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
Frederick S Nolte
The frequence of contagious conditions affecting the central nervous system (CNS) has been adding over the last several times. Among the reasons for the expansion of these conditions and the appearance of new neuropathogens are globalization, global warming, and the increased contiguity between humans and wild brutes due to mortal exertion analogous as deforestation. Neurotropic affecting normal brain function is shared by organisms analogous as contagions, bacteria, fungi, and freeloaders. Neuroinfections caused by these agents spark vulnerable responses, converting Neuroinflammation, excitotoxicity, and neurodegeneration. During neuroinfections, host cells release ATP as an extracellular pitfall signal withpro- seditious exertion. ATP is metabolized to its derivatives by ectonucleotidases analogous as CD39 and CD73; ATP and its metabolites modulate neuronal and vulnerable mechanisms through P1 and P2 purinergic receptors that are involved in pathophysiological mechanisms of neuroinfections. In this review we beat the salutary or pernicious goods of various factors of the purinergic signalling pathway in contagious conditions that affect the CNS, including mortal immunodeficiency contagion (HIV- 1) infection, herpes simplex contagion type 1(HSV- 1) infection, bacterial meningitis, sepsis, cryptococcosis, toxoplasmosis, and malaria. We also give a description of this signalling pathway in arising viral infections with neurological implications analogous as Zika and SARS- CoV- 2.