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1 network t-SNARE Sed5p, also functioned as a multicopy suppressor.
2 f Los1p in pre-tRNA splicing, we sought los1 multicopy suppressors.
3 tibodies, we found that the presence of this multicopy suppressor allowed the processing-defective La
4 Analysis of the suppression spectrum of this multicopy suppressor and peptide sequencing of the suppr
5 Proteus mirabilis, tatA was identified as a multicopy suppressor and restored extracellular signal p
10 Escherichia coli, is known to function as a multicopy suppressor for dnaJ mutations and to bind nons
11 e recently observed that KsgA functions as a multicopy suppressor for the cold-sensitive cell growth
12 isiae ZDS1 and ZDS2 genes were identified as multicopy suppressors in distinct genetic screens but we
14 RbfA, a 30S ribosome-binding factor, is a multicopy suppressor of a cold-sensitive C23U mutation o
15 complex), which was originally isolated as a multicopy suppressor of a cytochrome b mRNA translation
16 s cerevisiae was isolated independently as a multicopy suppressor of a dominant negative mutation in
18 he dksA gene was independently isolated as a multicopy suppressor of a mukB mutation, which is requir
21 encodes a putative Hsp90 co-chaperone, as a multicopy suppressor of a temperature-sensitive allele (
22 Sec20p, and SEC22 acts as an allele-specific multicopy suppressor of a temperature-sensitive ufe1 mut
24 pressor of yeast cbf5-1) was identified as a multicopy suppressor of cbf5-1 and subsequently was foun
27 dksA (dnaK suppressor) gene, which is also a multicopy suppressor of defects in the heat shock genes
28 richia coli msbA gene, first identified as a multicopy suppressor of htrB mutations, has been propose
29 ste 12 (Su(z)12), Extra Sex Combs (ESC), and Multicopy Suppressor of IRA 1 (MSI1), and functions in m
30 SI2 and SlSDG2, the orthologs of Arabidopsis MULTICOPY SUPPRESSOR OF IRA1 2 and SET DOMAIN GROUP 2, r
34 ally, the STM1 gene has been identified as a multicopy suppressor of mutations in several genes invol
35 accharomyces pombe mex67 gene (spmex67) as a multicopy suppressor of rae1-167 nup184-1 synthetic leth
40 We isolated a novel gene, alp16(+), as a multicopy suppressor of temperature-sensitive alp6-719 m
43 des C, C, and A to the 3' end of tRNAs, is a multicopy suppressor of the defect in tRNA nuclear expor
44 isolated the transcription factor MBP1 as a multicopy suppressor of the growth and alpha-factor resp
45 signal transduction.) AKR1 could serve as a multicopy suppressor of the lethality caused by either l
48 he pleiotropic drug resistance network, as a multicopy suppressor of the mitochondrial import defects
49 growth arrest identified the RAS2 gene as a multicopy suppressor of the PPS1p overexpression arrest.
51 e identified a truncated allele of dam1 as a multicopy suppressor of the sensitivity of cdc13-117 (cy
52 NA processing and degradation pathways, is a multicopy suppressor of the synthetic lethality and of t
54 ified the ribosome binding protein Stm1 as a multicopy suppressor of the temperature sensitivity of t
55 dentical to Cdm1, previously identified as a multicopy suppressor of the temperature-sensitive cdc1-P
58 ized open reading frame YER074W-A as a novel multicopy suppressor of the thermosensitive yip1-4 strai
59 strains, the ability of CDC42 to serve as a multicopy suppressor of the Ts- growth defect of deltabe
60 tudies confirm that LeMSI1 can function as a multicopy suppressor of the yeast ira1 mutant phenotype.
64 gene identified through a genetic screen for multicopy suppressors of a mutation in USO1, which suppr
66 ons are linked to CDC42, we screened for (i) multicopy suppressors of a Ts- cdc42 mutant, (ii) mutant
67 ta9 fatty acid desaturase of yeast, OLE1, as multicopy suppressors of an mga2Delta spt23 temperature-
70 ial proteins (e.g. MTCO3) were identified as multicopy suppressors of cdc13-1, suggesting the involve
71 gh three independent genome-wide screens for multicopy suppressors of each of the three Vpr activitie
72 We have identified OXA1 and TIM17 as novel multicopy suppressors of mtDNA instability in ilv5 cells
75 iated with Cpr7, a search was undertaken for multicopy suppressors of the cpr7Delta slow-growth pheno
76 aromyces cerevisiae genes, BMH1 and BMH2, as multicopy suppressors of the growth-inhibitory phenotype
78 otential targets for Cln3/CDK, we identified multicopy suppressors of the temperature sensitivity of
80 dentify functional partners, we screened for multicopy suppressors of the temperature-sensitive ydj1-
81 D23 and DDI1 were identified in a screen for multicopy suppressors of the temperature-sensitivity of
84 re we identify several HAL genes that act as multicopy suppressors of this sensitivity and are connec
85 rone system and its targets, we searched for multicopy suppressors of various temperature-sensitive m
90 acterized Sgls and uncovered a common set of multicopy suppressors, suggesting that these Sgls act by
91 tory developed a screen that identified five multicopy suppressors that can rescue lethal strains of
92 ia coli porin regulation was discovered from multicopy suppressors that permitted growth of cells exp
93 ture-sensitive ess1 mutants and identify six multicopy suppressors that rescue their mitotic-lethal p