Complex III staining in blue native polyacrylamide gels (Q49065871)

18 February 2018

title

Complex III staining in blue native polyacrylamide gels (English)

1 reference

18 February 2018

1 reference

1

1 reference

18 February 2018

author name string

Boel De Paepe

2

1 reference

18 February 2018

Sara Seneca

3

1 reference

18 February 2018

Willy Lissens

4

1 reference

18 February 2018

Heike Kotarsky

5

1 reference

18 February 2018

Linda De Meirleir

6

1 reference

18 February 2018

Vineta Fellman

7

1 reference

18 February 2018

Rudy Van Coster

8

1 reference

18 February 2018

publication date

12 April 2011

1 reference

18 February 2018

Journal of Inherited Metabolic Disease

published in

1 reference

18 February 2018

volume

34

1 reference

18 February 2018

issue

3

1 reference

18 February 2018

page(s)

741-747

1 reference

18 February 2018

Mitochondrial complex III deficiency associated with a homozygous mutation in UQCRQ

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

Electrophoresis techniques to investigate defects in oxidative phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

Respiratory-chain diseases related to complex III deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

A mutant mitochondrial respiratory chain assembly protein causes complex III deficiency in patients with tubulopathy, encephalopathy and liver failure.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

The GRACILE syndrome, a neonatal lethal metabolic disorder with iron overload

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

Missense mutations in the BCS1L gene as a cause of the Björnstad syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

An improved spectrophotometric method for a more specific and accurate assay of mitochondrial complex III activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

The epidemiology of mitochondrial disorders--past, present and future

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

High resolution clear native electrophoresis for in-gel functional assays and fluorescence studies of membrane protein complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

Quantification of muscle mitochondrial oxidative phosphorylation enzymes via histochemical staining of blue native polyacrylamide gels

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9315-7

Aberrant synthesis of ATP synthase resulting from a novel deletion in mitochondrial DNA in an African patient with progressive external ophthalmoplegia

21 January 2018

1 reference

12 December 2020

Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation

1 reference

12 December 2020

Evaluation of the mitochondrial respiratory chain and oxidative phosphorylation system using blue native gel electrophoresis

1 reference

12 December 2020

Screening of BCS1L mutations in severe neonatal disorders suspicious for mitochondrial cause

1 reference

12 December 2020

Three spectrophotometric assays for the measurement of the five respiratory chain complexes in minuscule biological samples

1 reference

12 December 2020

Abdominal pain and vomiting as first sign of mitochondrial disease

1 reference

12 December 2020

A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis

1 reference

12 December 2020

10.1007/S10545-011-9315-7

Identifiers

DOI

1 reference

18 February 2018

Dimensions Publication ID

1046728423

0 references

1 reference

18 February 2018