THOMAS LLOYD to Mice
This is a "connection" page, showing publications THOMAS LLOYD has written about Mice.
Connection Strength
0.233
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Loss of TDP-43 function and rimmed vacuoles persist after T cell depletion in a xenograft model of sporadic inclusion body myositis. Sci Transl Med. 2022 01 19; 14(628):eabi9196.
Score: 0.055
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TRPV4 disrupts mitochondrial transport and causes axonal degeneration via a CaMKII-dependent elevation of intracellular Ca2. Nat Commun. 2020 05 29; 11(1):2679.
Score: 0.049
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Characterizing local antibody responses in the muscle of inclusion body myositis patients. J Autoimmun. 2025 Jun; 154:103437.
Score: 0.017
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Seeding-competent TDP-43 persists in human patient and mouse muscle. Sci Transl Med. 2024 11 27; 16(775):eadp5730.
Score: 0.017
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Safety and efficacy of arimoclomol for inclusion body myositis: a multicentre, randomised, double-blind, placebo-controlled trial. Lancet Neurol. 2023 10; 22(10):900-911.
Score: 0.015
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Human pluripotent stem cell-derived myogenic progenitors undergo maturation to quiescent satellite cells upon engraftment. Cell Stem Cell. 2022 04 07; 29(4):610-619.e5.
Score: 0.014
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p53 is a central regulator driving neurodegeneration caused by C9orf72 poly(PR). Cell. 2021 02 04; 184(3):689-708.e20.
Score: 0.013
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Machine learning algorithms reveal unique gene expression profiles in muscle biopsies from patients with different types of myositis. Ann Rheum Dis. 2020 09; 79(9):1234-1242.
Score: 0.012
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TDP-43 and RNA form amyloid-like myo-granules in regenerating muscle. Nature. 2018 11; 563(7732):508-513.
Score: 0.011
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Mutant Huntingtin Disrupts the Nuclear Pore Complex. Neuron. 2017 Apr 05; 94(1):93-107.e6.
Score: 0.010
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Tdp-43 cryptic exons are highly variable between cell types. Mol Neurodegener. 2017 02 02; 12(1):13.
Score: 0.010
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Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis. Ann Neurol. 2017 Feb; 81(2):227-239.
Score: 0.010