Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Paola Cuccarolo"'
Autor:
Rossella Piras, Matteo Breno, Elisabetta Valoti, Marta Alberti, Paraskevas Iatropoulos, Caterina Mele, Elena Bresin, Roberta Donadelli, Paola Cuccarolo, Richard J. H. Smith, Ariela Benigni, Giuseppe Remuzzi, Marina Noris
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
C3 Glomerulopathy (C3G) and Immune Complex-Mediated Membranoproliferative glomerulonephritis (IC-MPGN) are rare diseases characterized by glomerular deposition of C3 caused by dysregulation of the alternative pathway (AP) of complement. In approximat
Externí odkaz:
https://doaj.org/article/bf5651269e7640a2b06033b39950716b
Autor:
Rossella Piras, Paraskevas Iatropoulos, Elena Bresin, Marta Todeschini, Sara Gastoldi, Elisabetta Valoti, Marta Alberti, Caterina Mele, Miriam Galbusera, Paola Cuccarolo, Ariela Benigni, Giuseppe Remuzzi, Marina Noris
Publikováno v:
Frontiers in Medicine, Vol 7 (2020)
Atypical hemolytic uremic syndrome (aHUS) is an ultra-rare disease characterized by microangiopathic hemolysis, thrombocytopenia, and renal impairment and is associated with dysregulation of the alternative complement pathway on the microvascular end
Externí odkaz:
https://doaj.org/article/9875cfb92ab846349f6c1740a5af9474
Autor:
Marta Columbaro, Silvia Ravera, Cristina Capanni, Isabella Panfoli, Paola Cuccarolo, Giorgia Stroppiana, Paolo Degan, Enrico Cappelli
Publikováno v:
PLoS ONE, Vol 9, Iss 7, p e104857 (2014)
Fanconi anemia (FA) is a genetic disorder characterised by chromosome instability, cytokine ipersensibility, bone marrow failure and abnormal haematopoiesis associated with acute myelogenous leukemia. Recent reports are contributing to characterize t
Externí odkaz:
https://doaj.org/article/bb87447a75bf4195807aabe1fda8a440
Autor:
Martina Dameri, Gabriella Cirmena, Francesco Ravera, Lorenzo Ferrando, Paola Cuccarolo, Mario Stabile, Giuseppe Nicolò Fanelli, Pier Vitale Nuzzo, Massimo Calabrese, Alberto Tagliafico, Alberto Ballestrero, Gabriele Zoppoli
Publikováno v:
Critical Reviews in Oncology/Hematology. 185:103963
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08723c123de18555c0c9b998e18d5337
https://doi.org/10.1016/j.critrevonc.2023.103963
https://doi.org/10.1016/j.critrevonc.2023.103963
Autor:
Daniela Calzia, Paolo Degan, Enrico Cappelli, Alberto Izzotti, Laura Ottaggio, Giorgia Chiappori, Sara Tavella, Paola Cuccarolo, Alessandro Cora
Publikováno v:
Journal of Cellular Physiology. 235:3508-3518
Muscle loss is a major problem for many in lifetime. Muscle and bone degeneration has also been observed in individuals exposed to microgravity and in unloading conditions. C2C12 myoblst cells are able to form myotubes, and myofibers and these cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6316e65b718e3950f370679c7891b4ef
https://doi.org/10.1002/jcp.29239
https://doi.org/10.1002/jcp.29239
Autor:
Paolo Degan, Paola Cuccarolo, Enrico Cappelli, Alberto Izzotti, Carlo Dufour, Daniela Calzia, Silvia Ravera, Alessandra Pulliero, Maria Grazia Longobardi
Publikováno v:
Metabolic Syndrome and Related Disorders. 17:53-59
Fanconi anemia (FA) is a complex tumor-prone disease defined by an entangled genotype and phenotype. Despite enormous efforts in the last 20 years, a comprehensive and integrated view of the disease is still missing. The aim of this pilot study was t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a32897b966b5fa5736ae4147fd58c3b
https://doi.org/10.1089/met.2018.0085
https://doi.org/10.1089/met.2018.0085
Autor:
Caterina Mele, Marta Alberti, Ebru Yılmaz Keskin, Giuseppe Remuzzi, Elisabetta Valoti, Marina Noris, Elena Bresin, Paola Cuccarolo, Camillo Carrara, Ariela Benigni, Yonca Açikgöz, Matteo Breno
Publikováno v:
Nephron. 142:264-270
A 6-month-old boy presented with acute renal failure, thrombocytopenia, and severe non-immune hemolytic anemia. Infection by Shiga-like toxin-producing Escherichia coli and other causes of microangiopathic hemolysis were ruled out, leading to a diagn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f29442dacef57102085d42e9f41b2810
https://doi.org/10.1159/000497823
https://doi.org/10.1159/000497823
Autor:
Marta Alberti, Paola Cuccarolo, Elisabetta Valoti, Caterina Mele, Paraskevas Iatropoulos, Miriam Galbusera, Ariela Benigni, Sara Gastoldi, Marina Noris, Rossella Piras, Marta Todeschini, Giuseppe Remuzzi, Elena Bresin
Publikováno v:
Frontiers in Medicine
Frontiers in Medicine, Vol 7 (2020)
Frontiers in Medicine, Vol 7 (2020)
Atypical hemolytic uremic syndrome (aHUS) is an ultra-rare disease characterized by microangiopathic hemolysis, thrombocytopenia, and renal impairment and is associated with dysregulation of the alternative complement pathway on the microvascular end
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1c05f25f5438b06afc13ecf4a012e65
http://europepmc.org/articles/PMC7670076
http://europepmc.org/articles/PMC7670076
Autor:
Rossella Piras, Annalisa Perna, Ariela Benigni, Luisa Murer, Paola Cuccarolo, Elisa Ferrari, Elisabetta Valoti, Roberta Donadelli, Valentina Portalupi, Matteo Breno, Caterina Mele, Miriam Galbusera, Marta Alberti, Sara Gastoldi, Giuseppe Remuzzi, Marina Vivarelli, Carmine Pecoraro, Elena Bresin, Marina Noris
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 74(1)
Rationale & Objective Although primary atypical hemolytic uremic syndrome (aHUS) is associated with abnormalities in complement genes and antibodies to complement factor H, the role of complement in secondary aHUS remains debatable. We evaluated the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74eff3cace7878cdaf159b08fc704b05
https://pubmed.ncbi.nlm.nih.gov/30851964
https://pubmed.ncbi.nlm.nih.gov/30851964
Autor:
Silvia Ravera, M. Illarcio, Isabella Panfoli, Martina Bartolucci, Paolo Degan, Daniela Calzia, E. Litamè, Alessandro Morelli, Paola Cuccarolo
Publikováno v:
Free Radical Research. 49:1156-1164
Oxidative phosphorylation (OXPHOS) is not only the main source of ATP for the cell, but also a major source of reactive oxygen species (ROS), which lead to oxidative stress. At present, mitochondria are considered the organelles responsible for the O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df2470d4203f8ae2c23673a42aeeeef8
https://doi.org/10.3109/10715762.2015.1050962
https://doi.org/10.3109/10715762.2015.1050962