(Q36811500)

English

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

scientific article published on February 1, 1992

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1732728%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

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 (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1732728%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

lactic acidosis

1 reference

based on heuristic

inferred from title

mitochondrial myopathy

1 reference

based on heuristic

inferred from title

protein biosynthesis

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1732728

11 November 2022

1 reference

10.1128/MCB.12.2.480-490.1992

https://api.crossref.org/works/10.1128/MCB.12.2.480-490.1992

11 November 2022

2

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17 September 2019

author name string

M. P. King

1

1 reference

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11 November 2022

M. Davidson

3

1 reference

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11 November 2022

E. A. Schon

4

1 reference

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11 November 2022

language of work or name

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publication date

1 February 1992

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17 September 2019

full work available at URL

http://mcb.asm.org/cgi/content/abstract/12/2/480

online access status

1 reference

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11 November 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1732728/?tool=EBI

online access status

1 reference

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11 November 2022

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/1732728/pdf/?tool=EBI

Portable Document Format

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11 November 2022

https://europepmc.org/articles/PMC364194

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

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11 November 2022

https://europepmc.org/articles/PMC364194?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1732728

11 November 2022

https://journals.asm.org/doi/pdf/10.1128/mcb.12.2.480-490.1992

1 reference

10.1128/MCB.12.2.480-490.1992

https://api.crossref.org/works/10.1128/MCB.12.2.480-490.1992

11 November 2022

Molecular and Cellular Biology

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1732728%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

12

1 reference

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17 September 2019

480-490

1 reference

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1732728%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1732728%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

Protein measurement with the Folin phenol reagent

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

29 September 2017

Sequence and organization of the human mitochondrial genome

1 reference

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29 September 2017

Isolation and characterization of full-length cDNA clones for human alpha-, beta-, and gamma-actin mRNAs: skeletal but not cytoplasmic actins have an amino-terminal cysteine that is subsequently removed

1 reference

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

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29 September 2017

Synthesis and turnover of mitochondrial ribonucleic acid in HeLa cells: the mature ribosomal and messenger ribonucleic acid species are metabolically unstable

1 reference

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29 September 2017

The General Structure of Transfer RNA Molecules

1 reference

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29 September 2017

Conversation of the Molecular Structure of Yeast Phenylalanine Transfer RNA in Two Crystal Forms

1 reference

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29 September 2017

Mitochondrial DNA and human evolution

1 reference

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29 September 2017

In vitro transcription of human mitochondrial DNA: accurate termination requires a region of DNA sequence that can function bidirectionally

1 reference

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29 September 2017

Isolation and mapping of a polymorphic DNA sequence pYNH24 on chromosome 2 (D2S44).

1 reference

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29 September 2017

Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

29 September 2017

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy

1 reference

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29 September 2017

A common mitochondrial DNA mutation in the t-RNA(Lys) of patients with myoclonus epilepsy associated with ragged-red fibers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

29 September 2017

Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

29 September 2017

mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

29 September 2017

Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

29 September 2017

RNA molecular weight determinations by gel electrophoresis under denaturing conditions, a critical reexamination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

29 September 2017

A lineage-specific gene encoding a major matrix protein of the sea urchin embryo spicule. II. Structure of the gene and derived sequence of the protein.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

27 June 2018

Termination of transcription in human mitochondria: identification and purification of a DNA binding protein factor that promotes termination

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

27 June 2018

Heteroplasmy of mitochondrial genomes in clonal cultures from patients with Kearns-Sayre syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

27 June 2018

Cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence for a nuclear DNA-encoded mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

27 June 2018

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

27 June 2018

Antimitochondrial autoantibodies of primary biliary cirrhosis as a novel probe in the study of 2-oxo acid dehydrogenases in patients with mitochondrial myopathies.

1 reference

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27 June 2018

A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

27 June 2018

Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

27 June 2018

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

27 June 2018

Fractionation of mitochondrial RNA from HeLa cells by high-resolution electrophoresis under strongly denaturing conditions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

27 June 2018

Compilation of tRNA sequences and sequences of tRNA genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

5 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=364194

5 September 2018

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1732728

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1732728

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A monoclonal antibody against cytochrome c oxidase distinguishes cardiac and skeletal muscle mitochondria

1 reference

https://pubmed.ncbi.nlm.nih.gov/1732728

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloned mycoplasma ribosomal RNA genes for the detection of mycoplasma contamination in tissue cultures

1 reference

https://pubmed.ncbi.nlm.nih.gov/1732728

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1128/MCB.12.2.480

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1732728%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

10.1128/MCB.12.2.480-490.1992

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1732728

11 November 2022

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1732728%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1732728%20AND%20SRC:MED&resulttype=core&format=json

17 September 2019

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