Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Maria Lina Massimino"'
Publikováno v:
Biology, Vol 12, Iss 12, p 1504 (2023)
Essential oils (EOs) are mixtures of volatile compounds, extracted from aromatic plants, with multiple activities including antioxidant and anti-inflammatory ones. EOs are complex mixtures easy to find on the market and with low costs. In this mini n
Externí odkaz:
https://doaj.org/article/8aa1b4bae6e44c0594cbacf1b0f1a8e3
Autor:
Alejandro Montoya-Gómez, Fiorella Tonello, Barbara Spolaore, Maria Lina Massimino, Leonel Montealegre-Sánchez, Andrés Castillo, Nelson Rivera Franco, María José Sevilla-Sánchez, Luis Manuel Solano-Redondo, Mildrey Mosquera-Escudero, Eliécer Jiménez-Charris
Publikováno v:
Cells, Vol 12, Iss 23, p 2715 (2023)
Despite advances in chemotherapeutic drugs used against cervical cancer, available chemotherapy treatments adversely affect the patient’s quality of life. For this reason, new molecules from natural sources with antitumor potential and few side eff
Externí odkaz:
https://doaj.org/article/f4cfc9c7ead043b1ad5aea96659ec82a
Autor:
Roberto Stella, Raphael Severino Bonadio, Stefano Cagnin, Roberta Andreotti, Maria Lina Massimino, Alessandro Bertoli, Caterina Peggion
Publikováno v:
Cells, Vol 12, Iss 23, p 2751 (2023)
Amyotrophic lateral sclerosis (ALS) is a motor neuron (MN) disease associated with progressive muscle atrophy, paralysis, and eventually death. Growing evidence demonstrates that the pathological process leading to ALS is the result of multiple alter
Externí odkaz:
https://doaj.org/article/03fe34f237694d3988d36e4adf46def8
Autor:
Caterina Peggion, Maria Lina Massimino, Roberto Stella, Raissa Bortolotto, Jessica Agostini, Arianna Maldi, Geppo Sartori, Fiorella Tonello, Alessandro Bertoli, Raffaele Lopreiato
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 15 (2021)
TDP-43 is a nuclear protein involved in pivotal processes, extensively studied for its implication in neurodegenerative disorders. TDP-43 cytosolic inclusions are a common neuropathologic hallmark in amyotrophic lateral sclerosis (ALS) and related di
Externí odkaz:
https://doaj.org/article/7141b76667ba49b8bcdd2988f374db35
Autor:
Caterina Peggion, Valeria Scalcon, Maria Lina Massimino, Kelly Nies, Raffaele Lopreiato, Maria Pia Rigobello, Alessandro Bertoli
Publikováno v:
Antioxidants, Vol 11, Iss 4, p 614 (2022)
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder characterized by the loss of motor neurons in the brain and spinal cord. While the exact causes of ALS are still unclear, the discovery that familial cases of ALS are related t
Externí odkaz:
https://doaj.org/article/ad498dad1edc435d8d0511aa29a8ced7
Autor:
Rosa Pia Norante, Maria Lina Massimino, Paolo Lorenzon, Agnese De Mario, Caterina Peggion, Mattia Vicario, Mattia Albiero, Maria Catia Sorgato, Raffaele Lopreiato, Alessandro Bertoli
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract A finely tuned Ca2+ homeostasis in restricted cell domains is of fundamental importance for neurons, where transient Ca2+ oscillations direct the proper coordination of electro-chemical signals and overall neuronal metabolism. Once such a pr
Externí odkaz:
https://doaj.org/article/8e299e8e280d44439975e49e38da4983
Publikováno v:
Toxicon. 170:99-107
Almost all animal venoms contain secretory phospholipases A2 (PLA2s), 14 kDa disulfide-rich enzymes that hydrolyze membrane phospholipids at the sn-2 position, releasing lysophospholipids and fatty acids. These proteins, depending on their sequence,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2c18e6ff6c160d8cc6df149778c91a2
https://doi.org/10.1016/j.toxicon.2019.09.019
https://doi.org/10.1016/j.toxicon.2019.09.019
Autor:
Alessandro Bertoli, Tito Calì, Maria Lina Massimino, Caterina Peggion, Raphael Severino Bonadio, Stefano Cagnin, Raffaele Lopreiato, Federica Lia
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 21
International Journal of Molecular Sciences, Vol 22, Iss 11853, p 11853 (2021)
Volume 22
Issue 21
International Journal of Molecular Sciences, Vol 22, Iss 11853, p 11853 (2021)
Mitochondria–ER contacts (MERCs), tightly regulated by numerous tethering proteins that act as molecular and functional connections between the two organelles, are essential to maintain a variety of cellular functions. Such contacts are often compr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56a13bcebc63e35c8b36985dd5996edb
https://pubmed.ncbi.nlm.nih.gov/34769284
https://pubmed.ncbi.nlm.nih.gov/34769284
Autor:
Maria Lina Massimino, Alessandro Bertoli, Raphael Severino Bonadio, Roberto Stella, Caterina Peggion, Stefano Cagnin
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 7028, p 7028 (2021)
Volume 22
Issue 13
International Journal of Molecular Sciences, Vol 22, Iss 7028, p 7028 (2021)
Volume 22
Issue 13
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease whose pathophysiology is largely unknown. Despite the fact that motor neuron (MN) death is recognized as the key event in ALS, astrocytes dysfunctionalities and neuroinfla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04f49d2683d428d26ea2f09361870ed6
https://pubmed.ncbi.nlm.nih.gov/34209958
https://pubmed.ncbi.nlm.nih.gov/34209958
Autor:
Enzo Spisni, Roberto Stella, Paolo Lorenzon, Alessandro Bertoli, Caterina Peggion, Maria Lina Massimino
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 7765, p 7765 (2020)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Prion diseases are rare transmissible neurodegenerative disorders caused by the accumulation of a misfolded isoform (PrPSc) of the cellular prion protein (PrPC) in the central nervous system (CNS). Neuropathological hallmarks of prion diseases are ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a656c7c444ac4e880cf80770206309db
https://www.mdpi.com/1422-0067/21/20/7765
https://www.mdpi.com/1422-0067/21/20/7765