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Article

NOTCH2 mutations in marginal zone lymphoma

1 Jan 2008

Abstract excerpt

status: Published

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18508802
DOI: 10.3324/haematol.11635

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Related research

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NOTCH2 mutations in marginal zone lymphomaPMID 18508802Read ↗

Clinical and diagnostic relevance of NOTCH2 -and KLF2 -mutations in splenic marginal zone lymphomaSemantic proximity Read ↗

NOTCH signaling in the pathogenesis of splenic marginal zone lymphoma-opportunities for therapy.Semantic proximity Read ↗

The coding genome of splenic marginal zone lymphoma: activation of NOTCH2 and other pathways regulating marginal zone development.Semantic proximity Read ↗

Marginal zone lymphomasSemantic proximity Read ↗

The genetics of nodal marginal zone lymphoma.Semantic proximity Read ↗

Systematic Review of Somatic Mutations in Splenic Marginal Zone Lymphoma.Semantic proximity Read ↗

Whole-exome sequencing in splenic marginal zone lymphoma reveals mutations in genes involved in marginal zone differentiation.Semantic proximity Read ↗

Whole-genome sequencing identifies recurrent somatic NOTCH2 mutations in splenic marginal zone lymphoma.Semantic proximity Read ↗

Role of Notch2 pathway in mature B cell malignanciesSemantic proximity Read ↗

Genetics and Prognostication in Splenic Marginal Zone Lymphoma: Revelations from Deep Sequencing.Semantic proximity Read ↗

KLF2 mutation is the most frequent somatic change in splenic marginal zone lymphoma and identifies a subset with distinct genotype.Semantic proximity Read ↗

High-throughput sequencing of nodal marginal zone lymphomas identifies recurrent BRAF mutations.Semantic proximity Read ↗

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