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

High-resolution oligonucleotide array-CGH pinpoints genes involved in cryptic losses in chronic lymphocytic leukemia

1 Jan 2007

Abstract excerpt

Although recurrent chromosomal alterations occur in chronic lymphocytic leukemia (CLL), relatively few affected tumor suppressors and oncogenes have been implicated. To improve genetic characterization of CLL, we performed high-resolution gene copy number analysis of 20 CLL patients using oligonucleotide array comparative genomic hybridization (aCGH). The most recurrent losses were observed in 13q and 11q with...

Read the complete abstract on PubMed

Topics

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

Share to Chronic Lymphocytic Leukemia Research
Share to Genomic variations and chromosomal abnormalities
Share to Immunodeficiency and Autoimmune Disorders

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

Source

Identifiers

PMID: 17901694
DOI: 10.1159/000106435

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

High-resolution oligonucleotide array-CGH pinpoints genes involved in cryptic losses in chronic lymphocytic leukemiaPMID 17901694Read ↗

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

High-resolution genomic profiling of chronic lymphocytic leukemia reveals new recurrent genomic alterations.Semantic proximity Read ↗

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

Molecular basis of chronic lymphocytic leukemia diagnosis and prognosisSemantic proximity Read ↗

The biology and clinical significance of acquired genomic copy number aberrations and recurrent gene mutations in chronic lymphocytic leukemia.Semantic proximity Read ↗

Array CGH analysis of chronic lymphocytic leukemia reveals frequent cryptic monoallelic and biallelic deletions of chromosome 22q11 that include the PRAME gene.Semantic proximity Read ↗

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

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

Genomic arrays identify high-risk chronic lymphocytic leukemia with genomic complexity: a multi-center studySemantic proximity Read ↗

The Heterogeneity of 13q Deletions in Chronic Lymphocytic Leukemia: Diagnostic Challenges and Clinical ImplicationsSemantic proximity Read ↗

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

Chronic lymphocytic leukemia: molecular heterogeneity revealed by high-throughput genomicsSemantic proximity Read ↗

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