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

A novel pathogenetic mutation in clonal eosinophilia.

Current hematology reports - 1 May 2004

Tefferi Ayalew

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 Remission Induction
Share to Benzamides
Share to Chromosomes, Human, Pair 4
Share to Eosinophilia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Imatinib Mesylate

Share to Inhibitory Concentration 50

Share to mRNA Cleavage and Polyadenylation Factors

Share to Receptor, Platelet-Derived Growth Factor alpha

Source

Identifiers

PMID: 15087067

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel pathogenetic mutation in clonal eosinophilia.PMID 15087067Read ↗

Eosinophilic disorders: Molecular pathogenesis, new classification, and modern therapySemantic proximity Read ↗

Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing.Semantic proximity Read ↗

Molecular Classification and Pathogenesis of Eosinophilic Disorders: 2005 UpdateSemantic proximity Read ↗

The Diagnostic Work-Up of Hypereosinophilia.Semantic proximity Read ↗

Cytogenetic and molecular genetic aspects of eosinophilic leukaemias.Semantic proximity Read ↗

Genetic and Molecular Contributors in Eosinophilic EsophagitisSemantic proximity Read ↗

Contemporary Classification and Diagnostic Evaluation of Hypereosinophilia.Semantic proximity Read ↗

Hypereosinophilic syndrome and clonal eosinophilia: point-of-care diagnostic algorithm and treatment update.Semantic proximity Read ↗

BRAF mutation as a novel driver of eosinophilic cystitis.Semantic proximity Read ↗

Autosomal-dominant hypohidrotic ectodermal dysplasia caused by a novel mutation.Semantic proximity Read ↗

Genomics of clonal evolution in a case of essential thrombocythemia.Semantic proximity Read ↗

Whole-exome sequencing and genome-wide methylation analyses identify novel disease associated mutations and methylation patterns in idiopathic hypereosinophilic syndrome.Semantic proximity Read ↗

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