Thomas Lloyd
Thomas Lloyd
Verified email at jhmi.edu
Title
Cited by
Cited by
Year
The C9orf72 repeat expansion disrupts nucleocytoplasmic transport
K Zhang, CJ Donnelly, AR Haeusler, JC Grima, JB Machamer, ...
Nature 525 (7567), 56-61, 2015
5252015
Hrs Regulates Endosome Membrane Invagination and Tyrosine Kinase Receptor Signaling in Drosophila
TE Lloyd, R Atkinson, MN Wu, Y Zhou, G Pennetta, HJ Bellen
Cell 108 (2), 261-269, 2002
4532002
Endophilin Mutations Block Clathrin-Mediated Endocytosis but Not Neurotransmitter Release
P Verstreken, O Kjaerulff, TE Lloyd, R Atkinson, Y Zhou, IA Meinertzhagen, ...
Cell 109 (1), 101-112, 2002
3202002
When cell biology meets development: endocytic regulation of signaling pathways
ES Seto, HJ Bellen, TE Lloyd
Genes & development 16 (11), 1314-1336, 2002
2622002
Syntaxin 1A interacts with multiple exocytic proteins to regulate neurotransmitter release in vivo
MN Wu, T Fergestad, TE Lloyd, Y He, K Broadie, HJ Bellen
Neuron 23 (3), 593-605, 1999
2141999
Crystal structure of the VHS and FYVE tandem domains of Hrs, a protein involved in membrane trafficking and signal transduction
Y Mao, A Nickitenko, X Duan, TE Lloyd, MN Wu, H Bellen, FA Quiocho
Cell 100 (4), 447-456, 2000
1822000
A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43
NA Lanson Jr, A Maltare, H King, R Smith, JH Kim, JP Taylor, TE Lloyd, ...
Human molecular genetics 20 (13), 2510-2523, 2011
1702011
Antibody levels correlate with creatine kinase levels and strength in anti–3‐hydroxy‐3‐methylglutaryl‐coenzyme A reductase–associated autoimmune myopathy
JL Werner, L Christopher‐Stine, SR Ghazarian, KS Pak, JE Kus, NR Daya, ...
Arthritis & Rheumatism 64 (12), 4087-4093, 2012
1632012
Increased frequency of DRB1* 11: 01 in anti–hydroxymethylglutaryl‐coenzyme A reductase–associated autoimmune myopathy
AL Mammen, D Gaudet, D Brisson, L Christopher‐Stine, TE Lloyd, ...
Arthritis care & research 64 (8), 1233-1237, 2012
1602012
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis
V Fridman, B Bundy, MM Reilly, D Pareyson, C Bacon, J Burns, J Day, ...
J Neurol Neurosurg Psychiatry 86 (8), 873-878, 2015
1502015
Flightless flies: Drosophila models of neuromuscular disease
TE Lloyd, JP Taylor
Annals of the New York Academy of Sciences 1184, e1, 2010
1382010
Mutant huntingtin disrupts the nuclear pore complex
JC Grima, JG Daigle, N Arbez, KC Cunningham, K Zhang, J Ochaba, ...
Neuron 94 (1), 93-107. e6, 2017
1252017
Evaluation and construction of diagnostic criteria for inclusion body myositis
TE Lloyd, AL Mammen, AA Amato, MD Weiss, M Needham, ...
Neurology 83 (5), 426-433, 2014
1192014
The p150Glued CAP-Gly domain regulates initiation of retrograde transport at synaptic termini
TE Lloyd, J Machamer, K O'Hara, JH Kim, SE Collins, MY Wong, B Sahin, ...
Neuron 74 (2), 344-360, 2012
1112012
A genome-wide search for synaptic vesicle cycle proteins in Drosophila
TE Lloyd, P Verstreken, EJ Ostrin, A Phillippi, O Lichtarge, HJ Bellen
Neuron 26 (1), 45-50, 2000
1112000
Stress granule assembly disrupts nucleocytoplasmic transport
K Zhang, JG Daigle, KM Cunningham, AN Coyne, K Ruan, JC Grima, ...
Cell 173 (4), 958-971. e17, 2018
1052018
Neuropeptide delivery to synapses by long-range vesicle circulation and sporadic capture
MY Wong, C Zhou, D Shakiryanova, TE Lloyd, DL Deitcher, ES Levitan
Cell 148 (5), 1029-1038, 2012
1052012
Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation
D Xu, W Shen, R Guo, Y Xue, W Peng, J Sima, J Yang, A Sharov, ...
Nature neuroscience 16 (9), 1238, 2013
942013
WIDE AWAKE mediates the circadian timing of sleep onset
S Liu, A Lamaze, Q Liu, M Tabuchi, Y Yang, M Fowler, R Bharadwaj, ...
Neuron 82 (1), 151-166, 2014
932014
Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathy
DN Herrmann, R Horvath, JE Sowden, M Gonzales, A Sanchez-Mejias, ...
The American Journal of Human Genetics 95 (3), 332-339, 2014
712014
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