Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marco A. Morales-Garza"'
Autor:
Shubham Patel, Faheem Ershad, Jimmy Lee, Lourdes Chacon‐Alberty, Yifan Wang, Marco A. Morales‐Garza, Arturo Haces‐Garcia, Seonmin Jang, Lei Gonzalez, Luis Contreras, Aman Agarwal, Zhoulyu Rao, Grace Liu, Igor R. Efimov, Yu Shrike Zhang, Min Zhao, Roslyn Rivkah Isseroff, Alamgir Karim, Abdelmotagaly Elgalad, Weihang Zhu, Xiaoyang Wu, Cunjiang Yu
Publikováno v:
Small, vol 18, iss 36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96b362516c8b657fd676666e1bf853d4
https://escholarship.org/uc/item/68n2d05k
https://escholarship.org/uc/item/68n2d05k
Autor:
Shubham Patel, Faheem Ershad, Jimmy Lee, Lourdes Chacon‐Alberty, Yifan Wang, Marco A. Morales‐Garza, Arturo Haces‐Garcia, Seonmin Jang, Lei Gonzalez, Luis Contreras, Aman Agarwal, Zhoulyu Rao, Grace Liu, Igor R. Efimov, Yu Shrike Zhang, Min Zhao, Roslyn Rivkah Isseroff, Alamgir Karim, Abdelmotagaly Elgalad, Weihang Zhu, Xiaoyang Wu, Cunjiang Yu
Publikováno v:
Small (Weinheim an der Bergstrasse, Germany). 18(36)
The need to develop wearable devices for personal health monitoring, diagnostics, and therapy has inspired the production of innovative on-demand, customizable technologies. Several of these technologies enable printing of raw electronic materials di
Autor:
Pedro Fernandez-Funez, Sergio Casas-Tinto, Yan Zhang, Melisa Gómez-Velazquez, Marco A Morales-Garza, Ana C Cepeda-Nieto, Joaquín Castilla, Claudio Soto, Diego E Rincon-Limas
Publikováno v:
PLoS Genetics, Vol 5, Iss 6, p e1000507 (2009)
Prion diseases are incurable neurodegenerative disorders in which the normal cellular prion protein (PrP(C)) converts into a misfolded isoform (PrP(Sc)) with unique biochemical and structural properties that correlate with disease. In humans, prion d
Externí odkaz:
https://doaj.org/article/806405e30d484048a35391af05dd857d
Autor:
Marco A. Morales-Garza, Caitlin Winebrenner, Doris A. Taylor, Mitalben Patel, Eric Chau, Farideh Beigi, Luiz C. Sampaio, Andrea S. Gobin
Publikováno v:
Journal of cellular physiology. 232(11)
Numerous protocols exist for isolating aortic endothelial and smooth muscle cells from small animals. However, establishing a protocol for isolating pure cell populations from large animal vessels that are more elastic has been challenging. We develo
Autor:
Martin R. Ramos-Gonzalez, Ricardo M. Cerda-Flores, Carlos D. Hernández-Castillo, Leonel Cantu-Martinez, Ricardo A. Rangel-Guerra, Marco A. Morales-Garza, Juan J.J. Vergara-Saavedra, Roberto Montes-de-Oca-Luna, Marcos J. Guerrero-Muñoz, Humberto González-González, Odila Saucedo-Cárdenas, Héctor R. Martínez
Publikováno v:
Neuroscience Letters. 468:264-266
Early- and late-onset Parkinson's disease (EOPD and LOPD) have been associated with mutations in the PARKIN gene. Several studies have reported association of Parkinson's disease (PD) with different polymorphisms in different ethnic populations. To s
In Vivo Generation of Neurotoxic Prion Protein: Role for Hsp70 in Accumulation of Misfolded Isoforms
Autor:
Ana Cecilia Cepeda-Nieto, Sergio Casas-Tintó, Melisa Gomez-Velazquez, Joaquín Castilla, Diego E. Rincon-Limas, Marco A. Morales-Garza, Yan Zhang, Pedro Fernandez-Funez, Claudio Soto
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 5, Iss 6, p e1000507 (2009)
PLoS Genetics, Vol 5, Iss 6, p e1000507 (2009)
Prion diseases are incurable neurodegenerative disorders in which the normal cellular prion protein (PrPC) converts into a misfolded isoform (PrPSc) with unique biochemical and structural properties that correlate with disease. In humans, prion disor