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Items: 1 to 20 of 96

1.

Heme oxygenase-1 promoter polymorphisms do not influence susceptibility to systemic sclerosis and its clinical phenotypes.

van Bon L, Broen JC, Schijvenaars MM, Rueda B, Simeón CP, Ortego-Centeno N, González-Gay MA, Radstake TR, Hunzelmann N, Riemekasten G, Witte T, Wagener FA, Vonk MC, Coenen MJ, Martin J.

Clin Exp Rheumatol. 2013 Mar-Apr;31(2 Suppl 76):186. No abstract available.

PMID:
23406650
2.

Association of a functional polymorphism in the matrix metalloproteinase-12 promoter region with systemic sclerosis in an Italian population.

Manetti M, Ibba-Manneschi L, Fatini C, Guiducci S, Cuomo G, Bonino C, Bazzichi L, Liakouli V, Giacomelli R, Abbate R, Bombardieri S, Montecucco C, Valentini G, Matucci-Cerinic M.

J Rheumatol. 2010 Sep;37(9):1852-7. doi: 10.3899/jrheum.100237.

PMID:
20595276
3.

Heme oxygenase-1 promoter polymorphisms and risk of spina bifida.

Fujioka K, Yang W, Wallenstein MB, Zhao H, Wong RJ, Stevenson DK, Shaw GM.

Birth Defects Res A Clin Mol Teratol. 2015 Sep;103(9):741-6. doi: 10.1002/bdra.23343.

PMID:
26173399
4.

Length polymorphism in heme oxygenase-1 and risk of CKD among patients with coronary artery disease.

Chen YH, Kuo KL, Hung SC, Hsu CC, Chen YH, Tarng DC.

J Am Soc Nephrol. 2014 Nov;25(11):2669-77. doi: 10.1681/ASN.2013111205.

5.

A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with systemic sclerosis in a large European cohort.

Bossini-Castillo L, Broen JC, Simeon CP, Beretta L, Vonk MC, Ortego-Centeno N, Espinosa G, Carreira P, Camps MT, Navarrete N, González-Escribano MF, Vicente-Rabaneda E, Rodríguez L, Tolosa C, Román-Ivorra JA, Gómez-Gracia I, García-Hernández FJ, Castellví I, Gallego M, Fernández-Nebro A, García-Portales R, Egurbide MV, Fonollosa V, de la Peña PG, Pros A, González-Gay MA, Hesselstrand R, Riemekasten G, Witte T, Coenen MJ, Koeleman BP, Houssiau F, Smith V, de Keyser F, Westhovens R, De Langhe E, Voskuyl AE, Schuerwegh AJ, Chee MM, Madhok R, Shiels P, Fonseca C, Denton C, Claes K, Padykov L, Nordin A, Palm O, Lie BA, Airó P, Scorza R, van Laar JM, Hunzelmann N, Kreuter A, Herrick A, Worthington J, Radstake TR, Martín J, Rueda B.

Ann Rheum Dis. 2011 Apr;70(4):638-41. doi: 10.1136/ard.2010.141838. Erratum in: Ann Rheum Dis. 2011 Aug;70(8):1520.

PMID:
21187296
6.

The role of heme oxygenase-1 in pulmonary disease.

Fredenburgh LE, Perrella MA, Mitsialis SA.

Am J Respir Cell Mol Biol. 2007 Feb;36(2):158-65. Review.

7.

Microsatellite polymorphism in the heme oxygenase-1 gene promoter and the risk of psoriasis in Taiwanese.

Chang YC, Wu WM, Tsai HY, Hsu LA.

Arch Dermatol Res. 2012 Nov;304(9):739-44. doi: 10.1007/s00403-012-1289-2.

PMID:
22965812
8.

Heme oxygenase-1 gene promoter polymorphism is associated with the development of necrotizing acute pancreatitis.

Gulla A, Evans BJ, Navenot JM, Pundzius J, Barauskas G, Gulbinas A, Dambrauskas Z, Arafat H, Wang ZX.

Pancreas. 2014 Nov;43(8):1271-6. doi: 10.1097/MPA.0000000000000171.

PMID:
25036905
9.
10.
11.

Effect of heme oxygenase-1 gene promoter polymorphism on cancer risk by histological subtype: A prospective study in arseniasis-endemic areas in Taiwan.

Wu MM, Lee CH, Hsu LI, Cheng WF, Lee TC, Wang YH, Chiou HY, Chen CJ.

Int J Cancer. 2016 Apr 15;138(8):1875-86. doi: 10.1002/ijc.29926.

PMID:
26566708
12.

Heme oxygenase-1 promoter polymorphisms and neonatal jaundice.

Kaplan M, Renbaum P, Hammerman C, Vreman HJ, Wong RJ, Stevenson DK.

Neonatology. 2014;106(4):323-9. doi: 10.1159/000365744.

PMID:
25277974
13.

Gene-gene interaction between heme oxygenase-1 and liver X receptor-beta and Alzheimer's disease risk.

Infante J, Rodríguez-Rodríguez E, Mateo I, Llorca J, Vázquez-Higuera JL, Berciano J, Combarros O.

Neurobiol Aging. 2010 Apr;31(4):710-4. doi: 10.1016/j.neurobiolaging.2008.05.025.

PMID:
18597895
14.

Heme oxygenase-1 promoter polymorphism is associated with risk of malignant mesothelioma.

Murakami A, Fujimori Y, Yoshikawa Y, Yamada S, Tamura K, Hirayama N, Terada T, Kuribayashi K, Tabata C, Fukuoka K, Tamaoki T, Nakano T.

Lung. 2012 Jun;190(3):333-7. doi: 10.1007/s00408-012-9371-2.

PMID:
22271370
15.

Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.

Bean CJ, Boulet SL, Ellingsen D, Pyle ME, Barron-Casella EA, Casella JF, Payne AB, Driggers J, Trau HA, Yang G, Jones K, Ofori-Acquah SF, Hooper WC, DeBaun MR.

Blood. 2012 Nov 1;120(18):3822-8. doi: 10.1182/blood-2011-06-361642.

16.

Association of heme oxygenase-1 GT-repeat polymorphism with blood pressure phenotypes and its relevance to future cardiovascular mortality risk: an observation based on arsenic-exposed individuals.

Wu MM, Chiou HY, Chen CL, Hsu LI, Lien LM, Wang CH, Hsieh YC, Wang YH, Hsueh YM, Lee TC, Cheng WF, Chen CJ.

Atherosclerosis. 2011 Dec;219(2):704-8. doi: 10.1016/j.atherosclerosis.2011.08.047.

PMID:
21945498
17.

Synergistic effect of two oxidative stress-related genes (heme oxygenase-1 and GSK3β) on the risk of Parkinson's disease.

Infante J, García-Gorostiaga I, Sánchez-Juan P, Sierra M, Martín-Gurpegui JL, Terrazas J, Mateo I, Rodríguez-Rodríguez E, Berciano J, Combarros O.

Eur J Neurol. 2010 May;17(5):760-2. doi: 10.1111/j.1468-1331.2009.02908.x.

PMID:
20039940
18.

Stromelysin promoter polymorphism is associated with systemic sclerosis.

Marasini B, Casari S, Zeni S, Turri O, Biondi ML.

Rheumatology (Oxford). 2001 Apr;40(4):475-6. No abstract available.

PMID:
11312392
19.

Association between heme oxygenase-1 gene promoter polymorphisms and metabolic syndrome in Iranians.

Javanmard SH, Keyhanian K, Loghmani P, Samety AA, Haghdoost F, Rafiei L, Talaei M, Asgari S, Jazi MH, Sarrafzadegan N.

Mol Biol Rep. 2012 Mar;39(3):3355-60. doi: 10.1007/s11033-011-1105-7.

PMID:
21725851
20.

Genetic analysis of heme oxygenase-1 (HO-1) in German Parkinson's disease patients.

Funke C, Tomiuk J, Riess O, Berg D, Soehn AS.

J Neural Transm (Vienna). 2009 Jul;116(7):853-9. doi: 10.1007/s00702-009-0237-6.

PMID:
19475336

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