Glycinergic Synapse Development, Plasticity, and Homeostasis in Zebrafish

per Ganser, Lisa R., Dallman, Julia E.
Publicat 2009

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

per Dallman, Julia E, Davis, Anna K, Moody, William J
Publicat 1998

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

per Dallman, Julia E, Dorman, Jennie B, Moody, William J
Publicat 2000

Spatial patterning of excitatory and inhibitory neuropil territories during spinal circuit development

per Yan, Qing, Zhai, Lu, Zhang, Bo, Dallman, Julia E.
Publicat a J Comp Neurol (2017)

A Conserved Role But Different Partners for the Transcriptional Corepressor CoREST in Fly and Mammalian Nervous System Formation

per Dallman, Julia E., Allopenna, Janet, Bassett, Andrew, Travers, Andrew, Mandel, Gail
Publicat a J Neurosci (2004)

The Gut-Brain-Microbiome Axis and Its Link to Autism: Emerging Insights and the Potential of Zebrafish Models

per James, David M., Davidson, Elizabeth A., Yanes, Julio, Moshiree, Baharak, Dallman, Julia E.
Publicat a Front Cell Dev Biol (2021)

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

per Kozol, Robert A., Abrams, Alexander J., James, David M., Buglo, Elena, Yan, Qing, Dallman, Julia E.
Publicat a Front Mol Neurosci (2016)

Synaptic Homeostasis in a Zebrafish Glial Glycine Transporter Mutant

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

Distinct phenotypes in zebrafish models of human startle disease()

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

Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease

per Buglo, Elena, Sarmiento, Evan, Martuscelli, Nicole Belliard, Sant, David W., Danzi, Matt C., Abrams, Alexander J., Dallman, Julia E., Züchner, Stephan
Publicat a PLoS One (2020)

Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism

per James, David M., Kozol, Robert A., Kajiwara, Yuji, Wahl, Adam L., Storrs, Emily C., Buxbaum, Joseph D., Klein, Mason, Moshiree, Baharak, Dallman, Julia E.
Publicat a Mol Autism (2019)

A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure

per Hung, Christina Y., Volkmar, Barbara, Baker, James D., Bauer, Johann W., Gussoni, Emanuela, Hainzl, Stefan, Klausegger, Alfred, Lorenzo, Jose, Mihalek, Ivana, Rittinger, Olaf, Tekin, Mustafa, Dallman, Julia E., Bodamer, Olaf A.
Publicat a PLoS One (2017)

Elevated preoptic brain activity in zebrafish glial glycine transporter mutants is linked to lethargy-like behaviors and delayed emergence from anesthesia

per Venincasa, Michael J., Randlett, Owen, Sumathipala, Sureni H., Bindernagel, Richard, Stark, Matthew J., Yan, Qing, Sloan, Steven A., Buglo, Elena, Meng, Qing Cheng, Engert, Florian, Züchner, Stephan, Kelz, Max B., Syed, Sheyum, Dallman, Julia E.
Publicat a Sci Rep (2021)

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

per 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.
Publicat a Hum Mol Genet (2015)

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

per 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
Publicat a Am J Hum Genet (2016)

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

per 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.
Publicat a Nat Genet (2015)