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Article

Impact of JAK2V617F mutation status, allele burden, and clearance after allogeneic stem cell transplantation for myelofibrosis.

Blood - 4 Nov 2010

Alchalby Haefaa, Badbaran Anita, Zabelina Tatjana, Kobbe Guido, Hahn Joachim, Wolff Daniel, Bornhäuser Martin, Thiede Christian, Baurmann Herrad, Bethge Wolfgang, Hildebrandt York, Bacher Ulrike, Fehse Boris, Zander Axel R, Kröger Nicolaus

Abstract excerpt

Allogeneic stem cell transplantation (ASCT) after reduced-intensity conditioning has become a reasonable treatment option for patients with advanced myelofibrosis. The role of characteristic molecular genetic abnormalities, such as JAK2V617F on outcome of ASCT, is not yet elucidated. In 139 of 162 myelofibrosis patients with known JAK2V617F mutation status who received ASCT after reduced-intensity conditioning,...

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Identifiers

PMID: 20489052
DOI: 10.1182/blood-2009-12-260588

Genes

JAK2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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