PLXNA2 Gene - GeneCards | PLXA2 Protein | PLXA2 Antibody
2024年12月25日 · PLXNA2 (Plexin A2) is a Protein Coding gene. Diseases associated with PLXNA2 include Gaba Aminotransferase Deficiency and Loeys-Dietz Syndrome 5. Among its …
PLXNA2 - Wikipedia
This plexin-A family member is thought to transduce signals from semaphorin-3A and -3C. [6] In some studies, the PLXNA2 gene is associated with schizophrenia. [7] and anxiety. PLXNA2 is …
PLXNA2 knockdown promotes M2 microglia polarization through ... - PubMed
Our study showed that PLXNA2 knockdown accelerated the recovery of motor function and cognitive ability after MCAO/R. In addition, PLXNA2 knockdown restrained proinflammatory …
丛素 A2（PLXNA2）基因 | MCE
信号蛋白的一个子集被 plexin-A/neuropilin 跨膜受体复合物识别，触发导致轴突排斥的细胞信号转导级联。 该 plexin-A 家族成员被认为可转导信号素 3A 和 -3C 的信号。 [RefSeq 提供，2008 …
PLXNA2 plexin A2 [Homo sapiens (human)] - Gene - NCBI
2025年2月8日 · Data suggest that Fyn tyrosine kinase (Fyn)-dependent phosphorylation at two critical tyrosines is a key feature of vertebrate plexin A1 (PlxnA1) and plexin A2 (PlxnA2) …
PLXNA2 - 华文百科
Plexin-A2 是一种 蛋白质，在人类中被 PLXNA2 基因 编码。 该基因编码了 plexin -apemaphorin 共受体 家族 的成员。 信号素是一个大型分泌或膜结合蛋白的家族，在神经系统发育过程中介导 …
PLXNA2人源基因|PLXNA2基因突变_致病性_靶点-RDDC官网
semaphorins是一大类可分泌或膜结合的蛋白质，在神经系统发育过程中对轴突路径的识别具有排斥作用。 一部分semaphorins被plexin-A/神经磷脂跨膜受体复合物识别，触发细胞信号转导级 …
Plxna2小鼠基因|Plxna2基因功能|Plxna2小鼠模型-RDDC官网
与人PLXNA2（plexin A2）正同源。 [由基因组资源联盟，2022年4月提供] Lineage-specific biology revealed by a finished genome assembly of the mouse. 具有相同的蛋白质结合活性， …
Plxna2 - plexin A2 基因 - MCE
Enables identical protein binding activity and semaphorin receptor activity. Involved in regulation of cell migration and semaphorin-plexin signaling pathway. Acts upstream of or within several …
PLXNA2 plexin A2 - NIH Genetic Testing Registry (GTR) - NCBI
2024年3月5日 · Clinical resource with information about PLXNA2, Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality., and …