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Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing

dc.contributor.authorArpagaus, Martineen_US
dc.contributor.authorBartels, Cynthia F.en_US
dc.contributor.authorDu, Bert N.en_US
dc.contributor.authorNogueira, Christine P.en_US
dc.contributor.authorLockridge, Oksanaen_US
dc.date.accessioned2006-09-11T14:32:34Z
dc.date.available2006-09-11T14:32:34Z
dc.date.issued1991-02en_US
dc.identifier.citationDu, Bert N.; Bartels, Cynthia F.; Nogueira, Christine P.; Arpagaus, Martine; Lockridge, Oksana; (1991). "Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing." Cellular and Molecular Neurobiology 11(1): 79-89. <http://hdl.handle.net/2027.42/44278>en_US
dc.identifier.issn0272-4340en_US
dc.identifier.issn1573-6830en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/44278
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2013061&dopt=citationen_US
dc.description.abstract1. New information identifying nucleotide alterations of human butyrylcholinesterase allows the use of more specific nomenclature for the variants commonly known as atypical, fluoride, silent, and K variant.en_US
dc.format.extent728297 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.otherSerum Cholinesteraseen_US
dc.subject.otherSilenten_US
dc.subject.otherLife Sciencesen_US
dc.subject.otherNeurosciencesen_US
dc.subject.otherAnimal Anatomy / Morphology / Histologyen_US
dc.subject.otherButyrylcholinesteraseen_US
dc.subject.otherPseudocholinesteraseen_US
dc.subject.otherAnionic Siteen_US
dc.subject.otherAtypicalen_US
dc.subject.otherFluoride Resistanten_US
dc.subject.otherK Varianten_US
dc.subject.otherSuccinylcholine Apneaen_US
dc.titleProposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencingen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumPharmacology Department, Medical Science I, M6322, University of Michigan Medical School, 48109-0626, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumPharmacology Department, Medical Science I, M6322, University of Michigan Medical School, 48109-0626, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumPharmacology Department, Medical Science I, M6322, University of Michigan Medical School, 48109-0626, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumPharmacology Department, Medical Science I, M6322, University of Michigan Medical School, 48109-0626, Ann Arbor, Michigan, USA; INRA, Génétique Moléculaire des Invertébrés, 123 Blvd. Francis Meilland, 06606, Antibes Cedex, Franceen_US
dc.contributor.affiliationumPharmacology Department, Medical Science I, M6322, University of Michigan Medical School, 48109-0626, Ann Arbor, Michigan, USA; Eppley Institute, University of Nebraska Medical Center, 600 South 42nd Street, 68198-6805, Omaha, Nebraska, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid2013061en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/44278/1/10571_2004_Article_BF00712801.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00712801en_US
dc.identifier.sourceCellular and Molecular Neurobiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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