Results 1 to 10 of about 2,827 (178)

Unraveling the Genetic Links Between Polycystic Kidney Disease and Hypertension Through ARL13B [PDF]

open access: goldInternational Journal of Nephrology and Renovascular Disease
Juan Chen,1,* Lei Song,2,* Shuqin Mei,1,* Jing Huang,3 Lili Fu,1 Chenchen Zhou,1 Xiaohua Hu,1 Liming Zhang,1 Cheng Xue,1,3 Zhiguo Mao1 1Kidney Institute, Division of Nephrology, Shanghai Changzheng Hospital, Second Military ...
Chen J   +9 more
doaj   +6 more sources

Loss of a primary cilia protein ARL13B promotes TGFβ-1 induced EMT of RPE in proliferative vitreoretinopathy via increasing Smad3 expression [PDF]

open access: goldFrontiers in Cell and Developmental Biology
BackgroundProliferative vitreoretinopathy (PVR) is a major complication of rhegmatogenous retinal detachment. Epithelial-mesenchymal transition (EMT) of retinal pigment epithelial (RPE) plays a central role in PVR pathogenesis.
Wenjun Sui   +25 more
doaj   +3 more sources

Knocking out ARL13B completely abolishes primary ciliogenesis in cell lines [PDF]

open access: yesScientific Reports
Small G protein ARL13B localizes to the cilium and plays essential roles in cilium biogenesis, organization, trafficking, and signaling. Here, we established multiple ARL13B knockout cell lines using the CRISPR/Cas9 system.
Divyanshu Mahajan, Hui Min Chia, Lei Lu
doaj   +3 more sources

ARL13B regulates Sonic hedgehog signaling from outside primary cilia [PDF]

open access: goldeLife, 2020
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 ARL13B is required within cilia, we knocked in a cilia-excluded variant of
Eduardo D Gigante   +4 more
doaj   +4 more sources

Axoneme polyglutamylation regulated by Joubert syndrome protein ARL13B controls ciliary targeting of signaling molecules [PDF]

open access: goldNature Communications, 2018
The small GTPase ARL13B is mutated in the human ciliopathy Joubert syndrome. Here the authors show that ARL13B and the RAB11 effector FIP5 promote import of tubulin glutamylase into cilia and as such axoneme polyglutamylation, which is demonstrated to be
Kai He   +10 more
doaj   +4 more sources

Postnatal Dynamic Ciliary ARL13B and ADCY3 Localization in the Mouse Brain [PDF]

open access: goldCells
Primary cilia are hair-like structures found on nearly all mammalian cell types, including cells in the developing and adult brain. A diverse set of receptors and signaling proteins localize within cilia to regulate many physiological and developmental ...
Katlyn K. Brewer   +5 more
doaj   +5 more sources

ARL13B controls male reproductive tract physiology through primary and Motile Cilia

open access: goldCommunications Biology
ARL13B is a small regulatory GTPase that controls ciliary membrane composition in both motile cilia and non-motile primary cilia. In this study, we investigated the role of ARL13B in the efferent ductules, tubules of the male reproductive tract essential
Céline Augière   +13 more
doaj   +4 more sources

Increasing Ciliary ARL13B Expression Drives Active and Inhibitor-Resistant Smoothened and GLI into Glioma Primary Cilia [PDF]

open access: goldCells, 2023
ADP-ribosylation factor-like protein 13B (ARL13B), a regulatory GTPase and guanine exchange factor (GEF), enriches in primary cilia and promotes tumorigenesis in part by regulating Smoothened (SMO), GLI, and Sonic Hedgehog (SHH) signaling.
Ping Shi   +8 more
doaj   +2 more sources

Enhanced Ciliogenesis of Human Bronchial Epithelial Cells by Simulated Microgravity [PDF]

open access: yesLife
Spaceflight induces a wide array of effects on the human body, notably including pathological changes mediated by alterations in gravity. Abnormalities in the formation of primary cilia (ciliogenesis) can lead to cell cycle arrest and decreased ...
Seung Hyun Bang   +7 more
doaj   +2 more sources

Differences in neuronal ciliation rate and ciliary content revealed by systematic imaging-based analysis of hiPSC-derived models across protocols [PDF]

open access: yesFrontiers in Cell and Developmental Biology
IntroductionCiliopathies are a group of human Mendelian disorders caused by dysfunction of primary cilia, small quasi-ubiquitous sensory organelles. Patients suffering from ciliopathies often display prominent neurodevelopmental phenotypes, underscoring ...
Walther Haenseler   +18 more
doaj   +2 more sources

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