PRND gene

Known as: DPL, prion-like protein doppel, PrPLP 
 
National Institutes of Health

Papers overview

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Highly Cited
2012
Highly Cited
2012
BACKGROUND Varying concentrations of blood components in platelet-rich plasma preparations may contribute to the variable results… (More)
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2012
2012
Article history: Received 13 October 2010 Received in revised form 12 February 2012 Accepted 10 March 2012 Available online 15… (More)
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Highly Cited
2007
Highly Cited
2007
The cellular prion protein, PrP(C), is neuroprotective in a number of settings and in particular prevents cerebellar degeneration… (More)
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2007
2007
The paper describes the implementation of a 380 MHz, 13 bit, direct digital synthesizer/mixer IC in 0.25mum CMOS technology. The… (More)
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Review
2005
Review
2005
DP (dipeptidyl peptidase) IV is the archetypal member of its six-member gene family. Four members of this family, DPIV, FAP… (More)
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Highly Cited
2005
Highly Cited
2005
While a beta-sheet-rich form of the prion protein (PrPSc) causes neurodegeneration, the biological activity of its precursor, the… (More)
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2003
2003
Disease-related amyloidogenic propensity has been unexpectedly found in proteins driven to adopt a monomeric uncomplexed state at… (More)
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Highly Cited
2002
Highly Cited
2002
The prion protein is a highly conserved glycoprotein expressed most highly in the synapse. Evidence has recently been put forward… (More)
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Highly Cited
2001
Highly Cited
2001
PrP knockout mice in which only the open reading frame was disrupted ('Zürich I') remained healthy. However, more extensive… (More)
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Highly Cited
1999
Highly Cited
1999
The novel locus Prnd is 16 kb downstream of the mouse prion protein (PrP) gene Prnp and encodes a 179 residue PrP-like protein… (More)
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