220 related articles for article (PubMed ID: 24192154)
1. Nitric oxide synthase polymorphisms, gene expression and lung function in chronic obstructive pulmonary disease.
Aminuddin F; Hackett TL; Stefanowicz D; Saferali A; Paré PD; Gulsvik A; Bakke P; Cho MH; Litonjua A; Lomas DA; Anderson WH; Beaty TH; Silverman EK; Sandford AJ
BMC Pulm Med; 2013 Nov; 13():64. PubMed ID: 24192154
[TBL] [Abstract][Full Text] [Related]
2. Association analysis of nitric oxide synthases: NOS1, NOS2A and NOS3 genes, with multiple sclerosis.
AlFadhli S; Mohammed EM; Al Shubaili A
Ann Hum Biol; 2013 Jul; 40(4):368-75. PubMed ID: 23826716
[TBL] [Abstract][Full Text] [Related]
3. [The relationship between resting heart rate and single nucleotide polymorphism at 3 sites of nitric oxide synthase gene in the Chinese Han nationality population].
Ma HX; Niu YH; Li ZY; Xie ZX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Dec; 23(6):670-2. PubMed ID: 17160951
[TBL] [Abstract][Full Text] [Related]
4. Single nucleotide polymorphisms in the NOS2 and NOS3 genes are associated with exhaled nitric oxide.
Dahgam S; Nyberg F; Modig L; Naluai AT; Olin AC
J Med Genet; 2012 Mar; 49(3):200-5. PubMed ID: 22368302
[TBL] [Abstract][Full Text] [Related]
5. Genetic influences on right ventricular systolic pressure (RVSP) in chronic obstructive pulmonary disease (COPD).
Shaw JG; Dent AG; Passmore LH; Burstow DJ; Bowman RV; Zimmerman PV; Fong KM; Yang IA
BMC Pulm Med; 2012 Jun; 12():25. PubMed ID: 22695028
[TBL] [Abstract][Full Text] [Related]
6. Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype.
Soldano KL; Garrett ME; Cope HL; Rusnak JM; Ellis NJ; Dunlap KL; Speer MC; Gregory SG; Ashley-Koch AE
Birth Defects Res B Dev Reprod Toxicol; 2013 Oct; 98(5):365-73. PubMed ID: 24323870
[TBL] [Abstract][Full Text] [Related]
7. Nitric oxide synthase enzymes in the airways of mice exposed to ovalbumin: NOS2 expression is NOS3 dependent.
Bratt JM; Williams K; Rabowsky MF; Last MS; Franzi LM; Last JA; Kenyon NJ
Mediators Inflamm; 2010; 2010():. PubMed ID: 20953358
[TBL] [Abstract][Full Text] [Related]
8. Nitric oxide synthase polymorphisms and asthma phenotypes in Chinese children.
Leung TF; Liu EK; Tang NL; Ko FW; Li CY; Lam CW; Wong GW
Clin Exp Allergy; 2005 Oct; 35(10):1288-94. PubMed ID: 16238787
[TBL] [Abstract][Full Text] [Related]
9. The -786 T/C polymorphism of NOS3 gene is a susceptibility marker of COPD among Tunisians that correlates with nitric oxide levels and airflow obstruction.
Ben Nasr H; Bchir S; Ben Anes A; Amri A; Sakhana Y; Benzarti M; Garrouch A; Tabka Z; Chahed K
Cytokine; 2017 May; 93():66-73. PubMed ID: 28526204
[TBL] [Abstract][Full Text] [Related]
10. Nitric oxide synthase (NOS) single nucleotide polymorphisms are associated with coronary heart disease and hypertension in the INTERGENE study.
Levinsson A; Olin AC; Björck L; Rosengren A; Nyberg F
Nitric Oxide; 2014 May; 39():1-7. PubMed ID: 24713495
[TBL] [Abstract][Full Text] [Related]
11. Genetic variants in nitric oxide synthase genes and the risk of male infertility in a Chinese population: a case-control study.
Yan L; Guo W; Wu S; Liu J; Zhang S; Shi L; Ji G; Gu A
PLoS One; 2014; 9(12):e115190. PubMed ID: 25517965
[TBL] [Abstract][Full Text] [Related]
12. Association of NOS2 and NOS3 gene polymorphisms with susceptibility to type 2 diabetes mellitus and diabetic nephropathy in the Chinese Han population.
Chen F; Li YM; Yang LQ; Zhong CG; Zhuang ZX
IUBMB Life; 2016 Jul; 68(7):516-25. PubMed ID: 27192959
[TBL] [Abstract][Full Text] [Related]
13. Expression of nitric oxide synthase isoforms in the ovine fetal brain: alteration by hormonal and hemodynamic stimuli.
Wood CE; Giroux D
J Soc Gynecol Investig; 2006 Jul; 13(5):329-37. PubMed ID: 16753312
[TBL] [Abstract][Full Text] [Related]
14. Association between polymorphisms of NOS1, NOS2 and NOS3 genes and suicide behavior: a systematic review and meta-analysis.
González-Castro TB; Genis-Mendoza AD; Tovilla-Zárate CA; Juárez-Rojop IE; López-Narvaez ML; Pérez-Hernández N; Rodríguez-Pérez JM; Martínez-Magaña JJ
Metab Brain Dis; 2019 Aug; 34(4):967-977. PubMed ID: 30900130
[TBL] [Abstract][Full Text] [Related]
15. Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.
Hancock DB; Martin ER; Vance JM; Scott WK
Neurogenetics; 2008 Oct; 9(4):249-62. PubMed ID: 18663495
[TBL] [Abstract][Full Text] [Related]
16. Genetic association between human chitinases and lung function in COPD.
Aminuddin F; Akhabir L; Stefanowicz D; Paré PD; Connett JE; Anthonisen NR; Fahy JV; Seibold MA; Burchard EG; Eng C; Gulsvik A; Bakke P; Cho MH; Litonjua A; Lomas DA; Anderson WH; Beaty TH; Crapo JD; Silverman EK; Sandford AJ
Hum Genet; 2012 Jul; 131(7):1105-14. PubMed ID: 22200767
[TBL] [Abstract][Full Text] [Related]
17. NOS3 Gene rs1799983 and rs2070744 Polymorphisms in Patients with Unstable Angina.
Pawlik A; Błaszczyk H; Rać M; Maciejewska-Skrendo A; Safranow K; Dziedziejko V
J Vasc Res; 2020; 57(3):136-142. PubMed ID: 32224624
[TBL] [Abstract][Full Text] [Related]
18. Compensatory lung growth in NOS3 knockout mice suggests synthase isoform redundancy.
Pokall S; Maldonado AR; Klanke CA; Katayama S; Morris LM; Vuletin JF; Lim FY; Crombleholme TM
Eur J Pediatr Surg; 2012 Apr; 22(2):148-56. PubMed ID: 22517523
[TBL] [Abstract][Full Text] [Related]
19. The Role of Single-Nucleotide Variants of
Shnayder NA; Petrova MM; Moskaleva PV; Shesternya PA; Pozhilenkova EA; Nasyrova RF
Molecules; 2021 Mar; 26(6):. PubMed ID: 33809023
[TBL] [Abstract][Full Text] [Related]
20. Association of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese.
Zhou Y; Yu H; Hou S; Fang J; Qin J; Yuan G; Kijlstra A; Yang P
Mol Vis; 2016; 22():311-8. PubMed ID: 27114698
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
