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Mss51p and Cox14p jointly regulate mitochondrial Cox1p expression in Saccharomyces cerevisiae
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instance of
scholarly article
1 reference
stated in
PubMed
PubMed ID
15306853
retrieved
1 December 2016
title
Mss51p and Cox14p jointly regulate mitochondrial Cox1p expression in Saccharomyces cerevisiae
(English)
1 reference
stated in
PubMed
PubMed ID
15306853
retrieved
1 December 2016
main subject
Saccharomyces cerevisiae
0 references
Cox14p YML129C
1 reference
stated in
GOA release 2020-03-11
Mss51p YLR203C
1 reference
stated in
GOA release 2020-03-11
Shy1p YGR112W
1 reference
stated in
GOA release 2020-03-11
mitochondrion
1 reference
based on heuristic
inferred from title
author
Alexander Tzagoloff
series ordinal
3
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author name string
Antoni Barrientos
series ordinal
1
0 references
Andrea Zambrano
series ordinal
2
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language of work or name
English
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publication date
1 September 2004
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published in
The EMBO Journal
1 reference
stated in
PubMed
PubMed ID
15306853
retrieved
1 December 2016
volume
23
0 references
page(s)
3472-82
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issue
17
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cites work
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SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome
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SHY1, the yeast homolog of the mammalian SURF-1 gene, encodes a mitochondrial protein required for respiration
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Characterization of COX17, a yeast gene involved in copper metabolism and assembly of cytochrome oxidase
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The product of the nuclear gene PET309 is required for translation of mature mRNA and stability or production of intron-containing RNAs derived from the mitochondrial COX1 locus of Saccharomyces cerevisiae
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One-step gene disruption in yeast
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High efficiency transformation of intact yeast cells using single stranded nucleic acids as a carrier
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[12] One-step gene disruption in yeast
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Mss51p promotes mitochondrial Cox1p synthesis and interacts with newly synthesized Cox1p.
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Shy1p is necessary for full expression of mitochondrial COX1 in the yeast model of Leigh's syndrome
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The MSS51 gene product is required for the translation of the COX1 mRNA in yeast mitochondria.
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27 November 2018
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PubMed
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based on heuristic
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SCO1 and SCO2 act as high copy suppressors of a mitochondrial copper recruitment defect in Saccharomyces cerevisiae
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/15306853
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Nuclear functions required for cytochrome c oxidase biogenesis in Saccharomyces cerevisiae. Characterization of mutants in 34 complementation groups
1 reference
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PubMed
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based on heuristic
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The biogenesis and assembly of photosynthetic proteins in thylakoid membranes1
1 reference
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PubMed
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https://pubmed.ncbi.nlm.nih.gov/15306853
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12 December 2020
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Isolation of highly purified mitochondria from Saccharomyces cerevisiae
1 reference
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PubMed
reference URL
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/SJ.EMBOJ.7600358
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1148999
OpenCitations bibliographic resource ID
1148999
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1148999
PMCID
516630
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1148999
PubMed ID
15306853
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1148999
ResearchGate publication ID
8404131
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