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Localization of the Gene for ATP Citrate Lyase (ACLY) Distal to Gastrin (GAS) and Proximal to D17S856 on Chromosome 17q12-q21
dc.contributor.authorCouch, Fergus J.en_US
dc.contributor.authorAbel, Kenneth J.en_US
dc.contributor.authorBrody, Lawrence C.en_US
dc.contributor.authorBoehnke, Michaelen_US
dc.contributor.authorCollins, Francis S.en_US
dc.contributor.authorWeber, Barbara L.en_US
dc.date.accessioned2006-04-10T18:09:01Z
dc.date.available2006-04-10T18:09:01Z
dc.date.issued1994-05-15en_US
dc.identifier.citationCouch, Fergus J., Abel, Kenneth J., Brody, Lawrence C., Boehnke, Michael, Collins, Francis S., Weber, Barbara L. (1994/05/15)."Localization of the Gene for ATP Citrate Lyase (ACLY) Distal to Gastrin (GAS) and Proximal to D17S856 on Chromosome 17q12-q21." Genomics 21(2): 444-446. <http://hdl.handle.net/2027.42/31578>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WG1-45NJXWS-4M/2/6c30ecfd2101d9643f857a8e84965ec2en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/31578
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8088842&dopt=citationen_US
dc.description.abstractThe gene encoding ATP-citrate lyase, designated ACLY, was mapped to human chromosome 17q12-q21 by PCR on a panel of human/rodent somatic cell hybrids and localized to 17q21.1 by PCH on a panel of radiation hybrids. The radiation hybrid panel indicates that the most likely position of ACLY on 17q21.1 is between gastrin (GAS) and D17S856 at a distance of 170-290 kb from the GAS locus.en_US
dc.format.extent186232 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleLocalization of the Gene for ATP Citrate Lyase (ACLY) Distal to Gastrin (GAS) and Proximal to D17S856 on Chromosome 17q12-q21en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumDepartment of Biostatistics, and Human Genetics, University of Michigan, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationumLaboratory of Gene Transfer, National Center for Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA; Human Genome Research, National Institutes of Health, Bethesda, Maryland, USA.en_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.en_US
dc.contributor.affiliationotherLaboratory of Gene Transfer, National Center for Human Genome Research, National Institutes of Health, Bethesda, Maryland, USA.en_US
dc.identifier.pmid8088842en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/31578/1/0000506.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1006/geno.1994.1293en_US
dc.identifier.sourceGenomicsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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