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(2010). Rat genomics methods and protocols (Vol. 1). New York, N.Y.: Humana Press.
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(2015). Mechanobiology of the Endothelium. CRC Press.
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Aalto, K., Autio, A., Kiss, E. A., Elima, K., Nymalm, Y., Veres, T. Z., et al. (2011). Siglec-9 is a novel leukocyte ligand for vascular adhesion protein-1 and can be used in PET imaging of inflammation and cancer. Blood, 118(13), 3725–3733.
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Aartsma-Rus, A. (2012). Exon Skipping. Humana PressInc.
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Abarrategui-Garrido, C., Martínez-Barricarte, R., López-Trascasa, M., de Córdoba, S. R., & Sánchez-Corral, P. (2009). Characterization of complement factor H-related (CFHR) proteins in plasma reveals novel genetic variations of CFHR1 associated with atypical hemolytic uremic syndrome. Blood, 114(19), 4261–4271.
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Abarrategui-Garrido, C., Melgosa, M., Peña-Carrión, A., de Jorge, E. G., de Cordoba, S. R., López Trascasa, M., et al. (2008). Mutations in Proteins of the Alternative Pathway of Complement and the Pathogenesis of Atypical Hemolytic Uremic Syndrome. Ajkd, 52(1), 171–180.
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Abascal, F., Juan, D., Jungreis, I., Martinez, L., Rigau, M., Rodriguez, J. M., et al. (2018). Loose ends: almost one in five human genes still have unresolved coding status. Nucleic Acids Res., .
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Abbasi, F., Azizi, F., Javaheri, M., Mosallanejad, A., Ebrahim-Habibi, A., & Ghafouri-Fard, S. (2015). Segregation of a novel homozygous 6 nucleotide deletion in GLUT2 gene in a Fanconi-Bickel syndrome family. Gene, 557(1), 103–105.
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Abbassi, V., Lowe, C. U., & Calcagno, P. L. (1968). Oculo-cerebro-renal syndrome. A review. Am J Dis Child, 115(2), 145–168.
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