264 related articles for article (PubMed ID: 37019623)
1. Diminished Neuronal ESCRT-0 Function Exacerbates AMPA Receptor Derangement and Accelerates Prion-Induced Neurodegeneration.
Lawrence JA; Aguilar-Calvo P; Ojeda-Juárez D; Khuu H; Soldau K; Pizzo DP; Wang J; Malik A; Shay TF; Sullivan EE; Aulston B; Song SM; Callender JA; Sanchez H; Geschwind MD; Roy S; Rissman RA; Trejo J; Tanaka N; Wu C; Chen X; Patrick GN; Sigurdson CJ
J Neurosci; 2023 May; 43(21):3970-3984. PubMed ID: 37019623
[TBL] [Abstract][Full Text] [Related]
2. Loss of hrs in the central nervous system causes accumulation of ubiquitinated proteins and neurodegeneration.
Tamai K; Toyoshima M; Tanaka N; Yamamoto N; Owada Y; Kiyonari H; Murata K; Ueno Y; Ono M; Shimosegawa T; Yaegashi N; Watanabe M; Sugamura K
Am J Pathol; 2008 Dec; 173(6):1806-17. PubMed ID: 19008375
[TBL] [Abstract][Full Text] [Related]
3. Absence of Apolipoprotein E is associated with exacerbation of prion pathology and promotes microglial neurodegenerative phenotype.
Pankiewicz JE; Lizińczyk AM; Franco LA; Diaz JR; Martá-Ariza M; Sadowski MJ
Acta Neuropathol Commun; 2021 Sep; 9(1):157. PubMed ID: 34565486
[TBL] [Abstract][Full Text] [Related]
4. Flow Cytometric Detection of PrP
Yamasaki T; Suzuki A; Hasebe R; Horiuchi M
J Virol; 2018 Jan; 92(1):. PubMed ID: 29046463
[TBL] [Abstract][Full Text] [Related]
5. Autophagy regulates exosomal release of prions in neuronal cells.
Abdulrahman BA; Abdelaziz DH; Schatzl HM
J Biol Chem; 2018 Jun; 293(23):8956-8968. PubMed ID: 29700113
[TBL] [Abstract][Full Text] [Related]
6. Prion protein post-translational modifications modulate heparan sulfate binding and limit aggregate size in prion disease.
Callender JA; Sevillano AM; Soldau K; Kurt TD; Schumann T; Pizzo DP; Altmeppen H; Glatzel M; Esko JD; Sigurdson CJ
Neurobiol Dis; 2020 Aug; 142():104955. PubMed ID: 32454127
[TBL] [Abstract][Full Text] [Related]
7. Neuronal Ndst1 depletion accelerates prion protein clearance and slows neurodegeneration in prion infection.
Aguilar-Calvo P; Malik A; Sandoval DR; Barback C; Orrù CD; Standke HG; Thomas OR; Dwyer CA; Pizzo DP; Bapat J; Soldau K; Ogawa R; Riley MB; Nilsson KPR; Kraus A; Caughey B; Iliff JJ; Vera DR; Esko JD; Sigurdson CJ
PLoS Pathog; 2023 Sep; 19(9):e1011487. PubMed ID: 37747931
[TBL] [Abstract][Full Text] [Related]
8. REST alleviates neurotoxic prion peptide-induced synaptic abnormalities, neurofibrillary degeneration and neuronal death partially via LRP6-mediated Wnt-β-catenin signaling.
Song Z; Zhu T; Zhou X; Barrow P; Yang W; Cui Y; Yang L; Zhao D
Oncotarget; 2016 Mar; 7(11):12035-52. PubMed ID: 26919115
[TBL] [Abstract][Full Text] [Related]
9. Neuroprotective and neurotoxic signaling by the prion protein.
Resenberger UK; Winklhofer KF; Tatzelt J
Top Curr Chem; 2011; 305():101-19. PubMed ID: 21598098
[TBL] [Abstract][Full Text] [Related]
10. Muskelin Coordinates PrP
Heisler FF; Pechmann Y; Wieser I; Altmeppen HC; Veenendaal L; Muhia M; Schweizer M; Glatzel M; Krasemann S; Kneussel M
Neuron; 2018 Sep; 99(6):1155-1169.e9. PubMed ID: 30174115
[TBL] [Abstract][Full Text] [Related]
11. Endogenous prion protein conversion is required for prion-induced neuritic alterations and neuronal death.
Cronier S; Carimalo J; Schaeffer B; Jaumain E; Béringue V; Miquel MC; Laude H; Peyrin JM
FASEB J; 2012 Sep; 26(9):3854-61. PubMed ID: 22661006
[TBL] [Abstract][Full Text] [Related]
12. At the centre of neuronal, synaptic and axonal pathology in murine prion disease: degeneration of neuroanatomically linked thalamic and brainstem nuclei.
Reis R; Hennessy E; Murray C; Griffin ÉW; Cunningham C
Neuropathol Appl Neurobiol; 2015 Oct; 41(6):780-97. PubMed ID: 25727649
[TBL] [Abstract][Full Text] [Related]
13. Prion disease is accelerated in mice lacking stress-induced heat shock protein 70 (HSP70).
Mays CE; Armijo E; Morales R; Kramm C; Flores A; Tiwari A; Bian J; Telling GC; Pandita TK; Hunt CR; Soto C
J Biol Chem; 2019 Sep; 294(37):13619-13628. PubMed ID: 31320473
[TBL] [Abstract][Full Text] [Related]
14. Prion-Associated Neurodegeneration Causes Both Endoplasmic Reticulum Stress and Proteasome Impairment in a Murine Model of Spontaneous Disease.
Otero A; Betancor M; Eraña H; Fernández Borges N; Lucas JJ; Badiola JJ; Castilla J; Bolea R
Int J Mol Sci; 2021 Jan; 22(1):. PubMed ID: 33466523
[TBL] [Abstract][Full Text] [Related]
15. ESCRT functions in autophagy and associated disease.
Rusten TE; Simonsen A
Cell Cycle; 2008 May; 7(9):1166-72. PubMed ID: 18418046
[TBL] [Abstract][Full Text] [Related]
16. RNA-seq and network analysis reveal unique glial gene expression signatures during prion infection.
Carroll JA; Race B; Williams K; Striebel J; Chesebro B
Mol Brain; 2020 May; 13(1):71. PubMed ID: 32381108
[TBL] [Abstract][Full Text] [Related]
17. Prion protein facilitates uptake of zinc into neuronal cells.
Watt NT; Taylor DR; Kerrigan TL; Griffiths HH; Rushworth JV; Whitehouse IJ; Hooper NM
Nat Commun; 2012; 3():1134. PubMed ID: 23072804
[TBL] [Abstract][Full Text] [Related]
18. Epigenetic Control of the Notch and Eph Signaling Pathways by the Prion Protein: Implications for Prion Diseases.
Hirsch TZ; Martin-Lannerée S; Reine F; Hernandez-Rapp J; Herzog L; Dron M; Privat N; Passet B; Halliez S; Villa-Diaz A; Lacroux C; Klein V; Haïk S; Andréoletti O; Torres JM; Vilotte JL; Béringue V; Mouillet-Richard S
Mol Neurobiol; 2019 Mar; 56(3):2159-2173. PubMed ID: 29998397
[TBL] [Abstract][Full Text] [Related]
19. Production of seedable Amyloid-β peptides in model of prion diseases upon PrP
Ezpeleta J; Baudouin V; Arellano-Anaya ZE; Boudet-Devaud F; Pietri M; Baudry A; Haeberlé AM; Bailly Y; Kellermann O; Launay JM; Schneider B
Nat Commun; 2019 Aug; 10(1):3442. PubMed ID: 31371707
[TBL] [Abstract][Full Text] [Related]
20. Lysosomal Quality Control in Prion Diseases.
Majumder P; Chakrabarti O
Mol Neurobiol; 2018 Mar; 55(3):2631-2644. PubMed ID: 28421536
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]