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

Detection of chromosomal aberrations in prostate cancer by fluorescence in situ hybridization (FISH).

European urology - 1 Dec 2003

Celep Figen, Karagüzel Ahmet, Ozgür Güner K, Yildiz Kadriye

Abstract excerpt

PURPOSE: Fluorescence in situ hybridization (FISH) is a powerful tool for quantitative analysis of chromosomes and genes and can be applied in a variety of specimens, including cell cultures, isolated nuclei from fresh and fixed tissues, and histological tissue sections. For detection of numerical chromosome aberrations, we examined prostatic cancer samples at our department. In addition, we also observed primary...

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
Share to Cohort Studies

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

Share to Culture Techniques

Share to In Situ Hybridization, Fluorescence

Share to Prostatic Neoplasms

Share to Risk Assessment

Share to Sensitivity and Specificity

Source

Identifiers

PMID: 14644118
DOI: 10.1016/s0302-2838(03)00414-7

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

Detection of chromosomal aberrations in prostate cancer by fluorescence in situ hybridization (FISH).PMID 14644118Read ↗

Chromosomal aberrations in prostate cancerSemantic proximity Read ↗

Molecular cytogenetics of prostate cancerSemantic proximity Read ↗

Fluorescence in situ hybridization evaluation of c-myc and androgen receptor gene amplification and chromosomal anomalies in prostate cancer in Japanese patientsSemantic proximity Read ↗

Comparative genomic hybridization reveals DNA copy number gains to frequently occur in human prostate cancer.Semantic proximity Read ↗

Spectral karyotype (SKY) analysis of human prostate carcinoma cell linesSemantic proximity Read ↗

Review of allelic loss and gain in prostate cancer.Semantic proximity Read ↗

Fluorescence in situ hybridization in surgical pathology: principles and applicationsSemantic proximity Read ↗

Chromosomal changes during development and progression of prostate adenocarcinomasSemantic proximity Read ↗

Simultaneously detection of genomic and expression alterations in prostate cancer using cDNA microarray.Semantic proximity Read ↗

Comparative genomic hybridization, allelic imbalance, and fluorescence in situ hybridization on chromosome 8 in prostate cancer.Semantic proximity Read ↗

Chromosomal aberrations in benign prostatic hyperplasia patients.Semantic proximity Read ↗

Differential chromosome allelic imbalance in the progression of human prostate cancer.Semantic proximity Read ↗

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