Glycinergic Synapse Development, Plasticity, and Homeostasis in Zebrafish

Por Ganser, Lisa R., Dallman, Julia E.
Publicado em 2009

Spontaneous activity regulates calcium-dependent K(+) current expression in developing ascidian muscle

Por Dallman, Julia E, Davis, Anna K, Moody, William J
Publicado em 1998

Action potential waveform voltage clamp shows significance of different Ca(2+) channel types in developing ascidian muscle

Por Dallman, Julia E, Dorman, Jennie B, Moody, William J
Publicado em 2000

Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish

Por Kozol, Robert A., Abrams, Alexander J., James, David M., Buglo, Elena, Yan, Qing, Dallman, Julia E.
Publicado no Front Mol Neurosci (2016)

Synaptic Homeostasis in a Zebrafish Glial Glycine Transporter Mutant

Por Mongeon, Rebecca, Gleason, Michelle R., Masino, Mark A., Fetcho, Joseph R., Mandel, Gail, Brehm, Paul, Dallman, Julia E.
Publicado em 2008

Distinct phenotypes in zebrafish models of human startle disease()

Por Ganser, Lisa R., Yan, Qing, James, Victoria M., Kozol, Robert, Topf, Maya, Harvey, Robert J., Dallman, Julia E.
Publicado em 2013

Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis

Por Kozol, Robert A., Cukier, Holly N., Zou, Bing, Mayo, Vera, De Rubeis, Silvia, Cai, Guiqing, Griswold, Anthony J., Whitehead, Patrice L., Haines, Jonathan L., Gilbert, John R., Cuccaro, Michael L., Martin, Eden R., Baker, James D., Buxbaum, Joseph D., Pericak-Vance, Margaret A., Dallman, Julia E.
Publicado no Hum Mol Genet (2015)

Cryptic Amyloidogenic Elements in the 3′ UTRs of Neurofilament Genes Trigger Axonal Neuropathy

Por Rebelo, Adriana P., Abrams, Alexander J., Cottenie, Ellen, Horga, Alejandro, Gonzalez, Michael, Bis, Dana M., Sanchez-Mejias, Avencia, Pinto, Milena, Buglo, Elena, Markel, Kasey, Prince, Jeffrey, Laura, Matilde, Houlden, Henry, Blake, Julian, Woodward, Cathy, Sweeney, Mary G., Holton, Janice L., Hanna, Michael, Dallman, Julia E., Auer-Grumbach, Michaela, Reilly, Mary M., Zuchner, Stephan
Publicado no Am J Hum Genet (2016)

Mutations in the UGO1-like protein SLC25A46 cause an optic atrophy spectrum disorder

Por Abrams, Alexander J., Hufnagel, Robert B., Rebelo, Adriana, Zanna, Claudia, Patel, Neville, Gonzalez, Michael A., Campeanu, Ion J., Griffin, Laurie B., Groenewald, Saskia, Strickland, Alleene V., Tao, Feifei, Speziani, Fiorella, Abreu, Lisa, Schüle, Rebecca, Caporali, Leonardo, La Morgia, Chiara, Maresca, Alessandra, Liguori, Rocco, Lodi, Raffaele, Ahmed, Zubair M., Sund, Kristen L., Wang, Xinjian, Krueger, Laura A., Peng, Yanyan, Prada, Carlos E., Prows, Cynthia A., Bove, Kevin, Schorry, Elizabeth K., Antonellis, Anthony, Zimmerman, Holly H., Abdul-Rahman, Omar A., Yang, Yaping, Downes, Susan M., Prince, Jeffery, Fontanesi, Flavia, Barrientos, Antonio, Nemeth, Andrea H., Carelli, Valerio, Huang, Taosheng, Zuchner, Stephan, Dallman, Julia E.
Publicado no Nat Genet (2015)