Molecular analysis of rearrangements in human ribosomal RNA gene clones
dc.contributor.author | Respess, James G. | en_US |
dc.contributor.author | Erickson, Jeanne | en_US |
dc.contributor.author | Rushford, Caroline L. | en_US |
dc.contributor.author | Jackson, David A. | en_US |
dc.contributor.author | Schmickel, Roy D. | en_US |
dc.date.accessioned | 2006-04-07T18:38:25Z | |
dc.date.available | 2006-04-07T18:38:25Z | |
dc.date.issued | 1983-10 | en_US |
dc.identifier.citation | Respess, James, Erickson, Jeanne, Rushford, Caroline, Jackson, David, Schmickel, Roy (1983/10)."Molecular analysis of rearrangements in human ribosomal RNA gene clones." Gene 24(2-3): 331-334. <http://hdl.handle.net/2027.42/25104> | en_US |
dc.identifier.uri | http://www.sciencedirect.com/science/article/B6T39-47VN2GX-GD/2/a7b81f441ddf8b78dc90bea2a61e11f1 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/25104 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6227528&dopt=citation | en_US |
dc.description.abstract | Human placental DNA, enriched for ribosomal sequences, was cloned in the phage vector [lambda]Charon 16A. Recombinants containing 28S rDNA sequences were isolated, and all were found to have deletions in the insert and/or vector DNA. Electron microscopic analysis was used to map the deletions and provide evidence that unstable forms of the recombinants can revert to the original vector or undergo further rearrangements. Specific deletions are manifested as previously unreported plaque phenotypes. | en_US |
dc.format.extent | 303890 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 | Molecular analysis of rearrangements in human ribosomal RNA gene clones | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Molecular, Cellular and Developmental Biology | en_US |
dc.subject.hlbsecondlevel | Genetics | 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 | Program in Cellular and Molecular Biology in the Health Sciences, University of Michigan Medical School, Ann Arbor, MI 48104, U.S.A. Tel. (313) 764-5428 | en_US |
dc.contributor.affiliationum | Program in Cellular and Molecular Biology in the Health Sciences, University of Michigan Medical School, Ann Arbor, MI 48104, U.S.A. Tel. (313) 764-5428 | en_US |
dc.contributor.affiliationum | Program in Cellular and Molecular Biology in the Health Sciences, University of Michigan Medical School, Ann Arbor, MI 48104, U.S.A. Tel. (313) 764-5428 | en_US |
dc.contributor.affiliationum | Program in Cellular and Molecular Biology in the Health Sciences, University of Michigan Medical School, Ann Arbor, MI 48104, U.S.A. Tel. (313) 764-5428 | en_US |
dc.contributor.affiliationum | Program in Cellular and Molecular Biology in the Health Sciences, University of Michigan Medical School, Ann Arbor, MI 48104, U.S.A. Tel. (313) 764-5428 | en_US |
dc.identifier.pmid | 6227528 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/25104/1/0000536.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1016/0378-1119(83)90094-X | en_US |
dc.identifier.source | Gene | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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