Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

about

Mitochondrial Genome Engineering: The Revolution May Not Be CRISPR-Ized.Dedicated surveillance mechanism controls G-quadruplex forming non-coding RNAs in human mitochondria.

P2860

Q47309962-E3B67D9E-6D0E-4321-834D-C54F1BA07A4C Q55434236-DF694E6C-23F2-44CE-A4C0-3F38B304DDF6

P2860

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

Item

http://www.wikidata.org/entity/Q47853362

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

@en

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

@nl

type

Item

label

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

@en

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

@nl

prefLabel

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

@en

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

@nl

P1476

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome

@en

P2093

Anders Paetau

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

Anu Suomalainen

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

Liliya Euro

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

Max Pohjanpelto

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

Pirjo Isohanni

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

Sanna Matilainen

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

Uwe Richter

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

P2860

PNPASE regulates RNA import into mitochondria

Mammalian polynucleotide phosphorylase is an intermembrane space RNase that maintains mitochondrial homeostasis

Defining the domains of human polynucleotide phosphorylase (hPNPaseOLD-35) mediating cellular senescence.

RNase P without RNA: identification and functional reconstitution of the human mitochondrial tRNA processing enzyme

Mitochondrial RNA Granules Are Centers for Posttranscriptional RNA Processing and Ribosome Biogenesis

Subacute necrotizing encephalomyelopathy in an infant

A mitochondrial protein compendium elucidates complex I disease biology

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Crystal structure of human polynucleotide phosphorylase: insights into its domain function in RNA binding and degradation

LRPPRC/SLIRP suppresses PNPase-mediated mRNA decay and promotes polyadenylation in human mitochondria

P304

3352-3361

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

P31

scholarly article

P356

10.1093/HMG/DDX221

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

P433

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

P478

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

P50

Christopher J Carroll

P577

2017-09-01T00:00:00Z

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

P698

28645153

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

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

about

P2860

P2860

Defective mitochondrial RNA processing due to PNPT1 variants causes Leigh syndrome.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698