Mouse models for mitochondrial diseases. - Test2 - elhamkhani - TriplyDB

Mouse models for mitochondrial diseases.

Mouse models for mitochondrial diseases.

http://www.wikidata.org/entity/Q38872626

about

Pharmacologic modeling of primary mitochondrial respiratory chain dysfunction in zebrafish.Genetic Counselling for Maternally Inherited Mitochondrial Disorders.The emerging role of immune dysfunction in mitochondrial diseases as a paradigm for understanding immunometabolism.

P2860

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P2860

Mouse models for mitochondrial diseases.

http://www.wikidata.org/entity/Q38872626

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Mouse models for mitochondrial diseases.

@en

type

label

Mouse models for mitochondrial diseases.

@en

prefLabel

Mouse models for mitochondrial diseases.

@en

P1433

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P1476

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P2093

Q38872626-FCB248CA-8A03-4277-9A7A-50B1241C34C5

P2860

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P31

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P1433

Human Molecular Genetics

P1476

Mouse models for mitochondrial diseases

@en

P2093

Benedetta Ruzzenente

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

P2860

Genome engineering using the CRISPR-Cas9 system

LRPPRC is necessary for polyadenylation and coordination of translation of mitochondrial mRNAs

Interaction of human SUV3 RNA/DNA helicase with BLM helicase; loss of the SUV3 gene results in mouse embryonic lethality

Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathy

Disruption of a mitochondrial RNA-binding protein gene results in decreased cytochrome b expression and a marked reduction in ubiquinol-cytochrome c reductase activity in mouse heart mitochondria

Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics.

NSUN4 is a dual function mitochondrial protein required for both methylation of 12S rRNA and coordination of mitoribosomal assembly

MTO1-deficient mouse model mirrors the human phenotype showing complex I defect and cardiomyopathy.

A conserved modified wobble nucleoside (mcm5s2U) in lysyl-tRNA is required for viability in yeast

Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

P31

scholarly article

P356

10.1093/HMG/DDW176

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P50

Metodi D Metodiev

P577

2016-06-21T00:00:00Z

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P698

27329762

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