Year |
Citation |
Score |
2023 |
Valentino RR, Scotton WJ, Roemer SF, Lashley T, Heckman MG, Shoai M, Martinez-Carrasco A, Tamvaka N, Walton RL, Baker MC, Macpherson HL, Real R, Soto-Beasley AI, Mok K, Revesz T, ... ... DeTure M, et al. Creating the Pick's disease International Consortium: Association study of H2 haplotype with risk of Pick's disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37163045 DOI: 10.1101/2023.04.17.23288471 |
0.3 |
|
2023 |
Oatman SR, Reddy JS, Quicksall Z, Carrasquillo MM, Wang X, Liu CC, Yamazaki Y, Nguyen TT, Malphrus K, Heckman M, Biswas K, Nho K, Baker M, Martens YA, Zhao N, ... ... DeTure M, et al. Genome-wide association study of brain biochemical phenotypes reveals distinct genetic architecture of Alzheimer's disease related proteins. Molecular Neurodegeneration. 18: 2. PMID 36609403 DOI: 10.1186/s13024-022-00592-2 |
0.379 |
|
2022 |
Meneses AD, Koga S, Li Z, O'Leary J, Li F, Chen K, Murakami A, Qiao W, Kurti A, Heckman MG, White L, Xie M, Chen Y, Finch NA, Lim MJ, ... ... DeTure MA, et al. APOE2 Exacerbates TDP-43 Related Toxicity in the Absence of Alzheimer Pathology. Annals of Neurology. PMID 36546684 DOI: 10.1002/ana.26580 |
0.337 |
|
2022 |
Seidler PM, Murray KA, Boyer DR, Ge P, Sawaya MR, Hu CJ, Cheng X, Abskharon R, Pan H, DeTure MA, Williams CK, Dickson DW, Vinters HV, Eisenberg DS. Structure-based discovery of small molecules that disaggregate Alzheimer's disease tissue derived tau fibrils in vitro. Nature Communications. 13: 5451. PMID 36114178 DOI: 10.1038/s41467-022-32951-4 |
0.468 |
|
2022 |
Jiang YX, Cao Q, Sawaya MR, Abskharon R, Ge P, DeTure M, Dickson DW, Fu JY, Ogorzalek Loo RR, Loo JA, Eisenberg DS. Amyloid fibrils in disease FTLD-TDP are composed of TMEM106B not TDP-43. Nature. PMID 35344984 DOI: 10.1038/s41586-022-04670-9 |
0.392 |
|
2022 |
Chang A, Xiang X, Wang J, Lee C, Arakhamia T, Simjanoska M, Wang C, Carlomagno Y, Zhang G, Dhingra S, Thierry M, Perneel J, Heeman B, Forgrave LM, DeTure M, et al. Homotypic fibrillization of TMEM106B across diverse neurodegenerative diseases. Cell. PMID 35247328 DOI: 10.1016/j.cell.2022.02.026 |
0.395 |
|
2021 |
Alquezar C, Schoch KM, Geier EG, Ramos EM, Scrivo A, Li KH, Argouarch AR, Mlynarski EE, Dombroski B, DeTure M, Dickson DW, Yokoyama JS, Cuervo AM, Burlingame AL, Schellenberg GD, et al. TSC1 loss increases risk for tauopathy by inducing tau acetylation and preventing tau clearance via chaperone-mediated autophagy. Science Advances. 7: eabg3897. PMID 34739309 DOI: 10.1126/sciadv.abg3897 |
0.393 |
|
2021 |
Muraoka S, Lin W, Takamatsu-Yukawa K, Hu J, Ikezu S, DeTure MA, Dickson DW, Emili A, Ikezu T. Enrichment of Phosphorylated Tau (Thr181) and Functionally Interacting Molecules in Chronic Traumatic Encephalopathy Brain-derived Extracellular Vesicles. Aging and Disease. 12: 1376-1388. PMID 34527416 DOI: 10.14336/AD.2020.1007 |
0.414 |
|
2021 |
Carlomagno Y, Manne S, DeTure M, Prudencio M, Zhang YJ, Hanna Al-Shaikh R, Dunmore JA, Daughrity LM, Song Y, Castanedes-Casey M, Lewis-Tuffin LJ, Nicholson KA, Wszolek ZK, Dickson DW, Fitzpatrick AWP, et al. The AD tau core spontaneously self-assembles and recruits full-length tau to filaments. Cell Reports. 34: 108843. PMID 33730588 DOI: 10.1016/j.celrep.2021.108843 |
0.573 |
|
2020 |
Wojtas AM, Carlomagno Y, Sens JP, Kang SS, Jensen TD, Kurti A, Baker KE, Berry TJ, Phillips VR, Castanedes MC, Awan A, DeTure M, De Castro CHF, Librero AL, Yue M, et al. Clusterin ameliorates tau pathology in vivo by inhibiting fibril formation. Acta Neuropathologica Communications. 8: 210. PMID 33261653 DOI: 10.1186/s40478-020-01079-1 |
0.531 |
|
2020 |
Hou X, Watzlawik JO, Cook C, Liu CC, Kang SS, Lin WL, DeTure M, Heckman MG, Diehl NN, Al-Shaikh FSH, Walton RL, Ross OA, Melrose HL, Ertekin-Taner N, Bu G, et al. Mitophagy alterations in Alzheimer's disease are associated with granulovacuolar degeneration and early tau pathology. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 33090691 DOI: 10.1002/alz.12198 |
0.335 |
|
2020 |
Liu CC, Yamazaki Y, Heckman MG, Martens YA, Jia L, Yamazaki A, Diehl NN, Zhao J, Zhao N, DeTure M, Davis MD, Felton LM, Qiao W, Li Y, Li H, et al. Tau and apolipoprotein E modulate cerebrovascular tight junction integrity independent of cerebral amyloid angiopathy in Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 32827351 DOI: 10.1002/Alz.12104 |
0.368 |
|
2020 |
Prudencio M, Humphrey J, Pickles S, Brown AL, Hill SE, Kachergus J, Shi J, Heckman M, Spiegel M, Cook C, Song Y, Yue M, Daughrity L, Carlomagno Y, Jansen-West K, ... ... DeTure M, et al. Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia. The Journal of Clinical Investigation. PMID 32790644 DOI: 10.1172/Jci139741 |
0.373 |
|
2020 |
Abskharon R, Seidler PM, Sawaya MR, Cascio D, Yang TP, Philipp S, Williams CK, Newell KL, Ghetti B, DeTure MA, Dickson DW, Vinters HV, Felgner PL, Nakajima R, Glabe CG, et al. Crystal structure of a conformational antibody that binds tau oligomers and inhibits pathological seeding by extracts from donors with Alzheimer's disease. The Journal of Biological Chemistry. PMID 32493775 DOI: 10.1074/Jbc.Ra120.013638 |
0.438 |
|
2020 |
Arakhamia T, Lee CE, Carlomagno Y, Duong DM, Kundinger SR, Wang K, Williams D, DeTure M, Dickson DW, Cook CN, Seyfried NT, Petrucelli L, Fitzpatrick AWP. Posttranslational Modifications Mediate the Structural Diversity of Tauopathy Strains. Cell. PMID 32032505 DOI: 10.1016/J.Cell.2020.01.027 |
0.543 |
|
2019 |
Seidler PM, Boyer DR, Murray KA, Yang TP, Bentzel M, Sawaya MR, Rosenberg G, Cascio D, Williams CK, Newell KL, Ghetti B, DeTure MA, Dickson DW, Vinters HV, Eisenberg DS. Structure-based inhibitors halt prion-like seeding by Alzheimer's disease- and tauopathy-derived brain tissue samples. The Journal of Biological Chemistry. PMID 31537646 DOI: 10.1074/Jbc.Ra119.009688 |
0.435 |
|
2019 |
DeTure MA, Dickson DW. The neuropathological diagnosis of Alzheimer's disease. Molecular Neurodegeneration. 14: 32. PMID 31375134 DOI: 10.1186/S13024-019-0333-5 |
0.316 |
|
2019 |
Koga S, Eric Ahlskog J, DeTure MA, Baker M, Roemer SF, Konno T, Rademakers R, Ross OA, Dickson DW. Coexistence of Progressive Supranuclear Palsy With Pontocerebellar Atrophy and Myotonic Dystrophy Type 1. Journal of Neuropathology and Experimental Neurology. PMID 31216016 DOI: 10.1093/Jnen/Nlz048 |
0.308 |
|
2019 |
Heckman MG, Brennan RR, Labbé C, Soto AI, Koga S, DeTure MA, Murray ME, Petersen RC, Boeve BF, van Gerpen JA, Uitti RJ, Wszolek ZK, Rademakers R, Dickson DW, Ross OA. Association of MAPT Subhaplotypes With Risk of Progressive Supranuclear Palsy and Severity of Tau Pathology. Jama Neurology. PMID 30882841 DOI: 10.1001/Jamaneurol.2019.0250 |
0.316 |
|
2019 |
Chung DC, Carlomagno Y, Cook CN, Jansen-West K, Daughrity L, Lewis-Tuffin LJ, Castanedes-Casey M, DeTure M, Dickson DW, Petrucelli L. Tau exhibits unique seeding properties in globular glial tauopathy. Acta Neuropathologica Communications. 7: 36. PMID 30845985 DOI: 10.1186/S40478-019-0691-9 |
0.565 |
|
2019 |
Croft CL, Cruz PE, Ryu DH, Ceballos-Diaz C, Strang KH, Woody BM, Lin WL, Deture M, Rodríguez-Lebrón E, Dickson DW, Chakrabarty P, Levites Y, Giasson BI, Golde TE. rAAV-based brain slice culture models of Alzheimer's and Parkinson's disease inclusion pathologies. The Journal of Experimental Medicine. PMID 30770411 DOI: 10.1084/Jem.20182184 |
0.303 |
|
2019 |
Carlomagno Y, Chung DC, Yue M, Kurti A, Avendano NM, Castanedes-Casey M, Hinkle KM, Jansen-West K, Daughrity LM, Tong J, Phillips V, Rademakers R, DeTure M, Fryer JD, Dickson DW, et al. Enhanced phosphorylation of T153 in soluble tau is a defining biochemical feature of the A152T tau risk variant. Acta Neuropathologica Communications. 7: 10. PMID 30674342 DOI: 10.1186/S40478-019-0661-2 |
0.493 |
|
2019 |
Eftekharzadeh B, Daigle JG, Kapinos LE, Coyne A, Schiantarelli J, Carlomagno Y, Cook C, Miller SJ, Dujardin S, Amaral AS, Grima JC, Bennett RE, Tepper K, DeTure M, Vanderburg CR, et al. Tau Protein Disrupts Nucleocytoplasmic Transport in Alzheimer's Disease. Neuron. 101: 349. PMID 30653936 DOI: 10.1016/J.Neuron.2018.12.031 |
0.383 |
|
2018 |
Eftekharzadeh B, Daigle JG, Kapinos LE, Coyne A, Schiantarelli J, Carlomagno Y, Cook C, Miller SJ, Dujardin S, Amaral AS, Grima JC, Bennett RE, Tepper K, DeTure M, Vanderburgh CR, et al. Tau Protein Disrupts Nucleocytoplasmic Transport in Alzheimer's Disease. Neuron. 99: 925-940.e7. PMID 30189209 DOI: 10.1016/J.Neuron.2018.07.039 |
0.535 |
|
2018 |
Kasanuki K, Ross OA, DeTure MA, Walton RL, Sanchez-Contreras M, Koga S, Murray ME, Rademakers R, Dickson DW. Relationships between lewy and tau pathologies in 375 consecutive non-Alzheimer's olfactory bulbs. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 29322556 DOI: 10.1002/Mds.27250 |
0.369 |
|
2017 |
Carlomagno Y, Chung DC, Yue M, Castanedes-Casey M, Madden BJ, Dunmore J, Tong J, DeTure M, Dickson DW, Petrucelli L, Cook C. An acetylation-phosphorylation switch that regulates tau aggregation propensity and function. The Journal of Biological Chemistry. PMID 28760828 DOI: 10.1074/Jbc.M117.794602 |
0.614 |
|
2016 |
Tacik P, DeTure MA, Yari C, Lin WL, Murray ME, Baker MC, Josephs KA, Boeve BF, Wszolek ZK, Graff-Radford NR, Parisi JE, Petrucelli L, Rademakers R, Isaacson RS, Heilman KM, et al. FTDP-17 with pick body-like inclusions associated with a novel tau mutation, p.E372G. Brain Pathology (Zurich, Switzerland). PMID 27529406 DOI: 10.1111/Bpa.12428 |
0.319 |
|
2016 |
Shinohara M, Murray ME, Frank RD, Shinohara M, DeTure M, Yamazaki Y, Tachibana M, Atagi Y, Davis MD, Liu CC, Zhao N, Painter MM, Petersen RC, Fryer JD, Crook JE, et al. Impact of sex and APOE4 on cerebral amyloid angiopathy in Alzheimer's disease. Acta Neuropathologica. PMID 27179972 DOI: 10.1007/S00401-016-1580-Y |
0.304 |
|
2015 |
Tacik P, DeTure M, Hinkle KM, Lin WL, Sanchez-Contreras M, Carlomagno Y, Pedraza O, Rademakers R, Ross OA, Wszolek ZK, Dickson DW. A Novel Tau Mutation in Exon 12, p.Q336H, Causes Hereditary Pick Disease. Journal of Neuropathology and Experimental Neurology. 74: 1042-52. PMID 26426266 DOI: 10.1097/Nen.0000000000000248 |
0.454 |
|
2015 |
Tacik P, DeTure M, Lin WL, Sanchez Contreras M, Wojtas A, Hinkle KM, Fujioka S, Baker MC, Walton RL, Carlomagno Y, Brown PH, Strongosky AJ, Kouri N, Murray ME, Petrucelli L, et al. A novel tau mutation, p.K317N, causes globular glial tauopathy. Acta Neuropathologica. 130: 199-214. PMID 25900293 DOI: 10.1007/S00401-015-1425-0 |
0.445 |
|
2014 |
Carlomagno Y, Zhang Y, Davis M, Lin WL, Cook C, Dunmore J, Tay W, Menkosky K, Cao X, Petrucelli L, Deture M. Casein kinase II induced polymerization of soluble TDP-43 into filaments is inhibited by heat shock proteins. Plos One. 9: e90452. PMID 24595055 DOI: 10.1371/Journal.Pone.0090452 |
0.413 |
|
2014 |
Kouri N, Carlomagno Y, Baker M, Liesinger AM, Caselli RJ, Wszolek ZK, Petrucelli L, Boeve BF, Parisi JE, Josephs KA, Uitti RJ, Ross OA, Graff-Radford NR, DeTure MA, Dickson DW, et al. Novel mutation in MAPT exon 13 (p.N410H) causes corticobasal degeneration. Acta Neuropathologica. 127: 271-82. PMID 24121548 DOI: 10.1007/S00401-013-1193-7 |
0.35 |
|
2014 |
Cook C, Carlomagno Y, Gendron TF, Dunmore J, Scheffel K, Stetler C, Davis M, Dickson D, Jarpe M, DeTure M, Petrucelli L. Acetylation of the KXGS motifs in tau is a critical determinant in modulation of tau aggregation and clearance. Human Molecular Genetics. 23: 104-16. PMID 23962722 DOI: 10.1093/Hmg/Ddt402 |
0.566 |
|
2013 |
Sahara N, DeTure M, Ren Y, Ebrahim AS, Kang D, Knight J, Volbracht C, Pedersen JT, Dickson DW, Yen SH, Lewis J. Characteristics of TBS-extractable hyperphosphorylated tau species: aggregation intermediates in rTg4510 mouse brain. Journal of Alzheimer's Disease : Jad. 33: 249-63. PMID 22941973 DOI: 10.3233/Jad-2012-121093 |
0.5 |
|
2012 |
Cook C, Gendron TF, Scheffel K, Carlomagno Y, Dunmore J, DeTure M, Petrucelli L. Loss of HDAC6, a novel CHIP substrate, alleviates abnormal tau accumulation. Human Molecular Genetics. 21: 2936-45. PMID 22492994 DOI: 10.1093/Hmg/Dds125 |
0.44 |
|
2010 |
Adams SJ, DeTure MA, McBride M, Dickson DW, Petrucelli L. Three repeat isoforms of tau inhibit assembly of four repeat tau filaments. Plos One. 5: e10810. PMID 20520830 DOI: 10.1371/Journal.Pone.0010810 |
0.394 |
|
2009 |
Adams SJ, Crook RJ, Deture M, Randle SJ, Innes AE, Yu XZ, Lin WL, Dugger BN, McBride M, Hutton M, Dickson DW, McGowan E. Overexpression of wild-type murine tau results in progressive tauopathy and neurodegeneration. The American Journal of Pathology. 175: 1598-609. PMID 19717642 DOI: 10.2353/Ajpath.2009.090462 |
0.474 |
|
2008 |
Hamano T, Gendron TF, Causevic E, Yen SH, Lin WL, Isidoro C, Deture M, Ko LW. Autophagic-lysosomal perturbation enhances tau aggregation in transfectants with induced wild-type tau expression. The European Journal of Neuroscience. 27: 1119-30. PMID 18294209 DOI: 10.1111/j.1460-9568.2008.06084.x |
0.566 |
|
2006 |
DeTure M, Granger B, Grover A, Hutton M, Yen SH. Evidence for independent mechanisms and a multiple-hit model of tau assembly. Biochemical and Biophysical Research Communications. 339: 858-64. PMID 16325769 DOI: 10.1016/J.Bbrc.2005.11.087 |
0.628 |
|
2005 |
Dinoto L, Deture MA, Purich DL. Structural insights into Alzheimer filament assembly pathways based on site-directed mutagenesis and S-glutathionylation of three-repeat neuronal Tau protein. Microscopy Research and Technique. 67: 156-63. PMID 16104002 DOI: 10.1002/Jemt.20195 |
0.774 |
|
2005 |
Ko LW, DeTure M, Sahara N, Chihab R, Vega IE, Yen SH. Recent advances in experimental modeling of the assembly of tau filaments. Biochimica Et Biophysica Acta. 1739: 125-39. PMID 15615632 DOI: 10.1016/j.bbadis.2004.09.004 |
0.565 |
|
2004 |
Ko LW, Rush T, Sahara N, Kersh JS, Easson C, Deture M, Lin WL, Connor YD, Yen SH. Assembly of filamentous tau aggregates in human neuronal cells. Journal of Alzheimer's Disease : Jad. 6: 605-22; discussion 6. PMID 15665401 |
0.56 |
|
2003 |
Grover A, England E, Baker M, Sahara N, Adamson J, Granger B, Houlden H, Passant U, Yen SH, DeTure M, Hutton M. A novel tau mutation in exon 9 (1260V) causes a four-repeat tauopathy. Experimental Neurology. 184: 131-40. PMID 14637086 DOI: 10.1016/S0014-4886(03)00393-5 |
0.559 |
|
2002 |
Ko LW, DeTure M, Sahara N, Chihab R, Yen SH. Cellular models for tau filament assembly. Journal of Molecular Neuroscience : Mn. 19: 311-6. PMID 12540057 |
0.562 |
|
2002 |
Sahara N, Lewis J, DeTure M, McGowan E, Dickson DW, Hutton M, Yen SH. Assembly of tau in transgenic animals expressing P301L tau: alteration of phosphorylation and solubility. Journal of Neurochemistry. 83: 1498-508. PMID 12472903 DOI: 10.1046/J.1471-4159.2002.01241.X |
0.524 |
|
2002 |
DeTure M, Ko LW, Easson C, Yen SH. Tau assembly in inducible transfectants expressing wild-type or FTDP-17 tau. The American Journal of Pathology. 161: 1711-22. PMID 12414518 DOI: 10.1016/S0002-9440(10)64448-3 |
0.591 |
|
2002 |
DeTure MA, Di Noto L, Purich DL. In vitro assembly of Alzheimer-like filaments. How a small cluster of charged residues in Tau and MAP2 controls filament morphology. The Journal of Biological Chemistry. 277: 34755-9. PMID 12023276 DOI: 10.1074/Jbc.M201201200 |
0.329 |
|
2000 |
DeTure M, Ko LW, Yen S, Nacharaju P, Easson C, Lewis J, van Slegtenhorst M, Hutton M, Yen SH. Missense tau mutations identified in FTDP-17 have a small effect on tau-microtubule interactions. Brain Research. 853: 5-14. PMID 10627302 DOI: 10.1016/S0006-8993(99)02124-1 |
0.615 |
|
1999 |
Di Noto L, DeTure MA, Purich DL. Disulfide-cross-linked tau and MAP2 homodimers readily promote microtubule assembly. Molecular Cell Biology Research Communications : McBrc. 2: 71-6. PMID 10527895 DOI: 10.1006/Mcbr.1999.0153 |
0.778 |
|
1999 |
Yen SH, Hutton M, DeTure M, Ko LW, Nacharaju P. Fibrillogenesis of tau: insights from tau missense mutations in FTDP-17. Brain Pathology (Zurich, Switzerland). 9: 695-705. PMID 10517508 DOI: 10.1111/J.1750-3639.1999.Tb00551.X |
0.554 |
|
1996 |
Zhang EY, DeTure MA, Bubb MR, Caviston TL, Erdos GW, Whittaker SD, Purich DL. Self-assembly of the brain MAP-2 microtubule-binding region into polymeric structures resembling Alzheimer filaments. Biochemical and Biophysical Research Communications. 229: 176-81. PMID 8954102 DOI: 10.1006/Bbrc.1996.1776 |
0.758 |
|
Low-probability matches (unlikely to be authored by this person) |
2002 |
Grover A, DeTure M, Yen SH, Hutton M. Effects on splicing and protein function of three mutations in codon N296 of tau in vitro. Neuroscience Letters. 323: 33-6. PMID 11911984 DOI: 10.1016/S0304-3940(02)00124-6 |
0.299 |
|
2023 |
Estades Ayuso V, Pickles S, Todd T, Yue M, Jansen-West K, Song Y, González Bejarano J, Rawlinson B, DeTure M, Graff-Radford NR, Boeve BF, Knopman DS, Petersen RC, Dickson DW, Josephs KA, et al. TDP-43-regulated cryptic RNAs accumulate in Alzheimer's disease brains. Molecular Neurodegeneration. 18: 57. PMID 37605276 DOI: 10.1186/s13024-023-00646-z |
0.298 |
|
2022 |
Jin Y, Li F, Sonoustoun B, Kondru NC, Martens YA, Qiao W, Heckman MG, Ikezu TC, Li Z, Burgess JD, Amerna D, O'Leary J, DeTure MA, Zhao J, McLean PJ, et al. APOE4 exacerbates α-synuclein seeding activity and contributes to neurotoxicity in Alzheimer's disease with Lewy body pathology. Acta Neuropathologica. PMID 35471463 DOI: 10.1007/s00401-022-02421-8 |
0.296 |
|
2020 |
Valentino RR, Koga S, Walton RL, Soto-Beasley AI, Kouri N, DeTure MA, Murray ME, Johnson PW, Petersen RC, Boeve BF, Uitti RJ, Wszolek ZK, Dickson DW, Ross OA, Heckman MG. MAPT subhaplotypes in corticobasal degeneration: assessing associations with disease risk, severity of tau pathology, and clinical features. Acta Neuropathologica Communications. 8: 218. PMID 33287913 DOI: 10.1186/s40478-020-01097-z |
0.285 |
|
2016 |
Tacik P, Sanchez-Contreras M, DeTure M, Murray ME, Rademakers R, Ross OA, Wszolek ZK, Parisi JE, Knopman DS, Petersen RC, Dickson DW. Clinicopathologic heterogeneity in FTDP-17 due to MAPT p.P301L mutation, including a patient with globular glial tauopathy. Neuropathology and Applied Neurobiology. PMID 27859539 DOI: 10.1111/Nan.12367 |
0.284 |
|
2010 |
Deture M, Hicks C, Petrucelli L. Targeting heat shock proteins in tauopathies. Current Alzheimer Research. 7: 677-84. PMID 20678072 |
0.275 |
|
2021 |
Crist AM, Hinkle KM, Wang X, Moloney CM, Matchett BJ, Labuzan SA, Frankenhauser I, Azu NO, Liesinger AM, Lesser ER, Serie DJ, Quicksall ZS, Patel TA, Carnwath TP, DeTure M, et al. Transcriptomic analysis to identify genes associated with selective hippocampal vulnerability in Alzheimer's disease. Nature Communications. 12: 2311. PMID 33875655 DOI: 10.1038/s41467-021-22399-3 |
0.266 |
|
2023 |
Koga S, Metrick MA, Golbe LI, Santambrogio A, Kim M, Soto-Beasley AI, Walton RL, Baker MC, De Castro CF, DeTure M, Russell D, Navia BA, Sandiego C, Ross OA, Vendruscolo M, et al. Case report of a patient with unclassified tauopathy with molecular and neuropathological features of both progressive supranuclear palsy and corticobasal degeneration. Acta Neuropathologica Communications. 11: 88. PMID 37264457 DOI: 10.1186/s40478-023-01584-z |
0.262 |
|
2010 |
Sahara N, DeTure M, Abdul-Shukkur E, Christensen S, Kang D, Knight J, Volbracht C, Petrucelli L, Yen S, Lewis J. P1-371: Characteristics of cytosolic hyperphosphorylated tau species in rTg4510 mouse brain Alzheimer's & Dementia. 6: S280-S281. DOI: 10.1016/J.Jalz.2010.05.925 |
0.259 |
|
2020 |
Morgan SA, Lavenir I, Fan J, Masuda-Suzukake M, Passarella D, DeTure MA, Dickson DW, Ghetti B, Goedert M. α-Synuclein filaments from transgenic mouse and human synucleinopathy-containing brains are major seed-competent species. The Journal of Biological Chemistry. PMID 32209651 DOI: 10.1074/Jbc.Ra119.012179 |
0.253 |
|
2015 |
Pottier C, Bieniek KF, Finch N, van de Vorst M, Baker M, Perkersen R, Brown P, Ravenscroft T, van Blitterswijk M, Nicholson AM, DeTure M, Knopman DS, Josephs KA, Parisi JE, Petersen RC, et al. Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease. Acta Neuropathologica. 130: 77-92. PMID 25943890 DOI: 10.1007/S00401-015-1436-X |
0.242 |
|
2017 |
DeTure M, Tacik P, Kouri N, Carlomagno Y, Ross K, Murray ME, Dickson DW. [P4-106]: GENETIC MUTATIONS IN MAPT AND SIGNIFICANT VARIABILITY IN TAU PROTEIN MODIFICATIONS INDICATE THE EXISTANCE OF A WIDE ARRAY OF STRAINS WITHIN AND ACROSS PRIMARY AND SECONDARY TAUOPATHIES Alzheimer's & Dementia. 13: P1298-P1298. DOI: 10.1016/J.Jalz.2017.06.1972 |
0.239 |
|
2020 |
Watzlawik JO, Hou X, Truban D, Ramnarine C, Barodia SK, Gendron TF, Heckman MG, DeTure M, Siuda J, Wszolek ZK, Scherzer CR, Ross OA, Bu G, Dickson DW, Goldberg MS, et al. Sensitive ELISA-based detection method for the mitophagy marker p-S65-Ub in human cells, autopsy brain, and blood samples. Autophagy. 1-16. PMID 33112198 DOI: 10.1080/15548627.2020.1834712 |
0.232 |
|
2015 |
Jones DR, Delenclos M, Baine AT, DeTure M, Murray ME, Dickson DW, McLean PJ. Transmission of Soluble and Insoluble α-Synuclein to Mice. Journal of Neuropathology and Experimental Neurology. 74: 1158-1169. PMID 26574670 DOI: 10.1097/Nen.0000000000000262 |
0.231 |
|
2021 |
Josephs KA, Duffy JR, Clark HM, Utianski RL, Strand EA, Machulda MM, Botha H, Martin PR, Pham NTT, Stierwalt J, Ali F, Buciuc M, Baker M, Fernandez De Castro CH, Spychalla AJ, ... ... DeTure MA, et al. A molecular pathology, neurobiology, biochemical, genetic and neuroimaging study of progressive apraxia of speech. Nature Communications. 12: 3452. PMID 34103532 DOI: 10.1038/s41467-021-23687-8 |
0.222 |
|
2022 |
Pickles S, Gendron TF, Koike Y, Yue M, Song Y, Kachergus JM, Shi J, DeTure M, Thompson EA, Oskarsson B, Graff-Radford NR, Boeve BF, Petersen RC, Wszolek ZK, Josephs KA, et al. Evidence of cerebellar TDP-43 loss of function in FTLD-TDP. Acta Neuropathologica Communications. 10: 107. PMID 35879741 DOI: 10.1186/s40478-022-01408-6 |
0.208 |
|
2021 |
Sayed FA, Kodama L, Fan L, Carling GK, Udeochu JC, Le D, Li Q, Zhou L, Wong MY, Horowitz R, Ye P, Mathys H, Wang M, Niu X, Mazutis L, ... ... DeTure MA, et al. AD-linked R47H- mutation induces disease-enhancing microglial states via AKT hyperactivation. Science Translational Medicine. 13: eabe3947. PMID 34851693 DOI: 10.1126/scitranslmed.abe3947 |
0.208 |
|
2014 |
Zhang YJ, Jansen-West K, Xu YF, Gendron TF, Bieniek KF, Lin WL, Sasaguri H, Caulfield T, Hubbard J, Daughrity L, Chew J, Belzil VV, Prudencio M, Stankowski JN, Castanedes-Casey M, ... ... DeTure M, et al. Aggregation-prone c9FTD/ALS poly(GA) RAN-translated proteins cause neurotoxicity by inducing ER stress. Acta Neuropathologica. 128: 505-24. PMID 25173361 DOI: 10.1007/S00401-014-1336-5 |
0.189 |
|
2020 |
Chen Z, Yan Yau W, Jaunmuktane Z, Tucci A, Sivakumar P, Gagliano Taliun SA, Turner C, Efthymiou S, Ibáñez K, Sullivan R, Bibi F, Athanasiou-Fragkouli A, Bourinaris T, Zhang D, Revesz T, ... ... DeTure M, et al. Neuronal intranuclear inclusion disease is genetically heterogeneous. Annals of Clinical and Translational Neurology. PMID 32777174 DOI: 10.1002/Acn3.51151 |
0.188 |
|
2014 |
DeTure M, Carlomagno Y, Zhang Y, Davis M, Lin W, Petrucelli L. P3-004: TDP-43 FILAMENT ASSEMBLY IS INHIBITED BY HEAT SHOCK PROTEINS Alzheimer's & Dementia. 10: P627-P628. DOI: 10.1016/J.Jalz.2014.05.1091 |
0.187 |
|
2023 |
Pickles S, Zanetti Alepuz D, Koike Y, Yue M, Tong J, Liu P, Zhou Y, Jansen-West K, Daughrity LM, Song Y, DeTure M, Oskarsson B, Graff-Radford NR, Boeve BF, Petersen RC, et al. CRISPR interference to evaluate modifiers of -mediated toxicity in FTD. Frontiers in Cell and Developmental Biology. 11: 1251551. PMID 37614226 DOI: 10.3389/fcell.2023.1251551 |
0.187 |
|
2019 |
Zhang YJ, Guo L, Gonzales PK, Gendron TF, Wu Y, Jansen-West K, O'Raw AD, Pickles SR, Prudencio M, Carlomagno Y, Gachechiladze MA, Ludwig C, Tian R, Chew J, DeTure M, et al. Heterochromatin anomalies and double-stranded RNA accumulation underlie poly(PR) toxicity. Science (New York, N.Y.). 363. PMID 30765536 DOI: 10.1126/Science.Aav2606 |
0.166 |
|
2020 |
Chitu V, Biundo F, Shlager GGL, Park ES, Wang P, Gulinello ME, Gokhan Ş, Ketchum HC, Saha K, DeTure MA, Dickson DW, Wszolek ZK, Zheng D, Croxford AL, Becher B, et al. Microglial Homeostasis Requires Balanced CSF-1/CSF-2 Receptor Signaling. Cell Reports. 30: 3004-3019.e5. PMID 32130903 DOI: 10.1016/J.Celrep.2020.02.028 |
0.157 |
|
2023 |
Sekiya H, Koga S, Murakami A, DeTure M, Ross OA, Uitti RJ, Cheshire WP, Wszolek ZK, Dickson DW. Frequency of Comorbid Pathologies and Their Clinical Impact in Multiple System Atrophy. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 37986699 DOI: 10.1002/mds.29670 |
0.148 |
|
2023 |
Zhang Z, Yu K, You Y, Jiang P, Wu Z, DeTure MA, Dickson DW, Ikezu S, Peng J, Ikezu T. Comprehensive characterization of human brain-derived extracellular vesicles using multiple isolation methods: Implications for diagnostic and therapeutic applications. Journal of Extracellular Vesicles. 12: e12358. PMID 37563857 DOI: 10.1002/jev2.12358 |
0.143 |
|
2021 |
Serrano GE, Walker JE, Arce R, Glass MJ, Vargas D, Sue LI, Intorcia AJ, Nelson CM, Oliver J, Papa J, Russell A, Suszczewicz KE, Borja CI, Belden C, Goldfarb D, ... ... Deture M, et al. Mapping of SARS-CoV-2 Brain Invasion and Histopathology in COVID-19 Disease. Medrxiv : the Preprint Server For Health Sciences. PMID 33619496 DOI: 10.1101/2021.02.15.21251511 |
0.135 |
|
2024 |
Luo H, Gustavsson EK, Macpherson H, Dominik N, Zhelcheska K, Montgomery K, Anderson C, Yau WY, Efthymiou S, Turner C, DeTure M, Dickson DW, Josephs KA, Revesz T, Lashley T, et al. Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022). Acta Neuropathologica Communications. 12: 2. PMID 38167323 DOI: 10.1186/s40478-023-01706-7 |
0.126 |
|
2022 |
Biundo F, Chitu V, Tindi J, Burghardt NS, Shlager GGL, Ketchum HC, DeTure MA, Dickson DW, Wszolek ZK, Khodakhah K, Stanley ER. Elevated granulocyte colony stimulating factor (CSF) causes cerebellar deficits and anxiety in a model of CSF-1 receptor related leukodystrophy. Glia. PMID 36433736 DOI: 10.1002/glia.24310 |
0.125 |
|
2004 |
Yen S, DeTure M, Sahara N, Ko L. S1-04-03 Cellular models for tauopathies Neurobiology of Aging. 25: S7. DOI: 10.1016/S0197-4580(04)80024-1 |
0.121 |
|
2021 |
Arakhamia T, Lee CE, Carlomagno Y, Kumar M, Duong DM, Wesseling H, Kundinger SR, Wang K, Williams D, DeTure M, Dickson DW, Cook CN, Seyfried NT, Petrucelli L, Steen JA, et al. Posttranslational Modifications Mediate the Structural Diversity of Tauopathy Strains. Cell. 184: 6207-6210. PMID 34890553 DOI: 10.1016/j.cell.2021.11.029 |
0.116 |
|
2010 |
López-Legentil S, Song B, DeTure M, Baden DG. Characterization and localization of a hybrid non-ribosomal peptide synthetase and polyketide synthase gene from the toxic dinoflagellate Karenia brevis. Marine Biotechnology (New York, N.Y.). 12: 32-41. PMID 19468793 DOI: 10.1007/S10126-009-9197-Y |
0.096 |
|
2022 |
Serrano GE, Walker JE, Tremblay C, Piras IS, Huentelman MJ, Belden CM, Goldfarb D, Shprecher D, Atri A, Adler CH, Shill HA, Driver-Dunckley E, Mehta SH, Caselli R, Woodruff BK, ... ... DeTure M, et al. SARS-CoV-2 Brain Regional Detection, Histopathology, Gene Expression, and Immunomodulatory Changes in Decedents with COVID-19. Journal of Neuropathology and Experimental Neurology. PMID 35818336 DOI: 10.1093/jnen/nlac056 |
0.084 |
|
2020 |
Crist AM, Hinkle KM, Wang X, Lesser ER, Azu NO, Moloney CM, Frankenhauser I, Labuzan SA, Matchett BJ, Liesinger AM, Serie D, DeTure M, Cook C, Petrucelli L, Petersen RC, et al. Investigating gene expression changes underlying selective hippocampal vulnerability in Alzheimer’s disease using a translational neuropathology approach Alzheimer's & Dementia. 16. DOI: 10.1002/alz.041199 |
0.08 |
|
2015 |
Prudencio M, Belzil VV, Batra R, Ross CA, Gendron TF, Pregent LJ, Murray ME, Overstreet KK, Piazza-Johnston AE, Desaro P, Bieniek KF, DeTure M, Lee WC, Biendarra SM, Davis MD, et al. Distinct brain transcriptome profiles in C9orf72-associated and sporadic ALS. Nature Neuroscience. 18: 1175-82. PMID 26192745 DOI: 10.1038/Nn.4065 |
0.076 |
|
2017 |
Prudencio M, Gonzales PK, Cook CN, Gendron TF, Daughrity LM, Song Y, Ebbert MTW, van Blitterswijk M, Zhang YJ, Jansen-West K, Baker MC, DeTure M, Rademakers R, Boylan KB, Dickson DW, et al. Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patients. Human Molecular Genetics. PMID 28637276 DOI: 10.1093/Hmg/Ddx233 |
0.074 |
|
2010 |
Cook CN, Dunmore J, Gendron T, Deture M, Petrucelli L. P1-372: Regulation of the Hsp90 chaperone complex by HDAC6 Alzheimer's & Dementia. 6: S281-S281. DOI: 10.1016/J.Jalz.2010.05.926 |
0.056 |
|
2021 |
Piras IS, Huentelman MJ, Walker JE, Arce R, Glass MJ, Vargas D, Sue LI, Intorcia AJ, Nelson CM, Suszczewicz KE, Borja CL, Desforges M, Deture M, Dickson DW, Beach TG, et al. Olfactory Bulb and Amygdala Gene Expression Changes in Subjects Dying with COVID-19. Medrxiv : the Preprint Server For Health Sciences. PMID 34545375 DOI: 10.1101/2021.09.12.21263291 |
0.056 |
|
2015 |
Pratico D, Giannopoulos P, Li J, Deture M, Dickson D. O2-05-04: The involvement of the 5lipoxygenase pathway in tauopathy Alzheimer's & Dementia. 11: P184-P185. DOI: 10.1016/J.Jalz.2015.07.157 |
0.03 |
|
2010 |
DeTure M, Petrucelli L. Targeting Heat Shock Proteins in Tauopathies Current Alzheimer Research. 999: 1-6. DOI: 10.2174/1567210206780722050 |
0.018 |
|
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