- SMS (gene)
Spermine synthase, also known as SMS, is a human
gene .cite web | title = Entrez Gene: SMS spermine synthase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6611| accessdate = ]PBB_Summary
section_title =
summary_text = The protein encoded by this gene belongs to the spermidine/spermine synthases family. This gene encodes a ubiquitous enzyme of polyamine metabolism.cite web | title = Entrez Gene: SMS spermine synthase| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6611| accessdate = ]References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Snyder RD, Robinson A |title=Recessive sex-linked mental retardation in the absence of other recognizable abnormalities. Report of a family. |journal=Clinical pediatrics |volume=8 |issue= 11 |pages= 669–74 |year= 1969 |pmid= 5823961 |doi=
*cite journal | author=Korhonen VP, Halmekytö M, Kauppinen L, "et al." |title=Molecular cloning of a cDNA encoding human spermine synthase. |journal=DNA Cell Biol. |volume=14 |issue= 10 |pages= 841–7 |year= 1995 |pmid= 7546290 |doi=
*cite journal | author=Arena JF, Schwartz C, Ouzts L, "et al." |title=X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12. |journal=Am. J. Med. Genet. |volume=64 |issue= 1 |pages= 50–8 |year= 1996 |pmid= 8826448 |doi= 10.1002/(SICI)1096-8628(19960712)64:1<50::AID-AJMG7>3.0.CO;2-V |doilabel=10.1002/(SICI)1096-8628(19960712)64:150::AID-AJMG73.0.CO;2-V
*cite journal | author=Grieff M, Whyte MP, Thakker RV, Mazzarella R |title=Sequence analysis of 139 kb in Xp22.1 containing spermine synthase and the 5' region of PEX. |journal=Genomics |volume=44 |issue= 2 |pages= 227–31 |year= 1997 |pmid= 9299240 |doi= 10.1006/geno.1997.4876
*cite journal | author= |title=Toward a complete human genome sequence. |journal=Genome Res. |volume=8 |issue= 11 |pages= 1097–108 |year= 1999 |pmid= 9847074 |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=Gevaert K, Goethals M, Martens L, "et al." |title=Exploring proteomes and analyzing protein processing by mass spectrometric identification of sorted N-terminal peptides. |journal=Nat. Biotechnol. |volume=21 |issue= 5 |pages= 566–9 |year= 2004 |pmid= 12665801 |doi= 10.1038/nbt810
*cite journal | author=Cason AL, Ikeguchi Y, Skinner C, "et al." |title=X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. |journal=Eur. J. Hum. Genet. |volume=11 |issue= 12 |pages= 937–44 |year= 2004 |pmid= 14508504 |doi= 10.1038/sj.ejhg.5201072
*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=Rush J, Moritz A, Lee KA, "et al." |title=Immunoaffinity profiling of tyrosine phosphorylation in cancer cells. |journal=Nat. Biotechnol. |volume=23 |issue= 1 |pages= 94–101 |year= 2005 |pmid= 15592455 |doi= 10.1038/nbt1046
*cite journal | author=Ross MT, Grafham DV, Coffey AJ, "et al." |title=The DNA sequence of the human X chromosome. |journal=Nature |volume=434 |issue= 7031 |pages= 325–37 |year= 2005 |pmid= 15772651 |doi= 10.1038/nature03440PBB_Controls
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