Penco S - Search Results

1

Molecular analysis of PDGFRA and PDGFRB genes by rapid single-strand conformation polymorphism (SSCP) in patients with core-binding factor leukaemias with KIT or FLT3 mutation.

Trojani A, Ripamonti CB, Penco S, Beghini A, Nadali G, Di Bona E, Viola A, Castagnola C, Colapietro P, Grillo G, Pezzetti L, Ravelli E, Patrosso MC, Marocchi A, Cuneo A, Ferrara F, Lazzarino M, Pizzolo G, Cairoli R, Morra E. Trojani A, et al. Among authors: penco s. Anticancer Res. 2008 Sep-Oct;28(5A):2745-51. Anticancer Res. 2008. PMID: 19035305 Free article.

2

New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.

Penco S, Buscema M, Patrosso MC, Marocchi A, Grossi E. Penco S, et al. BMC Bioinformatics. 2008 May 30;9:254. doi: 10.1186/1471-2105-9-254. BMC Bioinformatics. 2008. PMID: 18513389 Free PMC article.

3

Gene symbol: TYR. Disease: Albinism, oculocutaneous 1.

Patrosso MC, Lando G, Penco S. Patrosso MC, et al. Among authors: penco s. Hum Genet. 2008 Oct;124(3):294. Hum Genet. 2008. PMID: 18846608 No abstract available.

4

Genetic variations within KRIT1/CCM1, MGC4607/CCM2 and PDCD10/CCM3 in a large Italian family harbouring a Krit1/CCM1 mutation.

Pileggi S, Buscone S, Ricci C, Patrosso MC, Marocchi A, Brunori P, Battistini S, Penco S. Pileggi S, et al. Among authors: penco s. J Mol Neurosci. 2010 Oct;42(2):235-42. doi: 10.1007/s12031-010-9360-y. Epub 2010 Apr 24. J Mol Neurosci. 2010. PMID: 20419355

5

Molecular screening test in familial forms of cerebral cavernous malformation: the impact of the Multiplex Ligation-dependent Probe Amplification approach.

Penco S, Ratti R, Bianchi E, Citterio A, Patrosso MC, Marocchi A, Tassi L, La Camera A, Collice M. Penco S, et al. J Neurosurg. 2009 May;110(5):929-34. doi: 10.3171/2008.8.17640. J Neurosurg. 2009. PMID: 19199464

6

Phenotypic heterogeneity in a SOD1 G93D Italian ALS family: an example of human model to study a complex disease.

Penco S, Lunetta C, Mosca L, Maestri E, Avemaria F, Tarlarini C, Patrosso MC, Marocchi A, Corbo M. Penco S, et al. J Mol Neurosci. 2011 May;44(1):25-30. doi: 10.1007/s12031-010-9480-4. Epub 2010 Dec 1. J Mol Neurosci. 2011. PMID: 21120636

7

Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study.

Lando G, Mosca A, Bonora R, Azzario F, Penco S, Marocchi A, Panteghini M, Patrosso MC. Lando G, et al. Among authors: penco s. Pharmacogenetics. 2003 May;13(5):265-70. doi: 10.1097/00008571-200305000-00005. Pharmacogenetics. 2003. PMID: 12724618

8

Glutamate-cysteine ligase polymorphism, hypertension, and male sex are associated with cardiovascular events. Biochemical and genetic characterization of Italian subpopulation.

Campolo J, Penco S, Bianchi E, Colombo L, Parolini M, Caruso R, Sedda V, Patrosso MC, Cighetti G, Marocchi A, Parodi O. Campolo J, et al. Among authors: penco s. Am Heart J. 2007 Dec;154(6):1123-9. doi: 10.1016/j.ahj.2007.07.029. Epub 2007 Sep 6. Am Heart J. 2007. PMID: 18035085

9

SLC45A2 mutation frequency in Oculocutaneous Albinism Italian patients doesn't differ from other European studies.

Mauri L, Barone L, Al Oum M, Del Longo A, Piozzi E, Manfredini E, Stanzial F, Benedicenti F, Penco S, Patrosso MC. Mauri L, et al. Among authors: penco s. Gene. 2014 Jan 1;533(1):398-402. doi: 10.1016/j.gene.2013.09.053. Epub 2013 Oct 3. Gene. 2014. PMID: 24096233

10

Paraoxonase 1 L55M, Q192R and paraoxonase 2 S311C alleles in atherothrombosis.

Cozzi L, Campolo J, Parolini M, De Maria R, Patrosso MC, Marocchi A, Parodi O, Penco S. Cozzi L, et al. Among authors: penco s. Mol Cell Biochem. 2013 Feb;374(1-2):233-8. doi: 10.1007/s11010-012-1525-2. Epub 2012 Dec 6. Mol Cell Biochem. 2013. PMID: 23225229

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