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ARL13B encodes a member of the ADP-ribosylation factor-like family.
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loss of Arl13b leads to slow photoreceptor degeneration, but can be exacerbated by the loss of vangl2 (zeige VANGL2 ELISA Kits). Importantly, the data show that Arl13b can genetically and physically interact with Vangl2 (zeige VANGL2 ELISA Kits) and this association is important for normal photoreceptor structure.
Arl13b is an important effector of ciliary membrane biogenesis and ciliary length regulation.
Cilia localization is essential for in vivo functions of the Joubert syndrome protein arl13b.
the results show that palmitoylation plays a unique and critical role in controlling the localization, stability, abundance, and thus function of ARL13b. Pharmacological manipulation of protein palmitoylation may be a strategy to alter cilia function.
Our results show how Arl13b participates in Hedgehog (zeige SHH ELISA Kits) pathway activation in gastric cancer
Reduced primary cilia length and altered Arl13b expression are associated with deregulated chondrocyte Hedgehog (zeige SHH ELISA Kits) signaling in alkaptonuria (zeige HGD ELISA Kits).
ARL13B regulates IFT-A-mediated retrograde protein trafficking within cilia through its interaction with INPP5E.
Biochemical characterization of purified mammalian ARL13B protein indicates that it is an atypical GTPase and ARL3 guanine nucleotide exchange factor (GEF).(
Thus our data identify a novel ARL13B variant that causes JS and retinopathy and suggest an extension of the phenotypic spectrum of ARL13B mutations to obesity.
We conclude that MKS/NPHP modules comprise a TZ barrier to ARL-13 diffusion, whereas IFT genes predominantly facilitate ARL-13 ciliary entry and/or retention via active transport mechanisms.
X-ray crystallography of Arl13B demonstrates involvement of mutations R79Q and R200C in stabilizing intramolecular interactions.
Arl13b acts as the all-rounder in cilia formation and signaling (Review).
findings indicate that ARL13B, INPP5E, PDE6D, and CEP164 (zeige CEP164 ELISA Kits) form a distinct functional network that is involved in JBTS and NPHP but independent of the ones previously defined by NPHP and MKS proteins
Arl13b dysfunction resulted in hennin cell stagnation due to poor growth factor signaling and impaired detection of extracellular electrical gradients.
To investigate whether Arl13b has a role in ciliogenesis in mammalian kidney and whether loss of function of Arl13b leads to cystic kidneys in mammals, we generated a mouse model with kidney-specific conditional knockout of Arl13b Deletion of Arl13b in the distal nephron at the perinatal stage led to a cilia biogenesis defect and rapid kidney cyst formation
The authors show that the ciliary G-protein Arl13B, mutated in Joubert syndrome, is the guanine nucleotide exchange factor for Arl3, and its function is conserved in evolution
A new role for Arl13b in actin cytoskeleton remodeling through the interaction with Myh9 (zeige MYH9 ELISA Kits).
Early neuroepithelial deletion of ciliary Arl13b reversed the apical-basal polarity of radial progenitors & caused aberrant neuronal placement. Arl13b signaling in primary cilia is crucial for initial formation of a polarized radial glial scaffold.
guidance cue receptors essential for interneuronal migration localize to interneuronal primary cilia, but their concentration and dynamics are altered in the absence of Arl13b
By deleting Arl13b in mouse, we induced low-level constitutive GliA function at specific developmental stages and defined a crucial period prior to E10.5 when shifts in the level of GliA cause cells to change their fate
Study shows the cilia protein Arl13b is required for left right axis specification as its absence results in heterotaxia; the defect originates in the node where Cerl2 is not downregulated and asymmetric expression of Nodal is not maintained resulting in symmetric expression of both genes.
The role of Arl13b in ciliogenesis and it's interaction with Smo and Shh (zeige SHH ELISA Kits) proteins.Arl13b regulates the ciliary entry of Smo.
This gene encodes a member of the ADP-ribosylation factor-like family. The encoded protein is a small GTPase that contains both N-terminal and C-terminal guanine nucleotide-binding motifs. This protein is localized in the cilia and plays a role in cilia formation and in maintenance of cilia. Mutations in this gene are the cause of Joubert syndrome 8. Alternate splicing results in multiple transcript variants.
ADP-ribosylation factor-like protein 13B
, ADP-ribosylation factor-like 2-like 1
, ADP-ribosylation factor-like 13B
, ADP-ribosylation factor-like protein 13B-like
, ADP-ribosylation factor-like protein 2-like 1
, ARL2-like protein 1
, protein scorpion
, un-named hi459
, unm hi459