| Year |
Citation |
Score |
| 2023 |
Branch MR, Hsu CL, Ohnishi K, Shen WC, Lee E, Meisenhelder J, Winborn B, Sopher BL, Taylor JP, Hunter T, La Spada AR. MAP4K3 inhibits Sirtuin-1 to repress the LKB1-AMPK pathway to promote amino acid-dependent activation of the mTORC1 complex. Life Science Alliance. 6. PMID 37221017 DOI: 10.26508/lsa.202201525 |
0.5 |
|
| 2023 |
Holden SK, Bedenfield N, Taylor AS, Bayram E, Schwilk C, Fleisher J, Duda J, Shill H, Paulson HL, Stacy K, Wood J, Corsentino P, Sha SJ, Litvan I, Irwin DJ, ... ... Taylor JP, et al. Research Priorities of Individuals and Caregivers With Lewy Body Dementia: A Web-based Survey. Alzheimer Disease and Associated Disorders. 37: 50-58. PMID 36821177 DOI: 10.1097/WAD.0000000000000545 |
0.407 |
|
| 2022 |
Kim HJ, Mohassel P, Donkervoort S, Guo L, O'Donovan K, Coughlin M, Lornage X, Foulds N, Hammans SR, Foley AR, Fare CM, Ford AF, Ogasawara M, Sato A, Iida A, ... ... Taylor JP, et al. Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy. Nature Communications. 13: 2306. PMID 35484142 DOI: 10.1038/s41467-022-30015-1 |
0.377 |
|
| 2021 |
Nedelsky NB, Taylor JP. Pathological phase transitions in ALS-FTD impair dynamic RNA-protein granules. Rna (New York, N.Y.). PMID 34706979 DOI: 10.1261/rna.079001.121 |
0.81 |
|
| 2021 |
Beijer D, Kim HJ, Guo L, O'Donovan K, Mademan I, Deconinck T, Van Schil K, Fare CM, Drake LE, Ford AF, Kochański A, Kabzińska D, Dubuisson N, Van den Bergh P, Voermans NC, ... ... Taylor JP, et al. Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation. Jci Insight. 6. PMID 34291734 DOI: 10.1172/jci.insight.148363 |
0.334 |
|
| 2020 |
Zhang J, Velmeshev D, Hashimoto K, Huang YH, Hofmann JW, Shi X, Chen J, Leidal AM, Dishart JG, Cahill MK, Kelley KW, Liddelow SA, Seeley WW, Miller BL, Walther TC, ... ... Taylor JP, et al. Neurotoxic microglia promote TDP-43 proteinopathy in progranulin deficiency. Nature. PMID 32866962 DOI: 10.1038/S41586-020-2709-7 |
0.426 |
|
| 2020 |
Haenig C, Atias N, Taylor AK, Mazza A, Schaefer MH, Russ J, Riechers SP, Jain S, Coughlin M, Fontaine JF, Freibaum BD, Brusendorf L, Zenkner M, Porras P, Stroedicke M, ... ... Taylor JP, et al. Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains. Cell Reports. 32: 108050. PMID 32814053 DOI: 10.1016/J.Celrep.2020.108050 |
0.424 |
|
| 2020 |
Lee AK, Klein J, Fon Tacer K, Lord T, Oatley MJ, Oatley JM, Porter SN, Pruett-Miller SM, Tikhonova EB, Karamyshev AL, Wang YD, Yang P, Korff A, Kim HJ, Taylor JP, et al. Translational Repression of G3BP in Cancer and Germ Cells Suppresses Stress Granules and Enhances Stress Tolerance. Molecular Cell. PMID 32692974 DOI: 10.1016/J.Molcel.2020.06.037 |
0.314 |
|
| 2020 |
Yang P, Mathieu C, Kolaitis RM, Zhang P, Messing J, Yurtsever U, Yang Z, Wu J, Li Y, Pan Q, Yu J, Martin EW, Mittag T, Kim HJ, Taylor JP. G3BP1 Is a Tunable Switch that Triggers Phase Separation to Assemble Stress Granules. Cell. 181: 325-345.e28. PMID 32302571 DOI: 10.1016/J.Cell.2020.03.046 |
0.323 |
|
| 2020 |
Batlle C, Yang P, Coughlin M, Messing J, Pesarrodona M, Szulc E, Salvatella X, Kim HJ, Taylor JP, Ventura S. hnRNPDL Phase Separation Is Regulated by Alternative Splicing and Disease-Causing Mutations Accelerate Its Aggregation. Cell Reports. 30: 1117-1128.e5. PMID 31995753 DOI: 10.1016/J.Celrep.2019.12.080 |
0.44 |
|
| 2019 |
Farhan SMK, Howrigan DP, Abbott LE, Klim JR, Topp SD, Byrnes AE, Churchhouse C, Phatnani H, Smith BN, Rampersaud E, Wu G, Wuu J, Shatunov A, Iacoangeli A, Al Khleifat A, ... ... Taylor JP, et al. Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein. Nature Neuroscience. PMID 31768050 DOI: 10.1038/S41593-019-0530-0 |
0.389 |
|
| 2019 |
Taylor J, Lee SC. Mutations in Spliceosome Genes and Therapeutic Opportunities in Myeloid Malignancies. Genes, Chromosomes & Cancer. PMID 31334570 DOI: 10.1002/gcc.22784 |
0.311 |
|
| 2019 |
White MR, Mitrea DM, Zhang P, Stanley CB, Cassidy DE, Nourse A, Phillips AH, Tolbert M, Taylor JP, Kriwacki RW. C9orf72 Poly(PR) Dipeptide Repeats Disturb Biomolecular Phase Separation and Disrupt Nucleolar Function. Molecular Cell. PMID 30981631 DOI: 10.1016/J.Molcel.2019.03.019 |
0.365 |
|
| 2019 |
Wang B, Maxwell BA, Joo JH, Gwon Y, Messing J, Mishra A, Shaw TI, Ward AL, Quan H, Sakurada SM, Pruett-Miller SM, Bertorini T, Vogel P, Kim HJ, Peng J, ... Taylor JP, et al. ULK1 and ULK2 Regulate Stress Granule Disassembly Through Phosphorylation and Activation of VCP/p97. Molecular Cell. PMID 30979586 DOI: 10.1016/J.Molcel.2019.03.027 |
0.368 |
|
| 2019 |
Zhang P, Fan B, Yang P, Temirov J, Messing J, Kim HJ, Taylor JP. Chronic optogenetic induction of stress granules is cytotoxic and reveals the evolution of ALS-FTD pathology. Elife. 8. PMID 30893049 DOI: 10.7554/Elife.39578 |
0.407 |
|
| 2019 |
Nedelsky NB, Taylor JP. Bridging biophysics and neurology: aberrant phase transitions in neurodegenerative disease. Nature Reviews. Neurology. PMID 30890779 DOI: 10.1038/S41582-019-0157-5 |
0.793 |
|
| 2019 |
Mitra J, Guerrero EN, Hegde PM, Liachko NF, Wang H, Vasquez V, Gao J, Pandey A, Taylor JP, Kraemer BC, Wu P, Boldogh I, Garruto RM, Mitra S, Rao KS, et al. Motor neuron disease-associated loss of nuclear TDP-43 is linked to DNA double-strand break repair defects. Proceedings of the National Academy of Sciences of the United States of America. PMID 30770445 DOI: 10.1073/Pnas.1818415116 |
0.363 |
|
| 2019 |
Ralston SH, Taylor JP. Rare Inherited forms of Paget's Disease and Related Syndromes. Calcified Tissue International. PMID 30756140 DOI: 10.1007/S00223-019-00520-5 |
0.383 |
|
| 2018 |
Vogler TO, Wheeler JR, Nguyen ED, Hughes MP, Britson KA, Lester E, Rao B, Betta ND, Whitney ON, Ewachiw TE, Gomes E, Shorter J, Lloyd TE, Eisenberg DS, Taylor JP, et al. TDP-43 and RNA form amyloid-like myo-granules in regenerating muscle. Nature. 563: 508-513. PMID 30464263 DOI: 10.1038/S41586-018-0665-2 |
0.419 |
|
| 2018 |
Purice MD, Taylor JP. Linking hnRNP Function to ALS and FTD Pathology. Frontiers in Neuroscience. 12: 326. PMID 29867335 DOI: 10.3389/Fnins.2018.00326 |
0.815 |
|
| 2018 |
Guo L, Kim HJ, Wang H, Monaghan J, Freyermuth F, Sung JC, O'Donovan K, Fare CM, Diaz Z, Singh N, Zhang ZC, Coughlin M, Sweeny EA, DeSantis ME, Jackrel ME, ... ... Taylor JP, et al. Nuclear-Import Receptors Reverse Aberrant Phase Transitions of RNA-Binding Proteins with Prion-like Domains. Cell. 173: 677-692.e20. PMID 29677512 DOI: 10.1016/J.Cell.2018.03.002 |
0.404 |
|
| 2018 |
Zhang K, Daigle JG, Cunningham KM, Coyne AN, Ruan K, Grima JC, Bowen KE, Wadhwa H, Yang P, Rigo F, Taylor JP, Gitler AD, Rothstein JD, Lloyd TE. Stress Granule Assembly Disrupts Nucleocytoplasmic Transport. Cell. PMID 29628143 DOI: 10.1016/J.Cell.2018.03.025 |
0.362 |
|
| 2018 |
Nicolas A, Kenna KP, Renton AE, Ticozzi N, Faghri F, Chia R, Dominov JA, Kenna BJ, Nalls MA, Keagle P, Rivera AM, van Rheenen W, Murphy NA, van Vugt JJFA, Geiger JT, ... ... Taylor JP, et al. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. Neuron. 97: 1268-1283.e6. PMID 29566793 DOI: 10.1016/J.Neuron.2018.02.027 |
0.662 |
|
| 2018 |
Pottier C, Rampersaud E, Baker M, Wu G, Wuu J, McCauley JL, Zuchner S, Schule R, Bermudez C, Hussain S, Cooley A, Wallace M, Zhang J, Taylor JP, Benatar M, et al. Identification of compound heterozygous variants in OPTN in an ALS-FTD patient from the CReATe consortium: a case report. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-3. PMID 29558868 DOI: 10.1080/21678421.2018.1452947 |
0.386 |
|
| 2018 |
Dao TP, Kolaitis RM, Kim HJ, O'Donovan K, Martyniak B, Colicino E, Hehnly H, Taylor JP, Castañeda CA. Ubiquitin Modulates Liquid-Liquid Phase Separation of UBQLN2 via Disruption of Multivalent Interactions. Molecular Cell. PMID 29526694 DOI: 10.1016/J.Molcel.2018.02.004 |
0.344 |
|
| 2018 |
Badders NM, Korff A, Miranda HC, Vuppala PK, Smith RB, Winborn BJ, Quemin ER, Sopher BL, Dearman J, Messing J, Kim NC, Moore J, Freibaum BD, Kanagaraj AP, Fan B, ... ... Taylor JP, et al. Selective modulation of the androgen receptor AF2 domain rescues degeneration in spinal bulbar muscular atrophy. Nature Medicine. PMID 29505030 DOI: 10.1038/Nm.4500 |
0.591 |
|
| 2018 |
Wegmann S, Eftekharzadeh B, Tepper K, Zoltowska KM, Bennett RE, Dujardin S, Laskowski PR, MacKenzie D, Kamath T, Commins C, Vanderburg C, Roe AD, Fan Z, Molliex AM, Hernandez-Vega A, ... ... Taylor JP, et al. Tau protein liquid-liquid phase separation can initiate tau aggregation. The Embo Journal. PMID 29472250 DOI: 10.15252/Embj.201798049 |
0.337 |
|
| 2018 |
Lee Y, Jonson PH, Sarparanta J, Palmio J, Sarkar M, Vihola A, Evilä A, Suominen T, Penttilä S, Savarese M, Johari M, Minot MC, Hilton-Jones D, Maddison P, Chinnery P, ... ... Taylor JP, et al. TIA1 variant drives myodegeneration in multisystem proteinopathy with SQSTM1 mutations. The Journal of Clinical Investigation. PMID 29457785 DOI: 10.1172/Jci97103 |
0.453 |
|
| 2018 |
Wen J, Hübner J, Orisme W, Wu G, Tang B, Jia S, Easton J, Haupfear K, Freibaum BD, Kim HJ, High A, Peng J, Tatevossian RG, Taylor JP, Pfister SM, et al. Abstract PR08: Overexpression and mutations of CXorf67 in “infant-type” posterior fossa type-A ependymomas Cancer Research. 78. DOI: 10.1158/1538-7445.Pedca17-Pr08 |
0.358 |
|
| 2017 |
Hirsch-Reinshagen V, Pottier C, Nicholson AM, Baker M, Hsiung GR, Krieger C, Sengdy P, Boylan KB, Dickson DW, Mesulam M, Weintraub S, Bigio E, Zinman L, Keith J, Rogaeva E, ... ... Taylor JP, et al. Clinical and neuropathological features of ALS/FTD with TIA1 mutations. Acta Neuropathologica Communications. 5: 96. PMID 29216908 DOI: 10.1017/Cjn.2018.48 |
0.401 |
|
| 2017 |
Kim HJ, Taylor JP. Lost in Transportation: Nucleocytoplasmic Transport Defects in ALS and Other Neurodegenerative Diseases. Neuron. 96: 285-297. PMID 29024655 DOI: 10.1016/J.Neuron.2017.07.029 |
0.418 |
|
| 2017 |
Mackenzie IR, Nicholson AM, Sarkar M, Messing J, Purice MD, Pottier C, Annu K, Baker M, Perkerson RB, Kurti A, Matchett BJ, Mittag T, Temirov J, Hsiung GR, Krieger C, ... ... Taylor JP, et al. TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics. Neuron. 95: 808-816.e9. PMID 28817800 DOI: 10.1016/J.Neuron.2017.07.025 |
0.796 |
|
| 2017 |
Becker LA, Huang B, Bieri G, Ma R, Knowles DA, Jafar-Nejad P, Messing J, Kim HJ, Soriano A, Auburger G, Pulst SM, Taylor JP, Rigo F, Gitler AD. Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice. Nature. PMID 28405022 DOI: 10.1038/Nature22038 |
0.433 |
|
| 2017 |
Ishiguro T, Sato N, Ueyama M, Fujikake N, Sellier C, Kanegami A, Tokuda E, Zamiri B, Gall-Duncan T, Mirceta M, Furukawa Y, Yokota T, Wada K, Taylor JP, Pearson CE, et al. Regulatory Role of RNA Chaperone TDP-43 for RNA Misfolding and Repeat-Associated Translation in SCA31. Neuron. PMID 28343865 DOI: 10.1016/J.Neuron.2017.02.046 |
0.382 |
|
| 2017 |
Boeynaems S, Bogaert E, Kovacs D, Konijnenberg A, Timmerman E, Volkov A, Guharoy M, De Decker M, Jaspers T, Ryan VH, Janke AM, Baatsen P, Vercruysse T, Kolaitis RM, Daelemans D, ... Taylor JP, et al. Phase Separation of C9orf72 Dipeptide Repeats Perturbs Stress Granule Dynamics. Molecular Cell. 65: 1044-1055.e5. PMID 28306503 DOI: 10.1016/J.Molcel.2017.02.013 |
0.355 |
|
| 2017 |
Freibaum BD, Taylor JP. The Role of Dipeptide Repeats in C9ORF72-Related ALS-FTD. Frontiers in Molecular Neuroscience. 10: 35. PMID 28243191 DOI: 10.3389/Fnmol.2017.00035 |
0.445 |
|
| 2017 |
Taylor JP. A PR plug for the nuclear pore in amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences of the United States of America. PMID 28159889 DOI: 10.1073/Pnas.1621085114 |
0.416 |
|
| 2017 |
Paul KR, Molliex A, Cascarina S, Boncella AE, Taylor JP, Ross ED. The effects of mutations on the aggregation propensity of the human prion-like protein hnRNPA2B1. Molecular and Cellular Biology. PMID 28137911 DOI: 10.1128/Mcb.00652-16 |
0.383 |
|
| 2016 |
Lanman TA, Bakar D, Badders NM, Burke A, Kokkinis A, Shrader JA, Joe GO, Schindler AB, Bott LC, Harmison GG, Taylor JP, Fischbeck KH, Grunseich C. Sexual Reassignment Fails to Prevent Kennedy's Disease. Journal of Neuromuscular Diseases. 3: 121-125. PMID 27854206 DOI: 10.3233/Jnd-150128 |
0.585 |
|
| 2016 |
Taylor JP, Brown RH, Cleveland DW. Decoding ALS: from genes to mechanism. Nature. 539: 197-206. PMID 27830784 DOI: 10.1038/Nature20413 |
0.417 |
|
| 2016 |
Martinez FJ, Pratt GA, Van Nostrand EL, Batra R, Huelga SC, Kapeli K, Freese P, Chun SJ, Ling K, Gelboin-Burkhart C, Fijany L, Wang HC, Nussbacher JK, Broski SM, Kim HJ, ... ... Taylor JP, et al. Protein-RNA Networks Regulated by Normal and ALS-Associated Mutant HNRNPA2B1 in the Nervous System. Neuron. PMID 27773581 DOI: 10.1016/J.Neuron.2016.09.050 |
0.345 |
|
| 2016 |
Lee KH, Zhang P, Kim HJ, Mitrea DM, Sarkar M, Freibaum BD, Cika J, Coughlin M, Messing J, Molliex A, Maxwell BA, Kim NC, Temirov J, Moore J, Kolaitis RM, ... ... Taylor JP, et al. C9orf72 Dipeptide Repeats Impair the Assembly, Dynamics, and Function of Membrane-Less Organelles. Cell. 167: 774-788.e17. PMID 27768896 DOI: 10.1016/J.Cell.2016.10.002 |
0.398 |
|
| 2016 |
Marzahn MR, Marada S, Lee J, Nourse A, Kenrick S, Zhao H, Ben-Nissan G, Kolaitis RM, Peters JL, Pounds S, Errington WJ, Privé GG, Taylor JP, Sharon M, Schuck P, et al. Higher-order oligomerization promotes localization of SPOP to liquid nuclear speckles. The Embo Journal. 35: 1254-75. PMID 27220849 DOI: 10.15252/Embj.201593169 |
0.357 |
|
| 2016 |
Valentin-Vega YA, Wang YD, Parker M, Patmore DM, Kanagaraj A, Moore J, Rusch M, Finkelstein D, Ellison DW, Gilbertson RJ, Zhang J, Kim HJ, Taylor JP. Cancer-associated DDX3X mutations drive stress granule assembly and impair global translation. Scientific Reports. 6: 25996. PMID 27180681 DOI: 10.1038/Srep25996 |
0.406 |
|
| 2016 |
Ahmed M, Machado PM, Miller A, Spicer C, Herbelin L, He J, Noel J, Wang Y, McVey AL, Pasnoor M, Gallagher P, Statland J, Lu CH, Kalmar B, Brady S, ... ... Taylor JP, et al. Targeting protein homeostasis in sporadic inclusion body myositis. Science Translational Medicine. 8: 331ra41. PMID 27009270 DOI: 10.1126/Scitranslmed.Aad4583 |
0.386 |
|
| 2016 |
Bott LC, Badders NM, Chen KL, Harmison GG, Bautista E, Shih CC, Katsuno M, Sobue G, Taylor JP, Dantuma NP, Fischbeck KH, Rinaldi C. A small-molecule Nrf1 and Nrf2 activator mitigates polyglutamine toxicity in spinal and bulbar muscular atrophy. Human Molecular Genetics. PMID 26962150 DOI: 10.1093/Hmg/Ddw073 |
0.641 |
|
| 2016 |
Klionsky DJ, Abdelmohsen K, Abe A, Abedin J, Abeliovich H, Arozena AA, Adachi H, Adams CM, Adams PD, Adeli K, Adhihetty PJ, Adler SG, Agam G, Agarwal R, Aghi MK, ... ... Taylor JP, et al. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356 Autophagy. 12: 443-443. PMID 26902590 DOI: 10.1080/15548627.2016.1147886 |
0.507 |
|
| 2016 |
Klionsky DJ, Abdelmohsen K, Abe A, Abedin MJ, Abeliovich H, Acevedo Arozena A, Adachi H, Adams CM, Adams PD, Adeli K, Adhihetty PJ, Adler SG, Agam G, Agarwal R, Aghi MK, ... ... Taylor JP, et al. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy. 12: 1-222. PMID 26799652 DOI: 10.1080/15548627.2015.1100356 |
0.712 |
|
| 2016 |
Li S, Freibaum BD, Zhang P, Kim NC, Kolaitis RM, Molliex A, Kanagaraj AP, Yabe I, Tanino M, Tanaka S, Sasaki H, Ross ED, Taylor JP, Kim HJ. Genetic Interaction of hnRNPA2B1 and DNAJB6 in a Drosophila Model of Multisystem Proteinopathy. Human Molecular Genetics. PMID 26744327 DOI: 10.1093/Hmg/Ddv627 |
0.488 |
|
| 2015 |
Molliex A, Temirov J, Lee J, Coughlin M, Kanagaraj AP, Kim HJ, Mittag T, Taylor JP. Phase Separation by Low Complexity Domains Promotes Stress Granule Assembly and Drives Pathological Fibrillization. Cell. 163: 123-33. PMID 26406374 DOI: 10.1016/J.Cell.2015.09.015 |
0.394 |
|
| 2015 |
Coyne AN, Yamada SB, Siddegowda BB, Estes PS, Zaepfel BL, Johannesmeyer JS, Lockwood DB, Pham LT, Hart MP, Cassel JA, Freibaum B, Boehringer AV, Taylor JP, Reitz AB, Gitler AD, et al. Fragile X protein mitigates TDP-43 toxicity by remodeling RNA granules and restoring translation. Human Molecular Genetics. PMID 26385636 DOI: 10.1093/Hmg/Ddv389 |
0.436 |
|
| 2015 |
Freibaum BD, Lu Y, Lopez-Gonzalez R, Kim NC, Almeida S, Lee KH, Badders N, Valentine M, Miller BL, Wong PC, Petrucelli L, Kim HJ, Gao FB, Taylor JP. GGGGCC repeat expansion in C9orf72 compromises nucleocytoplasmic transport. Nature. 525: 129-33. PMID 26308899 DOI: 10.1038/Nature14974 |
0.441 |
|
| 2015 |
Taylor JP. Multisystem proteinopathy: Intersecting genetics in muscle, bone, and brain degeneration. Neurology. 85: 658-60. PMID 26208960 DOI: 10.1212/Wnl.0000000000001862 |
0.415 |
|
| 2015 |
Oh SY, He F, Krans A, Frazer M, Taylor JP, Paulson HL, Todd PK. RAN translation at CGG repeats induces ubiquitin proteasome system impairment in models of fragile X-associated tremor ataxia syndrome. Human Molecular Genetics. 24: 4317-26. PMID 25954027 DOI: 10.1093/Hmg/Ddv165 |
0.76 |
|
| 2015 |
Sanhueza M, Chai A, Smith C, McCray BA, Simpson TI, Taylor JP, Pennetta G. Network analyses reveal novel aspects of ALS pathogenesis. Plos Genetics. 11: e1005107. PMID 25826266 DOI: 10.1371/Journal.Pgen.1005107 |
0.789 |
|
| 2015 |
Scoto M, Rossor AM, Harms MB, Cirak S, Calissano M, Robb S, Manzur AY, MartÃnez Arroyo A, Rodriguez Sanz A, Mansour S, Fallon P, Hadjikoumi I, Klein A, Yang M, De Visser M, ... ... Taylor JP, et al. Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy. Neurology. 84: 668-79. PMID 25609763 DOI: 10.1212/Wnl.0000000000001269 |
0.33 |
|
| 2015 |
Scaramuzzino C, Casci I, Parodi S, Lievens PM, Polanco MJ, Milioto C, Chivet M, Monaghan J, Mishra A, Badders N, Aggarwal T, Grunseich C, Sambataro F, Basso M, Fackelmayer FO, ... Taylor JP, et al. Protein arginine methyltransferase 6 enhances polyglutamine-expanded androgen receptor function and toxicity in spinal and bulbar muscular atrophy. Neuron. 85: 88-100. PMID 25569348 DOI: 10.1016/J.Neuron.2014.12.031 |
0.411 |
|
| 2015 |
Oskarsson B, Wheelock V, Benatar M, Taylor JP, Joyce N, Chesak D, Jin LW. A case of familial ALS due to multi-system proteinopathy 1 and Huntington disease. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 16: 124-6. PMID 25205077 DOI: 10.3109/21678421.2014.952238 |
0.499 |
|
| 2015 |
Marzahn MR, Lee J, Palud A, Marada S, Nourse A, Taylor JP, Ogden SK, Mittag T. The Role of Protein Disorder and Self-Association in the Formation of Cellular Bodies Biophysical Journal. 108: 6a. DOI: 10.1016/J.Bpj.2014.11.047 |
0.375 |
|
| 2014 |
Gao FB, Taylor JP. RNA metabolism in neurological disease. Brain Research. 1584: 1-2. PMID 25248315 DOI: 10.1016/J.Brainres.2014.09.011 |
0.482 |
|
| 2014 |
Figley MD, Bieri G, Kolaitis RM, Taylor JP, Gitler AD. Profilin 1 associates with stress granules and ALS-linked mutations alter stress granule dynamics. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 8083-97. PMID 24920614 DOI: 10.1523/JNEUROSCI.0543-14.2014 |
0.304 |
|
| 2014 |
He F, Krans A, Freibaum BD, Taylor JP, Todd PK. TDP-43 suppresses CGG repeat-induced neurotoxicity through interactions with HnRNP A2/B1. Human Molecular Genetics. 23: 5036-51. PMID 24920338 DOI: 10.1093/Hmg/Ddu216 |
0.668 |
|
| 2014 |
Pinkus JL, Amato AA, Taylor JP, Greenberg SA. Abnormal distribution of heterogeneous nuclear ribonucleoproteins in sporadic inclusion body myositis. Neuromuscular Disorders : Nmd. 24: 611-6. PMID 24857366 DOI: 10.1016/J.Nmd.2014.04.012 |
0.382 |
|
| 2014 |
Johnson JO, Pioro EP, Boehringer A, Chia R, Feit H, Renton AE, Pliner HA, Abramzon Y, Marangi G, Winborn BJ, Gibbs JR, Nalls MA, Morgan S, Shoai M, Hardy J, ... ... Taylor JP, et al. Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis. Nature Neuroscience. 17: 664-6. PMID 24686783 DOI: 10.1038/Nn.3688 |
0.435 |
|
| 2014 |
Seelen M, Visser AE, Overste DJ, Kim HJ, Palud A, Wong TH, van Swieten JC, Scheltens P, Voermans NC, Baas F, de Jong JM, van der Kooi AJ, de Visser M, Veldink JH, Taylor JP, et al. No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy. Neurobiology of Aging. 35: 1956.e9-1956.e11. PMID 24612671 DOI: 10.1016/J.Neurobiolaging.2014.01.152 |
0.403 |
|
| 2014 |
Taylor JP. Neurodegenerative diseases: G-quadruplex poses quadruple threat. Nature. 507: 175-7. PMID 24598546 DOI: 10.1038/Nature13067 |
0.433 |
|
| 2014 |
Alami NH, Smith RB, Carrasco MA, Williams LA, Winborn CS, Han SS, Kiskinis E, Winborn B, Freibaum BD, Kanagaraj A, Clare AJ, Badders NM, Bilican B, Chaum E, Chandran S, ... ... Taylor JP, et al. Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations. Neuron. 81: 536-43. PMID 24507191 DOI: 10.1016/J.Neuron.2013.12.018 |
0.328 |
|
| 2013 |
Ramaswami M, Taylor JP, Parker R. Altered ribostasis: RNA-protein granules in degenerative disorders. Cell. 154: 727-36. PMID 23953108 DOI: 10.1016/J.Cell.2013.07.038 |
0.425 |
|
| 2013 |
Buchan JR, Kolaitis RM, Taylor JP, Parker R. Eukaryotic stress granules are cleared by autophagy and Cdc48/VCP function. Cell. 153: 1461-74. PMID 23791177 DOI: 10.1016/J.Cell.2013.05.037 |
0.423 |
|
| 2013 |
Fujita K, Nakamura Y, Oka T, Ito H, Tamura T, Tagawa K, Sasabe T, Katsuta A, Motoki K, Shiwaku H, Sone M, Yoshida C, Katsuno M, Eishi Y, Murata M, ... Taylor JP, et al. A functional deficiency of TERA/VCP/p97 contributes to impaired DNA repair in multiple polyglutamine diseases. Nature Communications. 4: 1816. PMID 23652004 DOI: 10.1038/Ncomms2828 |
0.62 |
|
| 2013 |
Benatar M, Wuu J, Fernandez C, Weihl CC, Katzen H, Steele J, Oskarsson B, Taylor JP. Motor neuron involvement in multisystem proteinopathy: implications for ALS. Neurology. 80: 1874-80. PMID 23635965 DOI: 10.1212/Wnl.0B013E3182929Fc3 |
0.471 |
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| 2013 |
Todd PK, Oh SY, Krans A, He F, Sellier C, Frazer M, Renoux AJ, Chen KC, Scaglione KM, Basrur V, Elenitoba-Johnson K, Vonsattel JP, Louis ED, Sutton MA, Taylor JP, et al. CGG repeat-associated translation mediates neurodegeneration in fragile X tremor ataxia syndrome. Neuron. 78: 440-55. PMID 23602499 DOI: 10.1016/J.Neuron.2013.03.026 |
0.799 |
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| 2013 |
Kim NC, Tresse E, Kolaitis RM, Molliex A, Thomas RE, Alami NH, Wang B, Joshi A, Smith RB, Ritson GP, Winborn BJ, Moore J, Lee JY, Yao TP, Pallanck L, ... ... Taylor JP, et al. VCP is essential for mitochondrial quality control by PINK1/Parkin and this function is impaired by VCP mutations. Neuron. 78: 65-80. PMID 23498974 DOI: 10.1016/J.Neuron.2013.02.029 |
0.789 |
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| 2013 |
Taylor JP. Neuroscience. RNA that gets RAN in neurodegeneration. Science (New York, N.Y.). 339: 1282-3. PMID 23493702 DOI: 10.1126/Science.1236450 |
0.409 |
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| 2013 |
Kim HJ, Kim NC, Wang YD, Scarborough EA, Moore J, Diaz Z, MacLea KS, Freibaum B, Li S, Molliex A, Kanagaraj AP, Carter R, Boylan KB, Wojtas AM, Rademakers R, ... ... Taylor JP, et al. Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS. Nature. 495: 467-73. PMID 23455423 DOI: 10.1038/Nature11922 |
0.485 |
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| 2013 |
Todd P, Oh S, Krans A, He F, Sellier C, Frazer M, Renoux A, Chen K, Scaglione K, Basrur V, Elenitoba-Johnson K, Vonsattel J, Louis E, Sutton M, Taylor J, et al. CGG Repeat-Associated Translation Mediates Neurodegeneration in Fragile X Tremor Ataxia Syndrome Neuron. 79: 402. DOI: 10.1016/j.neuron.2013.07.008 |
0.571 |
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| 2012 |
Klionsky DJ, Abdalla FC, Abeliovich H, Abraham RT, Acevedo-Arozena A, Adeli K, Agholme L, Agnello M, Agostinis P, Aguirre-Ghiso JA, Ahn HJ, Ait-Mohamed O, Ait-Si-Ali S, Akematsu T, Akira S, ... ... Taylor JP, et al. Guidelines for the use and interpretation of assays for monitoring autophagy. Autophagy. 8: 445-544. PMID 22966490 DOI: 10.4161/Auto.19496 |
0.686 |
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| 2012 |
Park YN, Zhao X, Norton M, Taylor JP, Eisenberg E, Greene LE. Huntingtin fragments and SOD1 mutants form soluble oligomers in the cell. Plos One. 7: e40329. PMID 22768276 DOI: 10.1371/Journal.Pone.0040329 |
0.356 |
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| 2012 |
Usenovic M, Tresse E, Mazzulli JR, Taylor JP, Krainc D. Deficiency of ATP13A2 leads to lysosomal dysfunction, α-synuclein accumulation, and neurotoxicity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 4240-6. PMID 22442086 DOI: 10.1523/Jneurosci.5575-11.2012 |
0.487 |
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| 2012 |
Messing A, Li R, Naidu S, Taylor JP, Silverman L, Flint D, van der Knaap MS, Brenner M. Archetypal and new families with Alexander disease and novel mutations in GFAP. Archives of Neurology. 69: 208-14. PMID 21987397 DOI: 10.1001/Archneurol.2011.1181 |
0.362 |
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| 2012 |
Majounie E, Traynor BJ, Chiò A, Restagno G, Mandrioli J, Benatar M, Taylor JP, Singleton AB. Mutational analysis of the VCP gene in Parkinson's disease. Neurobiology of Aging. 33: 209.e1-2. PMID 21920633 DOI: 10.1016/J.Neurobiolaging.2011.07.011 |
0.411 |
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| 2011 |
Mammen AL, Mahoney JA, St Germain A, Badders N, Taylor JP, Rosen A, Spinette S. A novel conserved isoform of the ubiquitin ligase UFD2a/UBE4B is expressed exclusively in mature striated muscle cells. Plos One. 6: e28861. PMID 22174917 DOI: 10.1371/Journal.Pone.0028861 |
0.302 |
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| 2011 |
Smith R, Taylor JP. Dissection and imaging of active zones in the Drosophila neuromuscular junction. Journal of Visualized Experiments : Jove. PMID 21559003 DOI: 10.3791/2676 |
0.333 |
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| 2011 |
Lanson NA, Maltare A, King H, Smith R, Kim JH, Taylor JP, Lloyd TE, Pandey UB. A Drosophila model of FUS-related neurodegeneration reveals genetic interaction between FUS and TDP-43. Human Molecular Genetics. 20: 2510-23. PMID 21487023 DOI: 10.1093/Hmg/Ddr150 |
0.475 |
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| 2011 |
Johnson JO, Mandrioli J, Benatar MG, Abramzon Y, Deerlin VMV, Trojanowski JQ, Gibbs JR, Brunetti M, Gronka S, Wuu J, Ding J, McCluskey L, Martinez-Lage M, Falcone D, Hernandez DG, ... ... Taylor JP, et al. Erratum exome sequencing reveals VCP mutations as a cause of familial ALS Neuron. 69. DOI: 10.1016/J.Neuron.2011.01.009 |
0.316 |
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| 2010 |
Todd PK, Oh SY, Krans A, Pandey UB, Di Prospero NA, Min KT, Taylor JP, Paulson HL. Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome. Plos Genetics. 6: e1001240. PMID 21170301 DOI: 10.1371/Journal.Pgen.1001240 |
0.781 |
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| 2010 |
Johnson JO, Mandrioli J, Benatar M, Abramzon Y, Van Deerlin VM, Trojanowski JQ, Gibbs JR, Brunetti M, Gronka S, Wuu J, Ding J, McCluskey L, Martinez-Lage M, Falcone D, Hernandez DG, ... ... Taylor JP, et al. Exome sequencing reveals VCP mutations as a cause of familial ALS. Neuron. 68: 857-64. PMID 21145000 DOI: 10.1016/J.Neuron.2010.11.036 |
0.423 |
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| 2010 |
Nedelsky NB, Pennuto M, Smith RB, Palazzolo I, Moore J, Nie Z, Neale G, Taylor JP. Native functions of the androgen receptor are essential to pathogenesis in a Drosophila model of spinobulbar muscular atrophy. Neuron. 67: 936-52. PMID 20869592 DOI: 10.1016/J.Neuron.2010.08.034 |
0.794 |
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| 2010 |
Ritson GP, Custer SK, Freibaum BD, Guinto JB, Geffel D, Moore J, Tang W, Winton MJ, Neumann M, Trojanowski JQ, Lee VM, Forman MS, Taylor JP. TDP-43 mediates degeneration in a novel Drosophila model of disease caused by mutations in VCP/p97. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 7729-39. PMID 20519548 DOI: 10.1523/Jneurosci.5894-09.2010 |
0.818 |
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| 2010 |
Lee JY, Nagano Y, Taylor JP, Lim KL, Yao TP. Disease-causing mutations in parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagy. The Journal of Cell Biology. 189: 671-9. PMID 20457763 DOI: 10.1083/Jcb.201001039 |
0.448 |
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| 2010 |
Palazzolo I, Nedelsky NB, Askew CE, Harmison GG, Kasantsev AG, Taylor JP, Fischbeck KH, Pennuto M. B2 attenuates polyglutamine-expanded androgen receptor toxicity in cell and fly models of spinal and bulbar muscular atrophy. Journal of Neuroscience Research. 88: 2207-16. PMID 20336775 DOI: 10.1002/Jnr.22389 |
0.789 |
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| 2010 |
Lloyd TE, Taylor JP. Flightless flies: Drosophila models of neuromuscular disease. Annals of the New York Academy of Sciences. 1184: e1-20. PMID 20329357 DOI: 10.1111/J.1749-6632.2010.05432.X |
0.417 |
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| 2010 |
La Spada AR, Taylor JP. Repeat expansion disease: progress and puzzles in disease pathogenesis. Nature Reviews. Genetics. 11: 247-58. PMID 20177426 DOI: 10.1038/Nrg2748 |
0.665 |
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| 2010 |
Custer SK, Neumann M, Lu H, Wright AC, Taylor JP. Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone. Human Molecular Genetics. 19: 1741-55. PMID 20147319 DOI: 10.1093/Hmg/Ddq050 |
0.369 |
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| 2010 |
Dachsel JC, Nishioka K, Vilariño-Güell C, Lincoln SJ, Soto-Ortolaza AI, Kachergus J, Hinkle KM, Heckman MG, Jasinska-Myga B, Taylor JP, Dickson DW, Gibson RA, Hentati F, Ross OA, Farrer MJ. Heterodimerization of Lrrk1-Lrrk2: Implications for LRRK2-associated Parkinson disease. Mechanisms of Ageing and Development. 131: 210-4. PMID 20144646 DOI: 10.1016/J.Mad.2010.01.009 |
0.308 |
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| 2010 |
Tresse E, Salomons FA, Vesa J, Bott LC, Kimonis V, Yao TP, Dantuma NP, Taylor JP. VCP/p97 is essential for maturation of ubiquitin-containing autophagosomes and this function is impaired by mutations that cause IBMPFD. Autophagy. 6: 217-27. PMID 20104022 DOI: 10.4161/Auto.6.2.11014 |
0.384 |
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| 2010 |
Batlevi Y, Martin DN, Pandey UB, Simon CR, Powers CM, Taylor JP, Baehrecke EH. Dynein light chain 1 is required for autophagy, protein clearance, and cell death in Drosophila. Proceedings of the National Academy of Sciences of the United States of America. 107: 742-7. PMID 20080745 DOI: 10.1073/Pnas.0907967107 |
0.435 |
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| 2010 |
Lee JY, Koga H, Kawaguchi Y, Tang W, Wong E, Gao YS, Pandey UB, Kaushik S, Tresse E, Lu J, Taylor JP, Cuervo AM, Yao TP. HDAC6 controls autophagosome maturation essential for ubiquitin-selective quality-control autophagy. The Embo Journal. 29: 969-80. PMID 20075865 DOI: 10.1038/Emboj.2009.405 |
0.406 |
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| 2010 |
McCray BA, Skordalakes E, Taylor JP. Disease mutations in Rab7 result in unregulated nucleotide exchange and inappropriate activation. Human Molecular Genetics. 19: 1033-47. PMID 20028791 DOI: 10.1093/Hmg/Ddp567 |
0.784 |
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| 2010 |
Freibaum BD, Chitta RK, High AA, Taylor JP. Global analysis of TDP-43 interacting proteins reveals strong association with RNA splicing and translation machinery. Journal of Proteome Research. 9: 1104-20. PMID 20020773 DOI: 10.1021/Pr901076Y |
0.444 |
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| 2009 |
Palazzolo I, Stack C, Kong L, Musaro A, Adachi H, Katsuno M, Sobue G, Taylor JP, Sumner CJ, Fischbeck KH, Pennuto M. Overexpression of IGF-1 in muscle attenuates disease in a mouse model of spinal and bulbar muscular atrophy. Neuron. 63: 316-28. PMID 19679072 DOI: 10.1016/J.Neuron.2009.07.019 |
0.543 |
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| 2009 |
Mojsilovic-Petrovic J, Nedelsky N, Boccitto M, Mano I, Georgiades SN, Zhou W, Liu Y, Neve RL, Taylor JP, Driscoll M, Clardy J, Merry D, Kalb RG. FOXO3a is broadly neuroprotective in vitro and in vivo against insults implicated in motor neuron diseases. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 8236-47. PMID 19553463 DOI: 10.1523/Jneurosci.1805-09.2009 |
0.798 |
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| 2009 |
Salajegheh M, Pinkus JL, Taylor JP, Amato AA, Nazareno R, Baloh RH, Greenberg SA. Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis. Muscle & Nerve. 40: 19-31. PMID 19533646 DOI: 10.1002/Mus.21386 |
0.367 |
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| 2009 |
Young JE, Garden GA, Martinez RA, Tanaka F, Sandoval CM, Smith AC, Sopher BL, Lin A, Fischbeck KH, Ellerby LM, Morrison RS, Taylor JP, La Spada AR. Polyglutamine-expanded androgen receptor truncation fragments activate a Bax-dependent apoptotic cascade mediated by DP5/Hrk. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 1987-97. PMID 19228953 DOI: 10.1523/Jneurosci.4072-08.2009 |
0.7 |
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| 2009 |
Salomons FA, Menéndez-Benito V, Böttcher C, McCray BA, Taylor JP, Dantuma NP. Selective accumulation of aggregation-prone proteasome substrates in response to proteotoxic stress. Molecular and Cellular Biology. 29: 1774-85. PMID 19158272 DOI: 10.1128/Mcb.01485-08 |
0.766 |
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| 2008 |
Nedelsky NB, Todd PK, Taylor JP. Autophagy and the ubiquitin-proteasome system: collaborators in neuroprotection. Biochimica Et Biophysica Acta. 1782: 691-9. PMID 18930136 DOI: 10.1016/J.Bbadis.2008.10.002 |
0.81 |
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| 2008 |
Klionsky DJ, Abeliovich H, Agostinis P, Agrawal DK, Aliev G, Askew DS, Baba M, Baehrecke EH, Bahr BA, Ballabio A, Bamber BA, Bassham DC, Bergamini E, Bi X, Biard-Piechaczyk M, ... ... Taylor JP, et al. Guidelines for the use and interpretation of assays for monitoring autophagy in higher eukaryotes. Autophagy. 4: 151-75. PMID 18188003 DOI: 10.4161/Auto.5338 |
0.571 |
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| 2008 |
McCray BA, Taylor JP. The role of autophagy in age-related neurodegeneration. Neuro-Signals. 16: 75-84. PMID 18097162 DOI: 10.1159/000109761 |
0.791 |
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| 2007 |
Pandey UB, Batlevi Y, Baehrecke EH, Taylor JP. HDAC6 at the intersection of autophagy, the ubiquitin-proteasome system and neurodegeneration. Autophagy. 3: 643-5. PMID 17912024 DOI: 10.4161/Auto.5050 |
0.481 |
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| 2007 |
Young JE, Gouw L, Propp S, Sopher BL, Taylor J, Lin A, Hermel E, Logvinova A, Chen SF, Chen S, Bredesen DE, Truant R, Ptacek LJ, La Spada AR, Ellerby LM. Proteolytic cleavage of ataxin-7 by caspase-7 modulates cellular toxicity and transcriptional dysregulation. The Journal of Biological Chemistry. 282: 30150-60. PMID 17646170 DOI: 10.1074/Jbc.M705265200 |
0.584 |
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| 2007 |
Melrose HL, Kent CB, Taylor JP, Dachsel JC, Hinkle KM, Lincoln SJ, Mok SS, Culvenor JG, Masters CL, Tyndall GM, Bass DI, Ahmed Z, Andorfer CA, Ross OA, Wszolek ZK, et al. A comparative analysis of leucine-rich repeat kinase 2 (Lrrk2) expression in mouse brain and Lewy body disease. Neuroscience. 147: 1047-58. PMID 17611037 DOI: 10.1016/J.Neuroscience.2007.05.027 |
0.305 |
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| 2007 |
Pandey UB, Nie Z, Batlevi Y, McCray BA, Ritson GP, Nedelsky NB, Schwartz SL, DiProspero NA, Knight MA, Schuldiner O, Padmanabhan R, Hild M, Berry DL, Garza D, Hubbert CC, ... ... Taylor JP, et al. HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS. Nature. 447: 859-63. PMID 17568747 DOI: 10.1038/Nature05853 |
0.766 |
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| 2007 |
Di Prospero NA, Sumner CJ, Penzak SR, Ravina B, Fischbeck KH, Taylor JP. Safety, tolerability, and pharmacokinetics of high-dose idebenone in patients with Friedreich ataxia. Archives of Neurology. 64: 803-8. PMID 17562928 DOI: 10.1001/Archneur.64.6.803 |
0.482 |
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| 2007 |
Guinto JB, Ritson GP, Taylor JP, Forman MS. Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy. Acta Neuropathologica. 114: 55-61. PMID 17457594 DOI: 10.1007/S00401-007-0224-7 |
0.808 |
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| 2007 |
Neumann M, Mackenzie IR, Cairns NJ, Boyer PJ, Markesbery WR, Smith CD, Taylor JP, Kretzschmar HA, Kimonis VE, Forman MS. TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations. Journal of Neuropathology and Experimental Neurology. 66: 152-7. PMID 17279000 DOI: 10.1096/Fasebj.21.5.A25 |
0.458 |
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| 2006 |
Taylor JP, Mata IF, Farrer MJ. LRRK2: a common pathway for parkinsonism, pathogenesis and prevention? Trends in Molecular Medicine. 12: 76-82. PMID 16406842 DOI: 10.1016/j.molmed.2005.12.004 |
0.326 |
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| 2006 |
Taylor J, Grote SK, Xia J, Vandelft M, Graczyk J, Ellerby LM, La Spada AR, Truant R. Ataxin-7 can export from the nucleus via a conserved exportin-dependent signal. The Journal of Biological Chemistry. 281: 2730-9. PMID 16314424 DOI: 10.1074/Jbc.M506751200 |
0.604 |
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| 2004 |
Piccioni F, Roman BR, Fischbeck KH, Taylor JP. A screen for drugs that protect against the cytotoxicity of polyglutamine-expanded androgen receptor. Human Molecular Genetics. 13: 437-46. PMID 14709594 DOI: 10.1093/Hmg/Ddh045 |
0.532 |
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| 2004 |
Xia J, Lee DH, Taylor J, Vandelft M, Truant R. Huntingtin contains a highly conserved nuclear export signal. Human Molecular Genetics. 12: 1393-403. PMID 12783847 DOI: 10.1093/hmg/ddg156 |
0.326 |
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| 2003 |
Sumner CJ, Huynh TN, Markowitz JA, Perhac JS, Hill B, Coovert DD, Schussler K, Chen X, Jarecki J, Burghes AH, Taylor JP, Fischbeck KH. Valproic acid increases SMN levels in spinal muscular atrophy patient cells. Annals of Neurology. 54: 647-54. PMID 14595654 DOI: 10.1002/Ana.10743 |
0.569 |
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| 2003 |
Taylor JP, Taye AA, Campbell C, Kazemi-Esfarjani P, Fischbeck KH, Min KT. Aberrant histone acetylation, altered transcription, and retinal degeneration in a Drosophila model of polyglutamine disease are rescued by CREB-binding protein. Genes & Development. 17: 1463-8. PMID 12815067 DOI: 10.1101/Gad.1087503 |
0.764 |
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| 2003 |
La Spada AR, Taylor JP. Polyglutamines placed into context. Neuron. 38: 681-4. PMID 12797953 DOI: 10.1016/S0896-6273(03)00328-3 |
0.655 |
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| 2003 |
Taylor JP, Tanaka F, Robitschek J, Sandoval CM, Taye A, Markovic-Plese S, Fischbeck KH. Aggresomes protect cells by enhancing the degradation of toxic polyglutamine-containing protein. Human Molecular Genetics. 12: 749-57. PMID 12651870 DOI: 10.1093/Hmg/Ddg074 |
0.62 |
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| 2002 |
Taylor JP, Fischbeck KH. Altered acetylation in polyglutamine disease: an opportunity for therapeutic intervention? Trends in Molecular Medicine. 8: 195-7. PMID 12067622 DOI: 10.1016/S1471-4914(02)02332-8 |
0.599 |
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| 2002 |
Taylor JP, Hardy J, Fischbeck KH. Toxic proteins in neurodegenerative disease. Science (New York, N.Y.). 296: 1991-5. PMID 12065827 DOI: 10.1126/Science.1067122 |
0.617 |
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| 2002 |
Caplen NJ, Taylor JP, Statham VS, Tanaka F, Fire A, Morgan RA. Rescue of polyglutamine-mediated cytotoxicity by double-stranded RNA-mediated RNA interference. Human Molecular Genetics. 11: 175-84. PMID 11809726 DOI: 10.1093/Hmg/11.2.175 |
0.358 |
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| 2000 |
McCampbell A, Taylor JP, Taye AA, Robitschek J, Li M, Walcott J, Merry D, Chai Y, Paulson H, Sobue G, Fischbeck KH. CREB-binding protein sequestration by expanded polyglutamine. Human Molecular Genetics. 9: 2197-202. PMID 10958659 DOI: 10.1093/Hmg/9.14.2197 |
0.806 |
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