Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Satish K Nemani"'
Autor:
Leonardo M Cortez, Satish K Nemani, Camilo Duque Velásquez, Aishwarya Sriraman, YongLiang Wang, Holger Wille, Debbie McKenzie, Valerie L Sim
Publikováno v:
PLoS Pathogens, Vol 17, Iss 6, p e1009703 (2021)
Prion diseases are transmissible neurodegenerative disorders that affect mammals, including humans. The central molecular event is the conversion of cellular prion glycoprotein, PrPC, into a plethora of assemblies, PrPSc, associated with disease. Dis
Externí odkaz:
https://doaj.org/article/6edcb27cf26947098ac2592983bba0b0
Autor:
Satish K. Nemani, Xiangzhu Xiao, Ignazio Cali, Laura Cracco, Gianfranco Puoti, Massimiliano Nigro, Jody Lavrich, Anuradha Bharara Singh, Brian S. Appleby, Valerie L. Sim, Silvio Notari, Witold K. Surewicz, Pierluigi Gambetti
Publikováno v:
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-12 (2020)
Abstract One of remarkable features of sporadic Creutzfeldt-Jakob disease (sCJD) is the great phenotypic variability. Understanding the molecular basis of this variability has important implications for the development of therapeutic approaches. It i
Externí odkaz:
https://doaj.org/article/c9ed097c798c49debd92f73c5be253e7
Autor:
Laura Cracco, Xiangzhu Xiao, Satish K. Nemani, Jody Lavrich, Ignazio Cali, Bernardino Ghetti, Silvio Notari, Witold K. Surewicz, Pierluigi Gambetti
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-9 (2019)
Abstract Despite their phenotypic heterogeneity, most human prion diseases belong to two broadly defined groups: Creutzfeldt-Jakob disease (CJD) and Gerstmann-Sträussler-Scheinker disease (GSS). While the structural characteristics of the disease-re
Externí odkaz:
https://doaj.org/article/ea9329de289a415c88f3286c662ceb27
Autor:
Irina Zemlyankina, Valerie L. Sim, Samia Hannaoui, Hermann Schaetzl, Pearl Cherry, Waqas Tahir, Tahir Ali, Satish K. Nemani, Sabine Gilch, Su Yeon Shim
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-14 (2021)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Prion diseases are fatal, infectious, and incurable neurodegenerative disorders caused by misfolding of the cellular prion protein (PrPC) into the infectious isoform (PrPSc). In humans, there are sporadic, genetic and infectious etiologies, with spor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dca56af104634176fd3d371d290bb1fa
https://doaj.org/article/df386e613c3148bea1070a9c620720db
https://doaj.org/article/df386e613c3148bea1070a9c620720db
Autor:
Fabio Moda, Claudio Soto, Fabrizio Tagliavini, Satish K. Nemani, Jody Lavrich, Diane Kofskey, Pierluigi Gambetti, Silvio Notari, Ignazio Cali, Brian S. Appleby
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-7 (2019)
Scientific Reports
Scientific Reports
The presence of abnormal, disease-related prion protein (PrPD) has recently been demonstrated by protein misfolding cyclic amplification (PMCA) in urine of patients affected with variant Creutzfeldt-Jakob disease (vCJD), a prion disease typically acq
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60650f79f7ba6fefb68460538696a18c
http://link.springer.com/article/10.1038/s41598-019-41694-0
http://link.springer.com/article/10.1038/s41598-019-41694-0
Autor:
Ignazio Cali, Pierluigi Gambetti, Tetsuyuki Kitamoto, Juan María Torres, Alba Marín-Moreno, Rabail Aslam, Satish K. Nemani, Manuel V. Camacho, Brian S. Appleby, Juan Carlos Espinosa
Publikováno v:
Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-11 (2021)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Digital.CSIC. Repositorio Institucional del CSIC
instname
11,Pág. Centro de Investigación en Sanidad Animal (CISA)
Current classifications of sporadic Creutzfeldt-Jakob disease (sCJD) identify five subtypes associated with different disease phenotypes. Most of these histopathological phenotypes (hist
Current classifications of sporadic Creutzfeldt-Jakob disease (sCJD) identify five subtypes associated with different disease phenotypes. Most of these histopathological phenotypes (hist
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d56b33df577569de08ea714f7b064be5
https://api.elsevier.com/content/abstract/scopus_id/85103159447
https://api.elsevier.com/content/abstract/scopus_id/85103159447
Autor:
Aishwarya Sriraman, Satish K. Nemani, Camilo Duque Velásquez, Leonardo M. Cortez, Holger Wille, YongLiang Wang, Valerie L. Sim, Debbie McKenzie
Publikováno v:
PLoS Pathogens
PLoS Pathogens, Vol 17, Iss 6, p e1009703 (2021)
PLoS Pathogens, Vol 17, Iss 6, p e1009703 (2021)
Prion diseases are transmissible neurodegenerative disorders that affect mammals, including humans. The central molecular event is the conversion of cellular prion glycoprotein, PrPC, into a plethora of assemblies, PrPSc, associated with disease. Dis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cabd2fc4aadb9dbd6dbd483ba2298f8a
https://pubmed.ncbi.nlm.nih.gov/34181702
https://pubmed.ncbi.nlm.nih.gov/34181702
Autor:
Ignazio, Cali, Juan Carlos, Espinosa, Satish K, Nemani, Alba, Marin-Moreno, Manuel V, Camacho, Rabail, Aslam, Tetsuyuki, Kitamoto, Brian S, Appleby, Juan Maria, Torres, Pierluigi, Gambetti
Publikováno v:
Acta Neuropathologica Communications
Current classifications of sporadic Creutzfeldt–Jakob disease (sCJD) identify five subtypes associated with different disease phenotypes. Most of these histopathological phenotypes (histotypes) co-distribute with distinct pairings of methionine (M)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a3bb5dd35625643c1649fda08ee8927e
https://pubmed.ncbi.nlm.nih.gov/33766126
https://pubmed.ncbi.nlm.nih.gov/33766126
Autor:
Massimiliano Nigro, Silvio Notari, Brian S. Appleby, Valerie L. Sim, Gianfranco Puoti, Pierluigi Gambetti, Satish K. Nemani, Jody Lavrich, Laura Cracco, Witold K. Surewicz, Ignazio Cali, Anuradha Bharara Singh, Xiangzhu Xiao
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-12 (2020)
Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-12 (2020)
One of remarkable features of sporadic Creutzfeldt-Jakob disease (sCJD) is the great phenotypic variability. Understanding the molecular basis of this variability has important implications for the development of therapeutic approaches. It is well es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ac7948af08cbea47736a3c26f9c6342
https://doi.org/10.1186/s40478-020-00966-x
https://doi.org/10.1186/s40478-020-00966-x
Autor:
Satish K. Nemani, Silvio Notari, Laura Cracco, Jody Lavrich, Ignazio Cali, Pierluigi Gambetti, Xiangzhu Xiao, Bernardino Ghetti, Witold K. Surewicz
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-9 (2019)
Acta Neuropathologica Communications
Acta Neuropathologica Communications
Despite their phenotypic heterogeneity, most human prion diseases belong to two broadly defined groups: Creutzfeldt-Jakob disease (CJD) and Gerstmann-Sträussler-Scheinker disease (GSS). While the structural characteristics of the disease-related pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4fc1f650bc5141f3185e542637a3227
https://doi.org/10.1186/s40478-019-0734-2
https://doi.org/10.1186/s40478-019-0734-2