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

Prevalence of CYLD mutations in Vietnamese patients with polycythemia vera.

Advances in clinical and experimental medicine : official organ Wroclaw Medical University - 1 Apr 2022

Trang Do Thi, Giang Nguyen Hoang, Trang Bui Kieu, Ngoc Nguyen Thy, Giang Nguyen Van, Canh Nguyen Xuan, Vuong Nguyen Ba, Xuan Nguyen Thi

Abstract excerpt

BACKGROUND: Polycythemia vera (PV) is characterized by increased proliferation and accumulation of erythroid and mature myeloid cells and megakaryocyte in the bone marrow and peripheral blood. The JAK2V617F mutation is present in most PV patients. Deubiquitinase (DUB) genes, including TNFAIP3 (A20), CYLD and Cezanne, function as negative regulators of inflammatory reaction through nuclear factor...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Deubiquitinating Enzyme CYLD

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Janus Kinase 2

Share to Mutation

Share to Polycythemia Vera

Share to Prevalence

Source

Identifiers

PMID: 35025147
DOI: 10.17219/acem/144027

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prevalence of CYLD mutations in Vietnamese patients with polycythemia vera.PMID 35025147Read ↗

Genetic Background of Polycythemia Vera.Semantic proximity Read ↗

A narrative review of the prevalence of polycythemia and its associated risk factors in Saudi Arabia.Semantic proximity Read ↗

Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera.Semantic proximity Read ↗

t(5;12)(q23-31;p13) with ETV6-ACSL6 gene fusion in polycythemia vera.Semantic proximity Read ↗

Genetic Characteristics of Polycythemia Vera and Essential Thrombocythemia in Korean Patients.Semantic proximity Read ↗

Clinical and molecular characterisation of a prospectively collected cohort of children and adolescents with polycythemia vera.Semantic proximity Read ↗

Identifying Six Novel Genetic Variants and Alterations in Peripheral T-cell Subsets in Porokeratosis PatientsSemantic proximity Read ↗

Spectrum mutations of PRF1, UNC13D, STX11, and STXBP2 genes in Vietnamese patients with hemophagocytic lymphohistiocytosis.Semantic proximity Read ↗

Association of JAK2V617F allele burden and clinical correlates in polycythemia vera: a systematic review and meta-analysis.Semantic proximity Read ↗

Novel pathogenic frameshift mutation in the POLH gene contributes to xeroderma pigmentosum variant type in a 16-year-old girl.Semantic proximity Read ↗

The Prevalence of JAK2 Exon 12 Mutations in Vietnamese Patients with JAK2 V617F-Negative Polycythemia Vera: Frequent or Rare?Semantic proximity Read ↗

Unanswered questions in polycythaemia vera.Semantic proximity Read ↗

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