Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Bice Strumbo"'
Autor:
Gianluigi Ardissino, Selena Longhi, Luigi Porcaro, Giulia Pintarelli, Bice Strumbo, Valentina Capone, Donata Cresseri, Giulia Loffredo, Francesca Tel, Stefania Salardi, Martina Sgarbanti, Laura Martelli, Evangeline Millicent Rodrigues, Nicolò Borsa-Ghiringhelli, Giovanni Montini, Manuela Seia, Massimo Cugno, Fabio Carfagna, Dario Consonni, Silvana Tedeschi
Publikováno v:
Kidney International Reports, Vol 6, Iss 6, Pp 1614-1621 (2021)
Introduction: Atypical hemolytic uremic syndrome (aHUS) is mainly due to complement regulatory gene abnormalities with a dominant pattern but incomplete penetrance. Thus, healthy carriers can be identified in any family of aHUS patients, but it is un
Externí odkaz:
https://doaj.org/article/9c4a411b84e947be84e68998d1311488
Autor:
Dalila Sahbani, Bice Strumbo, Silvana Tedeschi, Elena Conte, Giulia Maria Camerino, Elisa Benetti, Giovanni Montini, Gabriella Aceto, Giuseppe Procino, Paola Imbrici, Antonella Liantonio
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Type III and IV Bartter syndromes (BS) are rare kidney tubulopathies caused by loss-of-function mutations in the CLCNKB and BSND genes coding respectively for the ClC-Kb chloride channels and accessory subunit barttin. ClC-K channels are expressed in
Externí odkaz:
https://doaj.org/article/9c8a9393433b49a49177acba818535fc
Autor:
Selena Longhi, Massimo Cugno, Giulia Pintarelli, Donata Cresseri, Martina Sgarbanti, Francesca Tel, Fabio Carfagna, Manuela Seia, Stefania Salardi, Valentina Capone, Gianluigi Ardissino, Bice Strumbo, Dario Consonni, Giulia Loffredo, Laura Martelli, Giovanni Montini, Evangeline Millicent Rodrigues, Nicolò Borsa-Ghiringhelli, Luigi Porcaro, Silvana Tedeschi
Publikováno v:
Kidney International Reports
Kidney International Reports, Vol 6, Iss 6, Pp 1614-1621 (2021)
Kidney International Reports, Vol 6, Iss 6, Pp 1614-1621 (2021)
Introduction Atypical hemolytic uremic syndrome (aHUS) is mainly due to complement regulatory gene abnormalities with a dominant pattern but incomplete penetrance. Thus, healthy carriers can be identified in any family of aHUS patients, but it is unp
Autor:
Chiara Tamburello, Mirco Belingheri, Silvana Tedeschi, Massimo Cugno, Dario Consonni, Piergiorgio Messa, C. Beretta, Elena Grovetti, Sara Testa, Valentina Capone, Evangeline Millicent Rodrigues, Antenore Giussani, Gianluigi Ardissino, Stefania Salardi, Donata Cresseri, Michela Perrone, Lucrezia Furian, Samantha Griffini, Massimo Cardillo, Bice Strumbo, Francesca Tel, Grazia Corti, Martina Sgarbanti
Patients with atypical hemolytic uremic syndrome (aHUS) have long been considered ineligible for kidney transplantation (KTx) in several centers due to the high risk of disease recurrence, graft loss and life-threatening complications. The availabili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d4ca0d2b636b0bce28cdc81ec5d4693
http://hdl.handle.net/11577/3403229
http://hdl.handle.net/11577/3403229
Autor:
Antonella Liantonio, Giovanni Montini, Giuseppe Procino, Elena Conte, Elisa Benetti, Bice Strumbo, Giulia Maria Camerino, Gabriella Aceto, Paola Imbrici, Silvana Tedeschi, Dalila Sahbani
Publikováno v:
Frontiers in Pharmacology
Frontiers in Pharmacology, Vol 11 (2020)
Frontiers in Pharmacology, Vol 11 (2020)
Type III and IV Bartter syndromes (BS) are rare kidney tubulopathies caused by loss-of-function mutations in the CLCNKB and BSND genes coding respectively for the ClC-Kb chloride channels and accessory subunit barttin. ClC-K channels are expressed in
Autor:
Bice Strumbo, Gabriella Tedeschi, Emanuele Carosati, Gabriele Cruciani, Armando Negri, Simona Nonnis
Publikováno v:
Biochimie. 92:1335-1342
L-aspartate oxidase (LASPO) is a flavoenzyme catalyzing the first step in the de novo biosynthesis of NAD+. The enzyme oxidizes L-aspartate both under aerobic and anaerobic conditions using oxygen as well as fumarate as electron acceptor. In accordan
Publikováno v:
Fish Physiology and Biochemistry. 32:339-353
We report cloning and tissue expression of transcripts of a fourth fish-specific gene (SPRNB) encoding a prion protein (PrP)-related protein (Shadoo2) from two species, Cyprinus carpio (carp) and Danio rerio (zebrafish), as well as gene or partial tr
Publikováno v:
Comparative biochemistry and physiology. Part B, Biochemistrymolecular biology. 150(2)
Identification and characterization of a bovine cDNA and the corresponding gene coding for a novel protein structurally related to Zar1, therefore called Zar1-like, are here reported for the first time. Structure of Zar1-like is similar to Zar1 gene,
Autor:
Bice Strumbo, Lorenzo Sangiorgio, Jill E. Gready, Marko Premzl, Jennifer A. Marshall Graves, Tatjana Simonic
Publikováno v:
Gene. 314
We report evidence from cDNA isolation and expression analysis as well as analyses of genome, expressed sequence tag (EST), cDNA and expression databases for a new gene named SPRN (shadow of prion protein). SPRN comprises two exons, with the open rea
Publikováno v:
FEBS letters. 508(2)
Isolation and characterization of the cDNA coding for the 216-residue Xenopus laevis prion protein is reported. Existence of this protein in amphibians was suggested by an EST fragment (accession number BG813008), while a conclusive demonstration is