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Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase families
JOURNAL OF HUMAN GENETICS
Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes
JOURNAL OF HUMAN GENETICS
Scrapie removal using Planova((R)) virus removal filters
BIOLOGICALS
Disruption of neurotransmission in Drosophila mushroom body blocks retrieval but not acquisition of memory
NATURE
Conditional modification of behavior in drosophila by targeted expression of a temperature-sensitive shibire allele in defined neurons
JOURNAL OF NEUROBIOLOGY
Epidemiologic features of 65 Creutzfeldt-Jakob disease patients with a history of cadaveric dura mater transplantation in Japan
EPIDEMIOLOGY AND INFECTION
Construction of recombinant monoclonal antibodies from a chicken hybridomaline secreting specific antibody
CYTOTECHNOLOGY
The CHACM method for computing the characteristic polynomial of a polynomial matrix
IEICE TRANSACTIONS ON FUNDAMENTALS OF ELECTRONICS COMMUNICATIONS AND COMPUTER SCIENCES
Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu
NEUROSCIENCE LETTERS
The amnesiac gene product is expressed in two neurons in the Drosophila brain that are critical for memory
CELL
Proton magnetic resonance spectroscopy of a patient with Gerstmann-Straussler-Scheinker disease
NEURORADIOLOGY
Isolation and characterization of mutants for the vesicular acetylcholine transporter gene in Drosophila melanogaster
JOURNAL OF NEUROBIOLOGY
p300 mediates functional synergism between AF-1 and AF-2 of estrogen receptor alpha and beta by interacting directly with the N-terminal A/B domains
JOURNAL OF BIOLOGICAL CHEMISTRY
A chicken monoclonal antibody with specificity for the N-terminal of humanprion protein
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY
Efficient computation of the characteristic polynomial of a polynomial matrix
IEICE TRANSACTIONS ON FUNDAMENTALS OF ELECTRONICS COMMUNICATIONS AND COMPUTER SCIENCES
A novel phenotype in familial Creutzfeldt-Jakob disease: Prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein
ANNALS OF NEUROLOGY
Drosophila choline acetyltransferase temperature-sensitive mutants
NEUROCHEMICAL RESEARCH
Urocortin expression in the human central nervous system
CLINICAL ENDOCRINOLOGY
Increased 9,13-di-cis-retinoic acid in rat hepatic fibrosis: implication for a potential link between retinoid loss and TGF-beta mediated fibrogenesis in vivo
JOURNAL OF HEPATOLOGY
An inherited prion disease with a PrPP105L mutation - Clinicopathologic and PrP heterogeneity
NEUROLOGY
Wernicke encephalopathy-like symptoms as an early manifestation of Creutzfeldt-Jakob disease in a chronic alcoholic
JOURNAL OF THE NEUROLOGICAL SCIENCES
Molecular structure of dichloroacetaldehyde oxime by gas-phase electron diffraction combined with microwave spectroscopy
JOURNAL OF MOLECULAR STRUCTURE
Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting
ARCHIVES OF NEUROLOGY
Interaction of aluminum with PHF tau in Alzheimer's disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method
AMERICAN JOURNAL OF PATHOLOGY
Variant Gerstman-Straussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles
ACTA NEUROPATHOLOGICA
ON PUISEUX EXPANSION OF APPROXIMATE EIGENVALUES AND EIGENVECTORS
IEICE transactions on fundamentals of electronics, communications and computer science
COMPUTATION OF PRIMARY DECOMPOSITION WITH THE ZEROS OF AN IDEAL
IEICE transactions on fundamentals of electronics, communications and computer science
CODON-219 LYS ALLELE OF PRNP IS NOT FOUND IN SPORADIC CREUTZFELDT-JAKOB-DISEASE
Annals of neurology
PROTECTIVE PRION PROTEIN POLYMORPHISMS AGAINST SPORADIC CREUTZFELDT-JAKOB-DISEASE
Lancet
Molecular mechanism of a cross-talk between estrogen and growth-factor signaling pathways
ONCOLOGY
STRUCTURE AND ORGANIZATION OF THE DROSOPHILA CHOLINERGIC LOCUS
The Journal of biological chemistry
POTENT NOVEL NONSTEROIDAL ANDROGEN ANTAGONISTS WITH A PHTHALIMIDE SKELETON
Bioorganic & medicinal chemistry letters
HMB-45 AND TUBERIN IN HAMARTOMAS ASSOCIATED WITH TUBEROUS SCLEROSIS
Modern pathology
DURING SCRAPIE PRION PROPAGATION PROTEIN-X BINDS A DISCONTINUOUS EPITOPE ON THE CELLULAR PRION PROTEIN
Annals of neurology
THE HUMAN PRION DISEASES - FROM NEUROPATHOLOGY TO PATHOBIOLOGY AND MOLECULAR-GENETICS - FINAL REPORT OF AN EU CONCERTED ACTION
Neuropathology and applied neurobiology
AMYLOID BETA-PROTEIN (A-BETA) 1-40 BUT NOT A-BETA-1-42 CONTRIBUTES TOTHE EXPERIMENTAL FORMATION OF ALZHEIMER-DISEASE AMYLOID FIBRILS IN FAAT BRAIN
The Journal of neuroscience
TYPING PRION ISOFORMS
Nature
A JAPANESE FAMILY WITH A VARIANT OF GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE
Journal of Neurology, Neurosurgery and Psychiatry
UROCORTIN EXPRESSION IN HUMAN PITUITARY-GLAND AND PITUITARY-ADENOMA
The Journal of clinical endocrinology and metabolism
EFFECT OF DIMERIZATION OF THE D-GLUCOSE ANALOG OF MURAMYL DIPEPTIDE ON STIMULATION OF MACROPHAGE-LIKE CELLS
Carbohydrate research
ERC-55, A BINDING-PROTEIN FOR THE PAPILLOMA-VIRUS E6 ONCOPROTEIN, SPECIFICALLY INTERACTS WITH VITAMIN-D-RECEPTOR AMONG NUCLEAR RECEPTORS
Biochemical and biophysical research communications
EXPRESSION OF NEUROFIBROMATOSIS-2 PROTEIN IN HUMAN BRAIN-TUMORS - AN IMMUNOHISTOCHEMICAL STUDY
Acta Neuropathologica
THALAMIC FORM OF CREUTZFELDT-JAKOB-DISEASE OR FATAL INSOMNIA - REPORTOF A SPORADIC CASE WITH NORMAL PRION PROTEIN GENOTYPE
Acta Neuropathologica
IMMUNOHISTOLOGICAL EVALUATION OF CREUTZFELDT-JAKOB-DISEASE WITH REFERENCE TO THE TYPE PRPRES DEPOSITION
Clinical neuropathology
INTRON RETENTION GENERATES A NOVEL ISOFORM OF THE MURINE VITAMIN-D-RECEPTOR THAT ACTS IN A DOMINANT-NEGATIVE WAY ON THE VITAMIN-D SIGNALINGPATHWAY
Molecular and cellular biology
PUBLIC-HEALTH ISSUES AND CLINICAL AND NEUROLOGICAL CHARACTERISTICS OFTHE NEW VARIANT OF CREUTZFELDT-JAKOB-DISEASE AND OTHER HUMAN AND ANIMAL TRANSMISSIBLE SPONGIFORM ENCEPHALOPATHIES - MEMORANDUM FROM 2 WHO MEETINGS
Bulletin of the World Health Organization
FATAL FAMILIAL INSOMNIA WITH A MUTATION AT CODON-178 OF THE PRION PROTEIN GENE - FIRST REPORT FROM JAPAN
Neurology
EXPERIMENTAL TRANSMISSION OF CREUTZFELDT-JAKOB-DISEASE AND RELATED DISEASES TO RODENTS
Neurology
VASCULAR VARIANT OF PRION PROTEIN CEREBRAL AMYLOIDOSIS WITH TAU-POSITIVE NEUROFIBRILLARY TANGLES - THE PHENOTYPE OF THE STOP CODON-145 MUTATION IN PRNP
Proceedings of the National Academy of Sciences of the United Statesof America
A JAPANESE CASE OF CREUTZFELDT-JAKOB-DISEASE WITH A POINT MUTATION INTHE PRION PROTEIN GENE AT CODON-210
Journal of the neurological sciences
DIFFERENTIAL REGULATION OF CHOLINE-ACETYLTRANSFERASE EXPRESSION IN ADULT DROSOPHILA-MELANOGASTER BRAIN
Journal of neurobiology
HUMANIZED PRION PROTEIN KNOCK-IN BY CRE-INDUCED SITE-SPECIFIC RECOMBINATION IN THE MOUSE
Biochemical and biophysical research communications
MUTATION IN THE PRION PROTEIN GENE AT CODON-232 IN JAPANESE PATIENTS WITH CREUTZFELDT-JAKOB-DISEASE - A CLINICOPATHOLOGICAL, IMMUNOHISTOCHEMICAL AND TRANSMISSION STUDY
Acta Neuropathologica
THE ORIGINAL GERSTMANN-STRAUSSLER-SCHEINKER FAMILY OF AUSTRIA - DIVERGENT CLINICOPATHOLOGICAL PHENOTYPES BUT CONSTANT PRP GENOTYPE
Brain pathology
INHERITED PRION DISEASES AND TRANSMISSION TO RODENTS
Brain pathology
ALLELIC VARIATION OF APOLIPOPROTEIN-E IN JAPANESE SPORADIC CREUTZFELDT-JAKOB-DISEASE PATIENTS
Neuroscience letters
LOCALIZATION OF CHOLINE ACETYLTRANSFERASE-EXPRESSING NEURONS IN THE LARVAL VISUAL-SYSTEM OF DROSOPHILA-MELANOGASTER
Cell and tissue research
A POU HOMEO DOMAIN PROTEIN RELATED TO DPOU-19 PDM-1 BINDS TO THE REGULATORY DNA NECESSARY FOR VITAL EXPRESSION OF THE DROSOPHILA CHOLINE-ACETYLTRANSFERASE GENE/
The Journal of neuroscience
NEW VARIANT PRION PROTEIN IN A JAPANESE FAMILY WITH GERSTMANN-STRAUSSLER SYNDROME
Molecular brain research
APOLIPOPROTEIN-E IN CREUTZFELDT-JAKOB-DISEASE
Lancet
ACTIVATION OF THE ESTROGEN-RECEPTOR THROUGH PHOSPHORYLATION BY MITOGEN-ACTIVATED PROTEIN-KINASE
Science
SERIAL MRI IN EARLY CREUTZFELDT-JACOB DISEASE WITH A POINT MUTATION OF PRION PROTEIN AT CODON-180
Neuroradiology
FIRST EXPERIMENTAL TRANSMISSION OF FATAL FAMILIAL INSOMNIA
Nature
PRION PROTEIN AMYLOID ANGIOPATHY AND ALZHEIMER NEUROFIBRILLARY TANGLES IN PRNP STOP CODON-145
Journal of neuropathology and experimental neurology
REGULATION OF CHOLINE ACETYLTRANSFERASE LACZ FUSION GENE-EXPRESSION IN PUTATIVE CHOLINERGIC NEURONS OF DROSOPHILA-MELANOGASTER/
Journal of neurobiology
IMMUNOCYTOCHEMICAL STUDY OF CHOLINE-ACETYLTRANSFERASE IN DROSOPHILA-MELANOGASTER - AN ANALYSIS OF CIS-REGULATORY REGIONS CONTROLLING EXPRESSION IN THE BRAIN OF CDNA-TRANSFORMED FLIES
Journal of comparative neurology
PRION DISEASE WITH 144-BASE-PAIR INSERTION IN A JAPANESE FAMILY LINE
Acta Neuropathologica
HUMAN PRION DISEASES WITH VARIANT PRION PROTEIN
Philosophical transactions-Royal Society of London. Biological sciences
PRP GENE-MUTATIONS AND SUBTYPES OF HEREDITARY PRION
Neurobiology of aging
CREUTZFELDT-JAKOB-DISEASE TRANSMITTED BY A CADAVERIC DURA-MATER GRAFT
Neurosurgery
JAPANESE FAMILY WITH CREUTZFELDT-JAKOB-DISEASE WITH CODON-200 POINT MUTATION OF THE PRION PROTEIN GENE
Neurology
A VARIANT OF GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE CARRYING CODON-105 MUTATION WITH CODON-129 POLYMORPHISM OF THE PRION PROTEIN GENE - A CLINICOPATHOLOGICAL STUDY
Journal of the neurological sciences
TNF-BETA PRODUCED BY HUMAN T-LYMPHOTROPIC VIRUS TYPE I-INFECTED CELLSINFLUENCES THE PROLIFERATION OF HUMAN ENDOTHELIAL-CELLS AND FIBROBLASTS
The Journal of immunology
DETECTION OF HUMAN T-LYMPHOTROPHIC VIRUS TYPE-I (HTLV-I) PROVIRAL DNAAND ANALYSIS OF T-CELL RECEPTOR V-BETA CDR3 SEQUENCES IN SPINAL-CORD LESIONS OF HTLV-I-ASSOCIATED MYELOPATHY TROPICAL SPASTIC PARAPARESIS/
The Journal of experimental medicine
AN EXON-8-SPLICED OUT TRANSCRIPT OF NEUROFIBROMATOSIS-2 GENE IS CONSTITUTIVELY EXPRESSED IN VARIOUS HUMAN TISSUES
Journal of Biochemistry
SYNTHESIS OF 9E-LOCKED AND 9Z-LOCKED RETINOIC ACID ANALOGS AS LIGANDSFOR RAR AND RXR
Chemical and Pharmaceutical Bulletin
MIB1 STAINING INDEX AND SCORING OF HISTOLOGIC FEATURES IN MENINGIOMA - INDICATORS FOR THE PREDICTION OF BIOLOGIC POTENTIAL AND POSTOPERATIVE MANAGEMENT
Cancer
DISTRIBUTION OF PRION PROTEIN IN GERMAN PATIENTS WITH CREUTZFELDT-JAKOB-DISEASE IS DIFFERENT FROM THAT IN JAPANESE PATIENTS
Acta Neuropathologica
A NEW INHERITED PRION DISEASE (PRP-P105L MUTATION) SHOWING SPASTIC PARAPARESIS
Annals of neurology
ALZHEIMERS AMYLOID PRECURSOR PROTEIN MESSENGER-RNA WITHOUT EXON-15 ISUBIQUITOUSLY EXPRESSED EXCEPT IN THE RAT CENTRAL-NERVOUS-SYSTEM
Molecular brain research
IMMUNOHISTOCHEMICAL DISTRIBUTION OF AMYLOID PRECURSOR PROTEIN DURING NORMAL RAT DEVELOPMENT
Developmental brain research
A MISSENSE MUTATION AT CODON-105 WITH CODON-129 POLYMORPHISM OF THE PRION PROTEIN GENE IN A NEW VARIANT OF GERSTMANN-STRAUSSLER-SCHEINKER DISEASE
Neurology
SPECIES BARRIER PREVENTS AN ABNORMAL ISOFORM OF PRION PROTEIN FROM ACCUMULATING IN FOLLICULAR DENDRITIC CELLS OF MICE WITH CREUTZFELDT-JAKOB-DISEASE
Journal of virology
DOUBLE MUTATIONS AT CODON 180 AND CODON 232 OF THE PRNP GENE IN AN APPARENTLY SPORADIC CASE OF CREUTZFELDT-JAKOB-DISEASE
Journal of the neurological sciences
THE RAT CENTRAL-NERVOUS-SYSTEM EXPRESSES ALZHEIMERS AMYLOID PRECURSORPROTEIN APP(695), BUT NOT APP(677) (L-APP FORM)
Journal of neurochemistry
INTESTINAL PSEUDOOBSTRUCTION IN PATIENTS WITH AMYLOIDOSIS - CLINICOPATHOLOGICAL DIFFERENCES BETWEEN CHEMICAL TYPES OF AMYLOID PROTEIN
Gut
DEVELOPMENTS IN DIAGNOSIS FOR PRION DISEASES
British Medical Bulletin
AN AMBER MUTATION OF PRION PROTEIN IN GERSTMANN-STRAUSSLER SYNDROME WITH MUTANT PRP PLAQUES
Biochemical and biophysical research communications
ACCUMULATION OF ABNORMAL PRION PROTEIN IN MICE INFECTED WITH CREUTZFELDT-JAKOB-DISEASE VIA INTRAPERITONEAL ROUTE - A SEQUENTIAL STUDY
The American journal of pathology
WIDESPREAD DISTRIBUTION OF TAU IN THE ASTROCYTIC ELEMENTS OF GLIAL TUMORS
Acta Neuropathologica