Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.

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Human adenine nucleotide translocases physically and functionally interact with respirasomes.Cardiomyopathy-associated mutation in the ADP/ATP carrier reveals translation-dependent regulation of cytochrome c oxidase activity.

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Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.

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http://www.wikidata.org/entity/Q39860333

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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Deficiency in the mouse mitoch ...... ed with cardiac noncompaction.

@en

Deficiency in the mouse mitoch ...... ed with cardiac noncompaction.

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type

Item

label

Deficiency in the mouse mitoch ...... ed with cardiac noncompaction.

@en

Deficiency in the mouse mitoch ...... ed with cardiac noncompaction.

@nl

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Deficiency in the mouse mitoch ...... ed with cardiac noncompaction.

@en

Deficiency in the mouse mitoch ...... ed with cardiac noncompaction.

@nl

P1476

Deficiency in the mouse mitoch ...... ed with cardiac noncompaction.

@en

P2093

Adrian Flierl

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Alessia Angelin

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Douglas C Wallace

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Grant R MacGregor

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Jason E Kokoszka

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Katelyn M Sweeney

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Katrina G Waymire

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P2860

Suppression of adenine nucleotide translocase-2 by vector-based siRNA in human breast cancer cells induces apoptosis and inhibits tumor growth in vitro and in vivo

DNA sequences of two expressed nuclear genes for human mitochondrial ADP/ATP translocase

cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes

Two distinct genes for ADP/ATP translocase are expressed at the mRNA level in adult human liver

Cell death disguised: The mitochondrial permeability transition pore as the c-subunit of the F(1)F(O) ATP synthase

A human muscle adenine nucleotide translocator gene has four exons, is located on chromosome 4, and is differentially expressed.

Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy

The ADP/ATP translocator is not essential for the mitochondrial permeability transition pore

An uncoupling channel within the c-subunit ring of the F1FO ATP synthase is the mitochondrial permeability transition pore

Dimers of mitochondrial ATP synthase form the permeability transition pore

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1203-1212

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scholarly article

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10.1016/J.BBABIO.2016.03.026

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1857

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2016-04-02T00:00:00Z

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27048932

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5100012

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Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.

about

P2860

P2860

Deficiency in the mouse mitochondrial adenine nucleotide translocator isoform 2 gene is associated with cardiac noncompaction.

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label

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P932