Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Raffaella De Pace"'
Publikováno v:
Frontiers in Molecular Biosciences, Vol 11 (2024)
Externí odkaz:
https://doaj.org/article/7ed80102ef414ed5b0e52bf0cea6d80a
Autor:
Jérôme T. J. Nicol, Elisa Mazzoni, Maria Rosa Iaquinta, Raffaella De Pace, Pauline Gaboriaud, Natalia Maximova, Carolina Cason, Eleonora De Martino, Chiara Mazziotta, Pierre Coursaget, Antoine Touzé, Valentina Boz, Manola Comar, Mauro Tognon, Fernanda Martini
Publikováno v:
Frontiers in Immunology, Vol 14 (2024)
IntroductionHuman polyomaviruses (HPyVs) cause persistent/latent infections in a large fraction of the population. HPyV infections may cause severe diseases in immunocompromised patients. Malawi polyomavirus (MWPyV) is the 10th discovered human polyo
Externí odkaz:
https://doaj.org/article/e3c55885245249248e538565dc153943
Autor:
Xin Chen, Thomas Dong, Yuhui Hu, Raffaella De Pace, Rafael Mattera, Kathrin Eberhardt, Marvin Ziegler, Terry Pirovolakis, Mustafa Sahin, Juan S. Bonifacino, Darius Ebrahimi-Fakhari, Steven J. Gray
Publikováno v:
The Journal of Clinical Investigation, Vol 133, Iss 10 (2023)
Spastic paraplegia 50 (SPG50) is an ultrarare childhood-onset neurological disorder caused by biallelic loss-of-function variants in the AP4M1 gene. SPG50 is characterized by progressive spastic paraplegia, global developmental delay, and subsequent
Externí odkaz:
https://doaj.org/article/2bba6f1c88c84947824d953a3f8dcd7e
Autor:
Anika V. Prabhu, Insung Kang, Raffaella De Pace, Christopher A. Wassif, Hideji Fujiwara, Pamela Kell, Xuntian Jiang, Daniel S. Ory, Juan S. Bonifacino, Michael E. Ward, Forbes D. Porter
Publikováno v:
BMC Biology, Vol 19, Iss 1, Pp 1-12 (2021)
Abstract Background Niemann-Pick disease, type C (NPC) is a childhood-onset, lethal, neurodegenerative disorder caused by autosomal recessive mutations in the genes NPC1 or NPC2 and characterized by impaired cholesterol homeostasis, a lipid essential
Externí odkaz:
https://doaj.org/article/fbf727df91264aa1910bff5cd9a48708
Autor:
Raffaella De Pace, Dylan J. Britt, Jeffrey Mercurio, Arianne M. Foster, Lucas Djavaherian, Victoria Hoffmann, Daniel Abebe, Juan S. Bonifacino
Publikováno v:
Cell Reports, Vol 31, Iss 11, Pp 107775- (2020)
Summary: BORC is a multisubunit complex previously shown to promote coupling of mammalian lysosomes and C. elegans synaptic vesicle (SV) precursors (SVPs) to kinesins for anterograde transport of these organelles along microtubule tracks. We attempte
Externí odkaz:
https://doaj.org/article/6656a5725e454200933c06069beb0a9b
Autor:
Carlos M Guardia, Raffaella De Pace, Aritra Sen, Amra Saric, Michal Jarnik, David A Kolin, Ambarish Kunwar, Juan S Bonifacino
Publikováno v:
PLoS Biology, Vol 17, Iss 5, p e3000279 (2019)
We report the development and characterization of a method, named reversible association with motor proteins (RAMP), for manipulation of organelle positioning within the cytoplasm. RAMP consists of coexpressing in cultured cells (i) an organellar pro
Externí odkaz:
https://doaj.org/article/5ac32a12a8e441d4a457f7d9e2882e54
Autor:
Raffaella De Pace, Miguel Skirzewski, Markus Damme, Rafael Mattera, Jeffrey Mercurio, Arianne M Foster, Loreto Cuitino, Michal Jarnik, Victoria Hoffmann, H Douglas Morris, Tae-Un Han, Grazia M S Mancini, Andrés Buonanno, Juan S Bonifacino
Publikováno v:
PLoS Genetics, Vol 14, Iss 4, p e1007363 (2018)
The hereditary spastic paraplegias (HSP) are a clinically and genetically heterogeneous group of disorders characterized by progressive lower limb spasticity. Mutations in subunits of the heterotetrameric (ε-β4-μ4-σ4) adaptor protein 4 (AP-4) com
Externí odkaz:
https://doaj.org/article/8d246468754b439990a8441def5315a5
Autor:
Raffaella De Pace, Juan S. Bonifacino
Publikováno v:
Current Biology. 33:R143-R146
Autor:
Elisa Mazzoni, Maria Rosa Iaquinta, Maria Mosaico, Raffaella De Pace, Antonio D'Agostino, Mauro Tognon, Fernanda Martini
Publikováno v:
Tissue Engineering Part B: Reviews.
Autor:
Nilisha Fernando, Jaanam Gopalakrishnan, Adam Behensky, Lauren Reich, Chunhong Liu, Victor Bass, Michaella Bono, William Montgomery, Raffaella De Pace, Mary Mattapallil, Vijayaraj Nagarajan, Stephen Brooks, Dragan Maric, Rachel R Caspi, Dorian B. McGavern, Han-Yu Shih
Publikováno v:
bioRxiv
Alzheimer’s disease (AD) is the leading cause of dementia worldwide, but there are limited therapeutic options and no current cure. While the involvement of microglia in AD has been highly appreciated, the role of other innate and adaptive immune c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ceaa5940959f72294a3cbfb5c3e3e61
https://europepmc.org/articles/PMC10120715/
https://europepmc.org/articles/PMC10120715/