Zobrazeno 1 - 10
of 31
pro vyhledávání: '"VERONICA COSTA"'
Autor:
Veronica Costa, Stefan Aigner, Mirko Vukcevic, Evelyn Sauter, Katharina Behr, Martin Ebeling, Tom Dunkley, Arno Friedlein, Sannah Zoffmann, Claas A. Meyer, Frédéric Knoflach, Sebastian Lugert, Christoph Patsch, Fatiha Fjeldskaar, Laurie Chicha-Gaudimier, Anna Kiialainen, Paolo Piraino, Marc Bedoucha, Martin Graf, Sebastian Jessberger, Anirvan Ghosh, Josef Bischofberger, Ravi Jagasia
Publikováno v:
Cell Reports, Vol 15, Iss 1, Pp 86-95 (2016)
Hyperfunction of the mTORC1 pathway has been associated with idiopathic and syndromic forms of autism spectrum disorder (ASD), including tuberous sclerosis, caused by loss of either TSC1 or TSC2. It remains largely unknown how developmental processes
Externí odkaz:
https://doaj.org/article/c453283d07954edc80795548e6cfa550
Autor:
Roel Quintens, Sarvjeet Singh, Katleen Lemaire, Katrien De Bock, Mikaela Granvik, Anica Schraenen, Irene Olga Cornelia Maria Vroegrijk, Veronica Costa, Pieter Van Noten, Dennis Lambrechts, Stefan Lehnert, Leentje Van Lommel, Lieven Thorrez, Geoffroy De Faudeur, Johannes Anthonius Romijn, John Michael Shelton, Luca Scorrano, Henri Roger Lijnen, Peter Jacobus Voshol, Peter Carmeliet, Pradeep Puthenveetil Abraham Mammen, Frans Schuit
Publikováno v:
PLoS ONE, Vol 8, Iss 2, p e56719 (2013)
Oxidative phosphorylation in mitochondria is responsible for 90% of ATP synthesis in most cells. This essential housekeeping function is mediated by nuclear and mitochondrial genes encoding subunits of complex I to V of the respiratory chain. Althoug
Externí odkaz:
https://doaj.org/article/6e48974138964287b15012c484cb8268
Autor:
Miranda, Catarina Runa, Mendes, Pedro, Coelho, Pedro, Alvarez, Xenxo, Freitas, João, Dias, Miguel Sales, Orvalho, Verónica Costa
Each human face is unique. It has its own shape, topology, and distinguishing features. As such, developing and testing facial tracking systems are challenging tasks. The existing face recognition and tracking algorithms in Computer Vision mainly spe
Externí odkaz:
http://arxiv.org/abs/1506.00925
Autor:
Ravi Jagasia, Charlotte Bon, Soren V. Rasmussen, Solveig Badillo, Disa Tehler, Danièle Buchy, Marco Berrera, Megana Prasad, Marco Terrigno, Nikhil J. Pandya, Veronica Costa, Congwei Wang, Lykke Pedersen, Meghan T. Miller, Kamille Dumong Erichsen, Lars Joenson, Joerg Hipp, Azad Bonni, Lutz Müller, Annamaria Brändli-Baiocco, Thomas Kremer, Erich Koller, Marius C. Hoener
Angelman syndrome (AS) is a severe neurodevelopmental disorder caused by the loss of neuronal E3 ligase UBE3A with no available treatment. Restoring UBE3A levels via downregulation of the paternally cis-acting long non-coding antisense transcript (UB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25b371ef89b1857c8727fbfa1924bbe9
https://doi.org/10.1101/2022.06.09.495066
https://doi.org/10.1101/2022.06.09.495066
Autor:
Angelo Ferlazzo, Consuelo Celesti, Daniela Iannazzo, Claudio Ampelli, Daniele Giusi, Veronica Costantino, Giovanni Neri
Publikováno v:
ACS Omega, Vol 9, Iss 25, Pp 27085-27092 (2024)
Externí odkaz:
https://doaj.org/article/60684bdeab6f4c3b8c4c536a30019cc6
Autor:
Paul Lopatta, Ravi Jagasia, Rasmussen Søren Vestergaard, Tom Dunkley, Marco Berrera, Nikhil J. Pandya, Edwin Mientjes, Tania Distler, Ben Distel, Balazs Banfai, F. Isabella Zampeta, Ype Elgersma, Philip Grossen, Christoph Patsch, Martin Ebeling, Thomas Kremer, Sonja Meier, Yasmina Martí, A. Mattijs Punt, Congwei Wang, Veronica Costa, Manuel Tzouros, Marius C. Hoener
Publikováno v:
Cell Reports Medicine
Cell Reports Medicine, 2(8):100360. Cell Press
Cell Reports Medicine, 2(8):100360. Cell Press
Angelman syndrome (AS) is a neurodevelopmental disorder caused by the loss of maternal UBE3A, a ubiquitin protein ligase E3A. Here, we study neurons derived from patients with AS and neurotypical individuals, and reciprocally modulate UBE3A using ant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1738738cb51a3998314b1853efed0fa
https://doi.org/10.1016/j.xcrm.2021.100360
https://doi.org/10.1016/j.xcrm.2021.100360
Trata-se de dissertação baseada em estudo exploratório desenvolvido com a finalidade de investigar o potencial do SIEO - Sistema de Informação Especializado da Área de Odontologia para atuação na divulgação científica e outras ações visa
Autor:
Frédéric Knoflach, Sannah Jensen Zoffmann, Martin Ebeling, Mirko Vukcevic, Christoph Patsch, Claas A. Meyer, Tom Dunkley, Laurie Chicha-Gaudimier, Katharina Behr, Josef Bischofberger, Anna Kiialainen, Ravi Jagasia, Sebastian Jessberger, Veronica Costa, Paolo Piraino, Martin Graf, Fatiha Fjeldskaar, Marc Bedoucha, Sebastian Lugert, Stefan Aigner, Evelyn Sauter, Anirvan Ghosh, Arno Friedlein
Publikováno v:
Cell Reports, Vol 15, Iss 1, Pp 86-95 (2016)
SummaryHyperfunction of the mTORC1 pathway has been associated with idiopathic and syndromic forms of autism spectrum disorder (ASD), including tuberous sclerosis, caused by loss of either TSC1 or TSC2. It remains largely unknown how developmental pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9dcebef63545b1b30e464198171d1577
Autor:
Arno Friedlein, Sebastian Lugert, Stefan Aigner, Paul Cutler, Martin Ebeling, Veronica Costa, Meghan T. Miller, Paolo Piraino, Christoph Patsch, Ravi Jagasia, Tom Dunkley
Publikováno v:
PROTEOMICS - Clinical Applications. 9:684-694
Purpose Human pluripotent stem cell (hPSC)-derived cellular models have great potential to enable drug discovery and improve translation of preclinical insights to the clinic. We have developed a hPSC-derived neural precursor cell model for studying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d650c8f3f20ebc9d63c690d85d365d4
https://doi.org/10.1002/prca.201400150
https://doi.org/10.1002/prca.201400150