A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands von ESTIVILL, X, FARRALL, M, WATSON, E. K, WILLIAMSON, R, WAINWRIGHT, B. J, SCAMBLER, P. J, BELL, G. M, HAWLEY, K. M. F, LENCH, N. J, BATES, G. P, KRUYER, H. C, FREDERICK, P. A, STANIER, P

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Long-Term Dabigatran Treatment Delays Alzheimer’s Disease Pathogenesis in the TgCRND8 Mouse Model von Cortes-Canteli, Marta, Kruyer, Anna, Fernandez-Nueda, Irene, Marcos-Diaz, Ana, Ceron, Carlos, Richards, Allison T., Jno-Charles, Odella C., Rodriguez, Ignacio, Callejas, Sergio, Norris, Erin H., Sanchez-Gonzalez, Javier, Ruiz-Cabello, Jesus, Ibanez, Borja, Strickland, Sidney, Fuster, Valentin

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The GluK4 kainate receptor subunit regulates memory, mood, and excitotoxic neurodegeneration von Lowry, E.R, Kruyer, A, Norris, E.H, Cederroth, C.R, Strickland, S

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Hyperhomocysteinemia exacerbates Alzheimer's disease pathology by way of the β‐amyloid fibrinogen interaction von Chung, Y. C., Kruyer, A., Yao, Y., Feierman, E., Richards, A., Strickland, S., Norris, E. H.

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Hyperhomocysteinemia exacerbates Alzheimer's disease pathology by way of the [beta]-amyloid fibrinogen interaction von Chung, Y C, Kruyer, A, Yao, Y, Feierman, E, Richards, A, Strickland, S, Norris, E H

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Recurrent mutations in the NF1 gene are common among neurofibromatosis type 1 patients von Ars, E, Kruyer, H, Morell, M, Pros, E, Serra, E, Ravella, A, Estivill, X, Lázaro, C

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Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1 von ARS, E, SERRA, E, GARCIA, J, KRUYER, H, GAONA, A, LAZARO, C, ESTIVILL, X

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Confirmation of a double-hit model for the NF1 gene in benign neurofibromas von SERRA, E, PUIG, S, OTERO, D, GAONA, A, KRUYER, H, ARS, E, ESTIVILL, X, LAZARO, C

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Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patients von LAZARO, C, GAONA, A, AINSWORTH, P, TENCONI, R, VIDAUD, D, KRUYER, H, ARS, F, VOLPINI, V, ESTIVILL, X

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First prenatal diagnosis for Wolfram syndrome by molecular analysis of the WFS1 gene von Domènech, Enric, Kruyer, Helena, Gómez, Carolina, Calvo, Maria Teresa, Nunes, Virginia

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A Clinical Variant of Neurofibromatosis Type 1: Familial Spinal Neurofibromatosis with a Frameshift Mutation in the NF1 Gene von Ars, Elisabet, Kruyer, Helena, Gaona, Antonia, Casquero, Pilar, Rosell, Jordi, Volpini, Víctor, Serra, Eduard, Lázaro, Conxi, Estivill, Xavier

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Prenatal diagnosis of sporadic neurofibromatosis type 1 (NF1) by RNA and DNA analysis of a splicing mutation von Ars, Elisabet, Kruyer, Helena, Gaona, Antonia, Serra, Eduard, Lázaro, Conxi, Estivill, Xavier

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Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene von Tata, Frederick, Stanier, Philip, Wicking, Carol, Halford, Stephanie, Kruyer, Helena, Lench, Nicholas J., Scambler, Peter J., Hansen, Connie, Braman, Jeffrey C., Williamson, Robert, Wainwright, Brandon J.

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Molecular characterization of the breakpoints of a 12-kb deletion in the NF1 gene in a family showing germ-line mosaicism von LAZARO, C, GAONA, A, LYNCH, M, KRUYER, H, RAVELLA, A, ESTIVILL, X

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Two further cases of mutation R1947X in the NF1 gene : screening for a relatively common recurrent mutation von LAZARO, C, KRUYER, H, GAONA, A, ESTIVILL, X

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Response to exercise early after uncomplicated acute myocardial infarction in patients receiving no medication: Long-term follow-up von Koppes, Gerald M., Kruyer, William, Beckmann, Charles H., Jones, Frederic G.

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A new polymorphic locus, D7S411, isolated by cloning from preparative pulse-field gels is close to the mutation causing cystic fibrosis von Ramsay, M., Wainwright, B.J., Farrall, M., Estivill, X., Sutherland, H., Ho, M.-F., Davies, R., Halford, S., Tata, F., Wicking, C., Lench, N., Bauer, I., Ferec, C., Farndon, P., Kruyer, H., Stanier, P., Williamson, R., Scambler, P.J.

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Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met pJ3.11 von FARRALL, M, WATSON, E, LISSENS, W, SIMON, P, SCAMBLER, P, STANIER, P, VASSART, G, WORRALL, C, WILLIAMSON, R, WAINWRIGHT, B. J, BATES, G, BELL, G, BELL, J, DAVIES, K. A, ESTIVILL, X, KRUYER, H, LAW, H.-Y, LENCH, N

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Unusual response to intravenous verapamil in a patient with atrial fibrillation von Oliveros, R A, Kruyer, W B, Chilton, R J, Beckmann, C H, Boran, K J

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