Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Benedetta Mazzinghi"'
Publikováno v:
Kidney & Blood Pressure Research, Vol 49, Iss 1, Pp 258-265 (2024)
Background: Chronic kidney disease affects 10% of the world population, and it is associated with progression to end-stage kidney disease and increased morbidity and mortality. The advent of multi-omics technologies has expanded our knowledge on the
Externí odkaz:
https://doaj.org/article/280452f276f34d03aec72eb0e118cc5e
Autor:
Maria Elena Melica, Maria Lucia Angelotti, Giulia Antonelli, Anna Peired, Carolina Conte, Letizia De Chiara, Benedetta Mazzinghi, Elena Lazzeri, Laura Lasagni, Paola Romagnani
Publikováno v:
Bio-Protocol, Vol 13, Iss 16 (2023)
Kidney diseases are a global health concern. Modeling of kidney disease for translational research is often challenging because of species specificities or the postmitotic status of kidney epithelial cells that make primary cultures, for example podo
Externí odkaz:
https://doaj.org/article/747426ccb1264191b6ecaa4ce1ae1214
Autor:
Letizia De Chiara, Carolina Conte, Roberto Semeraro, Paula Diaz-Bulnes, Maria Lucia Angelotti, Benedetta Mazzinghi, Alice Molli, Giulia Antonelli, Samuela Landini, Maria Elena Melica, Anna Julie Peired, Laura Maggi, Marta Donati, Gilda La Regina, Marco Allinovi, Fiammetta Ravaglia, Daniele Guasti, Daniele Bani, Luigi Cirillo, Francesca Becherucci, Francesco Guzzi, Alberto Magi, Francesco Annunziato, Laura Lasagni, Hans-Joachim Anders, Elena Lazzeri, Paola Romagnani
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-19 (2022)
Acute kidney injury is frequent, often fatal and can leave survivors with chronic kidney disease. Here the authors show that tubular cell polyploidy reduces early fatality sustaining residual function but promotes chronic kidney disease, which can be
Externí odkaz:
https://doaj.org/article/a91d01abb8dc48d881536bd29de595fa
Autor:
Viviana Palazzo, Valentina Raglianti, Samuela Landini, Luigi Cirillo, Carmela Errichiello, Elisa Buti, Rosangela Artuso, Lucia Tiberi, Debora Vergani, Elia Dirupo, Paola Romagnani, Benedetta Mazzinghi, Francesca Becherucci
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 10, p 5641 (2022)
Bartter (BS) and Gitelman (GS) syndrome are autosomal recessive inherited tubulopathies, whose clinical diagnosis can be challenging, due to rarity and phenotypic overlap. Genotype–phenotype correlations have important implications in defining kidn
Externí odkaz:
https://doaj.org/article/2818652bb5fd4be39dacea57167e3e44
Autor:
Elena Lazzeri, Maria Lucia Angelotti, Anna Peired, Carolina Conte, Julian A. Marschner, Laura Maggi, Benedetta Mazzinghi, Duccio Lombardi, Maria Elena Melica, Sara Nardi, Elisa Ronconi, Alessandro Sisti, Giulia Antonelli, Francesca Becherucci, Letizia De Chiara, Ricardo Romero Guevara, Alexa Burger, Beat Schaefer, Francesco Annunziato, Hans-Joachim Anders, Laura Lasagni, Paola Romagnani
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-18 (2018)
The recovery of function upon acute kidney injury is thought to involve tubular cell dedifferentiation and proliferation. Here the authors show that Pax2+ progenitors regenerate tubules via cell division while other tubular cells support function rec
Externí odkaz:
https://doaj.org/article/fcd2644ead064a62bdd2370d3ecae9a3
Autor:
Laura Lasagni, Maria Lucia Angelotti, Elisa Ronconi, Duccio Lombardi, Sara Nardi, Anna Peired, Francesca Becherucci, Benedetta Mazzinghi, Alessandro Sisti, Simone Romoli, Alexa Burger, Beat Schaefer, Annamaria Buccoliero, Elena Lazzeri, Paola Romagnani
Publikováno v:
Stem Cell Reports, Vol 5, Iss 2, Pp 248-263 (2015)
Podocyte loss is a general mechanism of glomerular dysfunction that initiates and drives the progression of chronic kidney disease, which affects 10% of the world population. Here, we evaluate whether the regenerative response to podocyte injury infl
Externí odkaz:
https://doaj.org/article/ab64e26dfcaa406b9afd991e4b7623ba
Autor:
Francesca Becherucci, Samuela Landini, Viviana Palazzo, Luigi Cirillo, Valentina Raglianti, Gianmarco Lugli, Lucia Tiberi, Elia Dirupo, Stefania Bellelli, Tommaso Mazzierli, Jacopo Lomi, Fiammetta Ravaglia, Giulia Sansavini, Marco Allinovi, Domenico Giannese, Chiara Somma, Giuseppe Spatoliatore, Debora Vergani, Rosangela Artuso, Alberto Rosati, Calogero Cirami, Pietro Claudio Dattolo, Gesualdo Campolo, Letizia De Chiara, Laura Papi, Augusto Vaglio, Elena Lazzeri, Hans-Joachim Anders, Benedetta Mazzinghi, Paola Romagnani
Publikováno v:
Journal of the American Society of Nephrology. 34:706-720
Autor:
Maria Elena Melica, Giulia Antonelli, Roberto Semeraro, Maria Lucia Angelotti, Gianmarco Lugli, Samuela Landini, Fiammetta Ravaglia, Gilda La Regina, Carolina Conte, Letizia De Chiara, Anna Julie Peired, Benedetta Mazzinghi, Marta Donati, Alice Molli, Stefanie Steiger, Alberto Magi, Niccolò Bartalucci, Valentina Raglianti, Francesco Guzzi, Laura Maggi, Francesco Annunziato, Alexa Burger, Elena Lazzeri, Hans-Joachim Anders, Laura Lasagni, Paola Romagnani
Publikováno v:
Sci Transl Med
Science Translational Medicine
Science Translational Medicine
Crescentic glomerulonephritis is characterized by vascular necrosis and parietal epithelial cell hyperplasia in the space surrounding the glomerulus, resulting in the formation of crescents. Little is known about the molecular mechanisms driving this
Autor:
Francesca Becherucci, Luigi Cirillo, Samuela Landini, Viviana Palazzo, Valentina Raglianti, Gianmarco Lugli, Lucia Tiberi, Augusto Vaglio, Hans-Joachim Anders, Benedetta Mazzinghi, Paola Romagnani
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS With the spread of whole-exome sequencing techniques (WES), genetic kidney diseases are increasingly recognized across all age groups. However, accessibility, interpretation of results and costs limit the widespread of genomics us
Autor:
Luigi Cirillo, Francesca Becherucci, Stefania Bellelli, Benedetta Mazzinghi, Valentina Raglianti, Gianmarco Lugli, Samuela Landini, Viviana Palazzo, Lucia Tiberi, Augusto Vaglio, Hans-Joachim Anders, Paola Romagnani
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS In the last decade, the use of whole-exome sequencing techniques (WES) has provided many insights into inherited kidney diseases that are thought to represent at least 10%–15% of cases of end-stage CKD [1]. However, among others