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Abe, T., & Fujimori, T. (2013). Reporter mouse lines for fluorescence imaging. Dev. Growth Differ., 55(4), 390–405.
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Abe, T., Lu, X., Jiang, Y., Boccone, C. E., Qian, S., Vattem, K. M., et al. (2003). Site-directed mutagenesis of the active site of diacylglycerol kinase alpha: calcium and phosphatidylserine stimulate enzyme activity via distinct mechanisms. Biochem J, 375(Pt 3), 673–680.
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Abe-Dohmae, S. (2006). Serum amyloid A generates high density lipoprotein with cellular lipid in an ABCA1- or ABCA7-dependent manner. J Lip Res, 47(7), 1542–1550.
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Abe-Dohmae, S., Ikeda, Y., Matsuo, M., Hayashi, M., Okuhira, K., Ueda, K., et al. (2004). Human ABCA7 supports apolipoprotein-mediated release of cellular cholesterol and phospholipid to generate high density lipoprotein. J Biol Chem, 279(1), 604–611.
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Abecasis, G. (2010). Abecasis Lab GLF Tools.
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Abecasis, G. R., Cherny, S. S., Cookson, W. O., & Cardon, L. R. (2002). Merlin--rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet, 30(1), 97–101.
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Abelson, J. F., Kwan, K. Y., O’Roak, B. J., Baek, D. Y., Stillman, A. A., Morgan, T. M., et al. (2005). Sequence variants in SLITRK1 are associated with Tourette’s syndrome. Science, 310(5746), 317–320.
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Abeysinghe, S. S., Chuzhanova, N., & Cooper, D. N. (2006). Gross deletions and translocations in human genetic disease. Genome Dyn, 1, 17–34.
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Abeysinghe, S. S., Chuzhanova, N., Krawczak, M., Ball, E. V., & Cooper, D. N. (2003). Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs. Hum Mutat, 22(3), 229–244.
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Abeysinghe, S. S., Stenson, P. D., Krawczak, M., & Cooper, D. N. (2004). Gross Rearrangement Breakpoint Database (GRaBD). Hum Mutat, 23(3), 219–221.
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