The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking von Sewduth, Raj Nayan, Pandolfi, Silvia, Steklov, Mikhail, Sheryazdanova, Aidana, Zhao, Peihua, Criem, Nathan, Baietti, Maria F., Lechat, Benoit, Quarck, Rozeen, Impens, Francis, Sablina, Anna A.

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Fzd7 (Frizzled-7) Expressed by Endothelial Cells Controls Blood Vessel Formation Through Wnt/β-Catenin Canonical Signaling von Peghaire, C., Bats, M. L., Sewduth, R. N., Jeanningros, S., Jaspard, B., Couffinhal, T., Duplaa, C., Dufourcq, P.

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PDZRN3 destabilizes endothelial cell-cell junctions through a PKCζ-containing polarity complex to increase vascular permeability: Sci signal von Sewduth, R. N., Kovacic, H., Jaspard-Vinassa, B., Jecko, V., Wavasseur, T., Fritsch, N., Pernot, M., Jeanningros, S., Roux, E., Dufourcq, P., Couffinhal, T., Duplaa, C.

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Endothelial PDZRN3, controls vascular permeability through Wnt/PCP signaling and the PKC zeta dependent polarity complex von Sewduth, R., Kovacic, H., Jaspard-Vinassa, B., Wavasseur, T., Pernot, M., Gueniot, F., Couffinhal, T., Duplàa, C.

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Heterozygous deletion of a 2-Mb region including the dystroglycan gene in a patient with mild myopathy, facial hypotonia, oral-motor dyspraxia and white matter abnormalities von FROST, Amy R, BÖHM, Sabrina V, SEWDUTH, Raj N, JOSIFOVA, Dragana, OGILVIE, Caroline Mackie, IZATT, Louise, ROBERTS, Roland G

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Heterozygous deletion of a 2-megabase region including the dystroglycan gene in a patient with mild myopathy, facial hypotonia, oral-motor dyspraxia and white matter abnormalities von Roberts, Roland G, Frost, Amy R, Boehm, Sabrina V, Sewduth, Raj N, Josifova, Dragana, Ogilvie, Caroline Mackie, Izatt, Louise

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