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anti-Human VEGFB Anticorps:
anti-Mouse (Murine) VEGFB Anticorps:
anti-Rat (Rattus) VEGFB Anticorps:
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Mouse (Murine) Monoclonal VEGFB Primary Antibody pour IHC (p), IHC - ABIN258873
Rothhammer, Borucki, Tjon, Takenaka, Chao, Ardura-Fabregat, de Lima, Gutiérrez-Vázquez, Hewson, Staszewski, Blain, Healy, Neziraj, Borio, Wheeler, Dragin, Laplaud, Antel, Alvarez, Prinz, Quintana: Microglial control of astrocytes in response to microbial metabolites. dans Nature 2018
High plasma VEGF-B levels are associated with type 2 diabetes mellitus.
Data from clinical studies point out the changes in circulating or tissue expression levels of VEGF-B in obese compared with lean patients.
Cardiac transgenic vascular endothelial growth factor-B overexpression failed to protect heart transplants from ischemia-reperfusion injury.
renal VEGF-B expression correlates with the severity of Diabetic Kidney Disease.
Data show that metformin treatment reduces serum vascular endothelial growth factor B (VEGF-B) levels and ameliorates insulin (Montrer INS Anticorps) resistance.
VEGFA (Montrer VEGFA Anticorps) and VEGFB associated sub-network, kinase insert domain receptor (KDR (Montrer KDR Anticorps)), fibronectin 1 (FN1 (Montrer FN1 Anticorps)), transforming growth factor beta induced (TGFBI) and proliferating cell nuclear antigen (PCNA (Montrer PCNA Anticorps)) found to interact with at least two of the three hub genes.
Frameshift mutations of VEGFB gene is associated with stomach and colorectal cancers.
plasma VEGF (Montrer VEGFA Anticorps) levels before treatment were lower in patients with schizophrenia and that their VEGF (Montrer VEGFA Anticorps) levels increased after treatment.
fluid shear stress induces the synthesis of Insulin growth factor-2 and vascular endothelial growth factor (VEGF (Montrer VEGF Anticorps)) B and D, which in turn transactivate MMP-12 (Montrer MMP12 Anticorps).
MMP9 (Montrer MMP9 Anticorps) may activate VEGF-B via PI3K (Montrer PIK3CA Anticorps)/Akt (Montrer AKT1 Anticorps) signaling pathway.
the expression and role of VEGF-B in diabetic corneal neuropathy was examined by using type 1 diabetic mice and cultured trigeminal ganglion (TG) neurons.
Data suggest that dietary fatty acids create epigenetic/nutrigenomic changes in methylation levels of CpG island at Vegfb promoter and changes in Vegfb expression in white adipocytes in vivo and in vitro, with particular up-regulation of DNA methylation (Montrer HELLS Anticorps) by linoleic acid; Vegfb promoter methylation levels are closely related to Vegfb gene expression in visceral and subcutaneous adipose tissue.
PGC-1alpha is a master metabolic sensor that regulates the expression of Vegfa (Montrer VEGFA Anticorps) and Vegfb, coordinates blood vessels growth and fatty acid uptake with mitochondrial fatty acid oxidation.
These data therefore support a tightly controlled, paracrine signaling mechanism of VEGF-B to VEGFR1 (Montrer FLT1 Anticorps).
VEGFB-Induced Vascular Remodeling in Adipose Tissue Requires VEGF (Montrer VEGFA Anticorps)/VEGFR2 (Montrer KDR Anticorps). VEGFB-Induced Vascular Remodeling Improves Insulin (Montrer INS Anticorps) Supply, Signaling, and Function in Obese Mice.
VEGF-B is dispensable for normal cardiac function under unstressed conditions and for high fat diet-induced metabolic changes.
VEGF-B is a vascular remodeling factor promoting cancer metastasis.
Data indicate that vascular endothelial growth factor B knockout (Vegf-b-/-) mice showed impaired nerve repair with concomitant impaired trophic function.
Data indicate that VEGF-B is a high-affinity VEGFR-1 (Montrer FLT1 Anticorps) ligand that, unlike PlGF (Montrer PGF Anticorps), cannot efficiently induce signaling downstream of VEGFR-1 (Montrer FLT1 Anticorps).
PCR-SSCP and DNA sequencing methods were applied to reveal 3 SNPs and a duplication in the bovine VEGF-B gene among 675 samples belonging to three native Chinese cattle breeds.
This gene encodes a member of the PDGF (platelet-derived growth factor)/VEGF (vascular endothelial growth factor) family. The VEGF family members regulate the formation of blood vessels and are involved in endothelial cell physiology. This member is a ligand for VEGFR-1 (vascular endothelial growth factor receptor 1) and NRP-1 (neuropilin-1). Studies in mice showed that this gene was co-expressed with nuclear-encoded mitochondrial genes and the encoded protein specifically controlled endothelial uptake of fatty acids. Alternatively spliced transcript variants encoding distinct isoforms have been identified.