73 related articles for article (PubMed ID: 21889933)
1. High Resolution Melting Analysis (HRMA) for the identification of a rare UGT1A1 promoter polymorphism.
Minucci A; Mello E; Tripodi D; Concolino P; Zuppi C; Capoluongo E
Clin Biochem; 2011 Nov; 44(16):1359-60. PubMed ID: 21889933
[No Abstract] [Full Text] [Related]
2. Genotyping UGT1A1(TA)(n) polymorphism rare variants by high resolution melting curve analysis.
Ostanek B; Furlan D; Bratanič B
Clin Chim Acta; 2011 Feb; 412(5-6):489-90. PubMed ID: 21134365
[No Abstract] [Full Text] [Related]
3. Rapid UGT1A1 (TA)(n) genotyping by high resolution melting curve analysis for Gilbert's syndrome diagnosis.
Minucci A; Concolino P; Giardina B; Zuppi C; Capoluongo E
Clin Chim Acta; 2010 Feb; 411(3-4):246-9. PubMed ID: 19932091
[TBL] [Abstract][Full Text] [Related]
4. UGT1A1 (TA)n genotyping in sickle-cell disease: high resolution melting (HRM) curve analysis or direct sequencing, what is the best way?
Thomas V; Mazard B; Garcia C; Lacan P; Gagnieu MC; Joly P
Clin Chim Acta; 2013 Sep; 424():258-60. PubMed ID: 23827693
[TBL] [Abstract][Full Text] [Related]
5. Comprehensive analysis of UGT1A1 polymorphisms through high-resolution melting analysis and DNA sequencing.
Tsai SY; Er TK; Lin CW; Chang JG
Clin Lab; 2014; 60(6):1015-26. PubMed ID: 25016708
[TBL] [Abstract][Full Text] [Related]
6. Rapid, sensitive and inexpensive detection of SCN5A genetic variations by high resolution melting analysis.
Millat G; Chanavat V; Rodriguez-Lafrasse C; Rousson R
Clin Biochem; 2009 Apr; 42(6):491-9. PubMed ID: 19026623
[TBL] [Abstract][Full Text] [Related]
7. Bilirubin UDP-glucuronosyltransferase 1A1 (UGT1A1) gene promoter polymorphisms and HPRT, glycophorin A, and micronuclei mutant frequencies in human blood.
Grant DJ; Hall IJ; Eastmond DA; Jones IM; Bell DA
Mutat Res; 2004 May; 560(1):1-10. PubMed ID: 15099818
[TBL] [Abstract][Full Text] [Related]
8. Frequencies of UDP-glucuronosyltransferase 1 (UGT1A1) gene promoter polymorphisms among distinct ethnic groups from Brazil.
Fertrin KY; Gonçalves MS; Saad ST; Costa FF
Am J Med Genet; 2002 Mar; 108(2):117-9. PubMed ID: 11857560
[TBL] [Abstract][Full Text] [Related]
9. Evaluation of high-resolution melting analysis for screening the LDL receptor gene.
Laurie AD; George PM
Clin Biochem; 2009 Apr; 42(6):528-35. PubMed ID: 19118540
[TBL] [Abstract][Full Text] [Related]
10. UGT1A1 promoter polymorphisms and the development of hyperbilirubinemia and gallbladder disease in children with sickle cell anemia.
Carpenter SL; Lieff S; Howard TA; Eggleston B; Ware RE
Am J Hematol; 2008 Oct; 83(10):800-3. PubMed ID: 18756540
[TBL] [Abstract][Full Text] [Related]
11. Genotype frequencies of UDP-glucuronosyltransferase 1A1 promoter gene polymorphism in the population of healthy Croatian pre-scholars.
Marinković N; Pasalić D; Grsković B; Ferencak G; Honović L; Rukavina AS
Coll Antropol; 2008 Sep; 32(3):725-9. PubMed ID: 18982743
[TBL] [Abstract][Full Text] [Related]
12. Promoter length polymorphism in UGT1A1 and the risk of sporadic colorectal cancer.
Bajro MH; Josifovski T; Panovski M; Jankulovski N; Nestorovska AK; Matevska N; Petrusevska N; Dimovski AJ
Cancer Genet; 2012 Apr; 205(4):163-7. PubMed ID: 22559977
[TBL] [Abstract][Full Text] [Related]
13. The frequency of UDP-glucuronosyltransferase 1A1 promoter region (TA)7 polymorphism in newborns and it's relation with jaundice.
Muslu N; Turhan AB; Eskandari G; Atici A; Ozturk OG; Kul S; Atik U
J Trop Pediatr; 2007 Feb; 53(1):64-8. PubMed ID: 17166930
[TBL] [Abstract][Full Text] [Related]
14. Gilbert syndrome: the UGT1A1*28 promoter polymorphism as a biomarker of multifactorial diseases and drug metabolism.
Gil J; Sąsiadek MM
Biomark Med; 2012 Apr; 6(2):223-30. PubMed ID: 22448797
[TBL] [Abstract][Full Text] [Related]
15. Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects.
Takeuchi K; Kobayashi Y; Tamaki S; Ishihara T; Maruo Y; Araki J; Mifuji R; Itani T; Kuroda M; Sato H; Kaito M; Adachi Y
J Gastroenterol Hepatol; 2004 Sep; 19(9):1023-8. PubMed ID: 15304120
[TBL] [Abstract][Full Text] [Related]
16. High-throughput genotyping of mannose-binding lectin variants using high-resolution DNA-melting analysis.
Vossen RH; van Duijn M; Daha MR; den Dunnen JT; Roos A
Hum Mutat; 2010 Apr; 31(4):E1286-93. PubMed ID: 20127985
[TBL] [Abstract][Full Text] [Related]
17. A causal relationship between UDP-glucuronosyltransferase 1A1 promoter polymorphism and idiopathic hyperbilirubinemia in Turkish newborns.
Ergin H; Bican M; Atalay OE
Turk J Pediatr; 2010; 52(1):28-34. PubMed ID: 20402064
[TBL] [Abstract][Full Text] [Related]
18. Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia.
Chaar V; Kéclard L; Diara JP; Leturdu C; Elion J; Krishnamoorthy R; Clayton J; Romana M
Haematologica; 2005 Feb; 90(2):188-99. PubMed ID: 15710570
[TBL] [Abstract][Full Text] [Related]
19. Association of genetic polymorphisms in UGT1A1 with breast cancer and plasma hormone levels.
Guillemette C; De Vivo I; Hankinson SE; Haiman CA; Spiegelman D; Housman DE; Hunter DJ
Cancer Epidemiol Biomarkers Prev; 2001 Jun; 10(6):711-4. PubMed ID: 11401924
[TBL] [Abstract][Full Text] [Related]
20. UGT1A1 gene polymorphisms in North Indian neonates presenting with unconjugated hyperbilirubinemia.
Agrawal SK; Kumar P; Rathi R; Sharma N; DAS R; Prasad R; Narang A
Pediatr Res; 2009 Jun; 65(6):675-80. PubMed ID: 19430380
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
