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Biochemical and Biophysical Research Communications|February 6, 2007
The FBXW7 beta-form is suppressed in human glioma cellsZhaodi Gu, Kenichi Inomata, Kota Ishizawa, et al.Genetics|October 1, 1986
Latent Nonstructural Differentiation among Homologous Chromosomes at the Diploid Level: Chromosome 6B of AEGILOPS LONGISSIMAR S Kota, P E McGuire, J DvorákInteractive Cardiovascular and Thoracic Surgery|August 3, 2007
Strangulated intrapericardial herniation of the stomach after use of the right gastroepiploic artery for coronary artery bypass graftingYoshifumi Ikeda, Shoichi Tobari, Naomi Morita, et al.Interactive Cardiovascular and Thoracic Surgery|September 11, 2010
Rupture of Kommerell diverticulum after total arch replacementKota Agematsu, Tetsuyuki Ueda, Shuichi Hoshino, et al.Physical Chemistry Chemical Physics : PCCP|September 11, 2010
Theoretical study of the opsin shift of deprotonated retinal schiff base in the M state of bacteriorhodopsinKazuhiro J Fujimoto, Kota Asai, Jun-Ya HasegawaThe Biochemical Journal|July 28, 2010
Characterization of an ATP-regulated DNA-processing enzyme and thermotolerant phosphoesterase in the radioresistant bacterium Deinococcus radioduransSwathi Kota, C Vijaya Kumar, Hari S MisraOrganic Letters|August 11, 2010
Convenient RNA synthesis using a phosphoramidite possessing a biotinylated photocleavable groupKota Tomaya, Mayumi Takahashi, Noriaki Minakawa, et al.Biochemical and Biophysical Research Communications|April 20, 2010
Functional expression of 5-HT2A receptor in osteoblastic MC3T3-E1 cellsTakao Hirai, Kota Kaneshige, Teruko Kurosaki, et al.Molecular Cancer Therapeutics|April 1, 2010
Inhibition of aldose reductase prevents growth factor-induced G1-S phase transition through the AKT/phosphoinositide 3-kinase/E2F-1 pathway in human colon cancer cellsKota V Ramana, Ravinder Tammali, Satish K SrivastavaChemistry (Weinheim an Der Bergstrasse, Germany)|November 30, 2013
Asymmetric α-hydroxylation of a lactone with vinylogous pyridone by using a guanidine-urea bifunctional organocatalyst: catalytic enantioselective synthesis of a key intermediate for (20S)-camptothecin analoguesTatsuya Watanabe, Minami Odagi, Kota Furukori, et al.Pageof 827