Resultados de procura - Xander Nuttle

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  1. 1
    Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV

    Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNV por Michael H. Duyzend, Xander Nuttle, Bradley P. Coe, Carl Baker, Deborah A. Nickerson, Raphael Bernier, Evan E. Eichler

    Publicado 2015
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  2. 2
    The birth of a human-specific neural gene by incomplete duplication and gene fusion

    The birth of a human-specific neural gene by incomplete duplication and gene fusion por Max L. Dougherty, Xander Nuttle, Osnat Penn, Bradley J. Nelson, John Huddleston, Carl Baker, Lana Harshman, Michael H. Duyzend, Mario Ventura, Francesca Antonacci, Richard Sandstrom, Megan Y. Dennis, Evan E. Eichler

    Publicado 2017
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  3. 3
    Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editing

    Activation of the imprinted Prader-Willi syndrome locus by CRISPR-based epigenome editing por Dahlia Rohm, Joshua B. Black, Sean R. McCutcheon, Alejandro Barrera, Susan A. Berry, Daniel J. Morone, Xander Nuttle, Celine E. de Esch, Derek J.C. Tai, Michael E. Talkowski, Nahid Iglesias, Charles A. Gersbach

    Publicado 2025
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  4. 4
    Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication

    Evolution of Human-Specific Neural SRGAP2 Genes by Incomplete Segmental Duplication por Megan Y. Dennis, Xander Nuttle, Peter H. Sudmant, Francesca Antonacci, Tina Graves, Mikhail Nefedov, Jill A. Rosenfeld, Saba Sajjadian, Maika Malig, Holland Kotkiewicz, Cynthia J. Curry, Susan Shafer, Lisa G. Shaffer, Pieter J. de Jong, Richard K. Wilson, Evan E. Eichler

    Publicado 2012
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  5. 5
    The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals

    The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals por Giuliana Giannuzzi, Paul J. Schmidt, Eleonora Porcu, Gilles Willemin, Katherine M. Munson, Xander Nuttle, Rachel K. Earl, Jacqueline Chrast, Kendra Hoekzema, Davide Risso, Katrin Männik, Pasquelena De Nittis, Ethan Baratz, Yann Hérault, Xiang Gao, Caroline C. Philpott, Raphael Bernier, Zoltán Kutalik, Mark D. Fleming, Evan E. Eichler, Alexandre Reymond

    Publicado 2019
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  6. 6
    The evolution and population diversity of human-specific segmental duplications

    The evolution and population diversity of human-specific segmental duplications por Megan Y. Dennis, Lana Harshman, Bradley J. Nelson, Osnat Penn, Stuart Cantsilieris, John Huddleston, Francesca Antonacci, Kelsi Penewit, Laura Denman, Archana N. Raja, Carl Baker, Kenneth M. K. Mark, Maika Malig, Nicolette Janke, Claudia Y. Espinoza, Holly A.F. Stessman, Xander Nuttle, Kendra Hoekzema, Tina A. Lindsay-Graves, Richard K. Wilson, Evan E. Eichler

    Publicado 2017
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  7. 7
    Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models

    Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models por Derek J.C. Tai, Parisa Razaz, Serkan Erdin, Dadi Gao, Jennifer Wang, Xander Nuttle, Celine E. de Esch, Ryan L. Collins, Benjamin Currall, Kathryn O’Keefe, Nicholas D. Burt, Rachita Yadav, Lily Wang, Kiana Mohajeri, Tatsiana Aneichyk, Ashok Ragavendran, Alexei Stortchevoi, Elisabetta Morini, Weiyuan Ma, Diane Lucente, Alex Hastie, Raymond J. Kelleher, Roy H. Perlis, Michael E. Talkowski, James F. Gusella

    Publicado 2022
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  8. 8
    Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility

    Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility por Xander Nuttle, Giuliana Giannuzzi, Michael H. Duyzend, Joshua G. Schraiber, Iñigo Narvaiza, Peter H. Sudmant, Osnat Penn, Giorgia Chiatante, Maika Malig, John Huddleston, Christopher Benner, Francesca Camponeschi, Simone Ciofi‐Baffoni, Holly A.F. Stessman, Maria C. Marchetto, Laura Denman, Lana Harshman, Carl Baker, Archana N. Raja, Kelsi Penewit, Nicolette Janke, Weiliang Tang, Mario Ventura, Lucia Banci, Francesca Antonacci, Joshua M. Akey, Chris T. Amemiya, Fred H. Gage, Alexandre Reymond, Evan E. Eichler

    Publicado 2016
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  9. 9
    Human-specific <i>NOTCH</i>-like genes in a region linked to neurodevelopmental disorders affect cortical neurogenesis

    Human-specific <i>NOTCH</i>-like genes in a region linked to neurodevelopmental disorders affect cortical neurogenesis por Ian T. Fiddes, Gerrald A. Lodewijk, Meghan Mooring, Colleen M. Bosworth, Adam D. Ewing, Gary L. Mantalas, Adam M. Novak, Anouk van den Bout, Alex Bishara, Jimi L. Rosenkrantz, Ryan Lorig-Roach, Andrew R. Field, Maximillian Haeussler, Lotte Russo, Aparna Bhaduri, Tomasz J. Nowakowski, Alex A. Pollen, Max L. Dougherty, Xander Nuttle, Marie‐Claude Addor, Simon Zwolinski, Sol Katzman, Arnold Kreigstein, Evan E. Eichler, Sofie R. Salama, Frank M. J. Jacobs, David Haussler

    Publicado 2017
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  10. 10
    Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis

    Human-Specific NOTCH2NL Genes Affect Notch Signaling and Cortical Neurogenesis por Ian T. Fiddes, Gerrald A. Lodewijk, Meghan Mooring, Colleen M. Bosworth, Adam D. Ewing, Gary L. Mantalas, Adam M. Novak, Anouk van den Bout, Alex Bishara, Jimi L. Rosenkrantz, Ryan Lorig-Roach, Andrew R. Field, Maximilian Haeussler, Lotte Russo, Aparna Bhaduri, Tomasz J. Nowakowski, Alex A. Pollen, Max L. Dougherty, Xander Nuttle, Marie‐Claude Addor, Simon Zwolinski, Sol Katzman, Arnold R. Kriegstein, Evan E. Eichler, Sofie R. Salama, Frank M. J. Jacobs, David Haussler

    Publicado 2018
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  11. 11
    A cross-disorder dosage sensitivity map of the human genome

    A cross-disorder dosage sensitivity map of the human genome por Ryan L. Collins, Joseph Glessner, Eleonora Porcu, Maarja Lepamets, Rhonda Brandon, Christopher Lauricella, Lide Han, Theodore Morley, Lisa‐Marie Niestroj, Jacob C. Ulirsch, Selin Everett, Daniel P. Howrigan, Philip M. Boone, Jack Fu, Konrad J. Karczewski, Georgios Kellaris, Chelsea Lowther, Diane Lucente, Kiana Mohajeri, Margit Nõukas, Xander Nuttle, Kaitlin E. Samocha, Mi K. Trinh, Farid Ullah, Urmo Võsa, Matthew E. Hurles, Swaroop Aradhya, Erica E. Davis, Hilary K. Finucane, James F. Gusella, Aura Janze, Nicholas Katsanis, Ludmila Matyakhina, Benjamin M. Neale, D. B. Sanders, Stephanie Warren, Jennelle C. Hodge, Dennis Lal, Douglas M. Ruderfer, Jeanne Meck, Reedik Mägi, Tõnu Esko, Alexandre Reymond, Zoltán Kutalik, Hákon Hákonarson, Shamil Sunyaev, Harrison Brand, Michael E. Talkowski, Andres Metspalu, Reedik Mägi, Mari Nelis, Lili Milani, Tõnu Esko

    Publicado 2022
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