Julia E. Dallman

University of Miami, Coral Gables, FL 
Developmental neuroscience
"Julia Dallman"
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Rebelo AP, Abrams AJ, Cottenie E, et al. (2016) Cryptic Amyloidogenic Elements in the 3' UTRs of Neurofilament Genes Trigger Axonal Neuropathy. American Journal of Human Genetics
Abrams AJ, Hufnagel RB, Rebelo A, et al. (2015) Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nature Genetics. 47: 926-32
Kozol RA, Cukier HN, Zou B, et al. (2015) Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis. Human Molecular Genetics. 24: 4006-23
Wen R, Dallman JE, Li Y, et al. (2014) Knock-down DHDDS expression induces photoreceptor degeneration in zebrafish. Advances in Experimental Medicine and Biology. 801: 543-50
Mongeon R, Gleason MR, Masino MA, et al. (2008) Synaptic homeostasis in a zebrafish glial glycine transporter mutant. Journal of Neurophysiology. 100: 1716-23
Dallman JE, Allopenna J, Bassett A, et al. (2004) A conserved role but different partners for the transcriptional corepressor CoREST in fly and mammalian nervous system formation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 7186-93
Luna VM, Wang M, Ono F, et al. (2004) Persistent electrical coupling and locomotory dysfunction in the zebrafish mutant shocked. Journal of Neurophysiology. 92: 2003-9
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