Isoform pattern of 14-3-3 proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.

scientific article published in December 1999

Isoform pattern of 14-3-3 proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1046/J.1471-4159.1999.0732485.X
P698PubMed publication ID10582609
P5875ResearchGate publication ID12717908

P50authorMarkus OttoQ67390357
Johannes KornhuberQ17068400
Jens WiltfangQ42165310
P2093author name stringKretzschmar HA
Poser S
Zerr I
Steinacker P
Rüther E
Bodemer M
Aitken A
Bahn E
Baxter HC
P2860cites workDiagnostic criteria for sporadic Creutzfeldt-Jakob diseaseQ48934056
Antibodies against the major brain isoforms of 14-3-3 protein. An antibody specific for the N-acetylated amino-terminus of a protein.Q54649952
S-100 protein concentration in the cerebrospinal fluid of patients with Creutzfeldt-Jakob diseaseQ57274052
Diagnosis of Creutzfeldt-Jakob disease by two-dimensional gel electrophoresis of cerebrospinal fluidQ57274061
Elevated levels of tau-protein in cerebrospinal fluid of patients with Creutzfeldt–Jakob diseaseQ57781094
???Q56882731
Molecular cloning and expression of the transformation sensitive epithelial marker stratifin. A member of a protein family that has been involved in the protein kinase C signalling pathwayQ24309598
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4Q25938983
Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's DiseaseQ27860795
Novel proteinaceous infectious particles cause scrapieQ29547678
Diagnosis of Creutzfeldt-Jakob disease by measurement of S100 protein in serum: prospective case-control studyQ33754628
A new variant of Creutzfeldt-Jakob disease in the UK.Q34374893
A cellular gene encodes scrapie PrP 27-30 proteinQ34557641
14-3-3 proteins: a highly conserved, widespread family of eukaryotic proteinsQ35624026
Epidemiology of Creutzfeldt-Jakob diseaseQ40730013
Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clusteringQ41015587
Association of 14-3-3 proteins with centrosomesQ42817925
The assay development of a molecular marker for transmissible spongiform encephalopathies.Q45930864
Use of cerebrospinal fluid levels of 14-3-3 in predicting neurodegeneration in confirmed BSE symptomatic cattleQ47706321
14-3-3 and its possible role in co-ordinating multiple signalling pathwaysQ47986680
Purification of 14-3-3 protein and analysis of isoforms in chicken brain.Q48087654
Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted diseaseQ48126727
Protein kinase C inhibitor proteins. Purification from sheep brain and sequence similarity to lipocortins and 14-3-3 proteinQ48259445
Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples.Q48297442
A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathiesQ48480572
Detection of 14-3-3 protein in the cerebrospinal fluid supports the diagnosis of Creutzfeldt-Jakob diseaseQ48550821
The 14-3-3 brain protein in cerebrospinal fluid as a marker for transmissible spongiform encephalopathiesQ48913771
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectcerebrospinal fluidQ54196
patientQ181600
P304page(s)2485-2490
P577publication date1999-12-01
P1433published inJournal of NeurochemistryQ6295643
P1476titleIsoform pattern of 14-3-3 proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease.
P478volume73

Reverse relations

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