Yong Qian Wu - Publications

Affiliations: 
1991-1993 Pharmaceutical Sciences Wayne State University, Detroit, MI, United States 

8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Wu Y, Yang H, Cheng M, Shi J, Zhang W, Liu S, Zhang M. Calpain Inhibitor Calpeptin Alleviates Ischemia/Reperfusion-Induced Acute Kidney Injury Suppressing AIM2 Inflammasome and Upregulating Klotho Protein. Frontiers in Medicine. 9: 811980. PMID 35155498 DOI: 10.3389/fmed.2022.811980  0.313
2016 Wu Y, Xu J, El-Jouni W, Lu T, Li S, Wang Q, Tran M, Yu W, Wu M, Barrera IE, Bonventre JV, Zhou J, Denker BM, Kong T. Gα12 is required for renal cystogenesis induced by Pkd1 inactivation. Journal of Cell Science. PMID 27505895 DOI: 10.1242/jcs.190496  0.591
2015 Xu JX, Lu TS, Li S, Wu Y, Ding L, Denker BM, Bonventre JV, Kong T. Polycystin-1 and Gα12 regulate the cleavage of E-cadherin in kidney epithelial cells. Physiological Genomics. 47: 24-32. PMID 25492927 DOI: 10.1152/physiolgenomics.00090.2014  0.602
1995 Guo J, Wu YQ, Rattendi D, Bacchi CJ, Woster PM. S-(5′-deoxy-5′-adenosyl)-1-aminoxy-4-(methylsulfonio)-2- cyclopentene (AdoMao): An irreversible inhibitor of S-adenosylmethionine decarboxylase with potent in vitro antitrypanosomal activity Journal of Medicinal Chemistry. 38: 1770-1777. PMID 7752200 DOI: 10.1021/Jm00010A021  0.578
1995 Wu YQ, Woster PM. Irreversible inhibition of human S-adenosylmethionine decarboxylase by the pure diastereomeric forms of S-(5′-deoxy-5′-adenosyl)-1-ammonio-4-methylsulfonio-2-cyclopentene (AdoMac) Biochemical Pharmacology. 49: 1125-1133. PMID 7748194 DOI: 10.1016/0006-2952(95)98510-G  0.584
1993 Wu YQ, Woster PM. Preparation of the pure diastereomeric forms of S-(5'-deoxy-5'-adenosyl)-1-ammonio-4-methylsulfonio-2-cyclopentene and their evaluation as irreversible inhibitors of S-adenosylmethionine decarboxylase from Escherichia coli. Bioorganic & Medicinal Chemistry. 1: 349-60. PMID 8081865 DOI: 10.1016/S0968-0896(00)82141-0  0.588
1993 Guo JQ, Wu YQ, Farmer WL, Douglas KA, Woster PM, Garofalo J, Basshi CJ. Restricted rotation analogs of S-adenosylmethionine: synthesis, evaluation as inhibitors of S-adenosylmethionine decarboxylase, and potential use as selective antitrypanosomal agents Bioorganic and Medicinal Chemistry Letters. 3: 147-152. DOI: 10.1016/S0960-894X(01)80865-9  0.603
1993 Wu YQ, Lawrence T, Guo JQ, Woster PM. α-cyano-substituted analogoues of decarboxylated S-adenosylmethionine as enzyme activated, irreversible inhibitors of S-adenosylmethionine decarboxylase Bioorganic and Medicinal Chemistry Letters. 3: 2811-2816. DOI: 10.1016/S0960-894X(01)80770-8  0.599
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