当社グループは 3,000 以上の世界的なカンファレンスシリーズ 米国、ヨーロッパ、世界中で毎年イベントが開催されます。 1,000 のより科学的な学会からの支援を受けたアジア および 700 以上の オープン アクセスを発行ジャーナルには 50,000 人以上の著名人が掲載されており、科学者が編集委員として名高い
。オープンアクセスジャーナルはより多くの読者と引用を獲得
700 ジャーナル と 15,000,000 人の読者 各ジャーナルは 25,000 人以上の読者を獲得
Suresh Mathivanan
Intercellular interactions are pivotal for basic cellular activities and errors in either receiving or transmitting these signals are shown to cause pathological conditions. Whilst, such intercellular communications were once thought to be regulated by membrane surface molecules and/or soluble secreted proteins by stimulating the target cells through receptor mediated activation, increasing evidences suggest that extracellular microvesicles (EMVs) can also trigger such signaling events in the target cells. Exosomes and shedding microvesicles (SMVs) are classes of EMVs that are membrane enclosed organelles released by cells under physiological and pathological conditions [1-6]. Among the EMVs, exosomes are small (40-100 nm diameter) membraneous vesicles of endocytic origin while SMVs (also referred to as ectosomes) are large membranous vesicles (50-1000 nm diameter) that are shed directly from the plasma membrane (PM) [7]. Recent studies have shown that these EMVs mediate intercellular communication [8-10] and are shown to harbour mRNA, microRNA, proteins and lipids [8,11-14] based on the host cell.