140 related articles for article (PubMed ID: 33105931)
1. [Gene mutation pattern of Gilbert's syndrome combined with viral hepatitis and its relationship with the exploration of clinical data].
Ning HB; Jin HM; Liu CP; Peng Z; Li K; Xiao EH; Shang J
Zhonghua Gan Zang Bing Za Zhi; 2020 Oct; 28(10):855-860. PubMed ID: 33105931
[No Abstract] [Full Text] [Related]
2. 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]
3. Correlation of mutational analysis to clinical features in Taiwanese patients with Gilbert's syndrome.
Hsieh SY; Wu YH; Lin DY; Chu CM; Wu M; Liaw YF
Am J Gastroenterol; 2001 Apr; 96(4):1188-93. PubMed ID: 11316168
[TBL] [Abstract][Full Text] [Related]
4. TATA-box mutant in the promoter of the uridine diphosphate glucuronosyltransferase gene in Italian patients with Gilbert's syndrome.
Sampietro M; Lupica L; Perrero L; Romano R; Molteni V; Fiorelli G
Ital J Gastroenterol Hepatol; 1998 Apr; 30(2):194-8. PubMed ID: 9675658
[TBL] [Abstract][Full Text] [Related]
5. Restriction fragment length polymorphism effectively identifies exon 1 mutation of UGT1A1 gene in patients with Gilbert's Syndrome.
Shiu TY; Huang HH; Lin HH; Shih YL; Chu HC; Chang WK; Hsieh TY
Liver Int; 2015 Aug; 35(8):2050-6. PubMed ID: 25611851
[TBL] [Abstract][Full Text] [Related]
6. [A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome].
Kim YH; Yeon JE; Jung GM; Kim HJ; Kim JS; Byun KS; Bak YT; Lee CH
Taehan Kan Hakhoe Chi; 2002 Jun; 8(2):132-8. PubMed ID: 12499798
[TBL] [Abstract][Full Text] [Related]
7. [Clinical features and gene mutation profiles of patients with chronic hepatitis B and Gilbert's syndrome].
Ning H; Li K; Mao Z; Liu J; Xiao E; Kang Y; Shang J
Zhonghua Gan Zang Bing Za Zhi; 2015 Jan; 23(1):13-6. PubMed ID: 25751380
[TBL] [Abstract][Full Text] [Related]
8. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome.
Bosma PJ; Chowdhury JR; Bakker C; Gantla S; de Boer A; Oostra BA; Lindhout D; Tytgat GN; Jansen PL; Oude Elferink RP
N Engl J Med; 1995 Nov; 333(18):1171-5. PubMed ID: 7565971
[TBL] [Abstract][Full Text] [Related]
9. [Analysis of diagnostic value of UGT1A1 gene detection in Gilbert syndrome].
Zhang M; Li WN; Chen G; Xu X; Qi JY
Zhonghua Gan Zang Bing Za Zhi; 2021 Feb; 29(2):143-149. PubMed ID: 33685083
[No Abstract] [Full Text] [Related]
10. The combination of new missense mutation with [A(TA)7TAA] dinucleotide repeat in UGT1A1 gene promoter causes Gilbert's syndrome.
D'Angelo R; Rinaldi C; Donato L; Nicocia G; Sidoti A
Ann Clin Lab Sci; 2015; 45(2):202-5. PubMed ID: 25887876
[TBL] [Abstract][Full Text] [Related]
11. Compound heterozygous UGT1A1*28 and UGT1A1*6 or single homozygous UGT1A1*28 are major genotypes associated with Gilbert's syndrome in Chinese Han people.
Zhang M; Wang H; Huang Y; Xu X; Liu W; Ning Q; Chen T; Qi J
Gene; 2021 May; 781():145526. PubMed ID: 33631237
[TBL] [Abstract][Full Text] [Related]
12. Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome.
Monaghan G; Ryan M; Seddon R; Hume R; Burchell B
Lancet; 1996 Mar; 347(9001):578-81. PubMed ID: 8596320
[TBL] [Abstract][Full Text] [Related]
13. [Clinical and genetic analyses of UGT1A1 gene from a Chinese family with Gilbert's syndrome].
Peng XX; Jiang J
Zhonghua Yi Xue Za Zhi; 2010 Jun; 90(24):1690-3. PubMed ID: 20979879
[TBL] [Abstract][Full Text] [Related]
14. Gilbert's syndrome: High frequency of the (TA)7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene.
Farheen S; Sengupta S; Santra A; Pal S; Dhali GK; Chakravorty M; Majumder PP; Chowdhury A
World J Gastroenterol; 2006 Apr; 12(14):2269-75. PubMed ID: 16610035
[TBL] [Abstract][Full Text] [Related]
15. Rapid molecular diagnosis of the Gilbert's syndrome-associated exon 1 mutation within the UGT1A1 gene.
Hsieh TY; Shiu TY; Chu NF; Chao TY; Chu HC; Chang WK; Chao YC; Huang HH
Genet Mol Res; 2014 Jan; 13(1):670-9. PubMed ID: 24615032
[TBL] [Abstract][Full Text] [Related]
16. Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1.
Persico M; Persico E; Bakker CT; Rigato I; Amoroso A; Torella R; Bosma PJ; Tiribelli C; Ostrow JD
Hepatology; 2001 Mar; 33(3):627-32. PubMed ID: 11230743
[TBL] [Abstract][Full Text] [Related]
17. Donor liver uridine diphosphate (UDP)-glucuronosyltransferase-1A1 deficiency causing Gilbert's syndrome in liver transplant recipients.
Te HS; Schiano TD; Das S; Kuan SF; DasGupta K; Conjeevaram HS; Baker AL
Transplantation; 2000 May; 69(9):1882-6. PubMed ID: 10830226
[TBL] [Abstract][Full Text] [Related]
18. Genetic variation underlying common hereditary hyperbilirubinaemia (Gilbert's syndrome) and respiratory health in the 1946 British birth cohort.
Horsfall LJ; Hardy R; Wong A; Kuh D; Swallow DM
J Hepatol; 2014 Dec; 61(6):1344-51. PubMed ID: 25086287
[TBL] [Abstract][Full Text] [Related]
19. Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects.
Borlak J; Thum T; Landt O; Erb K; Hermann R
Hepatology; 2000 Oct; 32(4 Pt 1):792-5. PubMed ID: 11003624
[TBL] [Abstract][Full Text] [Related]
20. Dependence of blood biochemical parameters on various genotypes of the UGT1A1 gene associated with gilbert's syndrome.
Sidorenko DV; Nazarov VD; Volnikova EG; Kondrasheva EA; Peshkova NG; Kovaleva IS; Kokorina OS; Svatkovskaya IB; Lapin SV
Klin Lab Diagn; 2022 Feb; 67(2):69-75. PubMed ID: 35192750
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]