Enlisting rangers and scouts for reconnaissance and surveillance von Rybski, P.E., Papanikolopoulos, N.P., Stoeter, S.A., Krantz, D.G., Yesin, K.B., Gini, M., Voyles, R., Hougen, D.F., Nelson, B., Erickson, M.D.

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Sharing control [multiple miniature robots] von Rybski, P.E., Stoeter, S.A., Papanikolopoulos, N.P., Burt, I., Dahlin, T., Gini, M., Hougen, D.F., Krantz, D.G., Nageotte, F.

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System architecture for versatile autonomous and teleoperated control of multiple miniature robots von Rybski, P.E., Burt, I., Dahlin, T., Gini, M., Hougen, D.F., Krantz, D.G., Nageotte, F., Papanikolopoulos, N., Stoeter, S.A.

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Sharing control - multiple miniature robots von Rybski, P E, Stoeter, S A, Papanikolopoulos, N P, Burt, I, Dahlin, T, Gini, M, Hougen, D F, Krantz, D G, Nageotte, F

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Feedforward control (based on model inversion) and system performance prediction using high-fidelity nonlinear dynamic hydraulic system modeling von Hessburg, T.M., Krantz, D.G.

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3D integrated superconducting qubits von Rosenberg, D., Kim, D., Das, R., Yost, D., Gustavsson, S., Hover, D., Krantz, P., Melville, A., Racz, L., Samach, G. O., Weber, S. J., Yan, F., Yoder, J. L., Kerman, A. J., Oliver, W. D.

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Transcriptional dysregulation in NIPBL and cohesin mutant human cells von Liu, Jinglan, Zhang, Zhe, Bando, Masashige, Itoh, Takehiko, Deardorff, Matthew A, Clark, Dinah, Kaur, Maninder, Tandy, Stephany, Kondoh, Tatsuro, Rappaport, Eric, Spinner, Nancy B, Vega, Hugo, Jackson, Laird G, Shirahige, Katsuhiko, Krantz, Ian D

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Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis von Conlin, Laura K., Thiel, Brian D., Bonnemann, Carsten G., Medne, Livija, Ernst, Linda M., Zackai, Elaine H., Deardorff, Matthew A., Krantz, Ian D., Hakonarson, Hakon, Spinner, Nancy B.

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Demonstration of Density Matrix Exponentiation Using a Superconducting Quantum Processor von Kjaergaard, M., Schwartz, M. E., Greene, A., Samach, G. O., Bengtsson, A., O’Keeffe, M., McNally, C. M., Braumüller, J., Kim, D. K., Krantz, P., Marvian, M., Melville, A., Niedzielski, B. M., Sung, Y., Winik, R., Yoder, J., Rosenberg, D., Obenland, K., Lloyd, S., Orlando, T. P., Marvian, I., Gustavsson, S., Oliver, W. D.

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RAD21 Mutations Cause a Human Cohesinopathy von Deardorff, Matthew A., Wilde, Jonathan J., Albrecht, Melanie, Dickinson, Emma, Tennstedt, Stephanie, Braunholz, Diana, Mönnich, Maren, Yan, Yuqian, Xu, Weizhen, Gil-Rodríguez, María Concepcion, Clark, Dinah, Hakonarson, Hakon, Halbach, Sara, Michelis, Laura Daniela, Rampuria, Abhinav, Rossier, Eva, Spranger, Stephanie, Van Maldergem, Lionel, Lynch, Sally Ann, Gillessen-Kaesbach, Gabriele, Lüdecke, Hermann-Josef, Ramsay, Robert G., McKay, Michael J., Krantz, Ian D., Xu, Huiling, Horsfield, Julia A., Kaiser, Frank J.

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Neuronal genes deregulated in Cornelia de Lange Syndrome respond to removal and re-expression of cohesin von Weiss, Felix D., Calderon, Lesly, Wang, Yi-Fang, Georgieva, Radina, Guo, Ya, Cvetesic, Nevena, Kaur, Maninder, Dharmalingam, Gopuraja, Krantz, Ian D., Lenhard, Boris, Fisher, Amanda G., Merkenschlager, Matthias

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NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations von Gillis, Lynette A., McCallum, Jennifer, Kaur, Maninder, DeScipio, Cheryl, Yaeger, Dinah, Mariani, Allison, Kline, Antonie D., Li, Hui-hua, Devoto, Marcella, Jackson, Laird G., Krantz, Ian D.

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Electrochemical Measurements of Optogenetically Stimulated Quantal Amine Release from Single Nerve Cell Varicosities in Drosophila Larvae von Majdi, Soodabeh, Berglund, E. Carina, Dunevall, Johan, Oleinick, Alexander I., Amatore, Christian, Krantz, David E., Ewing, Andrew G.

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Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions von Aref-Eshghi, Erfan, Bend, Eric G., Colaiacovo, Samantha, Caudle, Michelle, Chakrabarti, Rana, Napier, Melanie, Brick, Lauren, Brady, Lauren, Carere, Deanna Alexis, Levy, Michael A., Kerkhof, Jennifer, Stuart, Alan, Saleh, Maha, Beaudet, Arthur L., Li, Chumei, Kozenko, Maryia, Karp, Natalya, Prasad, Chitra, Siu, Victoria Mok, Tarnopolsky, Mark A., Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Krantz, Ian D., Deardorff, Matthew A., Schwartz, Charles E., Sadikovic, Bekim

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p53 is required for brown adipogenic differentiation and has a protective role against diet-induced obesity von Molchadsky, A, Ezra, O, Amendola, P G, Krantz, D, Kogan-Sakin, I, Buganim, Y, Rivlin, N, Goldfinger, N, Folgiero, V, Falcioni, R, Sarig, R, Rotter, V

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Mutations in the human Jagged1 gene are responsible for Alagille syndrome von Oda, Takaya, Elkahloun, Abdel G, Pike, Brian L, Okajima, Kazuki, Krantz, Ian D, Genin, Anna, Piccoli, David A, Meltzer, Paul S, Spinner, Nancy B, Collins, Francis S, Chandrasekharappa, Settara C

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A phase III study evaluating the efficacy and safety of MBP8298 in secondary progressive MS von FREEDMAN, M. S, BAR-OR, A, FERENCZI, L, VERCO, T, OGER, J, TRABOULSEE, A, PATRY, D, YOUNG, C, OLSSON, T, LI, D, HARTUNG, H.-P, KRANTZ, M

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Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies von Miller, David T., Adam, Margaret P., Aradhya, Swaroop, Biesecker, Leslie G., Brothman, Arthur R., Carter, Nigel P., Church, Deanna M., Crolla, John A., Eichler, Evan E., Epstein, Charles J., Faucett, W. Andrew, Feuk, Lars, Friedman, Jan M., Hamosh, Ada, Jackson, Laird, Kaminsky, Erin B., Kok, Klaas, Krantz, Ian D., Kuhn, Robert M., Lee, Charles, Ostell, James M., Rosenberg, Carla, Scherer, Stephen W., Spinner, Nancy B., Stavropoulos, Dimitri J., Tepperberg, James H., Thorland, Erik C., Vermeesch, Joris R., Waggoner, Darrel J., Watson, Michael S., Martin, Christa Lese, Ledbetter, David H.

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Caveolin-1 controls mitochondrial damage and ROS production by regulating fission - fusion dynamics and mitophagy von Jiang, Ying, Krantz, Sarah, Qin, Xiang, Li, Shun, Gunasekara, Hirushi, Kim, Young-Mee, Zimnicka, Adriana, Bae, Misuk, Ma, Ke, Toth, Peter T., Hu, Ying, Shajahan-Haq, Ayesha N., Patel, Hemal H., Gentile, Saverio, Bonini, Marcelo G., Rehman, Jalees, Liu, Yiyao, Minshall, Richard D.

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Cornelia de Lange syndrome is caused by mutations in NIPBL , the human homolog of Drosophila melanogaster Nipped-B von Rappaport, Eric, Morris, Colleen A, Bamshad, Michael J, Calof, Anne L, Li, Hui-hua, Bottani, Armand, Gillis, Lynette A, Krantz, Ian D, Wasserman, Nora, DeScipio, Cheryl, Nowaczyk, Malgorzata J M, Lander, Arthur D, McCallum, Jennifer, Jukofsky, Lori, Devoto, Marcella, Kaur, Maninder, Kawauchi, Shimako, Yaeger, Dinah, Jackson, Laird G, Carey, John C, Toriello, Helga

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