Identification of two new single-nucleotide polymorphisms in FUT3 associated with the Lewis-null phenotype
dc.contributor.author | Cooling, Laura | en_US |
dc.contributor.author | Gu, Yuan | en_US |
dc.date.accessioned | 2010-06-01T21:37:52Z | |
dc.date.available | 2010-06-01T21:37:52Z | |
dc.date.issued | 2003-12 | en_US |
dc.identifier.citation | Cooling, Laura; Gu, Yuan (2003). "Identification of two new single-nucleotide polymorphisms in FUT3 associated with the Lewis-null phenotype." Transfusion 43(12): 1760-1761. <http://hdl.handle.net/2027.42/74680> | en_US |
dc.identifier.issn | 0041-1132 | en_US |
dc.identifier.issn | 1537-2995 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/74680 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=14674375&dopt=citation | en_US |
dc.format.extent | 133162 bytes | |
dc.format.extent | 3109 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | Blackwell Science Inc | en_US |
dc.rights | 2003 Blackwell Publishing Ltd. | en_US |
dc.title | Identification of two new single-nucleotide polymorphisms in FUT3 associated with the Lewis-null phenotype | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Oncology and Hematology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationother | Department of Epidemiology Tongji University Wuhan, China | en_US |
dc.identifier.pmid | 14674375 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/74680/1/j.0041-1132.2003.00593.x.pdf | |
dc.identifier.doi | 10.1111/j.0041-1132.2003.00593.x | en_US |
dc.identifier.source | Transfusion | en_US |
dc.identifier.citedreference | Spitalnik PF, Spitalnik SL. Human carbohydrate blood group systems. In: Dzik WH, Snyder EL, Stowell CP, Strauss RG, editors. Rossi's principles of transfusion medicine. 3rd ed. Philadelphia: Lippincott Williams & Wilkins; 2002 :92 - 110. | en_US |
dc.identifier.citedreference | Salomaa V, Pankow J, Heiss G, et al. Genetic background of Lewis negative blood group phenotype and its association with atherosclerotic disease in the NHLBI family heart study. J Int Med 2000; 247: 689 - 98. | en_US |
dc.identifier.citedreference | Liu TC, Chang JG, Lin SF, et al. Lewis (FUT3) genotypes in Taiwanese, Thai, and Filipino populations. Ann Hematol 2000; 79: 599 - 603. | en_US |
dc.identifier.citedreference | Pang H, Liu Y, Koda Y, et al. Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South Africa. Hum Genet 1998; 102: 675 - 80. | en_US |
dc.identifier.citedreference | Gu X, Preuss U, Gu T, Yu RK. Regulation of sialyltransferase activities by phosphorylation and dephosphorylation. J Neurochem 1995; 64: 2295 - 302. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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