185 related articles for article (PubMed ID: 24102512)
1. Association of NFE2L2 and KEAP1 haplotypes with amyotrophic lateral sclerosis.
Bergström P; von Otter M; Nilsson S; Nilsson AC; Nilsson M; Andersen PM; Hammarsten O; Zetterberg H
Amyotroph Lateral Scler Frontotemporal Degener; 2014 Mar; 15(1-2):130-7. PubMed ID: 24102512
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Association of KEAP1 and NFE2L2 polymorphisms with temporal lobe epilepsy and drug resistant epilepsy.
Liu Z; Yin X; Liu L; Tao H; Zhou H; Ma G; Cui L; Li Y; Zhang S; Xu Z; Yao L; Cai Z; Zhao B; Li K
Gene; 2015 Oct; 571(2):231-6. PubMed ID: 26149655
[TBL] [Abstract][Full Text] [Related]
4. Nrf2-encoding NFE2L2 haplotypes influence disease progression but not risk in Alzheimer's disease and age-related cataract.
von Otter M; Landgren S; Nilsson S; Zetterberg M; Celojevic D; Bergström P; Minthon L; Bogdanovic N; Andreasen N; Gustafson DR; Skoog I; Wallin A; Tasa G; Blennow K; Nilsson M; Hammarsten O; Zetterberg H
Mech Ageing Dev; 2010 Feb; 131(2):105-10. PubMed ID: 20064547
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Level and course of FEV1 in relation to polymorphisms in NFE2L2 and KEAP1 in the general population.
Siedlinski M; Postma DS; Boer JM; van der Steege G; Schouten JP; Smit HA; Boezen HM
Respir Res; 2009 Aug; 10(1):73. PubMed ID: 19671143
[TBL] [Abstract][Full Text] [Related]
7. Genetic variations and haplotype structures of transcriptional factor Nrf2 and its cytosolic reservoir protein Keap1 in Japanese.
Fukushima-Uesaka H; Saito Y; Maekawa K; Kamatani N; Kajio H; Kuzuya N; Noda M; Yasuda K; Sawada J
Drug Metab Pharmacokinet; 2007 Jun; 22(3):212-9. PubMed ID: 17603223
[TBL] [Abstract][Full Text] [Related]
8. Lack of association between nuclear factor erythroid-derived 2-like 2 promoter gene polymorphisms and oxidative stress biomarkers in amyotrophic lateral sclerosis patients.
LoGerfo A; Chico L; Borgia L; Petrozzi L; Rocchi A; D'Amelio A; Carlesi C; Caldarazzo Ienco E; Mancuso M; Siciliano G
Oxid Med Cell Longev; 2014; 2014():432626. PubMed ID: 24672634
[TBL] [Abstract][Full Text] [Related]
9. Nuclear erythroid 2-related factor 2-antioxidative response element signaling pathway in motor cortex and spinal cord in amyotrophic lateral sclerosis.
Sarlette A; Krampfl K; Grothe C; Neuhoff Nv; Dengler R; Petri S
J Neuropathol Exp Neurol; 2008 Nov; 67(11):1055-62. PubMed ID: 18957896
[TBL] [Abstract][Full Text] [Related]
10. KEAP1 Genetic Polymorphisms Associate with Breast Cancer Risk and Survival Outcomes.
Hartikainen JM; Tengström M; Winqvist R; Jukkola-Vuorinen A; Pylkäs K; Kosma VM; Soini Y; Mannermaa A
Clin Cancer Res; 2015 Apr; 21(7):1591-601. PubMed ID: 25589623
[TBL] [Abstract][Full Text] [Related]
11. Interaction of Genetic Variations in
Santos LR; Durães C; Ziros PG; Pestana A; Esteves C; Neves C; Carvalho D; Bongiovanni M; Renaud CO; Chartoumpekis DV; Habeos IG; Simões MS; Soares P; Sykiotis GP
Thyroid; 2019 Sep; 29(9):1302-1315. PubMed ID: 31426718
[No Abstract] [Full Text] [Related]
12. Paraoxonase promoter and intronic variants modify risk of sporadic amyotrophic lateral sclerosis.
Cronin S; Greenway MJ; Prehn JH; Hardiman O
J Neurol Neurosurg Psychiatry; 2007 Sep; 78(9):984-6. PubMed ID: 17702780
[TBL] [Abstract][Full Text] [Related]
13. Comprehensive assessment of genetic sequence variants in the antioxidant 'master regulator' NRF2 in idiopathic Parkinson's disease.
Todorovic M; Newman JR; Shan J; Bentley S; Wood SA; Silburn PA; Mellick GD
PLoS One; 2015; 10(5):e0128030. PubMed ID: 26010367
[TBL] [Abstract][Full Text] [Related]
14. Associations of the NRF2/KEAP1 pathway and antioxidant defense gene polymorphisms with chronic obstructive pulmonary disease.
Korytina GF; Akhmadishina LZ; Aznabaeva YG; Kochetova OV; Zagidullin NS; Kzhyshkowska JG; Zagidullin SZ; Viktorova TV
Gene; 2019 Apr; 692():102-112. PubMed ID: 30641209
[TBL] [Abstract][Full Text] [Related]
15. Nuclear factor erythroid 2-like 2 (Nrf2) expression in end-stage liver disease.
Kurzawski M; Dziedziejko V; Urasińska E; Post M; Wójcicki M; Miętkiewski J; Droździk M
Environ Toxicol Pharmacol; 2012 Jul; 34(1):87-95. PubMed ID: 22459801
[TBL] [Abstract][Full Text] [Related]
16. Hydrogen peroxide-mediated induction of SOD1 gene transcription is independent from Nrf2 in a cellular model of neurodegeneration.
Dell'Orco M; Milani P; Arrigoni L; Pansarasa O; Sardone V; Maffioli E; Polveraccio F; Bordoni M; Diamanti L; Ceroni M; Peverali FA; Tedeschi G; Cereda C
Biochim Biophys Acta; 2016 Feb; 1859(2):315-23. PubMed ID: 26619801
[TBL] [Abstract][Full Text] [Related]
17. Impaired antioxydative Keap1/Nrf2 system and the downstream stress protein responses in the motor neuron of ALS model mice.
Mimoto T; Miyazaki K; Morimoto N; Kurata T; Satoh K; Ikeda Y; Abe K
Brain Res; 2012 Mar; 1446():109-18. PubMed ID: 22353756
[TBL] [Abstract][Full Text] [Related]
18. NFE2L2 gene variants and susceptibility to childhood-onset asthma.
Córdova EJ; Jiménez-Morales S; Centeno F; Martinez-Hernández A; Martínez-Aguilar N; Del-Río-Navarro BE; Gómez-Vera J; Orozco L
Rev Invest Clin; 2011; 63(4):407-11. PubMed ID: 22364041
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.
Zou ZY; Cui LY; Sun Q; Li XG; Liu MS; Xu Y; Zhou Y; Yang XZ
Neurobiol Aging; 2013 Apr; 34(4):1312.e1-8. PubMed ID: 23046859
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
