scholarly article | Q13442814 |
review article | Q7318358 |
P6179 | Dimensions Publication ID | 1033326084 |
P356 | DOI | 10.1038/35094590 |
P698 | PubMed publication ID | 11584312 |
P2093 | author name string | Aguzzi A | |
Glatzel M | |||
Heppner FL | |||
Montrasio F | |||
Prinz M | |||
P2860 | cites work | Neuro-immune connection in spread of prions in the body? | Q57083714 |
The same prion strain causes vCJD and BSE | Q57092996 | ||
Turning off follicular dendritic cells | Q59068710 | ||
Reversion of prion protein conformational changes by synthetic b-sheet breaker peptides | Q59691802 | ||
Temporary inactivation of follicular dendritic cells delays neuroinvasion of scrapie | Q64447657 | ||
NGF modulates sympathetic innervation of lymphoid tissues | Q72037953 | ||
Prophylactic potential of pentosan polysulphate in transmissible spongiform encephalopathies | Q74452125 | ||
Lysosomotropic agents and cysteine protease inhibitors inhibit scrapie-associated prion protein accumulation | Q24525199 | ||
Branched polyamines cure prion-infected neuroblastoma cells | Q24529092 | ||
Impaired prion replication in spleens of mice lacking functional follicular dendritic cells | Q28144723 | ||
Mice devoid of PrP are resistant to scrapie | Q28249108 | ||
Abnormal development of peripheral lymphoid organs in mice deficient in lymphotoxin | Q28507630 | ||
Distinct roles for lymphotoxin-alpha and tumor necrosis factor in organogenesis and spatial organization of lymphoid tissue | Q28586439 | ||
Distinct roles in lymphoid organogenesis for lymphotoxins alpha and beta revealed in lymphotoxin beta-deficient mice | Q28587819 | ||
Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease | Q28588314 | ||
A route for prion neuroinvasion. | Q30328574 | ||
Immunoaffinity purification and neutralization of scrapie prion infectivity | Q33646402 | ||
Neuroinvasion by a Creutzfeldt-Jakob disease agent in the absence of B cells and follicular dendritic cells | Q33930758 | ||
Scrapie prion protein accumulation by scrapie-infected neuroblastoma cells abrogated by exposure to a prion protein antibody | Q33930771 | ||
Acridine and phenothiazine derivatives as pharmacotherapeutics for prion disease | Q33933969 | ||
Prions: health scare and biological challenge. | Q34185897 | ||
Doxycycline control of prion protein transgene expression modulates prion disease in mice | Q36527236 | ||
Ablation of the prion protein (PrP) gene in mice prevents scrapie and facilitates production of anti-PrP antibodies | Q36663046 | ||
Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system | Q36688984 | ||
Sleepless in Bologna: transmission of fatal familial insomnia | Q41052801 | ||
Methods of sympathetic degeneration and alteration | Q41364932 | ||
Bovine spongiform encephalopathy and early onset variant Creutzfeldt-Jakob disease | Q41652295 | ||
Surface lymphotoxin alpha/beta complex is required for the development of peripheral lymphoid organs | Q42196937 | ||
Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state | Q42675291 | ||
Prion (PrPSc)-specific epitope defined by a monoclonal antibody | Q42816365 | ||
Between cows and monkeys | Q43213308 | ||
Normal development and behaviour of mice lacking the neuronal cell-surface PrP protein | Q43522858 | ||
Sympathetic innervation of lymphoreticular organs is rate limiting for prion neuroinvasion | Q43702721 | ||
Transmissions to mice indicate that 'new variant' CJD is caused by the BSE agent | Q44592404 | ||
A B cell-deficient mouse by targeted disruption of the membrane exon of the immunoglobulin mu chain gene | Q46098688 | ||
Antibodies inhibit prion propagation and clear cell cultures of prion infectivity | Q46161882 | ||
The lymphotoxin beta receptor controls organogenesis and affinity maturation in peripheral lymphoid tissues | Q47713235 | ||
Amphotericin B delays the incubation period of scrapie in intracerebrally inoculated hamsters. | Q48263573 | ||
Prion research: the next frontiers | Q48540005 | ||
A crucial role for B cells in neuroinvasive scrapie. | Q48574532 | ||
Effectiveness of anthracycline against experimental prion disease in Syrian hamsters | Q48706421 | ||
Complement facilitates early prion pathogenesis | Q48930440 | ||
Normal host prion protein necessary for scrapie-induced neurotoxicity | Q49160879 | ||
Temporary depletion of complement component C3 or genetic deficiency of C1q significantly delays onset of scrapie. | Q54014234 | ||
Porphyrin and phthalocyanine antiscrapie compounds. | Q54061556 | ||
Potent inhibition of scrapie-associated PrP accumulation by congo red | Q54131452 | ||
Transepithelial prion transport by M cells | Q57083694 | ||
PrP expression in B lymphocytes is not required for prion neuroinvasion | Q57083708 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | prion protein family | Q24724413 |
P304 | page(s) | 745-749 | |
P577 | publication date | 2001-10-01 | |
P1433 | published in | Nature Reviews Neuroscience | Q2108225 |
P1476 | title | Interventional strategies against prion diseases | |
P478 | volume | 2 |
Q27641839 | A camelid antibody fragment inhibits the formation of amyloid fibrils by human lysozyme |
Q45140134 | Amyloid aggregates of the prion peptide PrP106-126 are destabilised by oxidation and by the action of dendrimers |
Q35877214 | Antiprion immunotherapy: to suppress or to stimulate? |
Q36579822 | Antiprion prophylaxis by gene transfer of a soluble prion antagonist |
Q38579674 | Biochemical aspects of dementias |
Q35548991 | CNS pathogenesis of prion diseases |
Q48959703 | Decrease in pathology and progression of scrapie after immunisation with synthetic prion protein peptides in hamsters. |
Q35892062 | Diagnosing prion diseases: needs, challenges and hopes |
Q27300832 | Effective gene therapy in a mouse model of prion diseases |
Q30979178 | Effects of beta-sheet breaker peptide polymers on scrapie-infected mouse neuroblastoma cells and their affinities to prion protein fragment PrP(81-145). |
Q64129780 | Elevated Levels of Tau Protein in Cerebrospinal Fluid of Patients With Probable Creutzfeldt-Jakob Disease |
Q47365495 | Human prion diseases: epidemiology and integrated risk assessment |
Q37569845 | Humoral immune response to native eukaryotic prion protein correlates with anti-prion protection. |
Q57083689 | Immunity against prions? |
Q36436176 | Inhibition of PrP(Sc) formation in scrapie infected N2a cells by 5,7,8-trimethyl-3,4-dihydro-2H-1,4-benzoxazine derivatives. |
Q40066046 | Intracellular accumulation of a mild-denatured monomer of the human PrP fragment 90-231, as possible mechanism of its neurotoxic effects |
Q44544140 | Isolation of drugs active against mammalian prions using a yeast-based screening assay |
Q24673105 | Lentivector-mediated RNAi efficiently suppresses prion protein and prolongs survival of scrapie-infected mice |
Q80373607 | Multiple antigenic peptides facilitate generation of anti-prion antibodies |
Q33843281 | Paracrine inhibition of prion propagation by anti-PrP single-chain Fv miniantibodies |
Q57083661 | Positioning of follicular dendritic cells within the spleen controls prion neuroinvasion |
Q35622996 | Prions and the immune system: a journey through gut, spleen, and nerves |
Q35714147 | Proteomic consequences of expression and pathological conversion of the prion protein in inducible neuroblastoma N2a cells |
Q40201448 | RNAi: a novel strategy for the treatment of prion diseases |
Q35990277 | Rational targeting for prion therapeutics. |
Q36626116 | Searching for anti-prion compounds: cell-based high-throughput in vitro assays and animal testing strategies |
Q48343268 | Soluble dimeric prion protein binds PrP(Sc) in vivo and antagonizes prion disease |
Q80820095 | Testing for prions: a novel protocol for vCJD prevalence studies |
Q33649832 | The prepared tau exon-specific antibodies revealed distinct profiles of tau in CSF of the patients with Creutzfeldt-Jakob disease |
Q24549130 | Transmissible Spongiform Encephalopathies Affecting Humans |
Q35038274 | Unfolding the role of protein misfolding in neurodegenerative diseases |
Q34534616 | What is the basis of transmissible spongiform encephalopathy induced neurodegeneration and can it be repaired? |