A pharmacological comparison of [ 3H]GBR12935 binding to rodent striatal and kidney homogenates: Binding to dopamine transporters? von Sharif, N.A., Nunes, J.L., Kalfayan, V., McClelland, D.L., Rosenkranz, R.P., Eglen, R.M., Whiting, R.L.

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A pharmacological comparison of ( super(3)H)GBR12935 binding to rodent striatal and kidney homogenates: Binding to dopamine transporters? von Sharif, NA, Nunes, J L, Kalfayan, V, McClelland, D L, Rosenkranz, R P, Eglen, R M, Whiting, R L

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NGS and Sanger screening for BRCA1/BRCA2, CHEK2 and TP53 in Argentinian high-risk breast/ovarian cancer families and bioinformatic studies: Initial results von Bruno, L., Jablonski, P., Ozkul, M., Mercado, G., Sendoya, J., Llera, A., Núñez, L., Valdez, R., Mansilla, D., Cólica, V., Kalfayan, P., Ruggiero, C., Reyes, M., Cerretini, R.

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Amplification of the X‐linked Drosophila chorion gene cluster requires a region upstream from the s38 chorion gene von Spradling, A.C., Cicco, D.V., Wakimoto, B.T., Levine, J.F., Kalfayan, L.J., Cooley, L.

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No difference in penetrance between truncating and missense/aberrant splicing pathogenic variants in MLH1 and MSH2: a prospective Lynch syndrome database study von Dominguez-Valentin, M., Plazzer, J.P., Sampson, J.R., Engel, C., Aretz, S., Jenkins, M.A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Macrae, F., Winship, I.M., Thomas, H., Evans, D.G., Burn, J., Greenblatt, M., Cappel, W.H.D.T.N., Sijmons, R.H., Nielsen, M., Bertario, L., Bonanni, B., Tibiletti, M.G., Cavestro, G.M., Lindblom, A., Valle, A. della, Lopez-Kostner, F., Alvarez, K., Gluck, N., Katz, L., Heinimann, K., Vaccaro, C.A., Nakken, S., Hovig, E., Green, K., Lalloo, F., Hill, J., Vasen, H.F.A., Perne, C., Buttner, R., Gorgens, H., Holinski-Feder, E., Morak, M., Holzapfel, S., Huneburg, R., Doeberitz, M.V., Loeffler, M., Rahner, N., Weitz, J., Steinke-Lange, V., Schmiegel, W., Vangala, D., Crosbie, E.J., Pineda, M., Navarro, M., Brunet, J., Moreira, L., Sanchez, A., Serra-Burriel, M., Mints, M., Kariv, R., Rosner, G., Pinero, T.A., Pavicic, W.H., Kalfayan, P., Broeke, S.W. ten, Mecklin, J.P., Pylvanainen, K., Renkonen-Sinisalo, L., Lepisto, A., Peltomaki, P., Hopper, J.L., Win, A.K., Buchanan, D.D., Lindor, N.M., Gallinger, S., Marchand, L. le, Newcomb, P.A., Figueiredo, J.C., Thibodeau, S.N., Therkildsen, C., Hansen, T.V.O., Lindberg, L., Rodland, E.A., Neffa, F., Esperon, P., Tjandra, D., Moslein, G., Seppala, T.T., Moller, P.

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Risk-reducing gynecological surgery in Lynch syndrome: results of an international survey from the prospective Lynch syndrome database von Dominguez-Valentin, M., Seppala, T.T., Engel, C., Aretz, S., Macrae, F., Winship, I., Capella, G., Thomas, H., Hovig, E., Nielsen, M., Sijmons, R.H., Bertario, L., Bonanni, B., Tibiletti, M.G., Cavestro, G.M., Mints, M., Gluck, N., Katz, L., Heinimann, K., Vaccaro, C.A., Green, K., Lalloo, F., Hill, J., Schmiegel, W., Vangala, D., Perne, C., Strauss, H.G., Tecklenburg, J., Holinski-Feder, E., Steinke-Lange, V., Mecklin, J.P., Plazzer, J.P., Pineda, M., Navarro, M., Vidal, J.B., Kariv, R., Rosner, G., Pinero, T.A., Gonzalez, M.L., Kalfayan, P., Sampson, J.R., Ryan, N.A.J., Evans, D.G., Moller, P., Crosbie, E.J.

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Risk-reducing gynecological surgery in Lynch syndrome: results of an international survey from the prospective Lynch syndrome database von Dominguez-Valentin, M., Seppälä, T.T., Engel, C., Aretz, S., Macrae, F., Winship, I., Capella, G., Thomas, H., Hovig, E., Nielsen, M., Sijmons, R.H., Bertario, L., Bonanni, B., Tibiletti, M.G., Cavestro, G.M., Mints, M., Gluck, N., Katz, L., Heinimann, K., Vaccaro, C.A., Green, K., Lalloo, F., Hill, J., Schmiegel, W., Vangala, D., Perne, C., Strauss, H.G., Tecklenburg, J., Holinski-Feder, E., Steinke-Lange, V., Mecklin, J.P., Plazzer, J.P., Pineda, M., Navarro, M., Vidal, J.B., Kariv, R., Rosner, G., Piñero, T.A., Gonzalez, M.L., Kalfayan, P., Sampson, J.R., Ryan, N.A.J., Evans, D.G., Moller, P., Crosbie, E.J.

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Uptake of hysterectomy and bilateral salpingooophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report von Seppala, T.T., Dominguez-Valentin, M., Crosbie, E.J., Engel, C., Aretz, S., Macrae, F., Winship, I., Capella, G., Thomas, H., Hovig, E., Nielsen, M., Sijmons, R.H., Bertario, L., Bonanni, B., Tibiletti, M.G., Cavestro, G.M., Mints, M., Gluck, N., Katz, L., Heinimann, K., Vaccaro, C.A., Green, K., Lalloo, F., Hill, J., Schmiegel, W., Vangala, D., Perne, C., Strauss, H.G., Tecklenburg, J., Holinski-Feder, E., Steinke-Lange, V., Mecklin, J.P., Plazzer, J.P., Pineda, M., Navarro, M., Vida, J.B., Kariv, R., Rosner, G., Pinero, T.A., Pavicic, W., Kalfayan, P., Broeke, S.W. ten, Jenkins, M.A., Sunde, L., Bernstein, I., Burn, J., Greenblatt, M., Cappel, W.H.D.T.N., Valle, A. della, Lopez-Koestner, F., Alvarez, K., Buttner, R., Gorgens, H., Morak, M., Holzapfel, S., Huneburg, R., Doeberitz, M.V., Loeffler, M., Redler, S., Weitz, J., Pylvanainen, K., Renkonen-Sinisalo, L., Lepisto, A., Hopper, J.L., Win, A.K., Lindor, N.M., Gallinger, S., Marchand, L.L., Newcomb, P.A., Figueiredo, J.C., Thibodeau, S.N., Therkildsen, C., Wadt, K.A.W., Mourits, M.J.E., Ketabi, Z., Denton, O.G., Rodland, E.A., Vasen, H., Neffa, F., Esperon, P., Tjandra, D., Moslein, G., Rokkones, E., Sampson, J.R., Evans, D.G., Moller, P.

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Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report von Dominguez-Valentin, M., Crosbie, E.J., Engel, C., Aretz, S., Macrae, F., Winship, I., Capella, G., Thomas, H., Nakken, S., Hovig, E., Nielsen, M., Sijmons, R.H., Bertario, L., Bonanni, B., Tibiletti, M.G., Cavestro, G.M., Mints, M., Gluck, N., Katz, L., Heinimann, K., Vaccaro, C.A., Green, K., Lalloo, F., Hill, J., Schmiegel, W., Vangala, D., Perne, C., Strauss, H.G., Tecklenburg, J., Holinski-Feder, E., Steinke-Lange, V., Mecklin, J.P., Plazzer, J.P., Pineda, M., Navarro, M., Vidal, J.B., Kariv, R., Rosner, G., Pinero, T.A., Gonzalez, M.L., Kalfayan, P., Ryan, N., Broeke, S.W. ten, Jenkins, M.A., Sunde, L., Bernstein, I., Burn, J., Greenblatt, M., Cappel, W.H.D.T.N., Valle, A. della, Lopez-Koestner, F., Alvarez, K., Buttner, R., Gorgens, H., Morak, M., Holzapfel, S., Huneburg, R., Doeberitz, M.V., Loeffler, M., Rahner, N., Weitz, J., Pylvanainen, K., Renkonen-Sinisalo, L., Lepisto, A., Auranen, A., Hopper, J.L., Win, A.K., Haile, R.W., Lindor, N.M., Gallinger, S., Marchand, L. le, Newcomb, P.A., Figueiredo, J.C., Thibodeau, S.N., Therkildsen, C., Okkels, H., Ketabi, Z., Denton, O.G., Rodland, E.A., Vasen, H., Neffa, F., Esperon, P., Tjandra, D., Moslein, G., Sampson, J.R., Evans, D.G., Seppala, T.T., Moller, P.

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Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database von Dominguez-Valentin, M., Sampson, J.R., Seppala, T.T., Broeke, S.W. ten, Plazzer, J.P., Nakken, S., Engel, C., Aretz, S., Jenkins, M.A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Thomas, H., Evans, D.G., Burn, J., Greenblatt, M., Hovig, E., Cappel, W.H.D.T.N.C., Sijmons, R.H., Bertario, L., Tibiletti, M.G., Cavestro, G.M., Lindblom, A., Valle, A. della, Lopez-Kostner, F., Gluck, N., Katz, L.H., Heinimann, K., Vaccaro, C.A., Buttner, R., Gorgens, H., Holinski-Feder, E., Morak, M., Holzapfel, S., Huneburg, R., Doeberitz, M.V., Loeffler, M., Rahner, N., Schackert, H.K., Steinke-Lange, V., Schmiegel, W., Vangala, D., Pylvanainen, K., Renkonen-Sinisalo, L., Hopper, J.L., Win, A.K., Haile, R.W., Lindor, N.M., Gallinger, S., Marchand, L. le, Newcomb, P.A., Figueiredo, J.C., Thibodeau, S.N., Wadt, K., Therkildsen, C., Okkels, H., Ketabi, Z., Moreira, L., Sanchez, A., Serra-Burriel, M., Pineda, M., Navarro, M., Blanco, I., Green, K., Lalloo, F., Crosbie, E.J., Hill, J., Denton, O.G., Frayling, I.M., Rodland, E.A., Vasen, H., Mints, M., Neffa, F., Esperon, P., Alvarez, K., Kariv, R., Rosner, G., Pinero, T.A., Gonzalez, M.L., Kalfayan, P., Tjandra, D., Winship, I.M., Macrae, F., Moslein, G., Mecklin, J.P., Nielsen, M., Moller, P.

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From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America von Alberto Vaccaro, C, Lopez-Kostner, F, Adriana, DV, Palmero, EI, Rossi, BM, Antelo, M, Solano, A, Carraro, DM, Forones, NM, Bohorquez, M, Lino-Silva, LS, Buleje, J, Spirandelli, F, Abe-Sandes, K, Nascimento, I, Sullcahuaman, Y, Sarroca, C, Laura Gonzalez, M, Ignacio Herrando, A, Alvarez, K, Neffa, F, Galvao, HC, Esperon, P, Golubicki, M, Cisterna, D, Cardoso, FC, Torrezan, GT, Aguiar Junior, S, Marques Pimenta, CA, da Cruz Formiga, MN, Santos, E, Sa, CU, Oliveira, EP, Fujita, R, Spirandelli, E, Jimenez, G, Cruz Guindalini, RS, Meira Velame de Azevedo, RG, Mario Bueno, LS, dos Santos Nogueira, ST, Torres Loarte, M, Padron, J, del Carmen Castro-Mujica, M, Sanchez del Monte, J, Caballero, C, Muneton Pena, CM, Pinto, J, Barletta-Carrillo, C, Angulo Melva, G, Pinero, T, Montenegro Beltran, P, Ashton-Prolla, P, Rodriguez, Y, Quispe, R, Teresa Rossi, N, Martin, C, Chialina, S, German Kalfayan, P, Carlos Bazo-Alvarez, J, Recalde Canete, A, Dominguez-Barrera, C, Nunez, L, Da Silva, SD, Balavarca, Y, Wernhoff, P, Plazzer, J-P, Moller, P, Hovig, E, Dominguez-Valentin, M

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Drosophila Chorion Gene Amplification: A Model System for the Study of Chromosome Replication von DeCicco, Diane V., Wakimoto, Barbara, Kalfayan, Laura, Levine, J., Spradling, A. C.

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Aspects of gene expression and its control - Drosophila chorion gene amplification: a model system for the study of chromosome replication von DeCicco, Diane V., Wakimoto, Barbara, Kalfayan, Laura, Levine, J., Spradling, A. C.

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