SEPT4 Antibody

1. In this review, we will discuss the recent advances of the tauopathy research, primarily focusing on its association with the early axonal manifestation of axonal transport defect, axonal mitochondrial stress, autophagic vesicle accumulation and the proceeding of axon destruction, and the pathogenic Tau spreading across the synapse. PMID: 29991349
2. Septin4 is a novel essential factor involved in oxidative stress induced vascular endothelial cell injury by interacting with apoptosis-related protein PARP1. PMID: 29366480
3. The data suggest that Sept4_i1 induces hepatic stellate cell apoptosis by inhibiting Akt and Bcl-2 expression and up-regulating PPAR-gamma expression. PMID: 25527525
4. results suggest that Septin4 may be involved in the process of activation of hepatic stellate cells by lipopolysaccharide stimulation. PMID: 23180367
5. Bradeion/SEPT4 transcript levels are significantly increased in patients with transitional cell bladder cancer.We hypothesize that Bradeion is directly involved in bladder cancer pathogenesis with the highest expression at early cancer stages. PMID: 22503047
6. Identification of a novel anti-apoptotic E3 ubiquitin ligase that ubiquitinates antagonists of inhibitor of apoptosis proteins SMAC, HtrA2, and ARTS. PMID: 23479728
7. these data suggests a tumor suppressor role of SEPT4_i1 in HCC through regulating hepatocellular carcinoma cell apoptosis. PMID: 21952823
8. The expression of SEPT4 is significantly decreased in the ejaculated sperm of idiopathic asthenozoospermia patients. PMID: 21898991
9. ARTS is localized at mitochondria and promotes programmed cell death (apoptosis). PMID: 21824006
10. role of Bradeion in colorectal neoplasms PMID: 12032658
11. Sept4 is involved in the formation of cytoplasmic inclusions as well as induction of cell death in alpha-synuclein-associated neurodegenerative disorders. PMID: 12695511
12. Data suggest that ARTS induces apoptosis by antagonizing IAPs, including XIAP. PMID: 15029247
13. SEPT8 and SEPT4 are localized surrounding alpha-granules. Activation of platelets by agonists resulted in the translocation of SEPT4 and SEPT8 to the platelet surface indicating a possible functional role of these proteins in platelet granular secretion PMID: 15116257
14. ARTS can function as a tumor suppressor protein in childhood acute lymphocytic leukemia. PMID: 15122323
15. high cellular levels of ARTS protein sensitize cells toward apoptosis PMID: 15837787
16. The data presented here suggest that ARTS P-loop is not frequently mutated in gastric, lung, and hepatocellular carcinomas, and that apoptosis deregulation in cancers is not dependent on the mutation of ARTS gene. PMID: 16376484
17. Finds somatic mutation in P-loop domains of proapoptotic ARTS genes uncommon in colon cancers. PMID: 16464805
18. define explicitly and characterize the domains of human SEPT4 PMID: 17105210
19. The Sept4 may be involved in PD as a dual susceptibility factor, as its insufficiency can diminish dopaminergic neurotransmission and enhance alpha-synuclein neurotoxicity. PMID: 17296554
20. interaction of kaposin A protein and the septin 4 variant was suggested as playing a possible role in the development of HHV-8-associated malignancies PMID: 17383018
21. SEPT9 sequence alternations causing hereditary neuralgic amyotrophy are associated with altered interactions with SEPT4/SEPT11 and resistance to Rho/Rhotekin-signaling PMID: 17546647
22. This protein may play an important role in the pathogenesis of schizophrenia and could be used as a marker for this disease. PMID: 17644312
23. Data report an intermediate structure of the GTPase domain of human SEPT4 (SEPT4-G) during unfolding transitions induced by temperature. PMID: 17764158
24. The stability and aggregation properties of the GTPase domain from human SEPT4. PMID: 18617022
25. Sporadic PD cases showed a statistically significant decrease of the fold change (FC) of SEPT4 (FC = 0.67, P = 0.054) gene expressions in the substantia nigra & amygdala (SEPT4: FC = 0.32, P = 0.007) versus healthy controls. PMID: 18951507
26. structural defects in sperm are not caused by abnormal transcription or point mutations of the TAT1 and SEPT4 genes; however, although both proteins are expressed, they are not properly localized at sperm annulus PMID: 19221096

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HGNC: 9165

OMIM: 603696

KEGG: hsa:5414

STRING: 9606.ENSP00000321674

UniGene: Hs.287518