نتایج جستجو برای: ژن prnp

تعداد نتایج: 16699  

Journal: :Trends in genetics : TIG 2004
Martin Kreitman Anna Di Rienzo

Natural selection is expected to leave distinctive signatures on patterns of neutral variation that are tightly linked to a site carrying an advantageous mutation. This notion is the basis for molecular population genetics approaches to the analysis of adaptations in the human genome. In principle, this is an attractive prospect; in practice, several complications and challenges make it difficu...

2013
Paul Shapshak

Human prion brain disease has been studied intensely since 1920. Examples of such diseases include Creutzfeldt-Jakob disease (CJD), fatal familial insomnia, Gerstmann-StrausslerScheinker disease, and Kuru. Central in the epidemiology and pathogenesis of prion diseases is the prion protein itself and the gene for this protein resides on chromosome 12, at locus 20pterp12. The prion protein is ter...

Journal: :Journal of Alzheimer's disease : JAD 2016
Emanuela Oldoni Giorgio G Fumagalli Maria Serpente Chiara Fenoglio Marta Scarioni Andrea Arighi Giuseppe Bruno Giuseppina Talarico Annamaria Confaloni Paola Piscopo Benedetta Nacmias Sandro Sorbi Innocenzo Rainero Elisa Rubino Lorenzo Pinessi Giuliano Binetti Roberta Ghidoni Luisa Benussi Giulia Grande Beatrice Arosio Devan Bursey John S Kauwe Sara Mg Cioffi Marina Arcaro Daniela Mari Claudio Mariani Elio Scarpini Daniela Galimberti

The missense P39L variant in the prion protein gene (PRNP) has recently been associated with frontotemporal dementia (FTD). Here, we analyzed the presence of the P39L variant in 761 patients with FTD and 719 controls and found a single carrier among patients. The patient was a 67-year-old male, with a positive family history for dementia, who developed apathy, short term memory deficit, and pos...

2017
Yo Ching Cheng Marco Musiani Maria Cavedon Sabine Gilch

Chronic wasting disease (CWD) is a prion disease found in deer, elk and moose in North America and since recently, wild reindeer in Norway. Caribou are at-risk to encounter CWD in areas such as Alberta, Canada, where the disease spreads toward caribou habitats. CWD susceptibility is modulated by species-specific polymorphisms in the prion protein gene (Prnp). We sequenced Prnp of woodland carib...

Journal: :Lancet 2004
Alexander H Peden Mark W Head Diane L Ritchie Jeanne E Bell James W Ironside

We report a case of preclinical variant Creutzfeldt-Jakob disease (vCJD) in a patient who died from a non-neurological disorder 5 years after receiving a blood transfusion from a donor who subsequently developed vCJD. Protease-resistant prion protein (PrP(res)) was detected by western blot, paraffin-embedded tissue blot, and immunohistochemistry in the spleen, but not in the brain. Immunohistoc...

2013
Rodolfo Villarreal-Calderon Maricela Franco-Lira Angélica González-Maciel Rafael Reynoso-Robles Lou Harritt Beatriz Pérez-Guillé Lara Ferreira-Azevedo Dan Drecktrah Hongtu Zhu Qiang Sun Ricardo Torres-Jardón Mariana Aragón-Flores Ana Calderón-Garcidueñas Philippe Diaz Lilian Calderón-Garcidueñas

Mexico City Metropolitan Area children and young adults exposed to high concentrations of air pollutants including fine and ultrafine particulate matter (PM) vs. clean air controls, exhibit myocardial inflammation and inflammasome activation with a differential right and left ventricular expression of key inflammatory genes and inflammasomes. We investigated the mRNA expression levels of the pr...

2012
Daniel McNaughton William Knight Rita Guerreiro Natalie Ryan Jessica Lowe Mark Poulter David J. Nicholl John Hardy Tamas Revesz James Lowe Martin Rossor John Collinge Simon Mead

Amyloid precursor protein gene (APP) duplications have been identified in screens of selected probands with early onset familial Alzheimer's disease (FAD). A causal role for copy number variation (CNV) in the prion protein gene (PRNP) in prion dementias is not known. We aimed to determine the prevalence of copy number variation in APP and PRNP in a large referral series, test a screening method...

2011
George Msalya Takeshi Shimogiri Shotaro Ohno Shin Okamoto Kotaro Kawabe Mitsuru Minezawa Yoshizane Maeda

BACKGROUND Prion protein (PrP) level plays the central role in bovine spongiform encephalopathy (BSE) susceptibility. Increasing the level of PrP decreases incubation period for this disease. Therefore, studying the expression of the cellular PrP or at least the messenger RNA might be used in selection for preventing the propagation of BSE and other prion diseases. Two insertion/deletion (indel...

2013
Maddalena D. Caiati Victoria F. Safiulina Giorgia Fattorini Sudhir Sivakumaran Giuseppe Legname Enrico Cherubini

The cellular form of prion protein PrP C is highly expressed in the brain, where it can be converted into its abnormally folded isoform PrP Sc to cause neurodegenerative diseases. Its predominant synaptic localization suggests a crucial role in synaptic signaling. Interestingly, PrP C is developmentally regulated and its high expression in the immature brain could be instrumental in regulating ...

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