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The protein encoded by INPP5E is an inositol 1,4,5-trisphosphate (InsP3) 5-phosphatase. De plus, nous expédions INPP5E Protéines (5) et beaucoup plus de produits pour cette protéine.
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Therefore our study identifies a compartmentalized PtdIns(3,4,5)P3/AKT (Montrer AKT1 Anticorps)/GSK3beta (Montrer GSK3b Anticorps) signaling axis at cilia in SHH (Montrer SHH Anticorps)-dependent medulloblastoma that is regulated by INPP5E to maintain tumor cell cilia, promote SHH (Montrer SHH Anticorps) signaling and thereby medulloblastoma progression.
we identify Inpp5e as an essential inhibitor of the PI3K/Akt (Montrer AKT1 Anticorps)/mTORC1 signaling axis in renal epithelial cells, and demonstrate a critical role for Inpp5e-dependent mTORC1 regulation in Polycystic kidney disease (PKD (Montrer PRKD1 Anticorps)) suppression
INPP5E localizes to centrosomes, chromosomes, and kinetochores in early mitosis and shuttles to the midzone spindle at mitotic exit.
INPP5E is an essential point of convergence between Hedgehog (Montrer SHH Anticorps) and phosphoinositide signaling at cilia that maintains transition zone function and Hedgehog (Montrer SHH Anticorps)-dependent embryonic development.
the affinity to PDE6delta and the release by Arl2 (Montrer ARL2 Anticorps)/3 in addition to a retention signal are the determinants for cargo sorting and enrichment at its destination.
PIPKIgamma and INPP5E localize to the centrosome and coordinate the initiation of ciliogenesis.
Inpp5e, through functional interactions with Rab20 (Montrer RAB20 Anticorps) on the phagosome, activates Rab5 (Montrer RAB5A Anticorps), which, in turn, increases PtdIns3P and delays phagosome acidification.
Inpp5e and SHIP1 (Montrer INPP5D Anticorps) exhibit specificity in regulating FcgammaR- versus CR3 (Montrer ITGAM Anticorps)-stimulated phagocytosis by controlling the amplitude and duration of PtdIns(3,4,5)P(3) at the phagocytic cup.
Inpp5e mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in the mouse.
we identify Inpp5e as an essential inhibitor of the PI3K (Montrer PIK3CA Anticorps)/Akt (Montrer AKT1 Anticorps)/mTORC1 signaling axis in renal epithelial cells, and demonstrate a critical role for Inpp5e-dependent mTORC1 regulation in Polycystic kidney disease (PKD (Montrer PRKD1 Anticorps)) suppression
ARL13B (Montrer ARL13B Anticorps) regulates IFT-A-mediated retrograde protein trafficking within cilia through its interaction with INPP5E.
In neuronal cells, INPP5E knockdown strongly inhibited autophagy by impairing the autophagosome-lysosome fusion step.
MKS1 (Montrer MKS1 Anticorps) functions in the transition zone at the base of the cilium to regulate ciliary INPP5E content.
These findings establish the first direct link between AURKA (Montrer AURKA Anticorps) and phosphoinositide signaling and suggest that the function of INPP5E in cilia is at least partly mediated by its interactions with AURKA (Montrer AURKA Anticorps)
Proteomic analysis identified INPP5E, whose mutations also lead to Joubert syndrome as novel prenyl-dependent cargo of PDE6D (Montrer PDE6D Anticorps). Mutant PDE6D (Montrer PDE6D Anticorps) shows reduced binding to INPP5E, which fails to localize to primary cilia in patient fibroblasts and tissues.
Identification of 12 different INPP5E mutations in patients with Joubert syndrome with an overall 2.7% mutation frequency.
The protein encoded by this gene is an inositol 1,4,5-trisphosphate (InsP3) 5-phosphatase. InsP3 5-phosphatases hydrolyze Ins(1,4,5)P3, which mobilizes intracellular calcium and acts as a second messenger mediating cell responses to various stimulation. Studies of the mouse counterpart suggest that this protein may hydrolyze phosphatidylinositol 3,4,5-trisphosphate and phosphatidylinositol 3,5-bisphosphate on the cytoplasmic Golgi membrane and thereby regulate Golgi-vesicular trafficking. Mutations in this gene cause Joubert syndrome\; a clinically and genetically heterogenous group of disorders characterized by midbrain-hindbrain malformation and various associated ciliopathies that include retinal dystrophy, nephronophthisis, liver fibrosis and polydactyly.
72 kDa inositol polyphosphate 5-phosphatase
, inositol polyphosphate-5-phosphatase, 72 kDa
, phosphatidylinositol 4,5-bisphosphate 5-phosphatase
, phosphatidylinositol polyphosphate 5-phosphatase type IV
, phosphatidylinositol-4,5-bisphosphate 5-phosphatase
, 5-phosphatase that induces arborization
, inositol polyphosphate 5-phosphatase
, phosphatidylinositol (4,5) bisphosphate 5-phosphatase
, inositol polyphosphate-5-phosphatase E
, peptidase (mitochondrial processing) alpha