B3GALTL
Beta-1,3-glucosyltransferase is an enzyme that in humans is encoded by the B3GALTL gene.[3][4][5][6]
References
- ↑ "Human PubMed Reference:".
- ↑ "Mouse PubMed Reference:".
- ↑ Heinonen TY, Pasternack L, Lindfors K, Breton C, Gastinel LN, Maki M, Kainulainen H (Aug 2003). "A novel human glycosyltransferase: primary structure and characterization of the gene and transcripts". Biochem Biophys Res Commun. 309 (1): 166–174. PMID 12943678. doi:10.1016/S0006-291X(03)01540-7.
- ↑ Sato T, Sato M, Kiyohara K, Sogabe M, Shikanai T, Kikuchi N, Togayachi A, Ishida H, Ito H, Kameyama A, Gotoh M, Narimatsu H (Nov 2006). "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". Glycobiology. 16 (12): 1194–1206. PMID 16899492. doi:10.1093/glycob/cwl035.
- ↑ Kozma K, Keusch JJ, Hegemann B, Luther KB, Klein D, Hess D, Haltiwanger RS, Hofsteenge J (Nov 2006). "Identification and characterization of abeta1,3-glucosyltransferase that synthesizes the Glc-beta1,3-Fuc disaccharide on thrombospondin type 1 repeats". J Biol Chem. 281 (48): 36742–36751. PMID 17032646. doi:10.1074/jbc.M605912200.
- ↑ "Entrez Gene: B3GALTL beta 1,3-galactosyltransferase-like".
External links
Further reading
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "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): 16899–16903. PMC 139241
. PMID 12477932. doi:10.1073/pnas.242603899.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–45. PMID 14702039. doi:10.1038/ng1285.
- Dunham A, Matthews LH, Burton J, et al. (2004). "The DNA sequence and analysis of human chromosome 13". Nature. 428 (6982): 522–528. PMC 2665288 . PMID 15057823. doi:10.1038/nature02379.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–2127. PMC 528928 . PMID 15489334. doi:10.1101/gr.2596504.
- Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. PMC 1356129 . PMID 16344560. doi:10.1101/gr.4039406.
- Lesnik Oberstein SA, Kriek M, White SJ, et al. (2006). "Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferase". Am. J. Hum. Genet. 79 (3): 562–566. PMC 1559553 . PMID 16909395. doi:10.1086/507567.