Julia E. Dallman - Publications

University of Miami, Coral Gables, FL 
Developmental neuroscience

31 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Kozol RA, James DM, Varela I, Sumathipala SH, Züchner S, Dallman JE. Restoring Shank3 in the rostral brainstem of shank3ab-/- zebrafish autism models rescues sensory deficits. Communications Biology. 4: 1411. PMID 34921227 DOI: 10.1038/s42003-021-02920-6  0.79
2021 James DM, Davidson EA, Yanes J, Moshiree B, Dallman JE. The Gut-Brain-Microbiome Axis and Its Link to Autism: Emerging Insights and the Potential of Zebrafish Models. Frontiers in Cell and Developmental Biology. 9: 662916. PMID 33937265 DOI: 10.3389/fcell.2021.662916  0.757
2021 Venincasa MJ, Randlett O, Sumathipala SH, Bindernagel R, Stark MJ, Yan Q, Sloan SA, Buglo E, Meng QC, Engert F, Züchner S, Kelz MB, Syed S, Dallman JE. Elevated preoptic brain activity in zebrafish glial glycine transporter mutants is linked to lethargy-like behaviors and delayed emergence from anesthesia. Scientific Reports. 11: 3148. PMID 33542258 DOI: 10.1038/s41598-021-82342-w  0.778
2020 Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA, ... ... Dallman J, et al. Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. Nature Genetics. PMID 32457452 DOI: 10.1038/S41588-020-0649-7  0.754
2020 Cortese A, Zhu Y, Rebelo AP, Negri S, Courel S, Abreu L, Bacon CJ, Bai Y, Bis-Brewer DM, Bugiardini E, Buglo E, Danzi MC, Feely SME, Athanasiou-Fragkouli A, Haridy NA, ... ... Dallman J, et al. Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes. Nature Genetics. PMID 32367058 DOI: 10.1038/S41588-020-0615-4  0.776
2020 Buglo E, Sarmiento E, Martuscelli NB, Sant DW, Danzi MC, Abrams AJ, Dallman JE, Züchner S. Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease. Plos One. 15: e0230566. PMID 32208444 DOI: 10.1371/Journal.Pone.0230566  0.788
2019 James DM, Kozol RA, Kajiwara Y, Wahl AL, Storrs EC, Buxbaum JD, Klein M, Moshiree B, Dallman JE. Intestinal dysmotility in a zebrafish () mutant model of autism. Molecular Autism. 10: 3. PMID 30733854 DOI: 10.1186/S13229-018-0250-4  0.772
2018 Bedell V, Buglo E, Marcato D, Pylatiuk C, Mikut R, Stegmaier J, Scudder W, Wray M, Züchner S, Strähle U, Peravali R, Dallman JE. Zebrafish: A Pharmacogenetic Model for Anesthesia. Methods in Enzymology. 602: 189-209. PMID 29588029 DOI: 10.1016/Bs.Mie.2018.02.004  0.768
2017 Hung CY, Volkmar B, Baker JD, Bauer JW, Gussoni E, Hainzl S, Klausegger A, Lorenzo J, Mihalek I, Rittinger O, Tekin M, Dallman JE, Bodamer OA. A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure. Plos One. 12: e0189324. PMID 29228025 DOI: 10.1371/Journal.Pone.0189324  0.347
2016 Yan Q, Zhai L, Zhang B, Dallman JE. Spatial patterning of excitatory and inhibitory neuropil territories during spinal circuit development. The Journal of Comparative Neurology. PMID 27997694 DOI: 10.1002/Cne.24152  0.603
2016 Kozol RA, Abrams AJ, James DM, Buglo E, Yan Q, Dallman JE. Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish. Frontiers in Molecular Neuroscience. 9: 55. PMID 27458342 DOI: 10.3389/Fnmol.2016.00055  0.763
2016 Rebelo AP, Abrams AJ, Cottenie E, Horga A, Gonzalez M, Bis DM, Sanchez-Mejias A, Pinto M, Buglo E, Markel K, Prince J, Laura M, Houlden H, Blake J, Woodward C, ... ... Dallman JE, et al. Cryptic Amyloidogenic Elements in the 3' UTRs of Neurofilament Genes Trigger Axonal Neuropathy. American Journal of Human Genetics. PMID 27040688 DOI: 10.1016/J.Ajhg.2016.02.022  0.775
2015 Abrams AJ, Hufnagel RB, Rebelo A, Zanna C, Patel N, Gonzalez MA, Campeanu IJ, Griffin LB, Groenewald S, Strickland AV, Tao F, Speziani F, Abreu L, Schüle R, Caporali L, ... ... Dallman JE, et al. Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder. Nature Genetics. 47: 926-32. PMID 26168012 DOI: 10.1038/Ng.3354  0.601
2015 Koenighofer M, Hung CY, McCauley JL, Dallman J, Back EJ, Mihalek I, Gripp KW, Sol-Church K, Rusconi P, Zhang Z, Shi GX, Andres DA, Bodamer OA. Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype. Clinical Genetics. PMID 25959749 DOI: 10.1111/Cge.12608  0.462
2015 Kozol RA, Cukier HN, Zou B, Mayo V, De Rubeis S, Cai G, Griswold AJ, Whitehead PL, Haines JL, Gilbert JR, Cuccaro ML, Martin ER, Baker JD, Buxbaum JD, Pericak-Vance MA, ... Dallman JE, et al. 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. PMID 25882707 DOI: 10.1093/Hmg/Ddv138  0.76
2014 Wen R, Dallman JE, Li Y, Züchner SL, Vance JM, Peričak-Vance MA, Lam BL. Knock-down DHDDS expression induces photoreceptor degeneration in zebrafish. Advances in Experimental Medicine and Biology. 801: 543-50. PMID 24664742 DOI: 10.1007/978-1-4614-3209-8_69  0.429
2014 Lam BL, Züchner SL, Dallman J, Wen R, Alfonso EC, Vance JM, Peričak-Vance MA. Mutation K42E in dehydrodolichol diphosphate synthase (DHDDS) causes recessive retinitis pigmentosa. Advances in Experimental Medicine and Biology. 801: 165-70. PMID 24664694 DOI: 10.1007/978-1-4614-3209-8_21  0.325
2013 Ganser LR, Yan Q, James VM, Kozol R, Topf M, Harvey RJ, Dallman JE. Distinct phenotypes in zebrafish models of human startle disease. Neurobiology of Disease. 60: 139-51. PMID 24029548 DOI: 10.1016/J.Nbd.2013.09.002  0.747
2013 Wen H, Linhoff MW, Hubbard JM, Nelson NR, Stensland D, Dallman J, Mandel G, Brehm P. Zebrafish calls for reinterpretation for the roles of P/Q calcium channels in neuromuscular transmission. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 7384-92. PMID 23616544 DOI: 10.1523/Jneurosci.5839-12.2013  0.741
2012 Yariz KO, Duman D, Seco CZ, Dallman J, Huang M, Peters TA, Sirmaci A, Lu N, Schraders M, Skromne I, Oostrik J, Diaz-Horta O, Young JI, Tokgoz-Yilmaz S, Konukseven O, et al. Mutations in OTOGL, encoding the inner ear protein otogelin-like, cause moderate sensorineural hearing loss. American Journal of Human Genetics. 91: 872-82. PMID 23122586 DOI: 10.1016/J.Ajhg.2012.09.011  0.334
2011 Züchner S, Dallman J, Wen R, Beecham G, Naj A, Farooq A, Kohli MA, Whitehead PL, Hulme W, Konidari I, Edwards YJ, Cai G, Peter I, Seo D, Buxbaum JD, et al. Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa. American Journal of Human Genetics. 88: 201-6. PMID 21295283 DOI: 10.1016/J.Ajhg.2011.01.001  0.349
2009 Ganser LR, Dallman JE. Glycinergic synapse development, plasticity, and homeostasis in zebrafish. Frontiers in Molecular Neuroscience. 2: 30. PMID 20126315 DOI: 10.3389/Neuro.02.030.2009  0.761
2008 Mongeon R, Gleason MR, Masino MA, Fetcho JR, Mandel G, Brehm P, Dallman JE. Synaptic homeostasis in a zebrafish glial glycine transporter mutant. Journal of Neurophysiology. 100: 1716-23. PMID 18715895 DOI: 10.1152/Jn.90596.2008  0.75
2004 Dallman JE, Allopenna J, Bassett A, Travers A, Mandel G. 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. PMID 15306652 DOI: 10.1523/Jneurosci.0238-04.2004  0.618
2004 Luna VM, Wang M, Ono F, Gleason MR, Dallman JE, Mandel G, Brehm P. Persistent electrical coupling and locomotory dysfunction in the zebrafish mutant shocked. Journal of Neurophysiology. 92: 2003-9. PMID 15201312 DOI: 10.1152/Jn.00454.2004  0.734
2003 Gleason MR, Higashijima S, Dallman J, Liu K, Mandel G, Fetcho JR. Translocation of CaM kinase II to synaptic sites in vivo. Nature Neuroscience. 6: 217-8. PMID 12563265 DOI: 10.1038/Nn1011  0.761
2000 Dallman JE, Dorman JB, Moody WJ. Action potential waveform voltage clamp shows significance of different Ca2+ channel types in developing ascidian muscle. The Journal of Physiology. 524: 375-86. PMID 10766919 DOI: 10.1111/J.1469-7793.2000.T01-1-00375.X  0.573
1999 Andrés ME, Burger C, Peral-Rubio MJ, Battaglioli E, Anderson ME, Grimes J, Dallman J, Ballas N, Mandel G. CoREST: a functional corepressor required for regulation of neural-specific gene expression. Proceedings of the National Academy of Sciences of the United States of America. 96: 9873-8. PMID 10449787 DOI: 10.1073/Pnas.96.17.9873  0.686
1998 Dallman JE, Davis AK, Moody WJ. Spontaneous activity regulates calcium-dependent K+ current expression in developing ascidian muscle. The Journal of Physiology. 511: 683-93. PMID 9714852 DOI: 10.1111/J.1469-7793.1998.683Bg.X  0.579
1996 Greaves AA, Davis AK, Dallman JE, Moody WJ. Co-ordinated modulation of Ca2+ and K+ currents during ascidian muscle development. The Journal of Physiology. 497: 39-52. PMID 8951710 DOI: 10.1113/Jphysiol.1996.Sp021748  0.564
1995 Davis A, Greaves A, Dallman J, Moody W. Comparison of ionic currents expressed in immature and mature muscle cells of an ascidian larva The Journal of Neuroscience. 15: 4875-4884. DOI: 10.1523/Jneurosci.15-07-04875.1995  0.577
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