Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
BMC Public Health|August 10, 2014
Physical activity differences between children from migrant and native originWim Labree, Freek Lötters, Dike van de Mheen, et al.
Scientific Reports|July 20, 2017
Dysregulated miRNAs and their pathogenic implications for the neurometabolic disease propionic acidemiaAna Rivera-Barahona, Alejandro Fulgencio-Covián, Celia Pérez-Cerdá, et al.
Neuroepidemiology|November 15, 2017
Increasing Incidence and Prevalence of Multiple Sclerosis in Puerto Rico (2013-2016)Angel Chinea, Carlos F Ríos-Bedoya, Ivonne Vicente, et al.
Translational Research : the Journal of Laboratory and Clinical Medicine|January 18, 2020
Pathogenic implications of dysregulated miRNAs in propionic acidemia related cardiomyopathyAlejandro Fulgencio-Covián, Esmeralda Alonso-Barroso, Adam J Guenzel, et al.
Frontiers in Plant Science|January 23, 2023
Phenotypic diversity and distinctiveness of the Belltall garlic landraceJoan Casals, Ana Rivera, Sonia Campo, et al.
European Journal of Immunology|February 14, 2023
STAT6 controls the stability and suppressive function of regulatory T cellsRubén D Arroyo-Olarte, Ana Rivera-Rugeles, Eduardo Nava-Lira, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 14, 2021
Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactylyDenise Horn, Elisa Fernández-Núñez, Ricardo Gomez-Carmona, et al.
Frontiers in Plant Science|December 20, 2018
Plant Genebanks: Present Situation and Proposals for Their Improvement. the Case of the Spanish NetworkMaría José Díez, Lucía De la Rosa, Isaura Martín, et al.
American Journal of Human Genetics|September 9, 2022
Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary ciliaAsier Iturrate, Ana Rivera-Barahona, Carmen-Lisset Flores, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 5, 2022
FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defectsAuriane Cospain, Ana Rivera-Barahona, Erwan Dumontet, et al.
Pageof 6