Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Maximiliano Presa"'
Autor:
Maximiliano Presa, Carolina Román
Publikováno v:
Rural History. :1-23
The literature about the nutrition transition has been discussing the existence of different paths. The case of Uruguay is introduced as a different case of transition. We focus on the period 1900–70 when the country shifted from an agricultural-ba
Autor:
Jone Lopez-Erauskin, Mariana Bravo-Hernandez, Maximiliano Presa, Michael W. Baughn, Ze’ev Melamed, Melinda S. Beccari, Ana Rita Agra de Almeida Quadros, Aamir Zuberi, Karen Ling, Oleksandr Platoshyn, Elkin Niño-Jara, I. Sandra Ndayambaje, Olatz Arnold-Garcia, Melissa McAlonis-Downes, Larissa Cabrera, Jonathan W. Artates, Jennifer Ryan, Frank Bennett, Paymaan Jafar-nejad, Frank Rigo, Martin Marsala, Cathleen M. Lutz, Don W. Cleveland, Clotilde Lagier-Tourenne
The human mRNA most affected by TDP-43 loss-of-function is transcribed from theSTMN2gene and encodes stathmin-2 (also known as SCG10), whose loss is a neurodegenerative disease hallmark. Here using multiplein vivoapproaches, including transient antis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a3fca87f97b78a3be286544a9b3838f6
https://doi.org/10.1101/2022.12.11.519794
https://doi.org/10.1101/2022.12.11.519794
Publikováno v:
Molecular Genetics and Metabolism. 138:107278
Autor:
Nicolina Cristina Sorrentino, Maximiliano Presa, Sergio Attanasio, Vincenzo Cacace, Martina Sofia, Aamir Zuberi, Jennifer Ryan, Somdatta Ray, Igor Petkovic, Karthikeyan Radhakrishnan, Lars Schlotawa, Andrea Ballabio, Cathleen Lutz, Nicola Brunetti‐Pierri
Multiple sulfatase deficiency (MSD) is an ultrarare lysosomal storage disorder due to deficiency of all known sulfatases. MSD is caused by mutations in the Sulfatase Modifying Factor 1 (SUMF1) gene encoding the enzyme responsible for the post-transla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::359ad552e9c60939652ca0a1098ebeaa
https://hdl.handle.net/11588/906865
https://hdl.handle.net/11588/906865
Autor:
Jennifer R. Dwyer, Jeremy J. Racine, Harold D. Chapman, Anna Quinlan, Maximiliano Presa, Grace A. Stafford, Ingo Schmitz, David V. Serreze
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 209(2)
Type 1 diabetes (T1D) in both humans and NOD mice is caused by T cell–mediated autoimmune destruction of pancreatic β cells. Increased frequency or activity of autoreactive T cells and failures of regulatory T cells (Tregs) to control these pathog
Autor:
Robert W. Burgess, Maximiliano Presa, Hannah Wilpan, Cathleen M. Lutz, Crystal Davis, Laurent P. Bogdanik, Guy M. Lenk, Steven J. Gray, Randy Walls, Rachel M. Bailey, Jenn Cook, Tara Murphy
Publikováno v:
J Clin Invest
Charcot-Marie-Tooth disease type 4J (CMT4J) is caused by recessive, loss-of-function mutations in FIG4, encoding a phosphoinositol(3,5)P2-phosphatase. CMT4J patients have both neuron loss and demyelination in the peripheral nervous system, with vacuo
Autor:
Maximiliano Presa, Rachel M. Bailey, Somdatta Ray, Lauren Bailey, Saurabh Tata, Tara Murphy, Harold Coombs, Steven J. Gray, Cathleen Lutz
Publikováno v:
Molecular Genetics and Metabolism. 135:S101
Autor:
Yuriko Tachida, Ashutosh Pandey, Seung Yeop Han, Hamed Jafar-Nejad, Joshua M Adams, Antonio Galeone, Maximiliano Presa, Hiroto Hirayama, Cathleen M. Lutz, Thomas Vaccari, Aamir Zuberi, Tadashi Suzuki, Markus Affolter, Shinya Matsuda
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd0a120e7b22d00fbf497820546fb3b8
https://doi.org/10.7554/elife.55596.sa2
https://doi.org/10.7554/elife.55596.sa2
Autor:
Ashutosh Pandey, Seung Yeop Han, Yuriko Tachida, Shinya Matsuda, Antonio Galeone, Aamir Zuberi, Markus Affolter, Maximiliano Presa, Tadashi Suzuki, Thomas Vaccari, Hiroto Hirayama, Cathleen M. Lutz, Hamed Jafar-Nejad, Joshua M Adams
Publikováno v:
eLife
eLife Sciences Publications, Ltd
eLife, Vol 9 (2020)
eLife Sciences Publications, Ltd
eLife, Vol 9 (2020)
During endoplasmic reticulum-associated degradation (ERAD), the cytoplasmic enzymeN-glycanase 1 (NGLY1) is proposed to removeN-glycans from misfoldedN-glycoproteins after their retrotranslocation from the ER to the cytosol. We previously reported tha
Autor:
Cristina Izquierdo, Angela Zarama Ortiz, Conchi Mora, Joan Verdaguer, Thomas Stratmann, Anna Montoya, Sara Malo, Maximiliano Presa, Nahir Garabatos
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-14 (2018)
Recercat. Dipósit de la Recerca de Catalunya
instname
Repositorio Abierto de la UdL
Universitad de Lleida
Scientific Reports
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Repositorio Abierto de la UdL
Universitad de Lleida
Scientific Reports
Dipòsit Digital de la UB
Universidad de Barcelona
Type 1 diabetes can be overcome by regulatory T cells (Treg) in NOD mice yet an efficient method to generate and maintain antigen-specific Treg is difficult to come by. Here, we devised a combination therapy of peptide/MHC tetramers and IL-2/anti-IL-