Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Susanna Tomasoni"'
Autor:
Luca Perico, Marta Todeschini, Federica Casiraghi, Marilena Mister, Anna Pezzotta, Tobia Peracchi, Susanna Tomasoni, Piera Trionfini, Ariela Benigni, Giuseppe Remuzzi
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
We examined the immune response in subjects previously infected with SARS-CoV2 and infection-naïve 9 months after primary 2-dose COVID-19 mRNA vaccination and 3 months after the booster dose in a longitudinal cohort of healthcare workers. Nine month
Externí odkaz:
https://doaj.org/article/c6dd1c6048334328923fb6f16ace37a3
Autor:
Luca Perico, Marina Morigi, Anna Pezzotta, Daniela Corna, Valerio Brizi, Sara Conti, Cristina Zanchi, Fabio Sangalli, Piera Trionfini, Sara Buttò, Christodoulos Xinaris, Susanna Tomasoni, Carlamaria Zoja, Giuseppe Remuzzi, Ariela Benigni, Barbara Imberti
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-18 (2021)
Abstract Abnormal kidney development leads to lower nephron number, predisposing to renal diseases in adulthood. In embryonic kidneys, nephron endowment is dictated by the availability of nephron progenitors, whose self-renewal and differentiation re
Externí odkaz:
https://doaj.org/article/348d577fe4874089875fa592c84cadd5
Autor:
Ariela Benigni, Susanna Tomasoni
Publikováno v:
Frontiers in Pharmacology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/19cdd07835ff47979db69c3044c0ca02
Publikováno v:
Stem Cell Research, Vol 57, Iss , Pp 102580- (2021)
Human induced pluripotent stem cells (iPSCs) have great promise in regenerative medicine. However, several limitations, including immune-incompatibility, have raised concerns regarding their clinical application. Recent studies have shown that human
Externí odkaz:
https://doaj.org/article/831fefabf399488f847c57f65799c790
Publikováno v:
Stem Cell Research, Vol 33, Iss , Pp 175-179 (2018)
Focal Segmental Glomerulosclerosis (FSGS) is the typical renal histologic lesion in familial steroid-resistant nephrotic syndrome, for which there is currently no treatment. Dysfunction of the glomerular podocyte, a specialized cell that forms the gl
Externí odkaz:
https://doaj.org/article/2992e83ce56b4b4abf3d93ea4d174c51
Autor:
Luca Perico, Susanna Tomasoni, Tobia Peracchi, Annalisa Perna, Anna Pezzotta, Giuseppe Remuzzi, Ariela Benigni
Publikováno v:
EBioMedicine, Vol 61, Iss , Pp 103069- (2020)
Background: Italy was the first western country to experience a large Coronavirus Disease 2019 (COVID-19) outbreak and the province of Bergamo experienced one of the deadliest COVID-19 outbreaks in the world. Following the peak of the epidemic in mid
Externí odkaz:
https://doaj.org/article/d8cb899df7834689b1f2030e2d369c20
Publikováno v:
Stem Cell Research, Vol 47, Iss , Pp 101881- (2020)
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, characterised by the development of multiple fluid-filled cysts in the kidneys and other organs. PKD1 and PKD2 are the two major causative genes encodi
Externí odkaz:
https://doaj.org/article/8b150a7e28904e458dc1b52042b27ef4
Publikováno v:
Stem Cell Research, Vol 42, Iss , Pp - (2020)
Autosomal dominant polycystic kidney disease (ADPKD) is the most prevalent inherited renal disease, characterized by multiple cysts that can lead to kidney failure resulting in end-stage renal disease. ADPKD is mainly caused by mutations in either th
Externí odkaz:
https://doaj.org/article/58ed6469b4ac464d870a597e20d67090
Autor:
Valentina Benedetti, Valerio Brizi, Patrizia Guida, Susanna Tomasoni, Osele Ciampi, Elena Angeli, Ugo Valbusa, Ariela Benigni, Giuseppe Remuzzi, Christodoulos Xinaris
Publikováno v:
EBioMedicine, Vol 33, Iss , Pp 253-268 (2018)
The lack of engineering systems able to faithfully reproduce complex kidney structures in vitro has made it difficult to efficiently model kidney diseases and development. Using polydimethylsiloxane (PDMS) scaffolds and a kidney-derived cell line we
Externí odkaz:
https://doaj.org/article/483f9c49b79b441694f3786eaf80902b
Autor:
Lorena Longaretti, Piera Trionfini, Valerio Brizi, Christodoulos Xinaris, Caterina Mele, Matteo Breno, Elena Romano, Roberta Giampietro, Giuseppe Remuzzi, Ariela Benigni, Susanna Tomasoni
Publikováno v:
Biomedicines, Vol 9, Iss 12, p 1808 (2021)
No effective treatments are available for familial steroid-resistant Focal Segmental Glomerulosclerosis (FSGS), characterized by proteinuria due to ultrastructural abnormalities in glomerular podocytes. Here, we studied a private PAX2 mutation identi
Externí odkaz:
https://doaj.org/article/08aef8f4506544499d69db0102459812