Epigenetic mechanisms modulate differences in Drosophila foraging behavior

par Anreiter, Ina, Kramer, Jamie M., Sokolowski, Marla B.
Publié dans Proc Natl Acad Sci U S A (2017)

Expression of Drosophila FOXO regulates growth and can phenocopy starvation

par Kramer, Jamie M, Davidge, Jason T, Lockyer, Joseph M, Staveley, Brian E
Publié 2003

Optimal RNA isolation method and primer design to detect gene knockdown by qPCR when validating Drosophila transgenic RNAi lines

par Mainland, Roslyn L., Lyons, Taylor A., Ruth, Mike M., Kramer, Jamie M.
Publié dans BMC Res Notes (2017)

The epigenetic regulator G9a attenuates stress-induced resistance and metabolic transcriptional programs across different stressors and species

par Riahi, Human, Fenckova, Michaela, Goruk, Kayla J., Schenck, Annette, Kramer, Jamie M.
Publié dans BMC Biol (2021)

Mushroom Body Specific Transcriptome Analysis Reveals Dynamic Regulation of Learning and Memory Genes After Acquisition of Long-Term Courtship Memory in Drosophila

par Jones, Spencer G., Nixon, Kevin C. J., Chubak, Melissa C., Kramer, Jamie M.
Publié dans G3 (Bethesda) (2018)

Drosophila Courtship Conditioning As a Measure of Learning and Memory

par Koemans, Tom S., Oppitz, Cornelia, Donders, Rogier A. T., van Bokhoven, Hans, Schenck, Annette, Keleman, Krystyna, Kramer, Jamie M.
Publié dans J Vis Exp (2017)

The Epigenetic Regulator G9a Mediates Tolerance to RNA Virus Infection in Drosophila

par Merkling, Sarah H., Bronkhorst, Alfred W., Kramer, Jamie M., Overheul, Gijs J., Schenck, Annette, Van Rij, Ronald P.
Publié dans PLoS Pathog (2015)

The histone methyltransferase G9a regulates tolerance to oxidative stress–induced energy consumption

par Riahi, Human, Brekelmans, Carlijn, Foriel, Sarah, Merkling, Sarah H., Lyons, Taylor A., Itskov, Pavel M., Kleefstra, Tjitske, Ribeiro, Carlos, van Rij, Ronald P., Kramer, Jamie M., Schenck, Annette
Publié dans PLoS Biol (2019)

Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a Drosophila Model for Intellectual Disability

par Vandewalle, Joke, Langen, Marion, Zschaetzsch, Marlen, Nijhof, Bonnie, Kramer, Jamie M., Brems, Hilde, Bauters, Marijke, Lauwers, Elsa, Srahna, Mohammed, Marynen, Peter, Verstreken, Patrik, Schenck, Annette, Hassan, Bassem A., Froyen, Guy
Publié 2013

Correction: Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a Drosophila Model for Intellectual Disability

par Vandewalle, Joke, Langen, Marion, Zschaetzsch, Marlen, Nijhof, Bonnie, Kramer, Jamie M., Brems, Hilde, Bauters, Marijke, Lauwers, Elsa, Srahna, Mohammed, Marynen, Peter, Verstreken, Patrik, Schenck, Annette, Hassan, Bassem A., Froyen, Guy
Publié 2014

Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules

par Kochinke, Korinna, Zweier, Christiane, Nijhof, Bonnie, Fenckova, Michaela, Cizek, Pavel, Honti, Frank, Keerthikumar, Shivakumar, Oortveld, Merel A.W., Kleefstra, Tjitske, Kramer, Jamie M., Webber, Caleb, Huynen, Martijn A., Schenck, Annette
Publié dans Am J Hum Genet (2016)

Epigenetic Regulation of Learning and Memory by Drosophila EHMT/G9a

par Kramer, Jamie M., Kochinke, Korinna, Oortveld, Merel A. W., Marks, Hendrik, Kramer, Daniela, de Jong, Eiko K., Asztalos, Zoltan, Westwood, J. Timothy, Stunnenberg, Hendrik G., Sokolowski, Marla B., Keleman, Krystyna, Zhou, Huiqing, van Bokhoven, Hans, Schenck, Annette
Publié 2011

Individual components of the SWI/SNF chromatin remodelling complex have distinct roles in memory neurons of the Drosophila mushroom body

par Chubak, Melissa C., Nixon, Kevin C. J., Stone, Max H., Raun, Nicholas, Rice, Shelby L., Sarikahya, Mohammed, Jones, Spencer G., Lyons, Taylor A., Jakub, Taryn E., Mainland, Roslyn L. M., Knip, Maria J., Edwards, Tara N., Kramer, Jamie M.
Publié dans Dis Model Mech (2019)

A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies

par Nixon, Kevin C.J., Rousseau, Justine, Stone, Max H., Sarikahya, Mohammed, Ehresmann, Sophie, Mizuno, Seiji, Matsumoto, Naomichi, Miyake, Noriko, Baralle, Diana, McKee, Shane, Izumi, Kosuke, Ritter, Alyssa L., Heide, Solveig, Héron, Delphine, Depienne, Christel, Titheradge, Hannah, Kramer, Jamie M., Campeau, Philippe M.
Publié dans Am J Hum Genet (2019)

CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation

par Mukhopadhyay, Arijit, Kramer, Jamie M., Merkx, Gerard, Lugtenberg, Dorien, Smeets, Dominique F., Oortveld, Merel A. W., Blokland, Ellen A. W., Agrawal, Jyoti, Schenck, Annette, van Bokhoven, Hans, Huys, Erik, Schoenmakers, Eric F., van Kessel, Ad Geurts, van Nouhuys, C. Erik, Cremers, Frans P. M.
Publié 2010

Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila

par Castells-Nobau, Anna, Eidhof, Ilse, Fenckova, Michaela, Brenman-Suttner, Dova B., Scheffer-de Gooyert, Jolanda M., Christine, Sheren, Schellevis, Rosa L., van der Laan, Kiran, Quentin, Christine, van Ninhuijs, Lisa, Hofmann, Falko, Ejsmont, Radoslaw, Fisher, Simon E., Kramer, Jamie M., Sigrist, Stephan J., Simon, Anne F., Schenck, Annette
Publié dans PLoS One (2019)

Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration

par Dubos, Aline, Castells-Nobau, Anna, Meziane, Hamid, Oortveld, Merel A.W., Houbaert, Xander, Iacono, Giovanni, Martin, Christelle, Mittelhaeuser, Christophe, Lalanne, Valérie, Kramer, Jamie M., Bhukel, Anuradha, Quentin, Christine, Slabbert, Jan, Verstreken, Patrik, Sigrist, Stefan J., Messaddeq, Nadia, Birling, Marie-Christine, Selloum, Mohammed, Stunnenberg, Henk G., Humeau, Yann, Schenck, Annette, Herault, Yann
Publié dans Hum Mol Genet (2015)

Identification of a novel synaptic protein, TMTC3, involved in periventricular nodular heterotopia with intellectual disability and epilepsy

par Farhan, Sali M K, Nixon, Kevin C J, Everest, Michelle, Edwards, Tara N, Long, Shirley, Segal, Dmitri, Knip, Maria J, Arts, Heleen H, Chakrabarti, Rana, Wang, Jian, Robinson, John F, Lee, Donald, Mirsattari, Seyed M, Rupar, C Anthony, Siu, Victoria M, Poulter, Michael O, Hegele, Robert A, Kramer, Jamie M
Publié dans Hum Mol Genet (2017)

Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder

par Koemans, Tom S., Kleefstra, Tjitske, Chubak, Melissa C., Stone, Max H., Reijnders, Margot R. F., de Munnik, Sonja, Willemsen, Marjolein H., Fenckova, Michaela, Stumpel, Connie T. R. M., Bok, Levinus A., Sifuentes Saenz, Margarita, Byerly, Kyna A., Baughn, Linda B., Stegmann, Alexander P. A., Pfundt, Rolph, Zhou, Huiqing, van Bokhoven, Hans, Schenck, Annette, Kramer, Jamie M.
Publié dans PLoS Genet (2017)

Disruption of an EHMT1-Associated Chromatin-Modification Module Causes Intellectual Disability

par Kleefstra, Tjitske, Kramer, Jamie M., Neveling, Kornelia, Willemsen, Marjolein H., Koemans, Tom S., Vissers, Lisenka E.L.M., Wissink-Lindhout, Willemijn, Fenckova, Michaela, van den Akker, Willem M.R., Kasri, Nael Nadif, Nillesen, Willy M., Prescott, Trine, Clark, Robin D., Devriendt, Koenraad, van Reeuwijk, Jeroen, de Brouwer, Arjan P.M., Gilissen, Christian, Zhou, Huiqing, Brunner, Han G., Veltman, Joris A., Schenck, Annette, van Bokhoven, Hans
Publié 2012