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Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS.
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
title
Fine mapping of mitochondrial RNAs derived from the mtDNA region containing a point mutation associated with MELAS
(English)
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
author
Yasutoshi Koga
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
author name string
M Davidson
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
E A Schon
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
M P King
series ordinal
4
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
language of work or name
English
0 references
publication date
1 February 1993
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
published in
Nucleic Acids Research
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
volume
21
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
page(s)
657-662
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
cites work
tRNA punctuation model of RNA processing in human mitochondria
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
Distinctive features of the 5'-terminal sequences of the human mitochondrial mRNAs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
Sequence and organization of the human mitochondrial genome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
Ribonucleic acid isolated by cesium chloride centrifugation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
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8 July 2018
Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
Termination of transcription in human mitochondria: identification and purification of a DNA binding protein factor that promotes termination
1 reference
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PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
Mitochondrial DNA mutations in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
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
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
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8 July 2018
A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
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
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
The mitochondrial tRNA(Leu)(UUR)) mutation in MELAS: a model for pathogenesis
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
8 July 2018
The pattern of transcription of the human mitochondrial rRNA genes reveals two overlapping transcription units
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
26 October 2018
Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=309166
retrieved
26 October 2018
Sequence analysis and precise mapping of the 3' ends of HeLa cell mitochondrial ribosomal RNAs
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7680123
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Secondary structure analysis of apolipoprotein II mRNA using enzymatic probes and reverse transcriptase. Evaluation of primer extension for high resolution structure mapping of mRNA
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/7680123
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1093/NAR/21.3.657
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
PMCID
309166
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
PubMed ID
7680123
1 reference
stated in
Europe PubMed Central
PMCID
309166
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7680123%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
ResearchGate publication ID
15519287
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