(Q41208355)

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Electrophoretic separation of multiprotein complexes from blood platelets and cell lines: technique for the analysis of diseases with defects in oxidative phosphorylation

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Europe PubMed Central

PubMed publication ID

28 September 2017

Electrophoretic separation of multiprotein complexes from blood platelets and cell lines: technique for the analysis of diseases with defects in oxidative phosphorylation (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

phosphorylation

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author name string

Schägger H

1

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Bentlage H

2

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Ruitenbeek W

3

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Pfeiffer K

4

1 reference

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PubMed publication ID

28 September 2017

Rotter S

5

1 reference

Europe PubMed Central

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28 September 2017

Rother C

6

1 reference

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28 September 2017

Böttcher-Purkl A

7

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28 September 2017

Lodemann E

8

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28 September 2017

publication date

1 April 1996

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28 September 2017

Electrophoresis

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28 September 2017

17

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28 September 2017

4

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Europe PubMed Central

PubMed publication ID

28 September 2017

709-714

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Europe PubMed Central

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28 September 2017

Complete localization of the intrachain disulphide bonds and the N-glycosylation points in the alpha-subunit of human platelet glycoprotein IIb.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

21 January 2018

Quantification of oxidative phosphorylation enzymes after blue native electrophoresis and two‐dimensional resolution: Normal complex I protein amounts in Parkinson's disease conflict with reduced catalytic activities

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Human diseases with defects in oxidative phosphorylation. 1. Decreased amounts of assembled oxidative phosphorylation complexes in mitochondrial encephalomyopathies

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Human diseases with defects in oxidative phosphorylation. 2. F1F0 ATP-synthase defects in Alzheimer disease revealed by blue native polyacrylamide gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

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The use of skin fibroblast cultures in the detection of respiratory chain defects in patients with lacticacidemia

1 reference

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7 January 2021

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Extreme variability of clinical symptoms among sibs in a MELAS family correlated with heteroplasmy for the mitochondrial A3243G mutation

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytochrome oxidase deficiency in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Binding of fibrinogen and von Willebrand factor to platelet glycoprotein IIb-IIIa complex

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Blue native electrophoresis for isolation of membrane protein complexes in enzymatically active form

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Platelet membrane glycoprotein IIb-IIIa complex: purification, characterization, and reconstitution into phospholipid vesicles

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

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Glanzmann thrombasthenia: deficient binding of von Willebrand factor to thrombin-stimulated platelets

1 reference

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7 January 2021

based on heuristic

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The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Native electrophoresis for isolation of mitochondrial oxidative phosphorylation protein complexes

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Isolation of the eleven protein subunits of the bc1 complex from beef heart

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

On the function of multiple subunits of cytochrome c oxidase from higher eukaryotes

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

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Fo membrane domain of ATP synthase from bovine heart mitochondria: purification, subunit composition, and reconstitution with F1-ATPase.

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of molecular masses and oligomeric states of protein complexes by blue native electrophoresis and isolation of membrane protein complexes by two-dimensional native electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Ubiquinol-cytochrome-c reductase from human and bovine mitochondria

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

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Altered properties of mitochondrial ATP-synthase in patients with a T-->G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial DNA mutations in human diseases: a review

1 reference

https://api.crossref.org/works/10.1002%2FELPS.1150170415

7 January 2021

based on heuristic

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Myopathology and a mitochondrial DNA deletion in the Pearson marrow and pancreas syndrome

1 reference

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7 January 2021

based on heuristic

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Identifiers

10.1002/ELPS.1150170415

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

ResearchGate publication ID

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