Association between matrix metalloproteinase-9 gene polymorphism and breast cancer in Brazilian women.
Clinics (Sao Paulo, Brazil)
VA Oliveira, DC Chagas, JR Amorim, RO Pereira, TA Nogueira, VML Borges, LM Campos-Verde, LM Martins, GP Rodrigues, EJ Nery Júnior, FA Sampaio, PV Lopes-Costa, JMCE Sousa, VC Silva, FCCD Silva, BBD Silva
Dataset of allele and genotype frequencies of the three functionally significant polymorphisms of the MMP genes in Russian patients with primary open-angle glaucoma, essential hypertension and peptic ulcer.
Data In Brief
O Minyaylo, D Starikova, M Moskalenko, I Ponomarenko, E Reshetnikov, V Dvornyk, M Churnosov
The relationship among GNB3 rs5443, PNPLA3 rs738409, GCKR rs780094 gene polymorphisms, type of maternal gestational weight gain and neonatal outcomes (STROBE-compliant article).
Medicine
C Mărginean, CO Mărginean, C Bănescu, LE Meliţ, F Tripon, M Iancu
The impact of changes in serum levels of metalloproteinase-2 and metalloproteinase-9 on pain perception in patients with disc herniation before and after surgery.
Journal Of Pain Research
P Kamieniak, J Bielewicz, J Kurzepa, B Daniluk, J Kocot, T Trojanowski
Association of matrix metalloproteinase 2 and matrix metalloproteinase 9 gene polymorphism in aggressive and nonaggressive odontogenic lesions: A pilot study.
Journal Of Oral And Maxillofacial Pathology : Jomfp
D Aloka, SK Padmakumar, S Sathyan, M Sebastian, M Banerjee, VT Beena
Variants in matrix metalloproteinase-9 gene are associated with hemorrhagic transformation in acute ischemic stroke patients with atherothrombosis, small artery disease, and cardioembolic stroke.
Brain And Behavior
X Yi, G Sui, Q Zhou, C Wang, J Lin, Z Chai, J Zhou
Matrix metalloproteinase-9 gene polymorphisms are associated with ischemic stroke severity and early neurologic deterioration in patients with atrial fibrillation.
Brain And Behavior
X Yi, Q Zhou, G Sui, D Fan, Y Zhang, M Shao, Z Han, H Luo, J Lin, J Zhou
The relationship between MMP9 and ADRA2A gene polymorphisms and mothers-newborns' nutritional status: an exploratory path model (STROBE compliant article).
Pediatric Research
CO Mărginean, C Mărginean, C Bănescu, LE Meliţ, F Tripon, M Iancu
Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease.
Nature Communications
C Yao, G Chen, C Song, J Keefe, M Mendelson, T Huan, BB Sun, A Laser, JC Maranville, H Wu, JE Ho, P Courchesne, A Lyass, MG Larson, C Gieger, J Graumann, AD Johnson, J Danesh, H Runz, SJ Hwang, C Liu, AS Butterworth, K Suhre, D Levy
Association of R279Q and C1562T polymorphisms of matrix metalloproteinase 9 gene and increased risk for myocardial infarction in patients with premature coronary artery disease.
Exome sequencing deciphers a germline MET mutation in familial epidermal growth factor receptor-mutant lung cancer.
Cancer Science
N Tode, T Kikuchi, T Sakakibara, T Hirano, A Inoue, S Ohkouchi, T Tamada, T Okazaki, A Koarai, H Sugiura, T Niihori, Y Aoki, K Nakayama, K Matsumoto, Y Matsubara, M Yamamoto, A Watanabe, T Nukiwa, M Ichinose
Germline Genetic Variants in TEK, ANGPT1, ANGPT2, MMP9, FGF2 and VEGFA Are Associated with Pathologic Complete Response to Bevacizumab in Breast Cancer Patients.
Plos One
I Makhoul, VK Todorova, ER Siegel, SW Erickson, I Dhakal, VR Raj, JY Lee, MS Orloff, RJ Griffin, RS Henry-Tillman, S Klimberg, LF Hutchins, SA Kadlubar
Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin.
Plos One
TE Galesloot, N Verweij, M Traglia, C Barbieri, F van Dijk, AJ Geurts-Moespot, D Girelli, LA Kiemeney, FC Sweep, MA Swertz, P van der Meer, C Camaschella, D Toniolo, SH Vermeulen, P van der Harst, DW Swinkels
No associations of a set of SNPs in the Vascular Endothelial Growth Factor (VEGF) and Matrix Metalloproteinase (MMP) genes with survival of colorectal cancer patients.
Cancer Medicine
LA Dan, S Werdyani, J Xu, K Shestopaloff, A Hyde, E Dicks, B Younghusband, J Green, P Parfrey, W Xu, S Savas
Matrix metalloproteinase 9 gene polymorphisms are associated with a multiple family history of gastric cancer.
Gastric Cancer : Official Journal Of The International Gastric Cancer Association And The Japanese Gastric Cancer Association
R Okada, M Naito, Y Hattori, T Seiki, K Wakai, H Nanri, M Watanabe, S Suzuki, TS Kairupan, N Takashima, H Mikami, K Ohnaka, Y Watanabe, S Katsuura-Kamano, M Kubo, N Hamajima, H Tanaka,
Genetic variants associated with colorectal brain metastases susceptibility and survival.
The Pharmacogenomics Journal
S Stremitzer, AS Berghoff, NB Volz, W Zhang, D Yang, S Stintzing, Y Ning, Y Sunakawa, S Yamauchi, A Sebio, S Matsusaka, S Okazaki, D Hanna, A Parekh, A Mendez, MD Berger, R El-Khoueiry, P Birner, M Preusser, HJ Lenz
A variant in the osteoprotegerin gene is associated with coronary atherosclerosis in patients with rheumatoid arthritis: results from a candidate gene study.
International Journal Of Molecular Sciences
CP Chung, JF Solus, A Oeser, C Li, P Raggi, JR Smith, CM Stein
The GC + CC genotype at position -418 in TIMP-2 promoter and the -1575GA/-1306CC genotype in MMP-2 is genetic predisposing factors for prevalence of moyamoya disease.
Bmc Neurology
YS Park, YJ Jeon, HS Kim, IB Han, SH Oh, DS Kim, NK Kim