Colapietro P - Search Results

1

Smith-Magenis syndrome and growth hormone deficiency.

Spadoni E, Colapietro P, Bozzola M, Marseglia GL, Repossi L, Danesino C, Larizza L, Maraschio P. Spadoni E, et al. Among authors: colapietro p. Eur J Pediatr. 2004 Jul;163(7):353-8. doi: 10.1007/s00431-004-1460-7. Epub 2004 May 8. Eur J Pediatr. 2004. PMID: 15138811 Free article.

2

Evidence for non-homologous end joining and non-allelic homologous recombination in atypical NF1 microdeletions.

Venturin M, Gervasini C, Orzan F, Bentivegna A, Corrado L, Colapietro P, Friso A, Tenconi R, Upadhyaya M, Larizza L, Riva P. Venturin M, et al. Among authors: colapietro p. Hum Genet. 2004 Jun;115(1):69-80. doi: 10.1007/s00439-004-1101-2. Epub 2004 Apr 21. Hum Genet. 2004. PMID: 15103551

3

From Whole Gene Deletion to Point Mutations of EP300-Positive Rubinstein-Taybi Patients: New Insights into the Mutational Spectrum and Peculiar Clinical Hallmarks.

Negri G, Magini P, Milani D, Colapietro P, Rusconi D, Scarano E, Bonati MT, Priolo M, Crippa M, Mazzanti L, Wischmeijer A, Tamburrino F, Pippucci T, Finelli P, Larizza L, Gervasini C. Negri G, et al. Among authors: colapietro p. Hum Mutat. 2016 Feb;37(2):175-83. doi: 10.1002/humu.22922. Epub 2015 Nov 4. Hum Mutat. 2016. PMID: 26486927

4

Differential cytogenomics and miRNA signature of the Acute Myeloid Leukaemia Kasumi-1 cell line CD34+38- compartment.

Pedranzini L, Mottadelli F, Ronzoni S, Rossella F, Ferracin M, Magnani I, Roversi G, Colapietro P, Negrini M, Pelicci PG, Larizza L. Pedranzini L, et al. Among authors: colapietro p. Leuk Res. 2010 Oct;34(10):1287-95. doi: 10.1016/j.leukres.2010.02.012. Epub 2010 Mar 12. Leuk Res. 2010. PMID: 20227111

5

Mapping of human WHN gene in a 17q11.2 YAC contig and identification of an intragenic STR.

Corrado L, Colapietro P, Larizza L, Riva P. Corrado L, et al. Among authors: colapietro p. Mol Cell Probes. 1999 Jun;13(3):199-202. doi: 10.1006/mcpr.1999.0237. Mol Cell Probes. 1999. PMID: 10369745

6

SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome.

Gervasini C, Grati FR, Lalatta F, Tabano S, Gentilin B, Colapietro P, De Toffol S, Frontino G, Motta F, Maitz S, Bernardini L, Dallapiccola B, Fedele L, Larizza L, Miozzo M. Gervasini C, et al. Among authors: colapietro p. Genet Med. 2010 Oct;12(10):634-40. doi: 10.1097/GIM.0b013e3181ed6185. Genet Med. 2010. PMID: 20847698 Free article.

7

STI 571 inhibition effect on KITAsn822Lys-mediated signal transduction cascade.

Beghini A, Bellini M, Magnani I, Colapietro P, Cairoli R, Morra E, Larizza L. Beghini A, et al. Among authors: colapietro p. Exp Hematol. 2005 Jun;33(6):682-8. doi: 10.1016/j.exphem.2005.03.007. Exp Hematol. 2005. PMID: 15911092 Free article.

8

NF1 exon 7 skipping and sequence alterations in exonic splice enhancers (ESEs) in a neurofibromatosis 1 patient.

Colapietro P, Gervasini C, Natacci F, Rossi L, Riva P, Larizza L. Colapietro P, et al. Hum Genet. 2003 Nov;113(6):551-4. doi: 10.1007/s00439-003-1009-2. Epub 2003 Sep 6. Hum Genet. 2003. PMID: 13680360

9

KIT activating mutations: incidence in adult and pediatric acute myeloid leukemia, and identification of an internal tandem duplication.

Beghini A, Ripamonti CB, Cairoli R, Cazzaniga G, Colapietro P, Elice F, Nadali G, Grillo G, Haas OA, Biondi A, Morra E, Larizza L. Beghini A, et al. Among authors: colapietro p. Haematologica. 2004 Aug;89(8):920-5. Haematologica. 2004. PMID: 15339674 Free article.

10

Distinct expression pattern of microtubule-associated protein/microtubule affinity-regulating kinase 4 in differentiated neurons.

Moroni RF, De Biasi S, Colapietro P, Larizza L, Beghini A. Moroni RF, et al. Among authors: colapietro p. Neuroscience. 2006 Nov 17;143(1):83-94. doi: 10.1016/j.neuroscience.2006.07.052. Epub 2006 Sep 14. Neuroscience. 2006. PMID: 16973293

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