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

Biallelic ETV6 rearrangements by recurrent translocations t(7;12)(p15;p13) and t(3;12)(q26.2;p13) in acute myeloid leukemia.

Leukemia research - 1 Nov 2011

Yamamoto Katsuya, Yakushijin Kimikazu, Funakoshi Yohei, Inui Yumiko, Okamura Atsuo, Matsuoka Hiroshi, Minami Hironobu

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 Antineoplastic Combined Chemotherapy Protocols
Share to Chromosomes, Human, Pair 12
Share to Chromosomes, Human, Pair 3

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 7

Share to ETS Translocation Variant 6 Protein

Share to Gene Rearrangement

Share to Proto-Oncogene Proteins c-ets

Share to Translocation, Genetic

Source

Identifiers

PMID: 21803420
DOI: 10.1016/j.leukres.2011.07.012

Genes

ETV6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Biallelic ETV6 rearrangements by recurrent translocations t(7;12)(p15;p13) and t(3;12)(q26.2;p13) in acute myeloid leukemia.PMID 21803420Read ↗

A Rare Case of ETV6/MECOM Rearrangement in Therapy-Related Acute Myeloid Leukemia with t(3;12) and Monosomy 7.Semantic proximity Read ↗

Acute myeloid leukemia bearing t(7;11)(p15;p15) is a distinct cytogenetic entity with poor outcome and a distinct mutation profile: comparative analysis of 493 adult patientsSemantic proximity Read ↗

<i>ETV6</i> rearrangements are recurrent in myeloid malignancies and are frequently associated with other genetic eventsSemantic proximity Read ↗

The Landscape of Secondary Genetic Rearrangements in Pediatric Patients with B-Cell Acute Lymphoblastic Leukemia with t(12;21)Semantic proximity Read ↗

FLT3 is fused to ETV6 in a myeloproliferative disorder with hypereosinophilia and a t(12;13)(p13;q12) translocationSemantic proximity Read ↗

Chronic myelocytic leukemia with eosinophilia, t(9;12)(q34;p13), and ETV6-ABL gene rearrangementSemantic proximity Read ↗

Mechanisms associated with t(7;12) acute myeloid leukaemia: from genetics to potential treatment targetsSemantic proximity Read ↗

Determination of ETV 6‐ RUNX 1 genomic breakpoint by next‐generation sequencingSemantic proximity Read ↗

The Diverse Roles of ETV6 Alterations in B-Lymphoblastic Leukemia and Other Hematopoietic Cancers.Semantic proximity Read ↗

Abnormalities of the der(12)t(12;21) in ETV6-RUNX1 acute lymphoblastic leukemia.Semantic proximity Read ↗

A large exon 6 break in V-form acute promyelocytic leukemia: relevance to clinical management.Semantic proximity Read ↗

B lymphoblastic leukemia with ETV6 amplification.Semantic proximity Read ↗

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