| Year |
Citation |
Score |
| 2024 |
Hanes CM, Mah KM, Steffen DM, Marcucci CG, Fuller LC, Burgess RW, Garrett AM, Weiner JA. A C-terminal motif containing a PKC phosphorylation site regulates γ-Protocadherin-mediated dendrite arborization in the cerebral cortex . Biorxiv : the Preprint Server For Biology. PMID 38328061 DOI: 10.1101/2024.01.25.577214 |
0.571 |
|
| 2023 |
Murray GC, Hines TJ, Tadenev ALD, Xu I, Züchner S, Burgess RW. Testing SIPA1L2 as a modifier of CMT1A using mouse models. Biorxiv : the Preprint Server For Biology. PMID 38076977 DOI: 10.1101/2023.11.30.569428 |
0.769 |
|
| 2023 |
Hines TJ, Bailey J, Liu H, Guntur AR, Seburn KL, Pratt SL, Funke JR, Tarantino LM, Burgess RW. A Novel ENU-Induced Mutation Causes Motor Deficits in Mice without Causing Peripheral Neuropathy. Biology. 12. PMID 37508383 DOI: 10.3390/biology12070953 |
0.76 |
|
| 2023 |
Murray GC, Bubier JA, Zinder OJ, Harris B, Clark J, Christopher MC, Hanley C, Tjong H, Li M, Ngan CY, Reinholdt L, Burgess RW, Tadenev ALD. An allelic series of spontaneous Rorb mutant mice exhibit a gait phenotype, changes in retina morphology and behavior, and gene expression signatures associated with the unfolded protein response. G3 (Bethesda, Md.). PMID 37300435 DOI: 10.1093/g3journal/jkad131 |
0.304 |
|
| 2023 |
Steffen DM, Hanes CM, Mah KM, Ramos PV, Bosch PJ, Hinz DC, Radley JJ, Burgess RW, Garrett AM, Weiner JA. A unique role for Protocadherin γC3 in promoting dendrite arborization through an Axin1-dependent mechanism. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 36604170 DOI: 10.1523/JNEUROSCI.0729-22.2022 |
0.751 |
|
| 2022 |
Martin PB, Holbrook SE, Hicks AN, Hines TJ, Bogdanik LP, Burgess RW, Cox GA. Clinically relevant mouse models of Charcot-Marie-Tooth Type 2S. Human Molecular Genetics. PMID 36413117 DOI: 10.1093/hmg/ddac283 |
0.784 |
|
| 2022 |
Peek SL, Bosch PJ, Bahl E, Iverson BJ, Parida M, Bais P, Manak JR, Michaelson JJ, Burgess RW, Weiner JA. p53-mediated neurodegeneration in the absence of the nuclear protein Akirin2. Iscience. 25: 103814. PMID 35198879 DOI: 10.1016/j.isci.2022.103814 |
0.554 |
|
| 2022 |
Hines TJ, Lutz C, Murray SA, Burgess RW. An Integrated Approach to Studying Rare Neuromuscular Diseases Using Animal and Human Cell-Based Models. Frontiers in Cell and Developmental Biology. 9: 801819. PMID 35047510 DOI: 10.3389/fcell.2021.801819 |
0.757 |
|
| 2021 |
Hines TJ, Tadenev ALD, Lone MA, Hatton CL, Bagasrawala I, Stum MG, Miers KE, Hornemann T, Burgess RW. Precision mouse models of Yars/dominant intermediate Charcot-Marie-Tooth disease type C and Sptlc1/hereditary sensory and autonomic neuropathy type 1. Journal of Anatomy. PMID 34875719 DOI: 10.1111/joa.13605 |
0.719 |
|
| 2021 |
Presa M, Bailey RM, Davis C, Murphy T, Cook J, Walls R, Wilpan H, Bogdanik L, Lenk GM, Burgess RW, Gray SJ, Lutz C. AAV9-mediated FIG4 delivery prolongs life span in Charcot Marie Tooth disease type 4J mouse model. The Journal of Clinical Investigation. PMID 33878035 DOI: 10.1172/JCI137159 |
0.348 |
|
| 2021 |
Stum MG, Tadenev ALD, Seburn KL, Miers KE, Poon PP, McMaster CR, Robinson C, Kane C, Silva KA, Cliften PF, Sundberg JP, Reinholdt LG, John SWM, Burgess RW. Genetic analysis of Pycr1 and Pycr2 in mice. Genetics. PMID 33734376 DOI: 10.1093/genetics/iyab048 |
0.318 |
|
| 2020 |
Racine JJ, Chapman HD, Doty R, Cairns BM, Hines TJ, Tadenev ALD, Anderson LC, Green T, Dyer ME, Wotton JM, Bichler Z, White JK, Ettinger R, Burgess RW, Serreze DV. T Cells from NOD- Mice Target Both Pancreatic and Neuronal Tissue. Journal of Immunology (Baltimore, Md. : 1950). PMID 32938729 DOI: 10.4049/Jimmunol.2000114 |
0.751 |
|
| 2019 |
Garrett AM, Bosch PJ, Steffen DM, Fuller LC, Marcucci CG, Koch AA, Bais P, Weiner JA, Burgess RW. CRISPR/Cas9 interrogation of the mouse Pcdhg gene cluster reveals a crucial isoform-specific role for Pcdhgc4. Plos Genetics. 15: e1008554. PMID 31877124 DOI: 10.1371/Journal.Pgen.1008554 |
0.742 |
|
| 2019 |
Morelli KH, Griffin LB, Pyne NK, Wallace LM, Fowler AM, Oprescu SN, Takase R, Wei N, Meyer-Schuman R, Mellacheruvu D, Kitzman JO, Kocen SG, Hines TJ, Spaulding EL, Lupski JR, ... ... Burgess RW, et al. Allele-specific RNA interference prevents neuropathy in Charcot-Marie-Tooth disease type 2D mouse models. The Journal of Clinical Investigation. PMID 31557132 DOI: 10.1172/Jci130600 |
0.769 |
|
| 2018 |
Garrett AM, Khalil A, Walton DO, Burgess RW. DSCAM promotes self-avoidance in the developing mouse retina by masking the functions of cadherin superfamily members. Proceedings of the National Academy of Sciences of the United States of America. PMID 30297418 DOI: 10.1073/Pnas.1809430115 |
0.665 |
|
| 2017 |
Sleigh JN, Dawes JM, West SJ, Wei N, Spaulding EL, Gómez-Martín A, Zhang Q, Burgess RW, Cader MZ, Talbot K, Yang XL, Bennett DL, Schiavo G. Trk receptor signaling and sensory neuron fate are perturbed in human neuropathy caused by Gars mutations. Proceedings of the National Academy of Sciences of the United States of America. PMID 28351971 DOI: 10.1073/Pnas.1614557114 |
0.335 |
|
| 2016 |
Garrett AM, Tadenev AL, Hammond YT, Fuerst PG, Burgess RW. Replacing the PDZ-interacting C-termini of DSCAM and DSCAML1 with epitope tags causes different phenotypic severity in different cell populations. Elife. 5. PMID 27637097 DOI: 10.7554/Elife.16144 |
0.68 |
|
| 2016 |
Bais P, Beebe K, Morelli KH, Currie ME, Norberg SN, Evsikov AV, Miers KE, Seburn KL, Guergueltcheva V, Kremensky I, Jordanova A, Bult CJ, Burgess RW. Metabolite profile of a mouse model of Charcot-Marie-Tooth type 2D neuropathy: implications for disease mechanisms and interventions. Biology Open. PMID 27288508 DOI: 10.1242/Bio.019273 |
0.311 |
|
| 2016 |
Burgess RW, Cox GA, Seburn KL. Neuromuscular Disease Models and Analysis. Methods in Molecular Biology (Clifton, N.J.). 1438: 349-94. PMID 27150099 DOI: 10.1007/978-1-4939-3661-8_19 |
0.323 |
|
| 2016 |
Garrett AM, Jucius TJ, Sigaud LP, Tang FL, Xiong WC, Ackerman SL, Burgess RW. Analysis of Expression Pattern and Genetic Deletion of Netrin5 in the Developing Mouse. Frontiers in Molecular Neuroscience. 9: 3. PMID 26858598 DOI: 10.3389/Fnmol.2016.00003 |
0.694 |
|
| 2015 |
Garrett AM, Burgess RW. Self-awareness in the retina. Elife. 4. PMID 26305501 DOI: 10.7554/Elife.10233 |
0.652 |
|
| 2015 |
Niehues S, Bussmann J, Steffes G, Erdmann I, Köhrer C, Sun L, Wagner M, Schäfer K, Wang G, Koerdt SN, Stum M, RajBhandary UL, Thomas U, Aberle H, Burgess RW, et al. Impaired protein translation in Drosophila models for Charcot-Marie-Tooth neuropathy caused by mutant tRNA synthetases. Nature Communications. 6: 7520. PMID 26138142 DOI: 10.1038/Ncomms8520 |
0.317 |
|
| 2015 |
Grice SJ, Sleigh JN, Motley WW, Liu JL, Burgess RW, Talbot K, Cader MZ. Dominant, toxic gain-of-function mutations in gars lead to non-cell autonomous neuropathology. Human Molecular Genetics. 24: 4397-406. PMID 25972375 DOI: 10.1093/Hmg/Ddv176 |
0.339 |
|
| 2014 |
Seburn KL, Morelli KH, Jordanova A, Burgess RW. Lack of neuropathy-related phenotypes in hint1 knockout mice. Journal of Neuropathology and Experimental Neurology. 73: 693-701. PMID 24918641 DOI: 10.1097/Nen.0000000000000085 |
0.331 |
|
| 2014 |
Sleigh JN, Grice SJ, Burgess RW, Talbot K, Cader MZ. Neuromuscular junction maturation defects precede impaired lower motor neuron connectivity in Charcot-Marie-Tooth type 2D mice. Human Molecular Genetics. 23: 2639-50. PMID 24368416 DOI: 10.1093/Hmg/Ddt659 |
0.358 |
|
| 2013 |
Weiner JA, Jontes JD, Burgess RW. Introduction to mechanisms of neural circuit formation. Frontiers in Molecular Neuroscience. 6: 12. PMID 23717261 DOI: 10.3389/Fnmol.2013.00012 |
0.566 |
|
| 2013 |
Bogdanik LP, Sleigh JN, Tian C, Samuels ME, Bedard K, Seburn KL, Burgess RW. Loss of the E3 ubiquitin ligase LRSAM1 sensitizes peripheral axons to degeneration in a mouse model of Charcot-Marie-Tooth disease. Disease Models & Mechanisms. 6: 780-92. PMID 23519028 DOI: 10.1242/Dmm.010942 |
0.372 |
|
| 2012 |
Schramm RD, Li S, Harris BS, Rounds RP, Burgess RW, Ytreberg FM, Fuerst PG. A novel mouse Dscam mutation inhibits localization and shedding of DSCAM. Plos One. 7: e52652. PMID 23300735 DOI: 10.1371/Journal.Pone.0052652 |
0.332 |
|
| 2012 |
Garrett AM, Tadenev AL, Burgess RW. DSCAMs: restoring balance to developmental forces. Frontiers in Molecular Neuroscience. 5: 86. PMID 22912601 DOI: 10.3389/Fnmol.2012.00086 |
0.652 |
|
| 2012 |
Bogdanik LP, Chapman HD, Miers KE, Serreze DV, Burgess RW. A MusD retrotransposon insertion in the mouse Slc6a5 gene causes alterations in neuromuscular junction maturation and behavioral phenotypes. Plos One. 7: e30217. PMID 22272310 DOI: 10.1371/journal.pone.0030217 |
0.317 |
|
| 2012 |
Burgess RW, Garrett AM, Tadenev AL. Contact is repulsive, but please note the "enclosed". Developmental Cell. 22: 5-6. PMID 22264725 DOI: 10.1016/J.Devcel.2011.12.017 |
0.645 |
|
| 2012 |
Maue RA, Burgess RW, Wang B, Wooley CM, Seburn KL, Vanier MT, Rogers MA, Chang CC, Chang TY, Harris BT, Graber DJ, Penatti CA, Porter DM, Szwergold BS, Henderson LP, et al. A novel mouse model of Niemann-Pick type C disease carrying a D1005G-Npc1 mutation comparable to commonly observed human mutations. Human Molecular Genetics. 21: 730-50. PMID 22048958 DOI: 10.1093/Hmg/Ddr505 |
0.329 |
|
| 2011 |
Davisson MT, Bronson RT, Tadenev AL, Motley WW, Krishnaswamy A, Seburn KL, Burgess RW. A spontaneous mutation in contactin 1 in the mouse. Plos One. 6: e29538. PMID 22242131 DOI: 10.1371/Journal.Pone.0029538 |
0.36 |
|
| 2011 |
Motley WW, Seburn KL, Nawaz MH, Miers KE, Cheng J, Antonellis A, Green ED, Talbot K, Yang XL, Fischbeck KH, Burgess RW. Charcot-Marie-Tooth-linked mutant GARS is toxic to peripheral neurons independent of wild-type GARS levels. Plos Genetics. 7: e1002399. PMID 22144914 DOI: 10.1371/Journal.Pgen.1002399 |
0.331 |
|
| 2011 |
Bogdanik LP, Burgess RW. A valid mouse model of AGRIN-associated congenital myasthenic syndrome. Human Molecular Genetics. 20: 4617-33. PMID 21890498 DOI: 10.1093/hmg/ddr396 |
0.344 |
|
| 2011 |
Garrett AM, Burgess RW. Candidate molecular mechanisms for establishing cell identity in the developing retina. Developmental Neurobiology. 71: 1258-72. PMID 21630473 DOI: 10.1002/Dneu.20926 |
0.682 |
|
| 2011 |
Stum M, McLaughlin HM, Kleinbrink EL, Miers KE, Ackerman SL, Seburn KL, Antonellis A, Burgess RW. An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations. Molecular and Cellular Neurosciences. 46: 432-43. PMID 21115117 DOI: 10.1016/J.Mcn.2010.11.006 |
0.334 |
|
| 2010 |
Burgess RW, Cox GA, Seburn KL. Neuromuscular disease models and analysis. Methods in Molecular Biology (Clifton, N.J.). 602: 347-93. PMID 20012408 DOI: 10.1007/978-1-60761-058-8_20 |
0.323 |
|
| 2009 |
Graf ER, Daniels RW, Burgess RW, Schwarz TL, DiAntonio A. Rab3 dynamically controls protein composition at active zones. Neuron. 64: 663-77. PMID 20005823 DOI: 10.1016/j.neuron.2009.11.002 |
0.605 |
|
| 2009 |
Fuerst PG, Bruce F, Tian M, Wei W, Elstrott J, Feller MB, Erskine L, Singer JH, Burgess RW. DSCAM and DSCAML1 function in self-avoidance in multiple cell types in the developing mouse retina. Neuron. 64: 484-97. PMID 19945391 DOI: 10.1016/J.Neuron.2009.09.027 |
0.307 |
|
| 2009 |
Achilli F, Bros-Facer V, Williams HP, Banks GT, AlQatari M, Chia R, Tucci V, Groves M, Nickols CD, Seburn KL, Kendall R, Cader MZ, Talbot K, van Minnen J, Burgess RW, et al. An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy. Disease Models & Mechanisms. 2: 359-73. PMID 19470612 DOI: 10.1242/Dmm.002527 |
0.336 |
|
| 2006 |
Seburn KL, Nangle LA, Cox GA, Schimmel P, Burgess RW. An active dominant mutation of glycyl-tRNA synthetase causes neuropathy in a Charcot-Marie-Tooth 2D mouse model. Neuron. 51: 715-26. PMID 16982418 DOI: 10.1016/J.Neuron.2006.08.027 |
0.35 |
|
| 2004 |
Burgess RW, Peterson KA, Johnson MJ, Roix JJ, Welsh IC, O'Brien TP. Evidence for a conserved function in synapse formation reveals Phr1 as a candidate gene for respiratory failure in newborn mice. Molecular and Cellular Biology. 24: 1096-105. PMID 14729956 DOI: 10.1128/MCB.24.3.1096-1105.2004 |
0.334 |
|
| 2002 |
Burgess RW, Dickman DK, Nunez L, Glass DJ, Sanes JR. Mapping sites responsible for interactions of agrin with neurons. Journal of Neurochemistry. 83: 271-84. PMID 12423238 DOI: 10.1046/j.1471-4159.2002.01102.x |
0.66 |
|
| 2002 |
Bhattacharya S, Stewart BA, Niemeyer BA, Burgess RW, McCabe BD, Lin P, Boulianne G, O'Kane CJ, Schwarz TL. Members of the synaptobrevin/vesicle-associated membrane protein (VAMP) family in Drosophila are functionally interchangeable in vivo for neurotransmitter release and cell viability. Proceedings of the National Academy of Sciences of the United States of America. 99: 13867-72. PMID 12364587 DOI: 10.1073/pnas.202335999 |
0.625 |
|
| 1999 |
Usui T, Shima Y, Shimada Y, Hirano S, Burgess RW, Schwarz TL, Takeichi M, Uemura T. Flamingo, a seven-pass transmembrane cadherin, regulates planar cell polarity under the control of Frizzled. Cell. 98: 585-95. PMID 10490098 DOI: 10.1016/S0092-8674(00)80046-X |
0.361 |
|
| 1998 |
Deitcher DL, Ueda A, Stewart BA, Burgess RW, Kidokoro Y, Schwarz TL. Distinct requirements for evoked and spontaneous release of neurotransmitter are revealed by mutations in the Drosophila gene neuronal-synaptobrevin. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 2028-39. PMID 9482790 DOI: 10.1523/Jneurosci.18-06-02028.1998 |
0.619 |
|
| 1997 |
Burgess RW, Deitcher DL, Schwarz TL. The synaptic protein syntaxin1 is required for cellularization of Drosophila embryos. The Journal of Cell Biology. 138: 861-75. PMID 9265652 DOI: 10.1083/jcb.138.4.861 |
0.417 |
|
| 1995 |
Parfitt K, Reist N, Li J, Burgess R, Deitcher D, DiAntonio A, Schwarz TL. Drosophila genetics and the functions of synaptic proteins. Cold Spring Harbor Symposia On Quantitative Biology. 60: 371-7. PMID 8824410 DOI: 10.1101/Sqb.1995.060.01.041 |
0.636 |
|
| 1993 |
Chin AC, Burgess RW, Wong BR, Schwarz TL, Scheller RH. Differential expression of transcripts from syb, a Drosophila melanogaster gene encoding VAMP (synaptobrevin) that is abundant in non-neuronal cells. Gene. 131: 175-81. PMID 8406010 DOI: 10.1016/0378-1119(93)90291-A |
0.422 |
|
| 1993 |
DiAntonio A, Burgess RW, Chin AC, Deitcher DL, Scheller RH, Schwarz TL. Identification and characterization of Drosophila genes for synaptic vesicle proteins. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 13: 4924-35. PMID 8229205 DOI: 10.1523/Jneurosci.13-11-04924.1993 |
0.673 |
|
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