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Julia Dallman
Julia Dallman
Verified email at bio.miami.edu
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Cited by
Year
CoREST: a functional corepressor required for regulation of neural-specific gene expression
ME Andrés, C Burger, MJ Peral-Rubio, E Battaglioli, ME Anderson, ...
Proceedings of the National Academy of Sciences 96 (17), 9873-9878, 1999
5761999
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder
AJ Abrams, RB Hufnagel, A Rebelo, C Zanna, N Patel, MA Gonzalez, ...
Nature genetics 47 (8), 926-932, 2015
2052015
Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa
S Züchner, J Dallman, R Wen, G Beecham, A Naj, A Farooq, MA Kohli, ...
The American Journal of Human Genetics 88 (2), 201-206, 2011
1892011
Crossing the blood–brain–barrier with transferrin conjugated carbon dots: A zebrafish model study
S Li, Z Peng, J Dallman, J Baker, AM Othman, PL Blackwelder, ...
Colloids and Surfaces B: Biointerfaces 145, 251-256, 2016
1292016
Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss
KO Yariz, D Duman, CZ Seco, J Dallman, M Huang, TA Peters, A Sirmaci, ...
The American Journal of Human Genetics 91 (5), 872-882, 2012
1222012
Translocation of CaM kinase II to synaptic sites in vivo
MR Gleason, S Higashijima, J Dallman, K Liu, G Mandel, JR Fetcho
Nature neuroscience 6 (3), 217-218, 2003
1092003
Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes
A Cortese, Y Zhu, AP Rebelo, S Negri, S Courel, L Abreu, CJ Bacon, ...
Nature genetics 52 (5), 473-481, 2020
1082020
Function over form: modeling groups of inherited neurological conditions in zebrafish
RA Kozol, AJ Abrams, DM James, E Buglo, Q Yan, JE Dallman
Frontiers in molecular neuroscience 9, 55, 2016
1002016
Tryptophan carbon dots and their ability to cross the blood-brain barrier
KJ Mintz, G Mercado, Y Zhou, Y Ji, SD Hettiarachchi, PY Liyanage, ...
Colloids and Surfaces B: Biointerfaces 176, 488-493, 2019
872019
Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of …
RA Kozol, HN Cukier, B Zou, V Mayo, S De Rubeis, G Cai, AJ Griswold, ...
Human molecular genetics 24 (14), 4006-4023, 2015
822015
A conserved role but different partners for the transcriptional corepressor CoREST in fly and mammalian nervous system formation
JE Dallman, J Allopenna, A Bassett, A Travers, G Mandel
Journal of Neuroscience 24 (32), 7186-7193, 2004
722004
Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism
DM James, RA Kozol, Y Kajiwara, AL Wahl, EC Storrs, JD Buxbaum, ...
Molecular autism 10, 1-15, 2019
592019
Cryptic amyloidogenic elements in the 3′ UTRs of neurofilament genes trigger axonal neuropathy
AP Rebelo, AJ Abrams, E Cottenie, A Horga, M Gonzalez, DM Bis, ...
The American Journal of Human Genetics 98 (4), 597-614, 2016
592016
Mutations in RIT1 cause Noonan syndrome – additional functional evidence and expanding the clinical phenotype
M Koenighofer, CY Hung, JL McCauley, J Dallman, EJ Back, I Mihalek, ...
Clinical genetics 89 (3), 359-366, 2016
532016
Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease
E Buglo, E Sarmiento, NB Martuscelli, DW Sant, MC Danzi, AJ Abrams, ...
PloS one 15 (3), e0230566, 2020
522020
“Dark” carbon dots specifically “light-up” calcified zebrafish bones
S Li, I Skromne, Z Peng, J Dallman, AO Al-Youbi, AS Bashammakh, ...
Journal of materials chemistry B 4 (46), 7398-7405, 2016
522016
Zebrafish calls for reinterpretation for the roles of P/Q calcium channels in neuromuscular transmission
H Wen, MW Linhoff, JM Hubbard, NR Nelson, D Stensland, J Dallman, ...
Journal of Neuroscience 33 (17), 7384-7392, 2013
352013
Spontaneous activity regulates calcium‐dependent K+ current expression in developing ascidian muscle
JE Dallman, AK Davis, WJ Moody
The Journal of physiology 511 (3), 683-693, 1998
351998
Synaptic homeostasis in a zebrafish glial glycine transporter mutant
R Mongeon, MR Gleason, MA Masino, JR Fetcho, G Mandel, P Brehm, ...
Journal of neurophysiology 100 (4), 1716-1723, 2008
322008
Persistent Electrical Coupling and Locomotory Dysfunction in the Zebrafish Mutant shocked
VM Luna, M Wang, F Ono, MR Gleason, JE Dallman, G Mandel, P Brehm
Journal of neurophysiology 92 (4), 2003-2009, 2004
262004
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