Entry
Name
Prion disease - Homo sapiens (human)
Description
Prion diseases, also termed transmissible spongiform encephalopathies (TSEs), are a group of fatal neurodegenerative diseases that affect humans and a number of other animal species. The etiology of these diseases is thought to be associated with the conversion of a normal protein, PrPC, into an infectious, pathogenic form, PrPSc. The conversion is induced by prion infections (for example, variant Creutzfeldt-Jakob disease (vCJD), iatrogenic CJD, Kuru), mutations (familial CJD, Gerstmann-Straussler-Scheinker syndrome, fatal familial insomnia (FFI)) or unknown factors (sporadic CJD (sCJD)), and is thought to occur after PrPC has reached the plasma membrane or is re-internalized for degradation. The PrPSc form shows greater protease resistance than PrPC and accumulates in affected individuals, often in the form of extracellular plaques. Pathways that may lead to neuronal death comprise oxidative stress, regulated activation of complement, ubiquitin-proteasome and endosomal-lysosomal systems, synaptic alterations and dendritic atrophy, corticosteroid response, and endoplasmic reticulum stress. In addition, the conformational transition could lead to the lost of a beneficial activity of the natively folded protein, PrPC.
Class
Human Diseases; Neurodegenerative disease
BRITE hierarchy
Pathway map
Ortholog table
Network
Element
N01197 Scrapie conformation PrPSc to 26S proteasome-mediated protein degradation
N01198 Scrapie conformation PrPSc to PERK-ATF4 signaling pathway
N01199 Scrapie conformation PrPSc to mGluR5-Ca2+ -apoptotic pathway
N01200 Scrapie conformation PrPSc to transport of calcium
N01201 Scrapie conformation PrPSc to VGCC-Ca2+ -apoptotic pathway
N01202 Oligomeric conformation PrPc to anterograde axonal transport
N01203 Scrapie conformation PrPSc to Notch singling pathway
N01205 Scrapie conformation PrPSc to PRNP-PI3K-NOX2 signaling pathway
Disease
Organism
Homo sapiens (human) [GN:
hsa ]
Gene
5621 PRNP; prion protein (Kanno blood group) [KO:K05634 ]
4684 NCAM1; neural cell adhesion molecule 1 [KO:K06491 ]
4685 NCAM2; neural cell adhesion molecule 2 [KO:K06491 ]
10963 STIP1; stress induced phosphoprotein 1 [KO:K09553 ]
581 BAX; BCL2 associated X, apoptosis regulator [KO:K02159 ]
2902 GRIN1; glutamate ionotropic receptor NMDA type subunit 1 [KO:K05208 ]
2903 GRIN2A; glutamate ionotropic receptor NMDA type subunit 2A [KO:K05209 ]
2904 GRIN2B; glutamate ionotropic receptor NMDA type subunit 2B [KO:K05210 ]
2905 GRIN2C; glutamate ionotropic receptor NMDA type subunit 2C [KO:K05211 ]
2906 GRIN2D; glutamate ionotropic receptor NMDA type subunit 2D [KO:K05212 ]
116443 GRIN3A; glutamate ionotropic receptor NMDA type subunit 3A [KO:K05213 ]
116444 GRIN3B; glutamate ionotropic receptor NMDA type subunit 3B [KO:K05214 ]
774 CACNA1B; calcium voltage-gated channel subunit alpha1 B [KO:K04849 ]
775 CACNA1C; calcium voltage-gated channel subunit alpha1 C [KO:K04850 ]
776 CACNA1D; calcium voltage-gated channel subunit alpha1 D [KO:K04851 ]
778 CACNA1F; calcium voltage-gated channel subunit alpha1 F [KO:K04853 ]
779 CACNA1S; calcium voltage-gated channel subunit alpha1 S [KO:K04857 ]
9451 EIF2AK3; eukaryotic translation initiation factor 2 alpha kinase 3 [KO:K08860 ] [EC:2.7.11.1 ]
1965 EIF2S1; eukaryotic translation initiation factor 2 subunit alpha [KO:K03237 ]
468 ATF4; activating transcription factor 4 [KO:K04374 ]
1649 DDIT3; DNA damage inducible transcript 3 [KO:K04452 ]
3708 ITPR1; inositol 1,4,5-trisphosphate receptor type 1 [KO:K04958 ]
3709 ITPR2; inositol 1,4,5-trisphosphate receptor type 2 [KO:K04959 ]
3710 ITPR3; inositol 1,4,5-trisphosphate receptor type 3 [KO:K04960 ]
5534 PPP3R1; protein phosphatase 3 regulatory subunit B, alpha [KO:K06268 ]
5535 PPP3R2; protein phosphatase 3 regulatory subunit B, beta [KO:K06268 ]
572 BAD; BCL2 associated agonist of cell death [KO:K02158 ]
7416 VDAC1; voltage dependent anion channel 1 [KO:K05862 ]
7417 VDAC2; voltage dependent anion channel 2 [KO:K15040 ]
7419 VDAC3; voltage dependent anion channel 3 [KO:K15041 ]
291 SLC25A4; solute carrier family 25 member 4 [KO:K05863 ]
292 SLC25A5; solute carrier family 25 member 5 [KO:K05863 ]
293 SLC25A6; solute carrier family 25 member 6 [KO:K05863 ]
83447 SLC25A31; solute carrier family 25 member 31 [KO:K05863 ]
317 APAF1; apoptotic peptidase activating factor 1 [KO:K02084 ]
4731 NDUFV3; NADH:ubiquinone oxidoreductase subunit V3 [KO:K03944 ]
4694 NDUFA1; NADH:ubiquinone oxidoreductase subunit A1 [KO:K03945 ]
4695 NDUFA2; NADH:ubiquinone oxidoreductase subunit A2 [KO:K03946 ]
4696 NDUFA3; NADH:ubiquinone oxidoreductase subunit A3 [KO:K03947 ]
4697 NDUFA4; NDUFA4 mitochondrial complex associated [KO:K03948 ]
56901 NDUFA4L2; NDUFA4 mitochondrial complex associated like 2 [KO:K03948 ]
4698 NDUFA5; NADH:ubiquinone oxidoreductase subunit A5 [KO:K03949 ]
4700 NDUFA6; NADH:ubiquinone oxidoreductase subunit A6 [KO:K03950 ]
4701 NDUFA7; NADH:ubiquinone oxidoreductase subunit A7 [KO:K03951 ]
4702 NDUFA8; NADH:ubiquinone oxidoreductase subunit A8 [KO:K03952 ]
4704 NDUFA9; NADH:ubiquinone oxidoreductase subunit A9 [KO:K03953 ]
4705 NDUFA10; NADH:ubiquinone oxidoreductase subunit A10 [KO:K03954 ]
4706 NDUFAB1; NADH:ubiquinone oxidoreductase subunit AB1 [KO:K03955 ]
126328 NDUFA11; NADH:ubiquinone oxidoreductase subunit A11 [KO:K03956 ]
55967 NDUFA12; NADH:ubiquinone oxidoreductase subunit A12 [KO:K11352 ]
51079 NDUFA13; NADH:ubiquinone oxidoreductase subunit A13 [KO:K11353 ]
4707 NDUFB1; NADH:ubiquinone oxidoreductase subunit B1 [KO:K03957 ]
4708 NDUFB2; NADH:ubiquinone oxidoreductase subunit B2 [KO:K03958 ]
4709 NDUFB3; NADH:ubiquinone oxidoreductase subunit B3 [KO:K03959 ]
4710 NDUFB4; NADH:ubiquinone oxidoreductase subunit B4 [KO:K03960 ]
4711 NDUFB5; NADH:ubiquinone oxidoreductase subunit B5 [KO:K03961 ]
4712 NDUFB6; NADH:ubiquinone oxidoreductase subunit B6 [KO:K03962 ]
4713 NDUFB7; NADH:ubiquinone oxidoreductase subunit B7 [KO:K03963 ]
4714 NDUFB8; NADH:ubiquinone oxidoreductase subunit B8 [KO:K03964 ]
4715 NDUFB9; NADH:ubiquinone oxidoreductase subunit B9 [KO:K03965 ]
4716 NDUFB10; NADH:ubiquinone oxidoreductase subunit B10 [KO:K03966 ]
54539 NDUFB11; NADH:ubiquinone oxidoreductase subunit B11 [KO:K11351 ]
4724 NDUFS4; NADH:ubiquinone oxidoreductase subunit S4 [KO:K03937 ]
4725 NDUFS5; NADH:ubiquinone oxidoreductase subunit S5 [KO:K03938 ]
4726 NDUFS6; NADH:ubiquinone oxidoreductase subunit S6 [KO:K03939 ]
4717 NDUFC1; NADH:ubiquinone oxidoreductase subunit C1 [KO:K03967 ]
4718 NDUFC2; NADH:ubiquinone oxidoreductase subunit C2 [KO:K03968 ]
6389 SDHA; succinate dehydrogenase complex flavoprotein subunit A [KO:K00234 ] [EC:1.3.5.1 ]
6390 SDHB; succinate dehydrogenase complex iron sulfur subunit B [KO:K00235 ] [EC:1.3.5.1 ]
6391 SDHC; succinate dehydrogenase complex subunit C [KO:K00236 ]
6392 SDHD; succinate dehydrogenase complex subunit D [KO:K00237 ]
7386 UQCRFS1; ubiquinol-cytochrome c reductase, Rieske iron-sulfur polypeptide 1 [KO:K00411 ] [EC:7.1.1.8 ]
7384 UQCRC1; ubiquinol-cytochrome c reductase core protein 1 [KO:K00414 ]
7385 UQCRC2; ubiquinol-cytochrome c reductase core protein 2 [KO:K00415 ]
7388 UQCRH; ubiquinol-cytochrome c reductase hinge protein [KO:K00416 ]
440567 UQCRHL; ubiquinol-cytochrome c reductase hinge protein like [KO:K00416 ]
7381 UQCRB; ubiquinol-cytochrome c reductase binding protein [KO:K00417 ]
27089 UQCRQ; ubiquinol-cytochrome c reductase complex III subunit VII [KO:K00418 ]
29796 UQCR10; ubiquinol-cytochrome c reductase, complex III subunit X [KO:K00419 ]
10975 UQCR11; ubiquinol-cytochrome c reductase, complex III subunit XI [KO:K00420 ]
4514 COX3; cytochrome c oxidase subunit III [KO:K02262 ]
4513 COX2; cytochrome c oxidase subunit II [KO:K02261 ]
84701 COX4I2; cytochrome c oxidase subunit 4I2 [KO:K02263 ]
1327 COX4I1; cytochrome c oxidase subunit 4I1 [KO:K02263 ]
9377 COX5A; cytochrome c oxidase subunit 5A [KO:K02264 ]
1329 COX5B; cytochrome c oxidase subunit 5B [KO:K02265 ]
1337 COX6A1; cytochrome c oxidase subunit 6A1 [KO:K02266 ]
1339 COX6A2; cytochrome c oxidase subunit 6A2 [KO:K02266 ]
1340 COX6B1; cytochrome c oxidase subunit 6B1 [KO:K02267 ]
1345 COX6C; cytochrome c oxidase subunit 6C [KO:K02268 ]
1346 COX7A1; cytochrome c oxidase subunit 7A1 [KO:K02270 ]
1347 COX7A2; cytochrome c oxidase subunit 7A2 [KO:K02270 ]
9167 COX7A2L; cytochrome c oxidase subunit 7A2 like [KO:K02270 ]
1349 COX7B; cytochrome c oxidase subunit 7B [KO:K02271 ]
1350 COX7C; cytochrome c oxidase subunit 7C [KO:K02272 ]
1351 COX8A; cytochrome c oxidase subunit 8A [KO:K02273 ]
498 ATP5F1A; ATP synthase F1 subunit alpha [KO:K02132 ]
509 ATP5F1C; ATP synthase F1 subunit gamma [KO:K02136 ]
513 ATP5F1D; ATP synthase F1 subunit delta [KO:K02134 ]
514 ATP5F1E; ATP synthase F1 subunit epsilon [KO:K02135 ]
515 ATP5PB; ATP synthase peripheral stalk-membrane subunit b [KO:K02127 ]
516 ATP5MC1; ATP synthase membrane subunit c locus 1 [KO:K02128 ]
517 ATP5MC2; ATP synthase membrane subunit c locus 2 [KO:K02128 ]
518 ATP5MC3; ATP synthase membrane subunit c locus 3 [KO:K02128 ]
10476 ATP5PD; ATP synthase peripheral stalk subunit d [KO:K02138 ]
539 ATP5PO; ATP synthase peripheral stalk subunit OSCP [KO:K02137 ]
522 ATP5PF; ATP synthase peripheral stalk subunit F6 [KO:K02131 ]
5701 PSMC2; proteasome 26S subunit, ATPase 2 [KO:K03061 ]
5700 PSMC1; proteasome 26S subunit, ATPase 1 [KO:K03062 ]
5704 PSMC4; proteasome 26S subunit, ATPase 4 [KO:K03063 ]
5706 PSMC6; proteasome 26S subunit, ATPase 6 [KO:K03064 ]
5702 PSMC3; proteasome 26S subunit, ATPase 3 [KO:K03065 ]
5705 PSMC5; proteasome 26S subunit, ATPase 5 [KO:K03066 ]
5708 PSMD2; proteasome 26S subunit ubiquitin receptor, non-ATPase 2 [KO:K03028 ]
5707 PSMD1; proteasome 26S subunit, non-ATPase 1 [KO:K03032 ]
5709 PSMD3; proteasome 26S subunit, non-ATPase 3 [KO:K03033 ]
5715 PSMD9; proteasome 26S subunit, non-ATPase 9 [KO:K06693 ]
5718 PSMD12; proteasome 26S subunit, non-ATPase 12 [KO:K03035 ]
5717 PSMD11; proteasome 26S subunit, non-ATPase 11 [KO:K03036 ]
9861 PSMD6; proteasome 26S subunit, non-ATPase 6 [KO:K03037 ]
5713 PSMD7; proteasome 26S subunit, non-ATPase 7 [KO:K03038 ]
5719 PSMD13; proteasome 26S subunit, non-ATPase 13 [KO:K03039 ]
5710 PSMD4; proteasome 26S subunit ubiquitin receptor, non-ATPase 4 [KO:K03029 ]
10213 PSMD14; proteasome 26S subunit, non-ATPase 14 [KO:K03030 ]
5714 PSMD8; proteasome 26S subunit, non-ATPase 8 [KO:K03031 ]
11047 ADRM1; ADRM1 26S proteasome ubiquitin receptor [KO:K06691 ]
7979 SEM1; SEM1 26S proteasome subunit [KO:K10881 ]
731 C8A; complement C8 alpha chain [KO:K03997 ]
732 C8B; complement C8 beta chain [KO:K03998 ]
733 C8G; complement C8 gamma chain [KO:K03999 ]
3312 HSPA8; heat shock protein family A (Hsp70) member 8 [KO:K03283 ]
3303 HSPA1A; heat shock protein family A (Hsp70) member 1A [KO:K03283 ]
3305 HSPA1L; heat shock protein family A (Hsp70) member 1 like [KO:K03283 ]
3304 HSPA1B; heat shock protein family A (Hsp70) member 1B [KO:K03283 ]
3310 HSPA6; heat shock protein family A (Hsp70) member 6 [KO:K03283 ]
5290 PIK3CA; phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha [KO:K00922 ] [EC:2.7.1.153 ]
5293 PIK3CD; phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta [KO:K00922 ] [EC:2.7.1.153 ]
5291 PIK3CB; phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta [KO:K00922 ] [EC:2.7.1.153 ]
5295 PIK3R1; phosphoinositide-3-kinase regulatory subunit 1 [KO:K02649 ]
5296 PIK3R2; phosphoinositide-3-kinase regulatory subunit 2 [KO:K02649 ]
8503 PIK3R3; phosphoinositide-3-kinase regulatory subunit 3 [KO:K02649 ]
1536 CYBB; cytochrome b-245 beta chain [KO:K21421 ] [EC:1.-.-.-]
1535 CYBA; cytochrome b-245 alpha chain [KO:K08009 ]
4689 NCF4; neutrophil cytosolic factor 4 [KO:K08012 ]
4688 NCF2; neutrophil cytosolic factor 2 [KO:K08010 ]
1385 CREB1; cAMP responsive element binding protein 1 [KO:K05870 ]
1386 ATF2; activating transcription factor 2 [KO:K04450 ]
10488 CREB3; cAMP responsive element binding protein 3 [KO:K09048 ]
90993 CREB3L1; cAMP responsive element binding protein 3 like 1 [KO:K09048 ]
64764 CREB3L2; cAMP responsive element binding protein 3 like 2 [KO:K09048 ]
84699 CREB3L3; cAMP responsive element binding protein 3 like 3 [KO:K09048 ]
148327 CREB3L4; cAMP responsive element binding protein 3 like 4 [KO:K09048 ]
9586 CREB5; cAMP responsive element binding protein 5 [KO:K09047 ]
1388 ATF6B; activating transcription factor 6 beta [KO:K09049 ]
6352 CCL5; C-C motif chemokine ligand 5 [KO:K12499 ]
7280 TUBB2A; tubulin beta 2A class IIa [KO:K07375 ]
Compound
Reference
Authors
Saa P, Harris DA, Cervenakova L
Title
Mechanisms of prion-induced neurodegeneration.
Journal
Reference
Authors
Goold R, McKinnon C, Tabrizi SJ
Title
Prion degradation pathways: Potential for therapeutic intervention.
Journal
Reference
Authors
Soto C, Satani N
Title
The intricate mechanisms of neurodegeneration in prion diseases.
Journal
Reference
Authors
Mays CE, Soto C
Title
The stress of prion disease.
Journal
Reference
Authors
Jones E, Mead S
Title
Genetic risk factors for Creutzfeldt-Jakob disease.
Journal
Reference
Authors
Kovacs GG, Budka H
Title
Prion diseases: from protein to cell pathology.
Journal
Reference
Authors
Campana V, Sarnataro D, Zurzolo C
Title
The highways and byways of prion protein trafficking.
Journal
Reference
Authors
Caughey B, Baron GS
Title
Prions and their partners in crime.
Journal
Reference
Authors
Chiesa R, Harris DA
Title
Prion diseases: what is the neurotoxic molecule?
Journal
Reference
Authors
Fasano C, Campana V, Zurzolo C
Title
Prions: protein only or something more? Overview of potential prion cofactors.
Journal
Reference
Authors
Roucou X, Gains M, LeBlanc AC
Title
Neuroprotective functions of prion protein.
Journal
Reference
Authors
Harris DA
Title
Cellular biology of prion diseases.
Journal
Clin Microbiol Rev 12:429-44 (1999)
Reference
Authors
Novakofski J, Brewer MS, Mateus-Pinilla N, Killefer J, McCusker RH
Title
Prion biology relevant to bovine spongiform encephalopathy.
Journal
Reference
Authors
Peggion C, Bertoli A, Sorgato MC
Title
Almost a century of prion protein(s): From pathology to physiology, and back to pathology.
Journal
Reference
Authors
Ryskalin L, Busceti CL, Biagioni F, Limanaqi F, Familiari P, Frati A, Fornai F
Title
Prion Protein in Glioblastoma Multiforme.
Journal
Reference
Authors
Ureshino RP, Erustes AG, Bassani TB, Wachilewski P, Guarache GC, Nascimento AC, Costa AJ, Smaili SS, Pereira GJDS
Title
The Interplay between Ca(2+) Signaling Pathways and Neurodegeneration.
Journal
Reference
Authors
Meneghetti E, Gasperini L, Virgilio T, Moda F, Tagliavini F, Benetti F, Legname G
Title
Prions Strongly Reduce NMDA Receptor S-Nitrosylation Levels at Pre-symptomatic and Terminal Stages of Prion Diseases.
Journal
Reference
Authors
Song Z, Zhao D, Yang L
Title
Molecular mechanisms of neurodegeneration mediated by dysfunctional subcellular organelles in transmissible spongiform encephalopathies.
Journal
Reference
Authors
Halliday M, Hughes D, Mallucci GR
Title
Fine-tuning PERK signaling for neuroprotection.
Journal
Reference
Authors
Hughes D, Halliday M
Title
What Is Our Current Understanding of PrP(Sc)-Associated Neurotoxicity and Its Molecular Underpinnings?
Journal
Reference
Authors
Hetz C, Mollereau B
Title
Disturbance of endoplasmic reticulum proteostasis in neurodegenerative diseases.
Journal
Reference
Authors
Hughes D, Mallucci GR
Title
The unfolded protein response in neurodegenerative disorders - therapeutic modulation of the PERK pathway.
Journal
Reference
Authors
Doyle KM, Kennedy D, Gorman AM, Gupta S, Healy SJ, Samali A
Title
Unfolded proteins and endoplasmic reticulum stress in neurodegenerative disorders.
Journal
Reference
Authors
Ferreiro E, Oliveira CR, Pereira CM
Title
The release of calcium from the endoplasmic reticulum induced by amyloid-beta and prion peptides activates the mitochondrial apoptotic pathway.
Journal
Reference
Authors
Ferreiro E, Resende R, Costa R, Oliveira CR, Pereira CM
Title
An endoplasmic-reticulum-specific apoptotic pathway is involved in prion and amyloid-beta peptides neurotoxicity.
Journal
Reference
Authors
Torres M, Encina G, Soto C, Hetz C
Title
Abnormal calcium homeostasis and protein folding stress at the ER: A common factor in familial and infectious prion disorders.
Journal
Reference
Authors
Ciechanover A, Kwon YT
Title
Degradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies.
Journal
Reference
Authors
Kristiansen M, Deriziotis P, Dimcheff DE, Jackson GS, Ovaa H, Naumann H, Clarke AR, van Leeuwen FW, Menendez-Benito V, Dantuma NP, Portis JL, Collinge J, Tabrizi SJ
Title
Disease-associated prion protein oligomers inhibit the 26S proteasome.
Journal
Reference
Authors
Wang HG, Pathan N, Ethell IM, Krajewski S, Yamaguchi Y, Shibasaki F, McKeon F, Bobo T, Franke TF, Reed JC.
Title
Ca2+-induced apoptosis through calcineurin dephosphorylation of BAD.
Journal
Reference
Authors
Hetz C, Russelakis-Carneiro M, Maundrell K, Castilla J, Soto C
Title
Caspase-12 and endoplasmic reticulum stress mediate neurotoxicity of pathological prion protein.
Journal
Reference
Authors
Zamponi E, Pigino GF
Title
Protein Misfolding, Signaling Abnormalities and Altered Fast Axonal Transport: Implications for Alzheimer and Prion Diseases.
Journal
Reference
Authors
Zamponi E, Buratti F, Cataldi G, Caicedo HH, Song Y, Jungbauer LM, LaDu MJ, Bisbal M, Lorenzo A, Ma J, Helguera PR, Morfini GA, Brady ST, Pigino GF
Title
Prion protein inhibits fast axonal transport through a mechanism involving casein kinase 2.
Journal
Reference
Authors
Schneider B, Pietri M, Pradines E, Loubet D, Launay JM, Kellermann O, Mouillet-Richard S
Title
Understanding the neurospecificity of Prion protein signaling.
Journal
Reference
Authors
Didonna A
Title
Prion protein and its role in signal transduction.
Journal
Reference
Authors
Shah SZA, Zhao D, Hussain T, Yang L
Title
The Role of Unfolded Protein Response and Mitogen-Activated Protein Kinase Signaling in Neurodegenerative Diseases with Special Focus on Prion Diseases.
Journal
Reference
Authors
Marella M, Gaggioli C, Batoz M, Deckert M, Tartare-Deckert S, Chabry J
Title
Pathological prion protein exposure switches on neuronal mitogen-activated protein kinase pathway resulting in microglia recruitment.
Journal
Reference
Authors
Ishikura N, Clever JL, Bouzamondo-Bernstein E, Samayoa E, Prusiner SB, Huang EJ, DeArmond SJ
Title
Notch-1 activation and dendritic atrophy in prion disease.
Journal
Reference
Authors
Dearmond SJ, Bajsarowicz K
Title
PrPSc accumulation in neuronal plasma membranes links Notch-1 activation to dendritic degeneration in prion diseases.
Journal
Reference
Authors
Hirsch TZ, Martin-Lanneree S, Reine F, Hernandez-Rapp J, Herzog L, Dron M, Privat N, Passet B, Halliez S, Villa-Diaz A, Lacroux C, Klein V, Haik S, Andreoletti O, Torres JM, Vilotte JL, Beringue V, Mouillet-Richard S
Title
Epigenetic Control of the Notch and Eph Signaling Pathways by the Prion Protein: Implications for Prion Diseases.
Journal
Reference
Authors
Aguzzi A, Zhu C
Title
Microglia in prion diseases.
Journal
Reference
Authors
Mabbott NA
Title
The complement system in prion diseases.
Journal
Reference
Authors
Mallucci G, Collinge J
Title
Rational targeting for prion therapeutics.
Journal
Related pathway
hsa04141 Protein processing in endoplasmic reticulum
hsa04610 Complement and coagulation cascades
KO pathway
LinkDB
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