Showing results (101-110 of 126) with videos related to

Sort By:
Pageof 13
Translational Research : the Journal of Laboratory and Clinical Medicine|July 28, 2018
MAFG is a potential therapeutic target to restore chemosensitivity in cisplatin-resistant cancer cells by increasing reactive oxygen speciesOlga Vera-Puente, Carlos Rodriguez-Antolin, Ana Salgado-Figueroa, et al.
Frontiers in Immunology|October 7, 2022
A catalog of the genetic causes of hereditary angioedema in the Canary Islands (Spain)Alejandro Mendoza-Alvarez, Eva Tosco-Herrera, Adrian Muñoz-Barrera, et al.
The Journal of Allergy and Clinical Immunology|November 7, 2022
The upper-airway microbiome as a biomarker of asthma exacerbations despite inhaled corticosteroid treatmentJavier Perez-Garcia, Mario González-Carracedo, Antonio Espuela-Ortiz, et al.
Cirugia Espanola|November 1, 2021
[Analysis of the broadcasting and perceived utility through the implementation of a virtual training platform during the pandemic]Raquel Sánchez-Santos, Salvador Morales-Conde, Jose Luis Ramos Rodriguez, et al.
Orphanet Journal of Rare Diseases|July 26, 2018
Improving the diagnosis of cobalamin and related defects by genomic analysis, plus functional and structural assessment of novel variantsSandra Brasil, Fátima Leal, Ana Vega, et al.
Science (New York, N.Y.)|January 4, 2014
Pregnenolone can protect the brain from cannabis intoxicationMonique Vallée, Sergio Vitiello, Luigi Bellocchio, et al.
Cirugia Espanola|July 9, 2022
Analysis of the broadcasting and perceived utility through the implementation of a virtual training platform during the pandemicRaquel Sánchez-Santos, Salvador Morales-Conde, Jose Luis Ramos Rodriguez, et al.
Nature Metabolism|November 26, 2024
Microviridae bacteriophages influence behavioural hallmarks of food addiction via tryptophan and tyrosine signalling pathwaysAnna Castells-Nobau, Irene Puig, Anna Motger-Albertí, et al.
Orphanet Journal of Rare Diseases|May 5, 2017
Diagnosis features of pediatric Gaucher disease patients in the era of enzymatic therapy, a national-base study from the Spanish Registry of Gaucher DiseaseMarcio Andrade-Campos, Pilar Alfonso, Pilar Irun, et al.
Nature Communications|July 6, 2024
The human VGLUT3-pT8I mutation elicits uneven striatal DA signaling, food or drug maladaptive consumption in male miceMathieu Favier, Elena Martin Garcia, Romain Icick, et al.
Pageof 13