<p>(A) Schematic showing the GFPu construct under control of the mouse prion promoter (PrP). GFPu protein is composed of GFP appended with a 16 amino acid C-terminal degradation signal, the CL-1 degron. (B) Western blot analysis and densitomeric quantification reveals no increase in steady-state levels of GFPu in 12 week R6/2 brains. α-tubulin was used as a loading control. (C) Expression of the GFPu transgene is unchanged in the 12-week-old R6/2 brain. Error bars represent the standard error of the mean.</p
The human cellular prion protein (PrPC) is a glycosylphosphatidylinositol (GPI) anchored membrane gl...
<p>Animals of the indicated genotypes were sacrificed at 10 weeks. Histological staining, order of i...
The prion protein has been implicated in a number of neurodegenerative diseases of the transmissible...
<p>Immunofluorescent staining of brain sections with anti-GFP antibody followed by quantitation of f...
<p>(A) The PrP protein coding sequence was replaced with GFP protein coding sequence. Rectangles rep...
(A) Representative blot of PrPGPIThy-1 L150 (generated for infection experiments) and WTPrPC mouse b...
<p>Though the transcript levels of pan-Gfap increase throughout development (p = 0.001, Oneway ANOVA...
Some prion protein mutations create anchorless molecules that cause Gerstmann–Sträussler–Scheinker (...
<p>At day 0, undifferentiated ALS-iPS-1 (A), C57-iPS-12 (B) and E14 (C) did not express GFP. GFP exp...
The conversion of the cellular prion protein (PrP(C)) to an abnormal and protease-resistant isoform ...
AbstractGlial fibrillary acidic protein (GFAP) is an intermediate filament protein specifically expr...
<p>(A) Western blot of APP and PrP<sup>C</sup> (antibody 6D11) in I5 (n = 3) and J20 (n = 2) transge...
<p>(A) In uninfected brains, GFP is observed in astrocyte-shaped cells, which are GFAP+ (B, C). In o...
We analyzed the relationship between pathogenic protein expression and perturbations to brain anatom...
<p>BrdU (100 mg/kg at E13.5) and GFP labeling in the cortex of P0 <i>Fgfr1<sup>f/f</sup>;Gad67-GFP+<...
The human cellular prion protein (PrPC) is a glycosylphosphatidylinositol (GPI) anchored membrane gl...
<p>Animals of the indicated genotypes were sacrificed at 10 weeks. Histological staining, order of i...
The prion protein has been implicated in a number of neurodegenerative diseases of the transmissible...
<p>Immunofluorescent staining of brain sections with anti-GFP antibody followed by quantitation of f...
<p>(A) The PrP protein coding sequence was replaced with GFP protein coding sequence. Rectangles rep...
(A) Representative blot of PrPGPIThy-1 L150 (generated for infection experiments) and WTPrPC mouse b...
<p>Though the transcript levels of pan-Gfap increase throughout development (p = 0.001, Oneway ANOVA...
Some prion protein mutations create anchorless molecules that cause Gerstmann–Sträussler–Scheinker (...
<p>At day 0, undifferentiated ALS-iPS-1 (A), C57-iPS-12 (B) and E14 (C) did not express GFP. GFP exp...
The conversion of the cellular prion protein (PrP(C)) to an abnormal and protease-resistant isoform ...
AbstractGlial fibrillary acidic protein (GFAP) is an intermediate filament protein specifically expr...
<p>(A) Western blot of APP and PrP<sup>C</sup> (antibody 6D11) in I5 (n = 3) and J20 (n = 2) transge...
<p>(A) In uninfected brains, GFP is observed in astrocyte-shaped cells, which are GFAP+ (B, C). In o...
We analyzed the relationship between pathogenic protein expression and perturbations to brain anatom...
<p>BrdU (100 mg/kg at E13.5) and GFP labeling in the cortex of P0 <i>Fgfr1<sup>f/f</sup>;Gad67-GFP+<...
The human cellular prion protein (PrPC) is a glycosylphosphatidylinositol (GPI) anchored membrane gl...
<p>Animals of the indicated genotypes were sacrificed at 10 weeks. Histological staining, order of i...
The prion protein has been implicated in a number of neurodegenerative diseases of the transmissible...