Cognosci 
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  • ||||||||||  COG 133 / Cognosci, COG1410 / Cognosci
    Journal:  Precise Modulation of Pericyte Dysfunction by a Multifunctional Nanoprodrug to Ameliorate Alzheimer's Disease. (Pubmed Central) -  Jun 4, 2024   
    Consequently, VLC@Cur-NPs markedly increased pericyte regeneration to form a positive feedback loop and thus improved neurovascular function and ultimately alleviated memory defects in APP/PS1 transgenic mice. We present a promising therapeutic strategy for AD that can precisely modulate pericytes and has the potential to treat other cerebrovascular diseases.
  • ||||||||||  COG 133 / Cognosci, COG1410 / Cognosci
    Journal:  ApoE Mimetic Peptide COG1410 Kills Mycobacterium smegmatis via Directly Interfering ClpC's ATPase Activity. (Pubmed Central) -  Mar 27, 2024   
    This study sheds light on a unique resistance mechanism against AMPs in mycobacteria, highlighting the pivotal role of ClpC in this process. Unraveling the interplay between COG1410 and ClpC enriches our understanding of AMP-bacterial interactions, offering potential insights for developing innovative strategies to combat antibiotic resistance.
  • ||||||||||  COG 133 / Cognosci, COG 112 / Cognosci
    Journal:  The role of ApoE in fatty acid transport from neurons to astrocytes under ischemia/hypoxia conditions. (Pubmed Central) -  Feb 27, 2024   
    In conclusion, ApoE plays an important role in mediating the transport of fatty acids from neurons to astrocytes under ischemia/hypoxia conditions, and this transport mechanism is ApoE isoform dependent. ApoE4 has a low transfer efficiency and may be a potential target for the clinical treatment of neonatal hypoxic-ischemic encephalopathy.
  • ||||||||||  COG 133 / Cognosci, COG 112 / Cognosci
    Journal:  Controlled Release of a Therapeutic Peptide in Sprayable Surgical Sealant for Prevention of Postoperative Abdominal Adhesions. (Pubmed Central) -  Mar 9, 2023   
    Two independent mouse models of cecal ligation and cecal anastomosis significantly reduced adhesion severity versus Seprafilm, COG133 liquid suspension, and no treatment control. The synergy of physical and chemical methods in a barrier material with proven preclinical studies highlights the value of COG133-loaded PLCL fiber mats in effectively dampening the formation of severe abdominal adhesions.
  • ||||||||||  COG 133 / Cognosci, COG 112 / Cognosci
    Journal, PD(L)-1 Biomarker, IO biomarker:  Inhibition of APOE potentiates immune checkpoint therapy for cancer. (Pubmed Central) -  Sep 30, 2022   
    Furthermore, APOE expression in cancer patients resistant to αPD-1 treatment significantly exceeded that in the sensitive group. For this reason, APOE is likely to be targeted for modifying tumor macrophage infiltrate and augmenting checkpoint immunotherapy.
  • ||||||||||  COG 133 / Cognosci, COG1410 / Cognosci
    Journal:  Apolipoprotein E mimetic peptide COG1410 combats pandrug-resistant Acinetobacter baumannii. (Pubmed Central) -  Sep 13, 2022   
    elegans infection model showed that combined therapy of COG1410 and polymyxin B was capable of significantly rescuing the infected nematodes. Taken together, our study demonstrates that COG1410 is a promising drug candidate in the battle against pandrug-resistant A. baumannii.
  • ||||||||||  COG 133 / Cognosci, COG 112 / Cognosci
    Journal:  COG133 Attenuates the Early Brain Injury Induced by Blood-Brain Barrier Disruption in Experimental Subarachnoid Hemorrhage. (Pubmed Central) -  May 6, 2022   
    In terms of molecular mechanism, COG133 inhibits blood-brain barrier destruction through the proinflammatory CypA-NF-κB-MMP9 pathway and reduces neuronal pyroptosis by inhibiting NLRP3 inflammasome activation. In conclusion, this study demonstrated that apoE-mimetic peptide, COG133, can play a neuroprotective role by protecting blood-brain barrier function and inhibiting brain cell pyroptosis to reduce early brain injury after subarachnoid hemorrhage.
  • ||||||||||  COG 133 / Cognosci, SF2523 / SignalRx, COG 112 / Cognosci
    Journal:  Polymeric nanomedicine for overcoming resistance mechanisms in hedgehog and Myc-amplified medulloblastoma. (Pubmed Central) -  Nov 17, 2021   
    Moreover, systemic administration of COG-133-NPs loaded with MDB5 and SF2523 resulted in decreased tumor burden compared to non-targeted drug-loaded NPs, without any hepatic toxicity. In conclusion, our nanomedicine of MDB5 and SF2523 offers a novel therapeutic strategy to treat chemoresistant MB.