نتایج جستجو برای: prnp

تعداد نتایج: 934  

Journal: :The New England journal of medicine 2009
Simon Mead Jerome Whitfield Mark Poulter Paresh Shah James Uphill Tracy Campbell Huda Al-Dujaily Holger Hummerich Jon Beck Charles A Mein Claudio Verzilli John Whittaker Michael P Alpers John Collinge

BACKGROUND Kuru is a devastating epidemic prion disease that affected a highly restricted geographic area of the Papua New Guinea highlands; at its peak, it predominantly affected adult women and children of both sexes. Its incidence has steadily declined since the cessation of its route of transmission, endocannibalism. METHODS We performed genetic and selected clinical and genealogic assess...

2012
Guangai Xue Yoko Aida Takashi Onodera Akikazu Sakudo

Transcription factors regulate gene expression by controlling the transcription rate. Some genes can repress their own expression to prevent over production of the corresponding protein, although the mechanism and significance of this negative feedback regulation remains unclear. In the present study, we describe negative feedback regulation of the bovine prion protein (PrP) gene PRNP in Japane...

2017
Timm Konold Laura J Phelan Ben R Donnachie Melanie J Chaplin Saira Cawthraw Lorenzo González

BACKGROUND A study to investigate transmission of classical scrapie via goat milk was carried out in sheep: firstly, lambs were challenged orally with goat scrapie brain homogenate to confirm transmission of scrapie from goats to sheep. In the second study phase, milk from scrapie-infected goats was fed to lambs. Lambs were selected according to their prion protein gene (PRNP) genotype, which w...

Journal: :Archives of neurology 2000
S Collins A Boyd A Fletcher K Byron C Harper C A McLean C L Masters

BACKGROUND The transmissible spongiform encephalopathies constitute a fascinating and biologically unique group of invariably fatal neurodegenerative disorders that affect both animals and humans. Creutzfeldt-Jakob disease (CJD), Gerstmann-Straussler-Scheinker syndrome, and fatal familial insomnia represent the more common human phenotypes. Excluding the small number of iatrogenically transmitt...

2015
Gaik-Siew Ch’ng Seong Soo A An Sun Oh Bae Eva Bagyinszky SangYun Kim

Alzheimer's disease (AD) is the most common form of dementia, which can be categorized into two main forms: early onset AD and late onset AD. The genetic background of early onset AD is well understood, and three genes, the APP, PSEN1, and PSEN2 have been identified as causative genes. In the current study, we tested three siblings from Malaysia who were diagnosed with early onset dementia, as ...

2007
Vilma Regina Martins Hélio Rodrigues Gomes Leila Chimelli Sergio Rosemberg Michele Christine Landemberger

The emergence of the new variant of Creutzfeldt-Jakob disease (vCJD) in the United Kingdom has raised concerns over the risks of this prion disease in other parts of the world. Since 2005, human prion diseases have been under compulsory notification in Brazil. It is well known that some polymorphisms within the cellular prion gene (PRNP) have been associated to a higher susceptibility to sporad...

Journal: :Journal of virology 2012
Kevin C Gough Claire A Baker Helen C Rees Linda A Terry John Spiropoulos Leigh Thorne Ben C Maddison

Preclinical sheep with the highly scrapie-susceptible VRQ/VRQ PRNP genotype secrete prions from the oral cavity. In order to further understand the significance of orally available prions, buccal swabs were taken from sheep with a range of PRNP genotypes and analyzed by serial protein misfolding cyclic amplification (sPMCA). Prions were detected in buccal swabs from scrapie-exposed sheep of gen...

2009
Simon Mead Mark Poulter James Uphill John Beck Jerome Whitfield Thomas EF Webb Tracy Campbell Gary Adamson Pelagia Deriziotis Sarah J Tabrizi Holger Hummerich Claudio Verzilli Michael P Alpers John C Whittaker John Collinge

BACKGROUND Human and animal prion diseases are under genetic control, but apart from PRNP (the gene that encodes the prion protein), we understand little about human susceptibility to bovine spongiform encephalopathy (BSE) prions, the causal agent of variant Creutzfeldt-Jakob disease (vCJD). METHODS We did a genome-wide association study of the risk of vCJD and tested for replication of our f...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Ryan J Monello Nathan L Galloway Jenny G Powers Sally A Madsen-Bouterse William H Edwards Mary E Wood Katherine I O'Rourke Margaret A Wild

Pathogens can exert a large influence on the evolution of hosts via selection for alleles or genotypes that moderate pathogen virulence. Inconsistent interactions between parasites and the host genome, such as those resulting from genetic linkages and environmental stochasticity, have largely prevented observation of this process in wildlife species. We examined the prion protein gene (PRNP) in...

2017
Gui-Ru Wu Tian-Chen Mu Zhen-Xing Gao Jun Wang Man-Sun Sy Chao-Yang Li

The expression of normal cellular prion protein (PrP) is required for the pathogenesis of prion diseases. However, the physiological functions of PrP remain ambiguous. Here, we identified PrP as being critical for tumor necrosis factor (TNF) α-triggered signaling in a human melanoma cell line, M2, and a pancreatic ductal cell adenocarcinoma cell line, BxPC-3. In M2 cells, TNFα up-regulates the ...

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