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Article

Rates of p16 ( MTS1 ) Mutations in Primary Tumors with 9p Loss

15 Jul 1994

Abstract excerpt

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Identifiers

PMID: 8023167
DOI: 10.1126/science.8023167

Provenance

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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

Rates of p16 ( MTS1 ) Mutations in Primary Tumors with 9p LossPMID 8023167Read ↗

Frequent somatic mutations and homozygous deletions of the p16 (MTS1) gene in pancreatic adenocarcinoma.Semantic proximity Read ↗

Frequent codeletion of p16/MTS1 and p15/MTS2 and genetic alterations in p16/MTS1 in pancreatic tumors.Semantic proximity Read ↗

Genomic changes of chromosomes 8p23.1 and 1q21: Novel mutations in malignant mesotheliomaSemantic proximity Read ↗

p16(MTS-1/CDKN2/INK4a) in Cancer ProgressionSemantic proximity Read ↗

Frequent Loss of 9p21 (p16INK4A) and Other Genomic Imbalances in Human Malignant Fibrous HistiocytomaSemantic proximity Read ↗

Codeletion of the genes for p16INK4, methylthioadenosine phosphorylase, interferon-α1, interferon-β1, and other 9p21 markers in human malignant cell linesSemantic proximity Read ↗

5' CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers.Semantic proximity Read ↗

Frequency of homozygous deletion at p16/CDKN2 in primary human tumoursSemantic proximity Read ↗

Infrequent methylation of CDKN2A(MTS1/p16) and rare mutation of both CDKN2A and CDKN2B(MTS2/p15) in primary astrocytic tumoursSemantic proximity Read ↗

Loss of heterozygosity at 9p21 loci and mutations of the MTS1 and MTS2 genes in human lung cancers.Semantic proximity Read ↗

Infrequent CDKN2 (MTS1/p16) gene alterations in human primary breast cancer.Semantic proximity Read ↗

p16 alterations and deletion mapping of 9p21-p22 in malignant mesothelioma.Semantic proximity Read ↗

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