Identification of specificity H-2.7 as an erythrocyte antigen: Control by an independent locus, H-2G , between the S and D regions
dc.contributor.author | David, Chella S. | en_US |
dc.contributor.author | Shreffler, Donald C. | en_US |
dc.contributor.author | Stimpfling, Jack H. | en_US |
dc.date.accessioned | 2006-09-11T18:08:57Z | |
dc.date.available | 2006-09-11T18:08:57Z | |
dc.date.issued | 1975-12 | en_US |
dc.identifier.citation | David, Chella S.; Stimpfling, Jack H.; Shreffler, Donald C.; (1975). "Identification of specificity H-2.7 as an erythrocyte antigen: Control by an independent locus, H-2G , between the S and D regions." Immunogenetics 2(1): 131-139. <http://hdl.handle.net/2027.42/46742> | en_US |
dc.identifier.issn | 1432-1211 | en_US |
dc.identifier.issn | 0093-7711 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/46742 | |
dc.description.abstract | Specificity H-2.7 is expressed predominantly on erythrocytes and controlled by a gene that maps within the H-2 gene complex at a locus, designated as H-2G , which apparently lies between regions S and D . Three phenotypes have been observed with respect to this antigen: a) positive by direct test and absorption (haplotypes H-2 f , H-2 j , H-2 p , H-2 s ); b) positive only by absorption ( H-2 k ); and c) negative ( H-2 b , H-2 d , H-2 q ). New crossover positions have been established for several H-2 recombinants based on classifications for the H-2G locus. | en_US |
dc.format.extent | 445080 bytes | |
dc.format.extent | 3115 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Springer-Verlag; Springer-Verlag New York Inc. | en_US |
dc.subject.other | Immunology | en_US |
dc.subject.other | Cell Biology | en_US |
dc.subject.other | Biomedicine | en_US |
dc.subject.other | Allergology | en_US |
dc.title | Identification of specificity H-2.7 as an erythrocyte antigen: Control by an independent locus, H-2G , between the S and D regions | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbsecondlevel | Biological Chemistry | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Human Genetics, University of Michigan, 48104, Ann Arbor, Michigan; McLaughlin Research Institute, Columbus Hospital, 59401, Great Falls, Montana | en_US |
dc.contributor.affiliationum | Department of Human Genetics, University of Michigan, 48104, Ann Arbor, Michigan; McLaughlin Research Institute, Columbus Hospital, 59401, Great Falls, Montana | en_US |
dc.contributor.affiliationum | Department of Human Genetics, University of Michigan, 48104, Ann Arbor, Michigan; McLaughlin Research Institute, Columbus Hospital, 59401, Great Falls, Montana | en_US |
dc.contributor.affiliationumcampus | Ann Arbor | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/46742/1/251_2005_Article_BF01572281.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1007/BF01572281 | en_US |
dc.identifier.source | Immunogenetics | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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