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

Clinical associations of CSNK1A1 mutation in myelodysplastic syndrome.

The Lancet. Haematology - 1 May 2015

Boultwood Jacqueline, Pellagatti Andrea

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 Mutation
Share to Myelodysplastic Syndromes
Share to Protein Serine-Threonine Kinases

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 26688092
DOI: 10.1016/S2352-3026(15)00070-8

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

Clinical associations of CSNK1A1 mutation in myelodysplastic syndrome.PMID 26688092Read ↗

The Impact of Somatic and Germline Mutations in Myelodysplastic Syndromes and Related Disorders.Semantic proximity Read ↗

Molecular genetic aspects of myelodysplastic syndromes.Semantic proximity Read ↗

Gene mutations in myelodysplastic syndromes.Semantic proximity Read ↗

IDH1 and IDH2 mutations in myelodysplastic syndromes and role in disease progressionSemantic proximity Read ↗

Congenital dyserythropoietic anemia type I mimicking myelodysplasia syndrome with a novel CDAN1 mutation.Semantic proximity Read ↗

CSNK1A1 mutations and isolated del(5q) abnormality in myelodysplastic syndrome: a retrospective mutational analysis.Semantic proximity Read ↗

Genetic abnormalities in myelodysplastic syndrome.Semantic proximity Read ↗

DNA repair gene variants are associated with an increased risk of myelodysplastic syndromes in a Czech population.Semantic proximity Read ↗

Fortuitous discovery of an NPM1 mutation in a myelodysplastic syndrome.Semantic proximity Read ↗

The Genetic Basis of Myelodysplastic SyndromesSemantic proximity Read ↗

A novel de novo mutation in CSNK2A1: reinforcing the link to neurodevelopmental abnormalities and dysmorphic features.Semantic proximity Read ↗

MUTATIONAL PROFILE ENABLES THE IDENTIFICATION OF A HIGH RISK SUBGROUP IN MYELODYSPLASTIC SYNDROMES WITH ISOLATED TRISOMY 8Semantic proximity Read ↗

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