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Article: Immunogenotyping in Hodgkin's disease

TitleImmunogenotyping in Hodgkin's disease
Authors
KeywordsImmunogenotyping
Gene rearrangement
Hodgkin's disease
Issue Date1988
Citation
Hematological Oncology, 1988, v. 6, n. 3, p. 239-245 How to Cite?
AbstractThis review presents and discusses the immunogenotypic findings in 112 cases of Hodgkin's disease (HD) and eight Hodgkin's cell lines. Clonal rearrangements of the T cell receptor γ and β chain, as well as immunoglobulin heavy and light chain genes, are detected in the majority of nodular sclerosis and lymphocytic depletion subtypes. Together with the recent immunophenotypic data, these findings are in favour of the view that HD is a disease of activated lymphoid cells. Further investigations will be necessary to characterize the morphology and immunophenotype of the clonally rearranged cell population which seems not to be confined to the Sternberg‐Reed and Hodgkin cell in every case. Prospective clinical studies including the genotype of HD cases have to be done in order to address the question of whether or not distinctive immunogenotypic profiles correlate with the clinical course of this lymphoproliferative disorder. Copyright © 1988 John Wiley & Sons, Ltd
Persistent Identifierhttp://hdl.handle.net/10722/292332
ISSN
2023 Impact Factor: 3.3
2023 SCImago Journal Rankings: 0.820
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorGriesser, Henrik-
dc.contributor.authorMak, Tak W.-
dc.date.accessioned2020-11-17T14:56:14Z-
dc.date.available2020-11-17T14:56:14Z-
dc.date.issued1988-
dc.identifier.citationHematological Oncology, 1988, v. 6, n. 3, p. 239-245-
dc.identifier.issn0278-0232-
dc.identifier.urihttp://hdl.handle.net/10722/292332-
dc.description.abstractThis review presents and discusses the immunogenotypic findings in 112 cases of Hodgkin's disease (HD) and eight Hodgkin's cell lines. Clonal rearrangements of the T cell receptor γ and β chain, as well as immunoglobulin heavy and light chain genes, are detected in the majority of nodular sclerosis and lymphocytic depletion subtypes. Together with the recent immunophenotypic data, these findings are in favour of the view that HD is a disease of activated lymphoid cells. Further investigations will be necessary to characterize the morphology and immunophenotype of the clonally rearranged cell population which seems not to be confined to the Sternberg‐Reed and Hodgkin cell in every case. Prospective clinical studies including the genotype of HD cases have to be done in order to address the question of whether or not distinctive immunogenotypic profiles correlate with the clinical course of this lymphoproliferative disorder. Copyright © 1988 John Wiley & Sons, Ltd-
dc.languageeng-
dc.relation.ispartofHematological Oncology-
dc.subjectImmunogenotyping-
dc.subjectGene rearrangement-
dc.subjectHodgkin's disease-
dc.titleImmunogenotyping in Hodgkin's disease-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/hon.2900060307-
dc.identifier.pmid3042582-
dc.identifier.scopuseid_2-s2.0-0023730979-
dc.identifier.volume6-
dc.identifier.issue3-
dc.identifier.spage239-
dc.identifier.epage245-
dc.identifier.eissn1099-1069-
dc.identifier.isiWOS:A1988P552700006-
dc.identifier.issnl0278-0232-

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