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
Kathina Boch
A type I trans membrane protein known as the polymeric immunoglobulin receptor (pIgR) is primarily made up of an intracellular area, a trans membrane region, and an extracellular region. Additionally, the repeating immunoglobulin-like (Ig-like) domains in the extracellular domain of pIgR increase in number with vertebrate evolution, from four in birds, amphibians, and reptiles to five in mammals [1]. It’s interesting to note that while pIgR can be expressed in the liver, respiratory system, intestines, and other organs, there are clear differences in pIgR expression levels between the same sites and different animals, as well as between different organs and physiological states within the same animal. The level of pIgR expression is significantly higher in the rodent liver than in the respiratory tract, and it is decreased or nonexistent in conditions like human lung cancer and rectal cancer. For instance, pIgR expression is higher in the mouse small intestine after weaning than before, whereas it only appears in the small intestine of rats after weaning [2].