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Book Chapter: Clonal Hematopoiesis and Its Functional Implications in MDS/AML

TitleClonal Hematopoiesis and Its Functional Implications in MDS/AML
Authors
Issue Date28-Sep-2023
PublisherSpringer Nature Singapore
Abstract

Clonal hematopoiesis (CH) is now a specifically recognized as a precursor myeloid neoplasm and comprised clonal hematopoiesis of indeterminate potential (CHIP) and clonal cytopenia of undetermined significance (CCUS). Various cohort studies have confirmed the association between CH and the subsequent development of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). In addition, there is recent evidence to show that CH is associated with highlighted inflammatory responses and may influence non-hematological disease states in the general population and in patients with hematological malignancies.


Persistent Identifierhttp://hdl.handle.net/10722/341849
ISBN

 

DC FieldValueLanguage
dc.contributor.authorSingh, Gill Harinder Harry-
dc.date.accessioned2024-03-26T05:37:40Z-
dc.date.available2024-03-26T05:37:40Z-
dc.date.issued2023-09-28-
dc.identifier.isbn9789819938094-
dc.identifier.urihttp://hdl.handle.net/10722/341849-
dc.description.abstract<p>Clonal hematopoiesis (CH) is now a specifically recognized as a precursor myeloid neoplasm and comprised clonal hematopoiesis of indeterminate potential (CHIP) and clonal cytopenia of undetermined significance (CCUS). Various cohort studies have confirmed the association between CH and the subsequent development of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). In addition, there is recent evidence to show that CH is associated with highlighted inflammatory responses and may influence non-hematological disease states in the general population and in patients with hematological malignancies.<br></p>-
dc.languageeng-
dc.publisherSpringer Nature Singapore-
dc.relation.ispartofPathogenesis and Treatment of Leukemia-
dc.titleClonal Hematopoiesis and Its Functional Implications in MDS/AML-
dc.typeBook_Chapter-
dc.identifier.doi10.1007/978-981-99-3810-0_28-
dc.identifier.eisbn9789819938100-

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