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Article

A frequent polymorphism in exon 1 of the p16/CDKN2 gene.

Molecular and cellular probes - 1 Dec 1995

Fueyo J, Gomez-Manzano C, Yung W K, Zhang W, Lee P S, Majumder S, Perhouse M, Levin V A, Kyritsis A P

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 8808318
DOI: 10.1006/mcpr.1995.0070

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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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A frequent polymorphism in exon 1 of the p16/CDKN2 gene.PMID 8808318Read ↗

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

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Absence of the L37P polymorphism in exon 1 of the CDKN2A gene.Semantic proximity Read ↗

Compilation of somatic mutations of the CDKN2 gene in human cancers: non-random distribution of base substitutions.Semantic proximity Read ↗

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Informative MspI polymorphism adjacent to exon 3 of the p16INK4 (MTS1) gene.Semantic proximity Read ↗

A single nucleotide polymorphism in the 3'untranslated region of the CDKN2A gene is common in sporadic primary melanomas but mutations in the CDKN2B, CDKN2C, CDK4 and p53 genes are rare.Semantic proximity Read ↗

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Polymorphic study of XRCC1 G28152A and XRCC1 C26304T in 10 Chinese populations.Semantic proximity Read ↗

Analysis of the Frequency of 10 Polymorphic Markers of CDKN2A and RB1 Genes in Russian Populations.Semantic proximity Read ↗

Analysis of the p16 gene status of non-familial dysplastic nevus syndrome patients.Semantic proximity Read ↗

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