Rapid proteasomal degradation of translocation-deficient UDP-glucuronosyltransferase 1A1 proteins in patients with Crigler–Najjar type II (Q44612271)

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4 December 2017

Rapid proteasomal degradation of translocation-deficient UDP-glucuronosyltransferase 1A1 proteins in patients with Crigler–Najjar type II (English)

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2003.09.072

20 March 2024

Rapid proteasomal degradation of translocation-deficient UDP-glucuronosyltransferase 1A1 proteins in patients with Crigler-Najjar type II (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14550264

20 March 2024

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2003.09.072

20 March 2024

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2003.09.072

20 March 2024

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2003.09.072

20 March 2024

author name string

Aki Ohnishi

1

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4 December 2017

Yoshikazu Emi

2

1 reference

4 December 2017

language of work or name

English

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publication date

1 October 2003

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4 December 2017

24 October 2003

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14550264

full work available at URL

20 March 2024

https://api.elsevier.com/content/article/PII:S0006291X03018692?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2003.09.072

https://api.elsevier.com/content/article/PII:S0006291X03018692?httpAccept=text/plain

20 March 2024

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2003.09.072

Biochemical and Biophysical Research Communications

20 March 2024

published in

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4 December 2017

310

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4 December 2017

735-741

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The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence

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2

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2003.09.072

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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4

1 reference

https://api.crossref.org/works/10.1016/J.BBRC.2003.09.072

Drug-responsive and tissue-specific alternative expression of multiple first exons in rat UDP-glucuronosyltransferase family 1 (UGT1) gene complex

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Biochemical and molecular aspects of genetic disorders of bilirubin metabolism

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Human UDP-glucuronosyltransferases: metabolism, expression, and disease

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Isolation and characterisation of a new hepatic bilirubin UDP-glucuronosyltransferase. Absence from Gunn rat liver

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

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Accelerated degradation of mislocalized UDP-glucuronosyltransferase family 1 (UGT1) proteins in Gunn rat hepatocytes

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Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 cases

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A mutation which disrupts the hydrophobic core of the signal peptide of bilirubin UDP-glucuronosyltransferase, an endoplasmic reticulum membrane protein, causes Crigler-Najjar type II.

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Inhibitors of the proteasome block the degradation of most cell proteins and the generation of peptides presented on MHC class I molecules

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Identifiers

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4 December 2017

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