Resultados da busca - Hakker, Inessa

Distinctive roles of different β-amyloid 42 aggregates in modulation of synaptic functions por Chiang, Hsueh-Cheng, Iijima, Koichi, Hakker, Inessa, Zhong, Yi

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Distinct Functional Domains of Neurofibromatosis Type 1 Regulate Immediate versus Long-Term Memory Formation por Ho, Ivan Shun, Hannan, Frances, Guo, Hui-Fu, Hakker, Inessa, Zhong, Yi

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Stereotyped Odor-Evoked Activity in the Mushroom Body of Drosophila Revealed by Green Fluorescent Protein-Based Ca(2+) Imaging por Wang, Yalin, Guo, Hui-Fu, Pologruto, Thomas A., Hannan, Frances, Hakker, Inessa, Svoboda, Karel, Zhong, Yi

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SMASH, a fragmentation and sequencing method for genomic copy number analysis por Wang, Zihua, Andrews, Peter, Kendall, Jude, Ma, Beicong, Hakker, Inessa, Rodgers, Linda, Ronemus, Michael, Wigler, Michael, Levy, Dan

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Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies por Jobanputra, Vaidehi, Andrews, Peter, Felice, Vanessa, Abhyankar, Avinash, Kozon, Lukasz, Robinson, Dino, London, Ferrah, Hakker, Inessa, Wrzeszczynski, Kazimierz, Ronemus, Michael

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Overexpression of Neprilysin Reduces Alzheimer Amyloid-β42 (Aβ42)-induced Neuron Loss and Intraneuronal Aβ42 Deposits but Causes a Reduction in cAMP-responsive Element-binding Pr... por Iijima-Ando, Kanae, Hearn, Stephen A., Granger, Linda, Shenton, Christopher, Gatt, Anthony, Chiang, Hsueh-Cheng, Hakker, Inessa, Zhong, Yi, Iijima, Koichi

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Aβ42 Mutants with Different Aggregation Profiles Induce Distinct Pathologies in Drosophila por Iijima, Koichi, Chiang, Hsueh-Cheng, Hearn, Stephen A., Hakker, Inessa, Gatt, Anthony, Shenton, Christopher, Granger, Linda, Leung, Amy, Iijima-Ando, Kanae, Zhong, Yi

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DNA copy number variations in children with vesicoureteral reflux and urinary tract infections por Liang, Dong, McHugh, Kirk M., Brophy, Pat D., Shaikh, Nader, Manak, J. Robert, Andrews, Peter, Hakker, Inessa, Wang, Zihua, Schwaderer, Andrew L., Hains, David S.

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Utility of single cell genomics in diagnostic evaluation of prostate cancer por Alexander, Joan, Kendall, Jude, McIndoo, Jean, Rodgers, Linda, Aboukhalil, Robert, Levy, Dan, Stepansky, Asya, Sun, Guoli, Chobardjiev, Lubomir, Riggs, Michael, Cox, Hilary, Hakker, Inessa, Nowak, Dawid G., Laze, Juliana, Llukani, Elton, Srivastava, Abhishek, Gruschow, Siobhan, Yadav, Shalini S., Robinson, Brian, Atwal, Gurinder, Trotman, Lloyd, Lepor, Herbert, Hicks, James, Wigler, Michael, Krasnitz, Alexander

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De Novo Gene Disruptions in Children on the Autistic Spectrum por Iossifov, Ivan, Ronemus, Michael, Levy, Dan, Wang, Zihua, Hakker, Inessa, Rosenbaum, Julie, Yamrom, Boris, Lee, Yoon-ha, Narzisi, Giuseppe, Leotta, Anthony, Kendall, Jude, Grabowska, Ewa, Ma, Beicong, Marks, Steven, Rodgers, Linda, Stepansky, Asya, Troge, Jennifer, Andrews, Peter, Bekritsky, Mitchell, Pradhan, Kith, Ghiban, Elena, Kramer, Melissa, Parla, Jennifer, Demeter, Ryan, Fulton, Lucinda L., Fulton, Robert S., Magrini, Vincent J., Ye, Kenny, Darnell, Jennifer C., Darnell, Robert B., Mardis, Elaine R., Wilson, Richard K., Schatz, Michael C., McCombie, W. Richard, Wigler, Michael

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The contribution of de novo coding mutations to autism spectrum disorder por Iossifov, Ivan, O’Roak, Brian J., Sanders, Stephan J., Ronemus, Michael, Krumm, Niklas, Levy, Dan, Stessman, Holly A., Witherspoon, Kali, Vives, Laura, Patterson, Karynne E., Smith, Joshua D., Paeper, Bryan, Nickerson, Deborah A., Dea, Jeanselle, Dong, Shan, Gonzalez, Luis E., Mandell, Jefferey D., Mane, Shrikant M., Murtha, Michael T., Sullivan, Catherine A., Walker, Michael F., Waqar, Zainulabedin, Wei, Liping, Willsey, A. Jeremy, Yamrom, Boris, Lee, Yoon-ha, Grabowska, Ewa, Dalkic, Ertugrul, Wang, Zihua, Marks, Steven, Andrews, Peter, Leotta, Anthony, Kendall, Jude, Hakker, Inessa, Rosenbaum, Julie, Ma, Beicong, Rodgers, Linda, Troge, Jennifer, Narzisi, Giuseppe, Yoon, Seungtai, Schatz, Michael C., Ye, Kenny, McCombie, W. Richard, Shendure, Jay, Eichler, Evan E., State, Matthew W., Wigler, Michael

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