Robert Burgess - Publications

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84 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
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  1
2019 Tadenev ALD, Burgess RW. Model validity for preclinical studies in precision medicine: precisely how precise do we need to be? Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 30953144 DOI: 10.1007/s00335-019-09798-0  0.36
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  1
2017 Morelli KH, Seburn KL, Schroeder DG, Spaulding EL, Dionne LA, Cox GA, Burgess RW. Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes. Cell Reports. 18: 3178-3191. PMID 28355569 DOI: 10.1016/j.celrep.2017.03.009  1
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  1
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  1
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  1
2016 Spaulding EL, Sleigh JN, Morelli KH, Pinter MJ, Burgess RW, Seburn KL. Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2d. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 3254-67. PMID 26985035 DOI: 10.1523/JNEUROSCI.1762-15.2016  1
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  1
2015 Fernandes KA, Bloomsburg SJ, Miller CJ, Billingslea SA, Merrill MM, Burgess RW, Libby RT, Fuerst PG. Novel axon projection after stress and degeneration in the Dscam mutant retina. Molecular and Cellular Neurosciences. 71: 1-12. PMID 26691152 DOI: 10.1016/j.mcn.2015.12.003  1
2015 Tadenev AL, Lopez GC, Wray A, Fuerst PG, Burgess RW. The role of DSCAMs in neurodevelopment and visual function in the mouse. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 47: 91. PMID 26531571 DOI: 10.1016/j.ijdevneu.2015.04.248  1
2015 He W, Bai G, Zhou H, Wei N, White NM, Lauer J, Liu H, Shi Y, Dumitru CD, Lettieri K, Shubayev V, Jordanova A, Guergueltcheva V, Griffin PR, Burgess RW, et al. CMT2D neuropathy is linked to the neomorphic binding activity of glycyl-tRNA synthetase. Nature. 526: 710-4. PMID 26503042 DOI: 10.1038/nature15510  1
2015 Garrett AM, Burgess RW. Self-awareness in the retina. Elife. 4. PMID 26305501 DOI: 10.7554/eLife.10233  1
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  1
2015 Fairfield H, Srivastava A, Ananda G, Liu R, Kircher M, Lakshminarayana A, Harris BS, Karst SY, Dionne LA, Kane CC, Curtain M, Berry ML, Ward-Bailey PF, Greenstein I, Byers C, ... ... Burgess R, et al. Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders. Genome Research. 25: 948-57. PMID 25917818 DOI: 10.1101/gr.186882.114  1
2015 Ekins S, Litterman NK, Arnold RJ, Burgess RW, Freundlich JS, Gray SJ, Higgins JJ, Langley B, Willis DE, Notterpek L, Pleasure D, Sereda MW, Moore A. A brief review of recent Charcot-Marie-Tooth research and priorities. F1000research. 4: 53. PMID 25901280 DOI: 10.12688/f1000research.6160.1  1
2014 Tezuka T, Inoue A, Hoshi T, Weatherbee SD, Burgess RW, Ueta R, Yamanashi Y. The MuSK activator agrin has a separate role essential for postnatal maintenance of neuromuscular synapses. Proceedings of the National Academy of Sciences of the United States of America. 111: 16556-61. PMID 25368159 DOI: 10.1073/pnas.1408409111  1
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  1
2014 Sleigh JN, Burgess RW, Gillingwater TH, Cader MZ. Morphological analysis of neuromuscular junction development and degeneration in rodent lumbrical muscles. Journal of Neuroscience Methods. 227: 159-65. PMID 24530702 DOI: 10.1016/j.jneumeth.2014.02.005  1
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  1
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  1
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  1
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  1
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  1
2012 Keeley PW, Sliff BJ, Lee SC, Fuerst PG, Burgess RW, Eglen SJ, Reese BE. Neuronal clustering and fasciculation phenotype in Dscam- and Bax-deficient mouse retinas. The Journal of Comparative Neurology. 520: 1349-64. PMID 22396220 DOI: 10.1002/cne.23033  1
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  1
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  1
2012 Fuerst PG, Bruce F, Rounds RP, Erskine L, Burgess RW. Cell autonomy of DSCAM function in retinal development. Developmental Biology. 361: 326-37. PMID 22063212 DOI: 10.1016/j.ydbio.2011.10.028  1
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  1
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  1
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  1
2011 Rauch SM, Huen K, Miller MC, Chaudry H, Lau M, Sanes JR, Johanson CE, Stopa EG, Burgess RW. Changes in brain β-amyloid deposition and aquaporin 4 levels in response to altered agrin expression in mice. Journal of Neuropathology and Experimental Neurology. 70: 1124-37. PMID 22082664 DOI: 10.1097/NEN.0b013e31823b0b12  1
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  1
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  1
2011 Blank M, Fuerst PG, Stevens B, Nouri N, Kirkby L, Warrier D, Barres BA, Feller MB, Huberman AD, Burgess RW, Garner CC. The Down syndrome critical region regulates retinogeniculate refinement. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 5764-76. PMID 21490218 DOI: 10.1523/JNEUROSCI.6015-10.2011  1
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  1
2011 Kasischke KA, Lambert EM, Panepento B, Sun A, Gelbard HA, Burgess RW, Foster TH, Nedergaard M. Two-photon NADH imaging exposes boundaries of oxygen diffusion in cortical vascular supply regions. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 31: 68-81. PMID 20859293 DOI: 10.1038/jcbfm.2010.158  1
2010 Sproule TJ, Sled JG, Wentzell J, Wang B, Henkelman RM, Roopenian DC, Burgess RW. A mouse model of heritable cerebrovascular disease. Plos One. 5: e15327. PMID 21217823 DOI: 10.1371/journal.pone.0015327  1
2010 Burgess RW, Fuerst PG. Distinct expression patterns of mitochondrially localized YFP in neuronal subsets in the retina of three transgenic mouse lines. Bmc Research Notes. 3: 253. PMID 20925942 DOI: 10.1186/1756-0500-3-253  1
2010 Fuerst PG, Harris BS, Johnson KR, Burgess RW. A novel null allele of mouse DSCAM survives to adulthood on an inbred C3H background with reduced phenotypic variability. Genesis (New York, N.Y. : 2000). 48: 578-84. PMID 20715164 DOI: 10.1002/dvg.20662  1
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  1
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  1
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  1
2009 Fuerst PG, Burgess RW. Adhesion molecules in establishing retinal circuitry. Current Opinion in Neurobiology. 19: 389-94. PMID 19660931 DOI: 10.1016/j.conb.2009.07.013  1
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  1
2009 Wooley CM, Xing S, Burgess RW, Cox GA, Seburn KL. Age, experience and genetic background influence treadmill walking in mice. Physiology & Behavior. 96: 350-61. PMID 19027767 DOI: 10.1016/j.physbeh.2008.10.020  1
2009 Bogdanik L, Burgess RW. Extracellular matrix molecules in neuromuscular junctions and central nervous system synapses The Sticky Synapse: Cell Adhesion Molecules and Their Role in Synapse Formation and Maintenance. 397-422. DOI: 10.1007/978-0-387-92708-4_20  1
2008 Wolfram T, Spatz JP, Burgess RW. Cell adhesion to agrin presented as a nanopatterned substrate is consistent with an interaction with the extracellular matrix and not transmembrane adhesion molecules. Bmc Cell Biology. 9: 64. PMID 19055842 DOI: 10.1186/1471-2121-9-64  1
2008 Patton BL, Wang B, Tarumi YS, Seburn KL, Burgess RW. A single point mutation in the LN domain of LAMA2 causes muscular dystrophy and peripheral amyelination. Journal of Cell Science. 121: 1593-604. PMID 18430779 DOI: 10.1242/jcs.015354  1
2008 Fuerst PG, Koizumi A, Masland RH, Burgess RW. Neurite arborization and mosaic spacing in the mouse retina require DSCAM. Nature. 451: 470-4. PMID 18216855 DOI: 10.1038/nature06514  1
2007 Harvey SJ, Jarad G, Cunningham J, Rops AL, van der Vlag J, Berden JH, Moeller MJ, Holzman LB, Burgess RW, Miner JH. Disruption of glomerular basement membrane charge through podocyte-specific mutation of agrin does not alter glomerular permselectivity. The American Journal of Pathology. 171: 139-52. PMID 17591961 DOI: 10.2353/ajpath.2007.061116  1
2007 Misgeld T, Kerschensteiner M, Bareyre FM, Burgess RW, Lichtman JW. Imaging axonal transport of mitochondria in vivo. Nature Methods. 4: 559-61. PMID 17558414 DOI: 10.1038/nmeth1055  1
2007 Fuerst PG, Rauch SM, Burgess RW. Defects in eye development in transgenic mice overexpressing the heparan sulfate proteoglycan agrin. Developmental Biology. 303: 165-80. PMID 17196957 DOI: 10.1016/j.ydbio.2006.11.033  1
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  1
2006 Burgess RW, Jucius TJ, Ackerman SL. Motor axon guidance of the mammalian trochlear and phrenic nerves: dependence on the netrin receptor Unc5c and modifier loci. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 5756-66. PMID 16723533 DOI: 10.1523/JNEUROSCI.0736-06.2006  1
2006 Burgess RW. The formation of the vertebrate neuromuscular junction: Roles for the extracellular matrix in synaptogenesis Molecular Mechanisms of Synaptogenesis. 13-27. DOI: 10.1007/978-0-387-32562-0_2  1
2005 Stacy RC, Demas J, Burgess RW, Sanes JR, Wong RO. Disruption and recovery of patterned retinal activity in the absence of acetylcholine. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 9347-57. PMID 16221843 DOI: 10.1523/JNEUROSCI.1800-05.2005  1
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  1
2003 Buffelli M, Burgess RW, Feng G, Lobe CG, Lichtman JW, Sanes JR. Genetic evidence that relative synaptic efficacy biases the outcome of synaptic competition. Nature. 424: 430-4. PMID 12879071 DOI: 10.1038/nature01844  1
2003 Lunyak V, Burgess R, Noskin L, Giliano N. Use of modified chromosomal immunoprecipitation for isolation of actively transcribed loci Molekulyarnaya Biologiya. 37: 156-163. DOI: 10.1023/A:1022353317744  1
2002 Burgess R, Luniak V, Noskin L, Giliano N. Identification of two new p53 target genes through implementation of the modified chromatin immunoprecipitation method and inverse PCR | Identifikatsiia dvukh novykh genov-mishenei p53 s ispol'zovaniem modifitsirovannogo metoda immunopretsipitatsii khromatina i invertirovannoi PTsR Molekulyarnaya Biologiya. 36: 1035-1043. PMID 12500542  1
2002 Misgeld T, Burgess RW, Lewis RM, Cunningham JM, Lichtman JW, Sanes JR. Roles of neurotransmitter in synapse formation: development of neuromuscular junctions lacking choline acetyltransferase. Neuron. 36: 635-48. PMID 12441053 DOI: 10.1016/S0896-6273(02)01020-6  1
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  1
2002 Lunyak VV, Burgess R, Prefontaine GG, Nelson C, Sze SH, Chenoweth J, Schwartz P, Pevzner PA, Glass C, Mandel G, Rosenfeld MG. Corepressor-dependent silencing of chromosomal regions encoding neuronal genes. Science (New York, N.Y.). 298: 1747-52. PMID 12399542 DOI: 10.1126/science.1076469  1
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  1
2002 Burgess R, Lunyak V, Rosenfeld MG. Signaling and transcriptional control of pituitary development Current Opinion in Genetics and Development. 12: 534-539. PMID 12200158 DOI: 10.1016/S0959-437X(02)00337-4  1
2002 Burgess R, Lunyak V, Noskin L, Giliano N. Identification of two p53 target genes by modified chromosomal immunoprecipitation and inverse PCR Molecular Biology. 36: 841-848. DOI: 10.1023/A:1021690111207  1
2001 Lin W, Burgess RW, Dominguez B, Pfaff SL, Sanes JR, Lee KF. Distinct roles of nerve and muscle in postsynaptic differentiation of the neuromuscular synapse. Nature. 410: 1057-64. PMID 11323662 DOI: 10.1038/35074025  1
2001 Terrado J, Burgess RW, DeChiara T, Yancopoulos G, Sanes JR, Kato AC. Motoneuron survival is enhanced in the absence of neuromuscular junction formation in embryos. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 3144-50. PMID 11312299  1
2001 Treier M, O'Connell S, Gleiberman A, Price J, Szeto DP, Burgess R, Chuang PT, McMahon AP, Rosenfeld MG. Hedgehog signaling is required for pituitary gland development. Development (Cambridge, England). 128: 377-86. PMID 11152636  1
2000 Burgess RW, Skarnes WC, Sanes JR. Agrin isoforms with distinct amino termini: differential expression, localization, and function. The Journal of Cell Biology. 151: 41-52. PMID 11018052 DOI: 10.1083/jcb.151.1.41  1
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  1
1999 Burgess RW, Nguyen QT, Son YJ, Lichtman JW, Sanes JR. Alternatively spliced isoforms of nerve- and muscle-derived agrin: their roles at the neuromuscular junction. Neuron. 23: 33-44. PMID 10402191 DOI: 10.1016/S0896-6273(00)80751-5  1
1998 Sanes JR, Apel ED, Burgess RW, Emerson RB, Feng G, Gautam M, Glass D, Grady RM, Krejci E, Lichtman JW, Lu JT, Massoulié J, Miner JH, Moscoso LM, Nguyen Q, et al. Development of the neuromuscular junction: genetic analysis in mice. Journal of Physiology, Paris. 92: 167-72. PMID 9789802 DOI: 10.1016/S0928-4257(98)80004-1  1
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  1
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  1
1996 Burgess R, Rawls A, Brown D, Bradley A, Olson EN. Requirement of the paraxis gene for somite formation and musculoskeletal patterning Nature. 384: 570-573. PMID 8955271 DOI: 10.1038/384570a0  1
1996 Olson EN, Brown D, Burgess R, Cserjesi P. A new subclass of helix-loop-helix transcription factors expressed in paraxial mesoderm and chondrogenic cell lineages Annals of the New York Academy of Sciences. 785: 108-118. PMID 8702115  1
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  1
1995 Staudinger J, Zhou J, Burgess R, Elledge SJ, Olson EN. PICK1: A perinuclear binding protein and substrate for protein kinase C isolated by the yeast two-hybrid system Journal of Cell Biology. 128: 263-271. PMID 7844141 DOI: 10.1083/jcb.128.3.263  1
1995 Burgess R, Cserjesi P, Ligon KL, Olson EN. Paraxis: a basic helix-loop-helix protein expressed in paraxial mesoderm and developing somites. Developmental Biology. 168: 296-306. PMID 7729571 DOI: 10.1006/dbio.1995.1081  1
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  1
1993 Olson EN, Burgess R, Staudinger J. Protein kinase C as a transducer of nuclear signals Cell Growth & Differentiation : the Molecular Biology Journal of the American Association For Cancer Research. 4: 699-705. PMID 8398911  1
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  1
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