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The Journal of Physiology|September 13, 2024
Protein kinase C epsilon contributes to chronic mechanoreflex sensitization in rats with heart failureAlec L E Butenas, Shannon K Parr, Joseph S Flax, et al.
Angewandte Chemie (International Ed. in English)|December 18, 2023
Metallacyclobuta-(2,3)-diene: A Bidentate Ligand for Stream-line Synthesis of First Row Transition Metal Catalysts for Cyclic Polymerization of PhenylacetyleneJohn B Russell, Debabrata Konar, Taylor M Keller, et al.
Journal of Endovascular Therapy : an Official Journal of the International Society of Endovascular Specialists|January 11, 2021
Health Care Utilization Following Inpatient Femoropopliteal Revascularization With Drug-Coated Balloon Angioplasty: A Nationwide Cohort AnalysisMichael I Gurin, Sebastian E Beyer, Mitchell Weinberg, et al.
Aerospace Medicine and Human Performance|August 1, 2026
Numerical Model of the Eye for Understanding Acute Microgravity-Induced Ocular ChangesDanielle J Carroll, Sara A Rothrock, Scott D Phillips, et al.
Organic Letters|November 4, 2010
Oligomers of a 5-carboxy-methanopyrrolidine β-amino acid. A search for orderGrant R Krow, Nian Liu, Matthew Sender, et al.
American Journal of Physiology. Heart and Circulatory Physiology|May 8, 2007
Urocortin prevents mitochondrial permeability transition in response to reperfusion injury indirectly by reducing oxidative stressPaul A Townsend, Sean M Davidson, Samantha J Clarke, et al.
Journal of Experimental Botany|April 21, 2011
MicroRNAs in the shoot apical meristem of soybeanChui E Wong, Ying-Tao Zhao, Xiu-Jie Wang, et al.
Journal of Affective Disorders|April 29, 2023
Change in cardiovascular health among adults with current or past major depressive disorder enrolled in intensive smoking cessation treatmentAllison J Carroll, Mark D Huffman, E Paul Wileyto, et al.
Psychiatry Research|March 21, 2012
Genetic association study of individual symptoms in depressionWoojae Myung, Jihye Song, Shinn-Won Lim, et al.
Journal of Medical Genetics|January 15, 2013
Whole-exome sequencing identifies a mutation in the mitochondrial ribosome protein MRPL44 to underlie mitochondrial infantile cardiomyopathyChristopher J Carroll, Pirjo Isohanni, Rosanna Pöyhönen, et al.
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