| scholarly article | Q13442814 |
| P2093 | author name string | Hiroshi Sato | |
| Seiji Kato | |||
| Osamu Kisaki | |||
| Hisahide Hiura | |||
| Tomohiro Samori | |||
| Kohei Shinohara | |||
| P2860 | cites work | Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS) | Q24635921 |
| Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II | Q28258225 | ||
| Dynamic allele-specific hybridization. A new method for scoring single nucleotide polymorphisms | Q28295310 | ||
| High-throughput SNP genotyping by allele-specific PCR with universal energy-transfer-labeled primers | Q28345927 | ||
| Pharmacogenetics and pharmacogenomics: why is this relevant to the clinical geneticist? | Q33818189 | ||
| The use of single-nucleotide polymorphism maps in pharmacogenomics | Q33913441 | ||
| Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER) | Q33948446 | ||
| Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays | Q35028100 | ||
| The novel bilirubin/phenol UDP-glucuronosyltransferase UGT1 gene locus: implications for multiple nonhemolytic familial hyperbilirubinemia phenotypes | Q35223429 | ||
| Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes | Q37378223 | ||
| Minisatellite repeat coding as a digital approach to DNA typing | Q39252911 | ||
| Investigation of the substrate specificity of a cloned expressed human bilirubin UDP-glucuronosyltransferase: UDP-sugar specificity and involvement in steroid and xenobiotic glucuronidation | Q41437632 | ||
| Methods for detection of point mutations: performance and quality assessment. IFCC Scientific Division, Committee on Molecular Biology Techniques | Q41525225 | ||
| Glucuronidation of 7-ethyl-10-hydroxycamptothecin (SN-38), an active metabolite of irinotecan (CPT-11), by human UGT1A1 variants, G71R, P229Q, and Y486D. | Q44251789 | ||
| UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer | Q44922991 | ||
| Rapid detection of UGT1A1 gene polymorphisms by newly developed Invader assay | Q44995510 | ||
| Single nucleotide polymorphism hunting in cyberspace | Q48021515 | ||
| Rapid, nonradioactive detection of mutations in the human genome by allele-specific amplification | Q69742037 | ||
| Detection of single-base changes using a bioluminometric primer extension assay | Q73051262 | ||
| Comprehensive UGT1A1 genotyping in a Japanese population by pyrosequencing | Q73552678 | ||
| The use of a genetic map of biallelic markers in linkage studies | Q73676260 | ||
| Electrophoretic detection of single-nucleotide polymorphisms | Q73686652 | ||
| Single-nucleotide polymorphism analysis by pyrosequencing | Q73775865 | ||
| Multicolor molecular beacons for allele discrimination | Q74109331 | ||
| Multiplex detection of single-nucleotide variations using molecular beacons | Q74618457 | ||
| Polymorphism identification and quantitative detection of genomic DNA by invasive cleavage of oligonucleotide probes | Q74649991 | ||
| Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II | Q74662198 | ||
| Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese | Q77452112 | ||
| From gels to chips: "minisequencing" primer extension for analysis of point mutations and single nucleotide polymorphisms | Q77794370 | ||
| Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism | Q77828485 | ||
| Irinotecan pharmacokinetics/pharmacodynamics and UGT1A genetic polymorphisms in Japanese: roles of UGT1A1*6 and *28 | Q80452767 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 85-91 | |
| P577 | publication date | 2010-01-01 | |
| P1433 | published in | Journal of Clinical Laboratory Analysis | Q15754724 |
| P1476 | title | High-throughput single-base mismatch detection for genotyping of UDP-glucuronosyltransferase (UGT1A1) with probe capture assay coupled with modified allele-specific primer extension reaction (MASPER) | |
| P478 | volume | 24 |
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