• GSK2194069 Camptothecin is a type of

  2021-10-09

  

  Camptothecin is a type of topo I inhibitor, and its prodrugs irinotecan and topotecan have been approved by the FDA for clinical cancer treatment. It has been reported that SAHA can enhance the cytotoxicity of camptothecin derivatives in several cancer cell lines20., 21., 22., 23., 24.. Taking the s

• br Methods br Results br

  2021-10-09

  

  Methods Results Discussion Peptide therapeutics represents a unique class of biopharmaceuticals that continues to evolve in drug discovery and development. We and others have been particularly interested in bioengineering innovative pGC-A and/or pGC-B peptide activators. This has been succe

• GPR is a G protein coupled receptor

  2021-10-09

  

  GPR55 is a G protein-coupled receptor that has pro-oncogenic properties and whose expression correlates with tumor aggressiveness and increased activation of extracellular signal-regulated kinase (ERK) cascade [12]. Elevated expression of GPR55 has been linked to aggressiveness in human pancreatic,

• With an ever increasing incidence rate of type diabetes and

  2021-10-09

  

  With an ever-increasing incidence rate of type 2 diabetes and obesity, it is imperative to develop new therapeutic regimes that may provide a benefit both in terms of efficacy and tolerability. The existing portfolio of drugs for the treatment of metabolic disorders, primarily type 2 diabetes and ob

• This resembles a vicious cycle since BBB disruption and infl

  2021-10-09

  

  This resembles a vicious cycle since BBB disruption and inflammation are thought to be caused by epilepsy, but other contributing factors are also known to be their cause, such as peripheral infection, autoimmunity, XL228 synthesis trauma and stroke that also underlie epilepsy [18]. Additional trigg

• Na K ATPase adenosine triphosphate ATP

  2021-10-09

  

  Na+/K+-ATPase, Potassium Canrenoate and astrocytic glutamate transporters act together to maintain sodium and potassium gradients and the proper activities of EAAT1 and EAAT2 (Rose et al., 2009; Sheean et al., 2013); nevertheless, in present study, Na+/K+-ATPase activity was shown to be increased a

• Na K ATPase adenosine triphosphate ATP

  2021-10-09

  

  Na+/K+-ATPase, 2881 and astrocytic glutamate transporters act together to maintain sodium and potassium gradients and the proper activities of EAAT1 and EAAT2 (Rose et al., 2009; Sheean et al., 2013); nevertheless, in present study, Na+/K+-ATPase activity was shown to be increased as from 24 h. It

• Introduction Human pathogenic Leishmania protozoa comprise

  2021-10-09

  

  Introduction Human pathogenic Leishmania protozoa comprise 20 different species that are distributed throughout the world and cause the disease leishmaniasis [1]. Transmission primarily occurs through the bite of a female sand fly and clinical manifestations of the disease span from cutaneous lesio

• Recently unimolecular multi functional peptides that combine

  2021-10-09

  

  Recently, unimolecular, multi-functional peptides that combine GLP-1RA activity with Tosedostat and/or GIP activity have been suggested as new therapeutic agents for glycaemic and weight control. In rodents, dual GIP and GLP-1 receptor agonists achieve significantly better glucose control and weigh

• WM-2474 br Materials and methods br Results br Discussion

  2021-10-09

  

  Materials and methods Results Discussion The global pandemic of T2DM has mandated a search for new types of therapeutic agent and several long-acting analogs of naturally occurring incretins, particularly derivatives of GLP-1, have already been adopted in clinical practice [29]. This study

• Primarily because secretase was a therapeutic target in

  2021-10-08

  

  Primarily because γ-secretase was a therapeutic target in AD, a plethora of γ-secretase inhibitors (GSIs) have been developed that effectively inhibit γ-secretase cleavage in humans [16]. Indeed, “druggability” of γ-secretase has not been an issue even when the identity of the target was unknown in

• Several small molecules such as erastin and RSL are

  2021-10-08

  

  Several small molecules, such as erastin and RSL3, are reported to induce ferroptosis in both normal and cancer VEGFR Tyrosine Kinase Inhibitor II [21,22]. We confirmed that erastin-induced growth inhibition is an ideal ferroptosis model for cardiomyocytes. The erastin inhibits the growth of H9c2 c

• We found the FAAH CC genotype only confers risk for

  2021-10-08

  

  We found the FAAH CC genotype only confers risk for anxiety if the CRFR1 minor allele combination is also present. Additionally, the FAAH AA/AC genotype was riskier than the CC if the three CRFR1 minor hyPerFUsion™ high-fidelity DNA polymerase were not present. This result is somewhat contrary to o

• Fig demonstrates placental amino acid transporter protein co

  2021-10-08

  

  Fig. 7 demonstrates placental amino Indomethacin synthesis transporter protein concentrations. While no change in the placental SNAT2 is effected in response to a high-fat diet in wt, a trend toward a reduction was seen in glut3 mice in response to a high-fat vs. chow diet (Fig. 7A and B). A high-f

• Immunohistochemistry analysis shown ghrelin and GHSR

  2021-10-08

  

  Immunohistochemistry analysis shown ghrelin and GHSR-1a immunostaining was located in the epithelial cells of Palomid 529 australia and ducts throughout the lactation, strong immunoreactive cells were detected in L30, L60 and L120 stage. The distribution of ghrelin has been shown in many tissues, i

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