Axonal transport disruption in peripheral nerve disease: From Jack’s discoveries as a resident to recent contributions

Por Lloyd, Thomas E.
Publicado no J Peripher Nerv Syst (2012)

Novel therapeutic approaches for inclusion body myositis

Por Lloyd, Thomas E.
Publicado no Curr Opin Rheumatol (2010)

Flightless Flies: Drosophila models of neuromuscular disease

Por Lloyd, Thomas E., Taylor, J. Paul
Publicado em 2010

Peripheral Neuropathy – Clinical and Electrophysiological Considerations

Por Chung, Tae, Prasad, Kalpana, Lloyd, Thomas E.
Publicado no Neuroimaging Clin N Am (2013)

The ALS gene FUS regulates synaptic transmission at the Drosophila neuromuscular junction

Por Machamer, James B., Collins, Sarah E., Lloyd, Thomas E.
Publicado em 2014

FIG4 regulates lysosome membrane homeostasis independent of phosphatase function

Por Bharadwaj, Rajnish, Cunningham, Kathleen M., Zhang, Ke, Lloyd, Thomas E.
Publicado no Hum Mol Genet (2016)

Nucleocytoplasmic transport in C9orf72-mediated ALS/FTD

Por Zhang, Ke, Grima, Jonathan C., Rothstein, Jeffery D., Lloyd, Thomas E.
Publicado no Nucleus (2016)

Neuropeptide Delivery to Synapses by Long Range Vesicle Circulation and Sporadic Capture

Por Wong, Man Yan, Zhou, Chaoming, Shakiryanova, Dinara, Lloyd, Thomas E., Deitcher, David L., Levitan, Edwin S.
Publicado em 2012

Myositis-specific autoantibodies are specific for myositis compared to genetic muscle disease

Por Mammen, Andrew L., Casciola-Rosen, Livia, Christopher-Stine, Lisa, Lloyd, Thomas E., Wagner, Kathryn R.
Publicado no Neurol Neuroimmunol Neuroinflamm (2015)

Evaluation and construction of diagnostic criteria for inclusion body myositis

Por Lloyd, Thomas E., Mammen, Andrew L., Amato, Anthony A., Weiss, Michael D., Needham, Merrilee, Greenberg, Steven A.
Publicado em 2014

Laing distal myopathy pathologically resembling inclusion body myositis

Por Roda, Ricardo H, Schindler, Alice B, Blackstone, Craig, Mammen, Andrew L, Corse, Andrea M, Lloyd, Thomas E
Publicado no Ann Clin Transl Neurol (2014)

Increased Frequency of DRB1*11:01 in Anti-HMG-CoA Reductase-Associated Autoimmune Myopathy

Por Mammen, Andrew L., Gaudet, Daniel, Brisson, Diane, Christopher-Stine, Lisa, Lloyd, Thomas E., Leffell, Mary S., Zachary, Andrea A.
Publicado em 2012

Overlapping features of polymyositis and inclusion body myositis in HIV-infected patients

Por Lloyd, Thomas E., Pinal-Fernandez, Iago, Michelle, E. Harlan, Christopher-Stine, Lisa, Pak, Katherine, Sacktor, Ned, Mammen, Andrew L.
Publicado no Neurology (2017)

A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43

Por Lanson, Nicholas A., Maltare, Astha, King, Hanna, Smith, Rebecca, Kim, Ji Han, Taylor, J. Paul, Lloyd, Thomas E., Pandey, Udai Bhan
Publicado no Hum Mol Genet (2011)

Cbl-associated protein regulates assembly and function of two tension-sensing structures in Drosophila

Por Bharadwaj, Rajnish, Roy, Madhuparna, Ohyama, Tomoko, Sivan-Loukianova, Elena, Delannoy, Michael, Lloyd, Thomas E., Zlatic, Marta, Eberl, Daniel F., Kolodkin, Alex L.
Publicado em 2013

Antibody Levels Correlate with Creatine Kinase Levels and Strength in Anti-HMG-CoA Reductase-Associated Autoimmune Myopathy

Por Werner, Jessie L., Christopher-Stine, Lisa, Ghazarian, Sharon R., Pak, Katherine S., Kus, Jordan E., Daya, Natalie R., Lloyd, Thomas E., Mammen, Andrew L.
Publicado em 2012

Calcium dysregulation, functional calpainopathy, and endoplasmic reticulum stress in sporadic inclusion body myositis

Por Amici, David R., Pinal-Fernandez, Iago, Mázala, Davi A. G., Lloyd, Thomas E., Corse, Andrea M., Christopher-Stine, Lisa, Mammen, Andrew L., Chin, Eva R.
Publicado no Acta Neuropathol Commun (2017)

The spectrum of muscle histopathologic findings in 42 weak scleroderma patients

Por Paik, Julie J., Wigley, Fredrick M., Lloyd, Thomas E., Corse, Andrea M., Casciola-Rosen, Livia, Shah, Ami A., Boin, Francesco, Hummers, Laura K., Mammen, Andrew L.
Publicado no Arthritis Care Res (Hoboken) (2015)

Cytosolic 5′-Nucleotidase 1A As a Target of Circulating Autoantibodies in Autoimmune Diseases

Por LLOYD, THOMAS E., CHRISTOPHER-STINE, LISA, PINAL-FERNANDEZ, IAGO, TINIAKOU, ELENI, PETRI, MICHELLE, BAER, ALAN, DANOFF, SONYE K., PAK, KATHERINE, CASCIOLA-ROSEN, LIVIA A., MAMMEN, ANDREW L.
Publicado no Arthritis Care Res (Hoboken) (2016)

Tdp-43 cryptic exons are highly variable between cell types

Por Jeong, Yun Ha, Ling, Jonathan P., Lin, Sophie Z., Donde, Aneesh N., Braunstein, Kerstin E., Majounie, Elisa, Traynor, Bryan J., LaClair, Katherine D., Lloyd, Thomas E., Wong, Philip C.
Publicado no Mol Neurodegener (2017)