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Animal Reproduction Science|December 8, 2004
Evaluation of gross anatomical features of cervix of tropical sheep using cervical silicone mouldsS M K Naqvi, G K Pandey, K K Gautam, et al.Journal of Clinical Pharmacology|April 18, 2001
Single-dose pharmacokinetics of atrasentan, an endothelin-A receptor antagonistE Samara, S Dutta, G Cao, et al.Cancer Biology & Therapy|June 16, 2004
Differential regulation of the protein tyrosine kinase activity following interleukin-2 (IL-2), interferron gamma (IFN-gamma) and SRBC administration in brain tumor-induced conditions: SRBC acting as a dual potentiator in regulating the cytokine profileM Bhattacharjee, S Sarkar, S Dutta, et al.ACS Applied Materials & Interfaces|March 10, 2021
Interfacial Engineering to Tailor the Properties of Multifunctional Ultralight Weight hBN-Polymer Composite AerogelsSehmus Ozden, Nikita S Dutta, Katelyn Randazzo, et al.Biochimica Et Biophysica Acta|June 9, 1995
Identification and evaluation of the role of endogenous tyrosine kinases in azoxymethane induction of proliferative processes in the colonic mucosa of ratsN K Relan, A Saeed, K Ponduri, et al.Free Radical Research Communications|January 1, 1989
Comparative toxicology of ozone and t-butyl hydroperoxide on isolated rat lungS Dutta, M Zimmer, H Sies, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 25, 2021
A systematic review and meta-analysis of efficacy and safety of Romosozumab in postmenopausal osteoporosisS Singh, S Dutta, S Khasbage, et al.Advances in Cancer Research|January 24, 2017
Applications of Mass Spectrometry Imaging to CancerG Arentz, P Mittal, C Zhang, et al.Laboratory Investigation; a Journal of Technical Methods and Pathology|November 1, 1995
Induction of EGF-receptor tyrosine kinase during early reparative phase of gastric mucosa and effects of agingN K Relan, S E Fligiel, S Dutta, et al.Journal of Medicinal Chemistry|July 1, 1986
Antagonists of substance P. Further modifications of substance P antagonists obtained by replacing either positions 7, 9 or 7, 8 and 11 of SP with D-amino acid residuesA S Dutta, J J Gormley, A S Graham, et al.Pageof 77