D’Arcangelo G, Miao GG, Chen SC, Soares HD, Morgan JI, Curran T (1995) A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 374(6524):719–723. doi:10.1038/374719a0
Article
PubMed
Google Scholar
Soriano E, Del Rio JA (2005) The cells of cajal-retzius: still a mystery one century after. Neuron 46(3):389–394. doi:10.1016/j.neuron.2005.04.019
CAS
Article
PubMed
Google Scholar
Groc L, Choquet D, Stephenson FA, Verrier D, Manzoni OJ, Chavis P (2007) NMDA receptor surface trafficking and synaptic subunit composition are developmentally regulated by the extracellular matrix protein reelin. J Neurosci 27(38):10165–10175. doi:10.1523/JNEUROSCI.1772-07.2007
CAS
Article
PubMed
Google Scholar
Rogers JT, Weeber EJ (2008) Reelin and apoE actions on signal transduction, synaptic function and memory formation. Neuron Glia Biol 4(3):259–270. doi:10.1017/S1740925X09990184
Article
PubMed
Google Scholar
Ohkubo N, Vitek MP, Morishima A, Suzuki Y, Miki T, Maeda N, Mitsuda N (2007) Reelin signals survival through Src-family kinases that inactivate BAD activity. J Neurochem 103(2):820–830. doi:10.1111/j.1471-4159.2007.04804.x
CAS
Article
PubMed
Google Scholar
Frotscher M (2010) Role for reelin in stabilizing cortical architecture. Trends Neurosci 33(9):407–414. doi:10.1016/j.tins.2010.06.001
CAS
Article
PubMed
Google Scholar
Pujadas L, Gruart A, Bosch C, Delgado L, Teixeira CM, Rossi D, de Lecea L, Martinez A et al (2010) Reelin regulates postnatal neurogenesis and enhances spine hypertrophy and long-term potentiation. J Neurosci 30(13):4636–4649. doi:10.1523/JNEUROSCI.5284-09.2010
CAS
Article
PubMed
Google Scholar
Beffert U, Weeber EJ, Morfini G, Ko J, Brady ST, Tsai LH, Sweatt JD, Herz J (2004) Reelin and cyclin-dependent kinase 5-dependent signals cooperate in regulating neuronal migration and synaptic transmission. J Neurosci 24(8):1897–1906. doi:10.1523/JNEUROSCI.4084-03.2004
CAS
Article
PubMed
Google Scholar
Stary CM, Xu L, Sun X, Ouyang YB, White RE, Leong J, Li J, Xiong X et al (2015) MicroRNA-200c contributes to injury from transient focal cerebral ischemia by targeting reelin. Stroke 46(2):551–556. doi:10.1161/STROKEAHA.114.007041
CAS
Article
PubMed
PubMed Central
Google Scholar
Won SJ, Kim SH, Xie L, Wang Y, Mao XO, Jin K, Greenberg DA (2006) Reelin-deficient mice show impaired neurogenesis and increased stroke size. Exp Neurol 198(1):250–259. doi:10.1016/j.expneurol.2005.12.008
CAS
Article
PubMed
Google Scholar
Cuchillo-Ibanez I, Balmaceda V, Botella-Lopez A, Rabano A, Avila J, Saez-Valero J (2013) Beta-amyloid impairs reelin signaling. PLoS One 8(8):e72297. doi:10.1371/journal.pone.0072297
CAS
Article
PubMed
PubMed Central
Google Scholar
Pujadas L, Rossi D, Andres R, Teixeira CM, Serra-Vidal B, Parcerisas A, Maldonado R, Giralt E et al (2014) Reelin delays amyloid-beta fibril formation and rescues cognitive deficits in a model of Alzheimer’s disease. Nat Commun 5:3443. doi:10.1038/ncomms4443
Article
PubMed
Google Scholar
Durakoglugil MS, Chen Y, White CL, Kavalali ET, Herz J (2009) Reelin signaling antagonizes beta-amyloid at the synapse. Proc Natl Acad Sci U S A 106(37):15938–15943. doi:10.1073/pnas.0908176106
CAS
Article
PubMed
PubMed Central
Google Scholar
Hiesberger T, Trommsdorff M, Howell BW, Goffinet A, Mumby MC, Cooper JA, Herz J (1999) Direct binding of reelin to VLDL receptor and ApoE receptor 2 induces tyrosine phosphorylation of disabled-1 and modulates tau phosphorylation. Neuron 24(2):481–489
CAS
Article
PubMed
Google Scholar
Trommsdorff M, Gotthardt M, Hiesberger T, Shelton J, Stockinger W, Nimpf J, Hammer RE, Richardson JA et al (1999) Reeler/disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2. Cell 97(6):689–701
CAS
Article
PubMed
Google Scholar
Bock HH, Herz J (2003) Reelin activates SRC family tyrosine kinases in neurons. Curr Biol 13(1):18–26
CAS
Article
PubMed
Google Scholar
Herz J, Chen Y (2006) Reelin, lipoprotein receptors and synaptic plasticity. Nat Rev Neurosci 7(11):850–859
CAS
Article
PubMed
Google Scholar
Beffert U, Morfini G, Bock HH, Reyna H, Brady ST, Herz J (2002) Reelin-mediated signaling locally regulates protein kinase B/Akt and glycogen synthase kinase 3beta. J Biol Chem 277(51):49958–49964. doi:10.1074/jbc.M209205200
CAS
Article
PubMed
Google Scholar
Park TJ, Curran T (2008) Crk and Crk-like play essential overlapping roles downstream of disabled-1 in the reelin pathway. J Neurosci 28(50):13551–13562. doi:10.1523/JNEUROSCI.4323-08.2008
CAS
Article
PubMed
PubMed Central
Google Scholar
Ma Y, Wu X, Li X, Fu J, Shen J, Li X, Wang H (2012) Corticosterone regulates the expression of neuropeptide Y and reelin in MLO-Y4 cells. Mol Cells 33(6):611–616. doi:10.1007/s10059-012-0053-y
CAS
Article
PubMed
PubMed Central
Google Scholar
Alvarez-Dolado M, Ruiz M, Del Rio JA, Alcantara S, Burgaya F, Sheldon M, Nakajima K, Bernal J et al (1999) Thyroid hormone regulates reelin and dab1 expression during brain development. J Neurosci 19(16):6979–6993
CAS
PubMed
Google Scholar
Lussier AL, Caruncho HJ, Kalynchuk LE (2009) Repeated exposure to corticosterone, but not restraint, decreases the number of reelin-positive cells in the adult rat hippocampus. Neurosci Lett 460(2):170–174. doi:10.1016/j.neulet.2009.05.050
CAS
Article
PubMed
Google Scholar
Buret L, van den Buuse M (2014) Corticosterone treatment during adolescence induces down-regulation of reelin and NMDA receptor subunit GLUN2C expression only in male mice: implications for schizophrenia. Int J Neuropsychopharmacol 17(8):1221–1232. doi:10.1017/S1461145714000121
CAS
Article
PubMed
Google Scholar
Miettinen R, Riedel A, Kalesnykas G, Kettunen HP, Puolivali J, Soininen H, Arendt T (2005) Reelin-immunoreactivity in the hippocampal formation of 9-month-old wildtype mouse: effects of APP/PS1 genotype and ovariectomy. J Chem Neuroanat 30(2–3):105–118. doi:10.1016/j.jchemneu.2005.06.003
CAS
Article
PubMed
Google Scholar
Rideau Batista Novais A, Guiramand J, Cohen-Solal C, Crouzin N, de Jesus Ferreira MC, Vignes M, Barbanel G, Cambonie G (2013) N-acetyl-cysteine prevents pyramidal cell disarray and reelin-immunoreactive neuron deficiency in CA3 after prenatal immune challenge in rats. Pediatr Res 73(6):750–755. doi:10.1038/pr.2013.40
Article
PubMed
Google Scholar
Palacios-Garcia I, Lara-Vasquez A, Montiel JF, Diaz-Veliz GF, Sepulveda H, Utreras E, Montecino M, Gonzalez-Billault C et al (2015) Prenatal stress down-regulates reelin expression by methylation of its promoter and induces adult behavioral impairments in rats. PLoS One 10(2):e0117680. doi:10.1371/journal.pone.0117680
Article
PubMed
PubMed Central
Google Scholar
Herring A, Donath A, Yarmolenko M, Uslar E, Conzen C, Kanakis D, Bosma C, Worm K et al (2012) Exercise during pregnancy mitigates Alzheimer-like pathology in mouse offspring. FASEB J 26(1):117–128. doi:10.1096/fj.11-193193
CAS
Article
PubMed
Google Scholar
Cotter D, Pariante CM (2002) Stress and the progression of the developmental hypothesis of schizophrenia. The British Journal of Psychiatry: The Journal of Mental Science 181:363–365
Article
Google Scholar
Pompili A, Arnone B, Gasbarri A (2012) Estrogens and memory in physiological and neuropathological conditions. Psychoneuroendocrinology 37(9):1379–1396. doi:10.1016/j.psyneuen.2012.01.007
CAS
Article
PubMed
Google Scholar
Tareen RS, Kamboj MK (2012) Role of endocrine factors in autistic spectrum disorders. Pediatr Clin N Am 59(1):75–88 . doi:10.1016/j.pcl.2011.10.013x
Article
Google Scholar
Forero DA, Casadesus G, Perry G, Arboleda H (2006) Synaptic dysfunction and oxidative stress in Alzheimer’s disease: emerging mechanisms. J Cell Mol Med 10(3):796–805
CAS
Article
PubMed
Google Scholar
Barron AM, Pike CJ (2012) Sex hormones, aging, and Alzheimer’s disease. Front Biosci 4:976–997
Google Scholar
Pamplona R, Naudi A, Gavin R, Pastrana MA, Sajnani G, Ilieva EV, Del Rio JA, Portero-Otin M et al (2008) Increased oxidation, glycoxidation, and lipoxidation of brain proteins in prion disease. Free Radic Biol Med 45(8):1159–1166. doi:10.1016/j.freeradbiomed.2008.07.009
CAS
Article
PubMed
Google Scholar
Fatemi SH, Kroll JL, Stary JM (2001) Altered levels of reelin and its isoforms in schizophrenia and mood disorders. Neuroreport 12(15):3209–3215
CAS
Article
PubMed
Google Scholar
Fatemi SH, Stary JM, Egan EA (2002) Reduced blood levels of reelin as a vulnerability factor in pathophysiology of autistic disorder. Cell Mol Neurobiol 22(2):139–152
CAS
Article
PubMed
Google Scholar
Herring A, Donath A, Steiner KM, Widera MP, Hamzehian S, Kanakis D, Kolble K, ElAli A et al (2012) Reelin depletion is an early phenomenon of Alzheimer’s pathology. J Alzheimers Dis 30(4):963–979. doi:10.3233/JAD-2012-112069
PubMed
Google Scholar
Botella-Lopez A, Burgaya F, Gavin R, Garcia-Ayllon MS, Gomez-Tortosa E, Pena-Casanova J, Urena JM, Del Rio JA et al (2006) Reelin expression and glycosylation patterns are altered in Alzheimer’s disease. Proc Natl Acad Sci U S A 103(14):5573–5578. doi:10.1073/pnas.0601279103
CAS
Article
PubMed
PubMed Central
Google Scholar
Saez-Valero J, Costell M, Sjogren M, Andreasen N, Blennow K, Luque JM (2003) Altered levels of cerebrospinal fluid reelin in frontotemporal dementia and Alzheimer’s disease. J Neurosci Res 72(1):132–136. doi:10.1002/jnr.10554
CAS
Article
PubMed
Google Scholar
Knuesel I, Nyffeler M, Mormede C, Muhia M, Meyer U, Pietropaolo S, Yee BK, Pryce CR et al (2009) Age-related accumulation of reelin in amyloid-like deposits. Neurobiol Aging 30(5):697–716. doi:10.1016/j.neurobiolaging.2007.08.011
CAS
Article
PubMed
Google Scholar
Schiffmann SN, Bernier B, Goffinet AM (1997) Reelin mRNA expression during mouse brain development. Eur J Neurosci 9(5):1055–1071
CAS
Article
PubMed
Google Scholar
Krstic D, Pfister S, Notter T, Knuesel I (2013) Decisive role of reelin signaling during early stages of Alzheimer’s disease. Neuroscience 246:108–116. doi:10.1016/j.neuroscience.2013.04.042
CAS
Article
PubMed
Google Scholar
Chin J, Massaro CM, Palop JJ, Thwin MT, Yu GQ, Bien-Ly N, Bender A, Mucke L (2007) Reelin depletion in the entorhinal cortex of human amyloid precursor protein transgenic mice and humans with Alzheimer’s disease. J Neurosci 27(11):2727–2733. doi:10.1523/JNEUROSCI.3758-06.2007
CAS
Article
PubMed
Google Scholar
Wirths O, Multhaup G, Czech C, Blanchard V, Tremp G, Pradier L, Beyreuther K, Bayer TA (2001) Reelin in plaques of beta-amyloid precursor protein and presenilin-1 double-transgenic mice. Neurosci Lett 316(3):145–148
CAS
Article
PubMed
Google Scholar
Doehner J, Madhusudan A, Konietzko U, Fritschy JM, Knuesel I (2010) Co-localization of reelin and proteolytic AbetaPP fragments in hippocampal plaques in aged wild-type mice. J Alzheimers Dis 19(4):1339–1357. doi:10.3233/JAD-2010-1333
CAS
Article
PubMed
Google Scholar
Kocherhans S, Madhusudan A, Doehner J, Breu KS, Nitsch RM, Fritschy JM, Knuesel I (2010) Reduced reelin expression accelerates amyloid-beta plaque formation and tau pathology in transgenic Alzheimer’s disease mice. J Neurosci 30(27):9228–9240. doi:10.1523/JNEUROSCI.0418-10.2010
CAS
Article
PubMed
Google Scholar
Botella-Lopez A, Cuchillo-Ibanez I, Cotrufo T, Mok SS, Li QX, Barquero MS, Dierssen M, Soriano E et al (2010) Beta-amyloid controls altered reelin expression and processing in Alzheimer’s disease. Neurobiol Dis 37(3):682–691. doi:10.1016/j.nbd.2009.12.006
CAS
Article
PubMed
Google Scholar
Lane-Donovan C, Philips GT, Wasser CR, Durakoglugil MS, Masiulis I, Upadhaya A, Pohlkamp T, Coskun C et al (2015) Reelin protects against amyloid beta toxicity in vivo. Sci Signal 8(384):ra67. doi:10.1126/scisignal.aaa6674
Article
PubMed
PubMed Central
Google Scholar
Herrmann US, Sonati T, Falsig J, Reimann RR, Dametto P, O’Connor T, Li B, Lau A et al (2015) Prion infections and anti-PrP antibodies trigger converging neurotoxic pathways. PLoS Pathog 11(2):e1004662. doi:10.1371/journal.ppat.1004662
CAS
Article
PubMed
PubMed Central
Google Scholar
Gavin R, Urena J, Rangel A, Pastrana MA, Requena JR, Soriano E, Aguzzi A, Del Rio JA (2008) Fibrillar prion peptide PrP(106-126) treatment induces Dab1 phosphorylation and impairs APP processing and Abeta production in cortical neurons. Neurobiol Dis 30(2):243–254. doi:10.1016/j.nbd.2008.02.001
CAS
Article
PubMed
Google Scholar
Gavin R, Ferrer I, del Rio JA (2010) Involvement of Dab1 in APP processing and beta-amyloid deposition in sporadic Creutzfeldt-Jakob patients. Neurobiol Dis 37(2):324–329. doi:10.1016/j.nbd.2009.10.010
CAS
Article
PubMed
Google Scholar
Bueler H, Fischer M, Lang Y, Bluethmann H, Lipp HP, DeArmond SJ, Prusiner SB, Aguet M et al (1992) Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein. Nature 356(6370):577–582
CAS
Article
PubMed
Google Scholar
Fischer M, Rulicke T, Raeber A, Sailer A, Moser M, Oesch B, Brandner S, Aguzzi A et al (1996) Prion protein (PrP) with amino-proximal deletions restoring susceptibility of PrP knockout mice to scrapie. EMBO J 15(6):1255–1264
CAS
PubMed
PubMed Central
Google Scholar
Steele AD, Emsley JG, Ozdinler PH, Lindquist S, Macklis JD (2006) Prion protein (PrPc) positively regulates neural precursor proliferation during developmental and adult mammalian neurogenesis. Proc Natl Acad Sci U S A 103(9):3416–3421. doi:10.1073/pnas.0511290103
CAS
Article
PubMed
PubMed Central
Google Scholar
Ordonez-Gutierrez L, Torres JM, Gavin R, Anton M, Arroba-Espinosa AI, Espinosa JC, Vergara C, Del Rio JA et al (2013) Cellular prion protein modulates beta-amyloid deposition in aged APP/PS1 transgenic mice. Neurobiol Aging 34(12):2793–2804. doi:10.1016/j.neurobiolaging.2013.05.019
CAS
Article
PubMed
Google Scholar
Cassard H, Torres JM, Lacroux C, Douet JY, Benestad SL, Lantier F, Lugan S, Lantier I et al (2014) Evidence for zoonotic potential of ovine scrapie prions. Nat Commun 5:5821. doi:10.1038/ncomms6821
CAS
Article
PubMed
Google Scholar
Padilla D, Beringue V, Espinosa JC, Andreoletti O, Jaumain E, Reine F, Herzog L, Gutierrez-Adan A et al (2011) Sheep and goat BSE propagate more efficiently than cattle BSE in human PrP transgenic mice. PLoS Pathog 7(3):e1001319. doi:10.1371/journal.ppat.1001319
CAS
Article
PubMed
PubMed Central
Google Scholar
Vilches S, Vergara C, Nicolas O, Mata A, Del Rio JA, Gavin R (2015) Domain-specific activation of death-associated intracellular signalling cascades by the cellular prion protein in neuroblastoma cells. Mol Neurobiol. doi:10.1007/s12035-015-9360-6
PubMed
Google Scholar
Carulla P, Bribian A, Rangel A, Gavin R, Ferrer I, Caelles C, Del Rio JA, Llorens F (2011) Neuroprotective role of PrPC against kainate-induced epileptic seizures and cell death depends on the modulation of JNK3 activation by GluR6/7-PSD-95 binding. Mol Biol Cell 22(17):3041–3054. doi:10.1091/mbc.E11-04-0321
CAS
Article
PubMed
PubMed Central
Google Scholar
Mingorance A, Fontana X, Sole M, Burgaya F, Urena JM, Teng FY, Tang BL, Hunt D et al (2004) Regulation of Nogo and Nogo receptor during the development of the entorhino-hippocampal pathway and after adult hippocampal lesions. Mol Cell Neurosci 26(1):34–49. doi:10.1016/j.mcn.2004.01.001
CAS
Article
PubMed
Google Scholar
Llorens F, Zafar S, Ansoleaga B, Shafiq M, Blanco R, Carmona M, Grau-Rivera O, Nos C et al (2015) Subtype and regional regulation of prion biomarkers in sporadic Creutzfeldt-Jakob disease. Neuropathol Appl Neurobiol 41(5):631–645. doi:10.1111/nan.12175
CAS
Article
PubMed
Google Scholar
Sandberg MK, Al-Doujaily H, Sharps B, De Oliveira MW, Schmidt C, Richard-Londt A, Lyall S, Linehan JM et al (2014) Prion neuropathology follows the accumulation of alternate prion protein isoforms after infective titre has peaked. Nat Commun 5:4347. doi:10.1038/ncomms5347
CAS
Article
PubMed
PubMed Central
Google Scholar
Forloni G, Angeretti N, Chiesa R, Monzani E, Salmona M, Bugiani O, Tagliavini F (1993) Neurotoxicity of a prion protein fragment. Nature 362(6420):543–546
CAS
Article
PubMed
Google Scholar
Brown DR (2000) Prion protein peptides: optimal toxicity and peptide blockade of toxicity. Mol Cell Neurosci 15(1):66–78
CAS
Article
PubMed
Google Scholar
Vilches S, Vergara C, Nicolas O, Sanclimens G, Merino S, Varon S, Acosta GA, Albericio F et al (2013) Neurotoxicity of prion peptides mimicking the central domain of the cellular prion protein. PLoS One 8(8):e70881. doi:10.1371/journal.pone.0070881
CAS
Article
PubMed
PubMed Central
Google Scholar
Vassallo N (2009) Properties and pathogenicity of prion-derived peptides. Protein Pept Lett 16(3):230–238
CAS
Article
PubMed
Google Scholar
Gavin R, Braun N, Nicolas O, Parra B, Urena JM, Mingorance A, Soriano E, Torres JM et al (2005) PrP(106-126) activates neuronal intracellular kinases and Egr1 synthesis through activation of NADPH-oxidase independently of PrPc. FEBS Lett 579(19):4099–4106. doi:10.1016/j.febslet.2005.06.037
CAS
Article
PubMed
Google Scholar
Duit S, Mayer H, Blake SM, Schneider WJ, Nimpf J (2010) Differential functions of ApoER2 and very low density lipoprotein receptor in reelin signaling depend on differential sorting of the receptors. J Biol Chem 285(7):4896–4908. doi:10.1074/jbc.M109.025973
CAS
Article
PubMed
Google Scholar
Schneider B, Mutel V, Pietri M, Ermonval M, Mouillet-Richard S, Kellermann O (2003) NADPH oxidase and extracellular regulated kinases 1/2 are targets of prion protein signaling in neuronal and non neuronal cells. Proc Natl Acad Sci U S A 100(23):13326–13331. doi:10.1073/pnas.2235648100
CAS
Article
PubMed
PubMed Central
Google Scholar
Pietri M, Caprini A, Mouillet-Richard S, Pradines E, Ermonval M, Grassi J, Kellermann O, Schneider B (2006) Overstimulation of PrPC signaling pathways by prion peptide 106-126 causes oxidative injury of bioaminergic neuronal cells. J Biol Chem 281(38):28470–28479. doi:10.1074/jbc.M602774200
CAS
Article
PubMed
Google Scholar
Vilches S, Vergara C, Nicolas O, Mata A, Del Rio JA, Gavin R (2016) Domain-specific activation of death-associated intracellular signalling cascades by the cellular prion protein in neuroblastoma cells. Mol Neurobiol 53(7):4438–4448. doi:10.1007/s12035-015-9360-6
CAS
Article
PubMed
Google Scholar
Alcantara S, Ruiz M, D’Arcangelo G, Ezan F, de Lecea L, Curran T, Sotelo C, Soriano E (1998) Regional and cellular patterns of reelin mRNA expression in the forebrain of the developing and adult mouse. J Neurosci 18(19):7779–7799
CAS
PubMed
Google Scholar
Guentchev M, Groschup MH, Kordek R, Liberski PP, Budka H (1998) Severe, early and selective loss of a subpopulation of GABAergic inhibitory neurons in experimental transmissible spongiform encephalopathies. Brain Pathol 8(4):615–623
CAS
Article
PubMed
Google Scholar
Cuchillo-Ibanez I, Balmaceda V, Mata-Balaguer T, Lopez-Font I, Saez-Valero J (2016) Reelin in Alzheimer’s disease, increased levels but impaired signaling: when more is less. J Alzheimers Dis. doi:10.3233/JAD-151193
PubMed
Google Scholar
Stranahan AM, Haberman RP, Gallagher M (2011) Cognitive decline is associated with reduced reelin expression in the entorhinal cortex of aged rats. Cereb Cortex 21(2):392–400. doi:10.1093/cercor/bhq106
Article
PubMed
Google Scholar
Stranahan AM, Salas-Vega S, Jiam NT, Gallagher M (2011) Interference with reelin signaling in the lateral entorhinal cortex impairs spatial memory. Neurobiol Learn Mem 96(2):150–155. doi:10.1016/j.nlm.2011.03.009
CAS
Article
PubMed
PubMed Central
Google Scholar
Devanathan V, Jakovcevski I, Santuccione A, Li S, Lee HJ, Peles E, Leshchyns’ka I, Sytnyk V et al (2010) Cellular form of prion protein inhibits reelin-mediated shedding of Caspr from the neuronal cell surface to potentiate Caspr-mediated inhibition of neurite outgrowth. J Neurosci 30(27):9292–9305. doi:10.1523/JNEUROSCI.5657-09.2010
CAS
Article
PubMed
Google Scholar
Rangel A, Madronal N, Gruart A, Gavin R, Llorens F, Sumoy L, Torres JM, Delgado-Garcia JM et al (2009) Regulation of GABA(a) and glutamate receptor expression, synaptic facilitation and long-term potentiation in the hippocampus of prion mutant mice. PLoS One 4(10):e7592. doi:10.1371/journal.pone.0007592
Article
PubMed
PubMed Central
Google Scholar
Carulla P, Llorens F, Matamoros-Angles A, Aguilar-Calvo P, Espinosa JC, Gavin R, Ferrer I, Legname G et al (2015) Involvement of PrP(C) in kainate-induced excitotoxicity in several mouse strains. Sci Rep 5:11971. doi:10.1038/srep11971
Article
PubMed
PubMed Central
Google Scholar
Benvegnu S, Roncaglia P, Agostini F, Casalone C, Corona C, Gustincich S, Legname G (2011) Developmental influence of the cellular prion protein on the gene expression profile in mouse hippocampus. Physiol Genomics 43(12):711–725. doi:10.1152/physiolgenomics.00205.2010
CAS
Article
PubMed
Google Scholar
Rubenstein R, Chang B, Petersen R, Chiu A, Davies P (2015) T-tau and P-tau in brain and blood from natural and experimental prion diseases. PLoS One 10(12):e0143103. doi:10.1371/journal.pone.0143103
Article
PubMed
PubMed Central
Google Scholar
Simon D, Herva ME, Benitez MJ, Garrido JJ, Rojo AI, Cuadrado A, Torres JM, Wandosell F (2014) Dysfunction of the PI3K-Akt-GSK-3 pathway is a common feature in cell culture and in vivo models of prion disease. Neuropathol Appl Neurobiol 40(3):311–326. doi:10.1111/nan.12066
CAS
Article
PubMed
Google Scholar
Newaz K, Sriram K, Bera D (2015) Identification of major signaling pathways in prion disease progression using network analysis. PLoS One 10(12):e0144389. doi:10.1371/journal.pone.0144389
Article
PubMed
PubMed Central
Google Scholar
Rizzardini M, Chiesa R, Angeretti N, Lucca E, Salmona M, Forloni G, Cantoni L (1997) Prion protein fragment 106-126 differentially induces heme oxygenase-1 mRNA in cultured neurons and astroglial cells. J Neurochem 68(2):715–720
CAS
Article
PubMed
Google Scholar
Keshvara L, Magdaleno S, Benhayon D, Curran T (2002) Cyclin-dependent kinase 5 phosphorylates disabled 1 independently of reelin signaling. J Neurosci 22(12):4869–4877
CAS
PubMed
Google Scholar
Llorens F, Schmitz M, Karch A, Cramm M, Lange P, Gherib K, Varges D, Schmidt C et al (2015) Comparative analysis of cerebrospinal fluid biomarkers in the differential diagnosis of neurodegenerative dementia. Alzheimers Dement. doi:10.1016/j.jalz.2015.10.009
PubMed
Google Scholar
Schmitz M, Ebert E, Stoeck K, Karch A, Collins S, Calero M, Sklaviadis T, Laplanche JL et al (2015) Validation of 14-3-3 protein as a marker in sporadic Creutzfeldt-Jakob disease diagnostic. Mol Neurobiol. doi:10.1007/s12035-015-9167-5
PubMed Central
Google Scholar
Miyashita A, Hatsuta H, Kikuchi M, Nakaya A, Saito Y, Tsukie T, Hara N, Ogishima S et al (2014) Genes associated with the progression of neurofibrillary tangles in Alzheimer’s disease. Transl Psychiatry 4:e396. doi:10.1038/tp.2014.35
CAS
Article
PubMed
PubMed Central
Google Scholar
Ferrer I (2002) Synaptic pathology and cell death in the cerebellum in Creutzfeldt-Jakob disease. Cerebellum 1(3):213–222. doi:10.1080/14734220260418448
CAS
Article
PubMed
Google Scholar
Clinton J, Forsyth C, Royston MC, Roberts GW (1993) Synaptic degeneration is the primary neuropathological feature in prion disease: a preliminary study. Neuroreport 4(1):65–68
CAS
Article
PubMed
Google Scholar