(Q73729911)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Point mutations in the mitochondrial tRNA(Lys) gene: implications for pathogenesis and mechanism (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

author name string

J P Masucci

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

E A Schon

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

M P King

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 September 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

Molecular and Cellular Biochemistry

6 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

174

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

1-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

215-219

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9309690%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1023/a:1006808524536

6 November 2019

exact match

0 references

cites work

Complementation of mutant and wild-type human mitochondrial DNAs coexisting since the mutation event and lack of complementation of DNAs introduced separately into a cell within distinct organelles

1 reference

12 December 2020

In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: two genotypes produce similar phenotypes.

1 reference

12 December 2020

Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNALeu(UUR) gene

1 reference

12 December 2020

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination

1 reference

12 December 2020

Lysyl-tRNA synthetase

1 reference

12 December 2020

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

1 reference

12 December 2020

Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)

1 reference

12 December 2020

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

1 reference

12 December 2020

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

12 December 2020

On the directional specificity of ribosome frameshifting at a "hungry" codon

1 reference

12 December 2020

A new mtDNA mutation in the tRNA(Lys) gene associated with myoclonic epilepsy and ragged-red fibers (MERRF)

1 reference

12 December 2020

Uncharged tRNA, protein synthesis, and the bacterial stringent response

1 reference

12 December 2020

In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria

1 reference

12 December 2020