Search Results - François V. Bolduc

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  1. 1
    Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature

    Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature by Francois D. Jacob, Vijay Ramaswamy, John Andersen, François V. Bolduc

    Published 2009
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  2. 2
    Excess protein synthesis in Drosophila Fragile X mutants impairs long-term memory

    Excess protein synthesis in Drosophila Fragile X mutants impairs long-term memory by François V. Bolduc, Kimberly Bell, Hilary Cox, Kendal Broadie, Tim Tully

    Published 2008
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  3. 3
    Insulin signaling is acutely required for long-term memory in Drosophila

    Insulin signaling is acutely required for long-term memory in Drosophila by Daniel B. Chambers, Alaura Androschuk, Cory Rosenfelt, Steven Langer, Mark Geoffrey Harding, François V. Bolduc

    Published 2015
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  4. 4
    A <i>Drosophila</i> model for Angelman syndrome

    A <i>Drosophila</i> model for Angelman syndrome by Yaning Wu, François V. Bolduc, Kimberly Bell, Tim Tully, Yanshan Fang, Amita Sehgal, Janice A. Fischer

    Published 2008
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  5. 5
    Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders

    Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders by Surya T. Madabattula, Joel C. Strautman, Andrew Bysice, Julia O’Sullivan, Alaura Androschuk, Cory Rosenfelt, Kacy Doucet, Guy A. Rouleau, François V. Bolduc

    Published 2015
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  6. 6
    Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders

    Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders by Surya T. Madabattula, Joel C. Strautman, Andrew Bysice, Julia O’Sullivan, Alaura Androschuk, Cory Rosenfelt, Kacy Doucet, Guy A. Rouleau, François V. Bolduc

    Published 2015
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  7. 7
    Insulin signaling misregulation underlies circadian and cognitive deficits in a Drosophila fragile X model

    Insulin signaling misregulation underlies circadian and cognitive deficits in a Drosophila fragile X model by Rachel E. Monyak, Dow Emerson, Brian P. Schoenfeld, Xiangzhong Zheng, Donald B. Chambers, Cory Rosenfelt, Steven Langer, Paul Hinchey, C.-H Choi, Thomas V. McDonald, François V. Bolduc, Amita Sehgal, Sean McBride, Thomas A. Jongens

    Published 2016
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  8. 8
    Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

    Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia by Ziv Gan‐Or, Naïma Bouslam, Nazha Birouk, Alexandra Lissouba, Daniel B. Chambers, Julie Vérièpe, Alaura Androschuk, Sandra B. Laurent, Daniel Rochefort, Dan Spiegelman, Alexandre Dionne‐Laporte, Anna Szuto, Meijiang Liao, Denise A. Figlewicz, Ahmed Bouhouche, Ali Benomar, Mohamed Yahyaoui, Réda Ouazzani, Grace Yoon, Nicolas Dupré, Oksana Suchowersky, François V. Bolduc, J. Alex Parker, Patrick A. Dion, Pierre Drapeau, Guy A. Rouleau, Bouchra Ouled Amar Bencheikh

    Published 2016
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  9. 9
    PDE-4 Inhibition Rescues Aberrant Synaptic Plasticity in<i>Drosophila</i>and Mouse Models of Fragile X Syndrome

    PDE-4 Inhibition Rescues Aberrant Synaptic Plasticity in<i>Drosophila</i>and Mouse Models of Fragile X Syndrome by Catherine H. Choi, Brian P. Schoenfeld, Eliana D Weisz, Aaron Bell, Daniel B. Chambers, Joseph Hinchey, Richard J. Choi, Paul Hinchey, Maria Kollaros, Michael Gertner, Neal Ferrick, Allison M. Terlizzi, Nicole L. Yohn, Eric Koenigsberg, David A. Liebelt, R. Suzanne Zukin, Newton H. Woo, Michael R. Tranfaglia, Natalia Louneva, Steven E. Arnold, Steven J. Siegel, François V. Bolduc, Thomas V. McDonald, Thomas A. Jongens, Sean McBride

    Published 2015
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  10. 10
    Multiple Drug Treatments That Increase cAMP Signaling Restore Long-Term Memory and Aberrant Signaling in Fragile X Syndrome Models

    Multiple Drug Treatments That Increase cAMP Signaling Restore Long-Term Memory and Aberrant Signaling in Fragile X Syndrome Models by Catherine H. Choi, Brian P. Schoenfeld, Aaron Bell, Joseph Hinchey, Cory Rosenfelt, Michael Gertner, Sean Campbell, Danielle Emerson, Paul Hinchey, Maria Kollaros, Neal Ferrick, Daniel B. Chambers, Steven Langer, Steven Sust, Aatika Malik, Allison M. Terlizzi, David A. Liebelt, David Ferreiro, Ali Sharma, Eric Koenigsberg, Richard J. Choi, Natalia Louneva, Steven E. Arnold, Robert E. Featherstone, Steven J. Siegel, R. Suzanne Zukin, Thomas V. McDonald, François V. Bolduc, Thomas A. Jongens, Sean McBride

    Published 2016
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  11. 11
    Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia

    Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic Paraplegia by Ralf A. Husain, Mona Grimmel, Matias Wagner, J. Christopher Hennings, Christian Marx, René G. Feichtinger, Abdelkrim Saadi, Kevin Rostásy, Florentine Radelfahr, Andrea Bevot, Marion Döbler‐Neumann, Hans Hartmann, Laurence Colleaux, Isabell Cordts, Xenia Kobeleva, Hossein Darvish, Somayeh Bakhtiari, Michael C. Kruer, Arnaud Besse, Andy Cheuk‐Him Ng, Diana Chiang, François V. Bolduc, Abbas Tafakhori, Shrikant Mane, Saghar Ghasemi Firouzabadi, Antje K. Huebner, Rebecca Buchert, Stefanie Beck‐Woedl, Amelie J. Müller, Lucia Laugwitz, Thomas Nägele, Zhao‐Qi Wang, Tim M. Strom, Marc Sturm, Thomas Meitinger, Thomas Klockgether, Olaf Rieß, Thomas Klopstock, Ulrich Brandl, Christian A. Hübner, Marcus Deschauer, Johannes A. Mayr, Penelope E. Bonnen, Ingeborg Krägeloh‐Mann, Saskia B. Wortmann, Tobias B. Haack

    Published 2020
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  12. 12
    PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production

    PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production by Frédéric Ebstein, Sébastien Küry, Victoria Most, Cory Rosenfelt, Marie‐Pier Scott‐Boyer, Geeske M. van Woerden, Thomas Besnard, Jonas Johannes Papendorf, Maja Studencka‐Turski, Tianyun Wang, Tzung‐Chien Hsieh, Richard Golnik, Dustin Baldridge, Cara Forster, Charlotte de Konink, Selina M. W. Teurlings, Virginie Vignard, Richard H. van Jaarsveld, Lesley C. Adès, Benjamin Cogné, Cyril Mignot, Wallid Deb, Marjolijn C.J. Jongmans, F. Sessions Cole, Marie‐José H. van den Boogaard, Jennifer Wambach, D.J. Wegner, Sandra Yang, Vickie Hannig, Jennifer Brault, Neda Zadeh, Bruce Bennetts, Boris Keren, Anne-Claire Gélineau, Zöe Powis, Meghan C. Towne, Kristine Bachman, Andrea Seeley, Anita Beck, Jennifer Morrison, Rachel Westman, Kelly Averill, Theresa Brunet, Judith Haasters, Melissa T. Carter, Matthew Osmond, Patricia G. Wheeler, Francesca Forzano, Shehla Mohammed, Yannis Trakadis, Andrea Accogli, Rachel Harrison, Yiran Guo, Hákon Hákonarson, Sophie Rondeau, Geneviève Baujat, Giulia Barcia, René G. Feichtinger, Johannes A. Mayr, Martin Preisel, Frédéric Laumonnier, Tilmann Kallinich, Alexej Knaus, Bertrand Isidor, Peter Krawitz, Uwe Völker, Elke Hammer, Arnaud Droit, Evan E. Eichler, Ype Elgersma, Peter W. Hildebrand, François V. Bolduc, Elke Krüger, Stéphane Bézieau

    Published 2023
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