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

JAK2 p.V617F Variants in Non-Blood DNA from Patients with Polycythemia Vera

Turkish journal of haematology : official journal of Turkish Society of Haematology - 31 Aug 2023

Mori Naoki, Ohwashi-Miyazaki Mari, Yoshinaga Kentaro, Shiseki Masayuki, Tanaka Junji

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 DNA
Share to Janus Kinase 2
Share to Mutation
Share to Polycythemia Vera

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Thrombocythemia, Essential

Source

Open in PubMed Open full text

Identifiers

PMID: 37278343
DOI: 10.4274/tjh.galenos.2023.2023-0159
PMCID: PMC10476263

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

JAK2 p.V617F Variants in Non-Blood DNA from Patients with Polycythemia VeraPMID 37278343Read ↗

Prevalance of JAK2 V617F and exon 12 mutations in polycythaemia veraSemantic proximity Read ↗

Molecular evidence of JAK2 p.V617F mutated pure erythroid leukemia arising from polycythemia vera.Semantic proximity Read ↗

JAK2 mutations in polycythemia vera--molecular mechanisms and clinical applications.Semantic proximity Read ↗

Genetic Background of Polycythemia Vera.Semantic proximity Read ↗

Bone marrow JAK2V617F allele burden and clinical correlates in polycythemia veraSemantic proximity Read ↗

Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis.Semantic proximity Read ↗

The disappearance of two alleles of JAK2 V617F from peripheral blood of a polycythaemia vera patient correlates with transformation into myelofibrosis.Semantic proximity Read ↗

JAK2V617F Exon-14 Mutation Driven Polycythemia Vera.Semantic proximity Read ↗

Features and Allele Frequency of JAK2 Exon 12-Mutated Polycythemia Vera in Comparison with JAK2V617F-Mutated Disease.Semantic proximity Read ↗

The clinical phenotype of wild-type, heterozygous, and homozygous JAK2V617F in polycythemia vera.Semantic proximity Read ↗

JAK2V617F variant allele frequency, non-driver mutations, single-nucleotide variants and polycythemia vera outcome.Semantic proximity Read ↗

Clinical profile of homozygous JAK2 617V>F mutation in patients with polycythemia vera or essential thrombocythemiaSemantic proximity Read ↗

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