Investigation of the molecular basis of the genetic deficiency of UDP-glucuronosyltransferase in Crigler-Najjar syndrome. (Q36816805)

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17 September 2019

review article

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title

Investigation of the molecular basis of the genetic deficiency of UDP-glucuronosyltransferase in Crigler-Najjar syndrome (English)

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17 September 2019

2

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17 September 2019

Michael Coughtrie

5

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17 September 2019

author name string

K J Robertson

1

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17 September 2019

L Sutherland

3

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17 September 2019

R Wooster

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17 September 2019

B Burchell

6

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17 September 2019

publication date

1 January 1991

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Journal of Inherited Metabolic Disease

17 September 2019

published in

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17 September 2019

volume

14

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17 September 2019

issue

4

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17 September 2019

page(s)

563-579

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https://scigraph.springernature.com/pub.10.1007/bf01797927

17 September 2019

exact match

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cites work

Analysis of bilirubin and bilirubin mono- and di-conjugates. Determination of their relative amounts in biological samples

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https://api.crossref.org/works/10.1007%2FBF01797927

Cloning of a human liver microsomal UDP-glucuronosyltransferase cDNA

21 January 2018

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An accurate and sensitive analysis by high-pressure liquid chromatography of conjugated and unconjugated bilirubin IX-alpha in various biological fluids

21 January 2018

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An investigation of the transverse topology of bilirubin UDP-glucuronosyltransferase in rat hepatic endoplasmic reticulum

21 January 2018

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Genetic deficiency of bilirubin glucuronidation in rats and humans

21 January 2018

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12 December 2020

UDP-glucuronyltransferase in perfused rat liver and in microsomes - III. Effects of galactosamine and carbon tetrachloride on the glucuronidation of 1-naphthol and bilirubin

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12 December 2020

Congenital familial nonhemolytic jaundice with kernicterus

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12 December 2020

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

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12 December 2020

Immunochemical analysis of uridine diphosphate-glucuronosyltransferase in four patients with the Crigler-Najjar syndrome type I.

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12 December 2020

The inadequacy of perinatal glucuronidation: immunoblot analysis of the developmental expression of individual UDP-glucuronosyltransferase isoenzymes in rat and human liver microsomes.

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12 December 2020

Determination of bilirubin glucuronide and assay of glucuronyltransferase with bilirubin as acceptor

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12 December 2020

Crigler-Najjar type II disease inheritance: a family study

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12 December 2020

Population studies on Gilbert's syndrome

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12 December 2020

The 3-methylcholanthrene-inducible UDP-glucuronosyltransferase deficiency in the hyperbilirubinemic rat (Gunn rat) is caused by a -1 frameshift mutation

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12 December 2020

Molecular pathology of glucose-6-phosphatase

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12 December 2020

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

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12 December 2020

The enantioselective glucuronidation of morphine in rats and humans. Evidence for the involvement of more than one UDP-glucuronosyltransferase isoenzyme

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12 December 2020

Topology and regulation of bilirubin UDP-glucuronyltransferase in sealed native microsomes from rat liver.

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12 December 2020

Liquid-chromatographic assay and identification of mono- and diester conjugates of bilirubin in normal serum

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12 December 2020

High-performance liquid chromatographic analysis of bile pigments as their native tetrapyrroles and as their dipyrrolic azosulfanilate derivatives

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12 December 2020

Isolation and sequencing of rat liver bilirubin UDP-glucuronosyltransferase cDNA: possible alternate splicing of a common primary transcript

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12 December 2020

Determination of bilirubin UDP-glucuronyl transferase activity in needle-biopsy specimens of human liver

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12 December 2020

Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity

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12 December 2020

Mechanism of the lack of induction of UDP-glucuronosyltransferase activity in Gunn rats by 3-methylcholanthrene. Identification of a truncated enzyme

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12 December 2020

Isolation and purification of rat liver morphine UDP-glucuronosyltransferase

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12 December 2020

STUDIES ON THE INHERITANCE OF CRIGLER--NAJJAR'S SYNDROME BY THE MENTHOL TEST

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12 December 2020

UDP-glucuronosyltransferases

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12 December 2020

Protein measurement with the Folin phenol reagent

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12 December 2020

Studies of UDP-glucuronyltransferase activities in human liver microsomes

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12 December 2020

Evidence indicating that UDP-N-acetylglucosamine does not appear to stimulate hepatic microsomal UDP-glucuronosyltransferase by interaction with the catalytic unit of the enzyme

1 reference

12 December 2020

Prolonged survival in three brothers with severe type 2 Crigler-Najjar syndrome. Ultrastructural and metabolic studies

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12 December 2020

Determination of morphine, morphine-3-glucuronide and (tentatively) morphine-6-glucuronide in plasma and urine using ion-pair high-performance liquid chromatography

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12 December 2020

Identifiers

DOI

10.1007/BF01797927

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1749222%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

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