Role of System Gly in glycine transport in monolayer cultures of liver cells
dc.contributor.author | Christensen, Halvor N. | en_US |
dc.contributor.author | Handlogten, Mary E. | en_US |
dc.date.accessioned | 2006-04-07T18:09:59Z | |
dc.date.available | 2006-04-07T18:09:59Z | |
dc.date.issued | 1981-01-15 | en_US |
dc.identifier.citation | Christensen, Halvor N., Handlogten, Mary E. (1981/01/15)."Role of System Gly in glycine transport in monolayer cultures of liver cells." Biochemical and Biophysical Research Communications 98(1): 102-107. <http://hdl.handle.net/2027.42/24480> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B6WBK-4F03B28-B0/2/f070bedf301cd888d54c406842fdb048 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/24480 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6163428&dopt=citation | en_US |
dc.description.abstract | The high-affinity component of glycine uptake by the hepatoma cell line HTC and by the ordinary rat hepatocyte corresponds to System Gly, the agency serving for glycine uptake by pigeon red blood cells and rabbit reticulocytes, and at most to only a minor extent to System ASC. This component was identified in HTC by its sensitivity to inhibition by sarcosine but scarcely by 2-(methylamino) isobutyric acid, by its insensitivity to lowering of the pH, and by the unique relation of its rate to the square of the Na+ concentration. The identity of the low-affinity component with System A was confirmed by opposite properties, and by its stimulation by insulin or amino acid starvation. Both components differed sharply from the System ASC uptake as measured with threonine. | en_US |
dc.format.extent | 364131 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 | Role of System Gly in glycine transport in monolayer cultures of liver cells | 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 The University of Michigan Medical School, Ann Arbor, Michigan 48109, USA | en_US |
dc.contributor.affiliationum | Department of Biological Chemistry The University of Michigan Medical School, Ann Arbor, Michigan 48109, USA | en_US |
dc.identifier.pmid | 6163428 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/24480/1/0000755.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0006-291X(81)91875-1 | en_US |
dc.identifier.source | Biochemical and Biophysical Research Communications | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.