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2002 2
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2008 3
2009 3
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2012 3
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2014 4
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Page 1
CDKN1C mutations: two sides of the same coin.
Eggermann T, Binder G, Brioude F, Maher ER, Lapunzina P, Cubellis MV, Bergadá I, Prawitt D, Begemann M. Eggermann T, et al. Among authors: cubellis mv. Trends Mol Med. 2014 Nov;20(11):614-22. doi: 10.1016/j.molmed.2014.09.001. Epub 2014 Sep 25. Trends Mol Med. 2014. PMID: 25262539 Review.
(Epi)genotype-phenotype correlations in Beckwith-Wiedemann syndrome.
Mussa A, Russo S, De Crescenzo A, Freschi A, Calzari L, Maitz S, Macchiaiolo M, Molinatto C, Baldassarre G, Mariani M, Tarani L, Bedeschi MF, Milani D, Melis D, Bartuli A, Cubellis MV, Selicorni A, Cirillo Silengo M, Larizza L, Riccio A, Ferrero GB. Mussa A, et al. Among authors: cubellis mv. Eur J Hum Genet. 2016 Feb;24(2):183-90. doi: 10.1038/ejhg.2015.88. Epub 2015 Apr 22. Eur J Hum Genet. 2016. PMID: 25898929 Free PMC article.
Gain of function in CDKN1C.
Riccio A, Cubellis MV. Riccio A, et al. Among authors: cubellis mv. Nat Genet. 2012 Jun 27;44(7):737-8. doi: 10.1038/ng.2336. Nat Genet. 2012. PMID: 22735584 No abstract available.
Taming molecular flexibility to tackle rare diseases.
Cubellis MV, Baaden M, Andreotti G. Cubellis MV, et al. Biochimie. 2015 Jun;113:54-8. doi: 10.1016/j.biochi.2015.03.018. Epub 2015 Apr 2. Biochimie. 2015. PMID: 25841341 Free PMC article.
60 results