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Published in Nature (London) (03.09.2015)
Published in Nature (London) (03.09.2015)
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Identification of distinctive interferon gene signatures in different types of myositis
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Mutant Huntingtin Disrupts the Nuclear Pore Complex
Grima, Jonathan C., Daigle, J. Gavin, Arbez, Nicolas, Cunningham, Kathleen C., Zhang, Ke, Ochaba, Joseph, Geater, Charlene, Morozko, Eva, Stocksdale, Jennifer, Glatzer, Jenna C., Pham, Jacqueline T., Ahmed, Ishrat, Peng, Qi, Wadhwa, Harsh, Pletnikova, Olga, Troncoso, Juan C., Duan, Wenzhen, Snyder, Solomon H., Ranum, Laura P.W., Thompson, Leslie M., Lloyd, Thomas E., Ross, Christopher A., Rothstein, Jeffrey D.
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WIDE AWAKE mediates the circadian timing of sleep onset
Liu, Sha, Lamaze, Angelique, Liu, Qili, Tabuchi, Masashi, Yang, Yong, Fowler, Melissa, Bharadwaj, Rajnish, Zhang, Julia, Bedont, Joseph, Blackshaw, Seth, Lloyd, Thomas E, Montell, Craig, Sehgal, Amita, Koh, Kyunghee, Wu, Mark N
Published in Neuron (Cambridge, Mass.) (02.04.2014)
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TDP-43 and RNA form amyloid-like myo-granules in regenerating muscle
Vogler, Thomas O., Wheeler, Joshua R., Nguyen, Eric D., Hughes, Michael P., Britson, Kyla A., Lester, Evan, Rao, Bhalchandra, Betta, Nicole Dalla, Whitney, Oscar N., Ewachiw, Theodore E., Gomes, Edward, Shorter, James, Lloyd, Thomas E., Eisenberg, David S., Taylor, J. Paul, Johnson, Aaron M., Olwin, Bradley B., Parker, Roy
Published in Nature (London) (01.11.2018)
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Lloyd, Thomas E, Mammen, Andrew L, Amato, Anthony A, Weiss, Michael D, Needham, Merrilee, Greenberg, Steven A
Published in Neurology (29.07.2014)
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Neuropeptide Delivery to Synapses by Long-Range Vesicle Circulation and Sporadic Capture
Wong, Man Yan, Zhou, Chaoming, Shakiryanova, Dinara, Lloyd, Thomas E., Deitcher, David L., Levitan, Edwin S.
Published in Cell (02.03.2012)
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Thigh muscle MRI in immune-mediated necrotising myopathy: extensive oedema, early muscle damage and role of anti-SRP autoantibodies as a marker of severity
Pinal-Fernandez, Iago, Casal-Dominguez, Maria, Carrino, John A, Lahouti, Arash H, Basharat, Pari, Albayda, Jemima, Paik, Julie J, Ahlawat, Shivani, Danoff, Sonye K, Lloyd, Thomas E, Mammen, Andrew L, Christopher-Stine, Lisa
Published in Annals of the rheumatic diseases (01.04.2017)
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Heterogeneity in gut microbiota drive polyphenol metabolism that influences α-synuclein misfolding and toxicity
Ho, Lap, Zhao, Danyue, Ono, Kenjiro, Ruan, Kai, Mogno, Ilaria, Tsuji, Mayumi, Carry, Eileen, Brathwaite, Justin, Sims, Steven, Frolinger, Tal, Westfall, Susan, Mazzola, Paolo, Wu, Qingli, Hao, Ke, Lloyd, Thomas E., Simon, James E., Faith, Jeremiah, Pasinetti, Giulio M.
Published in The Journal of nutritional biochemistry (01.02.2019)
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Increased frequency of DRB111:01 in anti–hydroxymethylglutaryl‐coenzyme A reductase–associated autoimmune myopathy
Mammen, Andrew L., Gaudet, Daniel, Brisson, Diane, Christopher‐Stine, Lisa, Lloyd, Thomas E., Leffell, Mary S., Zachary, Andrea A.
Published in Arthritis care & research (2010) (01.08.2012)
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Multi-omic analysis of selectively vulnerable motor neuron subtypes implicates altered lipid metabolism in ALS
Lee, Hojae, Lee, Jae Jin, Park, Na Young, Dubey, Sandeep Kumar, Kim, Taeyong, Ruan, Kai, Lim, Su Bin, Park, Seong-Hyun, Ha, Shinwon, Kovlyagina, Irina, Kim, Kyung-tai, Kim, Seongjun, Oh, Yohan, Kim, Hyesoo, Kang, Sung-Ung, Song, Mi-Ryoung, Lloyd, Thomas E., Maragakis, Nicholas J., Hong, Young Bin, Eoh, Hyungjin, Lee, Gabsang
Published in Nature neuroscience (01.12.2021)
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TFEB/Mitf links impaired nuclear import to autophagolysosomal dysfunction in C9-ALS
Cunningham, Kathleen M, Maulding, Kirstin, Ruan, Kai, Senturk, Mumine, Grima, Jonathan C, Sung, Hyun, Zuo, Zhongyuan, Song, Helen, Gao, Junli, Dubey, Sandeep, Rothstein, Jeffrey D, Zhang, Ke, Bellen, Hugo J, Lloyd, Thomas E
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Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy
Herrmann, David N., Horvath, Rita, Sowden, Janet E., Gonzales, Michael, Sanchez-Mejias, Avencia, Guan, Zhuo, Whittaker, Roger G., Almodovar, Jorge L., Lane, Maria, Bansagi, Boglarka, Pyle, Angela, Boczonadi, Veronika, Lochmüller, Hanns, Griffin, Helen, Chinnery, Patrick F., Lloyd, Thomas E., Littleton, J. Troy, Zuchner, Stephan
Published in American journal of human genetics (04.09.2014)
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Muscle Transcriptomics Shows Overexpression of Cadherin 1 in Inclusion Body Myositis
Ikenaga, Chiseko, Date, Hidetoshi, Kanagawa, Motoi, Mitsui, Jun, Ishiura, Hiroyuki, Yoshimura, Jun, Pinal‐Fernandez, Iago, Mammen, Andrew L., Lloyd, Thomas E., Tsuji, Shoji, Shimizu, Jun, Toda, Tatsushi, Goto, Jun
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The ALS gene FUS regulates synaptic transmission at the Drosophila neuromuscular junction
Machamer, James B, Collins, Sarah E, Lloyd, Thomas E
Published in Human molecular genetics (15.07.2014)
Published in Human molecular genetics (15.07.2014)
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Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis
Güttsches, Anne‐Katrin, Brady, Stefen, Krause, Kathryn, Maerkens, Alexandra, Uszkoreit, Julian, Eisenacher, Martin, Schreiner, Anja, Galozzi, Sara, Mertens‐Rill, Janine, Tegenthoff, Martin, Holton, Janice L., Harms, Matthew B., Lloyd, Thomas E., Vorgerd, Matthias, Weihl, Conrad C., Marcus, Katrin, Kley, Rudolf A.
Published in Annals of neurology (01.02.2017)
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Cytosolic 5′‐Nucleotidase 1A As a Target of Circulating Autoantibodies in Autoimmune Diseases
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.
Published in Arthritis care & research (2010) (01.01.2016)
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TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca2
Woolums, Brian M., McCray, Brett A., Sung, Hyun, Tabuchi, Masashi, Sullivan, Jeremy M., Ruppell, Kendra Takle, Yang, Yunpeng, Mamah, Catherine, Aisenberg, William H., Saavedra-Rivera, Pamela C., Larin, Bryan S., Lau, Alexander R., Robinson, Douglas N., Xiang, Yang, Wu, Mark N., Sumner, Charlotte J., Lloyd, Thomas E.
Published in Nature communications (29.05.2020)
Published in Nature communications (29.05.2020)
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Neuropathy-causing TRPV4 mutations disrupt TRPV4-RhoA interactions and impair neurite extension
McCray, Brett A., Diehl, Erika, Sullivan, Jeremy M., Aisenberg, William H., Zaccor, Nicholas W., Lau, Alexander R., Rich, Dominick J., Goretzki, Benedikt, Hellmich, Ute A., Lloyd, Thomas E., Sumner, Charlotte J.
Published in Nature communications (04.03.2021)
Published in Nature communications (04.03.2021)
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