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

Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia.

Leukemia - 1 Apr 2014

Kim Y, Schulz V P, Satake N, Gruber T A, Teixeira A M, Halene S, Gallagher P G, Krause D S

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 Chromosomes, Human, Pair 1
Share to Chromosomes, Human, Pair 22
Share to Exome
Share to Leukemia, Megakaryoblastic, Acute

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Matrix Metalloproteinase 8

Share to Oncogene Proteins, Fusion

Share to RNA-Binding Proteins

Share to Translocation, Genetic

Source

Open in PubMed Open full text

Identifiers

PMID: 24157583
DOI: 10.1038/leu.2013.314
PMCID: PMC3981934

Genes

MMP8

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 · 8 closest

Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia.PMID 24157583Read ↗

Single-molecule DNA sequencing of acute myeloid leukemia and myelodysplastic syndromes with multiple TP53 alterationsSemantic proximity Read ↗

Genomic landscape and clonal evolution of acute myeloid leukemia with t(8;21): an international study on 331 patientsSemantic proximity Read ↗

Identification of a novel Kmod -1 allele encoded by 977C>T (Pro326Leu).Semantic proximity Read ↗

Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemia.Semantic proximity Read ↗

Exome sequencing identifies MPL as a causative gene in familial aplastic anemia.Semantic proximity Read ↗

The translocation t(1;22)(p13;q13) is a nonrandom marker specifically associated with acute megakaryocytic leukemia in young childrenSemantic proximity Read ↗

A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia.Semantic proximity Read ↗

Clinical characterization of the mutational landscape of 24,639 real-world samples from patients with myeloid malignancies.Semantic proximity Read ↗

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