J. Wu

发表

FERRICYANIDE OXIDATION OF DIHYDROPYRIDINES AND ANALOGS

T. C. Bruice, M. Powell, J. Wu, 1984 .

Irreversible caspase inhibitors: tools for studying apoptosis.

L. Fritz, J. Wu, 1999, Methods.

Characterization of human type I and type II IMP dehydrogenases.

Y. Natsumeda, E. Papp, J. Wu, 1993, The Journal of biological chemistry.

Conformationally constrained inhibitors of caspase-1 (interleukin-1 beta converting enzyme) and of the human CED-3 homologue caspase-3 (CPP32, apopain).

K. Tomaselli, J. Krebs, J. Wu, 1998, Bioorganic & medicinal chemistry letters.

On the mechanism and inhibition of DNA cytosine methyltransferases.

D. Santi, J. Wu, Daniel V. Santi, 1985, Progress in clinical and biological research.

The mechanism of free base formation from DNA by bleomycin. A proposal based on site specific tritium release from Poly(dA.dU).

J. Stubbe, J. Kozarich, J. Wu, 1983, The Journal of biological chemistry.

A method for screening antisense oligodeoxyribonucleotides effective for mRNA translation-arrest.

K. Choo, J. Wu, L. Au, 1996, Journal of biochemistry.

Mechanism of hydrogen peroxide and hydroxyl free radical-induced intracellular acidification in cultured rat cardiac myoblasts.

S. M. Wang, Y. T. Lee, M. Wu, 1996, Circulation research.

Nonnucleoside inhibitors of HIV-1 reverse transcriptase: nevirapine as a prototype drug.

P. Grob, R. Ingraham, J. Wu, 1992, AIDS research and human retroviruses.

A potent fluorescent ATP-like inhibitor of cAMP-dependent protein kinase.

J. H. Wang, J. Wu, H. Chuan, 1989, The Journal of biological chemistry.

Stereochemical studies of the C-methylation of deoxycytidine catalyzed by HhaI methylase and the N-methylation of deoxyadenosine catalyzed by EcoRI methylase.

D. Santi, J. Wu, H. Floss, 1991, Archives of biochemistry and biophysics.

Mechanism of bleomycin: evidence for 4'-ketone formation in poly(dA-dU) associated exclusively with free base release.

J. Stubbe, J. Kozarich, J. Wu, 1985, Biochemistry.

Identification of the IMP binding site in the IMP dehydrogenase from Tritrichomonas foetus.

C. Wang, F. Whitby, J. Wu, 1995, Biochemistry.

Probing the active site of human IMP dehydrogenase using halogenated purine riboside 5'-monophosphates and covalent modification reagents.

K. Straub, J. Wu, L. Antonino, 1994, Biochemistry.

Chimeric human immunodeficiency virus type 1/type 2 reverse transcriptases display reversed sensitivity to nonnucleoside analog inhibitors.

A. Bacolla, J. Wu, C. Shih, 1991, Proceedings of the National Academy of Sciences of the United States of America.

Characterization of the binding site for nevirapine (BI-RG-587), a nonnucleoside inhibitor of human immunodeficiency virus type-1 reverse transcriptase.

S. Rogers, C. Pargellis, R. Ingraham, 1991, The Journal of biological chemistry.

Catalytic hydrolysis and synthesis of adenosine 5'-triphosphate by stereoisomers of covalently labeled F1-adenosinetriphosphatase and reconstituted submitochondrial particles.

J. H. Wang, J. Wu, J. Cesana, 1987, Biochemistry.

Geometric isomers of covalently labeled mitochondrial F1-adenosinetriphosphatase with different properties.

J. H. Wang, J. Wu, V. Joshi, 1986, Biochemistry.

Metabolism of 4'-azidothymidine. A compound with potent and selective activity against the human immunodeficiency virus.

J. Wu, M. S. Chen, R. Suttmann, 1992, The Journal of biological chemistry.

Specific inhibition of delta antigen by in vitro system by antisense oligodeoxynucleotide: implications for translation mechanism and treatment.

K. Choo, J. Wu, L. Au, 1997, Journal of virological methods.

5-Fluorocytosine in DNA is a mechanism-based inhibitor of HhaI methylase.

A. Matsuda, D. Santi, J. Wu, 1988, Biochemistry.

Human IMP dehydrogenase catalyzes the dehalogenation of 2-fluoro- and 2-chloroinosine 5'-monophosphate in the absence of NAD.

J. Wu, L. Antonino, 1994, Biochemistry.

Mechanism of bleomycin: evidence for a rate-determining 4'-hydrogen abstraction from poly(dA-dU) associated with the formation of both free base and base propenal.

J. Stubbe, J. Kozarich, J. Wu, 1985, Biochemistry.

Determination of the roles of active sites in F1-ATPase by controlled affinity labeling.

J. H. Wang, J. Wu, H. Chuan, 1989, Biochemistry.

Novel non-nucleoside inhibitors of HIV-1 reverse transcriptase. 2. Tricyclic pyridobenzoxazepinones and dibenzoxazepinones.

D. Mcneil, J. Wu, K. D. Hargrave, 1992, Journal of medicinal chemistry.

Inhibition of HIV-1 replication by a nonnucleoside reverse transcriptase inhibitor.

J. Adams, K. Grozinger, J. Wu, 1990, Science.

A novel dipyridodiazepinone inhibitor of HIV-1 reverse transcriptase acts through a nonsubstrate binding site.

J. Proudfoot, P. Grob, J. Wu, 1991, Biochemistry.

DNA degradation by bleomycin: evidence for 2'R-proton abstraction and for C-O bond cleavage accompanying base propenal formation.

J. Stubbe, J. Kozarich, J. Wu, 1986, Biochemistry.

Early metabolic inhibition‐induced intracellular sodium and calcium increase in rat cerebellar granule cells

M. Wu, J. Wu, Jiahn‐Chun Wu, 1999, The Journal of physiology.

EFFECTS OF GLUTATHIONE ON CHLOROPLAST MEMBRANE FLUIDITY AND THE GLUTATHIONE CIRCULATION SYSTEM IN YOUNG LOQUAT FRUITS UNDER LOW TEMPERATURE STRESS

J. Wu, Y. Ke, S. H. Sun, 2011 .

Choline and carnitine acetyltransferases of heart.

J. Wu, H. White, 1973, Biochemistry.

Structure-activity relationships for inhibition of inosine monophosphate dehydrogenase by nuclear variants of mycophenolic acid.

R. C. Hawley, B. Devens, C. González, 1996, Journal of medicinal chemistry.

Kinetic and catalytic mechanism of HhaI methyltransferase.

D. Santi, J. Wu, 1987, The Journal of biological chemistry.

Kinetics and inhibition of reverse transcriptase from human and simian immunodeficiency viruses

P. Marx, J. Wu, M. S. Chen, 1988, Antimicrobial Agents and Chemotherapy.

Rationally designed inhibitors of inosine monophosphate dehydrogenase.

K. Straub, E. Papp, J. Wu, 1997, Journal of medicinal chemistry.

The three-dimensional structure of caspase-8: an initiator enzyme in apoptosis.

M. Grütter, P. Mittl, S. D. Marco, 1999, Structure.

Isoelectric focusing of carnitine acetyltransferases isolated from tissues of man, rabbit and pigeon.

J. Wu, H. White, 1974, Comparative biochemistry and physiology. B, Comparative biochemistry.

Protein kinase C -activating isophthalate derivatives mitigate Alzheimer's disease-related cellular alterations

M. Hiltunen, J. Wu, Kaisa M. A. Paldanius, 2018, Neuropharmacology.

Caspase-8 specificity probed at subsite S(4): crystal structure of the caspase-8-Z-DEVD-cho complex.

M. Grütter, H. Blanchard, J. Wu, 2000, Journal of molecular biology.

Properties of catechol O-methyltransferases from brain and liver of rat and human.

J. Wu, H. White, 1975, The Biochemical journal.

Non-sialate inhibitor of influenza A/WSN/33 neuraminidase.

G. W. Peet, J. Wu, R. Eckner, 1995, Biochemistry.

Polypeptide linkages and resulting structural features as powerful chromogenic factors in the Lowry phenol reaction. Studies on a glycoprotein containing no Lowry phenol-reactive amino acids and on its desialylated and deglycosylated products.

A. M. Wu, J. Wu, A. Herp, 1978, The Biochemical journal.