نتایج جستجو برای: ژن prnp

تعداد نتایج: 16699  

2008
Emmanuelle Uro-Coste Hervé Cassard Stéphanie Simon Séverine Lugan Jean-Marc Bilheude Armand Perret-Liaudet James W. Ironside Stéphane Haik Christelle Basset-Leobon Caroline Lacroux Katell Peoch' Nathalie Streichenberger Jan Langeveld Mark W. Head Jacques Grassi Jean-Jacques Hauw Francois Schelcher Marie Bernadette Delisle Olivier Andréoletti

Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently subclassified according to the methionine/valine polymorphism at codon 129 of the PRNP gene and the proteinase K (PK) digested abnormal prion protein (PrPres)identified on Western blotting (type 1 or type 2). These biochemically distinct PrPres types have been considered to represent potential distinct prion strains. However, since c...

Journal: :Annals of neurology 2001
A Plaitakis A K Viskadouraki M Tzagournissakis I Zaganas S Verghese-Nikolakaki V Karagiorgis I Panagiotides C Kilindireas E Patsouris C Haberler H Budka T Sklaviadis

Since the spring of 1997, when the Neurology Department of the University Hospital of Crete admitted its first patient, nine cases (eight neuropathologically confirmed and one probable) of sporadic Creutzfeldt-Jakob disease (sCJD) have been recorded. This represents an annual incidence five-fold higher than expected based on the island's population (0.54 million). Molecular analysis of the prio...

2010
Matteo Busconi Corrado Fogher

In animals the prion disease includes sheep and goat scrapie and the bovine spongiform encephalopathy (BSE). While several polymorphisms of the prion (PRNP) gene have been identified in sheep and some of them have been associated with susceptibility to scrapie, few mutations are reported in cattle and no correlation with BSE have been demonstrated. Genetic screening for mutants in the PRNP gene...

2013
Bartholomew J. Naughton F. Jason Duncan Darren Murrey Tierra Ware Aaron Meadows Douglas M. McCarty Haiyan Fu

Mucopolysaccharidosis (MPS) IIIB is a devastating neuropathic lysosomal storage disease with complex pathology. This study identifies molecular signatures in peripheral blood that may be relevant to MPS IIIB pathogenesis using a mouse model. Genome-wide gene expression microarrays on pooled RNAs showed dysregulation of 2,802 transcripts in blood from MPS IIIB mice, reflecting pathological compl...

Journal: :The Journal of general virology 2003
Rona M Barron Val Thomson Declan King Jane Shaw David W Melton Jean C Manson

The PrP protein is central to the transmissible spongiform encephalopathies (TSEs), and the amino acid sequence of this protein in the host can influence both incubation time of disease and targeting of disease pathology. The N terminus of murine PrP has been proposed to be important in the replication of TSE agents, as mutations or deletions in that region can alter the efficiency of agent rep...

Journal: :American journal of nuclear medicine and molecular imaging 2016
Kacie D Deters Shannon L Risacher Karmen K Yoder Adrian L Oblak Frederick W Unverzagt Jill R Murrell Francine Epperson Eileen F Tallman Kimberly A Quaid Martin R Farlow Andrew J Saykin Bernardino Ghetti

Gerstmann-Sträussler-Scheinker Disease (GSS) is a familial neurodegenerative disorder characterized clinically by ataxia, parkinsonism, and dementia, and neuropathologically by deposition of diffuse and amyloid plaques composed of prion protein (PrP). The purpose of this study was to evaluate if [(11)C]Pittsburgh Compound B (PiB) positron emission tomography (PET) is capable of detecting PrP-am...

Journal: :Human molecular genetics 2005
Andreas Papassotiropoulos M Axel Wollmer Adriano Aguzzi Christoph Hock Roger M Nitsch Dominique J-F de Quervain

Human cognitive processes are highly variable across individuals and are influenced by both genetic and environmental factors. Although genetic variations affect short-term memory in humans, it is unknown whether genetic variability has also an impact on long-term memory. Because prion-like conformational changes may be involved in the induction of long-lasting synaptic plasticity, we examined ...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2006
Josef Priller Marco Prinz Mathias Heikenwalder Nicolas Zeller Petra Schwarz Frank L Heppner Adriano Aguzzi

Prion neuroinvasion is accompanied by maximal activation of microglia, the significance of which for pathogenesis is unknown. Here, we used bone marrow (BM) cells expressing GFP (green fluorescent protein) to study the turnover of microglia in mouse scrapie. We found that >or=50% of all brain microglia were replaced by BM-derived cells before clinical disease onset. In terminally sick mice, mic...

Journal: :Clinical chemistry 2006
Ekkehard Schütz Melanie Scharfenstein Bertram Brenig

BACKGROUND Scrapie is the transmissible spongiform encephalopathy in sheep. Because genetic variants of the ovine PrP gene (PRNP) can be associated with disease risk, the European Union initiated programs to eradicate high-risk PRNP genotypes from sheep livestock. For this purpose, reliable and cost-effective genotyping is needed. METHODS We amplified DNA to cover the 3 risk codons in exon 3 ...

Journal: :Anticancer research 2016
Chul Won Yun Seungpil Yun Jun Hee Lee Yong-Seok Han Yeo Min Yoon Daniel An Sang Hun Lee

BACKGROUND The putative functions of the cellular prion protein (PrP(c)) are believed to be associated with cell signaling, differentiation, survival, and cancer progression. With respect to cancer development and progression, elevations and mutations of PrP(c) expression have been shown to increase the risk for malignancy and metastasis in breast and colorectal cancer. Since both natural suppl...

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