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

FISH analysis of translocations involving the short arm of chromosome 9 in lymphoid malignancies.

Genes, chromosomes & cancer - 1 Aug 1997

Leblanc T, Derré J, Flexor M, Le Coniat M, Leroux D, Rimokh R, Larsen C J, Berger R

Abstract excerpt

Deletion of the short arm of chromosome 9 (9p), resulting in the loss of the p16INK4a/MTS1 gene, now called CDKN2, has been found to occur frequently in acute lymphoblastic leukemia, even in the absence of a microscopically visible deletion. In this study, we have used YAC probes encompassing the CDKN2 locus to analyze by fluorescence in situ hybridization patients with leukemia and lymphoma and translocations...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Alleles
Share to Blotting, Southern

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

Share to Carrier Proteins

Share to DNA, Neoplasm

Share to DNA Probes

Share to Karyotyping

Source

Identifiers

PMID: 9258663

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

FISH analysis of translocations involving the short arm of chromosome 9 in lymphoid malignancies.PMID 9258663Read ↗

Focal 9p instability in hematologic neoplasias revealed by comparative genomic hybridization and single-nucleotide polymorphism microarray analyses.Semantic proximity Read ↗

Characterization of chromosome 9 in human ovarian neoplasia identifies frequent genetic imbalance on 9q and rare alterations involving 9p, including CDKN2.Semantic proximity Read ↗

Targeted resequencing of 9p in acute lymphoblastic leukemia yields concordant results with array CGH and reveals novel genomic alterations.Semantic proximity Read ↗

Double jeopardy from a single translocation: deletions of the derivative chromosome 9 in chronic myeloid leukemiaSemantic proximity Read ↗

Two regions of deletion in 9p22- p24 in neuroblastoma are frequently observed in favorable tumors.Semantic proximity Read ↗

Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patientsSemantic proximity Read ↗

Allelic loss on chromosome 9q is associated with lymph node metastasis of primary breast cancer.Semantic proximity Read ↗

The gene for the cyclin-dependent-kinase-4 inhibitor, CDKN2A, is preferentially deleted in malignant mesotheliomaSemantic proximity Read ↗

Molecular and cytogenetic characterization of 9p– abnormalitiesSemantic proximity Read ↗

Frequent allele loss on 9p21-22 defines a smallest common region in the vicinity of the CDKN2 gene in sporadic breast cancer.Semantic proximity Read ↗

Homozygous deletions within human chromosome band 9p21 in melanoma.Semantic proximity Read ↗

Loss of heterozygosity at the 9p21-24 region and identification of BRM as a candidate tumor suppressor gene in head and neck squamous cell carcinoma.Semantic proximity Read ↗

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