Liver and intestinal fatty acid binding proteins in control and TGF beta 1 gene targeted deficient mice von Fontaine, R.N, Gossett, R.E, Schroeder, F, O'Toole, B.A, Doetschman, T, Kier, A.B

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Vitamin A Deficiency and Reproduction in Rhesus Monkeys1 von O'Toole, B.A., Fradkin, R., Warkany, J., Wilson, J.G., Mann, G.V.

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Vitamin A deficiency and reproduction in rhesus monkeys von O'Toole, B A, Fradkin, R, Warkany, J, Wilson, J G, Mann, G V

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Viral replication site distribution for rabbit hemorrhagic disease virus 2 in formalin-fixed, paraffin-embedded tissues via in situ hybridization von O’Toole, Alicia D., Zhang, Jian, Williams, Laura B. A., Brown, Corrie C.

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Detection of rabbit hemorrhagic disease virus 2 in formalin-fixed, paraffin-embedded tissues via in situ hybridization von O’Toole, Alicia D., Zhang, Jian, Williams, Laura B. A., Brown, Corrie C.

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CNS myelin induces regulatory functions of DC-SIGN-expressing, antigen-presenting cells via cognate interaction with MOG von García-Vallejo, J J, Ilarregui, J M, Kalay, H, Chamorro, S, Koning, N, Unger, W W, Ambrosini, M, Montserrat, V, Fernandes, R J, Bruijns, S C M, van Weering, J R T, Paauw, N J, O'Toole, T, van Horssen, J, van der Valk, P, Nazmi, K, Bolscher, J G M, Bajramovic, J, Dijkstra, C D, 't Hart, B A, van Kooyk, Y

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Iron and CF-related anemia: Expanding clinical and biochemical relationships von Gifford, A.H., Miller, S.D., Jackson, B.P., Hampton, T.H., O'Toole, G.A., Stanton, B.A., Parker, H.W.

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Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis von Thomas, A.C., Sinclair, C., Mahmud, N., Cullup, T., Mellerio, J.E., Harper, J., Dale, B.A., Turc-Carel, C., Hohl, D., McGrath, J.A., Vahlquist, A., Hellstrom-Pigg, M., Ganemo, A., Metcalfe, K., Mein, C.A., O'Toole, E.A, Kelsell, D.P.

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Factors identifying high-frequency and low-frequency health service utilization among substance-using adults von O'Toole, Thomas P., M.D, Pollini, Robin, Ph.D., M.P.H, Gray, Paulette, B.S, Jones, Theodore, B.A, Bigelow, George, Ph.D, Ford, Daniel E., M.D., M.P.H

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Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis: Novel and recurring ABCA12 mutations associated with HI von Thomas, A.C., Sinclair, C., Mahmud, N., Cullup, T., Mellerio, J.E., Harper, J., Dale, B.A., Turc-Carel, C., Hohl, D., McGrath, J.A., Vahlquist, A., Hellstrom-Pigg, M., Ganemo, A., Metcalfe, K., Mein, C.A., O’Toole, E.A, Kelsell, D.P.

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