Year |
Citation |
Score |
2020 |
Cunningham KM, Maulding K, Ruan K, Senturk M, Grima JC, Sung H, Zuo Z, Song H, Gao J, Dubey S, Rothstein JD, Zhang K, Bellen HJ, Lloyd TE. TFEB/Mitf links impaired nuclear import to autophagolysosomal dysfunction in C9-ALS. Elife. 9. PMID 33300868 DOI: 10.7554/eLife.59419 |
1 |
|
2020 |
Woolums BM, McCray BA, Sung H, Tabuchi M, Sullivan JM, Ruppell KT, Yang Y, Mamah C, Aisenberg WH, Saavedra-Rivera PC, Larin BS, Lau AR, Robinson DN, Xiang Y, Wu MN, ... ... Lloyd TE, et al. TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca. Nature Communications. 11: 2679. PMID 32471994 DOI: 10.1038/s41467-020-16411-5 |
0.72 |
|
2016 |
Chhabra A, Carrino JA, Farahani SJ, Thawait GK, Sumner CJ, Wadhwa V, Chaudhary V, Lloyd TE. Whole-body MR neurography: Prospective feasibility study in polyneuropathy and Charcot-Marie-Tooth disease. Journal of Magnetic Resonance Imaging : Jmri. PMID 27126998 DOI: 10.1002/jmri.25293 |
1 |
|
2015 |
Wu MN, Lloyd TE. Drosophila models of neurologic disease. Experimental Neurology. 274: 1-3. PMID 26566006 DOI: 10.1016/j.expneurol.2015.10.004 |
1 |
|
2015 |
Sanmaneechai O, Feely S, Scherer SS, Herrmann DN, Burns J, Muntoni F, Li J, Siskind CE, Day JW, Laura M, Sumner CJ, Lloyd TE, Ramchandren S, Shy RR, Grider T, et al. Genotype-phenotype characteristics and baseline natural history of heritable neuropathies caused by mutations in the MPZ gene. Brain : a Journal of Neurology. 138: 3180-92. PMID 26310628 DOI: 10.1093/brain/awv241 |
1 |
|
2015 |
Zhang K, Donnelly CJ, Haeusler AR, Grima JC, Machamer JB, Steinwald P, Daley EL, Miller SJ, Cunningham KM, Vidensky S, Gupta S, Thomas MA, Hong I, Chiu SL, Huganir RL, ... ... Lloyd TE, et al. The C9orf72 repeat expansion disrupts nucleocytoplasmic transport. Nature. 525: 56-61. PMID 26308891 DOI: 10.1038/nature14973 |
1 |
|
2015 |
Paik JJ, Wigley FM, Lloyd TE, Corse AM, Casciola-Rosen L, Shah AA, Boin F, Hummers LK, Mammen AL. The spectrum of muscle histopathologic findings in 42 weak scleroderma patients. Arthritis Care & Research. PMID 25989455 DOI: 10.1002/acr.22620 |
1 |
|
2015 |
Lloyd TE, Christopher-Stine L, Pinal-Fernandez I, Tiniakou E, Petri M, Baer A, Danoff S, Pak K, Casciola-Rosen L, Mammen AL. Cytosolic 5'-nucleotidase 1A is a common target of circulating autoantibodies in several autoimmune diseases. Arthritis Care & Research. PMID 25892010 DOI: 10.1002/acr.22600 |
1 |
|
2015 |
Fridman V, Bundy B, Reilly MM, Pareyson D, Bacon C, Burns J, Day J, Feely S, Finkel RS, Grider T, Kirk CA, Herrmann DN, Laurá M, Li J, Lloyd T, et al. CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 873-8. PMID 25430934 DOI: 10.1136/jnnp-2014-308826 |
1 |
|
2014 |
Wong CO, Chen K, Lin YQ, Chao Y, Duraine L, Lu Z, Yoon WH, Sullivan JM, Broadhead GT, Sumner CJ, Lloyd TE, Macleod GT, Bellen HJ, Venkatachalam K. A TRPV channel in Drosophila motor neurons regulates presynaptic resting Ca2+ levels, synapse growth, and synaptic transmission. Neuron. 84: 764-77. PMID 25451193 DOI: 10.1016/j.neuron.2014.09.030 |
1 |
|
2014 |
Herrmann DN, Horvath R, Sowden JE, Gonzalez M, Gonzales M, Sanchez-Mejias A, Guan Z, Whittaker RG, Almodovar JL, Lane M, Bansagi B, Pyle A, Boczonadi V, Lochmüller H, Griffin H, ... ... Lloyd TE, et al. Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy. American Journal of Human Genetics. 95: 332-9. PMID 25192047 DOI: 10.1016/J.AJHG.2014.09.012 |
1 |
|
2014 |
Lloyd TE, Mammen AL, Amato AA, Weiss MD, Needham M, Greenberg SA. Evaluation and construction of diagnostic criteria for inclusion body myositis. Neurology. 83: 426-33. PMID 24975859 DOI: 10.1212/WNL.0000000000000642 |
1 |
|
2014 |
Liu S, Lamaze A, Liu Q, Tabuchi M, Yang Y, Fowler M, Bharadwaj R, Zhang J, Bedont J, Blackshaw S, Lloyd TE, Montell C, Sehgal A, Koh K, Wu MN. WIDE AWAKE mediates the circadian timing of sleep onset. Neuron. 82: 151-66. PMID 24631345 DOI: 10.1016/j.neuron.2014.01.040 |
0.72 |
|
2014 |
Machamer JB, Collins SE, Lloyd TE. The ALS gene FUS regulates synaptic transmission at the Drosophila neuromuscular junction. Human Molecular Genetics. 23: 3810-22. PMID 24569165 DOI: 10.1093/hmg/ddu094 |
1 |
|
2014 |
Chung T, Prasad K, Lloyd TE. Peripheral neuropathy: clinical and electrophysiological considerations. Neuroimaging Clinics of North America. 24: 49-65. PMID 24210312 DOI: 10.1016/j.nic.2013.03.023 |
1 |
|
2014 |
Sullivan JM, Lloyd TE, Sumner CJ. Hereditary channelopathies caused by TRPV4 Mutations Pathologies of Calcium Channels. 413-440. DOI: 10.1007/978-3-642-40282-1_21 |
1 |
|
2013 |
Xu D, Shen W, Guo R, Xue Y, Peng W, Sima J, Yang J, Sharov A, Srikantan S, Yang J, Fox D, Qian Y, Martindale JL, Piao Y, Machamer J, ... ... Lloyd TE, et al. Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation. Nature Neuroscience. 16: 1238-47. PMID 23912945 DOI: 10.1038/nn.3479 |
1 |
|
2013 |
Bharadwaj R, Roy M, Ohyama T, Sivan-Loukianova E, Delannoy M, Lloyd TE, Zlatic M, Eberl DF, Kolodkin AL. Cbl-associated protein regulates assembly and function of two tension-sensing structures in Drosophila. Development (Cambridge, England). 140: 627-38. PMID 23293294 DOI: 10.1242/dev.085100 |
1 |
|
2012 |
Lloyd TE. Axonal transport disruption in peripheral nerve disease: From Jack's discoveries as a resident to recent contributions. Journal of the Peripheral Nervous System : Jpns. 17: 46-51. PMID 23279432 DOI: 10.1111/j.1529-8027.2012.00431.x |
1 |
|
2012 |
Werner JL, Christopher-Stine L, Ghazarian SR, Pak KS, Kus JE, Daya NR, Lloyd TE, Mammen AL. Antibody levels correlate with creatine kinase levels and strength in anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase-associated autoimmune myopathy. Arthritis and Rheumatism. 64: 4087-93. PMID 22933019 DOI: 10.1002/art.34673 |
1 |
|
2012 |
Lloyd TE, Machamer J, O'Hara K, Kim JH, Collins SE, Wong MY, Sahin B, Imlach W, Yang Y, Levitan ES, McCabe BD, Kolodkin AL. The p150(Glued) CAP-Gly domain regulates initiation of retrograde transport at synaptic termini. Neuron. 74: 344-60. PMID 22542187 DOI: 10.1016/j.neuron.2012.02.026 |
1 |
|
2012 |
Mammen AL, Gaudet D, Brisson D, Christopher-Stine L, Lloyd TE, Leffell MS, Zachary AA. Increased frequency of DRB1*11:01 in anti-hydroxymethylglutaryl-coenzyme A reductase-associated autoimmune myopathy. Arthritis Care & Research. 64: 1233-7. PMID 22422616 DOI: 10.1002/acr.21671 |
1 |
|
2012 |
Wadhwa V, Thakkar RS, Maragakis N, Höke A, Sumner CJ, Lloyd TE, Carrino JA, Belzberg AJ, Chhabra A. Sciatic nerve tumor and tumor-like lesions - uncommon pathologies. Skeletal Radiology. 41: 763-74. PMID 22410805 DOI: 10.1007/s00256-012-1384-7 |
1 |
|
2012 |
Wong MY, Zhou C, Shakiryanova D, Lloyd TE, Deitcher DL, Levitan ES. Neuropeptide delivery to synapses by long-range vesicle circulation and sporadic capture. Cell. 148: 1029-38. PMID 22385966 DOI: 10.1016/j.cell.2011.12.036 |
1 |
|
2011 |
Lanson NA, Maltare A, King H, Smith R, Kim JH, Taylor JP, Lloyd TE, Pandey UB. A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43. Human Molecular Genetics. 20: 2510-23. PMID 21487023 DOI: 10.1093/hmg/ddr150 |
1 |
|
2011 |
Lloyd TE, Chaudhry V. Treatment and Management of Hereditary Neuropathies Neuromuscular Disorders. 191-213. DOI: 10.1016/B978-1-4377-0372-6.00013-X |
1 |
|
2010 |
Lloyd TE. Novel therapeutic approaches for inclusion body myositis. Current Opinion in Rheumatology. 22: 658-64. PMID 20827206 DOI: 10.1097/BOR.0b013e32833f0f4a |
1 |
|
2010 |
Lloyd TE, Taylor JP. Flightless flies: Drosophila models of neuromuscular disease. Annals of the New York Academy of Sciences. 1184: e1-20. PMID 20329357 DOI: 10.1111/j.1749-6632.2010.05432.x |
1 |
|
2007 |
Jordan JD, Lloyd T, Pardo-Villamizar C. Case 16: chasing the dragon. Medgenmed : Medscape General Medicine. 9: 14. PMID 17955070 |
1 |
|
2002 |
Seto ES, Bellen HJ, Lloyd TE. When cell biology meets development: endocytic regulation of signaling pathways. Genes & Development. 16: 1314-36. PMID 12050111 DOI: 10.1101/gad.989602 |
1 |
|
2002 |
Verstreken P, Kjaerulff O, Lloyd TE, Atkinson R, Zhou Y, Meinertzhagen IA, Bellen HJ. Endophilin mutations block clathrin-mediated endocytosis but not neurotransmitter release. Cell. 109: 101-12. PMID 11955450 DOI: 10.1016/S0092-8674(02)00688-8 |
1 |
|
2002 |
Lloyd TE, Atkinson R, Wu MN, Zhou Y, Pennetta G, Bellen HJ. Hrs regulates endosome membrane invagination and tyrosine kinase receptor signaling in Drosophila. Cell. 108: 261-9. PMID 11832215 DOI: 10.1016/S0092-8674(02)00611-6 |
1 |
|
2001 |
Fergestad T, Wu MN, Schulze KL, Lloyd TE, Bellen HJ, Broadie K. Targeted mutations in the syntaxin H3 domain specifically disrupt SNARE complex function in synaptic transmission. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 9142-50. PMID 11717347 |
1 |
|
2001 |
Lloyd TE, Bellen HJ. pRIMing synaptic vesicles for fusion. Nature Neuroscience. 4: 965-6. PMID 11574826 DOI: 10.1038/nn1001-965 |
1 |
|
2001 |
Wu MN, Schulze KL, Lloyd TE, Bellen HJ. The ROP-syntaxin interaction inhibits neurotransmitter release. European Journal of Cell Biology. 80: 196-9. PMID 11302525 DOI: 10.1078/0171-9335-00143 |
1 |
|
2000 |
Lloyd TE, Verstreken P, Ostrin EJ, Phillippi A, Lichtarge O, Bellen HJ. A genome-wide search for synaptic vesicle cycle proteins in Drosophila. Neuron. 26: 45-50. PMID 10798391 |
1 |
|
2000 |
Mao Y, Nickitenko A, Duan X, Lloyd TE, Wu MN, Bellen H, Quiocho FA. Crystal structure of the VHS and FYVE tandem domains of Hrs, a protein involved in membrane trafficking and signal transduction. Cell. 100: 447-56. PMID 10693761 |
1 |
|
1999 |
Wu MN, Fergestad T, Lloyd TE, He Y, Broadie K, Bellen HJ. Syntaxin 1A interacts with multiple exocytic proteins to regulate neurotransmitter release in vivo. Neuron. 23: 593-605. PMID 10433270 DOI: 10.1016/S0896-6273(00)80811-9 |
1 |
|
1997 |
Lloyd TE, Yang L, Tang DN, Bennett T, Schober W, Lewis DE. Regulation of CD28 Costimulation in Human CD8+ T Cells Journal of Immunology. 158: 1551-1558. PMID 9029089 |
1 |
|
1995 |
Jeevan A, Bucana CD, Dong Z, Dizon VV, Thomas SL, Lloyd TE, Kripke ML. Ultraviolet radiation reduces phagocytosis and intracellular killing of mycobacteria and inhibits nitric oxide production by macrophages in mice Journal of Leukocyte Biology. 57: 883-890. PMID 7790771 |
1 |
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