Varaico: Literature-Extracted Genetic Variants

Gene:MMP9
Variant:p.Q279R
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MMP9

NM_004994.3:p.Q279R

Associated Papers

Analysis of the Role of Gene Variants in Matrix Metalloproteinases and Their Tissue Inhibitors in Bronchopulmonary Dysplasia (BPD): A Study in the Polish Population.

Szpecht D et al.

Current Issues in Molecular Biology, 2025

High-order single-nucleotide polymorphism interactions between selected anti-oxidant and protease genes influence North Indians' propensity for chronic obstructive pulmonary disease (COPD) and lung function parameters.

Kansal H et al.

Human Genomics, 2025

Proteogenomic Profiling of Treatment-Naïve Metastatic Malignant Melanoma.

Kuras M et al.

Cancers, 2025

40075679 (PubMed )
Supplement: cancers-17-00832-s001.zip › Table_S5._SAAVs.xlsx › Table_S5A

Genetic mutation and blue rubber bleb nevus syndrome: case reports and literature review.

Xing Y et al.

Frontiers in Genetics, 2025

Association of Matrix Metalloproteinases Polymorphisms with Glaucoma Risk, Glaucoma Phenotype, and Response to Treatment with Selective Laser Trabeculoplasty or Latanoprost.

Atanasovska Velkovska M et al.

International Journal of Molecular Sciences, 2024

39769228 (PubMed )
Supplement: ijms-25-13464-s001.zip › ijms-3311215-supplementary.pdf

The Association of MMP-2, MMP-9, and MMP-13 Gene Polymorphisms With Knee Osteoarthritis in the Greek Population.

Milaras C et al.

Cureus, 2024

Obesity-Dependent Association of the rs10454142 PPP1R21 with Breast Cancer.

Ponomarenko I et al.

Biomedicines, 2024

Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.

Yu H et al.

Elife, 2024

38277211 (PubMed )
Supplement: elife-89762-supp1.xlsx › Variants

Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.

Yu H et al.

Biorxiv : the Preprint Server for Biology, 2023

37292598 (PubMed )
Supplement: media-1.xlsx › Variants

Association between fibrosis-related gene polymorphism and long-term allograft outcome in renal transplant recipients.

Yin Y et al.

Bmc Medical Genomics, 2023

37867197 (PubMed )
Supplement: 12920_2023_1686_MOESM3_ESM.xlsx › Sheet1

Comprehensive Analysis of the Role of Gene Variants in Matrix Metalloproteinases and Their Tissue Inhibitors in Retinopathy of Prematurity: A Study in the Polish Population.

Choręziak-Michalak A et al.

International Journal of Molecular Sciences, 2023

New Genetically Determined Markers of the Functional State of the Cardiovascular System.

Kondakova EV et al.

Genes, 2023

Molecular Genetics of Thrombotic Myeloproliferative Neoplasms: Implications in Precision Oncology.

Chia YC et al.

Diagnostics (basel, Switzerland), 2023

Methodological quality assessment of genetic studies on brain arteriovenous malformation related hemorrhage: A cross-sectional study.

Jiang J et al.

Frontiers in Genetics, 2023

Gene polymorphisms of cyclin-dependent kinase inhibitor and matrix metalloproteinase-9 in Sudanese patients with esophageal squamous cell carcinoma.

Eltayeb MM et al.

Molecular Genetics & Genomic Medicine, 2022

Functionally significant polymorphisms of the MMP9 gene are associated with primary open-angle glaucoma in the population of Russia.

Ponomarenko I et al.

European Journal of Ophthalmology, 2022

Matrix Metalloproteinase Gene Polymorphisms Are Associated with Breast Cancer in the Caucasian Women of Russia.

Pavlova N et al.

International Journal of Molecular Sciences, 2022

The Modifying Effect of Obesity on the Association of Matrix Metalloproteinase Gene Polymorphisms with Breast Cancer Risk.

Pavlova N et al.

Biomedicines, 2022

Genetic susceptibility of bladder cancer in the Lebanese population.

Kourie HR et al.

Bmc Medical Genomics, 2022

36253817 (PubMed )
Supplement: 12920_2022_1372_MOESM1_ESM.xlsx › sheet_1

Effects of TIMP1 rs4898 Gene Polymorphism on Early-Onset Preeclampsia Development and Placenta Weight.

Mrozikiewicz AE et al.

Diagnostics (basel, Switzerland), 2022

Role of genetic polymorphisms in recurrent aphthous stomatitis: A systematic review and meta-analysis.

Yousefi H et al.

Cytokine, 2022

Germline Variants in Angiogenesis-Related Genes Contribute to Clinical Outcome in Head and Neck Squamous Cell Carcinoma.

Butkiewicz D et al.

Cancers, 2022

35406617 (PubMed )
Supplement: cancers-14-01844-s001.zip › cancers-1593018-supplementary.pdf

The polymorphisms of extracellular matrix-remodeling genes are associated with pelvic organ prolapse.

Li L et al.

International Urogynecology Journal, 2022

34973089 (PubMed )
Supplement: 192_2021_4917_MOESM1_ESM.xls › Sheet1

Novel Loss-of-Function Mutations in NPR2 Cause Acromesomelic Dysplasia, Maroteaux Type.

Wu J et al.

Frontiers in Genetics, 2022

35368703 (PubMed )
Supplement: DataSheet1.zip › 823861_SupMaterial › Data_Sheet_1.ZIP › raw_datas › patient_2__NGS_raw_data.xlsx › Sheet1

The risk of relapse in breast cancer patients is associated with MMP-9 gene polymorphism: a prospective study in a sample of the Iranian population.

Kohan L et al.

Nucleosides, Nucleotides & Nucleic Acids, 2022

Study on the Relationship between MMP-2, MMP-9 Gene Polymorphisms, and the Risk of Colorectal Cancer.

Peng S et al.

Evidence-based Complementary and Alternative Medicine : Ecam, 2022

Cardiovascular Pharmacogenomics: An Update on Clinical Studies of Antithrombotic Drugs in Brazilian Patients.

Hirata TDC et al.

Molecular Diagnosis & Therapy, 2021

Association of Matrix Metalloproteinase (MMP) Gene Polymorphisms With Knee Osteoarthritis: A Review of the Literature.

Milaras C et al.

Cureus, 2021

Functionally significant polymorphisms of the MMP-9 gene are associated with peptic ulcer disease in the Caucasian population of Central Russia.

Minyaylo O et al.

Scientific Reports, 2021

Interactions among variants in P53 apoptotic pathway genes are associated with neurologic deterioration and functional outcome after acute ischemic stroke.

Yi X et al.

Brain and Behavior, 2021

Peculiarities of Immune Regulation in Men of Perm Region with Atherosclerosis Related to Polymorphism of Candidate Genes.

Nikonoshina NA et al.

Bulletin of Experimental Biology and Medicine, 2021

Genetic Association between MMP9 and Choroidal Neovascularization in Age-Related Macular Degeneration.

Sohn EH et al.

Ophthalmology Science, 2021

Novel Data about Association of the Functionally Significant Polymorphisms of the MMP9 Gene with Exfoliation Glaucoma in the Caucasian Population of Central Russia.

Starikova D et al.

Ophthalmic Research, 2021

Association of the functionally significant polymorphisms of the MMP9 gene with H. pylori-positive gastric ulcer in the Caucasian population of Central Russia.

Dvornyk V et al.

Plos One, 2021

A protective polymorphism in MMP16, improved blood gas levels, and chronic obstructive pulmonary diseases: Family and two population-based studies.

Zhang Z et al.

Human Mutation, 2020

Role of matrix metalloproteinase-9 gene polymorphisms in glaucoma: A hospital-based study in Chinese patients.

Zhao F et al.

Journal of Clinical Laboratory Analysis, 2020

Matrix metalloproteinases as target genes for gene regulatory networks driving molecular and cellular pathways related to a multistep pathogenesis of cerebrovascular disease.

Polonikov A et al.

Journal of Cellular Biochemistry, 2019

Synergistic effects of TIMP2-418G/C and MMP9-1562C/T variants on the male infertility risk.

Roshankhah S et al.

Molecular Biology Reports, 2019

Cubilin Single Nucleotide Polymorphism Variants are Associated with Macroangiopathy While a Matrix Metalloproteinase-9 Single Nucleotide Polymorphism Flip-Flop may Indicate Susceptibility of Diabetic Nephropathy in Type-2 Diabetic Patients.

Albert C et al.

Nephron, 2019

Association of Matrix Metalloproteinase 9 (MMP-9) Polymorphisms with Asthma Risk: A Meta-Analysis.

Zou F et al.

Canadian Respiratory Journal, 2019

Evaluation of Matrix Metalloproteinase 9 Serum Concentration as a Biomarker in Malignant Mesothelioma.

Štrbac D et al.

Disease Markers, 2019

Comprehensive analysis of damage associated SNPs of MMP9 gene: A computational approach.

Bhatnager R et al.

Computational Biology and Chemistry, 2018

Matrix Metalloproteinases Polymorphisms as Baseline Risk Predictors in Malignant Pleural Mesothelioma.

Strbac D et al.

Radiology and Oncology, 2018

A matrix metalloproteinase 9 (MMP9) gene single nucleotide polymorphism is associated with predisposition to tick-borne encephalitis virus-induced severe central nervous system disease.

Barkhash AV et al.

Ticks and Tick-borne Diseases, 2018

Association of Polymorphism rs17576 of the Metalloproteinase 9 Gene with Gestational Diabetes in Euro-Brazilian Pregnant Women.

Costa CD et al.

Clinical Laboratory, 2018

The rs243866/243865 polymorphisms in MMP-2 gene and the relationship with BP control in obese resistant hypertensive subjects.

Ritter AMV et al.

Gene, 2018

Association of MMP-9 gene polymorphisms with nephrolithiasis patients.

Mehde AA et al.

Journal of Clinical Laboratory Analysis, 2018

A translational approach from an animal model identifies CD80 as a candidate gene for the study of bone phenotypes in postmenopausal women.

Panach L et al.

Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the Usa, 2017

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."