Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Maria Regoni"'
Publikováno v:
Bio-Protocol, Vol 11, Iss 15 (2021)
The Substantia Nigra pars compacta (SNc) is a midbrain dopaminergic nucleus that plays a key role in modulating motor and cognitive functions. It is crucially involved in several disorders, particularly Parkinson’s disease, which is characterized b
Externí odkaz:
https://doaj.org/article/fcbf8b4011e84b17b87b4d5f08531382
Publikováno v:
International Journal of Cardiology: Heart & Vasculature, Vol 21, Iss , Pp 80-86 (2018)
The prevalence of type 2 diabetes continues to increase and cardiovascular (CV) diseases remain the leading cause of death in diabetic patients. Diabetologists and Cardiologists have to work together in order to provide the best management to these p
Externí odkaz:
https://doaj.org/article/98eee03a64d7426e9d2931f9c0bcdde9
Publikováno v:
Cells, Vol 10, Iss 9, p 2260 (2021)
AMPA receptors (AMPARs) are ionotropic glutamate receptors that play a major role in excitatory neurotransmission. AMPARs are located at both presynaptic and postsynaptic plasma membranes. A huge number of studies investigated the role of postsynapti
Externí odkaz:
https://doaj.org/article/630eaeeacddd43c7a138da26853a6dce
Autor:
Guendalina Bastioli, Maria Regoni, Federico Cazzaniga, Chiara Maria Giulia De Luca, Edoardo Bistaffa, Letizia Zanetti, Fabio Moda, Flavia Valtorta, Jenny Sassone
Publikováno v:
Biomedicines, Vol 9, Iss 7, p 812 (2021)
Parkinson’s disease (PD) is the most common neurodegenerative movement disorder. The neuropathological hallmark of the disease is the loss of dopamine neurons of the substantia nigra pars compacta. The clinical manifestations of PD are bradykinesia
Externí odkaz:
https://doaj.org/article/290f36722bda466cb231cf59e0b22eeb
Autor:
Maria Regoni, Letizia Zanetti, Stefano Comai, Daniela Mercatelli, Salvatore Novello, Federica Albanese, Laura Croci, Gian Giacomo Consalez, Andrea Ciammola, Flavia Valtorta, Michele Morari, Jenny Sassone
Publikováno v:
Biomedicines, Vol 9, Iss 5, p 514 (2021)
Mutations in the PARK2 gene encoding the protein parkin cause autosomal recessive juvenile parkinsonism (ARJP), a neurodegenerative disease characterized by early dysfunction and loss of dopamine (DA) neurons in the substantia nigra pars compacta (SN
Externí odkaz:
https://doaj.org/article/12033736213a4a09a364896d9ec296cc
Parkinson’s disease is a neurodegenerative disorder characterized by the progressive dysfunction and loss of dopamine (DA) neurons of the substantia nigra pars compacta (SNc). Several pathways of programmed cell death are likely to play a role in D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26cbd7cbc1fd300c8ed579dc62a66d43
https://doi.org/10.22541/au.168534723.35545183/v1
https://doi.org/10.22541/au.168534723.35545183/v1
Autor:
Tsepo Goerttler, Letizia Zanetti, Maria Regoni, Karl Egger, Elias Kellner, Cornelius Deuschl, Christoph Kleinschnitz, Jenny Sassone, Stephan Klebe
ObjectivesAlexander disease (AD) is a rare disorder of the CNS. Diagnosis is based on clinical symptoms, typical MRI findings, and mutations in the glial fibrillary acid protein (GFAP) gene. In this case study, we describe a new mutation (p.L58P) in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5a823a748eff30d4042fa68b3339fb8
https://www.ncbi.nlm.nih.gov/pubmed/35620133
https://www.ncbi.nlm.nih.gov/pubmed/35620133
Publikováno v:
Bio Protoc
The Substantia Nigra pars compacta (SNc) is a midbrain dopaminergic nucleus that plays a key role in modulating motor and cognitive functions. It is crucially involved in several disorders, particularly Parkinson's disease, which is characterized by
Autor:
Daniela Mercatelli, G. Giacomo Consalez, Stefano Cattaneo, Renzo Bagnati, Alessio Di Fonzo, Michele Morari, Maria Passafaro, Jenny Sassone, Stefano Taverna, Laura Croci, Enrico Davoli, Andrea Ciammola, Letizia Zanetti, Alice Passoni, Giulia Maia Serratto, Salvatore Novello, Flavia Valtorta, Federica Albanese, Maria Regoni
Publikováno v:
Cell Death and Disease, Vol 11, Iss 11, Pp 1-11 (2020)
Cell Death & Disease
Cell Death & Disease
BackgroundMutations in the PARK2 gene encoding the protein parkin cause autosomal recessive juvenile parkinsonism (ARJP), a neurodegenerative disease characterized by dysfunction and death of dopamine (DA) neurons in the substantia nigra pars compact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa1eb6de2ad4e9f462cb80cc4ebe09aa
https://doi.org/10.21203/rs.3.rs-36149/v1
https://doi.org/10.21203/rs.3.rs-36149/v1
Autor:
Giovanna Dati, Jenny Sassone, Chiara Reale, Maria Teresa Pellecchia, Barbara Garavaglia, Maria Regoni
The vacuolar protein sorting 35 (VPS35) gene located on chromosome 16 has recently emerged as a cause of late-onset familial Parkinson’s disease (PD) (PARK17). The gene encodes a 796-residue protein nearly ubiquitously expressed in human tissues. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32a8eae64b3cd4637c5efa5d6db81cdf
http://hdl.handle.net/11386/4754064
http://hdl.handle.net/11386/4754064