anti-FOXO1 (FOXO1) 抗体产品概述

Human Forkhead Box O1 (FOXO1) interaction partners

1. LncRNA DANCR could inhibit osteoblast differentiation by regulating FOXO1 expression.

2. A significant correlation between the physical activity level and peripheral blood mononuclear cell SIRT1 (显示 SIRT1 抗体) and FOXO1 mRNA expression was found in COPD (显示 ARCN1 抗体) patients.

3. results indicate that FOXO1 inhibits gastric cancer (GC) growth and angiogenesis under hypoxic conditions via inactivation of the HIF-1alpha (显示 HIF1A 抗体)-VEGF (显示 VEGFA 抗体) pathway, possibly in association with SIRT1 (显示 SIRT1 抗体); thus, development of treatment modalities aiming at this pathway might be useful for treating GC

4. These results suggest that liraglutide may exert a renoprotective effect by a FoxO1-mediated upregulation of renal MnSOD (显示 SOD2 抗体) expression in the early DKD.

5. FOXO1, acetylation of FOXO1 and the following interaction between Ac-FOXO1 and Atg7 regulated the basal and serum starvation induced autophagy as evidenced by light chain 3 (LC3) accumulation and p62 degration.

6. PAX3 (显示 PAX3 抗体)-FOXO1 fusion protein serves as a driver mutation to initiate a cascade of mRNA and miRNA changes that ultimately reprogram proliferating myoblasts to induce the formation of alveolar rhabdomyosarcoma

7. Induced the nuclear accumulation of FOXO1.

8. The data indicate that Akt2 (显示 AKT2 抗体) ablation protects against cardiac aging through restored Foxo1-related autophagy and mitochondrial integrity.

9. the present study demonstrated that the expression of miR (显示 MLXIP 抗体)-196a in human liver cancer cells was upregulated; downregulation of miR (显示 MLXIP 抗体)-196a regulated human liver cancer cell biological functions which could benefit the clinical therapy of human liver cancer in the future

10. Inhibition of FOXO1 enhanced angiogenesis in human bio-engineered capillaries, and resulted in microvascular regeneration and improved function in mouse models of injury-repair.

Zebrafish Forkhead Box O1 (FOXO1) interaction partners

1. The findings reveal a novel mechanism by which Ca2 (显示 CA2 抗体)+ overload disrupts myofibril integrity by activating a Calcineurin-FoxO (显示 FOXO3 抗体)-MuRF1 (显示 TRIM63 抗体)-proteosome signaling pathway.

2. These results indicate that miR (显示 MYLIP 抗体)-182 functions as a FoxO1 inhibitor to antagonize osteoblast proliferation and differentiation, with a subsequent negative effect on osteogenesis.

3. gas6 (显示 GAS6 抗体) protects endothelial cells from apoptosis by a mechanism that involves PI3K-Akt (显示 AKT1 抗体)-dependent inactivation of FOXO1a.

Mouse (Murine) Forkhead Box O1 (FOXO1) interaction partners

1. Chimeric antigen receptor T cells releasing IL-18 (显示 IL18 抗体) convert to T-Bet(high) FoxO1(low) effectors that exhibit augmented activity against advanced solid tumors.

2. the molecular level, we confirmed, for the first time, that RES upregulated FoxO1 transcriptional activity by inhibiting the PI3K/AKT (显示 AKT1 抗体) signaling pathway, and hence promoted resistance to oxidative damage and restrained osteoclastogenesis. Inhibition of the PI3K/AKT (显示 AKT1 抗体) signaling pathway may be induced by RANKL (显示 TNFSF11 抗体).

3. FOXO1 is dispensable for naive T cell expression of TCF7 (显示 TCF7 抗体), it is essential for the expression of TCF7 (显示 TCF7 抗体) in a small subset of T cells within days following primary infection.

4. Foxo1 expression compromised embryonic stem cell self-renewal

5. we identified that Sirtuin 1 (SIRT1 (显示 SIRT1 抗体)), a deacetylase that suppresses FoxO1 acetylation in granulosa cell (GCs (显示 UGCG 抗体)), was downregulated by miR (显示 MLXIP 抗体)-181a and reversed the promoting effects of H2O2 and miR (显示 MLXIP 抗体)-181a on FoxO1 acetylation and GC apoptosis.

6. Study identified the roles of Foxo1 as a positive regulator and Foxp1 as a negative regulator of TH9 cell differentiation and antitumor activity.

7. miR (显示 MLXIP 抗体)-150-mediated suppression of Foxo1 regulates the balance between effector and memory cell differentiation

8. Inhibition of FOXO1 enhanced angiogenesis in human bio-engineered capillaries, and resulted in microvascular regeneration and improved function in mouse models of injury-repair.

9. Authors found that the repress effect of alphaMSH (显示 POMC 抗体) in adipocytes apoptosis is acting through Foxo1/mTORC2 (显示 CRTC2 抗体) pathway. These findings indicate that, alphaMSH (显示 POMC 抗体) has a strong inhibitory effect on ROS (显示 ROS1 抗体)-induced adipocyte apoptosis and underlying mechanism is interacting with key factors in mTOR (显示 FRAP1 抗体) signal pathway.

10. Sirt3 (显示 SIRT3 抗体) activation is essential to improve autophagy flux by reducing the acetylation modification on FoxO1, which in turn alleviates myocardial hypertrophy.

Pig (Porcine) Forkhead Box O1 (FOXO1) interaction partners

1. he knockdown of FoxO1 repressed lipogenesis by downregulating PDGFRalpha, and miR (显示 MYLIP 抗体)-34a inhibited adipogenesis through targeting PDGFRalpha.

2. These results indicate glycine enhances muscle protein mass under an inflammatory condition. The beneficial roles of glycine on the muscle are closely associated with maintaining Akt (显示 AKT1 抗体)-mTOR (显示 FRAP1 抗体)-FOXO1 signaling and suppressing the activation of TLR4 (显示 TLR4 抗体) and/or NOD2 (显示 NOD2 抗体) signaling pathways.

3. let-7g induces porcine granulosa cells apoptosis by inhibiting the MAP3K1 (显示 MAP3K1 抗体) gene, which promotes FoxO1 expression and dephosphorylation with nuclear accumulation.

4. inhibition of FoxO1 expression level caused by miR (显示 MYLIP 抗体)-15a/b over-expression had a positive effect on adipogenesis. Thus, we conclude that miR (显示 MYLIP 抗体)-15a/b promote adipogenesis in porcine pre-adipocyte via repressing FoxO1

5. Results show that FoxO1 likely regulates MyHC I (显示 MYH7 抗体) negatively and MyHC IIx and MyHC IIb (显示 MYH4 抗体) positively and may play a pivotal role in the determination of muscle fiber type.

6. Data suggest forkhead box protein O1 (FoxO1) involvement in the regulation of TNF-related apoptosis-inducing ligand TRAIL (显示 TNFSF10 抗体) and Fas ligand FasL (显示 FASL 抗体) expression during follicular atresia.

7. Data show that IL-4 (显示 IL4 抗体) induces upregulation of the junction protein claudin-5 (显示 CLDN5 抗体) in endothelial cells (ECs) through activation of Jak (显示 JAK3 抗体)/STAT6 (显示 STAT6 抗体) and phosphorylation and translocation of FoxO1 from the nucleus to the cytoplasm.

8. FoxO1 and C/EBPb (显示 CEBPB 抗体) regulate preadipocyte adipogenesis possibly through C/EBPb (显示 CEBPB 抗体)-> FoxO1-> C/EBPb (显示 CEBPB 抗体) feedback regulatory loop and FoxO1-C/EBPb (显示 CEBPB 抗体) protein complex.

9. FoxO1 delays and negatively regulates the porcine myoblast differentiation. It may also play a critical role in muscle fiber-type specification through the inhibition of myogenic regulation factors.

10. concluded that PI 3 (显示 PI3 抗体)-kinase and Akt (显示 AKT1 抗体) are activated after renal ischemia/reperfusion and that Akt (显示 AKT1 抗体) phosphorylation leads to phosphorylation of FKHR and FKHRL1 (显示 FOXO3 抗体), which may affect epithelial cell fate in acute renal failure.

Cow (Bovine) Forkhead Box O1 (FOXO1) interaction partners

1. This is the first study demonstrating a role for AMPK (显示 PRKAA1 抗体)-SIRT1 (显示 SIRT1 抗体)-FOXO1 signalling pathway in regulating apoptosis in bovine intramuscular adipocytes.

2. MicroRNA-183-96-182 cluster regulates bovine granulosa cell function by targeting FOXO1 gene.

3. downregulation of SIRT1 (显示 SIRT1 抗体) and FoxO1 were observed in the backfat tissue of Lilu cattle with increasing age

4. FOXO (显示 FOXO3 抗体) is a key regulator of ROS (显示 ROS1 抗体)-induced apoptosis in mammalian cells.

5. Protein kinase A-alpha directly phosphorylates FoxO1 in vascular endothelial cells to regulate expression of vascular cellular adhesion molecule (显示 NCAM1 抗体)-1 mRNA.

6. The results demonstrate pathways through which two different mediators, TNF-alpha (显示 TNF 抗体) and an advanced glycation endproduct, can induce pericyte apoptosis through activation of the transcription factor FOXO1.

Rhesus Monkey Forkhead Box O1 (FOXO1) interaction partners

1. FOXO1, 3, and 4 as well as their upstream regulator, AKT/p-AKT (显示 AKT1 抗体), was examined in rhesus macaque ovaries of three developmental stages: fetal, prepubertal, and adult

Xenopus laevis Forkhead Box O1 (FOXO1) interaction partners

1. FoxO1 translocation to the nucleus, and the increase in FoxO1 DNA binding activity in X. laevis liver strongly correlate with the up-regulation of manganese-dependent superoxide dismutase (显示 SOD1 抗体) and catalase (显示 CAT 抗体) mRNA and protein levels in this organ.