Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Janis Blevins"'
Autor:
Chae Kim, Tracy Haldiman, Krystyna Surewicz, Yvonne Cohen, Wei Chen, Janis Blevins, Man-Sun Sy, Mark Cohen, Qingzhong Kong, Glenn C Telling, Witold K Surewicz, Jiri G Safar
Publikováno v:
PLoS Pathogens, Vol 8, Iss 8, p e1002835 (2012)
The mammalian prions replicate by converting cellular prion protein (PrP(C)) into pathogenic conformational isoform (PrP(Sc)). Variations in prions, which cause different disease phenotypes, are referred to as strains. The mechanism of high-fidelity
Externí odkaz:
https://doaj.org/article/3f472084441c4b46aaa727eebbb80313
Autor:
Chae Kim, Tracy Haldiman, Yvonne Cohen, Wei Chen, Janis Blevins, Man-Sun Sy, Mark Cohen, Jiri G Safar
Publikováno v:
PLoS Pathogens, Vol 7, Iss 9, p e1002242 (2011)
The origin, range, and structure of prions causing the most common human prion disease, sporadic Creutzfeldt-Jakob disease (sCJD), are largely unknown. To investigate the molecular mechanism responsible for the broad phenotypic variability of sCJD, w
Externí odkaz:
https://doaj.org/article/35f9e59fe1d04881b47d177c898ad058
Autor:
Mark L. Cohen, Lawrence B. Schonberger, Pierluigi Gambetti, Raffaele Lodi, Marina Grisoli, Riccardo Pascuzzo, Gianmarco Castelli, Janis Blevins, Fabio M. Doniselli, Brian S. Appleby, Aymeric Stamm, Marco E. M. Moscatelli, Alberto Bizzi
Publikováno v:
Annals of Neurology
Objective: Sporadic Creutzfeldt–Jakob disease (sCJD) comprises several subtypes as defined by genetic and prion protein characteristics, which are associated with distinct clinical and pathological phenotypes. To date, no clinical test can reliably
Autor:
Sara Garbarino, Janis Blevins, Alberto Bizzi, Mark L. Cohen, Lawrence B. Schonberger, Riccardo Pascuzzo, Pierluigi Gambetti, Alexandra L. Young, Neil P. Oxtoby, Brian S. Appleby, Gianmarco Castelli, Daniel C. Alexander
Publikováno v:
Acta Neuropathologica
Sporadic Creutzfeldt–Jakob disease (sCJD) is a transmissible brain proteinopathy. Five main clinicopathological subtypes (sCJD-MM(V)1, -MM(V)2C, -MV2K, -VV1, and -VV2) are currently distinguished. Histopathological evidence suggests that the locali
Autor:
Anna Poleggi, John Collinge, Carla A. Ibrahim-Verbaas, Jean-Philippe Brandel, Emma Jones, Dimitriadis A, Anna Bartoletti-Stella, James Uphill, Christiane Stehmann, Mok Th, Gerard H. Jansen, Tracy Campbell, Zafar S, Holger Hummerich, van Duijn C, Jiri G. Safar, Ewa Golanska, Martinón-Torres F, Aili Golubjatnikov, Michael B. Coulthart, Zane Jaunmuktane, Beata Sikorska, Giuseppe Matullo, Miguel Calero, Jerome Whitfield, Sabina Capellari, Jean-Louis Laplanche, Kathleen Glisic, Gabor G. Kovacs, Richard Knight, Helen Speedy, Juan Ps, Olga Calero, Jean-Charles Lambert, Stéphane Haïk, Anna Ladogana, Akin Nihat, Stephanie A. Booth, Serena Aneli, Herbert Budka, Pawel P. Liberski, Piero Parchi, Shannon Sarros, Jacqueline M. Linehan, Sebastian Brandner, Maurizio Pocchiari, Ahmed P, Michael D. Geschwind, Fronztek K, Antonio Salas, Inga Zerr, Janis Blevins, Elodie Bouaziz-Amar, Brian S. Appleby, Steven J. Collins, P. Gambetti, Hata Karamujić-Čomić, Adriano Aguzzi, Philippe Amouyel, van der Lee S, Penny Norsworthy, Parmjit S. Jat, Liam Quinn, Emmanuelle Viré, Simon Mead
Mammalian prions are lethal pathogens composed of fibrillar assemblies of misfolded prion protein. Human prion diseases are rare and usually rapidly fatal neurodegenerative disorders, the most common being sporadic Creutzfeldt-Jakob disease (sCJD). V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cd854b0d6ee7d4a5ae9ac560ca64415
Autor:
Lawrence B. Schonberger, Riccardo Pascuzzo, Jiri G. Safar, Pierluigi Gambetti, Aaron Foutz, Marina Grisoli, Mark L. Cohen, Marco E. M. Moscatelli, Alberto Bizzi, Janis Blevins, Brian S. Appleby, Gianmarco Castelli, Raffaele Lodi
Publikováno v:
JAMA Neurol
Importance: Early diagnosis is a requirement for future treatment of prion diseases. Magnetic resonance imaging (MRI) with diffusion-weighted images and improved real-Time quaking-induced conversion (RT-QuIC) in cerebrospinal fluid (CSF) have emerged
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd98e91cd2d9c1a1ac16e520e6a435cc
http://hdl.handle.net/11585/799642
http://hdl.handle.net/11585/799642
Autor:
Gabor G. Kovacs, Stephanie A. Booth, Sebastian Brandner, Penny Norsworthy, Anna Ladogana, Akin Nihat, Herbert Budka, Saima Zafar, Helen Speedy, Antonio Salas, Parvin Ahmed, Holger Hummerich, Gerard H. Jansen, Tze How Mok, Michael D. Geschwind, Beata Sikorska, Maurizio Pocchiari, Christiane Stehmann, Sabina Capellari, Jean-Louis Laplanche, Sven J. van der Lee, Emma Jones, Jean-Charles Lambert, Olga Calero, Pierluigi Gambetti, Ewa Golanska, Serena Aneli, Richard Knight, Giuseppe Matullo, Pawel P. Liberski, Athanasios Dimitriadis, Jerome Whitfield, Hata Karamujić-Čomić, Federico Martinón-Torres, Emmanuelle Viré, Jiri G. Safar, Tracy Campbell, Pascual Sánchez-Juan, Katie Glisic, Anna Bartoletti-Stella, Carla A. Ibrahim-Verbaas, Adriano Aguzzi, Anna Poleggi, Aili Golubjatnikov, Karl Frontzek, Jean Phillipe Brandel, Phillipe Amouyel, Parmjit S. Jat, Zane Jaunmuktane, Simon Mead, Steven J. Collins, Inga Zerr, Liam Quinn, Piero Parchi, Janis Blevins, Elodie Bouaziz-Amar, Brian S. Appleby, Shannon Sarros, Jacqueline M. Linehan, Miguel Calero, Michael B. Coulthart, Stéphane Haïk, John Collinge, James Uphill, Cornelia M. van Duijn
Publikováno v:
The lancet / Neurology 19(10), 840-848 (2020). doi:10.1016/S1474-4422(20)30273-8
Lancet Neurol 2020; 19: 840?48
UCrea Repositorio Abierto de la Universidad de Cantabria
instname
Lancet Neurology, 19(10), 840-848. Lancet Publishing Group
The Lancet Neurology, 19(10), 840-848. Lancet Publishing Group
Jones, E, Hummerich, H, Viré, E, Uphill, J, Dimitriadis, A, Speedy, H, Campbell, T, Norsworthy, P, Quinn, L, Whitfield, J, Linehan, J, Jaunmuktane, Z, Brandner, S, Jat, P, Nihat, A, How Mok, T, Ahmed, P, Collins, S, Stehmann, C, Sarros, S, Kovacs, G G, Geschwind, M D, Golubjatnikov, A, Frontzek, K, Budka, H, Aguzzi, A, Karamujić-Čomić, H, van der Lee, S J, Ibrahim-Verbaas, C A, van Duijn, C M, Sikorska, B, Golanska, E, Liberski, P P, Calero, M, Calero, O, Sanchez-Juan, P, Salas, A, Martinón-Torres, F, Bouaziz-Amar, E, Haïk, S, Laplanche, J-L, Brandel, J-P, Amouyel, P, Lambert, J-C, Parchi, P, Bartoletti-Stella, A, Capellari, S, Poleggi, A, Ladogana, A, Pocchiari, M, Aneli, S, Matullo, G, Knight, R, Zafar, S, Zerr, I, Booth, S, Coulthart, M B, Jansen, G H, Glisic, K, Blevins, J, Gambetti, P, Safar, J, Appleby, B, Collinge, J & Mead, S 2020, ' Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease : a genome-wide association study ', Lancet Neurology, vol. 19, no. 10, pp. 840-848 . https://doi.org/10.1016/S1474-4422(20)30273-8
Lancet Neurol 2020; 19: 840?48
UCrea Repositorio Abierto de la Universidad de Cantabria
instname
Lancet Neurology, 19(10), 840-848. Lancet Publishing Group
The Lancet Neurology, 19(10), 840-848. Lancet Publishing Group
Jones, E, Hummerich, H, Viré, E, Uphill, J, Dimitriadis, A, Speedy, H, Campbell, T, Norsworthy, P, Quinn, L, Whitfield, J, Linehan, J, Jaunmuktane, Z, Brandner, S, Jat, P, Nihat, A, How Mok, T, Ahmed, P, Collins, S, Stehmann, C, Sarros, S, Kovacs, G G, Geschwind, M D, Golubjatnikov, A, Frontzek, K, Budka, H, Aguzzi, A, Karamujić-Čomić, H, van der Lee, S J, Ibrahim-Verbaas, C A, van Duijn, C M, Sikorska, B, Golanska, E, Liberski, P P, Calero, M, Calero, O, Sanchez-Juan, P, Salas, A, Martinón-Torres, F, Bouaziz-Amar, E, Haïk, S, Laplanche, J-L, Brandel, J-P, Amouyel, P, Lambert, J-C, Parchi, P, Bartoletti-Stella, A, Capellari, S, Poleggi, A, Ladogana, A, Pocchiari, M, Aneli, S, Matullo, G, Knight, R, Zafar, S, Zerr, I, Booth, S, Coulthart, M B, Jansen, G H, Glisic, K, Blevins, J, Gambetti, P, Safar, J, Appleby, B, Collinge, J & Mead, S 2020, ' Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease : a genome-wide association study ', Lancet Neurology, vol. 19, no. 10, pp. 840-848 . https://doi.org/10.1016/S1474-4422(20)30273-8
Background Human prion diseases are rare and usually rapidly fatal neurodegenerative disorders, the most common being sporadic Creutzfeldt-Jakob disease (sCJD). Variants in the PRNP gene that encodes prion protein are strong risk factors for sCJD but
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7233c1ef4905578810d4be7f91aaa40
Autor:
Xiaoqin Liu, Byron Caughey, Han Wang, Clive R. Hamlin, Mark L. Cohen, Jiri G. Safar, Wei Chen, Shulin Na Zhang, Pierluigi Gambetti, Lawrence B. Schonberger, Cameron Fausett, Curtis Tatsuoka, Yvonne Cohen, Aaron Foutz, Janis Blevins, Sheng Yang, Brian S. Appleby, Andrew G. Hughson
Publikováno v:
Annals of Neurology. 81:79-92
Objective—Several prion amplification systems have been proposed for detection of prions in cerebrospinal fluid (CSF), most recently, the measurements of prion seeding activity with second-generation real-time quaking-induced conversion (RT-QuIC).
Autor:
Ryan A. Maddox, Mark L. Cohen, Aleksandra Wrona, Kathleen Glisic, Janis Blevins, Brian S. Appleby, Lawrence B. Schonberger, Ermias D. Belay, Curtis Tatsuoka, Daniel D. Rhoads, Marissa Person, Aaron Foutz
Publikováno v:
Neurology. 95(8)
ObjectiveTo present the National Prion Disease Pathology Surveillance Center's (NPDPSC’s) experience using CSF real-time quaking-induced conversion (RT-QuIC) as a diagnostic test, to examine factors associated with false-negative RT-QuIC results, a
Autor:
Ryan A. Maddox, Janis Blevins, Brian S. Appleby, Joseph Y. Abrams, Lawrence B. Schonberger, Ermias D. Belay, Marissa Person
Publikováno v:
Neurology. 94(2)
ObjectiveTo report the incidence of prion disease in the United States.MethodsPrion disease decedents were retrospectively identified from the US national multiple cause-of-death data for 2003–2015 and matched with decedents in the National Prion D