Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Weitere Synonyme anzeigen
Wählen Sie die gewünschte Spezies
Human Neuregulin 1 Protein expressed in Human Cells - ABIN2004422
Holmes, Sliwkowski, Akita, Henzel, Lee, Park, Yansura, Abadi, Raab, Lewis: Identification of heregulin, a specific activator of p185erbB2. in Science (New York, N.Y.) 1992
Show all 2 Pubmed References
Human Neuregulin 1 Protein expressed in Wheat germ - ABIN1307066
Gu, Duce, Valova, Wong, Bush, Petrou, Wiley: P2X7 receptor-mediated scavenger activity of mononuclear phagocytes toward non-opsonized particles and apoptotic cells is inhibited by serum glycoproteins but remains active in cerebrospinal fluid. in The Journal of biological chemistry 2012
Data show that serum growth differentiation factor 15 (GDF15 (zeige GDF15 Proteine))levels were significantly higher in subjects with thyroid nodules compared with nodule negative subjects, and this was influenced by age.
Findings suggest that GDF15 (zeige GDF15 Proteine) induces tumor sphere formation through GDF15 (zeige GDF15 Proteine)-ERK1/2-GDF15 (zeige GDF15 Proteine) circuits, leading to maintenance of GDF15high cancer stem-like cells.
These authors demonstrate that blocking cardiomyocyte production of GDF15 (zeige GDF15 Proteine) normalizes circulating GDF15 (zeige GDF15 Proteine) level and restores liver growth hormone (zeige GH1 Proteine) signaling, establishing GDF15 (zeige GDF15 Proteine) as a bona fide heart-derived hormone that regulates pediatric body growth.
Authors demonstrated that GDF15 (zeige GDF15 Proteine) contributed to radioresistance of HNC (zeige MMP8 Proteine), as determined by both gain- and lost-of-functional experiments. Authors further showed that GDF15 (zeige GDF15 Proteine) facilitated the conversion of cancer stemness, as assessed by the promotion of CD44 (zeige CD44 Proteine)+ and ALDH1 (zeige ALDH1A1 Proteine)+ cell populations and spheroid cell formation.
this study, for the first time, demonstrates that GDF15 is a promising target for preventing cold I/R injury in heart transplantation. This study also shows that the resultant protective effects are mediated by the Foxo3 and NFkappaB signaling pathways
Using time-resolved-fluorescence energy transfer (TR-FRET), we demonstrated that in the presence of recombinant NRG1, binding of 9F7-F11 (zeige F11 Proteine) (a nonligand-competing anti-HER3 (zeige ERBB3 Proteine) antibody) to HER3 (zeige ERBB3 Proteine) is increased, whereas that of ligand-competing anti-HER3 (zeige ERBB3 Proteine) antibodies is decreased.
High circulating GDF-15 (zeige GDF15 Proteine) levels are predictive of secondary cardiovascular events in women but not in men with carotid atherosclerosis.
In patients with chronic obstructive pulmonary disease, high levels of GDF15 (zeige GDF15 Proteine) were independently associated with a higher yearly rate of exacerbations, higher mortality and increased decline in both FEV1 and FVC.
Data suggested NAG-1 (zeige GDF15 Proteine) protein as a crucial mediator of epithelial ovarian cancer (EOC) progression and resistance to the standard first-line chemotherapy against EOC, particularly in MyD88 (zeige MYD88 Proteine)-positive ovarian cancer stem-like cells.
Data suggest that SLC3A2 (zeige SLC3A2 Proteine)-NRG1 should be considered a therapeutic target for patients with invasive mucinous adenocarcinoma of the lung (IMA).
The manipulation of NRG1/ErbB4 (zeige ERBB4 Proteine) signaling in the present study revealed that NRG1/ErbB4 (zeige ERBB4 Proteine) activity in the hippocampus is critical for learning and memory.
Nrg1-I intramuscular injection enhanced muscle reinnervation by collateral sprouting
These results collectively suggest that sustained activation of Wnt (zeige WNT2 Proteine)/beta-catenin (zeige CTNNB1 Proteine) signaling in endothelial cells might be a cause of heart failure through suppressing neuregulin-ErbB (zeige EGFR Proteine) signaling.
These results suggest that the neuropsin (zeige KLK8 Proteine)-NRG1 signaling system has a role in pathological processes underlying temporal lobe epilepsy by regulating the activity of parvalbumin (zeige PVALB Proteine)-expressing interneurons, and that neuropsin (zeige KLK8 Proteine) regulates E/I balance and gamma oscillations through NRG1-ErbB4 (zeige ERBB4 Proteine) signaling toward parvalbumin (zeige PVALB Proteine)-expressing interneurons.
we show that the antifibrotic effect of neuregulin-1 is at least partially mediated through anti-inflammatory activity, linked to receptor tyrosine-protein kinase erbB-4 (zeige ERBB4 Proteine) activation in macrophages
Results show that at ventral hippocampus-nucleus accumbens synapses, presynaptic type III Nrg1 bidirectional signaling controls the establishment of ventral hippocampus-nucleus accumbens glutamatergic synapses. Type III Nrg1 back-signaling contributes to functional synaptic vesicle clustering and neurotransmitter vesicle release.
Results demonstrate for the first time a link between a mutation of a schizophrenia risk gene, neuregulin 1 and altered neuronal resonance properties in sensory cortex.
findings reveal molecular, cellular, and circuit mechanisms of NRG1/ErbB4 (zeige ERBB4 Proteine) in regulating the initiation of critical period visual cortical plasticity.
Data show that laminin alpha2beta1gamma1 (Lm211) can inhibit neuregulin 1 type III (Nrg1III) by limiting protein kinase A (PKA) activation, which is required to initiate myelination.
These results demonstrate for the first time in vivo interplay between Nrg1 and endocannabinoids in the brain.
Data suggest that epidermal growth factor receptor (zeige EGFR Proteine) B [ErbB (zeige EGFR Proteine)] isoforms and their ligands (epidermal growth factor (zeige EGF Proteine) [EGF (zeige EGF Proteine)], amphiregulin (zeige AREG Proteine) [AREG (zeige AREG Proteine)], and neuregulin-1 [NRG1]) are expressed in uteroplacental tissues in mid- and late-phases of pregnancy.
Cloning of a novel isoform of NRG1 (IgNRG1beta2) containing an immunoglobulin-like domain which is probably essential for efficient interaction with ErbB (zeige EGFR Proteine) receptors.
The present research focused on morphological distribution of Nrg1 and its receptors, ErbB2 (zeige ERBB2 Proteine) and ErbB4 (zeige ERBB4 Proteine), in main gastrointestinal tissues of the non-human primate rhesus monkey.
we observed the activation of Notch (zeige NOTCH1 Proteine) signaling in cardiomyocytes adjacent to those undergoing apical constriction, and we showed that this activation is positively regulated by Neuregulin signaling.
these results suggest that Nrg1 is not the primary effector of trabeculation and/or that other EGF (zeige EGF Proteine)-like ligand(s) activates the ErbB2 (zeige ERBB2 Proteine)/ErbB4 (zeige ERBB4 Proteine) pathway, either through functioning as the primary ligand or acting in a redundant manner. Overall, our work provides an example of cross-species differences in EGF (zeige EGF Proteine) family member requirements for an evolutionary conserved process.
Notch1 (zeige NOTCH1 Proteine) activation induces expression of ephrin b2a (efnb2a (zeige EFNB2 Proteine)) and neuregulin 1 (nrg1) in the endocardium to promote trabeculation and forced Notch (zeige NOTCH1 Proteine) activation in the absence of cardiac contraction rescues efnb2a (zeige EFNB2 Proteine) and nrg1 expression
These findings identify Nrg1 as a potent, induced mitogen for the endogenous adult heart regeneration program.
These results demonstrate that Nrg1 type III is an essential signal that controls Schwann cell migration to ensure that these glia are present in the correct numbers and positions in developing nerves.
ErbB3 (zeige ERBB3 Proteine) signaling is required for normal migration of trunk, but not cranial, neural crest cells
Disc1 (zeige DISC1 Proteine) and nrg1 function in controlling development of oligodendrocytes and neurones from olig2 (zeige OLIG2 Proteine)-expressing precursor cells.
NRG1 and PI3K functionally interact with ErbB2 (zeige ERBB2 Proteine) and ErbB3 (zeige ERBB3 Proteine) during regeneration
The protein encoded by this gene was originally identified as a 44-kD glycoprotein that interacts with the NEU/ERBB2 receptor tyrosine kinase to increase its phosphorylation on tyrosine residues. This protein is a signaling protein that mediates cell-cell interactions and plays critical roles in the growth and development of multiple organ systems. It is known that an extraordinary variety of different isoforms are produced from this gene through alternative promoter usage and splicing. These isoforms are tissue-specifically expressed and differ significantly in their structure, and thereby these isoforms are classified into types I, II, III, IV, V and VI. The gene dysregulation has been linked to diseases such as cancer, schizophrenia and bipolar disorder (BPD).
, NSAID (nonsteroidal anti-inflammatory drug)-activated protein 1
, NSAID-activated gene 1 protein
, NSAID-regulated gene 1 protein
, growth/differentiation factor 15
, macrophage inhibitory cytokine 1
, placental TGF-beta
, placental bone morphogenetic protein
, prostate differentiation factor
, pro-neuregulin-1, membrane-bound isoform
, type I neuregulin 1
, type III neuregulin 1
, neuregulin 1
, glial growth factor
, heregulin, alpha (45kD, ERBB2 p185-activator)
, neu differentiation factor
, neuregulin 1 type IV beta 1a
, neuregulin 1 type IV beta 3
, sensory and motor neuron derived factor
, neuregulin 1 type III beta 3
, membrane-bound isoform
, neuregulin 1 alpha isoform
, histidine-proline-rich glycoprotein