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
Sujitra Wongkasemjit
Trinucleotide rehash (TNR) sicknesses are brought about by the unusual extension of CXG (X = C, A, G and T) successions in genomes. We have revealed two little particles restricting to TNR, NCD, and NA, which firmly tie to CGG rehash (dependable grouping of delicate X disorder) and CAG rehash (Huntington's illness). The NMR design of NA restricting to the CAG/CAG group of three has been explained, yet the construction of NCD bound to the CGG/ CGG ternion still needed to be tended to. We here report the primary assurance of the NCD-CGG/CGG complex by NMR spectroscopy and the examination with the NA-CAG/CAG complex. While the NCD-CGG/CGG structure imparts the limiting qualities to that of the NA-CAG/CAG complicated, a tremendous distinction was found in the general design brought about by the underlying variance at the ligand-bound site. The NCD-CGG/CGG complex was proposed in the balance among stacked and crimped structures, even though NA-CAG/CAG complex has just the stacked designs [1]. The unique change of the NCD-CGG/CGG structure at the NCD-restricting site proposed space for streamlining in the linker design of NCD to acquire further developed liking to the CGG/CGG set of three.