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X D Ji

Showing results (31-40 of 54) with videos related to

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Journal of Medicinal Chemistry|October 9, 1999
Selective A(3) adenosine receptor antagonists: water-soluble 3, 5-diacyl-1,2,4-trialkylpyridinium salts and their oxidative generation from dihydropyridine precursorsR Xie, A H Li, X D Ji, et al.
Journal of Medicinal Chemistry|June 7, 1996
Synthesis and biological activities of flavonoid derivatives as A3 adenosine receptor antagonistsY Karton, J L Jiang, X D Ji, et al.
Zhonghua Yi Xue Za Zhi|May 14, 2026
[Prediction of recurrence-free survival of T1 glottic carcinoma based on enhanced CT anterior commissure invasion and tumor volume]H L Zhang, W F Li, L F Shen, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 1994
A mutant epidermal growth factor receptor common in human glioma confers enhanced tumorigenicityR Nishikawa, X D Ji, R C Harmon, et al.
Journal of Medicinal Chemistry|August 1, 1997
Structure-activity relationships of 4-(phenylethynyl)-6-phenyl-1,4-dihydropyridines as highly selective A3 adenosine receptor antagonistsJ Jiang, A M van Rhee, L Chang, et al.
Journal of Neuroscience Research|September 24, 1999
Differential expression of peroxiredoxin subtypes in human brain cell typesT A Sarafian, M A Verity, H V Vinters, et al.
Molecular and Cellular Biochemistry|January 12, 2000
Monoclonal anti-androgen receptor antibodies: production, characterization and potential diagnostic applicationsC C Shih, W J Young, C H Wang, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Stable isotope-labeled tryptophan as a precursor for studying the disposition of quinolinic acid in rabbitsR L Boni, M P Heyes, J D Bacher, et al.
Neuropharmacology|November 19, 1997
Pharmacological characterization of novel A3 adenosine receptor-selective antagonistsK A Jacobson, K S Park, J L Jiang, et al.
Journal of Molecular Recognition : JMR|December 1, 1989
Agonist derived molecular probes for A2 adenosine receptorsK A Jacobson, L K Pannell, X D Ji, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

Sort By:
Pageof 6
Journal of Medicinal Chemistry|October 9, 1999
Selective A(3) adenosine receptor antagonists: water-soluble 3, 5-diacyl-1,2,4-trialkylpyridinium salts and their oxidative generation from dihydropyridine precursorsR Xie, A H Li, X D Ji, et al.
Journal of Medicinal Chemistry|June 7, 1996
Synthesis and biological activities of flavonoid derivatives as A3 adenosine receptor antagonistsY Karton, J L Jiang, X D Ji, et al.
Zhonghua Yi Xue Za Zhi|May 14, 2026
[Prediction of recurrence-free survival of T1 glottic carcinoma based on enhanced CT anterior commissure invasion and tumor volume]H L Zhang, W F Li, L F Shen, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 1994
A mutant epidermal growth factor receptor common in human glioma confers enhanced tumorigenicityR Nishikawa, X D Ji, R C Harmon, et al.
Journal of Medicinal Chemistry|August 1, 1997
Structure-activity relationships of 4-(phenylethynyl)-6-phenyl-1,4-dihydropyridines as highly selective A3 adenosine receptor antagonistsJ Jiang, A M van Rhee, L Chang, et al.
Journal of Neuroscience Research|September 24, 1999
Differential expression of peroxiredoxin subtypes in human brain cell typesT A Sarafian, M A Verity, H V Vinters, et al.
Molecular and Cellular Biochemistry|January 12, 2000
Monoclonal anti-androgen receptor antibodies: production, characterization and potential diagnostic applicationsC C Shih, W J Young, C H Wang, et al.
Advances in Experimental Medicine and Biology|January 1, 1991
Stable isotope-labeled tryptophan as a precursor for studying the disposition of quinolinic acid in rabbitsR L Boni, M P Heyes, J D Bacher, et al.
Neuropharmacology|November 19, 1997
Pharmacological characterization of novel A3 adenosine receptor-selective antagonistsK A Jacobson, K S Park, J L Jiang, et al.
Journal of Molecular Recognition : JMR|December 1, 1989
Agonist derived molecular probes for A2 adenosine receptorsK A Jacobson, L K Pannell, X D Ji, et al.
Pageof 6