Todd McLaughlin - Publications

Affiliations: 
Salk Institute for Biological Studies, La Jolla, CA, United States 

21 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
2014 McLaughlin T, Lim YS, Santiago A, O'Leary DD. Multiple EphB receptors mediate dorsal-ventral retinotopic mapping via similar bi-functional responses to ephrin-B1. Molecular and Cellular Neurosciences. 63: 24-30. PMID 25051176 DOI: 10.1016/J.Mcn.2014.05.005  0.663
2014 Olsen O, Kallop DY, McLaughlin T, Huntwork-Rodriguez S, Wu Z, Duggan CD, Simon DJ, Lu Y, Easley-Neal C, Takeda K, Hass PE, Jaworski A, O'Leary DD, Weimer RM, Tessier-Lavigne M. Genetic analysis reveals that amyloid precursor protein and death receptor 6 function in the same pathway to control axonal pruning independent of β-secretase. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 6438-47. PMID 24806670 DOI: 10.1523/Jneurosci.3522-13.2014  0.643
2012 Simon DJ, Weimer RM, McLaughlin T, Kallop D, Stanger K, Yang J, O'Leary DD, Hannoush RN, Tessier-Lavigne M. A caspase cascade regulating developmental axon degeneration. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 17540-53. PMID 23223278 DOI: 10.1523/Jneurosci.3012-12.2012  0.603
2009 Nikolaev A, McLaughlin T, O'Leary DD, Tessier-Lavigne M. APP binds DR6 to trigger axon pruning and neuron death via distinct caspases. Nature. 457: 981-9. PMID 19225519 DOI: 10.1038/Nature07767  0.618
2008 Lim YS, McLaughlin T, Sung TC, Santiago A, Lee KF, O'Leary DD. p75(NTR) mediates ephrin-A reverse signaling required for axon repulsion and mapping. Neuron. 59: 746-58. PMID 18786358 DOI: 10.1016/J.Neuron.2008.07.032  0.677
2006 Hoopfer ED, McLaughlin T, Watts RJ, Schuldiner O, O'Leary DD, Luo L. Wlds protection distinguishes axon degeneration following injury from naturally occurring developmental pruning. Neuron. 50: 883-95. PMID 16772170 DOI: 10.1016/J.Neuron.2006.05.013  0.666
2005 McLaughlin T, O'Leary DD. Molecular gradients and development of retinotopic maps. Annual Review of Neuroscience. 28: 327-55. PMID 16022599 DOI: 10.1146/Annurev.Neuro.28.061604.135714  0.613
2005 O'Leary DD, McLaughlin T. Mechanisms of retinotopic map development: Ephs, ephrins, and spontaneous correlated retinal activity. Progress in Brain Research. 147: 43-65. PMID 15581697 DOI: 10.1016/S0079-6123(04)47005-8  0.704
2004 Yates PA, Holub AD, McLaughlin T, Sejnowski TJ, O'Leary DD. Computational modeling of retinotopic map development to define contributions of EphA-ephrinA gradients, axon-axon interactions, and patterned activity. Journal of Neurobiology. 59: 95-113. PMID 15007830 DOI: 10.1002/Neu.10341  0.703
2003 McLaughlin T, Torborg CL, Feller MB, O'Leary DD. Retinotopic map refinement requires spontaneous retinal waves during a brief critical period of development. Neuron. 40: 1147-60. PMID 14687549 DOI: 10.1016/S0896-6273(03)00790-6  0.612
2003 McLaughlin T, Hindges R, Yates PA, O'Leary DD. Bifunctional action of ephrin-B1 as a repellent and attractant to control bidirectional branch extension in dorsal-ventral retinotopic mapping. Development (Cambridge, England). 130: 2407-18. PMID 12702655 DOI: 10.1242/Dev.00467  0.682
2003 McLaughlin T, Hindges R, O'Leary DD. Regulation of axial patterning of the retina and its topographic mapping in the brain. Current Opinion in Neurobiology. 13: 57-69. PMID 12593983 DOI: 10.1016/S0959-4388(03)00014-X  0.687
2002 Hindges R, McLaughlin T, Genoud N, Henkemeyer M, O'Leary D. EphB forward signaling controls directional branch extension and arborization required for dorsal-ventral retinotopic mapping. Neuron. 35: 475-87. PMID 12165470 DOI: 10.1016/S0896-6273(02)00799-7  0.656
2001 Yates PA, Roskies AL, McLaughlin T, O'Leary DD. Topographic-specific axon branching controlled by ephrin-As is the critical event in retinotectal map development. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 8548-63. PMID 11606643 DOI: 10.1523/Jneurosci.21-21-08548.2001  0.699
2000 Erkman L, Yates PA, McLaughlin T, McEvilly RJ, Whisenhunt T, O'Connell SM, Krones AI, Kirby MA, Rapaport DH, Bermingham JR, O'Leary DD, Rosenfeld MG. A POU domain transcription factor-dependent program regulates axon pathfinding in the vertebrate visual system. Neuron. 28: 779-92. PMID 11163266 DOI: 10.1016/S0896-6273(00)00153-7  0.663
1999 McLaughlin T, O'Leary DD. Functional consequences of coincident expression of EphA receptors and ephrin-A ligands. Neuron. 22: 636-9. PMID 10230779 DOI: 10.1016/S0896-6273(00)80718-7  0.512
1999 O'Leary DD, Yates PA, McLaughlin T. Molecular development of sensory maps: representing sights and smells in the brain. Cell. 96: 255-69. PMID 9988220 DOI: 10.1016/S0092-8674(00)80565-6  0.54
1998 Frisén J, Yates PA, McLaughlin T, Friedman GC, O'Leary DD, Barbacid M. Ephrin-A5 (AL-1/RAGS) is essential for proper retinal axon guidance and topographic mapping in the mammalian visual system. Neuron. 20: 235-43. PMID 9491985 DOI: 10.1016/S0896-6273(00)80452-3  0.646
1997 Braisted JE, McLaughlin T, Wang HU, Friedman GC, Anderson DJ, O'leary DD. Graded and lamina-specific distributions of ligands of EphB receptor tyrosine kinases in the developing retinotectal system. Developmental Biology. 191: 14-28. PMID 9356168 DOI: 10.1006/Dbio.1997.8706  0.696
1997 Nakamoto M, Cheng H, Hansen MJ, Bergemann AD, Yoon CH, Friedman GC, McLaughlin T, O'Leary DD, Flanagan JG. S1-2 Eph receptors and their ligands in the development of retinotectal projection Neuroscience Research. 28: S3. DOI: 10.1016/S0168-0102(97)90003-1  0.305
1996 Nakamoto M, Cheng HJ, Friedman GC, McLaughlin T, Hansen MJ, Yoon CH, O'Leary DD, Flanagan JG. Topographically specific effects of ELF-1 on retinal axon guidance in vitro and retinal axon mapping in vivo. Cell. 86: 755-66. PMID 8797822 DOI: 10.1016/S0092-8674(00)80150-6  0.712
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