[HTML][HTML] FAM13A is a modifier gene of cystic fibrosis lung phenotype regulating rhoa activity, actin cytoskeleton dynamics and epithelial-mesenchymal transition

H Corvol, N Rousselet, KE Thompson, L Berdah… - Journal of Cystic …, 2018 - Elsevier
Background Cystic fibrosis (CF) lung disease severity is highly variable and dependent on
several factors including genetic modifiers. Family with sequence similarity 13 member A …

Bacterial lipopolysaccharide inhibits free thiamin uptake along the intestinal tract via interference with membrane expression of thiamin transporters 1 and 2

S Anthonymuthu, S Sabui, KI Manzon… - … of Physiology-Cell …, 2024 - journals.physiology.org
This study examined the effect of exposure of small and large intestinal epithelial cells to the
bacterial lipopolysaccharide (LPS) on uptake of free form of vitamin B1, ie, thiamin. The …

Silencing of CDC42 inhibits contraction and growth-related functions in prostate stromal cells, which is mimicked by ML141

R Wang, R Huang, Y Liu, A Tamalunas, CG Stief… - Life Sciences, 2023 - Elsevier
Background Prostate smooth muscle contraction and stromal growth may contribute to lower
urinary tract symptoms suggestive of benign prostatic hyperplasia, but are incompletely …

[HTML][HTML] CTNNAL1 deficiency suppresses CFTR expression in HDM-induced asthma mouse model through ROCK1-CAL signaling pathway: CTNNAL1 increases …

D Wu, J Zhu, F Yang, R Li, L Liu, D Liu… - Acta Biochimica et …, 2023 - ncbi.nlm.nih.gov
The downregulation of adhesion molecule catenin alpha-like 1 (CTNNAL1) in airway
epithelial cells of asthma patients and house dust mite (HDM)-induced asthma animal …

Unravelling druggable signalling networks that control F508del-CFTR proteostasis

RN Hegde, S Parashuraman, F Iorio, F Ciciriello… - Elife, 2015 - elifesciences.org
Cystic fibrosis (CF) is caused by mutations in CF transmembrane conductance regulator
(CFTR). The most frequent mutation (F508del-CFTR) results in altered proteostasis, that is …

Interaction of the small GTPase Cdc42 with arginine kinase restricts white spot syndrome virus in shrimp

JD Xu, HS Jiang, TD Wei, KY Zhang, XW Wang… - Journal of …, 2017 - Am Soc Microbiol
Many types of small GTPases are widely expressed in eukaryotes and have different
functions. As a crucial member of the Rho GTPase family, Cdc42 serves a number of …

Extracting insights from temporal data by integrating dynamic modeling and machine learning

R Ballweg, KA Engevik, MH Montrose, E Aihara… - Frontiers in …, 2020 - frontiersin.org
Biological processes are dynamic. As a result, temporal analyses are necessary to fully
understand the complex interactions that occurs within these systems. One example of a …

Progressive decline of T and B cell numbers and function in a patient with CDC42 deficiency

P Kashani, A Marwaha, S Feanny, VHD Kim… - Immunologic …, 2021 - Springer
Single allele mutations in the Cell Division Control protein 42 homolog (CDC42) gene were
recently shown to cause Takenouchi-Kosaki syndrome with diverse manifestations. These …

Cyclic stretch-induced the cytoskeleton rearrangement and gene expression of cytoskeletal regulators in human periodontal ligament cells

Y Wu, J Zhuang, D Zhao, F Zhang, J Ma… - Acta Odontologica …, 2017 - Taylor & Francis
Objective: This study aimed to explore the mechanism of the stretch-induced cell
realignment and cytoskeletal rearrangement by identifying several mechanoresponsive …

[HTML][HTML] The dosage-dependent effect exerted by the NM23-H1/H2 homolog NDK-1 on distal tip cell migration in C. elegans

Z Farkas, L Fancsalszky, É Saskői, A Gráf… - Laboratory …, 2018 - Elsevier
Abnormal regulation of cell migration and altered rearrangement of the cytoskeleton are
fundamental properties of metastatic cells. The first identified metastasis suppressor NM23 …