Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The mutant CALR allele burden in essential thrombocythemia at transformation to acute myeloid leukemia.

Blood cells, molecules & diseases - 1 Jun 2017

Langabeer Stephen E, Haslam Karl, Elhassadi Ezzat

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Antineoplastic Combined Chemotherapy Protocols
Share to Bone Marrow Cells
Share to Calreticulin
Share to Cell Transformation, Neoplastic

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Aberrations

Share to Karyotype

Share to Leukemia, Myeloid, Acute

Share to Thrombocythemia, Essential

Source

Identifiers

PMID: 28552475
DOI: 10.1016/j.bcmd.2017.05.004

Genes

CALR

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The mutant CALR allele burden in essential thrombocythemia at transformation to acute myeloid leukemia.PMID 28552475Read ↗

CALR mutation burden in essential thrombocythemia and disease outcome.Semantic proximity Read ↗

CALR-mutated essential thrombocythemia evolving to chronic myeloid leukemia with coexistent CALR mutation and BCR-ABL translocation.Semantic proximity Read ↗

Anagrelide and the CALR mutation allele burden in essential thrombocythemia.Semantic proximity Read ↗

A rare CALR variant mutation and a review of CALR in essential thrombocythemia.Semantic proximity Read ↗

Essential Thrombocythemia Associated With Germline JAK2 G571S Variant and Somatic CALR Type 1 Mutation.Semantic proximity Read ↗

The different variant allele frequencies of type I/type II mutations and the distinct molecular landscapes in CALR-mutant essential thrombocythaemia and primary myelofibrosis.Semantic proximity Read ↗

Myeloproliferative neoplasms with a low (<5%) CALR mutation allele burden.Semantic proximity Read ↗

Analysis of phenotype and outcome in essential thrombocythemia with CALR or JAK2 mutations.Semantic proximity Read ↗

Frequency and allele burden of CALR mutations in Chinese with essential thrombocythemia and primary myelofibrosis without JAK2(V617F) or MPL mutations.Semantic proximity Read ↗

CALR mutational status identifies different disease subtypes of essential thrombocythemia showing distinct expression profiles.Semantic proximity Read ↗

Assessing the thrombotic risk of patients with essential thrombocythemia in the genomic era.Semantic proximity Read ↗

Sequential mutational evaluation of CALR -mutated myeloproliferative neoplasms with thrombocytosis reveals an association between CALR allele burden evolution and disease progression.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.