Resultados da busca - Derek J.C. Tai

  • Mostrando 1 - 8 resultados de 8
Refinar Resultados
  1. 1
    SGK1 Phosphorylation of IκB Kinase α and p300 Up-regulates NF-κB Activity and Increases N-Methyl-D-aspartate Receptor NR2A and NR2B Expression

    SGK1 Phosphorylation of IκB Kinase α and p300 Up-regulates NF-κB Activity and Increases N-Methyl-D-aspartate Receptor NR2A and NR2B Expression por Derek J.C. Tai, Chia-Chen Su, Yun‐Li Ma, Eminy H.Y. Lee

    Publicado em 2008
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  2. 2
    MeCP2 SUMOylation rescues Mecp2-mutant-induced behavioural deficits in a mouse model of Rett syndrome

    MeCP2 SUMOylation rescues Mecp2-mutant-induced behavioural deficits in a mouse model of Rett syndrome por Derek J.C. Tai, Yen‐Chen Liu, Wei‐Lun Hsu, Yun‐Li Ma, Sin Jhong Cheng, Shau Y. Liu, Eminy H.Y. Lee

    Publicado em 2016
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  3. 3
    16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro

    16p11.2 deletion is associated with hyperactivation of human iPSC-derived dopaminergic neuron networks and is rescued by RHOA inhibition in vitro por Maria Sundberg, Hannah Pinson, Richard S. Smith, Kellen D. Winden, Pooja Venugopal, Derek J.C. Tai, James F. Gusella, Michael E. Talkowski, Christopher A. Walsh, Max Tegmark, Mustafa Şahin

    Publicado em 2021
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  4. 4
    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 em 2025
    Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  5. 5
    Statistical and functional convergence of common and rare variant risk for autism spectrum disorders at chromosome 16p

    Statistical and functional convergence of common and rare variant risk for autism spectrum disorders at chromosome 16p por Daniel J. Weiner, Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove, Jack Fu, Ajay Nadig, Caitlin E. Carey, Nikolas Baya, Jonas Bybjerg‐Grauholm, Sabina Berretta, Evan Z. Macosko, Jonathan Sebat, Luke J. O’Connor, David M. Hougaard, Anders D. Børglum, Michael E. Talkowski, Steve McCarroll, Elise Robinson

    Publicado em 2022
    Obter o texto integral Obter o texto integral
    Pré-impressão
    Salvar na lista
    Na minha lista:
  6. 6
    Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production

    Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production por Helen Chen, A. Kaitlyn Victor, Jonathon Klein, Klementina Fon Tacer, Derek J.C. Tai, Celine de Esch, Alexander Nuttle, Jamshid Temirov, Lisa C. Burnett, Michael Rosenbaum, Yiying Zhang, Li Ding, James J. Moresco, Jolene K. Diedrich, John R. Yates, Heather Tillman, Rudolph L. Leibel, Michael E. Talkowski, Daniel D. Billadeau, Lawrence T. Reiter, Patrick Ryan Potts

    Publicado em 2020
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  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 em 2022
    Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:
  8. 8
    Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

    Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p por Daniel J. Weiner, Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove, Jack Fu, Ajay Nadig, Caitlin E. Carey, Nikolas Baya, Jonas Bybjerg‐Grauholm, Preben Bo Mortensen, Thomas Werge, Ditte Demontis, Ole Mors, Merete Nordentoft, Thomas D. Als, Marie Bækvad‐Hansen, Anders Rosengren, Alexandra Havdahl, Anne Hedemand, Aarno Palotie, Aravinda Chakravarti, Dan E. Arking, Arvis Sulovari, Anna Starnawska, Bhooma Thiruvahindrapuram, Christiaan de Leeuw, Caitlin E. Carey, Christine Ladd‐Acosta, Celia van der Merwe, Bernie Devlin, Edwin H. Cook, Evan E. Eichler, Elisabeth Corfield, Gwen Dieleman, Gerard D. Schellenberg, Hákon Hákonarson, Hilary Coon, Isabel Dziobek, Jacob Vorstman, Jessica B. Girault, James S. Sutcliffe, Jinjie Duan, John I. Nürnberger, Joachim Hallmayer, Joseph D. Buxbaum, Joseph Piven, Lauren A. Weiss, Lea K. Davis, Magdalena Janecka, Manuel Mattheisen, Matthew W. State, Michael Gill, Mark J. Daly, Mohammed Uddin, Ole A. Andreassen, Peter Szatmari, Phil Hyoun Lee, Richard Anney, Stephan Ripke, Kyle F. Satterstrom, Susan L. Santangelo, Susan S. Kuo, Ludger Tebartz van Elst, Thomas Rolland, Thomas Bougeron, Tinca J. C. Polderman, Tychele N. Turner, Jack Underwood, Veera Manikandan, Vamsee Pillalamarri, Varun Warrier, Alexandra Philipsen, Andreas Reif, Anke Hinney, Bru Cormand, Claiton Henrique Dotto Bau, Diego Luiz Rovaris, Edmund Sonuga‐Barke, Elizabeth C. Corfield, Eugênio H. Grevet, Giovanni Abrahão Salum, Henrik Larsson, Jan Buitelaar, Jan Haavik, James J. McGough, Jonna Kuntsi, Josephine Elia, Klaus‐Peter Lesch, Marieke Klein, Mark A. Bellgrove, Martin Tesli, Patrick W. L. Leung, Pedro Mário Pan, Søren Dalsgaard, Sandra K. Loo, Sarah E. Medland, Stephen V. Faraone, Ted Reichborn‐Kjennerud

    Publicado em 2022
    Obter o texto integral Obter o texto integral
    Artigo
    Salvar na lista
    Na minha lista:

Ferramentas de busca: