kirk A, Morgan Gareth, Bejon Philip A, Sirugo Giorgio, O'Connell Maria A, Hanchard Neil, Kwiatkowski Dominic P, Prentice Andrew |
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Confirmation of an association between the TNF(-308) promoter polymorphism and stroke risk in children with sickle cell anemia.
Stroke; a journal of cerebral circulation 2007 Aug 38 (8): 2241-6. Hoppe Carolyn, Klitz William, D'Harlingue Katherine, Cheng Suzanne, Grow Michael, Steiner Lori, Noble Janelle, Adams Robert, Styles Lori, |
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Cytokine gene polymorphisms in acquired bone marrow failure.
American journal of hematology 2007 Aug 82 (8): 721-4. Gidvani Vinod, Ramkissoon Shakti, Sloand Elaine M, Young Neal |
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Clinical importance of transforming growth factor-beta but not of tumor necrosis factor-alpha gene polymorphisms in patients with the myelodysplastic syndrome belonging to the refractory anemia subtype.
Pathobiology : journal of immunopathology, molecular and cellular biology 2005 72 (3): 165-70. Balog Attila, Borbényi Zita, Gyulai Zsófia, Molnár Lenke, Mándi Yvet |
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Genetic polymorphisms in patients with myelodysplastic syndrome.
Acta microbiologica et immunologica Hungarica 2005 52 (3-4): 463-75. Gyulai Zsófia, Balog A, Borbényi Zita, Mándi Yvet |
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Gene interactions and stroke risk in children with sickle cell anemia.
Blood 2004 Mar 103 (6): 2391-6. Hoppe Carolyn, Klitz William, Cheng Suzanne, Apple Ray, Steiner Lori, Robles Lara, Girard Tom, Vichinsky Elliott, Styles Lori, |
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Tumor necrosis factor alpha, its soluble receptor I, and -308 gene promoter polymorphism in patients with rheumatoid arthritis with or without amyloidosis: implications for the pathogenesis of nephropathy and anemia of chronic disease in reactive amyloidosis.
Arthritis and rheumatism 2003 Nov 48 (11): 3068-76. Maury C P J, Liljeström M, Laiho K, Tiitinen S, Kaarela K, Hurme |
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The TNF2 allele is a risk factor to severe aplastic anemia independent of HLA-DR.
Human immunology 2003 Sep 64 (9): 896-901. Peng Jun, Liu Chuanfang, Zhu Kunli, Zhu Yuanyuan, Yu Yuan, Li Jie, Hou Ming, Chen Xueliang, Xu Conggao, Zhang Maoho |
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Clinical relevance of the TNF-alpha promoter/enhancer polymorphism in patients with aplastic anemia.
Annals of hematology 2002 Oct 81 (10): 566-9. Demeter Judit, Messer Gerald, Schrezenmeier Hube |
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- Page last updated:Apr 14, 2021
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