<p>PrP and 14-3-3 protein levels were analyzed in CSF samples obtained by lumbar puncture of 6 CJD patients (CJD-1 to CJD-6) at different time points during disease. Total protein content was assessed by Ponceau Red staining, the predominant band (albumin) is shown. The asterisk in samples from CJD-2, CJD-5 and CJD-6 indicates an additional PrP protein band detected between PrP band 1 and band 2.</p
Creutzfeldt-Jakob disease (CJD) belongs to a group of transmissible spongiform encephalopathies in w...
Every year, a large number of published studies present biomarkers for various neurological disorder...
Differential proteomic analysis has been performed on the cerebrospinal fluid (CSF) of six healthy a...
<p>CSF samples from CJD patients (N = 40) and non-CJD controls (N = 16), were obtained by lumbar pun...
<p>CSF samples from healthy control subjects (N = 3), CJD patients (N = 5), dementia patients (N = 3...
<p>CSF samples from CJD patients (N = 40) and non-CJD controls (N = 16), were obtained by lumbar pun...
<p><b>A.</b> The pattern of expression of PrP in two representative CSF samples (from one healthy co...
Cerebrospinal fluid (CSF) total prion protein (t-PrP) is decreased in sporadic Creutzfeldt-Jakob dis...
Creutzfeldt-Jakob disease (CJD) is the most frequent human Prion-related disorder (PrD). The detecti...
Creutzfeldt-Jakob disease (CJD) is the most frequent human Prion-related disorder (PrD). The detecti...
Cerebrospinal fluid (CSF) total prion protein (t-PrP) is decreased in sporadic Creutzfeldt-Jakob dis...
Creutzfeldt-Jakob disease (CJD) is the most frequent human Prion-related disorder (PrD). The detecti...
The clinical diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) is difficult, and reliable marke...
Creutzfeldt-Jakob disease (CJD) is a transmissible, fatal, neurodegenerative disease in humans. Rece...
(A) Western blots display the protein levels of four proteins PKM, CLU, KNG1 and PFN1 in N- and CSD-...
Creutzfeldt-Jakob disease (CJD) belongs to a group of transmissible spongiform encephalopathies in w...
Every year, a large number of published studies present biomarkers for various neurological disorder...
Differential proteomic analysis has been performed on the cerebrospinal fluid (CSF) of six healthy a...
<p>CSF samples from CJD patients (N = 40) and non-CJD controls (N = 16), were obtained by lumbar pun...
<p>CSF samples from healthy control subjects (N = 3), CJD patients (N = 5), dementia patients (N = 3...
<p>CSF samples from CJD patients (N = 40) and non-CJD controls (N = 16), were obtained by lumbar pun...
<p><b>A.</b> The pattern of expression of PrP in two representative CSF samples (from one healthy co...
Cerebrospinal fluid (CSF) total prion protein (t-PrP) is decreased in sporadic Creutzfeldt-Jakob dis...
Creutzfeldt-Jakob disease (CJD) is the most frequent human Prion-related disorder (PrD). The detecti...
Creutzfeldt-Jakob disease (CJD) is the most frequent human Prion-related disorder (PrD). The detecti...
Cerebrospinal fluid (CSF) total prion protein (t-PrP) is decreased in sporadic Creutzfeldt-Jakob dis...
Creutzfeldt-Jakob disease (CJD) is the most frequent human Prion-related disorder (PrD). The detecti...
The clinical diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) is difficult, and reliable marke...
Creutzfeldt-Jakob disease (CJD) is a transmissible, fatal, neurodegenerative disease in humans. Rece...
(A) Western blots display the protein levels of four proteins PKM, CLU, KNG1 and PFN1 in N- and CSD-...
Creutzfeldt-Jakob disease (CJD) belongs to a group of transmissible spongiform encephalopathies in w...
Every year, a large number of published studies present biomarkers for various neurological disorder...
Differential proteomic analysis has been performed on the cerebrospinal fluid (CSF) of six healthy a...