Our current understanding of prion biology and disease is largely based on studies performed on mammals, yet basic questions about the physiological function of prion proteins (PrPs) and the molecular nature of prion disorders remain elusive. To facilitate the establishment of non-mammalian models for prion research, we characterized the sequence, structural, and genomic homology between fish and other vertebrate PrPs, and analyzed the distinct molecular mechanisms that shaped the evolution of vertebrate PrP domains
International audienceThe prion protein (PrP) when misfolded into the pathogenic conformer PrPSc is ...
AbstractTransmissible spongiform encephalopathies (TSEs), otherwise known as prion disorders, are fa...
In the more than 20 years since its discovery, both the phylogenetic origin and cellular function of...
Recent findings of new genes in fish related to the prion protein (PrP) gene PRNP, including our rec...
Recent findings of new genes in fish related to the prion protein (PrP) gene PRNP, including our rec...
National audienceThe word prion (which stands for proteinaceous infectious agent) has originally bee...
Prion diseases are devastating neurological disorders caused by the propagation of particles contain...
Prion protein (PrP) sequences are until now available for only six of the 18 orders of placental mam...
© 2017 Bentham Science Publishers. More than thirty years have passed since the discovery of the pri...
The homologues of human disease genes are expected to contribute to better understanding of physiolo...
Among the diseases caused by protein misfolding is the family associated with the prion protein (PrP...
The prion protein (PrP) when misfolded into the pathogenic conformer PrPSc is the major causative ag...
The cellular prion protein PrPC is a ubiquitous GPI-anchored protein. While PrPC has been the focus ...
Prion disorders are a group of fatal neurodegenerative conditions of mammals. The key molecular even...
Prion protein (PrP) is best known for its involvement in prion diseases. A normal, dynamic isoform o...
International audienceThe prion protein (PrP) when misfolded into the pathogenic conformer PrPSc is ...
AbstractTransmissible spongiform encephalopathies (TSEs), otherwise known as prion disorders, are fa...
In the more than 20 years since its discovery, both the phylogenetic origin and cellular function of...
Recent findings of new genes in fish related to the prion protein (PrP) gene PRNP, including our rec...
Recent findings of new genes in fish related to the prion protein (PrP) gene PRNP, including our rec...
National audienceThe word prion (which stands for proteinaceous infectious agent) has originally bee...
Prion diseases are devastating neurological disorders caused by the propagation of particles contain...
Prion protein (PrP) sequences are until now available for only six of the 18 orders of placental mam...
© 2017 Bentham Science Publishers. More than thirty years have passed since the discovery of the pri...
The homologues of human disease genes are expected to contribute to better understanding of physiolo...
Among the diseases caused by protein misfolding is the family associated with the prion protein (PrP...
The prion protein (PrP) when misfolded into the pathogenic conformer PrPSc is the major causative ag...
The cellular prion protein PrPC is a ubiquitous GPI-anchored protein. While PrPC has been the focus ...
Prion disorders are a group of fatal neurodegenerative conditions of mammals. The key molecular even...
Prion protein (PrP) is best known for its involvement in prion diseases. A normal, dynamic isoform o...
International audienceThe prion protein (PrP) when misfolded into the pathogenic conformer PrPSc is ...
AbstractTransmissible spongiform encephalopathies (TSEs), otherwise known as prion disorders, are fa...
In the more than 20 years since its discovery, both the phylogenetic origin and cellular function of...