Processing of pro-opiomelanocortin-derived amidated joining peptide and glycine-extended precursor in monkey pituitary
dc.contributor.author | Fenger, Mogens | en_US |
dc.date.accessioned | 2006-04-10T14:45:50Z | |
dc.date.available | 2006-04-10T14:45:50Z | |
dc.date.issued | 1991-04-01 | en_US |
dc.identifier.citation | Fenger, Mogens (1991/04/01)."Processing of pro-opiomelanocortin-derived amidated joining peptide and glycine-extended precursor in monkey pituitary." Neuroscience Letters 124(2): 190-194. <http://hdl.handle.net/2027.42/29392> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B6T0G-485RM29-NG/2/108d821e595b82f1c203bff929048ece | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/29392 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2067719&dopt=citation | en_US |
dc.description.abstract | The molecular forms of proopiomelanocortin (POMC) derived amidated and C-terminal glycine-extended joining peptide from monkey (Macaca mulatta) pituitary were determined. The predominant forms of joining peptide found were the low molecular peptides POMC(76-105) and POMC(76-106), respectively. Significant amounts of N-terminally truncated POMC(78-105) and POMC(78-106) were also detected in the posterior-intermediate lobe. No N-terminal extended forms were detected. The relative amount of amidated joining peptide to total joining peptide was 6-35%. It is concluded that not only is the primary sequence of monkey and human POMC extremely conserved, but also the processing patterns are similar. The monkey therefore serves as a suitable model for studying regulation of the processing of POMC and the hypothalamus-pituitary-adrenal axis in man. | en_US |
dc.format.extent | 410925 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 | Processing of pro-opiomelanocortin-derived amidated joining peptide and glycine-extended precursor in monkey pituitary | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Public Health | en_US |
dc.subject.hlbsecondlevel | Psychology | en_US |
dc.subject.hlbsecondlevel | Neurosciences | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbtoplevel | Social Sciences | 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 | Mental Health Research Institute, University of Michigan, Ann Arbor, MI 48109, U.S.A.; National Institutes of Health, Bethesda, MD 20892, U.S.A. | en_US |
dc.identifier.pmid | 2067719 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/29392/1/0000463.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0304-3940(91)90091-7 | en_US |
dc.identifier.source | Neuroscience Letters | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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