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

Molecular allelokaryotyping of early-stage, untreated chronic lymphocytic leukemia.

Cancer - 15 Mar 2008

Lehmann Sören, Ogawa Seishi, Raynaud Sophie D, Sanada Masashi, Nannya Yasuhito, Ticchioni Michel, Bastard Christian, Kawamata Norihiko, Koeffler H Phillip

Abstract excerpt

BACKGROUND: To the authors' knowledge, genetic abnormalities in early-stage chronic lymphocytic leukemia (CLL) have not been examined fully. Single nucleotide polymorphism (SNP) genomic array (SNP-chip) is a new tool that can detect copy number changes and uniparental disomy (UPD) over the entire genome with very high resolution. METHODS: The authors performed SNP-chip analysis on 56 samples from patients with...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosome Aberrations
Share to Chromosomes, Human, Pair 13

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Flow Cytometry

Share to Immunoglobulin Heavy Chains

Share to In Situ Hybridization, Fluorescence

Share to Karyotyping

Share to Leukemia, Lymphocytic, Chronic, B-Cell

Share to ZAP-70 Protein-Tyrosine Kinase

Source

Identifiers

PMID: 18246537
DOI: 10.1002/cncr.23270

Genes

ATM

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular allelokaryotyping of early-stage, untreated chronic lymphocytic leukemia.PMID 18246537Read ↗

Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays.Semantic proximity Read ↗

Allelotyping in B-cell chronic lymphocytic leukemia (B-CLL).Semantic proximity Read ↗

Molecular diagnostics in chronic lymphocytic leukemia – Pathogenetic and clinical implicationsSemantic proximity Read ↗

Molecular allelokaryotyping of T-cell prolymphocytic leukemia cells with high density single nucleotide polymorphism arrays identifies novel common genomic lesions and acquired uniparental disomy.Semantic proximity Read ↗

A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL).Semantic proximity Read ↗

Integrative genomics analyses reveal molecularly distinct subgroups of B-cell chronic lymphocytic leukemia patients with 13q14 deletion.Semantic proximity Read ↗

Monoallelic and biallelic deletions of 13q14 in a group of CLL/SLL patients investigated by CGH Haematological Cancer and SNP array (8x60K)Semantic proximity Read ↗

The prognostic significance of various 13q14 deletions in chronic lymphocytic leukemia.Semantic proximity Read ↗

Large genomic aberrations detected by SNP array are independent prognosticators of a shorter time to first treatment in chronic lymphocytic leukemia patients with normal FISH.Semantic proximity Read ↗

Integrative genomic analysis implicates gain of PIK3CA at 3q26 and MYC at 8q24 in chronic lymphocytic leukemia.Semantic proximity Read ↗

Genetic Abnormalities in Chronic Lymphocytic Leukemia: Where We Are and Where We GoSemantic proximity Read ↗

Exploring the genetic landscape in chronic lymphocytic leukemia using high-resolution technologiesSemantic proximity Read ↗

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