The Toxicity of the PrP106-126 Prion Peptide on Cultured Photoreceptors Correlates with the Prion Protein Distribution in the Mammalian and Human Retina

This publication has 39 references indexed in Scilit:

• Abnormal prion protein in the retina of the most commonly occurring subtype of sporadic Creutzfeldt-Jakob disease
  British Journal of Ophthalmology, 2005
• Differences in Scrapie-Induced Pathology of the Retina and Brain in Transgenic Mice that Express Hamster Prion Protein in Neurons, Astrocytes, or Multiple Cell Types
  The American Journal of Pathology, 2004
• Sublethal Concentrations of Prion Peptide PrP106–126 or the Amyloid Beta Peptide of Alzheimer's Disease Activates Expression of Proapoptotic Markers in Primary Cortical Neurons
  Neurobiology of Disease, 2001
• New Insight into Abnormal Prion Protein Using Monoclonal Antibodies
  Biochemical and Biophysical Research Communications, 1999
• Syrian hamster prion protein (PrPC) is expressed in photoreceptor cells of the adult retina
  Neuroscience Letters, 1997
• The rod bipolar cell of the mammalian retina
  Visual Neuroscience, 1991
• Early electroretinogram alterations in Creutzfeldt-Jakob disease after growth hormone treatment
  The Lancet, 1991
• Localization of two calcium binding proteins, calbindin (28 kD) and parvalbumin (12 kD), in the vertebrate retina
  Journal of Comparative Neurology, 1990
• THE CORRELATION OF ELECTRORETINOGRAPHIC AND HISTOPATHOLOGICAL FINDINGS IN THE EYES OF MICE INFECTED WITH THE 79A STRAIN OF SCRAPIE
  Neuropathology and Applied Neurobiology, 1989
• Biochemical characterization of the major peanut‐agglutinin‐binding glycoproteins in vertebrate retinae
  Journal of Comparative Neurology, 1986