[cite web | title = Entrez Gene: UTP6 UTP6, small subunit (SSU) processome component, homolog (yeast)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55813| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*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=Jenne DE, Tinschert S, Stegmann E, "et al." |title=A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions. |journal=Genomics |volume=66 |issue= 1 |pages= 93–7 |year= 2000 |pmid= 10843809 |doi= 10.1006/geno.2000.6179
*cite journal | author=Wang Y, Han KJ, Pang XW, "et al." |title=Large scale identification of human hepatocellular carcinoma-associated antigens by autoantibodies. |journal=J. Immunol. |volume=169 |issue= 2 |pages= 1102–9 |year= 2002 |pmid= 12097419 |doi=
*cite journal | author=Scherl A, Couté Y, Déon C, "et al." |title=Functional proteomic analysis of human nucleolus. |journal=Mol. Biol. Cell |volume=13 |issue= 11 |pages= 4100–9 |year= 2003 |pmid= 12429849 |doi= 10.1091/mbc.E02-05-0271
*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=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=Venturin M, Bentivegna A, Moroni R, "et al." |title=Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval. |journal=Ann. Hum. Genet. |volume=69 |issue= Pt 5 |pages= 508–16 |year= 2005 |pmid= 16138909 |doi= 10.1111/j.1529-8817.2005.00203.x
*cite journal | author=Rual JF, Venkatesan K, Hao T, "et al." |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173–8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209
*cite journal | author=Piddubnyak V, Rigou P, Michel L, "et al." |title=Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patients. |journal=Cell Death Differ. |volume=14 |issue= 6 |pages= 1222–33 |year= 2007 |pmid= 17380155 |doi= 10.1038/sj.cdd.4402122
*cite journal | author=Douglas J, Cilliers D, Coleman K, "et al." |title=Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. |journal=Nat. Genet. |volume=39 |issue= 8 |pages= 963–5 |year= 2007 |pmid= 17632510 |doi= 10.1038/ng2083
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