(Q39625292)

13 September 2017

A human pathology-related mutation prevents import of an aminoacyl-tRNA synthetase into mitochondria (English)

1 reference

Laurence Maréchal-Drouard

13 September 2017

0 references

1 reference

6

object named as

Laurence Maréchal-Drouard

1 reference

13 September 2017

4

Gert C Scheper

1 reference

13 September 2017

Marie Messmer

1

1 reference

13 September 2017

Catherine Florentz

2

1 reference

13 September 2017

Hagen Schwenzer

3

1 reference

13 September 2017

Marjo S van der Knaap

5

1 reference

13 September 2017

Marie Sissler

7

1 reference

13 September 2017

language of work or name

English

0 references

publication date

1 February 2011

1 reference

13 September 2017

6

1 reference

based on heuristic

inferred from page(s)

published in

Biochemical Journal

1 reference

13 September 2017

433

1 reference

13 September 2017

3

1 reference

13 September 2017

441-446

1 reference

Nuclear genes and mitochondrial translation: a new class of genetic disease

13 September 2017

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Leukoencephalopathy with brainstem and spinal cord involvement and normal lactate: a new mutation in the DARS2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia--MLASA syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Long-range structural effects of a Charcot-Marie-Tooth disease-causing mutation in human glycyl-tRNA synthetase

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Toward the full set of human mitochondrial aminoacyl-tRNA synthetases: characterization of AspRS and TyrRS

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Mitochondrial processing peptidases

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Translocation of proteins into mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Mitochondrial protein-import machinery: correlating structure with function

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Multiple pathways for sorting mitochondrial precursor proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

On the mechanism of preprotein import by the mitochondrial presequence translocase

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Dual targeting is the rule for organellar aminoacyl-tRNA synthetases in Arabidopsis thaliana.

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Precursor protein is readily degraded in mitochondrial matrix space if the leader is not processed by mitochondrial processing peptidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

New functions of aminoacyl-tRNA synthetases beyond translation

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Mitochondrial protein import and human health and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Human deafness dystonia syndrome is a mitochondrial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

The Ala16Val genetic dimorphism modulates the import of human manganese superoxide dismutase into rat liver mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1042%2FBJ20101902

21 January 2018

Identifiers

DOI

10.1042/BJ20101902

1 reference

13 September 2017

1 reference