Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

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Ginsenoside Rd attenuates mitochondrial permeability transition and cytochrome C release in isolated spinal cord mitochondria: involvement of kinase-mediated pathways.

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Q33907618-6EC79F0C-A66A-4543-9683-AF68797E80C2

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Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

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http://www.wikidata.org/entity/Q50478827

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2014 nî lūn-bûn

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2014年の論文

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Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

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Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

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Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

@en

Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

@nl

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Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

@en

Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

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Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

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Alexandre Umpierrez Amaral

http://www.w3.org/2001/XMLSchema#string

Cristiane Cecatto

http://www.w3.org/2001/XMLSchema#string

Moacir Wajner

http://www.w3.org/2001/XMLSchema#string

Roger Frigério Castilho

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P2860

Ethylmalonic encephalopathy is caused by mutations in ETHE1, a gene encoding a mitochondrial matrix protein.

ETHE1 mutations are specific to ethylmalonic encephalopathy

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays

Mitochondrial permeability transition in acute neurodegeneration

Ethylmalonic encephalopathy: clinical and biochemical observations

Loss of cyclophilin D reveals a critical role for mitochondrial permeability transition in cell death

Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin

The ACADS gene variation spectrum in 114 patients with short-chain acyl-CoA dehydrogenase (SCAD) deficiency is dominated by missense variations leading to protein misfolding at the cellular level

Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy

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s12640-014-9460-5

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168-178

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scholarly article

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10.1007/S12640-014-9460-5

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P478

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Guilhian Leipnitz

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2014-02-21T00:00:00Z

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P698

24557940

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Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

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Ethylmalonic acid induces permeability transition in isolated brain mitochondria.

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P1476

P2093

P2860

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P1433

P1476

P2093

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