Results 21 to 30 of about 75,568 (261)

Modulation of the Pol II CTD Phosphorylation Code by Rac1 and Cdc42 Small GTPases in Cultured Human Cancer Cells and Its Implication for Developing a Synthetic-Lethal Cancer Therapy

open access: yesCells, 2020
Rho GTPases, including Rho, Cdc42, Rac and ROP subfamilies, are key signaling molecules in RNA polymerase II (Pol II) transcriptional control.
Bo Zhang   +4 more
doaj   +1 more source

Potential value of differential expression of CDC42 gene in adult and umbilical cord blood reticulocytes

open access: yesZhongguo shuxue zazhi, 2023
Objective To explore critical regulatory genes in the hemoglobin switch process by analyzing transcriptomic data from the GSE6236, GSE17639 and GSE35102 datasets.
Jinchao WANG, Genhao ZHANG
doaj   +1 more source

Targeting Cdc42 in cancer [PDF]

open access: yesExpert Opinion on Therapeutic Targets, 2013
The Rho GTPases are a family of proteins that control fundamental cellular processes in response to extracellular stimuli and internal programs. Rho GTPases function as molecular switches in which the GTP-bound proteins are active and GDP-bound proteins are inactive.
Luis E, Arias-Romero, Jonathan, Chernoff
openaire   +2 more sources

Cdc42 controls secretory granules morphology in rodent salivary glands in vivo

open access: yesCommunicative & Integrative Biology, 2020
We previously reported that the small GTPase Cdc42 negatively regulates endocytosis in the salivary gland of live mice. By using intravital subcellular microscopy, we showed that depletion of Cdc42 causes the mis-sorting of plasma membrane components ...
Akiko Shitara   +2 more
doaj   +1 more source

Gene targeting implicates Cdc42 GTPase in GPVI and non-GPVI mediated platelet filopodia formation, secretion and aggregation. [PDF]

open access: yesPLoS ONE, 2011
Cdc42 and Rac1, members of the Rho family of small GTPases, play critical roles in actin cytoskeleton regulation. We have shown previously that Rac1 is involved in regulation of platelet secretion and aggregation.
Huzoor Akbar   +7 more
doaj   +1 more source

Cdc42 is not essential for filopodium formation, directed migration, cell polarization, and mitosis in fibroblastoid cells [PDF]

open access: yes, 2005
Udgivelsesdato: 2005-OctCdc42 is a small GTPase involved in the regulation of the cytoskeleton and cell polarity. To test whether Cdc42 has an essential role in the formation of filopodia or directed cell migration, we generated Cdc42-deficient ...
CZUCHRA, A   +7 more
core   +1 more source

Regulation of cell protrusions by small GTPases during fusion of the neural folds

open access: yeseLife, 2016
Epithelial fusion is a crucial process in embryonic development, and its failure underlies several clinically important birth defects. For example, failure of neural fold fusion during neurulation leads to open neural tube defects including spina bifida.
Ana Rolo   +8 more
doaj   +1 more source

Cdc42 Promotes Axonogenesis of Primary Hippocampal Neurons by Inhibiting Glycogen Synthase Kinase-3β

open access: yesJournal of Integrative Neuroscience, 2022
Background: Progressive axon degeneration is a common pathological feature of neurodegenerative diseases. Cdc42 is a member of the Rho GTPase family that participates in axonogenesis.
Yu-Ting Li   +10 more
doaj   +1 more source

PTEN controls glandular morphogenesis through a juxtamembrane β-Arrestin1/ARHGAP21 scaffolding complex [PDF]

open access: yes, 2017
PTEN controls three-dimensional (3D) glandular morphogenesis by coupling juxtamembrane signalling to mitotic spindle machinery. While molecular mechanisms remain unclear, PTEN interacts through its C2 membrane-binding domain with the scaffold protein β ...
Anderson   +82 more
core   +3 more sources

Lipidation of small GTPase Cdc42 as regulator of its physiological and pathophysiological functions

open access: yesFrontiers in Physiology, 2023
The protein cell division cycle 42 (Cdc42) is a small GTPase of the Rho family regulating a plethora of physiological functions in a tissue, cell and subcellular-specific manner via participating in multiple signaling pathways.
Alexander Wirth, Evgeni Ponimaskin
doaj   +1 more source

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