(Q71890068)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8965724%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

Detection and analysis of mitochondrial DNA and RNA in muscle by in situ hybridization and single-fiber PCR (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8965724%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference

C T Moraes

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8965724%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

E A Schon

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8965724%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

publication date

1 January 1996

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8965724%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

published in

Methods in Enzymology

1 reference

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22 October 2019

volume

264

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8965724%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

page(s)

522-540

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8965724%20AND%20SRC:MED&resulttype=core&format=json

describes a project that uses

22 October 2019

in situ hybridization

1 reference

Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions

inferred from title

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB).

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNA(Leu(UUR)) gene an etiologic hot spot?

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

A mitochondrial tRNA anticodon swap associated with a muscle disease

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2896%2964046-4

7 January 2021

10.1016/S0076-6879(96)64046-4

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8965724%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference