Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Maddalena, Ripamonti"'
Autor:
Paolo Santambrogio, Anna Cozzi, Chiara Balestrucci, Maddalena Ripamonti, Valeria Berno, Eugenia Cammarota, Andrea Stefano Moro, Sonia Levi
Publikováno v:
Cell Death and Disease, Vol 15, Iss 5, Pp 1-10 (2024)
Abstract Disease models of neurodegeneration with brain iron accumulation (NBIA) offer the possibility to explore the relationship between iron dyshomeostasis and neurodegeneration. We analyzed hiPS-derived astrocytes from PANK2-associated neurodegen
Externí odkaz:
https://doaj.org/article/ac292067ea3c4ea49e49855dddee3311
Autor:
Erica Butti, Stefano Cattaneo, Marco Bacigaluppi, Marco Cambiaghi, Giulia Maria Scotti, Elena Brambilla, Francesca Ruffini, Giacomo Sferruzza, Maddalena Ripamonti, Fabio Simeoni, Laura Cacciaguerra, Aurora Zanghì, Angelo Quattrini, Riccardo Fesce, Paola Panina-Bordignon, Francesca Giannese, Davide Cittaro, Tanja Kuhlmann, Patrizia D’Adamo, Maria Assunta Rocca, Stefano Taverna, Gianvito Martino
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-23 (2022)
The physiological role of endogenous neural protenitor cells of the subventricular zone in adult stage is not fully understood. Here the authors show that in mice, these cells tune neuronal activity of the striatum via insulin-like growth factor bind
Externí odkaz:
https://doaj.org/article/531fd0239309440fae10ff19b71eab3c
Autor:
Paolo Santambrogio, Maddalena Ripamonti, Anna Cozzi, Marzia Raimondi, Chiara Cavestro, Ivano Di Meo, Alicia Rubio, Stefano Taverna, Valeria Tiranti, Sonia Levi
Publikováno v:
Cell Death and Disease, Vol 13, Iss 2, Pp 1-12 (2022)
Abstract Neurodegeneration associated with defective pantothenate kinase-2 (PKAN) is an early-onset monogenic autosomal-recessive disorder. The hallmark of the disease is the massive accumulation of iron in the globus pallidus brain region of patient
Externí odkaz:
https://doaj.org/article/7980b3f04e944f7d8ac44cb339971253
Autor:
Maddalena Ripamonti, Paolo Santambrogio, Gabriella Racchetti, Anna Cozzi, Ivano Di Meo, Valeria Tiranti, Sonia Levi
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 16 (2022)
PKAN disease is caused by mutations in the PANK2 gene, encoding the mitochondrial enzyme pantothenate kinase 2, catalyzing the first and key reaction in Coenzyme A (CoA) biosynthetic process. This disorder is characterized by progressive neurodegener
Externí odkaz:
https://doaj.org/article/342ff498975646968aa60d283f939dc2
Autor:
Anna Cozzi, Daniel I. Orellana, Paolo Santambrogio, Alicia Rubio, Cinzia Cancellieri, Serena Giannelli, Maddalena Ripamonti, Stefano Taverna, Giulia Di Lullo, Ermanna Rovida, Maurizio Ferrari, Gian Luca Forni, Chiara Fiorillo, Vania Broccoli, Sonia Levi
Publikováno v:
Stem Cell Reports, Vol 13, Iss 5, Pp 832-846 (2019)
Summary: Neuroferritinopathy (NF) is a movement disorder caused by alterations in the L-ferritin gene that generate cytosolic free iron. NF is a unique pathophysiological model for determining the direct consequences of cell iron dysregulation. We es
Externí odkaz:
https://doaj.org/article/1a80b9ac5a774715806543d0e61b3993
Publikováno v:
Cells, Vol 10, Iss 8, p 1969 (2021)
In 2001, a new type of human ferritin was identified by searching for homologous sequences to H-ferritin in the human genome. After the demonstration that this ferritin is located specifically in the mitochondrion, it was called mitochondrial ferriti
Externí odkaz:
https://doaj.org/article/27fb922c84ad491e95729f2643e85aa5
Autor:
Mattia Ferro, Jacopo Lamanna, Maddalena Ripamonti, Gabriella Racchetti, Alessandro Arena, Sara Spadini, Giovanni Montesano, Riccardo Cortese, Vincenzo Zimarino, Antonio Malgaroli
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
Visualization of synaptic activity in the living brain is challenging. This study devises a simple and efficient scheme that reports synaptic vesicle recycling in vivo using SynaptoZip, a genetically encoded sensor of past synaptic activities.
Externí odkaz:
https://doaj.org/article/972547f89abe41b0ab123373ee104007
Publikováno v:
Cellular and Molecular Life Sciences. 78:3355-3367
Neuroferritinopathy is a rare autosomal dominant inherited movement disorder caused by alteration of the L-ferritin gene that results in the production of a ferritin molecule that is unable to properly manage iron, leading to the presence of free red
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af6323b985d9c462306e0f6246fd6286
https://doi.org/10.1007/s00018-020-03747-w
https://doi.org/10.1007/s00018-020-03747-w
Autor:
Carsten Schulte, Maddalena Ripamonti, Elisa Maffioli, Martino Alfredo Cappelluti, Simona Nonnis, Luca Puricelli, Jacopo Lamanna, Claudio Piazzoni, Alessandro Podestà, Cristina Lenardi, Gabriella Tedeschi, Antonio Malgaroli, Paolo Milani
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 10 (2016)
The identification of biomaterials which promote neuronal maturation up to the generation of integrated neural circuits is fundamental for modern neuroscience. The development of neural circuits arises from complex maturative processes regulated by p
Externí odkaz:
https://doaj.org/article/84b92027557943129647cb626442e4fa
Autor:
Alicia Rubio, Serena Giannelli, Vania Broccoli, Maurizio Ferrari, Chiara Fiorillo, Daniel Orellana, Ermanna Rovida, Giulia Di Lullo, Paolo Santambrogio, Anna Cozzi, Cinzia Cancellieri, Stefano Taverna, Gian Luca Forni, Maddalena Ripamonti, Sonia Levi
Publikováno v:
Stem Cell Reports, Vol 13, Iss 5, Pp 832-846 (2019)
Stem Cell Reports
Stem Cell Reports
Summary Neuroferritinopathy (NF) is a movement disorder caused by alterations in the L-ferritin gene that generate cytosolic free iron. NF is a unique pathophysiological model for determining the direct consequences of cell iron dysregulation. We est
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01de26e5458b584eaa7c3e6d4ebdda03
http://www.sciencedirect.com/science/article/pii/S2213671119303315
http://www.sciencedirect.com/science/article/pii/S2213671119303315