Harris DA - Search Results

1

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. Clin Lab Med. 2003 Mar;23(1):175-86. doi: 10.1016/s0272-2712(02)00069-0. Clin Lab Med. 2003. PMID: 12733431 Review.

2

A mutant prion protein displays an aberrant membrane association when expressed in cultured cells.

Lehmann S, Harris DA. Lehmann S, et al. Among authors: harris da. J Biol Chem. 1995 Oct 13;270(41):24589-97. doi: 10.1074/jbc.270.41.24589. J Biol Chem. 1995. PMID: 7592679 Free article.

3

Mutant and infectious prion proteins display common biochemical properties in cultured cells.

Lehmann S, Harris DA. Lehmann S, et al. Among authors: harris da. J Biol Chem. 1996 Jan 19;271(3):1633-7. doi: 10.1074/jbc.271.3.1633. J Biol Chem. 1996. PMID: 8576163 Free article.

4

Two mutant prion proteins expressed in cultured cells acquire biochemical properties reminiscent of the scrapie isoform.

Lehmann S, Harris DA. Lehmann S, et al. Among authors: harris da. Proc Natl Acad Sci U S A. 1996 May 28;93(11):5610-4. doi: 10.1073/pnas.93.11.5610. Proc Natl Acad Sci U S A. 1996. PMID: 8643624 Free PMC article.

5

Identification of intermediate steps in the conversion of a mutant prion protein to a scrapie-like form in cultured cells.

Daude N, Lehmann S, Harris DA. Daude N, et al. Among authors: harris da. J Biol Chem. 1997 Apr 25;272(17):11604-12. doi: 10.1074/jbc.272.17.11604. J Biol Chem. 1997. PMID: 9111077 Free article.

6

Evidence for a six-transmembrane domain structure of presenilin 1.

Lehmann S, Chiesa R, Harris DA. Lehmann S, et al. Among authors: harris da. J Biol Chem. 1997 May 2;272(18):12047-51. doi: 10.1074/jbc.272.18.12047. J Biol Chem. 1997. PMID: 9115271 Free article.

7

A wild-type prion protein does not acquire properties of the scrapie isoform when coexpressed with a mutant prion protein in cultured cells.

Lehmann S, Daude N, Harris DA. Lehmann S, et al. Among authors: harris da. Brain Res Mol Brain Res. 1997 Dec 1;52(1):139-45. doi: 10.1016/s0169-328x(97)00231-3. Brain Res Mol Brain Res. 1997. PMID: 9450686

8

Copper stimulates endocytosis of the prion protein.

Pauly PC, Harris DA. Pauly PC, et al. Among authors: harris da. J Biol Chem. 1998 Dec 11;273(50):33107-10. doi: 10.1074/jbc.273.50.33107. J Biol Chem. 1998. PMID: 9837873 Free article.

9

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: harris da. Neuron. 1998 Dec;21(6):1339-51. doi: 10.1016/s0896-6273(00)80653-4. Neuron. 1998. PMID: 9883727 Free article.

10

Prion proteins carrying pathogenic mutations are resistant to phospholipase cleavage of their glycolipid anchors.

Narwa R, Harris DA. Narwa R, et al. Among authors: harris da. Biochemistry. 1999 Jul 6;38(27):8770-7. doi: 10.1021/bi990736c. Biochemistry. 1999. PMID: 10393552

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