Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Dongrui Zhou

Molecular Probes for Identification of UDP-glucuronosyltransferase 1 Gene Polymorphisms for Gilbert's Syndrome Diagnosis

Biomedical Research

2018

English

Related publications

Identification of a Novel Deletion in UDP-glucuronosyltransferase Gene in a Patient With Crigler–Najjar Syndrome Type I

Blood Cells, Molecules, and Diseases

English

Genotyping of the UDP-Glucuronosyltransferase (UGT) 1A7 Gene Revisited

English

Variations in the UDP-glucuronosyltransferase 1A1 Gene for the Development of Unconjugated Hyperbilirubinemia in Taiwanese

English

Identification of a Genetic Alteration in the Code for Bilirubin UDP-glucuronosyltransferase in the UGT1 Gene Complex of a Crigler-Najjar Type I Patient.

Journal of Clinical Investigation

Medicine

1992

English

Sequence Variations in the UDP-glucuronosyltransferase 2B7 (UGT2B7) Gene: Identification of 10 Novel Single Nucleotide Polymorphisms (SNPs) and Analysis of Their Relevance to Morphine Glucuronidation in Cancer Patients

Pharmacogenomics Journal

English

Ligand Orientation Governs Conjugation Capacity of UDP-glucuronosyltransferase 1A1

Journal of Biochemistry

English

Cloning and Characterization of the Human UDP-glucuronosyltransferase 1A8, 1A9, and 1A10 Gene Promoters

Journal of Biological Chemistry

English

The UDP-Glucuronosyltransferase 2B17 Gene Deletion Polymorphism: Sex-Specific Association With Urinary 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanol Glucuronidation Phenotype and Risk for Lung Cancer

Cancer Epidemiology Biomarkers and Prevention

English

Immune Response to Lentiviral Bilirubin UDP-glucuronosyltransferase Gene Transfer in Fetal and Neonatal Rats

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Dongrui Zhou

Molecular Probes for Identification of UDP-glucuronosyltransferase 1 Gene Polymorphisms for Gilbert's Syndrome Diagnosis

Related publications

Identification of a Novel Deletion in UDP-glucuronosyltransferase Gene in a Patient With Crigler–Najjar Syndrome Type I

Genotyping of the UDP-Glucuronosyltransferase (UGT) 1A7 Gene Revisited

Variations in the UDP-glucuronosyltransferase 1A1 Gene for the Development of Unconjugated Hyperbilirubinemia in Taiwanese

Identification of a Genetic Alteration in the Code for Bilirubin UDP-glucuronosyltransferase in the UGT1 Gene Complex of a Crigler-Najjar Type I Patient.

Sequence Variations in the UDP-glucuronosyltransferase 2B7 (UGT2B7) Gene: Identification of 10 Novel Single Nucleotide Polymorphisms (SNPs) and Analysis of Their Relevance to Morphine Glucuronidation in Cancer Patients

Ligand Orientation Governs Conjugation Capacity of UDP-glucuronosyltransferase 1A1

Cloning and Characterization of the Human UDP-glucuronosyltransferase 1A8, 1A9, and 1A10 Gene Promoters

The UDP-Glucuronosyltransferase 2B17 Gene Deletion Polymorphism: Sex-Specific Association With Urinary 4-(Methylnitrosamino)-1-(3-Pyridyl)-1-Butanol Glucuronidation Phenotype and Risk for Lung Cancer

Immune Response to Lentiviral Bilirubin UDP-glucuronosyltransferase Gene Transfer in Fetal and Neonatal Rats