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Article

Frequent deletions of FHIT and FRA3B in Barrett's metaplasia and esophageal adenocarcinomas

2 Oct 1997

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Share to Cancer-related gene regulation
Share to Gastrointestinal Tumor Research and Treatment
Share to Tracheal and airway disorders

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9349498
DOI: 10.1038/sj.onc.1201330

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Frequent deletions of FHIT and FRA3B in Barrett's metaplasia and esophageal adenocarcinomasPMID 9349498Read ↗

Deletion at fragile sites is a common and early event in Barrett's esophagus.Semantic proximity Read ↗

Do FHIT gene alterations play a role in human solid tumors?Semantic proximity Read ↗

Genome-wide catalogue of chromosomal aberrations in barrett's esophagus and esophageal adenocarcinoma: a high-density single nucleotide polymorphism array analysis.Semantic proximity Read ↗

Genetic and Epigenetic Alterations in Barrett’s Esophagus and Esophageal AdenocarcinomaSemantic proximity Read ↗

Common fragile genes and digestive tract cancers.Semantic proximity Read ↗

Fragile Genes That Are Frequently Altered in Cancer: Players Not Passengers.Semantic proximity Read ↗

Anomalous transcripts and allelic deletions of the FHIT gene in human esophageal cancer.Semantic proximity Read ↗

Complex structural rearrangements are present in high-grade dysplastic Barrett’s oesophagus samplesSemantic proximity Read ↗

Chromosomal Imbalances in Barrett's Adenocarcinoma and the Metaplasia-Dysplasia-Carcinoma SequenceSemantic proximity Read ↗

Inactivation of p16, RUNX3, and HPP1 occurs early in Barrett's-associated neoplastic progression and predicts progression riskSemantic proximity Read ↗

FHIT alterations in breast cancer.Semantic proximity Read ↗

Mapping of homozygous deletions in verified esophageal adenocarcinoma cell lines and xenografts.Semantic proximity Read ↗

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