Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Quetzalli Denisse Angeles-López"'
Autor:
Pablo Eliasib Martínez-Gopar, Quetzalli Denisse Angeles-López, Gabriela Rodríguez-Manzo, Marian Jesabel Pérez-Rodríguez, Francisca Pérez-Severiano, Luis Tristán-López, René Garduño-Gutiérrez, Claudia González-Espinosa
Publikováno v:
Journal of Neurochemistry. 160:256-270
Huntington´s disease (HD) is a pathological condition that can be studied in mice by the administration of quinolinic acid (QUIN), an agonist of the N-methyl-d-aspartate receptor (NMDAR) that induces NMDAR-mediated cytotoxicity and neuroinflammation
Autor:
Quetzalli Denisse Angeles-López, Adriana Morales-Martínez, Argelia Sánchez-Chinchillas, Miguel Hernández-Cerón, Francisca Pérez-Severiano, José Segovia-Vila
Publikováno v:
I: Experimental therapeutics – preclinical.
Autor:
José Segovia, Richard L. Magin, Daniel Deyoung, Lucia García-Lara, Manish Amin, Quetzalli Denisse Angeles-López, Rodolfo G. Gatto, Carina Weissmann, Libia Catalina Salinas Castellanos, Osvaldo D. Uchitel, Thomas H. Mareci
Publikováno v:
Neurobiology of Aging. 102:32-49
Diffusion MRI (dMRI) has been able to detect early structural changes related to neurological symptoms present in Huntington's disease (HD). However, there is still a knowledge gap to interpret the biological significance at early neuropathological s
Autor:
José Segovia, Francisca Pérez-Severiano, Quetzalli Denisse Angeles-López, Nicolás Aguirre-Pineda, Guillermo Elizondo-Azuela, Rolando Castañeda-Arellano, Lucia García-Lara
Publikováno v:
Behavioural Brain Research. 408:113230
Huntington's disease (HD) is an inherited neurodegenerative disorder caused by an abnormal CAG repeat expansion in the huntingtin gene coding for a protein with an elongated polyglutamine sequence. HD patients present choreiform movements, which are