Human Genome Epidemiology Literature Finder
Records 1 - 14 (of 14 Records) |
Query Trace: Syndrome and MMP9[original query] |
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Matrix metalloproteinase 9 (MMP-9) gene polymorphism and MMP-9 plasma levels in primary Sjogren's syndrome. Rheumatology (Oxford, England) 2004 Dec 43 (12): 1476-9. Hulkkonen J, Pertovaara M, Antonen J, Pasternack A, Hurme M, Pöllänen P, Lehtimäki |
Genetic polymorphisms of macrophage-mediators in Guillain-Barré syndrome. Journal of neuroimmunology 2007 Oct 190 (1-2): 127-30. Geleijns Karin, Emonts Marieke, Laman Jon D, van Rijs Wouter, van Doorn Pieter A, Hermans Peter W M, Jacobs Bart |
Role of functional single nucleotide polymorphisms of MMP1, MMP2, and MMP9 in open angle glaucomas. Molecular vision 2010 16 1764-70. Mossböck Georg, Weger Martin, Faschinger Christoph, Zimmermann Christine, Schmut Otto, Renner Wilfried, El-Shabrawi Yos |
The selected genetic polymorphisms of metalloproteinases MMP2, 7, 9 and MMP inhibitor TIMP2 in sarcoidosis. Medical science monitor : international medical journal of experimental and clinical research 2011 Oct 17 (10): CR598-607. Piotrowski Wojciech J, Górski Pawe?, Pietras Tadeusz, Fendler Wojciech, Szemraj Janu |
Variations in matrix metalloproteinase-1, -3, and -9 genes and the risk of acute coronary syndrome and coronary artery disease in the Chinese Han population. Coronary artery disease 2013 Jan . Xu X, Wang L, Xu C, Zhang P, Yong F, Liu H, Wang J, Shi Y |
High serum level of matrix metalloproteinase 9 and promoter polymorphism - 1562 C:T as a new risk factor for metabolic syndrome. DNA and cell biology 2014 Nov 33 (11): 816-22. Yadav Suraj S, Mandal Raju K, Singh Manish K, Verma Archna, Dwivedi Pradeep, Sethi Rishi, Usman Kauser, Khattri Sanj |
[Analysis of genotype combinations at the polymorphic points of the promoter regions of the genes of three matrix metalloproteinases and the gene of vascular endothelial growth factor (VEGF) in patients with history of acute myocardial infarction]. Terapevticheski? arkhiv 2014 86 (4): 19-24. Shevchenko A V, Konenkov V I, Prokof'ev V F, Pokushalov E |
Association of Nitric Oxide Synthase and Matrix Metalloprotease Single Nucleotide Polymorphisms with Preeclampsia and Its Complications. PloS one 2015 10 (8): e0136693. Leonardo Daniela P, Albuquerque Dulcinéia M, Lanaro Carolina, Baptista Letícia C, Cecatti José G, Surita Fernanda G, Parpinelli Mary A, Costa Fernando F, Franco-Penteado Carla F, Fertrin Kleber Y, Costa Maria Lau |
Splenomegaly and Its Associations with Genetic Polymorphisms and Treatment Outcome in Colorectal Cancer Patients Treated with Adjuvant FOLFOX. Cancer research and treatment : official journal of Korean Cancer Association 2016 Jul 48 (3): 990-7. Kim Mi-Jung, Han Sae-Won, Lee Dae-Won, Cha Yongjun, Lee Kyung-Hun, Kim Tae-Yong, Oh Do-Youn, Kim Se Hyung, Im Seock-Ah, Bang Yung-Jue, Kim Tae-Y |
Association of matrix metalloproteinase-9 polymorphism with severity of Guillain-Barré syndrome. Journal of the neurological sciences 2020 May 415 116908. Hayat Shoma, Ahmad Oyishee, Mahmud Ishtiaq, Howlader Md Zakir Hossain, Islam Zhahir |
Association of single nucleotide polymorphisms in the CD209, MMP9, TNFA and IFNG genes with susceptibility to Japanese encephalitis in children from North India. Gene 2021 9 808 145962. Deval Hirawati, Alagarasu Kalichamy, Srivastava Neha, Bachal Rupali, Mittal Mahima, Agrawal Apoorv, Bote Minal, Gondhalekar Aniket, Bondre Vijay P, Kant Raj |
Possibilities of Multilayer Perceptron in Complexing Risk Factors of Diabetic Foot Syndrome. Bulletin of experimental biology and medicine 2022 Aug 173 (4): 415-418. Troitskaya N I, Shapovalov K G, Mudrov V |
Association of the matrix metalloproteinases (MMPs) family gene polymorphisms and the risk of coronavirus disease 2019 (COVID-19); implications of contribution for development of neurological symptoms in the COVID-19 patients. Molecular biology reports 2022 11 50 (1): 173-183. Ramezani Samaneh, Ezzatifar Fatemeh, Hojjatipour Tahereh, Hemmatzadeh Maryam, Shabgah Arezoo Gowhari, Navashenaq Jamshid Gholizadeh, Aslani Saeed, Shomali Navid, Arabi Mohsen, Babaie Farhad, Jadidi-Niaragh Farhad, Hosseinzadeh Ramin, Feizisani Fahimeh, Khodayar Sara, Safari Roghaiyeh, Mohammadi Ham |
Influence of matrix metalloproteinase 9 variant rs17576 on ischemic stroke risk and severity in acute coronary syndrome. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2024 6 33 (8): 107824. Neda M Bogari, Hind Mansour Naffadi, Ahmad O Babalghith, Zohor Asaad Azher, Iman Sabri Abumansour, Ehab M Melibary, Muneera Qattan, Amaal M Alluhaibi, Amr A Amin, Mustafa Bogari, Dema Neda Bogari, Rami Obaid, Reem M All |
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