GRACE: An Autonomous Robot for the AAAI Robot Challenge von Simmons, Reid, Goldberg, Dani, Goode, Adam, Montemerlo, Michael, Roy, Nicholas, Sellner, Brennan, Urmson, Chris, Schultz, Alan, Abramson, Myriam, Adams, William, Atrash, Amin, Bugajska, Magda, Coblenz, Michael, MacMahon, Matt, Perzanowski, Dennis, Horswill, Ian, Zubek, Robert, Kortenkamp, David, Wolfe, Bryn, Milam, Tod, Maxwell, Bruce

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Huxley: A flexible robot control architecture for autonomous underwater vehicles von Goldberg, D.

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Unmanned underwater vehicle von Key, Jr., William H, Smith, Jeffrey M, Godin, Samuel D, Goldberg, Dani, Baker, Leonard M

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Evaluating the Dynamics of Agent-Environment Interaction von Goldberg,Dani

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UNMANNED UNDERWATER VEHICLE von Godin Samuel D, Key, JR. William H, Baker Leonard M, Goldberg Dani, Smith Jeffrey M

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Robust Behavior-Based Control for Distributed Multi-Robot Collection Tasks von Goldberg,Dani, Mataric,Maja J

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Swarming Unmanned Underwater Vehicles von Goldberg, Dani, Seereeram, Sanjeev, Key, Bill

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GRACE and GEORGE: Autonomous Robots for the AAAI Robot Challenge von Simmons, Reid, Bruce, Allison, Goldberg, Dani, Goode, Adam, Schultz, Alan, Adams, William, Horswill, Ian, Kortenkamp, David, Wolfe, Bryn, Maxwell, Bruce

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GRACE: An Autonomous Robot for the AAAI Robot Challenge von Simmons, Reid, Goldberg, Dani, Goode, Adam, Montemerlo, Michael, Roy, Nicholas, Schultz, Alan C, Abramson, Myriam, Horswill, Ian, Kortenkamp, David, Maxwell, Bruce

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Comparing models of delivery for cancer genetics services among patients receiving primary care who meet criteria for genetic evaluation in two healthcare systems: BRIDGE randomize... von Kaphingst, Kimberly A, Kohlmann, Wendy, Chambers, Rachelle Lorenz, Goodman, Melody S, Bradshaw, Richard, Chan, Priscilla A, Chavez-Yenter, Daniel, Colonna, Sarah V, Espinel, Whitney F, Everett, Jessica N, Gammon, Amanda, Goldberg, Eric R, Gonzalez, Javier, Hagerty, Kelsi J, Hess, Rachel, Kehoe, Kelsey, Kessler, Cecilia, Kimball, Kadyn E, Loomis, Shane, Martinez, Tiffany R, Monahan, Rachel, Schiffman, Joshua D, Temares, Dani, Tobik, Katie, Wetter, David W, Mann, Devin M, Kawamoto, Kensaku, Del Fiol, Guilherme, Buys, Saundra S, Ginsburg, Ophira

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Solanum pennellii (LA5240) backcross inbred lines (BILs) for high resolution mapping in tomato von Torgeman, Shai, Pleban, Tzili, Goldberg, Yael, Ferrante, Paola, Aprea, Giuseppe, Giuliano, Giovanni, Yichie, Yoav, Fisher, Josef, Zemach, Itay, Koch, Amit, Rochsar, Edan, Oved, Matan, Bandel, Kfir, Zamir, Dani

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Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants von Kayumi, Sayaka, Pérez-Jurado, Luis A., Palomares, María, Rangu, Sneha, Sheppard, Sarah E., Chung, Wendy K., Kruer, Michael C., Kharbanda, Mira, Amor, David J., McGillivray, George, Cohen, Julie S., García-Miñaúr, Sixto, van Eyk, Clare L., Harper, Kelly, Jolly, Lachlan A., Webber, Dani L., Barnett, Christopher P., Santos-Simarro, Fernando, Pacio-Míguez, Marta, Pozo, Angela del, Bakhtiari, Somayeh, Deardorff, Matthew, Dubbs, Holly A., Izumi, Kosuke, Grand, Katheryn, Gray, Christopher, Mark, Paul R., Bhoj, Elizabeth J., Li, Dong, Ortiz-Gonzalez, Xilma R., Keena, Beth, Zackai, Elaine H., Goldberg, Ethan M., Perez de Nanclares, Guiomar, Pereda, Arrate, Llano-Rivas, Isabel, Arroyo, Ignacio, Fernández-Cuesta, María Ángeles, Thauvin-Robinet, Christel, Faivre, Laurence, Garde, Aurore, Mazel, Benoit, Bruel, Ange-Line, Tress, Michael L., Brilstra, Eva, Fine, Amena Smith, Crompton, Kylie E., Stegmann, Alexander P.A., Sinnema, Margje, Stevens, Servi C.J., Nicolai, Joost, Lesca, Gaetan, Lion-François, Laurence, Haye, Damien, Chatron, Nicolas, Piton, Amelie, Nizon, Mathilde, Cogne, Benjamin, Srivastava, Siddharth, Bassetti, Jennifer, Muss, Candace, Gripp, Karen W., Procopio, Rebecca A., Millan, Francisca, Morrow, Michelle M., Assaf, Melissa, Moreno-De-Luca, Andres, Joss, Shelagh, Hamilton, Mark J., Bertoli, Marta, Foulds, Nicola, McKee, Shane, MacLennan, Alastair H., Gecz, Jozef, Corbett, Mark A.

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Mice Deficient in the alpha 7 Neuronal Nicotinic Acetylcholine Receptor Lack alpha -Bungarotoxin Binding Sites and Hippocampal Fast Nicotinic Currents von Orr-Urtreger, Avi, Goldner, Finn M, Saeki, Mayuko, Lorenzo, Isabel, Goldberg, Leah, De Biasi, Mariella, Dani, John A, Patrick, James W, Beaudet, Arthur L

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Genomic and phenotypic characterization of 404 individuals with neurodevelopmental disorders caused by CTNNB1 variants von Kayumi, Sayaka, Pérez-Jurado, Luis A, Palomares, María, Rangu, Sneha, Sheppard, Sarah E, Chung, Wendy K, Kruer, Michael C, Kharbanda, Mira, Amor, David J, McGillivray, George, Cohen, Julie S, García-Miñaúr, Sixto, van Eyk, Clare L, Harper, Kelly, Jolly, Lachlan A, Webber, Dani L, Barnett, Christopher P, Santos-Simarro, Fernando, Pacio-Míguez, Marta, Pozo, Angela Del, Bakhtiari, Somayeh, Deardorff, Matthew, Dubbs, Holly A, Izumi, Kosuke, Grand, Katheryn, Gray, Christopher, Mark, Paul R, Bhoj, Elizabeth J, Li, Dong, Ortiz-Gonzalez, Xilma R, Keena, Beth, Zackai, Elaine H, Goldberg, Ethan M, Perez de Nanclares, Guiomar, Pereda, Arrate, Llano-Rivas, Isabel, Arroyo, Ignacio, Fernández-Cuesta, María Ángeles, Thauvin-Robinet, Christel, Faivre, Laurence, Garde, Aurore, Mazel, Benoit, Bruel, Ange-Line, Tress, Michael L, Brilstra, Eva, Fine, Amena Smith, Crompton, Kylie E, Stegmann, Alexander P A, Sinnema, Margje, Stevens, Servi C J, Nicolai, Joost, Lesca, Gaetan, Lion-François, Laurence, Haye, Damien, Chatron, Nicolas, Piton, Amelie, Nizon, Mathilde, Cogne, Benjamin, Srivastava, Siddharth, Bassetti, Jennifer, Muss, Candace, Gripp, Karen W, Procopio, Rebecca A, Millan, Francisca, Morrow, Michelle M, Assaf, Melissa, Moreno-De-Luca, Andres, Joss, Shelagh, Hamilton, Mark J, Bertoli, Marta, Foulds, Nicola, McKee, Shane, MacLennan, Alastair H, Gecz, Jozef, Corbett, Mark A

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Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity von Baris, Hagit N., Barnes-Kedar, Inbal, Toledano, Helen, Halpern, Marisa, Hershkovitz, Dov, Lossos, Alexander, Lerer, Israela, Peretz, Tamar, Kariv, Revital, Cohen, Shlomi, Half, Elizabeth E., Magal, Nurit, Drasinover, Valerie, Wimmer, Katharina, Goldberg, Yael, Bercovich, Dani, Levi, Zohar

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Longitudinal phase 2 clinical trials of live, attenuated tularemia vaccine in healthy research laboratory workers von Saunders, David L., Pierson, Benjamin C., Haller, Jeannine, Norris, Sarah, Cardile, Anthony P., Reisler, Ronald B., Okwesili, Arthur C., Boudreau, Ellen, Rusnak, Janice, Danner, Denise K., Purcell, Bret K., Barth, James F., Tompkins, Erin L., Downs, Isaac L., Liggett, Dani, Pettit, Patricia, Pratt, Tami, Goldberg, Mark, Kortepeter, Mark G., Guerena, Fernando B., Aldis, John W., Keshtkar-Jahromi, Maryam, Pittman, Phillip R.

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Constitutional Mismatch Repair Deficiency in Israel: High Proportion of Founder Mutations in MMR Genes and Consanguinity: CMMRD, Founder Mutations, and Consanguinity in Israel von Baris, Hagit N., Barnes-Kedar, Inbal, Toledano, Helen, Halpern, Marisa, Hershkovitz, Dov, Lossos, Alexander, Lerer, Israela, Peretz, Tamar, Kariv, Revital, Cohen, Shlomi, Half, Elizabeth E., Magal, Nurit, Drasinover, Valerie, Wimmer, Katharina, Goldberg, Yael, Bercovich, Dani, Levi, Zohar

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Two BRCA1/2 founder mutations in Jews of Sephardic origin von Sagi, Michal, Eilat, Avital, Ben Avi, Liat, Goldberg, Yael, Bercovich, Dani, Hamburger, Tamar, Peretz, Tamar, Lerer, Israela

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Independent Sets in Random Graphs from the Weighted Second Moment Method von Dani, Varsha, Moore, Cristopher

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Mutation spectrum in HNPCC in the Israeli population von Goldberg, Yael, Porat, Rinnat M., Kedar, Inbal, Shochat, Chen, Sagi, Michal, Eilat, Avital, Mendelson, Suzan, Hamburger, Tamar, Nissan, Aviram, Hubert, Ayala, Kadouri, Luna, Pikarski, Eli, Lerer, Israela, Abeliovich, Dvorah, Bercovich, Dani, Peretz, Tamar

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