Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Keyshla Y. Negron-Rios"'
Autor:
Stephanie S. Sandoval-Pistorius, Julia E. Gerson, Nyjerus Liggans, Jaimie H. Ryou, Kulin Oak, Xingli Li, Keyshla Y. Negron-Rios, Svetlana Fischer, Henry Barsh, Emily V. Crowley, Mary E. Skinner, Lisa M. Sharkey, Sami J. Barmada, Henry L. Paulson
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-14 (2023)
Abstract The key protein implicated in Parkinson’s disease and other synucleinopathies is α-synuclein, and a post-translationally modified form of the protein, phosphorylated at serine 129 (pS129), is a principal component in Lewy bodies, a pathol
Externí odkaz:
https://doaj.org/article/eaddfd74f32f410b9eea3dbbd5fece4b
Autor:
Lisa M. Sharkey, Stephanie S. Sandoval-Pistorius, Shannon J. Moore, Julia E. Gerson, Robert Komlo, Svetlana Fischer, Keyshla Y. Negron-Rios, Emily V. Crowley, Francisco Padron, Ronak Patel, Geoffrey G. Murphy, Henry L. Paulson
Publikováno v:
Neurobiology of Disease, Vol 143, Iss , Pp 105016- (2020)
The ubiquitin-binding proteasomal shuttle protein UBQLN2 is implicated in common neurodegenerative disorders due to its accumulation in disease-specific aggregates and, when mutated, directly causes familial frontotemporal dementia/amyotrophic latera
Externí odkaz:
https://doaj.org/article/4abe4f08dbae4d1ba1c9c18d4d34cd8e
Autor:
Stephanie S, Sandoval-Pistorius, Julia E, Gerson, Nyjerus, Liggans, Jaimie H, Ryou, Kulin, Oak, Xingli, Li, Keyshla Y, Negron-Rios, Svetlana, Fischer, Henry, Barsh, Emily V, Crowley, Mary E, Skinner, Lisa M, Sharkey, Sami J, Barmada, Henry L, Paulson
Publikováno v:
Scientific reports. 13(1)
The key protein implicated in Parkinson's disease and other synucleinopathies is α-synuclein, and a post-translationally modified form of the protein, phosphorylated at serine 129 (pS129), is a principal component in Lewy bodies, a pathological hall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fbd7bd50449312be17b1c9a238f86ee7
https://pubmed.ncbi.nlm.nih.gov/36609661
https://pubmed.ncbi.nlm.nih.gov/36609661
Autor:
Julia E. Gerson, Emily V. Crowley, Shannon J. Moore, Svetlana Fischer, Robert Komlo, Geoffrey G. Murphy, Ronak Patel, Lisa M. Sharkey, Stephanie S. Sandoval-Pistorius, Keyshla Y. Negron-Rios, Henry L. Paulson, Francisco Padron
Publikováno v:
Neurobiol Dis
Neurobiology of Disease, Vol 143, Iss, Pp 105016-(2020)
Neurobiology of Disease, Vol 143, Iss, Pp 105016-(2020)
The ubiquitin-binding proteasomal shuttle protein UBQLN2 is implicated in common neurodegenerative disorders due to its accumulation in disease-specific aggregates and, when mutated, directly causes familial frontotemporal dementia/amyotrophic latera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f289b41bd2723460de3d5c5ceb3c7850
https://doi.org/10.1016/j.nbd.2020.105016
https://doi.org/10.1016/j.nbd.2020.105016