TNF-α −308 G/A variant and susceptibility to chronic obstructive pulmonary disease: A systematic review and meta-analysis-Reference-Cited by-同舟云学术

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TNF-α −308 G/A variant and susceptibility to chronic obstructive pulmonary disease: A systematic review and meta-analysis

Published:2019-11 Issue: Volume:123 Page:154763
ISSN:1043-4666
Container-title:Cytokine
language:en
Short-container-title:Cytokine

Author:

Salimi Asl Mohammad,Ahmadi Ali,Salimian Jafar,Shohani Sepideh,Azimzadeh Jamalkandi Sadegh^ORCID,Ghanei Mostafa

Publisher

Elsevier BV

Subject

Molecular Biology,Hematology,Biochemistry,Immunology,Immunology and Allergy

Reference57 articles.

1. Burden and clinical features of chronic obstructive pulmonary disease (COPD);Pauwels;Lancet,2004

2. Standards for the diagnosis and care of patients with chronic obstructive pulmonary disease;Celli;Am. J. Respir. Crit. Care Med.,1995

3. Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease, 2014.

4. Tumor necrosis factors: developments during the last decade;Aggarwal;Eur. Cytokine Netw.,1996

5. Cellular and molecular characteristics of inflammation in chronic bronchitis;Sun;Eur. J. Clin. Invest.,1998

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1. Tumor necrosis factor‑α ‑308 G/A genetic polymorphism in patients with chronic obstructive pulmonary disease presenting with hyperactive airways;Biomedical Reports;2024-06-12

2. Association between single-nucleotide polymorphism of cytokines genes and chronic obstructive pulmonary disease: A systematic review and meta-analysis;Cytokine;2023-11

3. Risk of Tumor Necrosis Factor Alpha Inhibitors Usage and Related Adverse Effects;The Journal of Neurobehavioral Sciences;2023

4. Genetic Variants Associated with Chronic Obstructive Pulmonary Disease Risk: Cumulative Epidemiological Evidence from Meta-Analyses and Genome-Wide Association Studies;Canadian Respiratory Journal;2022-06-09

5. Association Between TNF-α-308, +489, −238 Polymorphism, and COPD Susceptibility: An Updated Meta-Analysis and Trial Sequential Analysis;Frontiers in Genetics;2022-01-21

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