Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Gabriele Dati"'
Autor:
Paola Zaratin, Deborah Bertorello, Roberta Guglielmino, Danilo Devigili, Giampaolo Brichetto, Valentina Tageo, Gabriele Dati, Stephanie Kramer, Mario Alberto Battaglia, Monica Di Luca
Publikováno v:
Health Research Policy and Systems, Vol 20, Iss 1, Pp 1-9 (2022)
Abstract The COVID-19 pandemic has unmasked even more clearly the need for research and care to form a unique and interdependent ecosystem, a concept which has emerged in recent years. In fact, to address urgent and unexpected missions such as “fig
Externí odkaz:
https://doaj.org/article/0f9d975d9e4a4fc0b5958a897e08b0a1
Autor:
Paola Saveri, Pietro Fratta, Sophie Belin, Francesca Ornaghi, Michael E. Shy, Angelo Quattrini, Patrizia D'Adamo, M. Laura Feltri, Desirée Zambroni, Lawrence Wrabetz, Gabriele Dati
Publikováno v:
Human Molecular Genetics
Protein Zero (P0) is the major structural protein in peripheral myelin and mutations in the Myelin Protein Zero (Mpz) gene produce wide ranging hereditary neuropathy phenotypes. To gain insight in the mechanisms underlying a particularly severe form,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::815b9b8055816fb4222611eea8ba4430
Autor:
Giuseppe Digilio, Gabriele Dati, Valeria Catanzaro, Linda Chaabane, Silvia Rizzitelli, Evelina Cittadino, Concetta V. Gringeri, Silvio Aime, Valeria Menchise
Publikováno v:
Contrast Media & Molecular Imaging. 7:175-184
Two novel Gd-based contrast agents (CAs) for the molecular imaging of matrix metalloproteinases (MMPs) were synthetized and characterized in vitro and in vivo. These probes were based on the PLG*LWAR peptide sequence, known to be hydrolyzed between G
Autor:
Concetta V, Gringeri, Valeria, Menchise, Silvia, Rizzitelli, Evelina, Cittadino, Valeria, Catanzaro, Gabriele, Dati, Linda, Chaabane, Giuseppe, Digilio, Silvio, Aime
Publikováno v:
Contrast mediamolecular imaging. 7(2)
Two novel Gd-based contrast agents (CAs) for the molecular imaging of matrix metalloproteinases (MMPs) were synthetized and characterized in vitro and in vivo. These probes were based on the PLG*LWAR peptide sequence, known to be hydrolyzed between G
Autor:
Gringeri, Concetta V., Valeria, Menchise, Rizzitelli, Silvia, Cittadino, Evelina, Valeria, Catanzaro, Gabriele, Dati, Linda, Chaabane, Giuseppe, Digilio, Aime, Silvio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______970::4adaad9428225fee477985831b18ebce
http://hdl.handle.net/2318/132582
http://hdl.handle.net/2318/132582
Autor:
Maria Pannese, Alessandro Bertolo, Simona Capossela, Linda Chaabane, Gabriele Dati, Stefano Biffo, Patrizia D'Adamo, Veronica Bianchi, Luca Muzio, Antonello Mallamaci, Claudia Godi, Letterio S. Politi
Publikováno v:
The American journal of pathology. 180(3)
Protein synthesis is a tightly regulated, energy-consuming process. The control of mRNA translation into protein is fundamentally important for the fine-tuning of gene expression; additionally, precise translational control plays a critical role in m
Autor:
Alessandro, Nodari, Stefano C, Previtali, Gabriele, Dati, Simona, Occhi, Felipe A, Court, Cristina, Colombelli, Desirée, Zambroni, Giorgia, Dina, Ubaldo, Del Carro, Kevin P, Campbell, Angelo, Quattrini, Lawrence, Wrabetz, M Laura, Feltri
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 28(26)
Schwann cells integrate signals deriving from the axon and the basal lamina to myelinate peripheral nerves. Integrin alpha6beta4 is a laminin receptor synthesized by Schwann cells and displayed apposed to the basal lamina. alpha6beta4 integrin expres
Autor:
Stefano C. Previtali, Daniele Imperiale, Pietro Fratta, Robin L. Avila, Klaus V. Toyka, Jürgen Zielasek, Elisa Tinelli, Daniel A. Kirschner, M. Laura Feltri, Maurizio D'Antonio, Albee Messing, Lawrence Wrabetz, Gabriele Dati, Maria Pennuto, Angelo Quattrini
Missense mutations in 22 genes account for one-quarter of Charcot–Marie–Tooth (CMT) hereditary neuropathies.Myelin Protein Zero(MPZ,P0) mutations produce phenotypes ranging from adult demyelinating (CMT1B) to early onset [Déjérine-Sottas syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dd5c8d634e60b94a70445577a103068
http://hdl.handle.net/11577/3257901
http://hdl.handle.net/11577/3257901
Autor:
Lawrence Wrabetz, Gabriele Dati, Annalisa Bolis, C. Yan Cheng, Alessandra Bolino, Simona Bussini, Maria Laura Feltri, Dolores D. Mruk, Stefano C. Previtali, Giorgia Dina, Stefano Amadio, Angelo Quattrini, Ubaldo Del Carro
Publikováno v:
The Journal of Cell Biology
Mutations in MTMR2, the myotubularin-related 2 gene, cause autosomal recessive Charcot-Marie-Tooth (CMT) type 4B1, a demyelinating neuropathy with myelin outfolding and azoospermia. MTMR2 encodes a ubiquitously expressed phosphatase whose preferred s