हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।
ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं
Maolian Gong
Understanding the regulation of pancreatic development is fundamental for the identification of novel therapeutic options for the highly prevalent diabetic patients all over the world. GATA6 mutations are associated with a broad pancreatic phenotype spectrum from severe pancreas agenesis and neonatal diabetes to the adult onset of diabetes. Many studies in mice verified the critical roles of GATA6 in pancreas development, however, phenotypes disparity is very large between human and mice. To understand the underlying mechanism of the human phenotypes, using human Pluripotent Stem Cells (hPSCs) to model the GATA6 deficiency in vitro becomes to be a very efficient research strategy. Deficient GATA6 gene dosage disrupts the differentiation of human pancreatic progenitors, leads to impaired formation of pancreatic β-like cells and the pancreas. Except for the gene dosage, GATA6 was identified activating transcription in its nearby genes temporally, which further activates cardiomyocyte and endoderm gene network through chromatin binding in intergenic regions without a GATA-binding motif. The elucidation of the GATA6 function in the pancreas can indicate a novel therapy strategy i.e. stem cell therapy.