2024年12月2日 · L’Institut des Sciences Moléculaires de Marseille (iSm2) forme un centre de recherche multidisciplinaire au cœur de la chimie moléculaire en agissant principalement à l’interface avec la biologie et affichant la volonté d'orienter une partie de ses recherches à l'interface avec la Physique.

The Sectéra Iridium ® Security Module 2 (ISM2) is a sleek, small form factor encryption module that provides NSA Certified protection of classified voice and data communications. The module is covert – it fits completely inside the Iridium 9575A handset and provides end-to-end security for information classified Top Secret and below.

2024年12月25日 · Complete information for ISM2 gene (Protein Coding), Isthmin 2, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

2024年12月2日 · The Institute of Molecular Sciences of Marseille (iSm2) forms a multidisciplinary research center at the heart of molecular chemistry, primarily acting at the interface with biology and displaying the desire to direct part of its research at the interface with Physics.

Isthmin (ISM) is a secreted protein family with two members, namely ISM1 and ISM2, both containing a TSR1 domain followed by an AMOP domain. Its broad expression pattern suggests diverse functions in developmental and physiological processes.

该基因编码的蛋白质包含 1 型血小板反应蛋白结构域，该结构域存在于血小板反应蛋白、许多参与补体途径的蛋白质以及细胞外基质蛋白中。 已观察到编码不同同种型的两种选择性剪接的转录物变体。 [RefSeq 提供，2009 年 3 月] The protein encoded by this gene contains a type 1 thrombospondin domain, which is present in thrombospondin, a number of proteins involved in the complement pathway, as well as in extracellular matrix proteins.

2020年10月13日 · ISM2 protein is decreased in the circulation and placenta in patients with preeclampsia. Circulating ISM2 protein was measured in 30 women with normotensive pregnancy (Control), 21 patients with gestational hypertension (GH) and 30 patients with preeclampsia (PE).

2022年12月21日 · Isthmin (ISM) is a secreted protein family with two members, namely ISM1 and ISM2, both containing a TSR1 domain followed by an AMOP domain. Its broad expression pattern suggests diverse functions in developmental and physiological processes. Over the past few years, multiple studies have focused on …

expression of ISM2 is significantly associated with poor prognosis. More importantly, a couple of in-vitro and in-vivo assays verified the vital significance of ISM2 in the progression of CRC. Furthermore, the silence of ISM2 induced more CD8+ T …

这个基因编码的蛋白质包含一个类型1血栓素域，存在于血栓素中，一些与补体途径有关的蛋白质以及细胞外基质蛋白质。 已经观察到了两种可变剪接的转录变异体，它们编码不同的异构体。 [由RefSeq，2009年3月提供] 该基因暂未发现相关的转录本和蛋白质序列信息。 该模块正在开发中，请耐心等待我们的数据更新。 Haploinsufficiency of the Notch Ligand DLL1 Causes Variable Neurodevelopmental Disorders.