Citations (25)
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Amel Ben Anes, Hela Ben Nasr, Abdelhamid Garrouche, Sarra Bchir, Zaineb Dhaouefi, Elyes Chabchoub, Zouhair Tabka & Karim Chahed. (2019) The Cu/Zn superoxide dismutase +35A/C (rs2234694) variant correlates with altered levels of protein carbonyls and glutathione and associates with severity of COPD in a Tunisian population. Free Radical Research 53:3, pages 293-303.
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Bo Gong, Yi Shi, Chao Qu, Zimeng Ye, Yilin Yin, Chang Tan, Ping Shuai, Jing Li, Xiaoxin Guo, Yilian Cheng, Zhenglin Yang, Ying Lin & Xiaoqi Liu. (2018) Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population. Ophthalmic Genetics 39:1, pages 35-40.
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Khaled K. Abu-Amero, Altaf A. Kondkar, Ahmed Mousa, Essam A. Osman & Saleh A. Al-Obeidan. (2013) Analysis of Catalase SNP rs1001179 in Saudi patients with Primary Open Angle Glaucoma. Ophthalmic Genetics 34:4, pages 223-228.
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Articles from other publishers (22)
Marcin Kosmalski, Izabela Szymczak-Pajor, Józef Drzewoski & Agnieszka Śliwińska. (2023) Non-Alcoholic Fatty Liver Disease Is Associated with a Decreased Catalase (CAT) Level, CT Genotypes and the T Allele of the -262 C/T CAT Polymorphism. Cells 12:18, pages 2228.
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Larissa Alves Maciel, Patrício Lopes de Araújo Leite, Patrick Anderson Santos, Lucas Pinheiro Barbosa, Sara Duarte Gutierrez, Lysleine Alves Deus, Márcia Cristiane Araújo, Samuel da Silva Aguiar, Thiago Santos Rosa, John E. Lewis & Herbert Gustavo Simões. (2023) Intensity of Depression Symptoms Is Negatively Associated with Catalase Activity in Master Athletes. International Journal of Environmental Research and Public Health 20:5, pages 4397.
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Dipak A. Kadam, Saurabh D. Kalamkar, Amit Saraf, Imran Pathan, Jhankar Acharya, Komal Pekhale, Yogesh Shouche, Kavita Lole, Saroj Ghaskadbi & Richa Ashma. (2022) SNPs in the catalase promoter: a study based on Indian diabetic individuals. International Journal of Diabetes in Developing Countries 43:1, pages 155-162.
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Kanchan V. Pipal, Manju Mamtani, Ashwini A. Patel, Sujeet G. Jaiswal, Manisha T. Jaisinghani & Hemant Kulkarni. (2022) Susceptibility Loci for Type 2 Diabetes in the Ethnically Endogamous Indian Sindhi Population: A Pooled Blood Genome-Wide Association Study. Genes 13:8, pages 1298.
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Maria Bove, Adriano Lama, Stefania Schiavone, Claudio Pirozzi, Paolo Tucci, Vladyslav Sikora, Giovanna Trinchese, Gaetano Corso, Maria Grazia Morgese & Luigia Trabace. (2022) Social isolation triggers oxidative status and impairs systemic and hepatic insulin sensitivity in normoglycemic rats. Biomedicine & Pharmacotherapy 149, pages 112820.
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Makedonka Atanasovska Velkovska, Katja Goričar, Tanja Blagus, Vita Dolžan & Barbara Cvenkel. (2021) Association of Genetic Polymorphisms in Oxidative Stress and Inflammation Pathways with Glaucoma Risk and Phenotype. Journal of Clinical Medicine 10:5, pages 1148.
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Rok Herman, Mojca Jensterle, Andrej Janež, Katja Goričar & Vita Dolžan. (2020) Genetic Variability in Antioxidative and Inflammatory Pathways Modifies the Risk for PCOS and Influences Metabolic Profile of the Syndrome. Metabolites 10:11, pages 439.
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Yuan Sun, Suiyan Li, Hongwei Liu, Yan Gong, Huai Bai, Wei Huang, Qingqing Liu, Linbo Guan & Ping Fan. (2019) Association of GPx1 P198L and CAT C-262T Genetic Variations With Polycystic Ovary Syndrome in Chinese Women. Frontiers in Endocrinology 10.
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Nisa Decharatchakul, Chatri Settasatian, Nongnuch Settasatian, Nantarat Komanasin, Upa Kukongviriyapan, Phongsak Intharaphet & Vichai Senthong. (2019)
Association of genetic polymorphisms in
SOD2
,
SOD3
,
GPX3
, and
GSTT1
with hypertriglyceridemia and low HDL-C level in subjects with high risk of coronary artery disease
. PeerJ 7, pages e7407.
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Mohammad Reza Salahshoor, Maryam Sohrabi, Faramarz Jalili, Parnian Jalili, Negin Rezavand, Lida Haghnazari & Cyrus Jalili. (2018)
No evidence for a major effect of three common polymorphisms of the
GPx1
,
MnSOD
, and
CAT
genes on PCOS susceptibility
. Journal of Cellular Biochemistry 120:2, pages 2362-2369.
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César Hernández-Guerrero, Alicia Parra-Carriedo, Diana Ruiz-de-Santiago, Oscar Galicia-Castillo, Mario Buenrostro-Jáuregui & Carmen Díaz-Gutiérrez. (2018) Genetic polymorphisms of antioxidant enzymes CAT and SOD affect the outcome of clinical, biochemical, and anthropometric variables in people with obesity under a dietary intervention. Genes & Nutrition 13:1.
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Rohia Alili, Valérie Nivet-Antoine, Antonin Saldmann, Jean-Louis Golmard, Charles-Henry Cottart, Christelle Laguillier, Philippe Giral, Jean-Louis Beaudeux, Jean-Luc Bouillot, Christine Poitou, Karine Clément & Marylise Hébert-Schuster. (2018) Human catalase gene promoter haplotype and cardiometabolic improvement after bariatric surgery. Gene 656, pages 17-21.
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Matthew W. Wong, Nady Braidy, Anne Poljak, Russell Pickford, Madhav Thambisetty & Perminder S. Sachdev. (2017) Dysregulation of lipids in Alzheimer's disease and their role as potential biomarkers. Alzheimer's & Dementia 13:7, pages 810-827.
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Antonis Goulas, Dimitrios Agapakis, Athanassios Apostolidis, Dimitra Gouda, Sotirios Anastassiadis, Christina Trakatelli, Christos Savopoulos & Apostolos I. Hatzitolios. (2016) Association of the Common Catalase Gene Polymorphism rs1001179 With Glycated Hemoglobin and Plasma Lipids in Hyperlipidemic Patients. Biochemical Genetics 55:1, pages 77-86.
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L Góth. (2016) Blood Catalase Activities, Catalase Gene Polymorphisms and Acatalasemia Mutations in Hungarian Patients with Diabetes Mellitus. Global Journal of Obesity, Diabetes and Metabolic Syndrome, pages 001-005.
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Mostafa Saadat & Shekoofeh Saadat. (2014) Genetic Polymorphism of CAT C-262 T and Susceptibility to Breast Cancer, a Case–Control Study and Meta-Analysis of the Literatures. Pathology & Oncology Research 21:2, pages 433-437.
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Terez Nagy, Erika Paszti, Miklos Kaplar, Harjit Pal Bhattoa & Laszlo Goth. (2015) Further acatalasemia mutations in human patients from Hungary with diabetes and microcytic anemia. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 772, pages 10-14.
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Jintana Sirivarasai, Sukhumpun Kaojarern, Suwannee Chanprasertyothin, Pachara Panpunuan, Krittaya Petchpoung, Aninthita Tatsaneeyapant, Krongtong Yoovathaworn, Thunyachai Sura, Sming Kaojarern & Piyamit Sritara. (2015) Environmental Lead Exposure, Catalase Gene, and Markers of Antioxidant and Oxidative Stress Relation to Hypertension: An Analysis Based on the EGAT Study. BioMed Research International 2015, pages 1-9.
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Natsuko Taniguchi, Satoshi Konno, Akira Isada, Takeshi Hattori, Hirokazu Kimura, Kaoruko Shimizu, Yukiko Maeda, Hironi Makita, Nobuyuki Hizawa & Masaharu Nishimura. (2014) Association of the CAT-262C>T polymorphism with asthma in smokers and the nonemphysematous phenotype of chronic obstructive pulmonary disease. Annals of Allergy, Asthma & Immunology 113:1, pages 31-36.e2.
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Khaled K Abu-Amero, Taif Anwar Azad, Ahmed Mousa, Essam A Osman, Tahira Sultan & Saleh A Al-Obeidan. (2013) A catalase promoter variant rs1001179 is associated with visual acuity but not with primary angle closure glaucoma in Saudi patients. BMC Medical Genetics 14:1.
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Kamel Mohammedi, Thiago A. Patente, Naïma Bellili-Muñoz, Fathi Driss, Maria Beatriz Monteiro, Ronan Roussel, Elizabeth J. Pavin, Nathalie Seta, Frédéric Fumeron, Mirela J. Azevedo, Luis H. Canani, Samy Hadjadj, Michel Marre, Maria Lúcia Corrêa-Giannella & Gilberto Velho. (2013) Catalase activity, allelic variations in the catalase gene and risk of kidney complications in patients with type 1 diabetes. Diabetologia 56:12, pages 2733-2742.
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László Góth & Teréz Nagy. (2013) Inherited catalase deficiency: Is it benign or a factor in various age related disorders?. Mutation Research/Reviews in Mutation Research 753:2, pages 147-154.
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