Results 111 to 120 of about 6,019 (214)

Precursor ion scanning for detection and structural characterization of heterogeneous glycopeptide mixtures

, 2002
The structure of N-linked glycans is determined by a complex, anabolic, intracellular pathway but the exact role of individual glycans is not always clear.
Gill, A C, Lilley, Kathryn, Ritchie, Mark A, Deery, Michael J, Lilley, K, Gill, Andrew C, Ritchie, M A, Deery, M J   +7 more
core   +1 more source

Human transmissible spongiform encephalopathy: Case report

Iatreia, 2014
We report the case of a 64 year-old woman with motor and cognitive deterioration that progressed rapidly during eight months. She was unsuccessfully treated with quinacrine, and died in a terminal status, by septic shock secondary to bronchopneumonia by ...
Duque Velásquez, Camilo , Garzón Álzate, Ánderson , Villegas Lanau, Andrés , Escobar Velásquez, Laura Marcela , Zea Lopera, Julián , Lopera, Francisco , Rodas González, Juan David   +6 more
doaj  

Final results of project on feline spongiform encephalopathy [PDF]

, 2006
Feline spongiform encephalopathy (FSE) is a transmissible spongiform encephalopathy associated with the accumulation of an abnormal isoform of the prion protein (PrPsc) in the Central Nervous System.
Perazzini, Alice Zaira, Cantile, Carlo, Porcario, Chiara, Casalone, Cristina, Castagnaro, Massimo, Loria, Ruggero Giudo, Mandara, Maria Teresa, Caramelli, Maria, Ligios, Ciriaco, Iulini, Barbara   +9 more
core   +1 more source

Prion protein PrP nucleic acid binding and mobilization implicates retroelements as the replicative component of transmissible spongiform encephalopathy. [PDF]

Arch Virol, 2020
Lathe R, Darlix JL.
europepmc   +1 more source

Proteins as markers of TSE infection in sheep blood

, 2008
Transmissible spongiform encephalopathies (TSEs) are a group of fatal infectious neurodegenerative diseases affecting both humans and agricultural animals. TSE transmission via blood transfusion has been demonstrated experimentally in rodent, primate and
Martin, Joanne
core  

PrP-C1 fragment in cattle brains reveals features of the transmissible spongiform encephalopathy associated PrP(sc).

, 2017
Three different types of bovine spongiform encephalopathy (BSE) are known and supposedly caused by distinct prion strains: the classical (C-) BSE type that was typically found during the BSE epidemic, and two relatively rare atypical BSE types, termed H ...
Serra, Fabienne Heirangi, Seuberlich, Torsten, Lüthi, Ramona, Czub, Stefanie, Gray, John, Müller, Joachim, Dudas, Sandor   +6 more
core   +1 more source

Transmissible spongiform encephalopathies [PDF]

Journal of Medical Microbiology, 1995
openaire   +2 more sources

Efficient transmission and characterization of creutzfeldt-jakob disease strains in bank voles.

, 2006
Transmission of prions between species is limited by the "species barrier," which hampers a full characterization of human prion strains in the mouse model.
Bari Michele A. Di, Boyle, Aileen, Lipp Hans-Peter, Gabriele Vaccari, Maurizio Pocchiari, Cardone Franco, Sbriccoli Marco, Claudia Cartoni, Sbriccoli, Marco, Boyle Aileen, Dell'Omo, Giacomo, Nonno, Romolo, Di Bari, Michele A, Nonno Romolo, Franco Cardone, Galeno, Roberta, Marco Sbriccoli, Paola Fazzi, Vaccari Gabriele, Cartoni, Claudia, Cardone, Franco, Galeno Roberta, Loredana Ingrosso, Roberta Galeno, Fazzi, Paola, Lipp, Hans-Peter, Fazzi Paola, Michele A Di Bari, Ingrosso Loredana, Hans-Peter Lipp, Ingrosso, Loredana, Pocchiari, Maurizio, Umberto Agrimi, Pocchiari Maurizio, Vaccari, Gabriele, Agrimi, Umberto, Giacomo Dell'Omo, Moira Bruce, Aileen Boyle, Dell'Omo Giacomo, Agrimi Umberto, Bruce Moira, Bruce, Moira, Romolo Nonno, Cartoni Claudia   +44 more
core   +1 more source

Prion Seeding Activity in Plant Tissues Detected by RT-QuIC

Pathogens
Prion diseases such as scrapie, bovine spongiform encephalopathy (BSE), and chronic wasting disease (CWD) affect domesticated and wild herbivorous mammals. Animals afflicted with CWD, the transmissible spongiform encephalopathy of cervids (deer, elk, and
Kate Burgener, Stuart Siegfried Lichtenberg, Daniel P. Walsh, Heather N. Inzalaco, Aaron Lomax, Joel A. Pedersen   +5 more
doaj   +1 more source

The 37kDa/67kDa laminin receptor as a therapeutic target in prion diseases: potency of antisense LRP RNA, siRNAs specific for LRP mRNA and a LRP decoy mutant [PDF]

, 2006
Prion diseases are a group of rare, fatal neurodegenerative diseases, also known as transmissible spongiform encephalopathies (TSEs), that affect both animals and humans and include bovine spongiform encephalopathy (BSE) in cattle, scrapie in sheep ...
Vana, Karen
core