Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 47 Records) |
Query Trace: Syndrome and IL10[original query] |
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Hypertriglyceridemia-induced pancreatitis and risk of persistent systemic inflammatory response syndrome. The American journal of the medical sciences 2014 12 349 (3): 206-11. Bosques-Padilla Francisco J, Vázquez-Elizondo Genaro, González-Santiago Omar, Del Follo-Martínez Lourdes, González Oscar P, González-González Jose A, Maldonado-Garza Héctor J, Garza-González Elvi |
Peripheral blood-derived cytokine gene polymorphisms and metabolic profile in women with polycystic ovary syndrome. Cytokine 2015 Jun . Sóter Mirelle O, Ferreira Cláudia N, Sales Mariana F, Candido Ana L, Reis Fernando M, Milagres Kátia S, Ronda Carla, Silva Ieda O, Sousa Marinez O, Gomes Karina |
Analysis of IL10 haplotypes in primary Sjögren's syndrome patients from Western Mexico: Relationship with mRNA expression, IL-10 soluble levels, and autoantibodies. Human immunology 2015 Jul 76 (7): 473-9. Vázquez-Villamar M, Palafox-Sánchez C A, Muñoz-Valle J F, Valle Y, Orozco-Barocio G, Hernández-Bello J, Oregon-Romero |
A meta-analysis of immunogenetic Case-Control Association Studies in irritable bowel syndrome. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2015 May 27 (5): 717-27. Czogalla B, Schmitteckert S, Houghton L A, Sayuk G S, Camilleri M, Olivo-Diaz A, Spiller R, Wouters M M, Boeckxstaens G, Bermejo J Lorenzo, Niesler |
Clinical associations of host genetic variations in the genes of cytokines in critically ill patients. Clinical and experimental immunology 2015 Jun 180 (3): 531-41. Belopolskaya O B, Smelaya T V, Moroz V V, Golubev A M, Salnikova L |
Interleukin 10 (- 1082 G/A) and (- 819 C/T) gene polymorphisms in Egyptian women with polycystic ovary syndrome (PCOS). Meta gene 2016 Sep 9 254-8. Talaat Roba M, Mohamed Yasmin A, Mohamad Ehab H, Elsharkawy Marwa, Guirgis Adel |
Cytokine-related and sodium channel polymorphism as candidate predisposing factors for childhood encephalopathy FIRES/AERRPS. Journal of the neurological sciences 2016 Sep 368 272-6. Saitoh M, Kobayashi K, Ohmori I, Tanaka Y, Tanaka K, Inoue T, Horino A, Ohmura K, Kumakura A, Takei Y, Hirabayashi S, Kajimoto M, Uchida T, Yamazaki S, Shiihara T, Kumagai T, Kasai M, Terashima H, Kubota M, Mizuguchi |
[THE RELATIONSHIP BETWEEN POLYMORPHISMS OF G-1082A AND C-592A LOCI OF THE IL10 GENE AND MULTIFOCAL ATHEROSCLEROSIS IN PATIENTS WITH ACUTE CORONARY SYNDROME WITHOUT SEGMENT ST ELEVATION]. Klinicheskaia meditsina 2016 3 93 (11): 28-34. Berns S A, Shmidt E A, Makeeva O A, Golikova A A, Ivanova T B, Nagirnyak O A, Barbarash O |
Candidate gene variants of the immune system and sudden infant death syndrome. International journal of legal medicine 2016 Mar . Fard Delnaz, Läer Katharina, Rothämel Thomas, Schürmann Peter, Arnold Matthias, Cohen Marta, Vennemann Mechtild, Pfeiffer Heidi, Bajanowski Thomas, Pfeufer Arne, Dörk Thilo, Klintschar Micha |
Contribution of IL-10 and its -592 A/C polymorphism to cognitive functions in first-episode drug-naive schizophrenia. Brain, behavior, and immunity 2016 Mar . Xiu Mei Hong, Tian Li, Chen Song, Tan Yun Long, Chen Da Chun, Chen Jing, Chen Nan, De Yang Fu, Licinio Julio, Kosten Thomas R, Soares Jair C, Zhang Xiang Ya |
HPA axis dysregulation, NR3C1 polymorphisms and glucocorticoid receptor isoforms imbalance in metabolic syndrome. Diabetes/metabolism research and reviews 2016 Aug . Martins Clarissa Silva, Elias Daniel, Colli Leandro Machado, Couri Carlos Eduardo, Souza Manoel Carlos L A, Moreira Ayrton C, Foss Milton C, Elias Lucila L K, de Castro Margar |
Association of anti-inflammatory cytokine IL10 polymorphisms with motoric cognitive risk syndrome in an Ashkenazi Jewish population. Neurobiology of aging 2017 10 58 238.e1-238.e8. Sathyan Sanish, Barzilai Nir, Atzmon Gil, Milman Sofiya, Ayers Emmeline, Verghese J |
Influence of IL1B, IL6 and IL10 gene variants and plasma fatty acid interaction on metabolic syndrome risk in a cross-sectional population-based study. Clinical nutrition (Edinburgh, Scotland) 2017 Feb . Maintinguer Norde Marina, Oki Erica, Ferreira Carioca Antonio Augusto, Teixeira Damasceno Nágila Raquel, Fisberg Regina Mara, Lobo Marchioni Dirce Maria, Rogero Marcelo Mace |
Interaction between Herpes Virus Infections and IL10 and Risk of Bone Marrow Suppression. International journal of organ transplantation medicine 2018 11 9 (3): 119-125. Yaghobi R, Alizadeh F, Khodavandi |
Genetic variations in inflammation-related genes and their influence on the susceptibility of pediatric acute lung injury in a Chinese population. Gene 2018 Nov . Zhao Xinqian, He Jing, Xie Guoyan, Xu Song, Xie Jun, Chen Youyuan, Wu H |
Association between interleukin-10 genetic variant (-1082G>A) with detection and severity of respiratory distress syndrome in preterm neonates. International journal of immunogenetics 2019 Sep . Al-Shaer Osama S, Behiry Eman G, Elsadek Akram E, Salama Shaimaa |
Interleukin 10 gene polymorphisms and frailty syndrome in elderly Mexican people: (Sadem study). Molecular genetics & genomic medicine 2019 Aug e918. Juárez-Cedillo Teresa, Vargas-Alarcón Gilberto, Martínez-Rodríguez Nancy, Juárez-Cedillo Enrique, Fragoso José Manuel, Escobedo-de-la-Peña Jor |
Functional dyspepsia susceptibility is associated with TGFB1 gene polymorphisms (RS4803455, RS1800469) in H pylori-negative Chinese population. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2019 Aug e13681. Cheung Cynthia K Y, Lan Lin Lin, Chan Yawen, Yuen Kay, Cheong Pui Kuan, Fang Fanny, Wu Justin C |
SNP variations in IL10, TNF? and TNFAIP3 genes in patients with dry eye syndrome and Sjogren's syndrome. Journal of inflammation (London, England) 2019 16 6. Ben-Eli Hadas, Gomel Nir, Aframian Doron Jacob, Abu-Seir Rania, Perlman Riki, Ben-Chetrit Eldad, Mevorach Dror, Kleinstern Geffen, Paltiel Ora, Solomon Abrah |
STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren's Syndrome: Association with Disease Susceptibility and Clinical Aspects. Journal of immunology research 2019 2019 7682827. Colafrancesco Serena, Ciccacci Cinzia, Priori Roberta, Latini Andrea, Picarelli Giovanna, Arienzo Francesca, Novelli Giuseppe, Valesini Guido, Perricone Carlo, Borgiani Pao |
Common Inflammation-Related Candidate Gene Variants and Acute Kidney Injury in 2647 Critically Ill Finnish Patients. Journal of clinical medicine 2019 Mar 8 (3): . Vilander Laura M, Vaara Suvi T, Kaunisto Mari A, Pettilä Ville, Study Group The Finna |
Candidate single nucleotide polymorphisms of irritable bowel syndrome: a systemic review and meta-analysis. BMC gastroenterology 2019 Oct 19 (1): 165. Zhu Shiwei, Wang Ben, Jia Qiong, Duan Lipi |
Common genetic susceptibility loci link PFAPA syndrome, Behçet's disease, and recurrent aphthous stomatitis. Proceedings of the National Academy of Sciences of the United States of America 2020 6 117 (25): 14405-14411. Manthiram Kalpana, Preite Silvia, Dedeoglu Fatma, Demir Selcan, Ozen Seza, Edwards Kathryn M, Lapidus Sivia, Katz Alexander E, , Feder Henry M, Lawton Maranda, Licameli Greg R, Wright Peter F, Le Julie, Barron Karyl S, Ombrello Amanda K, Barham Beverly, Romeo Tina, Jones Anne, Srinivasalu Hemalatha, Mudd Pamela A, DeBiasi Roberta L, Gül Ahmet, Marshall Gary S, Jones Olcay Y, Chandrasekharappa Settara C, Stepanovskiy Yuriy, Ferguson Polly J, Schwartzberg Pamela L, Remmers Elaine F, Kastner Daniel |
[Predicting the development of adverse events in patients with acute coronary syndrome including genetics in the long-term follow-up]. Kardiologiia 2020 Mar 60 (4): 77-85. Shmidt E A, Berns S A, Ponasenko A V, Klimenkova A V, Tumanova S A, Litvinova M N, Barbarash O |
SNPs and transcriptional activity of genes of innate and adaptive immunity at the maternal-fetal interface in woman with preterm labour, associated with preterm premature rupture of membranes. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2020 73 (1): 25-30. Lyubomirskaya Ekaterina S, Kamyshnyi Alexandr M, Krut Yuriy Ya, Smiianov Vladyslav A, Fedoniuk Larisa Ya, Romanyuk Lidiya B, Kravets Natalya Ya, Mochulska Oksana |
A First Step for the Molecular Characterization of Neurological Involvement of Behçet Syndrome: an Italian Pivotal Study. Journal of molecular neuroscience : MN 2020 11 71 (6): 1284-1289. Padula Maria Carmela, Leccese Pietro, Lascaro Nancy, Padula Angela Anna, Carbone Teresa, Martelli Giuseppe, D'Angelo Salvato |
Pattern recognition receptor CD14 gene polymorphisms in alcohol use disorder patients and its Influence on liver disease susceptibility. Frontiers in immunology 2022 13 975027. Roy Neelanjana, Nadda Neeti, Kumar Hem, Prasad Chandreswar, Kumar Jha Jyotish, Pandey Hem Chandra, Vanamail Perumal, Saraya Anoop, Balhara Yatan Pal Singh, Shalimar , Nayak Baibaswa |
Sex and Gender Differences in Overlap Syndrome of Functional Gastrointestinal Disorder and Effect of Genetic Polymorphisms in South Korea: A Long-term Follow-up Study. Journal of neurogastroenterology and motility 2022 1 28 (1): 145-158. Lee Ju Yup, Kim Nayoung, Park Ji Hyun, Yu Jeong Eun, Song Yun Jeong, Yoon Jung Won, Lee Dong |
Association between interleukin-10 gene polymorphisms (rs1800871, rs1800872, and rs1800896) and severity of infection in different SARS-CoV-2 variants. Human genomics 2023 3 17 (1): 19. Abbood Sattar Jabbar Abbood, Anvari Enayat, Fateh Abolfa |
Association between genetic variants in TREM1, CXCL10, IL4, CXCL8 and TLR7 genes with the occurrence of congenital Zika syndrome and severe microcephaly. Scientific reports 2023 3 13 (1): 3466. Santos Camilla Natália Oliveira, Magalhães Lucas Sousa, Fonseca Adriana Barbosa de Lima, Bispo Ana Jovina Barreto, Porto Roseane Lima Santos, Alves Juliana Cardoso, Dos Santos Cliomar Alves, de Carvalho Jaira Vanessa, da Silva Angela Maria, Teixeira Mauro Martins, de Almeida Roque Pacheco, Dos Santos Priscila Lima, de Jesus Amélia Ribei |
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- Page last updated:Apr 22, 2024
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