Xuetao Chen

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Bi-acetylated l-stepholidine (l-SPD-A), a novel derivate of l-stepholidine (l-SPD), possesses a pharmacological profile of D(1)/5-HT(1A) agonism and D(2) antagonism. In the present study, we examined the potential antipsychotic effect of l-SPD-A in a phencyclidine (PCP)-induced rat model of schizophrenia. Pretreatment with l-SPD-A blocked acute PCP-induced(More)
This is an " accepted article " , which is a version which has been revised by the author to incorporate review suggestions, and which has been accepted by IEEE for publication. be obtained for all other uses, in any current or future media, including reprinting/republishing this material for advertising or promotional purposes, creating new collective(More)
—Telecommunication usage has skyrocketed in recent years and will continue to grow as developing world reaches to wireless as the communication medium of choice. The telecommunications world is only now addressing the significant environmental impact it is creating as well as the incredible cost on power usage. This realization has led to a push towards(More)
Assumptions • No buffer considered • Delay hiding techniques • Channel variances are heterogeneous • Power-Clock-frequency relation P c : available computing power. f: clock frequency. n' : exponent parameter in power-frequency relation in computing process. a : parameter in power-frequency relation in computing process. Intuition • The WDC network is(More)
BACKGROUND There has been an increasing trend in the incidence of stroke worldwide in recent years, and the number of studies focusing on the risk factors for stroke has also increased every year. To comprehensively evaluate the risk factors of stroke identified in prospective Western and Asian cohort studies. METHODS Population-based cohort studies on(More)
AIM Nanobody is an antibody fragment consisting of a single monomeric variable antibody domain, which can be used for a variety of biotechnological and therapeutic purposes. The aim of this work was to isolate and characterize a human signal domain antibody against VEGFR-2 domain3 (VEGFR D3) from a phage display library. METHODS To produce(More)
A series of apomorphine ((-)-1, APO)-derived analogues ((+/-)-3, (-)-4-(-)-6) were designed and synthesized by hybridizing APO with a privileged 2-aminothiazole functionality which was lent from the orally available anti-parkinsonian drug, pramipexole (2). Among these hybridized compounds, catecholic aporphine (-)-6 shows good affinity at the D(2) receptor(More)
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