B3GALTL

B3GALTL

Beta 1,3-galactosyltransferase-like, also known as B3GALTL, is a human gene.cite web | title = Entrez Gene: B3GALTL beta 1,3-galactosyltransferase-like| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=145173| accessdate = ]

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References

Further reading

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*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=Heinonen TY, Pasternack L, Lindfors K, "et al." |title=A novel human glycosyltransferase: primary structure and characterization of the gene and transcripts. |journal=Biochem. Biophys. Res. Commun. |volume=309 |issue= 1 |pages= 166–74 |year= 2003 |pmid= 12943678 |doi=
*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=Dunham A, Matthews LH, Burton J, "et al." |title=The DNA sequence and analysis of human chromosome 13. |journal=Nature |volume=428 |issue= 6982 |pages= 522–8 |year= 2004 |pmid= 15057823 |doi= 10.1038/nature02379
*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=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=Sato T, Sato M, Kiyohara K, "et al." |title=Molecular cloning and characterization of a novel human beta1,3-glucosyltransferase, which is localized at the endoplasmic reticulum and glucosylates O-linked fucosylglycan on thrombospondin type 1 repeat domain. |journal=Glycobiology |volume=16 |issue= 12 |pages= 1194–206 |year= 2007 |pmid= 16899492 |doi= 10.1093/glycob/cwl035
*cite journal | author=Lesnik Oberstein SA, Kriek M, White SJ, "et al." |title=Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase. |journal=Am. J. Hum. Genet. |volume=79 |issue= 3 |pages= 562–6 |year= 2006 |pmid= 16909395 |doi= 10.1086/507567
*cite journal | author=Kozma K, Keusch JJ, Hegemann B, "et al." |title=Identification and characterization of abeta1,3-glucosyltransferase that synthesizes the Glc-beta1,3-Fuc disaccharide on thrombospondin type 1 repeats. |journal=J. Biol. Chem. |volume=281 |issue= 48 |pages= 36742–51 |year= 2007 |pmid= 17032646 |doi= 10.1074/jbc.M605912200

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  • Peters-Plus-Syndrom — Das Peters Plus Syndrom ist eine mit lediglich etwa 20 dokumentierten Fallbeispielen seit der Abgrenzungsbeschreibung 1984 sehr seltene Entwicklungsstörung im vorderen Augenabschnitt. Alternativ wird sie als Krause Kivlin Syndrom bezeichnet.… …   Deutsch Wikipedia

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