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Elevated levels of two tRNA species bypass the requirement for elongator complex in transcription and exocytosis.
Esberg A, Huang B, Johansson MJ, Byström AS. Esberg A, et al. Among authors: bystrom as. Mol Cell. 2006 Oct 6;24(1):139-48. doi: 10.1016/j.molcel.2006.07.031. Mol Cell. 2006. PMID: 17018299
Mutational analysis of conserved positions potentially important for initiator tRNA function in Saccharomyces cerevisiae.
von Pawel-Rammingen U, Aström S, Byström AS. von Pawel-Rammingen U, et al. Among authors: bystrom as. Mol Cell Biol. 1992 Apr;12(4):1432-42. doi: 10.1128/mcb.12.4.1432. Mol Cell Biol. 1992. PMID: 1549105 Free PMC article.
Surprisingly, nucleoside changes in base pairs 3-70, 12-23, 31-39, and 29-41, as well as expanding loop I by inserting an A at position 17 (A17) had no effect on the tester strain. ...
Surprisingly, nucleoside changes in base pairs 3-70, 12-23, 31-39, and 29-41, as well as expanding loop I by inserting an A at …
Cloning, nucleotide sequence, and regulation of MET14, the gene encoding the APS kinase of Saccharomyces cerevisiae.
Korch C, Mountain HA, Byström AS. Korch C, et al. Among authors: bystrom as. Mol Gen Genet. 1991 Sep;229(1):96-108. doi: 10.1007/BF00264218. Mol Gen Genet. 1991. PMID: 1654509
This is the same as the consensus sequence of the Centromere DNA Element I (CDEI) that binds the Centromere Promoter Factor I (CPFI) and of two regulatory elements of the PHO5 gene to which the yeast protein PHO4 binds. ...
This is the same as the consensus sequence of the Centromere DNA Element I (CDEI) that binds the Centromere Promoter Factor I (CPFI) …
Four major transcriptional responses in the methionine/threonine biosynthetic pathway of Saccharomyces cerevisiae.
Mountain HA, Byström AS, Larsen JT, Korch C. Mountain HA, et al. Among authors: bystrom as. Yeast. 1991 Nov;7(8):781-803. doi: 10.1002/yea.320070804. Yeast. 1991. PMID: 1789001
Four major responses were evident: strong repression by methionine of MET3, MET5 and MET14, as previously described for MET3, MET2 and MET25; weak repression by methionine of MET6; weak stimulation by methionine but no response to threonine was seen for THR1, HOM2 and HOM3 …
Four major responses were evident: strong repression by methionine of MET3, MET5 and MET14, as previously described for MET3, MET2 an …
A chicken beta-actin gene can complement a disruption of the Saccharomyces cerevisiae ACT1 gene.
Karlsson R, Aspenström P, Byström AS. Karlsson R, et al. Among authors: bystrom as. Mol Cell Biol. 1991 Jan;11(1):213-7. doi: 10.1128/mcb.11.1.213. Mol Cell Biol. 1991. PMID: 1986221 Free PMC article.
Non-autogenous control of ribosomal protein synthesis from the trmD operon in Escherichia coli.
Wikström PM, Byström AS, Björk GR. Wikström PM, et al. Among authors: bystrom as. J Mol Biol. 1988 Sep 5;203(1):141-52. doi: 10.1016/0022-2836(88)90098-8. J Mol Biol. 1988. PMID: 2460631
Overproduced tRNA(m1G37)methyltransferase and 21,000 Mr protein were as stable as E. coli total protein, whereas the two ribosomal proteins were degraded to a large extent. ...
Overproduced tRNA(m1G37)methyltransferase and 21,000 Mr protein were as stable as E. coli total protein, whereas the two ribos …
Prevention of translational frameshifting by the modified nucleoside 1-methylguanosine.
Björk GR, Wikström PM, Byström AS. Björk GR, et al. Among authors: bystrom as. Science. 1989 May 26;244(4907):986-9. doi: 10.1126/science.2471265. Science. 1989. PMID: 2471265
Differentially expressed trmD ribosomal protein operon of Escherichia coli is transcribed as a single polycistronic mRNA species.
Byström AS, von Gabain A, Björk GR. Byström AS, et al. J Mol Biol. 1989 Aug 20;208(4):575-86. doi: 10.1016/0022-2836(89)90149-6. J Mol Biol. 1989. PMID: 2478711
Furthermore, earlier experiments have shown the existence of differential expression as well as non-co-ordinate regulation within the operon. ...
Furthermore, earlier experiments have shown the existence of differential expression as well as non-co-ordinate regulation wit …
Multiple molecular determinants for retrotransposition in a primer tRNA.
Keeney JB, Chapman KB, Lauermann V, Voytas DF, Aström SU, von Pawel-Rammingen U, Byström A, Boeke JD. Keeney JB, et al. Among authors: bystrom a. Mol Cell Biol. 1995 Jan;15(1):217-26. doi: 10.1128/mcb.15.1.217. Mol Cell Biol. 1995. PMID: 7528326 Free PMC article.
Retroviruses and long terminal repeat-containing retroelements use host-encoded tRNAs as primers for the synthesis of minus strong-stop DNA, the first intermediate in reverse transcription of the retroelement RNA. ...Finally, we have used interspecies hybrid initiator tRNA …
Retroviruses and long terminal repeat-containing retroelements use host-encoded tRNAs as primers for the synthesis of minus strong-st …
Modulation of tRNA(iMet), eIF-2, and eIF-2B expression shows that GCN4 translation is inversely coupled to the level of eIF-2.GTP.Met-tRNA(iMet) ternary complexes.
Dever TE, Yang W, Aström S, Byström AS, Hinnebusch AG. Dever TE, et al. Among authors: bystrom as. Mol Cell Biol. 1995 Nov;15(11):6351-63. doi: 10.1128/mcb.15.11.6351. Mol Cell Biol. 1995. PMID: 7565788 Free PMC article.
Consistent with eIF-2 functioning in translation as part of a ternary complex composed of eIF-2, GTP, and Met-tRNA(iMet), reduced gene dosage of initiator tRNA(Met) mimicked phosphorylation of eIF-2 alpha and stimulated GCN4 translation. ...Analysis of eIF-2 alpha phosphor …
Consistent with eIF-2 functioning in translation as part of a ternary complex composed of eIF-2, GTP, and Met-tRNA(iMet), reduced gen …
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