Piccardo P - Search Results

1

GFP-tagged prion protein is correctly localized and functionally active in the brains of transgenic mice.

Barmada S, Piccardo P, Yamaguchi K, Ghetti B, Harris DA. Barmada S, et al. Among authors: piccardo p. Neurobiol Dis. 2004 Aug;16(3):527-37. doi: 10.1016/j.nbd.2004.05.005. Neurobiol Dis. 2004. PMID: 15262264

2

A murine model of a familial prion disease.

Harris DA, Chiesa R, Drisaldi B, Quaglio E, Migheli A, Piccardo P, Ghetti B. Harris DA, et al. Among authors: piccardo p. Clin Lab Med. 2003 Mar;23(1):175-86. doi: 10.1016/s0272-2712(02)00069-0. Clin Lab Med. 2003. PMID: 12733431 Review.

3

Molecular distinction between pathogenic and infectious properties of the prion protein.

Chiesa R, Piccardo P, Quaglio E, Drisaldi B, Si-Hoe SL, Takao M, Ghetti B, Harris DA. Chiesa R, et al. Among authors: piccardo p. J Virol. 2003 Jul;77(13):7611-22. doi: 10.1128/jvi.77.13.7611-7622.2003. J Virol. 2003. PMID: 12805461 Free PMC article.

4

Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein.

Stewart RS, Piccardo P, Ghetti B, Harris DA. Stewart RS, et al. Among authors: piccardo p. J Neurosci. 2005 Mar 30;25(13):3469-77. doi: 10.1523/JNEUROSCI.0105-05.2005. J Neurosci. 2005. PMID: 15800202 Free PMC article.

5

Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice.

Li A, Piccardo P, Barmada SJ, Ghetti B, Harris DA. Li A, et al. Among authors: piccardo p. EMBO J. 2007 Jun 6;26(11):2777-85. doi: 10.1038/sj.emboj.7601726. Epub 2007 May 17. EMBO J. 2007. PMID: 17510630 Free PMC article.

6

A transgenic model of a familial prion disease.

Harris DA, Chiesa R, Drisaldi B, Quaglio E, Migheli A, Piccardo P, Ghetti B. Harris DA, et al. Among authors: piccardo p. Arch Virol Suppl. 2000;(16):103-12. doi: 10.1007/978-3-7091-6308-5_9. Arch Virol Suppl. 2000. PMID: 11214912 Review.

7

Primary myopathy and accumulation of PrPSc-like molecules in peripheral tissues of transgenic mice expressing a prion protein insertional mutation.

Chiesa R, Pestronk A, Schmidt RE, Tourtellotte WG, Ghetti B, Piccardo P, Harris DA. Chiesa R, et al. Among authors: piccardo p. Neurobiol Dis. 2001 Apr;8(2):279-88. doi: 10.1006/nbdi.2001.0400. Neurobiol Dis. 2001. PMID: 11300723

8

Neurological illness in transgenic mice expressing a prion protein with an insertional mutation.

Chiesa R, Piccardo P, Ghetti B, Harris DA. Chiesa R, et al. Among authors: piccardo p. Neuron. 1998 Dec;21(6):1339-51. doi: 10.1016/s0896-6273(00)80653-4. Neuron. 1998. PMID: 9883727 Free article.

9

Accumulation of protease-resistant prion protein (PrP) and apoptosis of cerebellar granule cells in transgenic mice expressing a PrP insertional mutation.

Chiesa R, Drisaldi B, Quaglio E, Migheli A, Piccardo P, Ghetti B, Harris DA. Chiesa R, et al. Among authors: piccardo p. Proc Natl Acad Sci U S A. 2000 May 9;97(10):5574-9. doi: 10.1073/pnas.97.10.5574. Proc Natl Acad Sci U S A. 2000. PMID: 10805813 Free PMC article.

10

Cellular and transgenic models of familial prion diseases.

Harris DA, Chiesa R, Migheli A, Piccardo P, Ghetti B. Harris DA, et al. Among authors: piccardo p. Methods Mol Med. 2001;59:149-61. doi: 10.1385/1-59259-134-5:149. Methods Mol Med. 2001. PMID: 21374503

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