DPAGT1
DPAGT1 (Dolichyl-phosphate N-acetylglucosaminephosphotransferase 1) هوَ بروتين يُشَفر بواسطة جين DPAGT1 في الإنسان.[1][2]
المراجع
- "Entrez Gene: DPAGT1 dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)"، مؤرشف من الأصل في 05 ديسمبر 2010.
- "A sequence-tagged site map of human chromosome 11"، Genomics، 17 (3): 699–725، ديسمبر 1993، doi:10.1006/geno.1993.1392، PMID 8244387.
قراءة متعمقة
- Freeze HH (2002)، "Update and perspectives on congenital disorders of glycosylation"، Glycobiology، 11 (12): 129R–143R، doi:10.1093/glycob/11.12.129R، PMID 11805072.
- Freeze HH (2003)، "Human disorders in N-glycosylation and animal models"، Biochim. Biophys. Acta، 1573 (3): 388–93، doi:10.1016/S0304-4165(02)00408-7، PMID 12417423.
- "New disorders in carbohydrate metabolism: congenital disorders of glycosylation and their impact on the endocrine system"، Reviews in endocrine & metabolic disorders، 4 (1): 103–13، 2003، doi:10.1023/A:1021883605280، PMID 12618564.
- "Dolichol-linked glycoprotein synthesis in developing mammalian brain: maturational changes of the N-acetylglucosaminylphosphotransferase"، Brain Res.، 430 (2): 277–84، 1987، doi:10.1016/0165-3806(87)90160-x، PMID 3038274.
- "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.
- "Normalization and subtraction: two approaches to facilitate gene discovery"، Genome Res.، 6 (9): 791–806، 1997، doi:10.1101/gr.6.9.791، PMID 8889548.
- "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.
- "Cloning and functional expression of the human GlcNAc-1-P transferase, the enzyme for the committed step of the dolichol cycle, by heterologous complementation in Saccharomyces cerevisiae"، Glycobiology، 8 (1): 77–85، 1998، doi:10.1093/glycob/8.1.77، PMID 9451016.
- "Regulation of UDP-N-acetylglucosamine:dolichyl-phosphate N-acetylglucosamine-1-phosphate transferase by retinoic acid in P19 cells"، Biochem. J.، 338 (2): 561–8، 1999، doi:10.1042/0264-6021:3380561، PMC 1220086، PMID 10024536.
- "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، PMC 139241، PMID 12477932.
- "Genomic structure of the human UDP-GlcNAc:dolichol-P GlcNAc-1-P transferase gene"، DNA Seq.، 13 (5): 245–50، 2003، doi:10.1080/1042517021000017126، PMID 12592703.
- "Congenital disorder of glycosylation Ic in patients of Indian origin"، Mol. Genet. Metab.، 79 (3): 221–8، 2004، doi:10.1016/S1096-7192(03)00089-1، PMID 12855228.
- "Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type Ij"، Hum. Mutat.، 22 (2): 144–50، 2004، doi:10.1002/humu.10239، PMID 12872255.
- "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، PMC 528928، PMID 15489334.
- بوابة علم الأحياء الخلوي والجزيئي
- بوابة طب
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