(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)

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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

Europe PubMed Central

PubMed publication ID

28 September 2017

Rotter S

5

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Rother C

6

1 reference

Europe PubMed Central

PubMed publication ID

28 September 2017

Böttcher-Purkl A

7

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Europe PubMed Central

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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

PubMed publication ID

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

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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

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7 January 2021

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

1 reference

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

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

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

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

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Cytochrome oxidase deficiency in Alzheimer's disease

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

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

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

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

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

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Native electrophoresis for isolation of mitochondrial oxidative phosphorylation protein complexes

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

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

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

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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

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Ubiquinol-cytochrome-c reductase from human and bovine mitochondria

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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

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Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies

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Mitochondrial DNA mutations in human diseases: a review

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

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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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