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283 related items for PubMed ID: 25625535
1. Association of HMOX1 gene promoter polymorphisms with hyperbilirubinemia in the early neonatal period. Katayama Y, Yokota T, Zhao H, Wong RJ, Stevenson DK, Taniguchi-Ikeda M, Nakamura H, Iijima K, Morioka I. Pediatr Int; 2015 Aug; 57(4):645-9. PubMed ID: 25625535 [Abstract] [Full Text] [Related]
2. Association between genetic polymorphism of heme oxygenase 1 promoter and neonatal hyperbilirubinemia: a meta-analysis. Zhou JF, Luo JY, Zhu WB, Yang CY, Zeng YL, Qiu XL. J Matern Fetal Neonatal Med; 2021 Jan; 34(1):12-23. PubMed ID: 30700176 [Abstract] [Full Text] [Related]
3. Neonatal hyperbilirubinemia in Japanese neonates: analysis of the heme oxygenase-1 gene and fetal hemoglobin composition in cord blood. Kanai M, Akaba K, Sasaki A, Sato M, Harano T, Shibahara S, Kurachi H, Yoshida T, Hayasaka K. Pediatr Res; 2003 Aug; 54(2):165-71. PubMed ID: 12736395 [Abstract] [Full Text] [Related]
4. Heme oxygenase-1 gene variants and hyperbilirubinemia risk in North Indian newborns. Tiwari PK, Sethi A, Basu S, Raman R, Kumar A. Eur J Pediatr; 2013 Dec; 172(12):1627-32. PubMed ID: 23877636 [Abstract] [Full Text] [Related]
5. Heme oxygenase-1 genetic variants and the conundrum of hyperbilirubinemia in African-American newborns. Schutzman DL, Gatien E, Ajayi S, Wong RJ. J Perinatol; 2018 Apr; 38(4):345-350. PubMed ID: 29302043 [Abstract] [Full Text] [Related]
7. Association of (GT)n repeats promoter polymorphism of heme oxygenase-1 gene with serum bilirubin levels in healthy Indian adults. D'Silva S, Borse V, Colah RB, Ghosh K, Mukherjee MB. Genet Test Mol Biomarkers; 2011 Apr; 15(4):215-8. PubMed ID: 21198350 [Abstract] [Full Text] [Related]
8. HMOX1 promoter (GT)n polymorphim is associated with childhood-onset systemic lupus erythematosus but not with juvenile rheumatoid arthritis in a Mexican population. Córdova EJ, Martínez-Hernández A, Ramírez-Bello J, Velázquez-Cruz R, Centeno F, Baca V, Orozco L. Clin Exp Rheumatol; 2012 Apr; 30(2):297-301. PubMed ID: 22338608 [Abstract] [Full Text] [Related]
9. Polymorphisms in the Haem Oxygenase-1 promoter are not associated with severity of Plasmodium falciparum malaria in Ghanaian children. Hansson HH, Maretty L, Balle C, Goka BQ, Luzon E, Nkrumah FN, Schousboe ML, Rodrigues OP, Bygbjerg IC, Kurtzhals JA, Alifrangis M, Hempel C. Malar J; 2015 Apr 11; 14():153. PubMed ID: 25888733 [Abstract] [Full Text] [Related]
10. The relationship between hyperbilirubinemia and the promoter region and first exon of UGT1A1 gene polymorphisms in Vietnamese newborns. Nguyen TT, Zhao W, Yang X, Zhong DN. Pediatr Res; 2020 Dec 11; 88(6):940-944. PubMed ID: 32126570 [Abstract] [Full Text] [Related]
11. Prolonged unconjugated hyperbilirubinaemia associated with the haem oxygenase-1 gene promoter polymorphism. Bozkaya OG, Kumral A, Yesilirmak DC, Ulgenalp A, Duman N, Ercal D, Ozkan H. Acta Paediatr; 2010 May 11; 99(5):679-683. PubMed ID: 20121710 [Abstract] [Full Text] [Related]
12. HMOX1 promoter polymorphism modulates the relationship between disease activity and joint damage in rheumatoid arthritis. Wagener FA, Toonen EJ, Wigman L, Fransen J, Creemers MC, Radstake TR, Coenen MJ, Barrera P, van Riel PL, Russel FG. Arthritis Rheum; 2008 Nov 11; 58(11):3388-93. PubMed ID: 18975324 [Abstract] [Full Text] [Related]
13. Heme oxygenase-1 gene promoter polymorphism is associated with risk of gastric adenocarcinoma and lymphovascular tumor invasion. Lo SS, Lin SC, Wu CW, Chen JH, Yeh WI, Chung MY, Lui WY. Ann Surg Oncol; 2007 Aug 11; 14(8):2250-6. PubMed ID: 17520317 [Abstract] [Full Text] [Related]
14. [OATP 1B1 T521C/A388G is an important polymorphism gene related to neonatal hyperbilirubinemia]. Zhang HX, Zhao X, Yang Z, Peng CY, Long R, Li GN, Li J, He ZK. Zhonghua Er Ke Za Zhi; 2010 Sep 11; 48(9):650-5. PubMed ID: 21092521 [Abstract] [Full Text] [Related]
15. Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants. Zhou Y, Wang SN, Li H, Zha W, Wang X, Liu Y, Sun J, Peng Q, Li S, Chen Y, Jin L. PLoS One; 2014 Sep 11; 9(8):e104251. PubMed ID: 25102181 [Abstract] [Full Text] [Related]
16. Association of serum bilirubin and promoter variations in HMOX1 and UGT1A1 genes with sporadic colorectal cancer. Jirásková A, Novotný J, Novotný L, Vodicka P, Pardini B, Naccarati A, Schwertner HA, Hubácek JA, Puncochárová L, Šmerhovský Z, Vítek L. Int J Cancer; 2012 Oct 01; 131(7):1549-55. PubMed ID: 22212955 [Abstract] [Full Text] [Related]
17. Subjects with coronary artery disease and reduced ejection fraction have longer (GT)n repeats in the heme-oxygenase 1 gene promoter. Liang KW, Lee WJ, Lee WL, Wu JP, Lee IT, Wang JS, Sheu WH. Heart Vessels; 2021 May 01; 36(5):615-620. PubMed ID: 33388910 [Abstract] [Full Text] [Related]
18. The role of UGT1A1 promoter polymorphism and exon-1 mutations in neonatal jaundice. Halis H, Ergin H, Köseler A, Atalay EÖ. J Matern Fetal Neonatal Med; 2017 Nov 01; 30(22):2658-2664. PubMed ID: 27842454 [Abstract] [Full Text] [Related]
19. Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan. Weng YH, Chiu YW, Cheng SW, Yang CY. BMC Pediatr; 2016 Aug 24; 16(1):144. PubMed ID: 27557546 [Abstract] [Full Text] [Related]
20. Association between the Specific UGT1A1 Promoter Sequence Variant (c-3279T>G) and Unconjugated Neonatal Hyperbilirubinemia. Tomerak RH, Helal NF, Shaker OG, Yousef MA. J Trop Pediatr; 2016 Dec 24; 62(6):457-463. PubMed ID: 27318112 [Abstract] [Full Text] [Related] Page: [Next] [New Search]