219 related articles for article (PubMed ID: 26377032)
1. Performance of In Silico Tools for the Evaluation of UGT1A1 Missense Variants.
Rodrigues C; Santos-Silva A; Costa E; Bronze-da-Rocha E
Hum Mutat; 2015 Dec; 36(12):1215-25. PubMed ID: 26377032
[TBL] [Abstract][Full Text] [Related]
2. Prediction of deleterious non-synonymous single-nucleotide polymorphisms of human uridine diphosphate glucuronosyltransferase genes.
Di YM; Chan E; Wei MQ; Liu JP; Zhou SF
AAPS J; 2009 Sep; 11(3):469-80. PubMed ID: 19572200
[TBL] [Abstract][Full Text] [Related]
3. A bioinformatics approach for the phenotype prediction of nonsynonymous single nucleotide polymorphisms in human cytochromes P450.
Wang LL; Li Y; Zhou SF
Drug Metab Dispos; 2009 May; 37(5):977-91. PubMed ID: 19204079
[TBL] [Abstract][Full Text] [Related]
4. Phenotype prediction of deleterious nonsynonymous single nucleotide polymorphisms in human alcohol metabolism-related genes: a bioinformatics study.
Wang LL; Yang AK; Li Y; Liu JP; Zhou SF
Alcohol; 2010 Aug; 44(5):425-38. PubMed ID: 20804942
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Using SIFT and PolyPhen to predict loss-of-function and gain-of-function mutations.
Flanagan SE; Patch AM; Ellard S
Genet Test Mol Biomarkers; 2010 Aug; 14(4):533-7. PubMed ID: 20642364
[TBL] [Abstract][Full Text] [Related]
7. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.
Kadakol A; Ghosh SS; Sappal BS; Sharma G; Chowdhury JR; Chowdhury NR
Hum Mutat; 2000 Oct; 16(4):297-306. PubMed ID: 11013440
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Crigler-Najjar syndrome in The Netherlands: identification of four novel UGT1A1 alleles, genotype-phenotype correlation, and functional analysis of 10 missense mutants.
Sneitz N; Bakker CT; de Knegt RJ; Halley DJ; Finel M; Bosma PJ
Hum Mutat; 2010 Jan; 31(1):52-9. PubMed ID: 19830808
[TBL] [Abstract][Full Text] [Related]
10. Prediction of deleterious functional effects of non-synonymous single nucleotide polymorphisms in human nuclear receptor genes using a bioinformatics approach.
Liu YH; Li CG; Zhou SF
Drug Metab Lett; 2009 Dec; 3(4):242-86. PubMed ID: 20050372
[TBL] [Abstract][Full Text] [Related]
11. A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome.
Nakagawa T; Mure T; Yusoff S; Ono E; Kusuma Harahap IS; Morikawa S; Morioka I; Takeshima Y; Nishio H; Matsuo M
Kobe J Med Sci; 2011 Jul; 57(1):E26-31. PubMed ID: 22169899
[TBL] [Abstract][Full Text] [Related]
12. Phenotype prediction of non-synonymous single-nucleotide polymorphisms in human ATP-binding cassette transporter genes.
Wang LL; Liu YH; Meng LL; Li CG; Zhou SF
Basic Clin Pharmacol Toxicol; 2011 Feb; 108(2):94-114. PubMed ID: 20849526
[TBL] [Abstract][Full Text] [Related]
13. Phenotype prediction of nonsynonymous single nucleotide polymorphisms in human phase II drug/xenobiotic metabolizing enzymes: perspectives on molecular evolution.
Hao D; Xiao P; Chen S
Sci China Life Sci; 2010 Oct; 53(10):1252-62. PubMed ID: 20953949
[TBL] [Abstract][Full Text] [Related]
14. Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.
Canu G; Minucci A; Zuppi C; Capoluongo E
Blood Cells Mol Dis; 2013 Apr; 50(4):273-80. PubMed ID: 23403257
[TBL] [Abstract][Full Text] [Related]
15. Compound heterozygosity of a novel exon 3 frameshift (p.R357P fs*24) mutation and Y486D mutation in exon 5 of the UGT1A1 gene in a Thai infant with Crigler-Najjar syndrome type 2.
Tesapirat L; Nilyanimit P; Wanlapakorn N; Poovorawan Y
Genet Mol Res; 2015 Apr; 14(2):3293-9. PubMed ID: 25966095
[TBL] [Abstract][Full Text] [Related]
16. Computational prediction of the effects of non-synonymous single nucleotide polymorphisms in human DNA repair genes.
Nakken S; Alseth I; Rognes T
Neuroscience; 2007 Apr; 145(4):1273-9. PubMed ID: 17055652
[TBL] [Abstract][Full Text] [Related]
17. Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome.
Sutomo R; Laosombat V; Sadewa AH; Yokoyama N; Nakamura H; Matsuo M; Nishio H
Pediatr Int; 2002 Aug; 44(4):427-32. PubMed ID: 12139570
[TBL] [Abstract][Full Text] [Related]
18. Statistical geometry based prediction of nonsynonymous SNP functional effects using random forest and neuro-fuzzy classifiers.
Barenboim M; Masso M; Vaisman II; Jamison DC
Proteins; 2008 Jun; 71(4):1930-9. PubMed ID: 18186470
[TBL] [Abstract][Full Text] [Related]
19. In-Silico Analyses of Nonsynonymous Variants in the BRCA1 Gene.
Arshad S; Ishaque I; Mumtaz S; Rashid MU; Malkani N
Biochem Genet; 2021 Dec; 59(6):1506-1526. PubMed ID: 33945048
[TBL] [Abstract][Full Text] [Related]
20. Performance of mutation pathogenicity prediction tools on missense variants associated with 46,XY differences of sex development.
Montenegro LR; Lerário AM; Nishi MY; Jorge AAL; Mendonca BB
Clinics (Sao Paulo); 2021; 76():e2052. PubMed ID: 33503178
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
