Show simple item record

Removal of High-Molecular-Weight DNA by Carboxylated Magnetic Beads Enhances the Detection of Mutated K-ras DNA in Urine

dc.contributor.authorSu, Ying-Hsiuen_US
dc.contributor.authorSong, Janeten_US
dc.contributor.authorWang, Zhilien_US
dc.contributor.authorWang, Xiao-Heen_US
dc.contributor.authorWang, Mengjunen_US
dc.contributor.authorBrenner, Dean E.en_US
dc.contributor.authorBlock, Timothy M.en_US
dc.date.accessioned2010-06-01T22:13:58Z
dc.date.available2010-06-01T22:13:58Z
dc.date.issued2008-08en_US
dc.identifier.citationSu, Ying-Hsiu; Song, Janet; Wang, Zhili; Wang, Xiao-He; Wang, Mengjun; Brenner, Dean E.; Block, Timothy M. (2008). "Removal of High-Molecular-Weight DNA by Carboxylated Magnetic Beads Enhances the Detection of Mutated K-ras DNA in Urine." Annals of the New York Academy of Sciences 1137(1 Circulating Nucleic Acids in Plasma and Serum V ): 82-91. <http://hdl.handle.net/2027.42/75249>en_US
dc.identifier.issn0077-8923en_US
dc.identifier.issn1749-6632en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/75249
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18837929&dopt=citationen_US
dc.format.extent270366 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Incen_US
dc.rights© 2008 New York Academy of Sciencesen_US
dc.subject.otherCirculating DNAen_US
dc.subject.otherDisease Biomarkeren_US
dc.subject.otherK-ras Mutationen_US
dc.subject.otherColon Canceren_US
dc.titleRemoval of High-Molecular-Weight DNA by Carboxylated Magnetic Beads Enhances the Detection of Mutated K-ras DNA in Urineen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelScience (General)en_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Internal Medicine and Pharmacology, 2150B Cancer and Geriatrics Center, University of Michigan Medical Center, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherDepartment of Microbiology and Immunology, College of Medicine, Drexel University, Doylestown, Pennsylvania, USAen_US
dc.contributor.affiliationotherNucleic Acid/Protein Research Core Facility, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USAen_US
dc.identifier.pmid18837929en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/75249/1/annals.1448.019.pdf
dc.identifier.doi10.1196/annals.1448.019en_US
dc.identifier.sourceAnnals of the New York Academy of Sciencesen_US
dc.identifier.citedreferenceSu, Y.H. et al. 2004. Human urine contains small, 150 to 250 nucleotide-sized, soluble DNA derived from the circulation and may be useful in the detection of colorectal cancer. J. Mol. Diagn. 6: 101 – 107.en_US
dc.identifier.citedreferenceBotezatu, I. et al. 2000. Genetic analysis of DNA excreted in urine: a new approach for detecting specific genomic DNA sequences from cells dying in an organism. Clin. Chem. 46: 1078 – 1084.en_US
dc.identifier.citedreferenceSerdyuk, O.I. et al. 2001. Detection of mutant k-ras sequences in the urine of cancer patients. Bull. Exp. Biol. Med. 131: 283 – 284.en_US
dc.identifier.citedreferenceDeAngelis, M. et al. 1995. Solid-phase reversible immobilization for the isolation of PCR products. Nucl. Acids Res. 23: 4742 – 4743.en_US
dc.identifier.citedreferenceHawkins, T. et al. 1994. DNA purification and isolation using a solid-phase. Nucl. Acids Res. 22: 4543 – 4544.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


Files in this item

Show simple item record

Remediation of Harmful Language

The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.

Accessibility

If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.