(Q54620011)

1 June 2018

title

Comparison between medium-chain acyl-CoA dehydrogenase mutant proteins overexpressed in bacterial and mammalian cells. (English)

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1 June 2018

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2

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1 June 2018

Brage Storstein Andresen

3

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1 June 2018

author name string

Jensen TG

1

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1 June 2018

Lund TB

4

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1 June 2018

Kristensen TJ

5

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1 June 2018

Jensen UB

6

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1 June 2018

Winther V

7

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1 June 2018

Kølvraa S

8

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1 June 2018

Gregersen N

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1 June 2018

Bolund L

10

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1 June 2018

publication date

1 January 1995

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1 June 2018

published in

Human Mutation

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1 June 2018

volume

6

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1 June 2018

issue

3

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1 June 2018

page(s)

226-231

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1 June 2018

Co-overexpression of bacterial GroESL chaperonins partly overcomes non-productive folding and tetramer assembly of E. coli-expressed human medium-chain acyl-CoA dehydrogenase (MCAD) carrying the prevalent disease-causing K304E mutation.

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

Characterization of wild-type human medium-chain acyl-CoA dehydrogenase (MCAD) and mutant enzymes present in MCAD-deficient patients by two-dimensional gel electrophoresis: evidence for post-translational modification of the enzyme.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Immunochemical characterization of variant medium-chain acyl-CoA dehydrogenase in fibroblasts from patients with medium-chain acyl-CoA dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Low-density lipoprotein receptor point mutation results in expression of both active and inactive surface forms of the same mutant receptor

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

GroE heat-shock proteins promote assembly of foreign prokaryotic ribulose bisphosphate carboxylase oligomers in Escherichia coli.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coli

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Biosynthesis of variant medium chain acyl-CoA dehydrogenase in cultured fibroblasts from patients with medium chain acyl-CoA dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Biosynthesis of four rat liver mitochondrial acyl-CoA dehydrogenases: in vitro synthesis, import into mitochondria, and processing of their precursors in a cell-free system and in cultured cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Crystal structures of medium-chain acyl-CoA dehydrogenase from pig liver mitochondria with and without substrate

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Improved site-directed mutagenesis method using PCR.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

The mechanism of Z alpha 1-antitrypsin accumulation in the liver

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

The common variant of cystic fibrosis transmembrane conductance regulator is recognized by hsp70 and degraded in a pre-Golgi nonlysosomal compartment

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060305

7 January 2021

Identifiers

DOI

10.1002/HUMU.1380060305

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1 June 2018

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1 June 2018