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dc.contributor.authorQuesenberry, Peter J.
dc.contributor.authorHabibian, Houri K.
dc.contributor.authorDooner, Mark S.
dc.contributor.authorZhong, Suju
dc.contributor.authorReilly, Judith
dc.contributor.authorPeters, Stefan O.
dc.contributor.authorBecker, Pamela S.
dc.contributor.authorGrimaldi, Christina I.
dc.contributor.authorCarlson, Jane E.
dc.contributor.authorReddy, G. Prem Veer
dc.contributor.authorNilsson, Susan K.
dc.contributor.authorStewart, F. Marc
dc.date2022-08-11T08:09:35.000
dc.date.accessioned2022-08-23T16:36:41Z
dc.date.available2022-08-23T16:36:41Z
dc.date.issued1998-05-28
dc.date.submitted2009-03-31
dc.identifier.citationTrans Am Clin Climatol Assoc. 1998;109:19-25; discussion 25-6.
dc.identifier.issn0065-7778 (Print)
dc.identifier.pmid9601124
dc.identifier.urihttp://hdl.handle.net/20.500.14038/38841
dc.description.abstractThese observations suggest several immediate clinical strategies. In gene therapy, approaches could be targeted to obtain cycling of hematopoietic stem cells and gene-carrying retrovirus vector integration followed by engraftment at an appropriate time interval which favors engraftment. The same type of approach can be utilized for stem cell expansion approaches. Alternatively marrow or peripheral stem cell engraftment can be obtained with minimal to no toxicity in allochimeric strategies in such diseases as sickle cell anemia or thalassemia. A similar approach could be useful in obtaining cell engraftment with minimal toxicity in therapies employing cellular immune (T-cell and NK-cell) attack against cancer. These areas of clinical application are outline in Table 3.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=9601124&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194341/?tool=pubmed
dc.subjectAnimals
dc.subjectCell Differentiation
dc.subjectCytokines
dc.subjectFemale
dc.subjectGene Therapy
dc.subjectHematopoiesis
dc.subjectHematopoietic Stem Cell Transplantation
dc.subjectHematopoietic Stem Cells
dc.subjectHumans
dc.subjectMale
dc.subjectMice
dc.subjectMice, Inbred BALB C
dc.subjectModels, Biological
dc.subjectPhenotype
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleChiaroscuro hematopoietic stem cell
dc.typeJournal Article
dc.source.journaltitleTransactions of the American Clinical and Climatological Association
dc.source.volume109
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/1681
dc.identifier.contextkey805502
html.description.abstract<p>These observations suggest several immediate clinical strategies. In gene therapy, approaches could be targeted to obtain cycling of hematopoietic stem cells and gene-carrying retrovirus vector integration followed by engraftment at an appropriate time interval which favors engraftment. The same type of approach can be utilized for stem cell expansion approaches. Alternatively marrow or peripheral stem cell engraftment can be obtained with minimal to no toxicity in allochimeric strategies in such diseases as sickle cell anemia or thalassemia. A similar approach could be useful in obtaining cell engraftment with minimal toxicity in therapies employing cellular immune (T-cell and NK-cell) attack against cancer. These areas of clinical application are outline in Table 3.</p>
dc.identifier.submissionpathoapubs/1681
dc.contributor.departmentCancer Center
dc.source.pages19-25; discussion 25-6


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