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Items: 1 to 20 of 36

1.

The neurodegeneration sequence in prion diseases: evidence from functional, morphological and ultrastructural studies of the GABAergic system.

Bouzamondo-Bernstein E, Hopkins SD, Spilman P, Uyehara-Lock J, Deering C, Safar J, Prusiner SB, Ralston HJ 3rd, DeArmond SJ.

J Neuropathol Exp Neurol. 2004 Aug;63(8):882-99.

2.

Synaptic pathology in Alzheimer's disease: a review of ultrastructural studies.

Scheff SW, Price DA.

Neurobiol Aging. 2003 Dec;24(8):1029-46. Review.

PMID:
14643375
3.

Do disorders of movement cause movement disorders and dementia?

Goldstein LS.

Neuron. 2003 Oct 9;40(2):415-25. Review.

4.

Cell death, Bcl-2, Bax, and the cerebellum.

Vogel MW.

Cerebellum. 2002 Dec;1(4):277-87. Review.

PMID:
12879966
5.

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.

J Virol. 2003 Jul;77(13):7611-22.

6.

Synaptic changes characterize early behavioural signs in the ME7 model of murine prion disease.

Cunningham C, Deacon R, Wells H, Boche D, Waters S, Diniz CP, Scott H, Rawlins JN, Perry VH.

Eur J Neurosci. 2003 May;17(10):2147-55.

PMID:
12786981
7.

Mechanisms of cell death in neurodegenerative diseases: fashion, fiction, and facts.

Graeber MB, Moran LB.

Brain Pathol. 2002 Jul;12(3):385-90. Review. Erratum in: Brain Pathol. 2002 Oct; 12(4):522..

PMID:
12146806
8.

Naturally secreted oligomers of amyloid beta protein potently inhibit hippocampal long-term potentiation in vivo.

Walsh DM, Klyubin I, Fadeeva JV, Cullen WK, Anwyl R, Wolfe MS, Rowan MJ, Selkoe DJ.

Nature. 2002 Apr 4;416(6880):535-9.

PMID:
11932745
9.

BAX contributes to apoptotic-like death following neonatal hypoxia-ischemia: evidence for distinct apoptosis pathways.

Gibson ME, Han BH, Choi J, Knudson CM, Korsmeyer SJ, Parsadanian M, Holtzman DM.

Mol Med. 2001 Sep;7(9):644-55.

10.

Changes in cortical and striatal neurons predict behavioral and electrophysiological abnormalities in a transgenic murine model of Huntington's disease.

Laforet GA, Sapp E, Chase K, McIntyre C, Boyce FM, Campbell M, Cadigan BA, Warzecki L, Tagle DA, Reddy PH, Cepeda C, Calvert CR, Jokel ES, Klapstein GJ, Ariano MA, Levine MS, DiFiglia M, Aronin N.

J Neurosci. 2001 Dec 1;21(23):9112-23.

11.

Huntingtin aggregate-associated axonal degeneration is an early pathological event in Huntington's disease mice.

Li H, Li SH, Yu ZX, Shelbourne P, Li XJ.

J Neurosci. 2001 Nov 1;21(21):8473-81.

12.

Onset of accumulation of PrPres in murine ME7 scrapie in relation to pathological and PrP immunohistochemical changes.

Jeffrey M, Martin S, Barr J, Chong A, Fraser JR.

J Comp Pathol. 2001 Jan;124(1):20-8.

PMID:
11428185
13.

Prion diseases of humans and animals: their causes and molecular basis.

Collinge J.

Annu Rev Neurosci. 2001;24:519-50. Review.

PMID:
11283320
14.

Prion and prejudice: normal protein and the synapse.

Brown DR.

Trends Neurosci. 2001 Feb;24(2):85-90. Review.

PMID:
11164938
15.

Apoptosis in the nervous system.

Yuan J, Yankner BA.

Nature. 2000 Oct 12;407(6805):802-9. Review.

PMID:
11048732
16.
17.

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.

Proc Natl Acad Sci U S A. 2000 May 9;97(10):5574-9.

18.

Neurodegeneration in Lurcher mice occurs via multiple cell death pathways.

Doughty ML, De Jager PL, Korsmeyer SJ, Heintz N.

J Neurosci. 2000 May 15;20(10):3687-94.

19.

Synapse loss associated with abnormal PrP precedes neuronal degeneration in the scrapie-infected murine hippocampus.

Jeffrey M, Halliday WG, Bell J, Johnston AR, MacLeod NK, Ingham C, Sayers AR, Brown DA, Fraser JR.

Neuropathol Appl Neurobiol. 2000 Feb;26(1):41-54.

PMID:
10736066
20.
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