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The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.

Mitochondrial creatine kinase in human health and disease

Open access
Schlattner, Uwe, Tokarska-Schlattner, Malgorzata, Wallimann, Theo·2006·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Abstract

Mitochondrial creatine kinase (MtCK), together with cytosolic creatine kinase isoenzymes and the highly diffusible CK reaction product, phosphocreatine, provide a temporal and spatial energy buffer to maintain cellular energy homeostasis. Mitochondrial proteolipid complexes containing MtCK form microcompartments that are involved in channeling energy in form of phosphocreatine rather than ATP into the cytosol. Under situations of compromised cellular energy state, which are often linked to ischemia, oxidative stress and calcium overload, two characteristics of mitochondrial creatine kinase are particularly relevant: its exquisite susceptibility to oxidative modifications and the compensatory up-regulation of its gene expression, in some cases leading to accumulation of crystalline MtCK inclusion bodies in mitochondria that are the clinical hallmarks for mitochondrial cytopathies. Both of these events may either impair or reinforce, respectively, the functions of mitochondrial MtCK complexes in cellular energy supply and protection of mitochondria form the so-called permeability transition leading to apoptosis or necrosis.

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Crossref · 10.1016/j.bbadis.2005.09.004

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Metadata

Authors
Schlattner, U., Tokarska-Schlattner, M., & Wallimann, T.
Venue
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Publisher
Elsevier BV
Published
2006-02
Volume
1762
Issue
2
Pages
164-180
ISSN
0925-4439 (ISSN-L)
OpenAlex
W2134017403
Cited by
622
References
14
FWCI
7.72
Type
journal article
Language
en
Open access
bronze

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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