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

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

Por Yan, Qing, Zhai, Lu, Zhang, Bo, Dallman, Julia E.
Publicado no J Comp Neurol (2017)

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

Por Dallman, Julia E., Allopenna, Janet, Bassett, Andrew, Travers, Andrew, Mandel, Gail
Publicado no J Neurosci (2004)

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

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

Por Buglo, Elena, Sarmiento, Evan, Martuscelli, Nicole Belliard, Sant, David W., Danzi, Matt C., Abrams, Alexander J., Dallman, Julia E., Züchner, Stephan
Publicado no PLoS One (2020)

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

Por James, David M., Kozol, Robert A., Kajiwara, Yuji, Wahl, Adam L., Storrs, Emily C., Buxbaum, Joseph D., Klein, Mason, Moshiree, Baharak, Dallman, Julia E.
Publicado no Mol Autism (2019)

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

Por 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.
Publicado no PLoS One (2017)

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

Por 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.
Publicado no 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

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)