| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Weissmann C | |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | molecular biology | Q7202 |
| P1104 | number of pages | 9 | |
| P304 | page(s) | 3-11 | |
| P577 | publication date | 1996-06-01 | |
| P1433 | published in | FEBS Letters | Q1388051 |
| P1476 | title | The Ninth Datta Lecture. Molecular biology of transmissible spongiform encephalopathies | |
| P478 | volume | 389 |
| Q32067033 | A diagnostic test for scrapie-infected sheep using a capillary electrophoresis immunoassay with fluorescent-labeled peptides |
| Q84522846 | A novel mutation I215V in the PRNP gene associated with Creutzfeldt-Jakob and Alzheimer's diseases in three patients with divergent clinical phenotypes |
| Q59690434 | Allelic origin of the abnormal prion protein isoform in familial prion diseases |
| Q48168864 | Amino acid sequence of the Felis catus prion protein |
| Q33368981 | Antagonistic interactions between yeast chaperones Hsp104 and Hsp70 in prion curing |
| Q39365772 | Assessment of the PrPc Amino-Terminal Domain in Prion Species Barriers |
| Q44391303 | Atypical effect of salts on the thermodynamic stability of human prion protein |
| Q41652295 | Bovine spongiform encephalopathy and early onset variant Creutzfeldt-Jakob disease |
| Q34640695 | Bovine spongiform encephalopathy: is it an autoimmune disease due to bacteria showing molecular mimicry with brain antigens? |
| Q44488493 | Capillary isoelectric focusing of the scrapie prion protein |
| Q28359731 | Changing a single amino acid in the N-terminus of murine PrP alters TSE incubation time across three species barriers |
| Q44805548 | Characterization of recombinant, membrane-attached full-length prion protein |
| Q40307214 | Checking the pH-induced conformational transition of prion protein by molecular dynamics simulations: effect of protonation of histidine residues |
| Q42597838 | Combination of the somatic cell nuclear transfer method and RNAi technology for the production of a prion gene-knockdown calf using plasmid vectors harboring the U6 or tRNA promoter |
| Q51770160 | Detailed biophysical characterization of the acid-induced PrP(c) to PrP(β) conversion process. |
| Q44174343 | Disease-associated F198S mutation increases the propensity of the recombinant prion protein for conformational conversion to scrapie-like form |
| Q35053001 | Ex vivo propagation of infectious sheep scrapie agent in heterologous epithelial cells expressing ovine prion protein |
| Q48784818 | Familial mutations and the thermodynamic stability of the recombinant human prion protein |
| Q48674028 | Flexibility of the murine prion protein and its Asp178Asn mutant investigated by molecular dynamics simulations |
| Q44009134 | Folding and intrinsic stability of deletion variants of PrP(121-231), the folded C-terminal domain of the prion protein |
| Q34305029 | Folding dynamics and energetics of recombinant prion proteins |
| Q24533260 | Genetic and environmental factors affecting the de novo appearance of the [PSI+] prion in Saccharomyces cerevisiae |
| Q73966978 | Human prion proteins expressed in Escherichia coli and purified by high-affinity column refolding |
| Q48721370 | Identification of the prion protein allotypes which accumulate in the brain of sporadic and familial Creutzfeldt-Jakob disease patients |
| Q41831450 | Impact of methionine oxidation as an initial event on the pathway of human prion protein conversion |
| Q41844502 | Influence of the N-terminal domain on the aggregation properties of the prion protein |
| Q38837529 | Interplay of buried histidine protonation and protein stability in prion misfolding |
| Q43539798 | Lack of evidence to support the association of the human prion gene with schizophrenia |
| Q36724125 | Marked decrease of neuropeptide Y Y2 receptor binding sites in the hippocampus in murine prion disease |
| Q33842432 | Markedly increased susceptibility to natural sheep scrapie of transgenic mice expressing ovine prp. |
| Q44886629 | Methionine 129 variant of human prion protein oligomerizes more rapidly than the valine 129 variant: implications for disease susceptibility to Creutzfeldt-Jakob disease. |
| Q47832900 | Molecular dynamics simulation of temperature induced unfolding of animal prion protein |
| Q54559823 | NMR characterization of the full-length recombinant murine prion protein, mPrP(23-231). |
| Q27620845 | NMR solution structure of the human prion protein |
| Q27625393 | NMR structures of three single-residue variants of the human prion protein |
| Q36688984 | Normal host prion protein (PrPC) is required for scrapie spread within the central nervous system |
| Q35917933 | Overexpression of the SUP45 gene encoding a Sup35p-binding protein inhibits the induction of the de novo appearance of the [PSI+] prion |
| Q91967822 | PAD-Beads enrichment enhances detection of PrPSc using real-time quaking-induced conversion |
| Q34471219 | PrP polymorphisms tightly control sheep prion replication in cultured cells |
| Q60044694 | Preparation of lyophilized recombinant prion protein for TSE diagnosis by RT-QuIC |
| Q36317308 | Prion protein NMR structure and familial human spongiform encephalopathies |
| Q36654584 | Prion protein NMR structure and species barrier for prion diseases |
| Q33756704 | Prion protein NMR structures of elk and of mouse/elk hybrids |
| Q48174350 | Prion protein: a role in sleep regulation? |
| Q28776299 | Prion protein: evolution caught en route |
| Q36236422 | Prion-inducing domain 2-114 of yeast Sup35 protein transforms in vitro into amyloid-like filaments |
| Q92248207 | Proteinase K resistant cores of prions and amyloids |
| Q49844410 | Real-Time Quaking-Induced Conversion Detection of Bovine Spongiform Encephalopathy Prions in a Subclinical Steer |
| Q54559827 | Recombinant full-length murine prion protein, mPrP(23-231): purification and spectroscopic characterization. |
| Q35884369 | Scrapie infectivity correlates with converting activity, protease resistance, and aggregation of scrapie-associated prion protein in guanidine denaturation studies. |
| Q47861173 | Sequence-dependent dynamical instability of the human prion protein: a comparative simulation study |
| Q73067776 | Sleep and sleep regulation in normal and prion protein-deficient mice |
| Q42675291 | Specific binding of normal prion protein to the scrapie form via a localized domain initiates its conversion to the protease-resistant state |
| Q34306690 | Spongiform encephalopathies: insights from transgenic models |
| Q41840813 | Stability and conformational properties of doppel, a prion-like protein, and its single-disulphide mutant. |
| Q41987801 | Sulphated glycosaminoglycans prevent the neurotoxicity of a human prion protein fragment |
| Q34533438 | The Functional Role of Prion Protein (PrPC) on Autophagy |
| Q27642560 | The Octapeptide Repeats in Mammalian Prion Protein Constitute a pH-dependent Folding and Aggregation Site |
| Q43600364 | The Val-210-Ile pathogenic Creutzfeldt-Jakob disease mutation increases both the helical and aggregation propensities of a sequence corresponding to helix-3 of PrP(C). |
| Q44755150 | The effect of disease-associated mutations on the folding pathway of human prion protein |
| Q38847495 | The formation, function and regulation of amyloids: insights from structural biology |
| Q46020428 | The prion folding problem. |
| Q43466267 | The prionoses and other conformational disorders |
| Q24643343 | The protein product of the het-s heterokaryon incompatibility gene of the fungus Podospora anserina behaves as a prion analog |
| Q34177517 | The role of dimerization in prion replication |
| Q31538196 | The role of disulfide bridge in the folding and stability of the recombinant human prion protein |
| Q57794386 | Thermodynamic characterization for the denatured state of bovine prion protein and the BSE Associated variant E211K |
| Q34305023 | Three-dimensional structures of prion proteins |
| Q35122356 | Three-dimensional structures of the prion protein and its doppel |
| Q48357484 | Transgenic and knockout mice in research on prion diseases |
| Q41570752 | Transgenic animals as models of neurodegenerative diseases in humans |
| Q41874945 | Translation termination efficiency can be regulated in Saccharomyces cerevisiae by environmental stress through a prion-mediated mechanism |
| Q36978208 | Ultrasensitive detection of pathological prion protein aggregates by dual-color scanning for intensely fluorescent targets |
| Q36287456 | Use of bovine recombinant prion protein and real-time quaking-induced conversion to detect cattle transmissible mink encephalopathy prions and discriminate classical and atypical L- and H-Type bovine spongiform encephalopathy. |
| Q72990483 | Use of capillary electrophoresis and fluorescent labeled peptides to detect the abnormal prion protein in the blood of animals that are infected with a transmissible spongiform encephalopathy |
| Q48612578 | Use of capillary sodium dodecyl sulfate gel electrophoresis to detect the prion protein extracted from scrapie-infected sheep. |
| Q41642296 | Yeast prions: inheritance by seeded protein polymerization? |
| Q86691495 | [Is Parkinson's disease a prion disease?] |
Search more.