MTO1

MTO1

Mitochondrial translation optimization 1 homolog (S. cerevisiae), also known as MTO1, is a human gene.cite web | title = Entrez Gene: MTO1 mitochondrial translation optimization 1 homolog (S. cerevisiae)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=25821| accessdate = ]

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References

Further reading

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*cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=
*cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, "et al." |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=
*cite journal | author=Lai CH, Chou CY, Ch'ang LY, "et al." |title=Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics. |journal=Genome Res. |volume=10 |issue= 5 |pages= 703–13 |year= 2000 |pmid= 10810093 |doi=
*cite journal | author=Li X, Li R, Lin X, Guan MX |title=Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation. |journal=J. Biol. Chem. |volume=277 |issue= 30 |pages= 27256–64 |year= 2002 |pmid= 12011058 |doi= 10.1074/jbc.M203267200
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Mungall AJ, Palmer SA, Sims SK, "et al." |title=The DNA sequence and analysis of human chromosome 6. |journal=Nature |volume=425 |issue= 6960 |pages= 805–11 |year= 2003 |pmid= 14574404 |doi= 10.1038/nature02055
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Bykhovskaya Y, Mengesha E, Wang D, "et al." |title=Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3. |journal=Mol. Genet. Metab. |volume=83 |issue= 3 |pages= 199–206 |year= 2005 |pmid= 15542390 |doi= 10.1016/j.ymgme.2004.07.009
*cite journal | author=Krull M, Brosius J, Schmitz J |title=Alu-SINE exonization: en route to protein-coding function. |journal=Mol. Biol. Evol. |volume=22 |issue= 8 |pages= 1702–11 |year= 2005 |pmid= 15901843 |doi= 10.1093/molbev/msi164

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  • GTPBP3 — GTP binding protein 3 (mitochondrial), also known as GTPBP3, is a human gene.cite web | title = Entrez Gene: GTPBP3 GTP binding protein 3 (mitochondrial)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

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