نتائج البحث - Hakker, Inessa

Distinctive roles of different β-amyloid 42 aggregates in modulation of synaptic functions حسب 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 حسب 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 حسب 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 حسب 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 حسب 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... حسب 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 حسب 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 حسب 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 حسب 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 حسب 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 حسب 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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