Prion protein accumulation and neuroprotection in hypoxic brain damage.
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J. Bell | A. McNeill | J. Ironside | M. Head | A. Fotheringham | I. Davies | N. McLennan | Paul M. Brennan | D. Ritchie | Alun Williams | F. Brannan | K. Rennison | N. Mclennan | J. Bell
[1] David R. Brown,et al. Lack of prion protein expression results in a neuronal phenotype sensitive to stress , 2002, Journal of neuroscience research.
[2] S. Haswell,et al. Metal imbalance and compromised antioxidant function are early changes in prion disease. , 2002, The Biochemical journal.
[3] J. Bell,et al. In situ hybridization analysis of PrP mRNA in human CNS tissues , 2001, Neuropathology and applied neurobiology.
[4] I. Izquierdo,et al. Imbalance of antioxidant defense in mice lacking cellular prion protein. , 2001, Free radical biology & medicine.
[5] H. Budka,et al. Marked increase of neuronal prion protein immunoreactivity in Alzheimer's disease and human prion diseases , 2001, Acta Neuropathologica.
[6] E. Mackenzie,et al. The ischaemic penumbra , 2001, Current opinion in neurology.
[7] Mark A. Smith,et al. Increased levels of oxidative stress markers detected in the brains of mice devoid of prion protein , 2001, Journal of neurochemistry.
[8] A. Giese,et al. Prion-induced neuronal damage--the mechanisms of neuronal destruction in the subacute spongiform encephalopathies. , 2001, Current topics in microbiology and immunology.
[9] A. Favier,et al. Prion infection impairs the cellular response to oxidative stress. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[10] R. Ce. Nonpathogenic prion protein (PrPc) acts as a cell-surface signal transducer. , 2000 .
[11] C. Davies,et al. Oedema and glial cell involvement in the aged mouse brain after permanent focal ischaemia , 2000, Neuropathology and applied neurobiology.
[12] M. Sy,et al. Prion disease: A loss of antioxidant function? , 2000, Biochemical and biophysical research communications.
[13] H. Budka,et al. Evidence for Oxidative Stress in Experimental Prion Disease , 2000, Neurobiology of Disease.
[14] Subrata Ghosh,et al. Cellular prion protein is expressed in the human enteric nervous system , 2000, Nature Medicine.
[15] M. Smith,et al. Oxidative stress in Alzheimer's disease. , 2000, Biochimica et biophysica acta.
[16] K. Brown,et al. Detection of PrP in extraneural tissues , 2000, Microscopy research and technique.
[17] M. Esiri,et al. Prion protein immunoreactivity in brain samples from an unselected autopsy population: findings in 200 consecutive cases , 2000, Neuropathology and applied neurobiology.
[18] M. Kao,et al. Heat shock modulates prion protein expression in human NT‐2 cells , 2000, Neuroreport.
[19] C. Reilly. Nonpathogenic prion protein (PrPc) acts as a cell-surface signal transducer. , 2000, Journal of neurology.
[20] M. Papadopoulos,et al. An introduction to the changes in gene expression that occur after cerebral ischaemia. , 2000, British journal of neurosurgery.
[21] J. Hescheler,et al. Redox-regulation of intrinsic prion expression in multicellular prostate tumor spheroids. , 1999, Free radical biology & medicine.
[22] K. Beyreuther,et al. Prion protein-deficient neurons reveal lower glutathione reductase activity and increased susceptibility to hydrogen peroxide toxicity. , 1999, The American journal of pathology.
[23] P. Schürmann,et al. Evidence of Presynaptic Location and Function of the Prion Protein , 1999, The Journal of Neuroscience.
[24] S. Whatley,et al. Circadian regulation of prion protein messenger RNA in the rat forebrain: a widespread and synchronous rhythm , 1999, Neuroscience.
[25] S. Love. Oxidative Stress in Brain Ischemia , 1999, Brain pathology.
[26] Stanley B. Prusiner,et al. Nobel Lecture: Prions , 1998 .
[27] E. Tschachler,et al. Human keratinocytes express cellular prion-related protein in vitro and during inflammatory skin diseases. , 1998, The American journal of pathology.
[28] Mehmet,et al. Expression of amyloid precursor protein (β‐APP) in the neonatal brain following hypoxic ischaemic injury , 1998, Neuropathology and applied neurobiology.
[29] B. Faucheux,et al. Cellular prion protein localization in rodent and primate brain , 1998, The European journal of neuroscience.
[30] H. Kretzschmar,et al. Effects of Copper on Survival of Prion Protein Knockout Neurons and Glia , 1998, Journal of neurochemistry.
[31] J. Satoh,et al. Constitutive and Cytokine‐inducible Expression of Prion Protein Gene in Human Neural Cell Lines , 1998, Journal of neuropathology and experimental neurology.
[32] D. Westaway,et al. The cellular prion protein binds copper in vivo , 1997, Nature.
[33] H. Kretzschmar,et al. Effects of oxidative stress on prion protein expression in pc12 cells , 1997, International Journal of Developmental Neuroscience.
[34] P. Achermann,et al. Altered circadian activity rhythms and sleep in mice devoid of prion protein , 1996, Nature.
[35] M. Beal,et al. Aging, energy, and oxidative stress in neurodegenerative diseases , 1995, Annals of neurology.
[36] G. Majno,et al. Apoptosis, oncosis, and necrosis. An overview of cell death. , 1995, The American journal of pathology.
[37] M. Palmer,et al. Prion protein is necessary for normal synaptic function , 1994, Nature.
[38] D. Stephenson,et al. Amyloid precursor protein accumulates in regions of neurodegeneration following focal cerebral ischemia in the rat , 1992, Brain Research.
[39] M. Kaufman,et al. The priori protein gene: a role in mouse embryogenesis? , 2005 .
[40] S. Prusiner,et al. Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein , 1992, Nature.
[41] N. Cashman,et al. Nearly ubiquitous tissue distribution of the scrapie agent precursor protein , 1992, Neurology.
[42] Neil R. Cashman,et al. Cellular isoform of the scrapie agent protein participates in lymphocyte activation , 1990, Cell.
[43] P. McBride,et al. Precise targeting of the pathology of the sialoglycoprotein, PrP, and vacuolar degeneration in mouse scrapie , 1989, Neuroscience Letters.