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The Journal of Biological Chemistry|September 25, 2003
Tuba, a novel protein containing bin/amphiphysin/Rvs and Dbl homology domains, links dynamin to regulation of the actin cytoskeletonMarco A Salazar, Adam V Kwiatkowski, Lorenzo Pellegrini, et al.Journal of Cell Science|March 20, 2015
Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALSSimona Rossi, Alessia Serrano, Valeria Gerbino, et al.The Journal of Investigative Dermatology|March 1, 2014
Nectin-4 mutations causing ectodermal dysplasia with syndactyly perturb the rac1 pathway and the kinetics of adherens junction formationPaola Fortugno, Emmanuelle Josselin, Konstantinos Tsiakas, et al.Journal of Cellular Physiology|September 25, 2024
An inherited TBX3 alteration in a prenatal case of ulnar-mammary syndrome: Clinical assessment and functional characterization in Drosophila melanogasterIrene Bottillo, Andrea D'Alessandro, Maria Pia Ciccone, et al.Developmental Cell|December 25, 2012
Biochemical membrane lipidomics during Drosophila developmentXue Li Guan, Gianluca Cestra, Guanghou Shui, et al.Cell Death and Differentiation|May 28, 2025
DNA damage response defects induced by the formation of TDP-43 and mutant FUS cytoplasmic inclusions and their pharmacological rescueStefania Modafferi, Stefania Farina, Francesca Esposito, et al.Brain : a Journal of Neurology|May 8, 2021
Biallelic mutations in RNF220 cause laminopathies featuring leukodystrophy, ataxia and deafnessAntonella Sferra, Paola Fortugno, Marialetizia Motta, et al.Cell Reports|September 7, 2025
ADSL deficiency is a secondary mitochondrial disease affecting organelle homeostasis and ERK2/AKT signaling in a linear genotype-phenotype relationMatteo Bordi, Beatrice Testa, Claudia Compagnucci, et al.Pageof 3