(Q43623400)

25 November 2017

title

Assay of mitochondrial ATP synthesis in animal cells (English)

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25 November 2017

Manfredi G

1

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25 November 2017

Spinazzola A

series ordinal

2

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25 November 2017

Checcarelli N

series ordinal

3

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25 November 2017

Naini A

series ordinal

4

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25 November 2017

publication date

1 January 2001

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25 November 2017

published in

Methods in Cell Biology

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25 November 2017

volume

65

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25 November 2017

page(s)

133-145

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Kinetics of the firefly luciferase catalyzed reactions

25 November 2017

cites work

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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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7 January 2021

Decreased ATP synthesis is phenotypically expressed during increased energy demand in fibroblasts containing mitochondrial tRNA mutations

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7 January 2021

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

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Principles of carrier catalysis elucidated by comparing two similar membrane translocators from mitochondria, the ADP/ATP carrier and the uncoupling protein

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7 January 2021

Functional characterization of mitochondrial oxidative phosphorylation in saponin-skinned human muscle fibers

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P1,P5-Di(Adenosine-5′)Pentaphosphate(Ap5A) as an Inhibitor of Adenylate Kinase in Studies of Fragmented Sarcoplasmic Reticulum from Bullfrog Skeletal Muscle1

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7 January 2021

Adenosine triphosphate: Continuous measurement in mitochondrial suspensions by firefly luciferase luminescence

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Continuous measurement and rapid kinetics of ATP synthesis in rat liver mitochondria, mitoplasts and inner membrane vesicles determined by firefly-luciferase luminescence

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Regulatory effects of ATP and luciferin on firefly luciferase activity

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7 January 2021

Continuous monitoring of ATP levels in living insulin secreting cells expressing cytosolic firefly luciferase

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Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 gene.

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The mitochondrial DNA mutation at 8993 associated with NARP slows the rate of ATP synthesis in isolated lymphoblast mitochondria

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Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

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7 January 2021

Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome

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7 January 2021

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7 January 2021

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Mitochondrial oxidative phosphorylation in digitonin-permeabilized chorionic villus fibroblasts: a new method with potential for prenatal diagnosis

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Prenatal diagnosis of systemic disorders of the respiratory chain in cultured chorionic villus fibroblasts by study of ATP-synthesis in digitonin-permeabilized cells

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A luminometric method for the determination of ATP and phosphocreatine in single human skeletal muscle fibres

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SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome

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7 January 2021

10.1016/S0091-679X(01)65008-8

Identifiers

DOI

1 reference

25 November 2017

1 reference