(Q44594109)

English

Misfolding, degradation, and aggregation of variant proteins. The molecular pathogenesis of short chain acyl-CoA dehydrogenase (SCAD) deficiency

scientific article published on 23 September 2003

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Misfolding, degradation, and aggregation of variant proteins. The molecular pathogenesis of short chain acyl-CoA dehydrogenase (SCAD) deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

5

object named as

Lars Bolund

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

author name string

Christina Bak Pedersen

1

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Peter Bross

2

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Vibeke Stenbroen Winter

3

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Thomas Juhl Corydon

4

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Kim Bartlett

6

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Niels Gregersen

8

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

language of work or name

0 references

publication date

23 September 2003

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

number of pages

10

1 reference

based on heuristic

inferred from page(s)

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

278

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

48

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

47449-47458

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

Molecular cloning and nucleotide sequence of complementary DNAs encoding human short chain acyl-coenzyme A dehydrogenase and the study of the molecular basis of human short chain acyl-coenzyme A dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Short-chain acyl-coenzyme A dehydrogenase deficiency. Clinical and biochemical studies in two patients

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase gene

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Genetic deficiency of short-chain acyl-coenzyme A dehydrogenase in cultured fibroblasts from a patient with muscle carnitine deficiency and severe skeletal muscle weakness

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Transient organic aciduria and persistent lacticacidemia in a patient with short-chain acyl-coenzyme A dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Short chain acyl-coenzyme A dehydrogenase (SCAD) deficiency. Immunochemical demonstration of molecular heterogeneity due to variant SCAD with differing stability

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Ethylmalonic aciduria is associated with an amino acid variant of short chain acyl-coenzyme A dehydrogenase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Purification and characterization of two polymorphic variants of short chain acyl-CoA dehydrogenase reveal reduction of catalytic activity and stability of the Gly185Ser enzyme

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

A mitochondrial specific stress response in mammalian cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Short-chain acyl-coenzyme A dehydrogenase deficiency in mice.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Molecular chaperones in cellular protein folding

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Molecular chaperones and mitochondrial protein folding

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Defining the eukaryotic cytosolic chaperonin-binding sites in human tubulins

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Mutational screen identifies critical amino acid residues of beta-actin mediating interaction between its folding intermediates and eukaryotic cytosolic chaperonin CCT.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Mutant Cu/Zn-superoxide dismutase proteins have altered solubility and interact with heat shock/stress proteins in models of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Kinetic partitioning of protein folding and aggregation.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

The structural basis of protein folding and its links with human disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Molecular basis of the neurodegenerative disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Alternate aggregation pathways of the Alzheimer beta-amyloid peptide. An in vitro model of preamyloid.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Neurodegenerative disorders of protein aggregation

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Protein folding and disease: a view from the first Horizon Symposium.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Crystal structure of rat short chain acyl-CoA dehydrogenase complexed with acetoacetyl-CoA: comparison with other acyl-CoA dehydrogenases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

The requirement of matrix ATP for the import of precursor proteins into the mitochondrial matrix and intermembrane space.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Short-chain acyl-CoA dehydrogenase deficiency in a 16-year-old girl with severe muscle wasting and scoliosis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Protein folding in mitochondria requires complex formation with hsp60 and ATP hydrolysis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Grp78 Is Involved in Retention of Mutant Low Density Lipoprotein Receptor Protein in the Endoplasmic Reticulum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

A new case of short-chain acyl-CoA dehydrogenase deficiency with isolated ethylmalonic aciduria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Mild or absent clinical signs in twin sisters with short-chain acyl-CoA dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Acute fatty liver of pregnancy associated with short-chain acyl-coenzyme A dehydrogenase deficiency

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: one of the variant alleles, 511C-->T, is present at an unexpectedly high frequency in the general population, as was the case for 625G-->A, to

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Effects of two mutations detected in medium chain acyl-CoA dehydrogenase (MCAD)-deficient patients on folding, oligomer assembly, and stability of MCAD enzyme

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Studies on the Effects of Saturated and Unsaturated Short-Chain Monocarboxylic Acids on the Energy Metabolism of Rat Liver Mitochondria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Aggregation of misfolded proteins can be a selective process dependent upon peptide composition

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M309514200

21 January 2018

Identifiers

10.1074/JBC.M309514200

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

4 December 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q44594109&oldid=2110966932"