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Inherited disorders of bilirubin metabolism
scientific article (publication date: 2003)
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instance of
scholarly article
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review article
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stated in
Europe PubMed Central
title
Inherited disorders of bilirubin metabolism
(English)
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author name string
Piter Jabik Bosma
series ordinal
1
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language of work or name
English
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publication date
January 2003
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published in
Journal of Hepatology
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volume
38
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issue
1
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page(s)
107-17
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cites work
Properties and Composition of the Bile Pigment giving a Direct Diazo Reaction
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Direct-reacting bilirubin, bilirubin glucuronide, in serum, bile and urine
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The excretion of bilirubin as a diglucuronide giving the direct van den Bergh reaction
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Uridine compounds in glucuronic acid metabolism. I. The formation of glucuronides in liver suspensions
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Congenital jaundice in rats, due to a defect in glucuronide formation
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The synthesis of bilirubin glucuronide in animal and human liver
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The pathologic dyes
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The enzymatic conversion of heme to bilirubin by microsomal heme oxygenase
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Chronic unconjugated hyperbilirubinemia without overt signs of hemolysis in adolescents and adults
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Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity
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A Biochemical Lesion in Congenital, Non-obstructive, Non-hæmolytic Jaundice
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Substrates and products of purified rat liver bilirubin UDP-glucuronosyltransferase
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Thirteen UDPglucuronosyltransferase genes are encoded at the human UGT1 gene complex locus
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Sequence of exons and the flanking regions of human bilirubin-UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I
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7 January 2021
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Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient
1 reference
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7 January 2021
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Identification of defect in the genes for bilirubin UDP-glucuronosyl-transferase in a patient with Crigler-Najjar syndrome type II
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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A mutation in bilirubin uridine 5'-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type II
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7 January 2021
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Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Assignment of the human UDP glucuronosyltransferase gene (UGT1A1) to chromosome region 2q37
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Effects of phenobarbital on bilirubin metabolism and its response to phototherapy in the jaundiced Gunn rat
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7 January 2021
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The differential diagnosis of Crigler-Najjar disease, types 1 and 2, by bile pigment analysis
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
based on heuristic
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Crigler-Najjar syndrome type II is inherited both as a dominant and as a recessive trait
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7 January 2021
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Homodimerization of human bilirubin-uridine-diphosphoglucuronate glucuronosyltransferase-1 (UGT1A1) and its functional implications
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Oral calcium phosphate: a new therapy for Crigler-Najjar disease?
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7 January 2021
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Treatment of the Crigler-Najjar syndrome type I with hepatocyte transplantation
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Gene therapy for inherited hyperbilirubinemias
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia
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7 January 2021
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[Prevalence of Gilbert's syndrome in Germany]
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Bilirubin glucuronide formation in vitro; demonstration of a defect in Gilbert's disease
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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inferred from DOI database lookup
Hepatic Bilirubin UDP-Glucuronyl Transferase Activity in Liver Disease and Gilbert's Syndrome
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Unconjugated Bilirubin and an Increased Proportion of Bilirubin Monoconjugates in the Bile of Patients with Gilbert's Syndrome and Crigler-Najjar Disease
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Detection of Gilbert's syndrome in patients with hemolysis. A method using radioactive chromium.
1 reference
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7 January 2021
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Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Predicted homozygous mis-sense mutation in Gilbert's syndrome
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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The genetic basis of Gilbert's syndrome
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Bilirubin is an antioxidant of possible physiological importance
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Serum bilirubin and risk of ischemic heart disease in middle-aged British men
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Induction of human UDP-glucuronosyltransferase UGT1A1 by flavonoids-structural requirements
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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In vitro induction of bilirubin conjugation in primary rat hepatocyte culture
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Gilbert syndrome associated with beta-thalassemia
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Alteration of drug metabolism in Gilbert's syndrome
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Investigation of the substrate specificity of a cloned expressed human bilirubin UDP-glucuronosyltransferase: UDP-sugar specificity and involvement in steroid and xenobiotic glucuronidation
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Endogenous hormones and breast cancer risk
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7 January 2021
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Kinetics and metabolism of paracetamol and phenacetin
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7 January 2021
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Normal pathways for glucuronidation, sulphation and oxidation of paracetamol in Gilbert's syndrome
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7 January 2021
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Decreased glucuronidation and increased bioactivation of acetaminophen in Gilbert's syndrome
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7 January 2021
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Paracetamol glucuronidation by recombinant rat and human phenol UDP-glucuronosyltransferases
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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UDP-glucuronosyltransferase (UGT1A1*28 and UGT1A6*2) polymorphisms in Caucasians and Asians: relationships to serum bilirubin concentrations
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Genetic polymorphism in the human UGT1A6 (planar phenol) UDP-glucuronosyltransferase: pharmacological implications
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Antitumor activity of a camptothecin derivative, CPT-11, against human tumor xenografts in nude mice
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
based on heuristic
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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
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
based on heuristic
inferred from DOI database lookup
Relationship between development of diarrhea and the concentration of SN-38, an active metabolite of CPT-11, in the intestine and the blood plasma of athymic mice following intraperitoneal administration of CPT-11.
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Severe CPT-11 toxicity in patients with Gilbert's syndrome: two case reports
1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Phase I clinical and pharmacogenetic study of weekly TAS-103 in patients with advanced cancer
1 reference
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7 January 2021
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7 January 2021
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1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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1 reference
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https://api.crossref.org/works/10.1016%2FS0168-8278%2802%2900359-8
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7 January 2021
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Identifiers
DOI
10.1016/S0168-8278(02)00359-8
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4468486
OpenCitations bibliographic resource ID
4468486
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4468486
PubMed publication ID
12480568
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
4468486
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