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Page 1
The spindle checkpoint requires cyclin-dependent kinase activity.
Genes Dev. 2003 Oct 15;17(20):2520-5. doi: 10.1101/gad.267603.
Genes Dev. 2003.
PMID: 14561775
Free PMC article.
A case of premature ovarian failure in a 33-year-old woman.
Colao E, Granata T, Vismara MF, Bombardiere F, Nocera D, Luciano E, Perrotti N, Malatesta P.
Colao E, et al. Among authors: nocera d.
Case Rep Genet. 2013;2013:573841. doi: 10.1155/2013/573841. Epub 2013 Jan 29.
Case Rep Genet. 2013.
PMID: 23509644
Free PMC article.
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Non-Invasive Prenatal Test Analysis Opens a Pandora's Box: Identification of Very Rare Cases of SRY-Positive Healthy Females, Segregating for Three Generations Thanks to Preferential Inactivation of the XqYp Translocated Chromosome.
Politi C, Grillone K, Nocera D, Colao E, Bellisario ML, Loddo S, Catino G, Novelli A, Perrotti N, Rodolfo I, Malatesta P.
Politi C, et al. Among authors: nocera d.
Genes (Basel). 2024 Jan 16;15(1):103. doi: 10.3390/genes15010103.
Genes (Basel). 2024.
PMID: 38254992
Free PMC article.
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Functional characterization of p.Pro409His variant in HNF1A, a hypomorphic mutation involved in pancreatic β-cell dysfunction.
Nocera D, Menniti M, Belviso S, Bond HM, Lanzillotta D, Spoleti CB, Guagliardi MR, Malatesta P, Trapasso F, Irace C, Perrotti N, Iuliano R.
Nocera D, et al.
Acta Diabetol. 2019 Aug;56(8):883-888. doi: 10.1007/s00592-019-01298-6. Epub 2019 Apr 9.
Acta Diabetol. 2019.
PMID: 30963309
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Identification of a new mutation in the gene coding for hairless protein responsible for alopecia universalis: The importance of direct gene sequencing.
Nucara S, Colao E, Mangone G, Baudi F, Fabiani F, Nocera D, Passafaro G, Longo T, Laria AE, Malatesta P, Amato R, Trapasso F, Perrotti N.
Nucara S, et al. Among authors: nocera d.
Dermatol Online J. 2011 Jan 15;17(1):3.
Dermatol Online J. 2011.
PMID: 21272494
Free article.
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