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Abhinand, C. S., Raju, R., Soumya, S. J., Arya, P. S., & Sudhakaran, P. R. (2016). VEGF-A/VEGFR2 signaling network in endothelial cells relevant to angiogenesis. J Cell Commun Signal, 10(4), 347–354.
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Abouelhoda, M., Faquih, T., El-Kalioby, M., & Alkuraya, F. S. (2016). Revisiting the morbid genome of Mendelian disorders. Genome Biol, 17(1), 235.
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Adams, M. C., Evans, J. P., Henderson, G. E., & Berg, J. S. (2016). The promise and peril of genomic screening in the general population. Genet Med, 18(6), 593–599.
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Adams, S. R., Mackey, M. R., Ramachandra, R., Palida Lemieux, S. F., Steinbach, P., Bushong, E. A., et al. (2016). Multicolor Electron Microscopy for Simultaneous Visualization of Multiple Molecular Species. Cell Chem Biol, .
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Adrovic, A., Canpolat, N., Caliskan, S., Sever, L., Kıykım, E., Agbas, A., et al. (2016). Cobalamin C defect-hemolytic uremic syndrome caused by new mutation in MMACHC. Pediatr Int, 58(8), 763–765.
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Afroze, B., & Chen, M. (2016). Fanconi-Bickel Syndrome: Two Pakistani Patients Presenting with Hypophosphatemic Rickets. J Pediatr Genet, 5(3), 161–166.
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Agarwal, A., Dong, Z., Harris, R., Murray, P., Parikh, S. M., Rosner, M. H., et al. (2016). Cellular and Molecular Mechanisms of AKI. Journal of the American Society of Nephrology, 27(5), 1288–1299.
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Aguet, F., & Ardlie, K. G. (2016). Tissue Specificity of Gene Expression. Current Genetic Medicine Reports, .
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Aguet, F., Brown, A. A., Castel, S., Davis, J. R., & Mohammadi…, P. (2016). Local genetic effects on gene expression across 44 human tissues. BiorXiv, .
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Agus, Z. S. (2016). Mechanisms and causes of hypomagnesemia. Curr Opin Nephrol Hypertens, 25(4), 301–307.
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