(Q28324082)

English

Molecular basis for the lack of bilirubin-specific and 3-methylcholanthrene-inducible UDP-glucuronosyltransferase activities in Gunn rats. The two isoforms are encoded by distinct mRNA species that share an identical single base deletion

scientific article published on September 25, 1991

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Molecular basis for the lack of bilirubin-specific and 3-methylcholanthrene-inducible UDP-glucuronosyltransferase activities in Gunn rats. The two isoforms are encoded by distinct mRNA species that share an identical single base deletion (English)

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10.1016/S0021-9258(18)55268-6

https://api.crossref.org/works/10.1016/S0021-9258(18)55268-6

7 November 2022

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10.1016/S0021-9258(18)55268-6

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author name string

J. Roy-Chowdhury

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Europe PubMed Central

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7 November 2022

T. J. Huang

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7 November 2022

K. Kesari

3

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7 November 2022

M. Lederstein

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7 November 2022

I. M. Arias

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Europe PubMed Central

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7 November 2022

N. Roy-Chowdhury

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Europe PubMed Central

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publication date

25 September 1991

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full work available at URL

http://intl.jbc.org/cgi/content/abstract/266/27/18294

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7 November 2022

https://api.elsevier.com/content/article/PII:S0021925818552686?httpAccept=text/xml

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10.1016/S0021-9258(18)55268-6

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7 November 2022

https://api.elsevier.com/content/article/PII:S0021925818552686?httpAccept=text/plain

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7 November 2022

Journal of Biological Chemistry

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266

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27

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18294-8

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Substrate specificity and characterization of rat liver p-nitrophenol, 3 alpha-hydroxysteroid and 17 beta-hydroxysteroid UDP-glucuronosyltransferases

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10.1016/S0021-9258(18)55268-6

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7 November 2022

Characterization and regulation of rat liver UDP glucuronosyltransferases

3

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10.1016/S0021-9258(18)55268-6

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7 November 2022

Substrates and products of purified rat liver bilirubin UDP-glucuronosyltransferase

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10.1016/S0021-9258(18)55268-6

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7 November 2022

Properties of a 3-methylcholanthrene-inducible phenol UDP-glucuronosyltransferase from rat liver

6

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10.1016/S0021-9258(18)55268-6

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7 November 2022

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

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10.1016/S0021-9258(18)55268-6

https://api.crossref.org/works/10.1016/S0021-9258(18)55268-6

7 November 2022

Constitutional nonhemolytic hyperbilirubinemia in the rat: defect of bilirubin conjugation

10

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10.1016/S0021-9258(18)55268-6

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7 November 2022

Reactivation of a pure defective UDP-glucuronyltransferase from homozygous gunn rat liver

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10.1016/S0021-9258(18)55268-6

https://api.crossref.org/works/10.1016/S0021-9258(18)55268-6

7 November 2022

Drug Metabolism and Disposition

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10

590

author name string

Watkins

publication date

1982

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10.1016/S0021-9258(18)55268-6

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7 November 2022

Isolation of multiple normal and functionally defective forms of uridine diphosphate-glucuronosyltransferase from inbred Gunn rats

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10.1016/S0021-9258(18)55268-6

https://api.crossref.org/works/10.1016/S0021-9258(18)55268-6

7 November 2022

Induction deficiency of the microsomal UDPglucuronosyltransferase by 3-methylcholanthrene in Gunn rats

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10.1016/S0021-9258(18)55268-6

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7 November 2022

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

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10.1016/S0021-9258(18)55268-6

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7 November 2022

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

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10.1016/S0021-9258(18)55268-6

https://api.crossref.org/works/10.1016/S0021-9258(18)55268-6

7 November 2022

DNA sequencing with chain-terminating inhibitors

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10.1016/S0021-9258(18)55268-6

https://api.crossref.org/works/10.1016/S0021-9258(18)55268-6

7 November 2022

Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia

28

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10.1016/S0021-9258(18)55268-6

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7 November 2022

Aberrant splicing and missense mutations cause steroid 21-hydroxylase [P-450(C21)] deficiency in humans: possible gene conversion products

29

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10.1016/S0021-9258(18)55268-6

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7 November 2022

Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency

30

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7 November 2022

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