HRAS and the Costello syndrome von Rauen, KA

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Dermatological findings in 61 mutation-positive individuals with cardiofaciocutaneous syndrome von Siegel, D.H., McKenzie, J., Frieden, I.J., Rauen, K.A.

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Dermatological phenotype in Costello syndrome: consequences of Ras dysregulation in development von Siegel, D.H., Mann, J.A., Krol, A.L., Rauen, K.A.

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The association between juvenile xanthogranulomas in neurofibromatosis type 1 patients and the development of leukaemia: A systematic review von Meyer, S. N., Vaughn, A., Li, Y., Studer, A. C., Rauen, K. A., Kiuru, M.

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Comparison of hair manifestations in cardio‐facio‐cutaneous and Costello syndromes highlights the influence of the RAS pathway on hair growth von Urban, J., Qi, L., Zhao, H., Rybak, I., Rauen, K.A., Kiuru, M.

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Craniofacial and dental development in cardio-facio-cutaneous syndrome: the importance of Ras signaling homeostasis von Goodwin, AF, Oberoi, S, Landan, M, Charles, C, Groth, J, Martinez, A, Fairley, C, Weiss, LA, Tidyman, WE, Klein, OD, Rauen, KA

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Disruption of 3D Tissue Integrity Facilitates Adenovirus Infection by Deregulating the Coxsackievirus and Adenovirus Receptor von Anders, M., Hansen, R., R. -X. Ding, Rauen, K. A., Bissell, M. J., Korn, W. Michael

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Germline mutation in BRAF codon 600 is compatible with human development: de novo p.V600G mutation identified in a patient with CFC syndrome von Champion, KJ, Bunag, C, Estep, AL, Jones, JR, Bolt, CH, Rogers, RC, Rauen, KA, Everman, DB

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Patient-derived iPSCs show premature neural differentiation and neuron type-specific phenotypes relevant to neurodevelopment von Yeh, E, Dao, D Q, Wu, Z Y, Kandalam, S M, Camacho, F M, Tom, C, Zhang, W, Krencik, R, Rauen, K A, Ullian, E M, Weiss, L A

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Periventricular heterotopia associated with chromosome 5p anomalies von SHEEN, V. L, WHELESS, J. W, SHERR, E. H, BODELL, A, BRAVERMAN, E, COTTER, P. D, RAUEN, K. A, GLENN, O, WEISIGER, K, PACKMAN, S, WALSH, C. A

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Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH von Klein, OD, Cotter, PD, Moore, MW, Zanko, A, Gilats, M, Epstein, CJ, Conte, F, Rauen, KA

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Deletion of MAP2K2/MEK2: a novel mechanism for a RASopathy? von Nowaczyk, M.J.M., Thompson, B.A., Zeesman, S., Moog, U., Sanchez-Lara, P.A., Magoulas, P.L., Falk, R.E., Hoover-Fong, J.E., Batista, D.A.S., Amudhavalli, S.M., White, S.M., Graham, G.E., Rauen, K.A.

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Expression of the coxsackievirus- and adenovirus receptor in gastrointestinal cancer correlates with tumor differentiation von Korn, W M, Macal, M, Christian, C, Lacher, M D, McMillan, A, Rauen, K A, Warren, R S, Ferrell, L

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Sex and gender differences in Alzheimer's disease: current challenges and implications for clinical practice: Position paper of the Dementia and Cognitive Disorders Panel of the Eu... von Ferretti, M T, Martinkova, J, Biskup, E, Benke, T, Gialdini, G, Nedelska, Z, Rauen, K, Mantua, V, Religa, D, Hort, J, Santuccione Chadha, A, Schmidt, R

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Congenital diaphragmatic hernia in Smith–Magenis syndrome: A possible locus at chromosome 17p11.2 von Sanford, E.F., Bermudez‐Wagner, K., Jeng, L.J.B., Rauen, K.A., Slavotinek, Anne M.

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400 Mutational landscape of melanocytic tumors from RASopathy patients von Young, L.J., Meyer, S., Tavernetti, J., Simmons, E., Rauen, K., McPherson, J., Kiuru, M.

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1186 Melanoma in neurofibromatosis type 1: A systematic review von Meyer, S.N., Simmons, E., Studer, A., Rauen, K., Kiuru, M.

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Kinase-activating and kinase-impaired cardio-facio-cutaneous syndrome alleles have activity during zebrafish development and are sensitive to small molecule inhibitors von Anastasaki, Corina, Estep, Anne L., Marais, Richard, Rauen, Katherine A., Patton, E. Elizabeth

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346 Hair alterations in the setting of germline RAS pathway mutations von Urban, J., Kiuru, M., Rauen, K.

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416 Regulation of the number of melanocytic nevi by the RAS pathway in cardio-facio-cutaneous and Costello syndromes von Kiuru, M., Urban, J., Rybak, I., Terrell, J., Rauen, K.

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