「CEREVISIAE」の共起表現(1語右で並び替え)

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共起表現

「CEREVISIAE」の共起表現一覧(1語右で並び替え)

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PSI+] and [URE3] phenotypes in Saccharomyces	cerevisiae, a form of budding yeast, were caused by pri
In the budding yeast Saccharomyces	cerevisiae, actin filaments are the major structural co
The yeast Saccharomyces	cerevisiae acts on the starch and ferments it.
esearch studied baker's yeast (Saccharomyces	cerevisiae) and is one of two robot scientists working
unctionally related to SWI/SNF complex in S.	cerevisiae and Drosophila; the latter is thought to fac
alized growing vats for the production of S.	cerevisiae, and in the United States around the turn of
breviated to CWP1 is a gene of Saccharomyces	cerevisiae and the Saccharomyces cerevisiae Saccharomyc
Cell Wall Protein, produced by Saccharomyces	cerevisiae and Saccharomyces pastorianus during cell li
he snoRNA identified in yeast (Saccharomyces	cerevisiae) and called snR66 .
into the molecular genetics of Saccharomyces	cerevisiae and Vitis vinifera.
e also been well studied in budding yeast S.	cerevisiae and in the fungus Neurospora crassa.
ke beer are the top-fermenting Saccharomyces	cerevisiae and bottom-fermenting Saccharomyces uvarum.
mannan and glucan formation in Saccharomyces	cerevisiae and used for the analysis of mRNA stability.
most commonly used yeasts are Saccharomyces	cerevisiae and Schizosaccharomyces pombe, although rese
s such as Candida albicans and Saccharomyces	cerevisiae and molds such as Aspergillus niger.
ucor spp, and yeasts including Saccharomyces	cerevisiae, and Saccharomycopsis fibuliger, Endomycopsi
prokaryotes, and more recently, in yeast (S.	cerevisiae) and in Tetrahymena thermophila.
he family contains the species Saccharomyces	cerevisiae, arguably the most economically important fu
res derived from barm, usually Saccharomyces	cerevisiae, became ancestral to most forms of brewer's
R and XDH respectively were introduced to S.	cerevisiae by means of genetic engineering.
Extended exposure to S.	cerevisiae can result in hypersensitivity.
s protein is highly similar to Saccharomyces	cerevisiae Cdc14, a protein tyrosine phosphatase involv
imilar to the gene products of Saccharomyces	cerevisiae cdc28, and Schizosaccharomyces pombe cdc2, a
is highly similar to the gene products of S.	cerevisiae cdc28, and S. pombe cdc2, also known as Cdk1
Saccharomyces	cerevisiae contains one desaturase, Ole1p, which induce
	Cerevisiae), Dcp2 is joined by the decapping activator
Homologues of the Saccharomyces	cerevisiae Ero1 proteins have been found in all eukaryo
n (ChIP) assays showed that in Saccharomyces	cerevisiae, even when SER3 was being repressed, TATA-bi
y the use of yeasts other than Saccharomyces	cerevisiae for fermentation.
e (SUPT16H) which is 36% identical to the S.	cerevisiae gene Spt16 and the 80 kDa subunit is human S
o two groups; the ale strains (Saccharomyces	cerevisiae, generally used for ale and stout) and the l
eukaryotes, the budding yeast Saccharomyces	cerevisiae has the best characterised replication origi
ne in 1982 and a yeast species Saccharomyces	cerevisiae in 1986 before finally Battini et al. sequen
se II trancription, subunit 12 homolog of S.	cerevisiae, is one of several subunits in the mammalian
ugar, and the amount of yeast, Saccharomyces	cerevisiae, is regulated by the European Commission (Re
ene responsible for trehalase activity in S.	cerevisiae is NTH1.
The GC-content of Yeast (Saccharomyces	cerevisiae) is 38%, and that of another common model or
se lactose is unfermentable by Saccharomyces	cerevisiae, it adds sweetness, body, and calories to th
ught to have diverged from the Saccharomyces	cerevisiae lineage between 300 million and 1 billion ye
ded by this gene is similar to Saccharomyces	cerevisiae LYS5, which is required for the activation o
annel which is related in sequence to the S.	cerevisiae MID-1 stretch-activated channel.
cations include baker's yeast (Saccharomyces	cerevisiae), mustard weed/thale cress (Arabidopsis thal
iclopirox's mechanism, several Saccharomyces	cerevisiae mutants were screened and tested.
In Saccharomyces	cerevisiae NatA Acetyltransferase interacts with the Su
S.	cerevisiae on the other hand can not ferment D-xylose t
le-domain antibody in E. coli, Saccharomyces	cerevisiae or other suitable organisms.
Oxysterol binding proteins OSBP, S.	cerevisiae OSH1 and YHR073w.
d in cell cultures, ethanol in Saccharomyces	cerevisiae), oxygen limitation (anaerobiosis).
phenomenon whereby the yeast, Saccharomyces	cerevisiae, produces ethanol (alcohol) aerobically in t
een designed to find kinases that altered S.	cerevisiae proliferation when overexpressed.
shares strong similarity with Saccharomyces	cerevisiae protein Cdc27, and the gene product of Schiz
Like the distantly related Saccharomyces	cerevisiae, S. pombe is a significant model organism in
transport and use, the S. pastorianus and S.	cerevisiae species are closely related within the Sacch
3 complements cdc28 mutants of Saccharomyces	cerevisiae suggesting that it may be involved in cell c
certain model organisms such as the yeast S.	cerevisiae, the nematode C. elegans and the fruit fly D
In S.	cerevisiae, the copper uptake genes CTR1, CTR2, and CTR
RUF1-8 found in Saccharomyces	cerevisiae, though three of these were later reclassifi
Genus Metavirus; type species: Saccharomyces	cerevisiae Ty3 virus
a voile (veil) of active yeast Saccharomyces	cerevisiae type bayanus on its surface.
S.	cerevisiae was the model organism used during the two-h
aker's yeast is of the species Saccharomyces	cerevisiae, which is the same species commonly used in
n Escherichia coli and HIS3 in Saccharomyces	cerevisiae) will survive on these media.
ubtilis, as well as strains of Saccharomyces	cerevisiae with mutations that impair arginine biosynth
ted fatty acid biosynthesis in Saccharomyces	cerevisiae without having an effect on sterol formation
t is the human ortholog of the Saccharomyces	cerevisiae YVH1 protein tyrosine phosphatase.

共起表現

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「CEREVISIAE」の共起表現一覧(1語右で並び替え)