Keywords: PrP; prion protein; PrPC; normal cellular isoform of PrP; PrPSc; abnormal misfolded isoform of PrP; CJD; Creutzfeldt Jakob disease; sCJD; sporadic CJD; dCJD; dura mater graft-associated CJD; p-dCJD; plaque-type dCJD; np-dCJD; non-plaque-type dCJD; 129M/M;
مقالات ISI (ترجمه نشده)
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Keywords: AA; amino acid; Aβo; oligomeric β-amyloid; Aβ; β-amyloid; AD; Alzheimer's disease; α7nAChR; α7 nicotinic acetylcholine receptor; ALS; amyotrophic lateral sclerosis; APLP1; amyloid beta precursor-like protein 1; APP; amyloid precursor protein; β-A
Keywords: α-Syn; α-synuclein; Aβ; beta-amyloid; AD; Alzheimer's disease; AON; anterior olfactory nucleus; ALS; amyotrophic lateral sclerosis; APP; amyloid precursor protein; CBD; corticobasal degeneration; CJD; Creutzfeldt-Jakob disease; DLB; dementia with Lewy
Keywords: Aβ; amyloid β peptide; AD; Alzheimerʹs Disease; ALS; amyotrophic lateral sclerosis; Amb; Amphotericin B; BBB; blood-brain barrier; CJD; Creutzfeld Jakob disease; CSF; cerebral spinal fluid; DCS; D-Cycloserine; DOX; Doxorubicin; GA; Geldanamycin; GAPDH;
Keywords: A1PI; Virus; Prions; Safety; Purity; Stability; ADA; anti-drug antibody; A1PI; alpha1-proteinase inhibitor; B19V; parvovirus B19; BVDV; bovine viral diarrhea virus; CJD; Creutzfeldt-Jakob-Disease; CPV; canine parvovirus; DTT; dithiothreitol; EMA; European
Keywords: CDC; Centers for Disease Control and Prevention; CJD; Creutzfeldt-Jakob disease; HCV; hepatitis C virus; HIV; human immunodeficiency virus; HSV; herpes simplex virus; PFU; plaque-forming unit; ppm; parts per million; vCJD; variant Creutzfeldt-Jakob diseas
Keywords: Creutzfeldt-Jakob disease; Overlap Parasomnias; Status Dissociatus; Videopolisomnography; CJD; Creutzfeldt-Jakob Disease; CSF; cerebrospinal fluid; CT; computed tomography; EEG; electroencephalogram; EMG; electromyogram; EOG; electroculogram; MRI; Magneti
Keywords: α-syn; α-synuclein; Aβ; β-amyloid; AD; Alzheimer's disease; ADAMs; a disintegrin and metalloproteinases; ALS; amyotrophic lateral sclerosis; BSE; bovine spongiform encephalopathy; CJD; Creutzfeldt-Jakob disease; CNS; central nervous system; CSF; cer
Keywords: Prion infection; Scrapie; CJD; Aging; Age-related; Incubation period; Gene expression; Inflammation; PrP; Neurodegeneration;
Keywords: BSE; bovine spongiform encephalopathy; cAMP; cyclic adenosine monophosphate; CJD; Creutzfeldt-Jakob disease; CSF; cerebrospinal fluid; EM; electron microscopy; ER; endoplasmic reticulum; ERK1/2; extracellular signal-regulated protein kinases 1 and 2; GPI;
Keywords: AMPA; α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid; BSE; bovine spongiform encephalopathy; CJD; Creutzfeldt-Jakob disease; vCJD; the variant of CJD; F14; PrP knockout fusion cell line; F21; wild-type fusion cell line; ICP-MS; inductively-coupled
Keywords: AD; Alzheimer's disease; PD; Parkinson's disease; HD; Huntington's disease; CJD; Creutzfeld-Jacob disease; mAb; monoclonal antibody; scFv; single-chain Fv; VH; variable domain of the heavy chain; VL; variable domain of the light chain; VHH; variable dom
Keywords: Luminal endoscope; Decontamination; Prion; CJD;
Keywords: AA; ascorbic acid; BSE; Bovine spongiform encephalopathies; B3LYP; Becke 3 parameter Lee Yang Parr; BP86; Becke Perdew86; CD; Circular dichroism; CJD; Creutzfeldt-Jakob disease; CPMD; Car-Parrinello molecular dynamics; DFT; Density functional theory;
ASGE guideline for infection control during GI endoscopy
Keywords: ASGE; American Society for Gastrointestinal Endoscopy; CDC; Centers for Disease Control and Prevention; CJD; Creutzfeldt-Jacob disease; CRE; carbapenem-resistant Enterobacteriaceae; FDA; U.S. Food and Drug Administration; HBV; hepatitis B virus; HCV; hepa
Residue-specific mobility changes in soluble oligomers of the prion protein define regions involved in aggregation
Keywords: Prion protein; Protein misfolding; Beta oligomer; Solution NMR; PrPSc; infectious particle of misfolded prion protein; PrP; prion protein; PrPc; cellular prion protein; BSE; bovine spongiform encephalopathy; CWD; chronic wasting disease; CJD; Creutzfeldt
Non-cell-autonomous actions of α-synuclein: Implications in glial synucleinopathies
Keywords: Astrocyte; Microglia; Neurodegeneration; Neuroinflammation; Parkinson disease; Protein aggregation; Multiple system atrophy; AD; Alzheimer disease; CJD; Creutzfeldt-Jakob disease; CNP; 3â²-cyclic nucleotide 3â²-phosphodiesterase; CSF; cerebrospinal fl
Oligodendrogliopathy in neurodegenerative diseases with abnormal protein aggregates: The forgotten partner
Keywords: 5-HT; 5-hydroxytryptamine; Aβ; β-amyloid; ABCA8; ATP binding cassette subfamily A member 8; AD; Alzheimer's disease; ADP; adenosine diphosphate; AGD; argyrophilic grain disease; ALS; amyotrophic lateral sclerosis; AMBRA-1; autophagy and beclin 1 regul
Neuroanatomical correlates of prion disease progression - a 3T longitudinal voxel-based morphometry study
Keywords: Prion disease; Structural MRI; Longitudinal voxel based morphometry; 3T MRI; CJD;
Modulation of proteostasis by transcription factor NRF2 and impact in neurodegenerative diseases
Keywords: α-SYN; alpha synuclein; β-TrCP; β-transducin repeat containing E3 ubiquitin protein ligase; Aβ; amyloid beta; AD; Alzheimer's disease; ALS; amyotrophic lateral sclerosis; AMPK; AMP-activated protein kinase; ARE; antioxidant response element; ASK1; apo
l-Arginine ethylester enhances in vitro amplification of PrPSc in macaques with atypical L-type bovine spongiform encephalopathy and enables presymptomatic detection of PrPSc in the bodily fluids
Keywords: Atypical bovine spongiform encephalopathy; Protein misfolding cyclic amplification; Arginine ethylester; Bodily fluid; Nonhuman primate; PrPSc; Pathogenic form of prion protein; PrPC; cellular prion protein; CJD; Creutzfeldt-Jakob disease; BSE; Bovine s
Inherited mtDNA variations are not strong risk factors in human prion disease
Keywords: Prion; CJD; Mitochondrial; GWAS;
Polo-like kinase 3 (PLK3) mediates the clearance of the accumulated PrP mutants transiently expressed in cultured cells and pathogenic PrPSc in prion infected cell line via protein interaction
Keywords: PLKs; polo-like kinases; KD; kinase domain; PBD; polo-box domain; TSE; transmissible spongiform encephalopathies; CJD; Creutzfeldt-Jakob disease; GSS; Gerstmann-Straüssler-Scheinker; FFI; fatal familial insomnia; BSE; bovine spongiform encephalopat
Special Needs Populations: Perioperative Care of the Patient With Creutzfeldt-Jakob Disease
Keywords: Creutzfeldt-Jakob disease; CJD; prion; neurosurgery; diagnostic biopsy; infection prevention; disinfection and sterilization;
Molecular cloning and sequence analysis of prion protein gene in Xiji donkey in China
Keywords: TSEs; transmissible spongiform encephalopathies; CJD; Creutzfeldt-Jakob disease; vCJD; variant Creutzfeldt-Jakob diseases; BSE; bovine spongiform encephalopathy; CWD; chronic wasting disease; FME; feline spongiform encephalopathy; TME; mink spongiform
Dysregulation of brain olfactory and taste receptors in AD, PSP and CJD, and AD-related model
Keywords: AD; Alzheimer's disease; ADYLC3; adenylyl cyclase 3; ATP; adenosine triphosphate; cAMP; cyclic adenosine monophosphate; CJD; Creutzfeldt-Jakob disease; CNG; cyclic nucleotide-gated; Gnal; olfactory G protein; GUS-β; β-glucuronidase; HSD; Honestly Si
Anaesthesia and intensive care for patients with transmissible diseases
Keywords: Anaesthesia; CJD; hepatitis B; hepatitis C; HIV; intensive care
Soil-mediated prion transmission: Is local soil-type a key determinant of prion disease incidence?
Keywords: PrP protein; Transmissible spongiform encephalopathy; N-terminus; BSE; CJD; Fate
Characterization of the glycated human cerebrospinal fluid proteome
Keywords: AD; Alzheimer's disease; AGEs; Advanced glycation end products; ALS; Amyotrophic lateral sclerosis; BAC; Boronate affinity chromatography; β2M; Beta-2 microglobulin; CID; Collision-induced dissociation; CJD; Creutzfeld-Jakob disease; CML; Nε-(carboxym
Molecular cloning and polymorphism analysis of the prion protein gene in Tan sheep of Ningxia, China
Keywords: TSE; transmissible spongiform encephalopathies; CJD; Creutzfeldt-Jakob disease; BSE; bovine spongiform encephalopathy; PrP; prion protein; PrPc; cellular prion protein; PRNP; prion protein gene; SNPs; single nucleotide polymorphisms; ARQ; A136R154Q171;
Synthesis of 9-substituted 2,3,4,9-tetrahydro-1H-carbazole derivatives and evaluation of their anti-prion activity in TSE-infected cells
Keywords: Prion diseases; Transmissible spongiform encephalopathies; Anti-prion compound; 2,3,4,9-Tetrahydro-1H-carbazole; Ring-opening reaction; Structure-activity relationships; TSEs; transmissible spongiform encephalopathies; CJD; Creutzfeldt-Jakob disease;
Alteration of the endocannabinoid system in mouse brain during prion disease
Keywords: prion; endocannabinoid; cannabinoid receptor; neurodegenerative disease; brain; mouse; AEA; arachidonoylethanolamide or anandamide; CBD; cannabidiol; CBR; cannabinoid receptor; CJD; Creutzfeldt-Jakob disease; GAPDH; glyceraldehyde-3-phosphate dehydrogenas
14-3-3 proteins in neurodegeneration
Keywords: TH; tyrosine hydroxylase; 3â²UTR; three prime untranslated region; CSF; cerebrospinal fluid; 2D-PAGE; two-dimensional polyacrylamide gel electrophoresis; PD; Parkinson disease; AD; Alzheimer disease; CJD; Creutzfeldt-Jakob disease; MSA; multiple system a
Cortical propagation of Creutzfeldt–Jakob disease with codon 180 mutation
Keywords: CJD; Prion; Codon 180; MRI; Pathology; Immunohistochemistry; Ultrastructure; Axonal transport
Putaminal volume and diffusion in early familial Creutzfeldt–Jakob Disease
Keywords: Putamen; VOI; ADC; CJD; E200K; FIRST; FSL; SPM
The effects of prion protein expression on metal metabolism
Keywords: CTR1; CTR2; NRAMP; DMT-1; Manganese; Copper; Prion; CJD; Scrapie
Binding of 14-3-3 proteins to a single stranded oligodeoxynucleotide aptamer
Keywords: Aptamer; 14-3-3; TSE; CJD; Affinity; Protein–DNA interaction
Bone marrow stroma cells are susceptible to prion infection
Keywords: Prion protein; CJD; BSE; Bone marrow stromal cell; MSC
A monoclonal antibody (1D12) defines novel distribution patterns of prion protein (PrP) as granules in nucleus
Keywords: BSE; CJD; Prion; Western blot; Immunohistochemistry
Increased oxidation, glycoxidation, and lipoxidation of brain proteins in prion disease
Keywords: AASA; aminoadipic semialdehyde; BSE; bovine spongiform encephalopathy; CEL; N-É-carboxyethyllysine; CJD; Creutzfeldt-Jakob disease; CML; N-É-carboxymethyllysine; DBI; double bond index; GSA; glutamic semialdehyde, 4-HNE, 4-hydroxynonenal; MCO; metal-cat
Elevated manganese levels in blood and CNS in human prion disease
Keywords: Prion; Manganese; CJD; Neurodegeneration
Infection control during GI endoscopy
Keywords: AER; automatic endoscope reprocessor; ASGE; American Society for Gastrointestinal Endoscopy; CDC; Centers for Disease Control; CJD; Creutzfeldt-Jacob disease; ESGE; European Society of Gastrointestinal Endoscopy; FDA; U.S. Food and Drug Administration; HB
CRBL cells: Establishment, characterization and susceptibility to prion infection
Keywords: PrP; prion protein; PrPC; cellular prion protein; PrPSc; scrapie prion protein disease; CJD; Creutzfeldt-Jakob; p53â/â; p53 null; CRBL; a cell line established from the cerebellum; N2a; Neuro2a; ScN2a; scrapie-infected N2a; SMB; scrapie-infected mouse
The ubiquitin-proteasome system in spongiform degenerative disorders
Keywords: AD; Alzheimer's disease; AgRP; Agouti related protein; AIDS; acquired immune deficiency syndrome; APP; amyloid precursor protein; ASPA; aspartoacylase gene; Atrn; attractin; BSE; bovine spongiform encephalopathy; CD; Canavan's spongiform leukodystroph
Anti-GAD antibody cerebellar ataxia mimicking Creutzfeldt–Jakob disease
Keywords: 14-3-3; Glutamic acid decarboxylase antibody; CJD; Cerebellar ataxia; Anti-GAD65
Halting the spread of human prion disease - exceptional measures for an exceptional problem
Keywords: BSE; CJD; Prion; Surgery; Decontamination;
Understanding the natural variability of prion diseases
Keywords: Prions; CJD; Neurodegeneration
Molecular subtype-specific clinical diagnosis of prion diseases
Keywords: Dementia; CJD; Subtype; 14-3-3; Transthyretin; MRI
Developmental expression of PrP in the post-implantation embryo
Keywords: Prnp; gene encoding the prion protein; PrP; prion protein; PrPC; normal, cellular prion protein; SHa; Syrian hamster; Tg; transgenic; Mo; mouse; CJD; Creutzfeldt-Jakob disease; Prion; Prnp; Expression regulation; Transgenic mice; β-galactosidase;
C1q binding and complement activation by prions and amyloids
Keywords: Alzheimer; Amyloid; C1q; Prion; Scrapie; Transmissible spongiform encephalopathy; Aβ; amyloid β peptide; AD; Alzheimer's disease; APP; amyloid precursor protein; BSE; bovine spongiform encephalopathy; CJD; Creutzfeld-Jacob disease; FBD; familial Briti