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Proceedings of the National Academy of Sciences of the United States of America|August 19, 1997
P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphataseM P Myers, J P Stolarov, C Eng, et al.The Journal of Biological Chemistry|August 10, 1977
Reversible activation of hepatic adenylate cyclase by guanyl-5'-yl-(alpha,beta-methylene)diphosphonate and guanyl-5'-yl imidodiphosphateC Londos, M C Lin, A F Welton, et al.Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry|August 11, 2006
Characterization of O2-CeO2 interactions using in situ Raman spectroscopy and first-principle calculationsY M Choi, Harry Abernathy, Hsin-Tsung Chen, et al.Nature Chemistry|November 24, 2011
Roaming-mediated isomerization in the photodissociation of nitrobenzeneMichael L Hause, Nuradhika Herath, Rongshun Zhu, et al.The Journal of Biological Chemistry|March 25, 1985
Glucagon-stimulated phosphorylation of rat liver glycogen synthase in isolated hepatocytesA Akatsuka, T J Singh, H Nakabayashi, et al.The Journal of Membrane Biology|November 1, 1988
Identification and comparison of bile acid-binding polypeptides in ileal basolateral membraneM C Lin, S L Weinberg, W Kramer, et al.Genes, Chromosomes & Cancer|August 10, 1999
Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 and VBP1) mutation and loss in renal-cell carcinoma developmentS C Clifford, S Walsh, K Hewson, et al.Oncogene|February 18, 1999
Over-representation of a germline RET sequence variant in patients with sporadic medullary thyroid carcinoma and somatic RET codon 918 mutationO Gimm, D S Neuberg, D J Marsh, et al.American Journal of Hematology|January 24, 2015
Genome-wide association study follow-up identifies cyclin A2 as a regulator of the transition through cytokinesis during terminal erythropoiesisLeif S Ludwig, Hyunjii Cho, Aoi Wakabayashi, et al.Human Molecular Genetics|August 1, 1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung diseaseT Attié, A Pelet, P Edery, et al.Pageof 71