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The protein encoded by NEUROG3 is a basic helix-loop-helix (bHLH) transcription factor involved in neurogenesis. Additionally we are shipping Neurogenin 3 Antibodies (116) and Neurogenin 3 Proteins (6) and many more products for this protein.
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These results provide new detail regarding the Ngn3 transcriptional network operating in endocrine progenitor cells to specify a beta (show SUCLA2 ELISA Kits) cell phenotype
ChIP experiments confirmed that Pdx1 (show PDX1 ELISA Kits) activates the expression of the downstream transcription factors, Ngn3 and Pax6 (show PAX6 ELISA Kits), by combined with the promoter regions of insulin (Insulin (show INS ELISA Kits)-P), Ngn3 (Ngn3-P), and Pax6 (Pax6 (show PAX6 ELISA Kits)-P).
NGN3 expression in the adult human exocrine pancreas marks a dedifferentiating cell population.
conclude that NEUROG3 is essential for endocrine pancreas development in humans and that as little as 10% NEUROG3 is sufficient for formation of pancreatic endocrine cells
NEUROG3 deficiency produces a rare clinical syndrome characterised by severe malabsorptive diarrhoea from early life and mild diabetes with a variable age of onset.
Activation of the developmental pathway neurogenin-3/microRNA-7a regulates cholangiocyte proliferation in response to injury.
The expression of transcription factor Ngn3 and pancreatic mesenchymal microenvironment are important and necessary to promote pancreatic progenitors differentiated to islet cells regardless of pancreatic development or islets regeneration.
Recessively inherited NEUROG-3 mutations were originally identified in three patients with unexplained congenital malabsorptive diarrhea and an absence of EC.
Prospectively isolated NGN3-expressing progenitors from human embryonic stem cells give rise to pancreatic endocrine cells.
Data indicate associations of SNPs in eight loci CXCR4, HHEX, FOXA2, NGN3, TCF7L2, FLJ39370 (C4orf32), LOC646279 (RPL21P7) and THADA with body mass index (BMI) and weight.
Ngn3-mediated pancreatic duct-to-endocrine cell reprogramming was measured employing genome wide mRNA profiling.
Duplication of pre-existing beta-cells is not the sole source of new beta-cells during pregnancy; Ngn3 may be involved in this process.
data demonstrate that HIF1-alpha (show HIF1A ELISA Kits) negatively controls beta cell differentiation in vivo by regulating NGN3 expression, and that this effect is mediated by signals from blood vessels.
Data indicate that all neurogenin 3 (Neurog3)-tuberous sclerosis complex 1 (Tsc1 (show TSC1 ELISA Kits))-/- mice developed notable adenocarcinoma-like lesions in pancreas starting from the age of 100 days old.
Hnf1b plays a crucial role in the regulatory networks that control pancreatic MPC expansion, acinar cell identity, duct morphogenesis and generation of endocrine precursors.
The role of neurogenin 3 and PD-L1 (show CD274 ELISA Kits) in the genesis of neo-islets in NOD mice is reported.
Neurog3 establishes the posterior boundary of the serotonergic system by actively suppressing serotonergic specification in the spinal cord.
Insm1 (show INSM1 ELISA Kits) works to promote endocrine cell differentiation in a pathway that involves Neurog3 and Ripply3 (show DSCR6 ELISA Kits)
three transcription factors, PDX1 (show PDX1 ELISA Kits), NGN3 and MAFA (show MAFA ELISA Kits), are very important in pancreatic development. Overexpression of these three factors can reprogram both pancreatic exocrine and SOX9 (show SOX9 ELISA Kits)-positive cells of the liver into cells resembling pancreatic beta cells
The role of Ngn3 in the specification of hypothalamic neurons controlling energy balance, is reported.
The control of endocrine cell fate is instead fulfilled by two basic helix-loop-helix factors, Ascl1b and Neurod1 (show NEUROD1 ELISA Kits) and NEUROG3 is not the unique pancreatic endocrine cell fate determinant in vertebrates.
Nkx2.2 coordinately activates NeuroD1 with Ngn3 in the endocrine progenitor cell and plays a role in the maintenance of NeuroD1 expression to regulate beta cell function in the mature islet.
The protein encoded by this gene is a basic helix-loop-helix (bHLH) transcription factor involved in neurogenesis. The encoded protein likely acts as a heterodimer with another bHLH protein. Defects in this gene are a cause of congenital malabsorptive diarrhea 4 (DIAR4).
, class A basic helix-loop-helix protein 7
, protein atonal homolog 5
, Neurogenin 3 (Atonal protein homolog 5) (Helix-loop-helix protein mATH-4B) (MATH4B)
, atonal homolog 5
, helix-loop-helix protein mATH-4B
, transcriptional regulator, Relax
, atonal homolog 4