173 related articles for article (PubMed ID: 30641209)
21. The association of genetic polymorphisms of hypoxia inducible factor-1 alpha and vascular endothelial growth factor with increased risk of chronic obstructive pulmonary disease: A case-control study.
Yu ZG; Wang BZ; Cheng ZZ
Kaohsiung J Med Sci; 2017 Sep; 33(9):433-441. PubMed ID: 28865600
[TBL] [Abstract][Full Text] [Related]
22. Impact on the Clinical Evolution of Patients with COVID-19 Pneumonia and the Participation of the
Soto ME; Fuentevilla-Álvarez G; Palacios-Chavarría A; Vázquez RRV; Herrera-Bello H; Moreno-Castañeda L; Torres-Paz YE; González-Moyotl NJ; Pérez-Torres I; Aisa-Alvarez A; Manzano-Pech L; Pérez-Torres I; Huesca-Gómez C; Gamboa R
Int J Mol Sci; 2022 Dec; 24(1):. PubMed ID: 36613859
[TBL] [Abstract][Full Text] [Related]
23. Genetic associations of Nrf2-encoding NFE2L2 variants with Parkinson's disease - a multicenter study.
von Otter M; Bergström P; Quattrone A; De Marco EV; Annesi G; Söderkvist P; Wettinger SB; Drozdzik M; Bialecka M; Nissbrandt H; Klein C; Nilsson M; Hammarsten O; Nilsson S; Zetterberg H
BMC Med Genet; 2014 Dec; 15():131. PubMed ID: 25496089
[TBL] [Abstract][Full Text] [Related]
24. Nrf2 expression is increased in peripheral blood mononuclear cells derived from mild-moderate ex-smoker COPD patients with persistent oxidative stress.
Fratta Pasini AM; Ferrari M; Stranieri C; Vallerio P; Mozzini C; Garbin U; Zambon G; Cominacini L
Int J Chron Obstruct Pulmon Dis; 2016; 11():1733-43. PubMed ID: 27555763
[TBL] [Abstract][Full Text] [Related]
25. [Polymorphic Variants of Glutamate Receptor (GRIK5, GRIN2B) and Serotonin Receptor (HTR2A) Genes Are Associated with Chronic Obstructive Pulmonary Disease].
Korytina GF; Akhmadishina LZ; Kochetova OV; Aznabaeva YG; Zagidullin SZ; Victorova TV
Mol Biol (Mosk); 2017; 51(4):603-614. PubMed ID: 28900078
[TBL] [Abstract][Full Text] [Related]
26. Relationship of vitamin D binding protein polymorphisms and lung function in Korean chronic obstructive pulmonary disease.
Jung JY; Choi DP; Won S; Lee Y; Shin JH; Kim YS; Kim SK; Oh YM; Suh I; Lee SD
Yonsei Med J; 2014 Sep; 55(5):1318-25. PubMed ID: 25048491
[TBL] [Abstract][Full Text] [Related]
27. Polymorphism in the Promoter Region of NFE2L2 Gene Is a Genetic Marker of Susceptibility to Cirrhosis Associated with Alcohol Abuse.
Nunes Dos Santos K; Florentino RM; França A; Lima Filho ACM; Santos MLD; Missiaggia D; Fonseca MC; Brasil Costa I; Vidigal PVT; Nathanson MH; Lemos FO; Leite MF
Int J Mol Sci; 2019 Jul; 20(14):. PubMed ID: 31340446
[TBL] [Abstract][Full Text] [Related]
28. Nrf2: friend and foe in preventing cigarette smoking-dependent lung disease.
Müller T; Hengstermann A
Chem Res Toxicol; 2012 Sep; 25(9):1805-24. PubMed ID: 22686525
[TBL] [Abstract][Full Text] [Related]
29. Genetic variation in antioxidant enzymes, cigarette smoking, and longitudinal change in lung function.
Tang W; Bentley AR; Kritchevsky SB; Harris TB; Newman AB; Bauer DC; Meibohm B; Cassano PA;
Free Radic Biol Med; 2013 Oct; 63():304-12. PubMed ID: 23688726
[TBL] [Abstract][Full Text] [Related]
30. Four SNPs and Systemic Level of FOXP3 in Smokers and Patients with Chronic Obstructive Pulmonary Disease.
Chu S; Zhong X; Zhang J; Lai X; Xie J; Li Y
COPD; 2016 Dec; 13(6):760-766. PubMed ID: 27310557
[TBL] [Abstract][Full Text] [Related]
31. Association Studies of HSPA1A and HSPA1L Gene Polymorphisms With Schizophrenia.
Kowalczyk M; Kucia K; Owczarek A; Suchanek-Raif R; Merk W; Paul-Samojedny M; Kowalski J
Arch Med Res; 2018 Jul; 49(5):342-349. PubMed ID: 30342847
[TBL] [Abstract][Full Text] [Related]
32. Genetic analysis of NFE2L2 promoter variation in Taiwanese Parkinson's disease.
Chen YC; Wu YR; Wu YC; Lee-Chen GJ; Chen CM
Parkinsonism Relat Disord; 2013 Feb; 19(2):247-50. PubMed ID: 23176750
[TBL] [Abstract][Full Text] [Related]
33. Nrf2-Keap1 signaling in oxidative and reductive stress.
Bellezza I; Giambanco I; Minelli A; Donato R
Biochim Biophys Acta Mol Cell Res; 2018 May; 1865(5):721-733. PubMed ID: 29499228
[TBL] [Abstract][Full Text] [Related]
34. Candidate genes for COPD in two large data sets.
Bakke PS; Zhu G; Gulsvik A; Kong X; Agusti AG; Calverley PM; Donner CF; Levy RD; Make BJ; Paré PD; Rennard SI; Vestbo J; Wouters EF; Anderson W; Lomas DA; Silverman EK; Pillai SG
Eur Respir J; 2011 Feb; 37(2):255-63. PubMed ID: 20562129
[TBL] [Abstract][Full Text] [Related]
35. Association of Nrf2-encoding NFE2L2 haplotypes with Parkinson's disease.
von Otter M; Landgren S; Nilsson S; Celojevic D; Bergström P; Håkansson A; Nissbrandt H; Drozdzik M; Bialecka M; Kurzawski M; Blennow K; Nilsson M; Hammarsten O; Zetterberg H
BMC Med Genet; 2010 Mar; 11():36. PubMed ID: 20196834
[TBL] [Abstract][Full Text] [Related]
36. Identification of genetic variants in the TNF promoter associated with COPD secondary to tobacco smoking and its severity.
Reséndiz-Hernández JM; Sansores RH; Hernández-Zenteno Rde J; Vargas-Alarcón G; Colín-Barenque L; Velázquez-Uncal M; Camarena A; Ramírez-Venegas A; Falfán-Valencia R
Int J Chron Obstruct Pulmon Dis; 2015; 10():1241-51. PubMed ID: 26170653
[TBL] [Abstract][Full Text] [Related]
37. Association of hsp70-2 (+1267A/G), hsp70-hom (+2437T/C), HMOX-1 (number of GT repeats) and TNF-alpha (+489G/A) polymorphisms with COPD in Croatian population.
Matokanović M; Rumora L; Popović-Grle S; Čepelak I; Čulić O; Barišić K
Clin Biochem; 2012 Jul; 45(10-11):770-4. PubMed ID: 22542718
[TBL] [Abstract][Full Text] [Related]
38. Association of the CAT-262C>T polymorphism with asthma in smokers and the nonemphysematous phenotype of chronic obstructive pulmonary disease.
Taniguchi N; Konno S; Isada A; Hattori T; Kimura H; Shimizu K; Maeda Y; Makita H; Hizawa N; Nishimura M
Ann Allergy Asthma Immunol; 2014 Jul; 113(1):31-36.e2. PubMed ID: 24824229
[TBL] [Abstract][Full Text] [Related]
39. Gene-expression signature regulated by the KEAP1-NRF2-CUL3 axis is associated with a poor prognosis in head and neck squamous cell cancer.
Namani A; Matiur Rahaman M; Chen M; Tang X
BMC Cancer; 2018 Jan; 18(1):46. PubMed ID: 29306329
[TBL] [Abstract][Full Text] [Related]
40. Keap1/Nrf2 pathway in kidney cancer: frequent methylation of KEAP1 gene promoter in clear renal cell carcinoma.
Fabrizio FP; Costantini M; Copetti M; la Torre A; Sparaneo A; Fontana A; Poeta L; Gallucci M; Sentinelli S; Graziano P; Parente P; Pompeo V; De Salvo L; Simone G; Papalia R; Picardo F; Balsamo T; Flammia GP; Trombetta D; Pantalone A; Kok K; Paranita F; Muscarella LA; Fazio VM
Oncotarget; 2017 Feb; 8(7):11187-11198. PubMed ID: 28061437
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
