Glycinergic Synapse Development, Plasticity, and Homeostasis in Zebrafish

gan Ganser, Lisa R., Dallman, Julia E.
Cyhoeddwyd 2009

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

gan Dallman, Julia E, Davis, Anna K, Moody, William J
Cyhoeddwyd 1998

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

gan Dallman, Julia E, Dorman, Jennie B, Moody, William J
Cyhoeddwyd 2000

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

gan Yan, Qing, Zhai, Lu, Zhang, Bo, Dallman, Julia E.
Cyhoeddwyd yn J Comp Neurol (2017)

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

gan Dallman, Julia E., Allopenna, Janet, Bassett, Andrew, Travers, Andrew, Mandel, Gail
Cyhoeddwyd yn J Neurosci (2004)

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

gan James, David M., Davidson, Elizabeth A., Yanes, Julio, Moshiree, Baharak, Dallman, Julia E.
Cyhoeddwyd yn Front Cell Dev Biol (2021)

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

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

Synaptic Homeostasis in a Zebrafish Glial Glycine Transporter Mutant

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

Distinct phenotypes in zebrafish models of human startle disease()

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

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

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

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

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

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

gan 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.
Cyhoeddwyd yn PLoS One (2017)

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

gan 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.
Cyhoeddwyd yn 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

gan 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.
Cyhoeddwyd yn Hum Mol Genet (2015)

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

gan 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
Cyhoeddwyd yn Am J Hum Genet (2016)

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

gan 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.
Cyhoeddwyd yn Nat Genet (2015)