RPP30

RPP30

Ribonuclease P/MRP 30kDa subunit, also known as RPP30, is a human gene.cite web | title = Entrez Gene: RPP30 ribonuclease P/MRP 30kDa subunit| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10556| accessdate = ]

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References

Further reading

PBB_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=Bonaldo MF, Lennon G, Soares MB |title=Normalization and subtraction: two approaches to facilitate gene discovery. |journal=Genome Res. |volume=6 |issue= 9 |pages= 791–806 |year= 1997 |pmid= 8889548 |doi=
*cite journal | author=Eder PS, Kekuda R, Stolc V, Altman S |title=Characterization of two scleroderma autoimmune antigens that copurify with human ribonuclease P. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=94 |issue= 4 |pages= 1101–6 |year= 1997 |pmid= 9037013 |doi=
*cite journal | author=Stolc V, Altman S |title=Rpp1, an essential protein subunit of nuclear RNase P required for processing of precursor tRNA and 35S precursor rRNA in Saccharomyces cerevisiae. |journal=Genes Dev. |volume=11 |issue= 18 |pages= 2414–25 |year= 1997 |pmid= 9308968 |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=Jarrous N, Eder PS, Guerrier-Takada C, "et al." |title=Autoantigenic properties of some protein subunits of catalytically active complexes of human ribonuclease P. |journal=RNA |volume=4 |issue= 4 |pages= 407–17 |year= 1998 |pmid= 9630247 |doi=
*cite journal | author=Jiang T, Guerrier-Takada C, Altman S |title=Protein-RNA interactions in the subunits of human nuclear RNase P. |journal=RNA |volume=7 |issue= 7 |pages= 937–41 |year= 2001 |pmid= 11455963 |doi=
*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=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Welting TJ, van Venrooij WJ, Pruijn GJ |title=Mutual interactions between subunits of the human RNase MRP ribonucleoprotein complex. |journal=Nucleic Acids Res. |volume=32 |issue= 7 |pages= 2138–46 |year= 2004 |pmid= 15096576 |doi= 10.1093/nar/gkh539
*cite journal | author=Deloukas P, Earthrowl ME, Grafham DV, "et al." |title=The DNA sequence and comparative analysis of human chromosome 10. |journal=Nature |volume=429 |issue= 6990 |pages= 375–81 |year= 2004 |pmid= 15164054 |doi= 10.1038/nature02462
*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=Andersen JS, Lam YW, Leung AK, "et al." |title=Nucleolar proteome dynamics. |journal=Nature |volume=433 |issue= 7021 |pages= 77–83 |year= 2005 |pmid= 15635413 |doi= 10.1038/nature03207
*cite journal | author=Kimura K, Wakamatsu A, Suzuki Y, "et al." |title=Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. |journal=Genome Res. |volume=16 |issue= 1 |pages= 55–65 |year= 2006 |pmid= 16344560 |doi= 10.1101/gr.4039406
*cite journal | author=Wimplinger I, Morleo M, Rosenberger G, "et al." |title=Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome. |journal=Am. J. Hum. Genet. |volume=79 |issue= 5 |pages= 878–89 |year= 2006 |pmid= 17033964 |doi= 10.1086/508474
*cite journal | author=Olsen JV, Blagoev B, Gnad F, "et al." |title=Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. |journal=Cell |volume=127 |issue= 3 |pages= 635–48 |year= 2006 |pmid= 17081983 |doi= 10.1016/j.cell.2006.09.026

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