Fruit flies and intellectual disability

Por Bolduc, François V., Tully, Tim
Publicado em 2009

From Learning to Memory: What Flies Can Tell Us about Intellectual Disability Treatment

Por Androschuk, Alaura, Al-Jabri, Basma, Bolduc, Francois V.
Publicado no Front Psychiatry (2015)

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

Por Jacob, Francois Dominique, Ramaswamy, Vijay, Andersen, John, Bolduc, Francois V
Publicado em 2009

Fragile X Mental Retardation 1 and Filamin A Interact Genetically in Drosophila Long-Term Memory

Por Bolduc, François V., Bell, Kimberly, Rosenfelt, Cory, Cox, Hilary, Tully, Tim
Publicado em 2010

Excess protein synthesis in Drosophila Fragile X mutants impairs long-term memory

Por Bolduc, François V., Bell, Kimberly, Cox, Hilary, Broadie, Kendal, Tully, Tim
Publicado em 2008

An assay for social interaction in Drosophila fragile X mutants

Por Bolduc, Francois V., Valente, Dan, Nguyen, Antoinette T., Mitra, Partha P., Tully, Tim
Publicado em 2010

Genomic characterization of chromosome 8 pericentric trisomy

Por Vander Pluym, Juliana H, O’Sullivan, Julia, Andrew, Gail, Bolduc, Francois V
Publicado no Clin Case Rep (2015)

Reversible white matter lesions associated with mutant EHMT1 and Kleefstra syndrome

Por He, Xu, Caluseriu, Oana, Srivastava, Ratika, Denny, Anne Marie, Bolduc, Francois V.
Publicado no Neurol Genet (2016)

Insulin signaling is acutely required for long-term memory in Drosophila

Por Chambers, Daniel B., Androschuk, Alaura, Rosenfelt, Cory, Langer, Steven, Harding, Mark, Bolduc, Francois V.
Publicado no Front Neural Circuits (2015)

Recurrent Diplopia in a Pediatric Patient with Bickerstaff Brainstem Encephalitis

Por McLeod, Scott A., Wee, Wallace, Jacob, Francois D., Chapados, Isabelle, Bolduc, Francois V.
Publicado no Case Rep Neurol Med (2016)

A Drosophila model for Angelman syndrome

Por Wu, Yaning, Bolduc, Francois V., Bell, Kimberly, Tully, Tim, Fang, Yanshan, Sehgal, Amita, Fischer, Janice A.
Publicado em 2008

Conserved pharmacological rescue of hereditary spastic paraplegia-related phenotypes across model organisms

Por Julien, Carl, Lissouba, Alexandra, Madabattula, Surya, Fardghassemi, Yasmin, Rosenfelt, Cory, Androschuk, Alaura, Strautman, Joel, Wong, Clement, Bysice, Andrew, O'sullivan, Julia, Rouleau, Guy A., Drapeau, Pierre, Parker, J. Alex, Bolduc, François V.
Publicado no Hum Mol Genet (2016)

Cognitive Enhancement in Infants Associated with Increased Maternal Fruit Intake During Pregnancy: Results from a Birth Cohort Study with Validation in an Animal Model()

Por Bolduc, Francois V., Lau, Amanda, Rosenfelt, Cory S., Langer, Steven, Wang, Nan, Smithson, Lisa, Lefebvre, Diana, Alexander, R. Todd, Dickson, Clayton T., Li, Liang, Becker, Allan B., Subbarao, Padmaja, Turvey, Stuart E., Pei, Jacqueline, Sears, Malcolm R., Mandhane, Piush J.
Publicado no EBioMedicine (2016)

Insulin Signaling Misregulation underlies Circadian and Cognitive Deficits in a Drosophila Fragile X Model

Por Monyak, Rachel E., Emerson, Danielle, Schoenfeld, Brian P., Zheng, Xiangzhong, Chambers, Daniel B., Rosenfelt, Cory, Langer, Steven, Hinchey, Paul, Choi, Catherine H., McDonald, Thomas V., Bolduc, Francois V., Sehgal, Amita, McBride, Sean M.J., Jongens, Thomas A.
Publicado no Mol Psychiatry (2016)

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Por Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuck, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexandre, Szuto, Anna, Liao, Meijiang, Figlewicz, Denise A., Bouhouche, Ahmed, Benomar, Ali, Yahyaoui, Mohamed, Ouazzani, Reda, Yoon, Grace, Dupré, Nicolas, Suchowersky, Oksana, Bolduc, Francois V., Parker, J. Alex, Dion, Patrick A., Drapeau, Pierre, Rouleau, Guy A., Bencheikh, Bouchra Ouled Amar
Publicado no Am J Hum Genet (2016)

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia

Por Gan-Or, Ziv, Bouslam, Naima, Birouk, Nazha, Lissouba, Alexandra, Chambers, Daniel B., Vérièpe, Julie, Androschuk, Alaura, Laurent, Sandra B., Rochefort, Daniel, Spiegelman, Dan, Dionne-Laporte, Alexandre, Szuto, Anna, Liao, Meijiang, Figlewicz, Denise A., Bouhouche, Ahmed, Benomar, Ali, Yahyaoui, Mohamed, Ouazzani, Reda, Yoon, Grace, Dupré, Nicolas, Suchowersky, Oksana, Bolduc, Francois V., Parker, J. Alex, Dion, Patrick A., Drapeau, Pierre, Rouleau, Guy A., Bencheikh, Bouchra Ouled Amar
Publicado no Am J Hum Genet (2016)

PDE-4 Inhibition Rescues Aberrant Synaptic Plasticity in Drosophila and Mouse Models of Fragile X Syndrome

Por Choi, Catherine H., Schoenfeld, Brian P., Weisz, Eliana D., Bell, Aaron J., Chambers, Daniel B., Hinchey, Joseph, Choi, Richard J., Hinchey, Paul, Kollaros, Maria, Gertner, Michael J., Ferrick, Neal J., Terlizzi, Allison M., Yohn, Nicole, Koenigsberg, Eric, Liebelt, David A., Zukin, R. Suzanne, Woo, Newton H., Tranfaglia, Michael R., Louneva, Natalia, Arnold, Steven E., Siegel, Steven J., Bolduc, Francois V., McDonald, Thomas V., Jongens, Thomas A., McBride, Sean M. J.
Publicado no J Neurosci (2015)

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

Por Choi, Catherine H., Schoenfeld, Brian P., Bell, Aaron J., Hinchey, Joseph, Rosenfelt, Cory, Gertner, Michael J., Campbell, Sean R., Emerson, Danielle, Hinchey, Paul, Kollaros, Maria, Ferrick, Neal J., Chambers, Daniel B., Langer, Steven, Sust, Steven, Malik, Aatika, Terlizzi, Allison M., Liebelt, David A., Ferreiro, David, Sharma, Ali, Koenigsberg, Eric, Choi, Richard J., Louneva, Natalia, Arnold, Steven E., Featherstone, Robert E., Siegel, Steven J., Zukin, R. Suzanne, McDonald, Thomas V., Bolduc, Francois V., Jongens, Thomas A., McBride, Sean M. J.
Publicado no Front Behav Neurosci (2016)