G Salloum, AR Bresnick, JM Backer - Biochemical Journal, 2023 - portlandpress.com
Macropinocytosis is defined as an actin-dependent but coat-and dynamin-independent endocytic uptake process, which generates large intracellular vesicles (macropinosomes) …
The development and progression of oral cavity squamous cell carcinoma (OSCC) involves complex cellular mechanisms that contribute to the low five-year survival rate of …
C Casalou, A Ferreira, DC Barral - Frontiers in Cell and …, 2020 - frontiersin.org
The Adenosine diphosphate-Ribosylation Factor (ARF) family belongs to the RAS superfamily of small GTPases and is involved in a wide variety of physiological processes …
ED Gigante, MR Taylor, AA Ivanova, RA Kahn… - Elife, 2020 - elifesciences.org
ARL13B is a regulatory GTPase highly enriched in cilia. Complete loss of Arl13b disrupts cilia architecture, protein trafficking and Sonic hedgehog signaling. To determine whether …
K Hua, RJ Ferland - Cellular and Molecular Life Sciences, 2018 - Springer
Primary cilia are immotile organelles known for their roles in development and cell signaling. Defects in primary cilia result in a range of disorders named ciliopathies. Because this …
K He, X Ma, T Xu, Y Li, A Hodge, Q Zhang… - Nature …, 2018 - nature.com
Tubulin polyglutamylation is a predominant axonemal post-translational modification. However, if and how axoneme polyglutamylation is essential for primary cilia and contribute …
C Casalou, A Faustino, DC Barral - Small GTPases, 2016 - Taylor & Francis
Members of the ADP-ribosylation factor (Arf) family of small GTP-binding (G) proteins regulate several aspects of membrane trafficking, such as vesicle budding, tethering and …
Whereas human dendritic cells (DCs) are largely resistant to productive infection with HIV-1, they have a unique ability to take up the virus and transmit it efficiently to T lymphocytes …
C Seixas, SY Choi, N Polgar… - Molecular biology of …, 2016 - Am Soc Cell Biol
Arl13b belongs to the ADP-ribosylation factor family within the Ras superfamily of regulatory GTPases. Mutations in Arl13b cause Joubert syndrome, which is characterized by …