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Results: 1 to 20 of 116

1.

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 Aug 7;9(8):e104251. doi: 10.1371/journal.pone.0104251. eCollection 2014.

PMID:
25102181
[PubMed - in process]
Free PMC Article
2.

A Systematic Evaluation of Short Tandem Repeats in Lipid Candidate Genes: Riding on the SNP-Wave.

Lamina C, Haun M, Coassin S, Kloss-Brandstätter A, Gieger C, Peters A, Grallert H, Strauch K, Meitinger T, Kedenko L, Paulweber B, Kronenberg F.

PLoS One. 2014 Jul 22;9(7):e102113. doi: 10.1371/journal.pone.0102113. eCollection 2014.

PMID:
25050552
[PubMed - in process]
Free PMC Article
3.

Body fat percentage is a major determinant of total bilirubin independently of UGT1A1*28 polymorphism in young obese.

Belo L, Nascimento H, Kohlova M, Bronze-da-Rocha E, Fernandes J, Costa E, Catarino C, Aires L, Mansilha HF, Rocha-Pereira P, Quintanilha A, Rêgo C, Santos-Silva A.

PLoS One. 2014 Jun 5;9(6):e98467. doi: 10.1371/journal.pone.0098467. eCollection 2014.

PMID:
24901842
[PubMed - in process]
Free PMC Article
4.

Two unrelated patients with rare Crigler-Najjar syndrome type I: two novel mutations and a patient with loss of heterozygosity of UGT1A1 gene.

Li Y, Qu YJ, Zhong XM, Cao YY, Jin LM, Bai JL, Ma X, Jin YW, Wang H, Zhang YL, Song F.

J Zhejiang Univ Sci B. 2014 May;15(5):474-81. doi: 10.1631/jzus.B1300233.

PMID:
24793765
[PubMed - in process]
Free PMC Article
5.

Molecular Analysis of the UGT1A1 Gene in Korean Patients with Crigler-Najjar Syndrome Type II.

Ko JS, Chang JY, Moon JS, Yang HR, Seo JK.

Pediatr Gastroenterol Hepatol Nutr. 2014 Mar;17(1):37-40. doi: 10.5223/pghn.2014.17.1.37. Epub 2014 Mar 31.

PMID:
24749086
[PubMed]
Free PMC Article
6.

Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.

Maruo Y, Morioka Y, Fujito H, Nakahara S, Yanagi T, Matsui K, Mori A, Sato H, Tukey RH, Takeuchi Y.

J Pediatr. 2014 Jul;165(1):36-41.e1. doi: 10.1016/j.jpeds.2014.01.060. Epub 2014 Mar 17.

PMID:
24650397
[PubMed - in process]
Free PMC Article
7.

Serum bilirubin concentration in healthy adult North-Europeans is strictly controlled by the UGT1A1 TA-repeat variants.

Kringen MK, Piehler AP, Grimholt RM, Opdal MS, Haug KB, Urdal P.

PLoS One. 2014 Feb 28;9(2):e90248. doi: 10.1371/journal.pone.0090248. eCollection 2014.

PMID:
24587300
[PubMed - in process]
Free PMC Article
8.

Association between inherited monogenic liver disorders and chronic hepatitis C.

Piekuse L, Kreile M, Zarina A, Steinberga Z, Sondore V, Keiss J, Lace B, Krumina A.

World J Hepatol. 2014 Feb 27;6(2):92-7. doi: 10.4254/wjh.v6.i2.92.

PMID:
24575168
[PubMed]
Free PMC Article
9.

PharmGKB summary: very important pharmacogene information for UGT1A1.

Barbarino JM, Haidar CE, Klein TE, Altman RB.

Pharmacogenet Genomics. 2014 Mar;24(3):177-83. doi: 10.1097/FPC.0000000000000024. No abstract available.

PMID:
24492252
[PubMed - in process]
Free PMC Article
10.

Differences in UGT1A1, UGT1A7, and UGT1A9 polymorphisms between Uzbek and Japanese populations.

Maeda H, Hazama S, Shavkat A, Okamoto K, Oba K, Sakamoto J, Takahashi K, Oka M, Nakamura D, Tsunedomi R, Okayama N, Mishima H, Kobayashi M.

Mol Diagn Ther. 2014 Jun;18(3):333-42. doi: 10.1007/s40291-014-0083-6.

PMID:
24453052
[PubMed - in process]
Free PMC Article
11.

Bone scintigraphy in Ollier's disease: A rare case report.

Khan SH, Rather TA, Koul PA, Makhdoomi R, Bhat AR, Malik D, Manohar R.

Indian J Nucl Med. 2013 Oct;28(4):226-9. doi: 10.4103/0972-3919.121968.

PMID:
24379533
[PubMed]
Free PMC Article
12.

Comprehensive variant screening of the UGT gene family.

Kim JY, Cheong HS, Park BL, Kim LH, Namgoong S, Kim JO, Kim HD, Kim YH, Chung MW, Han SY, Shin HD.

Yonsei Med J. 2014 Jan;55(1):232-9. doi: 10.3349/ymj.2014.55.1.232.

PMID:
24339312
[PubMed - indexed for MEDLINE]
Free PMC Article
13.
14.

Personalizing colon cancer therapeutics: targeting old and new mechanisms of action.

Kline CL, El-Deiry WS.

Pharmaceuticals (Basel). 2013 Aug 21;6(8):988-1038. doi: 10.3390/ph6080988.

PMID:
24276379
[PubMed]
Free PMC Article
15.

The effect of UGT1A1 promoter polymorphism in the development of hyperbilirubinemia and cholelithiasis in hemoglobinopathy patients.

AlFadhli S, Al-Jafer H, Hadi M, Al-Mutairi M, Nizam R.

PLoS One. 2013 Oct 30;8(10):e77681. doi: 10.1371/journal.pone.0077681. eCollection 2013.

PMID:
24204915
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene.

Chaouch L, Talbi E, Moumni I, Ben Chaabene A, Kalai M, Chaouachi D, Mallouli F, Ghanem A, Abbes S.

Dis Markers. 2013;35(2):67-72. doi: 10.1155/2013/173474. Epub 2013 Jul 28.

PMID:
24167350
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

New insights in bilirubin metabolism and their clinical implications.

Sticova E, Jirsa M.

World J Gastroenterol. 2013 Oct 14;19(38):6398-407. doi: 10.3748/wjg.v19.i38.6398. Review.

PMID:
24151358
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Distribution of selected gene polymorphisms of UGT1A1 in a Saudi population.

Alkharfy KM, Alghamdi AM, Bagulb KM, Al-Jenoobi FI, Al-Mohizea AM, Al-Muhsen S, Halwani R, Parvez MK, Al-Dosari MS.

Arch Med Sci. 2013 Aug 30;9(4):731-8. doi: 10.5114/aoms.2013.37012. Epub 2013 Aug 20.

PMID:
24049537
[PubMed]
Free PMC Article
19.

Characterization of raloxifene glucuronidation: potential role of UGT1A8 genotype on raloxifene metabolism in vivo.

Sun D, Jones NR, Manni A, Lazarus P.

Cancer Prev Res (Phila). 2013 Jul;6(7):719-30. doi: 10.1158/1940-6207.CAPR-12-0448. Epub 2013 May 16.

PMID:
23682072
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study.

Cox AJ, Ng MC, Xu J, Langefeld CD, Koch KL, Dawson PA, Carr JJ, Freedman BI, Hsu FC, Bowden DW.

Atherosclerosis. 2013 Jul;229(1):155-60. doi: 10.1016/j.atherosclerosis.2013.04.008. Epub 2013 Apr 19.

PMID:
23642732
[PubMed - indexed for MEDLINE]
Free PMC Article

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