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

Sézary syndrome is a unique cutaneous T-cell lymphoma as identified by an expanded gene signature including diagnostic marker molecules CDO1 and DNM3

22 Nov 2007

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 Cutaneous lymphoproliferative disorders research
Share to Lymphoma Diagnosis and Treatment
Share to Phytochemical compounds biological activities

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 18033314
DOI: 10.1038/sj.leu.2405044

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Sézary syndrome is a unique cutaneous T-cell lymphoma as identified by an expanded gene signature including diagnostic marker molecules CDO1 and DNM3PMID 18033314Read ↗

Sézary syndrome: old enigmas, new targets.Semantic proximity Read ↗

Single-cell analysis of Sézary syndrome reveals novel markers and shifting gene profiles associated with treatmentSemantic proximity Read ↗

Genomic profiling of Sézary syndrome identifies alterations of key T cell signaling and differentiation genes.Semantic proximity Read ↗

Improved Sézary cell detection and novel insights into immunophenotypic and molecular heterogeneity in Sézary syndromeSemantic proximity Read ↗

Single-Cell Profiling Reveals Targetable Malignant T-Cell Subtypes and Immune Evasion Pathways in Sézary SyndromeSemantic proximity Read ↗

Sézary syndrome originates from heavily mutated hematopoietic progenitorsSemantic proximity Read ↗

Sézary Syndrome: Translating Genetic Diversity into Personalized Medicine.Semantic proximity Read ↗

The mutational landscape of cutaneous T cell lymphoma and Sézary syndrome.Semantic proximity Read ↗

Integrated genomic analyses of cutaneous T-cell lymphomas reveal the molecular bases for disease heterogeneity.Semantic proximity Read ↗

CD158k and PD-1 expressions define heterogeneous subtypes of Sezary syndromeSemantic proximity Read ↗

Phenotypic plasticity of malignant T cells in blood and skin of a Sézary syndrome patient revealed by single cell transcriptomicsSemantic proximity Read ↗

Genome-Wide Analysis of Cutaneous T-Cell Lymphomas Identifies Three Clinically Relevant ClassesSemantic proximity Read ↗

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