Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Alessandra Renieri"'
Autor:
Joaquin Manrique, Valentina Villani, Stefano Da Sacco, Laura Perin, Roger E. De Filippo, Alessandra Renieri, Astgik Petrosyan, Andrea Angeletti, Paolo Cravedi
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-17 (2019)
Nature Communications
Nature Communications
In this work we model the glomerular filtration barrier, the structure responsible for filtering the blood and preventing the loss of proteins, using human podocytes and glomerular endothelial cells seeded into microfluidic chips. In long-term cultur
Autor:
Andrea Angeletti, Stefano Da Sacco, Paolo Cravedi, Roger E. De Filippo, Alessandra Renieri, Astgik Petrosyan, Joaquin Manrique, Valentina Villani, Laura Perin
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-1 (2019)
Nature Communications
Nature Communications
In this work we model the glomerular filtration barrier, the structure responsible for filtering the blood and preventing the loss of proteins, using human podocytes and glomerular endothelial cells seeded into microfluidic chips. In long-term cultur
Autor:
Andrea Accogli, Anna Maria Pinto, Paolo Toti, Valeria Morbidoni, Eva Trevisson, Francesca Ariani, Sonia De Francesco, Elisa Gelli, Maria Antonietta Mencarelli, Alessandra Renieri, Theodora Hadjistilianou, Elisa Frullanti, Valeria Capra, Elena Gusson, Gaia Roversi, Valentina Imperatore
Retinoblastoma is the most common eye cancer in children. Numerous families have been described displaying reduced penetrance and expressivity. An extensive molecular characterization of seven families led us to characterize the two main mechanisms i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d431709091ba0134957e4b054a7804a5
http://hdl.handle.net/10281/197606
http://hdl.handle.net/10281/197606
Autor:
Tommaso Patriarchi, Mario Costa, Elisa Landucci, Johannes W. Hell, Alessandra Renieri, Francesco Olimpico, Francesca Ariani, Elisa Frullanti, Sonia Amabile, Caterina Lo Rizzo, Flora M. Vaccarino, Ilaria Meloni
Publikováno v:
European journal of human genetics : EJHG, vol 24, iss 6
Rett syndrome (RTT) is a severe neurodevelopmental disorder associated with mutations in either MECP2, CDKL5 or FOXG1. The precise molecular mechanisms that lead to the pathogenesis of RTT have yet to be elucidated. We recently reported that expressi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90b5d79ab82f4952e506c11493389ef6
https://europepmc.org/articles/PMC4820038/
https://europepmc.org/articles/PMC4820038/
Autor:
Anna Bartolini, Sonia Amabile, Elisa Landucci, Gabriella Livide, Luca Massimino, Francesca Ariani, Elisa Frullanti, Ilaria Meloni, Francesca Mari, Alessandra Renieri, Flora M. Vaccarino, Maria Grazia Lolli
Foxg1 gene encodes for a transcription factor essential for telencephalon development in the embryonic mammalian forebrain. Its complete absence is embryonic lethal while Foxg1 heterozygous mice are viable but display microcephaly, altered hippocampa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be33d190026726a28041e9a6a8641b1
https://europepmc.org/articles/PMC4717204/
https://europepmc.org/articles/PMC4717204/