Functional analysis of CDKN2A/p16INK4a 5′-UTR variants predisposing to melanoma

Functional, structural, and genetic evaluation of 20CDKN2Agerm line mutations identified in melanoma-prone families or patients

(2009) Caroline Kannengiesser et al.   HUMAN MUTATION

Clinical genetic testing for familial melanoma in Italy: A cooperative study

(2009) William Bruno et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY

CDKN2A and MC1R analysis in amelanotic and pigmented melanoma

(2009) Paola Ghiorzo et al.   MELANOMA RESEARCH

Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans

(2009) S. E. Calvo et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma

(2008) F Lesueur et al.   BRITISH JOURNAL OF CANCER

Genetics of melanoma predisposition

(2008) J. Lin et al.   BRITISH JOURNAL OF DERMATOLOGY

A Translational Profiling Approach for the Molecular Characterization of CNS Cell Types

(2008) Myriam Heiman et al.   CELL

Genomic rearrangements of the CDKN2A locus are infrequent in Italian malignant melanoma families without evidence of CDKN2A/CDK4 point mutations

(2008) Marina Vignoli et al.   MELANOMA RESEARCH

CDKN2A mutations and MC1R variants in Italian patients with single or multiple primary melanoma

(2008) L. Pastorino et al.   Pigment Cell & Melanoma Research

The Polycomb Protein and E3 Ubiquitin Ligase Ring1B Harbors an IRES in its Highly Conserved 5′ UTR

(2008) Erwin Boutsma et al.   PLoS One