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Human Mutation|March 5, 2009
Functional, structural, and genetic evaluation of 20 CDKN2A germ line mutations identified in melanoma-prone families or patientsCaroline Kannengiesser, Sharon Brookes, Anna Gutierrez del Arroyo, et al.
The EMBO Journal|March 5, 2013
Interplay between Homeobox proteins and Polycomb repressive complexes in p16INK⁴a regulationNadine Martin, Nikolay Popov, Francesca Aguilo, et al.
Molecular Cell|December 13, 2005
Involvement of MINK, a Ste20 family kinase, in Ras oncogene-induced growth arrest in human ovarian surface epithelial cellsBarbara Nicke, Julie Bastien, Sophia J Khanna, et al.
European Journal of Human Genetics : EJHG|April 18, 2003
A single Mediterranean, possibly Jewish, origin for the Val59Gly CDKN2A mutation in four melanoma-prone familiesEmanuel Yakobson, Shlomit Eisenberg, Ruth Isacson, et al.
Cell Stem Cell|January 10, 2012
MicroRNA regulation of Cbx7 mediates a switch of Polycomb orthologs during ESC differentiationAna O'Loghlen, Ana M Muñoz-Cabello, Alexandre Gaspar-Maia, et al.
The Journal of Clinical Endocrinology and Metabolism|April 3, 2008
The role of the aryl hydrocarbon receptor-interacting protein gene in familial and sporadic pituitary adenomasChrysanthia A Leontiou, Maria Gueorguiev, Jacqueline van der Spuy, et al.
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