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Article

The JAK2 V617F mutation identifies a subgroup of MDS patients with isolated deletion 5q and a proliferative bone marrow

13 Apr 2006

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 16617322
DOI: 10.1038/sj.leu.2404215

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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.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

The JAK2 V617F mutation identifies a subgroup of MDS patients with isolated deletion 5q and a proliferative bone marrowPMID 16617322Read ↗

U2AF1 mutations in primary myelofibrosis are strongly associated with anemia and thrombocytopenia despite clustering with JAK2V617F and normal karyotypeSemantic proximity Read ↗

JAK2 V617F: a single mutation in the myeloproliferative group of disorders.Semantic proximity Read ↗

Isolated del(5q) in myeloid malignancies: clinicopathologic and molecular features in 143 consecutive patients.Semantic proximity Read ↗

Both expanded and uncultured mesenchymal stem cells from MDS patients are genomically abnormal, showing a specific genetic profile for the 5q− syndromeSemantic proximity Read ↗

MPN patients with low mutant JAK2 allele burden show late expansion restricted to erythroid and megakaryocytic lineagesSemantic proximity Read ↗

Myelodysplastic Disease Associated with Deletions of Chromosome 5q RegionSemantic proximity Read ↗

Involvement of deleted chromosome 5 in complex chromosomal aberrations in newly diagnosed myelodysplastic syndromes (MDS) is correlated with extremely adverse prognosisSemantic proximity Read ↗

Acute myeloid leukemia with isolated del(5q) is associated with IDH1/IDH2 mutations and better prognosis when compared to acute myeloid leukemia with complex karyotype including del(5q).Semantic proximity Read ↗

Hematological MalignanciesSemantic proximity Read ↗

Refractory anemia with ringed sideroblasts associated with marked thrombocytosis (RARS-T), another myeloproliferative condition characterized by JAK2 V617F mutation.Semantic proximity Read ↗

Monosomal karyotype in MDS: explaining the poor prognosis?Semantic proximity Read ↗

Bone Marrow Morphology Associated With Germline RUNX1 Mutations in Patients With Familial Platelet Disorder With Associated Myeloid MalignancySemantic proximity Read ↗

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