Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Elisa Tinelli"'
Publikováno v:
Agathón, Vol 15 (2024)
Compared to other industrial fields, the construction sector, although encouraged by a framework of international policies that push towards spreading circular economy principles, still needs to adopt new ‘closed cycle’ resource management models
Externí odkaz:
https://doaj.org/article/b4644e9cd63540e5a6e4bfb7814dc9b7
Autor:
Christopher J. Minnis, StJohn Townsend, Julia Petschnigg, Elisa Tinelli, Jürg Bähler, Claire Russell, Sara E. Mole
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Juvenile CLN3 disease is a recessively inherited paediatric neurodegenerative disorder, with most patients homozygous for a 1-kb intragenic deletion in CLN3. The btn1 gene is the Schizosaccharomyces pombe orthologue of CLN3. Here, we have ex
Externí odkaz:
https://doaj.org/article/6527e4bac2b54420a484033fbe621105
Autor:
Elisa Tinelli
Publikováno v:
Italies, Vol 24, Pp 63-73 (2021)
L’analyse a pour objet le Paradoxe III (Meglio è d’esser ignorante che dotto) dans la collection des Paradoxes d’Ortensio Lando (1543), dans le but d’en souligner la structure argumentative basée sur le paradigme de la sancta rusticitas, ai
Externí odkaz:
https://doaj.org/article/f6c426a340284845900abec033cd9e8c
Autor:
Christopher J. Minnis, StJohn Townsend, Julia Petschnigg, Elisa Tinelli, Jürg Bähler, Claire Russell, Sara E. Mole
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-3 (2021)
Externí odkaz:
https://doaj.org/article/96da108b24f34e5ca18dd0cb24c426b5
Autor:
Elisa Tinelli
Publikováno v:
Studi Giraldiani, Vol 3, Iss 0, Pp 297-304 (2017)
Externí odkaz:
https://doaj.org/article/83f819979bcd4249a28f49d24c63f295
Autor:
Daniel Gerber, Monica Ghidinelli, Elisa Tinelli, Christian Somandin, Joanne Gerber, Jorge A Pereira, Andrea Ommer, Gianluca Figlia, Michaela Miehe, Lukas G Nägeli, Vanessa Suter, Valentina Tadini, Páris NM Sidiropoulos, Carsten Wessig, Klaus V Toyka, Ueli Suter
Publikováno v:
eLife, Vol 8 (2019)
Myelination requires extensive plasma membrane rearrangements, implying that molecules controlling membrane dynamics play prominent roles. The large GTPase dynamin 2 (DNM2) is a well-known regulator of membrane remodeling, membrane fission, and vesic
Externí odkaz:
https://doaj.org/article/af9ab6773f8547549f402cbb9cb83ae6
Autor:
Elisa Tinelli
Publikováno v:
Italies, Vol 24, Pp 63-73 (2021)
L’analyse a pour objet le Paradoxe III (Meglio è d’esser ignorante che dotto) dans la collection des Paradoxes d’Ortensio Lando (1543), dans le but d’en souligner la structure argumentative basée sur le paradigme de la sancta rusticitas, ai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3876ace8453a7364784ae2fab9d42f9
https://doi.org/10.4000/italies.8098
https://doi.org/10.4000/italies.8098
Autor:
Julia Petschnigg, Jürg Bähler, Claire Russell, StJohn Townsend, Sara E. Mole, Elisa Tinelli, Christopher J. Minnis
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-3 (2021)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b5009fbdc84f9a4998086ca4b7794da
https://doaj.org/article/96da108b24f34e5ca18dd0cb24c426b5
https://doaj.org/article/96da108b24f34e5ca18dd0cb24c426b5
Autor:
Claire Russell, Jürg Bähler, Elisa Tinelli, StJohn Townsend, Sara E. Mole, Julia Petschnigg, Christopher J. Minnis
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Juvenile CLN3 disease is a recessively inherited paediatric neurodegenerative disorder, with most patients homozygous for a 1-kb intragenic deletion in CLN3. The btn1 gene is the Schizosaccharomyces pombe orthologue of CLN3. Here, we have extended th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6e45eede73a5b8251c520b4ea02ed2d
http://europepmc.org/articles/PMC7973434
http://europepmc.org/articles/PMC7973434
Autor:
Joanne Gerber, Elisa Tinelli, Jorge A. Pereira, Monica Ghidinelli, Klaus V. Toyka, Ueli Suter, Daniel Gerber, Shuo Lin, Luigi Tortola, Francesco Santarella, Markus A. Rüegg, Manfred Kopf, Andrea Ommer, Sven Bachofner
Publikováno v:
Human Molecular Genetics, 29 (8)
Human Molecular Genetics
Human Molecular Genetics
Some mutations affecting dynamin 2 (DNM2) can cause dominantly inherited Charcot–Marie–Tooth (CMT) neuropathy. Here, we describe the analysis of mice carrying the DNM2 K562E mutation which has been associated with dominant-intermediate CMT type B
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d0c82595153162878edd1a1a87ce517
https://hdl.handle.net/20.500.11850/418646
https://hdl.handle.net/20.500.11850/418646
