Biology:UTP6
From HandWiki
 Generic protein structure example |
U3 small nucleolar RNA-associated protein 6 homolog is a protein that in humans is encoded by the UTP6 gene.[1][2][3]
See also
- Fibrillarin
- Small nucleolar RNA U3
- RCL1
- RRP9
- UTP11L
- UTP14A
- UTP15
References
- ↑ "A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions". Genomics 66 (1): 93–7. Jul 2000. doi:10.1006/geno.2000.6179. PMID 10843809.
- ↑ "Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval". Ann Hum Genet 69 (Pt 5): 508–16. Sep 2005. doi:10.1111/j.1529-8817.2005.00203.x. PMID 16138909.
- ↑ "Entrez Gene: UTP6 UTP6, small subunit (SSU) processome component, homolog (yeast)". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55813.
Further reading
- "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1–2): 171–4. 1994. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1–2): 149–56. 1997. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- "Large scale identification of human hepatocellular carcinoma-associated antigens by autoantibodies.". J. Immunol. 169 (2): 1102–9. 2002. doi:10.4049/jimmunol.169.2.1102. PMID 12097419.
- "Functional proteomic analysis of human nucleolus.". Mol. Biol. Cell 13 (11): 4100–9. 2003. doi:10.1091/mbc.E02-05-0271. PMID 12429849.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. 2003. doi:10.1073/pnas.242603899. PMID 12477932. Bibcode: 2002PNAS...9916899M.
- "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. 2004. doi:10.1038/ng1285. PMID 14702039.
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. 2004. doi:10.1101/gr.2596504. PMID 15489334.
- "Nucleolar proteome dynamics.". Nature 433 (7021): 77–83. 2005. doi:10.1038/nature03207. PMID 15635413. Bibcode: 2005Natur.433...77A.
- "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173–8. 2005. doi:10.1038/nature04209. PMID 16189514. Bibcode: 2005Natur.437.1173R.
- "Positive regulation of apoptosis by HCA66, a new Apaf-1 interacting protein, and its putative role in the physiopathology of NF1 microdeletion syndrome patients.". Cell Death Differ. 14 (6): 1222–33. 2007. doi:10.1038/sj.cdd.4402122. PMID 17380155.
- "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.". Nat. Genet. 39 (8): 963–5. 2007. doi:10.1038/ng2083. PMID 17632510.
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