Evidence for a hepatic transport system not responsive to glucagon or theophylline
dc.contributor.author | Harrison, Lester I. | en_US |
dc.contributor.author | Christensen, Halvor N. | en_US |
dc.date.accessioned | 2006-04-17T16:27:46Z | |
dc.date.available | 2006-04-17T16:27:46Z | |
dc.date.issued | 1971-04-02 | en_US |
dc.identifier.citation | Harrison, Lester I., Christensen, Halvor N. (1971/04/02)."Evidence for a hepatic transport system not responsive to glucagon or theophylline." Biochemical and Biophysical Research Communications 43(1): 119-125. <http://hdl.handle.net/2027.42/33672> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B6WBK-4G0VTNW-1S/2/eef5faa428b80ffd840ac58eb5c7460b | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/33672 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=5579936&dopt=citation | en_US |
dc.description.abstract | SummaryIn experiments designed to examine which transport systems are responsive to the adenine cyclase system, young rats received isotopically labeled, non-metabolizable amino acid analogs, selected for specificity to known transport systems. After allowing 38 hr for the amino acid to be distributed, glucagon or theophylline were injected intraperitoneally. Two amino acids typically reactive with a Na+-dependent transport system for neutral amino acids, and one with a system for cationic amino acids, showed sharply elevated hepatic levels, relative to the plasma. Levels for the first group also rose in the diaphragm. A model amino acid typically reactive with a Na+-insensitive transport system underwent no change in its distribution during 2 to 6 hr. | en_US |
dc.format.extent | 375007 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | Elsevier | en_US |
dc.title | Evidence for a hepatic transport system not responsive to glucagon or theophylline | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Natural Resources and Environment | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbsecondlevel | Ecology and Evolutionary Biology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Biological Chemistry, University of Michigan Ann Arbor, Michigan 48104, USA | en_US |
dc.contributor.affiliationum | Department of Biological Chemistry, University of Michigan Ann Arbor, Michigan 48104, USA | en_US |
dc.identifier.pmid | 5579936 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/33672/1/0000182.pdf | en_US |
dc.identifier.source | Biochemical and Biophysical Research Communications | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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