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N-terminal sequence of human leukocyte glycoprotein Mol: conservation across species and homology to platelet IIb/IIIa

dc.contributor.authorPierce, Mark W.en_US
dc.contributor.authorRemold-O'Donnell, Eileenen_US
dc.contributor.authorTodd, Robert F. IIIen_US
dc.contributor.authorArnaout, M. Aminen_US
dc.date.accessioned2006-04-07T19:22:38Z
dc.date.available2006-04-07T19:22:38Z
dc.date.issued1986-12-12en_US
dc.identifier.citationPierce, Mark W., Remold-O'Donnell, Eileen, Todd, III, Robert F., Arnaout, M. Amin (1986/12/12)."N-terminal sequence of human leukocyte glycoprotein Mol: conservation across species and homology to platelet IIb/IIIa." Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology 874(3): 368-371. <http://hdl.handle.net/2027.42/25944>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T21-47PNXRR-HP/2/dfa6c5a8ea254837ca6eb04a74cfb3d8en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25944
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3539202&dopt=citationen_US
dc.description.abstractMo1 and gp160-gp93 are two surface membrane glycoprotein heterodimers present on granulocytes and monocytes derived from humans and guinea pigs, respectively. We purified both antigens and found that their alpha subunits had identical N-termini which were significantly homologous to the alpha subunit of the human adhesion platelet glycoprotein IIb/IIIa.en_US
dc.format.extent291609 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleN-terminal sequence of human leukocyte glycoprotein Mol: conservation across species and homology to platelet IIb/IIIaen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumHematology/Oncology Unit, University of Michigan, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherHoward Hughes Medical Institute Laboratories and Diabetes Unit and Medical Services, Massachusetts General Hospital, Boston, MA, USAen_US
dc.contributor.affiliationotherCenter for Blood Research, The Childrens Hospital, Harvard Medical School, Boston, MA, USAen_US
dc.contributor.affiliationotherDivisions of Immunology & Nephrology, The Childrens Hospital, Harvard Medical School, Boston, MA, USAen_US
dc.identifier.pmid3539202en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25944/1/0000006.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0167-4838(86)90037-3en_US
dc.identifier.sourceBiochimica et Biophysica Actaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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