Colapietro P - Search Results

1

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.

2

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

3

Distribution and high frequency of novel alleles at NF1 polymorphic markers in the Italian population.

Natacci F, Colapietro P, Riva P, Corrado L, Rossi LN, Maninetti MM, Casciati MC, Zambrino Ca, Lanzi G, Larizza L. Natacci F, et al. Among authors: colapietro p. Mol Cell Probes. 1999 Dec;13(6):415-20. doi: 10.1006/mcpr.1999.0268. Mol Cell Probes. 1999. PMID: 10657145

4

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

5

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

6

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.

7

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.

8

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.

9

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

10

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients.

Bentivegna A, Milani D, Gervasini C, Castronovo P, Mottadelli F, Manzini S, Colapietro P, Giordano L, Atzeri F, Divizia MT, Uzielli ML, Neri G, Bedeschi MF, Faravelli F, Selicorni A, Larizza L. Bentivegna A, et al. Among authors: colapietro p. BMC Med Genet. 2006 Oct 19;7:77. doi: 10.1186/1471-2350-7-77. BMC Med Genet. 2006. PMID: 17052327 Free PMC article.

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