MOCOS


MOCOS

Molybdenum cofactor sulfurase, also known as MOCOS, is a human gene.cite web | title = Entrez Gene: MOCOS molybdenum cofactor sulfurase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55034| 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=Ichida K, Matsumura T, Sakuma R, "et al." |title=Mutation of human molybdenum cofactor sulfurase gene is responsible for classical xanthinuria type II. |journal=Biochem. Biophys. Res. Commun. |volume=282 |issue= 5 |pages= 1194–200 |year= 2001 |pmid= 11302742 |doi= 10.1006/bbrc.2001.4719
*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=Yamamoto T, Moriwaki Y, Takahashi S, "et al." |title=Identification of a new point mutation in the human molybdenum cofactor sulferase gene that is responsible for xanthinuria type II. |journal=Metab. Clin. Exp. |volume=52 |issue= 11 |pages= 1501–4 |year= 2003 |pmid= 14624414 |doi=
*cite journal | author=Beausoleil SA, Jedrychowski M, Schwartz D, "et al." |title=Large-scale characterization of HeLa cell nuclear phosphoproteins. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 33 |pages= 12130–5 |year= 2004 |pmid= 15302935 |doi= 10.1073/pnas.0404720101
*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=Beausoleil SA, Villén J, Gerber SA, "et al." |title=A probability-based approach for high-throughput protein phosphorylation analysis and site localization. |journal=Nat. Biotechnol. |volume=24 |issue= 10 |pages= 1285–92 |year= 2006 |pmid= 16964243 |doi= 10.1038/nbt1240
*cite journal | author=Peretz H, Naamati MS, Levartovsky D, "et al." |title=Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria. |journal=Mol. Genet. Metab. |volume=91 |issue= 1 |pages= 23–9 |year= 2007 |pmid= 17368066 |doi= 10.1016/j.ymgme.2007.02.005

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