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Article

Identification of MPL W515L/K mutations in patients with primary myelofibrosis and essential thrombocythaemia by allele-specific polymerase chain reaction.

Acta haematologica - 1 Jan 2009

Daly Sarah, Conneally Eibhlin, Langabeer Stephen E

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Share to DNA Mutational Analysis
Share to Janus Kinase 2
Share to Mutation, Missense
Share to Point Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polymerase Chain Reaction

Share to Primary Myelofibrosis

Share to Receptors, Thrombopoietin

Share to Thrombocythemia, Essential

Source

Identifiers

PMID: 19521067
DOI: 10.1159/000224333

Genes

MPL

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of MPL W515L/K mutations in patients with primary myelofibrosis and essential thrombocythaemia by allele-specific polymerase chain reaction.PMID 19521067Read ↗

Detection of an MPLW515 mutation in a case with features of both essential thrombocythemia and refractory anemia with ringed sideroblasts and thrombocytosis.Semantic proximity Read ↗

Essential thrombocythemia with MPL W515S mutation.Semantic proximity Read ↗

Detection of MPL mutations by a novel allele-specific PCR-based strategy.Semantic proximity Read ↗

Characteristics and clinical correlates of MPL 515W>L/K mutation in essential thrombocythemia.Semantic proximity Read ↗

MPL mutations in myeloproliferative disorders: analysis of the PT-1 cohort.Semantic proximity Read ↗

MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients.Semantic proximity Read ↗

JAK2 V617F and MPL W515L/K mutations in Korean patients with essential thrombocythemia.Semantic proximity Read ↗

Detection of MPLW515L/K mutations and determination of allele frequencies with a single-tube PCR assay.Semantic proximity Read ↗

Screening and monitoring of MPL W515L mutation with real-time PCR in patients with myelofibrosis undergoing allogeneic-SCTSemantic proximity Read ↗

MPL W515L/K mutations in 343 Chinese adults with JAK2V617F mutation-negative chronic myeloproliferative disorders detected by a newly developed RQ-PCR based on TaqMan MGB probes.Semantic proximity Read ↗

A sensitive detection method for MPLW515L or MPLW515K mutation in chronic myeloproliferative disorders with locked nucleic acid-modified probes and real-time polymerase chain reaction.Semantic proximity Read ↗

MPL exon 10 mutations other than canonical MPL W515L/K mutations identified by in-house MPL exon 10 direct sequencing in essential thrombocythemia.Semantic proximity Read ↗

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