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Variation in coding exons of two electrophoretic alleles at the pigtail macaque carbonic anhydrase I locus as determined by direct, double-stranded sequencing of polymerase chain reaction (PCR) products

dc.contributor.authorBergenhem, Nils C. H.en_US
dc.contributor.authorVenta, Patrick J.en_US
dc.contributor.authorHopkins, Penelope J.en_US
dc.contributor.authorTashian, Richard E.en_US
dc.date.accessioned2006-09-11T14:22:13Z
dc.date.available2006-09-11T14:22:13Z
dc.date.issued1992-06en_US
dc.identifier.citationBergenhem, Nils C. H.; Venta, Patrick J.; Hopkins, Penelope J.; Tashian, Richard E.; (1992). "Variation in coding exons of two electrophoretic alleles at the pigtail macaque carbonic anhydrase I locus as determined by direct, double-stranded sequencing of polymerase chain reaction (PCR) products." Biochemical Genetics 30 (5-6): 279-287. <http://hdl.handle.net/2027.42/44158>en_US
dc.identifier.issn1573-4927en_US
dc.identifier.issn0006-2928en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44158
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1616482&dopt=citationen_US
dc.description.abstractTwo, electrophoretically distinct, forms of carbonic anhydrase I (CA Ia and CA Ib) are found at high polymorphic frequencies in red cells of natural populations of pigtail macaques, Macaca nemestrina , from southeast Asia. By use of the polymerase chain reaction, exons of the CA I gene were amplified from homozygous ( a/a, b/b ) and heterozygous ( a/b ) animals. Direct sequencing of the amplified DNA from four animals revealed differences between the a and the b electrophoretic alleles ranging from three to six nucleotides, and from one to three differences within each allele. These results indicate a greater genetic variability at the CA I locus in this macaque species than previously realized.en_US
dc.format.extent498917 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherPolymerase Chain Reactionen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherHuman Geneticsen_US
dc.subject.otherMedical Microbiologyen_US
dc.subject.otherZoologyen_US
dc.subject.otherMacaca Nemestrinaen_US
dc.subject.otherCarbonic Anhydrase I Locusen_US
dc.subject.otherDNA Sequencingen_US
dc.subject.otherAllelic Variationen_US
dc.titleVariation in coding exons of two electrophoretic alleles at the pigtail macaque carbonic anhydrase I locus as determined by direct, double-stranded sequencing of polymerase chain reaction (PCR) productsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, 48109-0618, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, 48109-0618, Ann Arbor, Michigan; Small Animal Clinical Sciences, College of Veterinary Medicine, Michigan State University, 48824-1314, East Lansing, Michiganen_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, 48109-0618, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Human Genetics, University of Michigan Medical School, 48109-0618, Ann Arbor, Michigan; Department of Molecular and Experimental Medicine, Research Institute of Scripps Clinic, 10666 North Torrey Pines Road, 92037, La Jolla, Californiaen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid1616482en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44158/1/10528_2004_Article_BF00553755.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00553755en_US
dc.identifier.sourceBiochemical Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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