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
Zhanxiang Zhou
The workshop brought along scientists from pharmaceutical, academic, health authority, and contract analysis organizations to debate novel approaches and current challenges for the utilization of in vitro protein unharness assays (cras) for the identification of protein unharness syndrome (CRS) potential of novel antibody (mab) medical specialty. Topics conferred encompassed a regulative perspective on protein unharness and assessment, case studies relating to the translatability of diagnosis protein knowledge to the clinic, and therefore the latest state of the science of cras, as well as comparisons between mab medical specialty at intervals one platform and across many assay platforms, a completely unique physiological assay platform, and assay improvement approaches like determination of fcr expression profiles and use of applied mathematics tests [1]. The info and approaches conferred confirmed that multiple CRA platforms area unit in use for identification of CRS potential which the selection of a specific CRA platform is very hooked in to the provision of resources for individual laboratories (e.g. Positive and negative controls, range of human blood donors), the assay through-put needed, and therefore the mechanism-of-action of the therapeutic candidate to be tested. Workshop participants united that a lot of knowledge on the prognosticative performance of CRA platforms is required, and current efforts to check in vitro assay results with clinical protein assessments were mentioned. In summary, several laboratories still focus analysis efforts on the advance of the translatability of current CRA platforms still explore novel approaches which can result in a lot of correct, and probably patient-specific, CRS prediction within the future [2].