(Q71853052)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603536%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Heteroplasmic mitochondrial tRNA(Lys) mutation and its complementation in MERRF patient-derived mitochondrial transformants (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603536%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

Heteroplasmic mitochondrial tRNALys mutation and its complementation in MERRF patient-derived mitochondrial transformants (English)

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

8 June 2024

1 reference

M. Yoneda

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603536

8 June 2024

T. Miyatake

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603536

8 June 2024

G. Attardi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7603536

8 June 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7603536

8 June 2024

publication date

1 January 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603536%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

21 October 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmus.880181420

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

https://onlinelibrary.wiley.com/doi/full/10.1002/mus.880181420

8 June 2024

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

Muscle & nerve. Supplement

8 June 2024

published in

volume

3

page(s)

S95-101

publication date

1995

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7603536

8 June 2024

volume

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603536%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

S95-101

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603536%20AND%20SRC:MED&resulttype=core&format=json

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

21 October 2019

cites work

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1126/SCIENCE.2814477

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

3

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

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

8 June 2024

4

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction

8 June 2024

5

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

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

8 June 2024

7

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

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

8 June 2024

8

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

Quantitation of mitochondrial DNA carrying tRNALys mutation in MERRF patients

8 June 2024

10

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

Uniform tissue distribution of tRNA(Lys) mutation in mitochondrial DNA in MERRF patients

8 June 2024

11

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

8 June 2024

12

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

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

8 June 2024

13

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

Simple detection of tRNALys mutation in myoclonus epilepsy associated with ragged-red fibers (MERRF) by polymerase chain reaction with a mismatched primer

8 June 2024

15

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

A MERRF/MELAS overlap syndrome associated with a new point mutation in the mitochondrial DNA tRNA(Lys) gene

8 June 2024

16

1 reference

https://api.crossref.org/works/10.1002/MUS.880181420

8 June 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7603536%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference