Associated Papers
Genomic alterations in ovarian endometriosis and subsequently diagnosed ovarian carcinoma.
Linder A et al.
Human Reproduction (oxford, England), 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
Genetic Polymorphisms Involved in Bladder Cancer: A Global Review.
Kourie HR et al.
Oncology Reviews, 2023
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
Genetic susceptibility of bladder cancer in the Lebanese population.
Kourie HR et al.
Bmc Medical Genomics, 2022
The polymorphisms of extracellular matrix-remodeling genes are associated with pelvic organ prolapse.
Li L et al.
International Urogynecology Journal, 2022
Integration of Transcriptome and Exome Genotyping Identifies Significant Variants with Autism Spectrum Disorder.
Almandil NB et al.
Pharmaceuticals (basel, Switzerland), 2022
Analysis of ALK, IDH1, IDH2 and MMP8 somatic mutations in differentiated thyroid cancers.
Murugan AK et al.
Molecular and Clinical Oncology, 2021
Why does SARS-CoV-2 hit in different ways? Host genetic factors can influence the acquisition or the course of COVID-19.
Monticelli M et al.
European Journal of Medical Genetics, 2021
Polymorphisms of the matrix metalloproteinase genes are associated with essential hypertension in a Caucasian population of Central Russia.
Moskalenko M et al.
Scientific Reports, 2021
Impacts of Chemokine (C-X-C Motif) Receptor 2 C1208T Polymorphism on Cancer Susceptibility.
Zhou J et al.
Journal of Immunology Research, 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
Genomic profiling of colorectal cancer with isolated lung metastasis.
Zhang N et al.
Cancer Cell International, 2020
MMP-8 C-799 T, Lys460Thr, and Lys87Glu variants are not related to risk of cancer.
Zhang LF et al.
Bmc Medical Genetics, 2019
Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromes.
Soukupova J et al.
Plos One, 2018
DiMeX: A Text Mining System for Mutation-Disease Association Extraction.
Mahmood AS et al.
Plos One, 2016
MMP-8 genotypes influence the inflammatory response in human endotoxemia.
Rella JM et al.
Inflammation, 2014
Uncommon GNAQ, MMP8, AKT3, EGFR, and PIK3R1 mutations in thyroid cancers.
Murugan AK et al.
Endocrine Pathology, 2011
Missense polymorphisms in matrix metalloproteinase genes and skin cancer risk.
Nan H et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2008
Matrix metalloproteinase polymorphisms are associated with bladder cancer invasiveness.
Kader AK et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2007
Matrix metalloproteinase polymorphisms and bladder cancer risk.
Kader AK et al.
Cancer Research, 2006