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Roy Parker - Publications

Affiliations: 
Chemistry and Biochemistry University of Colorado, Boulder, Boulder, CO, United States 
Area:
Control of mRNA Function in Eukaryotic Cells
Website:
http://chem.colorado.edu/index.php?option=com_content&view=article&id=576&Itemid=185

240 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Shehata SI, Watkins JM, Burke JM, Parker R. Mechanisms and consequences of mRNA destabilization during viral infections. Virology Journal. 21: 38. PMID 38321453 DOI: 10.1186/s12985-024-02305-1  0.366
2023 Ripin N, Parker R. Formation, function, and pathology of RNP granules. Cell. 186: 4737-4756. PMID 37890457 DOI: 10.1016/j.cell.2023.09.006  0.306
2023 Huynh TN, Parker R. The PARN, TOE1, and USB1 RNA deadenylases and their roles in non-coding RNA regulation. The Journal of Biological Chemistry. 299: 105139. PMID 37544646 DOI: 10.1016/j.jbc.2023.105139  0.36
2023 Shehata SI, Parker R. SARS-CoV-2 Nsp1 mediated mRNA degradation requires mRNA interaction with the ribosome. Rna Biology. 20: 444-456. PMID 37415298 DOI: 10.1080/15476286.2023.2231280  0.531
2022 Burke JM, Ripin N, Ferretti MB, St Clair LA, Worden-Sapper ER, Salgado F, Sawyer SL, Perera R, Lynch KW, Parker R. RNase L activation in the cytoplasm induces aberrant processing of mRNAs in the nucleus. Plos Pathogens. 18: e1010930. PMID 36318584 DOI: 10.1371/journal.ppat.1010930  0.377
2022 Khong A, Matheny T, Huynh TN, Babl V, Parker R. Limited effects of mA modification on mRNA partitioning into stress granules. Nature Communications. 13: 3735. PMID 35768440 DOI: 10.1038/s41467-022-31358-5  0.412
2022 Decker CJ, Burke JM, Mulvaney PK, Parker R. RNA is required for the integrity of multiple nuclear and cytoplasmic membrane-less RNP granules. The Embo Journal. e110137. PMID 35355287 DOI: 10.15252/embj.2021110137  0.321
2021 Corbet GA, Burke JM, Parker R. ADAR1 limits stress granule formation through both translation-dependent and translation-independent mechanisms. Journal of Cell Science. PMID 34397095 DOI: 10.1242/jcs.258783  0.355
2021 Burke JM, St Clair LA, Perera R, Parker R. SARS-CoV-2 infection triggers widespread host mRNA decay leading to an mRNA export block. Rna (New York, N.Y.). PMID 34315815 DOI: 10.1261/rna.078923.121  0.427
2021 Burke JM, Gilchrist AR, Sawyer SL, Parker R. RNase L limits host and viral protein synthesis via inhibition of mRNA export. Science Advances. 7. PMID 34088676 DOI: 10.1126/sciadv.abh2479  0.384
2021 Burke JM, St Clair LA, Perera R, Parker R. Rapid decay of host basal mRNAs during SARS-CoV-2 infection perturbs host antiviral mRNA biogenesis and export. Biorxiv : the Preprint Server For Biology. PMID 33907748 DOI: 10.1101/2021.04.19.440452  0.369
2020 Matheny T, Van Treeck B, Huynh TN, Parker R. RNA partitioning into stress granules is based on the summation of multiple interactions. Rna (New York, N.Y.). PMID 33199441 DOI: 10.1261/rna.078204.120  0.323
2020 Shukla S, Jeong HC, Sturgeon CM, Parker R, Batista LFZ. Chemical inhibition of PAPD5/7 rescues telomerase function and hematopoiesis in dyskeratosis congenita. Blood Advances. 4: 2717-2722. PMID 32559291 DOI: 10.1182/Bloodadvances.2020001848  0.367
2020 Xing W, Muhlrad D, Parker R, Rosen MK. A quantitative inventory of yeast P body proteins reveals principles of composition and specificity. Elife. 9. PMID 32553117 DOI: 10.7554/Elife.56525  0.324
2020 Moon SL, Morisaki T, Stasevich TJ, Parker R. Coupling of translation quality control and mRNA targeting to stress granules. The Journal of Cell Biology. 219. PMID 32520986 DOI: 10.1083/Jcb.202004120  0.498
2020 Corbet GA, Parker R. RNP Granule Formation: Lessons from P-Bodies and Stress Granules. Cold Spring Harbor Symposia On Quantitative Biology. PMID 32482896 DOI: 10.1101/Sqb.2019.84.040329  0.435
2020 Tauber D, Tauber G, Parker R. Mechanisms and Regulation of RNA Condensation in RNP Granule Formation. Trends in Biochemical Sciences. PMID 32475683 DOI: 10.1016/J.Tibs.2020.05.002  0.42
2020 Lee JE, Cathey PI, Wu H, Parker R, Voeltz GK. Endoplasmic reticulum contact sites regulate the dynamics of membraneless organelles. Science (New York, N.Y.). 367. PMID 32001628 DOI: 10.1126/Science.Aay7108  0.307
2020 Cirillo L, Cieren A, Barbieri S, Khong A, Schwager F, Parker R, Gotta M. UBAP2L Forms Distinct Cores that Act in Nucleating Stress Granules Upstream of G3BP1. Current Biology : Cb. PMID 31956030 DOI: 10.1016/J.Cub.2019.12.020  0.393
2020 Tauber D, Tauber G, Khong A, Van Treeck B, Pelletier J, Parker R. Modulation of RNA Condensation by the DEAD-Box Protein eIF4A. Cell. PMID 31928844 DOI: 10.1016/J.Cell.2019.12.031  0.444
2020 Brocard M, Iadevaia V, Klein P, Hall B, Lewis G, Lu J, Burke J, Willcocks MM, Parker R, Goodfellow IG, Ruggieri A, Locker N. Norovirus infection results in eIF2α independent host translation shut-off and remodels the G3BP1 interactome evading stress granule formation. Plos Pathogens. 16: e1008250. PMID 31905230 DOI: 10.1371/Journal.Ppat.1008250  0.367
2020 Burke JM, Lester ET, Tauber D, Parker R. RNase L promotes the formation of unique ribonucleoprotein granules distinct from stress granules. The Journal of Biological Chemistry. PMID 31896577 DOI: 10.1074/Jbc.Ra119.011638  0.417
2019 Khong A, Parker R. The Landscape of Eukaryotic mRNPs. Rna (New York, N.Y.). PMID 31879280 DOI: 10.1261/Rna.073601.119  0.595
2019 Decker CJ, Steiner HR, Hoon-Hanks LL, Morrison JH, Haist KC, Stabell AC, Poeschla EM, Morrison TE, Stenglein MD, Sawyer SL, Parker R. dsRNA-Seq: Identification of Viral Infection by Purifying and Sequencing dsRNA. Viruses. 11. PMID 31615058 DOI: 10.3390/V11100943  0.346
2019 Matheny T, Rao B, Parker R. Transcriptome-wide comparison of stress granules and P-bodies reveals that translation plays a major role in RNA partitioning. Molecular and Cellular Biology. PMID 31591142 DOI: 10.1128/Mcb.00313-19  0.396
2019 Burke JM, Moon SL, Matheny T, Parker R. RNase L Reprograms Translation by Widespread mRNA Turnover Escaped by Antiviral mRNAs. Molecular Cell. PMID 31494035 DOI: 10.1016/J.Molcel.2019.07.029  0.526
2019 Baron DM, Matheny T, Lin YC, Leszyk JD, Kenna K, Gall KV, Santos DP, Tischbein M, Funes S, Hayward LJ, Kiskinis E, Landers JE, Parker R, Shaffer SA, Bosco DA. Quantitative proteomics identifies proteins that resist translational repression and become dysregulated in ALS-FUS. Human Molecular Genetics. PMID 30806671 DOI: 10.1093/Hmg/Ddz048  0.375
2019 Shukla S, Bjerke GA, Muhlrad D, Yi R, Parker R. The RNase PARN Controls the Levels of Specific miRNAs that Contribute to p53 Regulation. Molecular Cell. PMID 30770239 DOI: 10.1016/J.Molcel.2019.01.010  0.342
2019 Fok WC, Shukla S, Vessoni AT, Brenner KA, Parker R, Sturgeon CM, Batista LFZ. Posttranscriptional modulation of TERC by PAPD5 inhibition rescues hematopoietic development in dyskeratosis congenita. Blood. PMID 30728146 DOI: 10.1182/Blood-2018-11-885368  0.369
2019 Tauber D, Parker R. 15-Deoxy-Δ-prostaglandin J2 promotes phosphorylation of eukaryotic initiation factor 2α and activates the integrated stress response. The Journal of Biological Chemistry. PMID 30723157 DOI: 10.1074/Jbc.Ra118.007138  0.316
2019 Van Treeck B, Parker R. Principles of Stress Granules Revealed by Imaging Approaches. Cold Spring Harbor Perspectives in Biology. 11. PMID 30709880 DOI: 10.1101/Cshperspect.A033068  0.343
2019 Moon SL, Morisaki T, Khong A, Lyon K, Parker R, Stasevich TJ. Multicolour single-molecule tracking of mRNA interactions with RNP granules. Nature Cell Biology. PMID 30664789 DOI: 10.1038/S41556-018-0263-4  0.558
2019 Parker R, Updike DL. Decision letter: Recruitment of mRNAs to P granules by condensation with intrinsically-disordered proteins Elife. DOI: 10.7554/Elife.52896.Sa1  0.393
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, ... ... Parker R, 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  0.36
2018 Khong A, Parker R. mRNP architecture in translating and stress conditions reveals an ordered pathway of mRNP compaction. The Journal of Cell Biology. PMID 30322972 DOI: 10.1083/Jcb.201806183  0.591
2018 Moon SL, Parker R. Analysis of eIF2B bodies and their relationships with stress granules and P-bodies. Scientific Reports. 8: 12264. PMID 30115954 DOI: 10.1038/S41598-018-30805-Y  0.371
2018 Mittag T, Parker R. Multiple Modes of Protein-Protein Interactions Promote RNP Granule Assembly. Journal of Molecular Biology. PMID 30099026 DOI: 10.1016/J.Jmb.2018.08.005  0.367
2018 Van Treeck B, Parker R. Emerging Roles for Intermolecular RNA-RNA Interactions in RNP Assemblies. Cell. 174: 791-802. PMID 30096311 DOI: 10.1016/J.Cell.2018.07.023  0.413
2018 Braselmann E, Wierzba AJ, Polaski JT, Chromiński M, Holmes ZE, Hung ST, Batan D, Wheeler JR, Parker R, Jimenez R, Gryko D, Batey RT, Palmer AE. A multicolor riboswitch-based platform for imaging of RNA in live mammalian cells. Nature Chemical Biology. PMID 30061719 DOI: 10.1038/S41589-018-0103-7  0.401
2018 Bakthavachalu B, Huelsmeier J, Sudhakaran IP, Hillebrand J, Singh A, Petrauskas A, Thiagarajan D, Sankaranarayanan M, Mizoue L, Anderson EN, Pandey UB, Ross E, VijayRaghavan K, Parker R, Ramaswami M. RNP-Granule Assembly via Ataxin-2 Disordered Domains Is Required for Long-Term Memory and Neurodegeneration. Neuron. 98: 754-766.e4. PMID 29772202 DOI: 10.1016/J.Neuron.2018.04.032  0.582
2018 Moon SL, Parker R. EIF2B2 mutations in Vanishing White Matter Disease hyper- suppress translation and delay recovery during the integrated stress response. Rna (New York, N.Y.). PMID 29632131 DOI: 10.1261/Rna.066563.118  0.36
2018 Van Treeck B, Protter DSW, Matheny T, Khong A, Link CD, Parker R. RNA self-assembly contributes to stress granule formation and defining the stress granule transcriptome. Proceedings of the National Academy of Sciences of the United States of America. PMID 29483269 DOI: 10.1073/Pnas.1800038115  0.446
2018 Protter DSW, Rao BS, Van Treeck B, Lin Y, Mizoue L, Rosen MK, Parker R. Intrinsically Disordered Regions Can Contribute Promiscuous Interactions to RNP Granule Assembly. Cell Reports. 22: 1401-1412. PMID 29425497 DOI: 10.1016/J.Celrep.2018.01.036  0.358
2017 Khong A, Jain S, Matheny T, Wheeler JR, Parker R. Isolation of mammalian stress granule cores for RNA-Seq analysis. Methods (San Diego, Calif.). PMID 29196162 DOI: 10.1016/J.Ymeth.2017.11.012  0.403
2017 Tutucci E, Vera M, Biswas J, Garcia J, Parker R, Singer RH. An improved MS2 system for accurate reporting of the mRNA life cycle. Nature Methods. PMID 29131164 DOI: 10.1038/Nmeth.4502  0.528
2017 Khong A, Matheny T, Jain S, Mitchell SF, Wheeler JR, Parker R. The Stress Granule Transcriptome Reveals Principles of mRNA Accumulation in Stress Granules. Molecular Cell. PMID 29129640 DOI: 10.1016/J.Molcel.2017.10.015  0.476
2017 Rao BS, Parker R. Numerous interactions act redundantly to assemble a tunable size of P bodies in Saccharomyces cerevisiae. Proceedings of the National Academy of Sciences of the United States of America. PMID 29078371 DOI: 10.1073/Pnas.1712396114  0.426
2017 Harigaya Y, Parker R. Erratum to: the link between adjacent codon pairs and mRNA stability. Bmc Genomics. 18: 704. PMID 28886693 DOI: 10.1186/S12864-017-4088-5  0.498
2017 Shukla S, Parker R. PARN modulates Y RNA stability, 3' end formation and its modification. Molecular and Cellular Biology. PMID 28760775 DOI: 10.1128/Mcb.00264-17  0.436
2017 Harigaya Y, Parker R. The link between adjacent codon pairs and mRNA stability. Bmc Genomics. 18: 364. PMID 28486986 DOI: 10.1186/S12864-017-3749-8  0.512
2017 Wheeler JR, Jain S, Kong A, Parker R. Isolation of yeast and mammalian stress granule cores. Methods (San Diego, Calif.). PMID 28457979 DOI: 10.1016/J.Ymeth.2017.04.020  0.34
2017 Parker R. Decision letter: Non-invasive measurement of mRNA decay reveals translation initiation as the major determinant of mRNA stability Elife. DOI: 10.7554/Elife.32536.078  0.5
2016 Walters RW, Matheny T, Mizoue LS, Rao BS, Muhlrad D, Parker R. Identification of NAD+ capped mRNAs in Saccharomyces cerevisiae. Proceedings of the National Academy of Sciences of the United States of America. PMID 28031484 DOI: 10.1073/Pnas.1619369114  0.536
2016 Harigaya Y, Parker R. Analysis of the association between codon optimality and mRNA stability in Schizosaccharomyces pombe. Bmc Genomics. 17: 895. PMID 27825301 DOI: 10.1186/S12864-016-3237-6  0.451
2016 Harigaya Y, Parker R. Codon optimality and mRNA decay. Cell Research. PMID 27811910 DOI: 10.1038/Cr.2016.127  0.44
2016 Poornima G, Shah S, Vignesh V, Parker R, Rajyaguru PI. Arginine methylation promotes translation repression activity of eIF4G-binding protein, Scd6. Nucleic Acids Research. PMID 27613419 DOI: 10.1093/Nar/Gkw762  0.376
2016 Wheeler JR, Matheny T, Jain S, Abrisch R, Parker R. Distinct stages in stress granule assembly and disassembly. Elife. 5. PMID 27602576 DOI: 10.7554/Elife.18413  0.378
2016 Banani SF, Rice AM, Peeples WB, Lin Y, Jain S, Parker R, Rosen MK. Compositional Control of Phase-Separated Cellular Bodies. Cell. PMID 27374333 DOI: 10.1016/J.Cell.2016.06.010  0.355
2016 Protter DS, Parker R. Principles and Properties of Stress Granules. Trends in Cell Biology. PMID 27289443 DOI: 10.1016/J.Tcb.2016.05.004  0.365
2016 Shukla S, Parker R. Hypo- and Hyper-Assembly Diseases of RNA-Protein Complexes. Trends in Molecular Medicine. PMID 27263464 DOI: 10.1016/J.Molmed.2016.05.005  0.363
2016 Eshleman N, Liu G, McGrath K, Parker R, Buchan JR. Defects in THO/TREX-2 function cause accumulation of novel cytoplasmic mRNP granules that can be cleared by autophagy. Rna (New York, N.Y.). PMID 27251550 DOI: 10.1261/Rna.057224.116  0.454
2016 Garcia JF, Parker R. Ubiquitous accumulation of 3' mRNA decay fragments in Saccharomyces cerevisiae mRNAs with chromosomally integrated MS2 arrays. Rna (New York, N.Y.). 22: 657-9. PMID 27090788 DOI: 10.1261/Rna.056325.116  0.449
2016 Mitchell SF, Parker R. Identification of Endogenous mRNA-Binding Proteins in Yeast Using Crosslinking and PolyA Enrichment. Methods in Molecular Biology (Clifton, N.J.). 1421: 153-63. PMID 26965264 DOI: 10.1007/978-1-4939-3591-8_13  0.548
2016 Shukla S, Schmidt JC, Goldfarb KC, Cech TR, Parker R. Inhibition of telomerase RNA decay rescues telomerase deficiency caused by dyskerin or PARN defects. Nature Structural & Molecular Biology. PMID 26950371 DOI: 10.1038/Nsmb.3184  0.444
2016 Lasda E, Parker R. Circular RNAs Co-Precipitate with Extracellular Vesicles: A Possible Mechanism for circRNA Clearance. Plos One. 11: e0148407. PMID 26848835 DOI: 10.1371/Journal.Pone.0148407  0.312
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, ... ... Parker R, 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  0.314
2016 Jain S, Wheeler JR, Walters RW, Agrawal A, Barsic A, Parker R. ATPase-Modulated Stress Granules Contain a Diverse Proteome and Substructure. Cell. PMID 26777405 DOI: 10.1016/J.Cell.2015.12.038  0.344
2015 Mitchell SF, Parker R. Modifications on Translation Initiation. Cell. 163: 796-8. PMID 26544933 DOI: 10.1016/J.Cell.2015.10.056  0.36
2015 Lin Y, Protter DS, Rosen MK, Parker R. Formation and Maturation of Phase-Separated Liquid Droplets by RNA-Binding Proteins. Molecular Cell. PMID 26412307 DOI: 10.1016/J.Molcel.2015.08.018  0.369
2015 Walters RW, Parker R. Coupling of Ribostasis and Proteostasis: Hsp70 Proteins in mRNA Metabolism. Trends in Biochemical Sciences. 40: 552-9. PMID 26410596 DOI: 10.1016/J.Tibs.2015.08.004  0.539
2015 Walters RW, Muhlrad D, Garcia J, Parker R. Differential effects of Ydj1 and Sis1 on Hsp70-mediated clearance of stress granules in Saccharomyces cerevisiae. Rna (New York, N.Y.). 21: 1660-71. PMID 26199455 DOI: 10.1261/Rna.053116.115  0.359
2015 Garcia JF, Parker R. MS2 coat proteins bound to yeast mRNAs block 5' to 3' degradation and trap mRNA decay products: implications for the localization of mRNAs by MS2-MCP system. Rna (New York, N.Y.). 21: 1393-5. PMID 26092944 DOI: 10.1261/Rna.051797.115  0.437
2015 Mitchell SF, Parker R. In vivo cross-linking followed by polyA enrichment to identify yeast mRNA binding proteins. Methods in Molecular Biology (Clifton, N.J.). 1259: 35-47. PMID 25579578 DOI: 10.1007/978-1-4939-2214-7_3  0.538
2014 Lasda E, Parker R. Circular RNAs: diversity of form and function. Rna (New York, N.Y.). 20: 1829-42. PMID 25404635 DOI: 10.1261/Rna.047126.114  0.423
2014 Shukla S, Parker R. Quality control of assembly-defective U1 snRNAs by decapping and 5'-to-3' exonucleolytic digestion. Proceedings of the National Academy of Sciences of the United States of America. 111: E3277-86. PMID 25071210 DOI: 10.1073/Pnas.1412614111  0.377
2014 Mitchell SF, Parker R. Principles and properties of eukaryotic mRNPs. Molecular Cell. 54: 547-58. PMID 24856220 DOI: 10.1016/J.Molcel.2014.04.033  0.583
2014 Harigaya Y, Parker R. Fragile X mental retardation protein and the ribosome. Molecular Cell. 54: 330-2. PMID 24813710 DOI: 10.1016/J.Molcel.2014.04.027  0.336
2014 Decker CJ, Parker R. Analysis of double-stranded RNA from microbial communities identifies double-stranded RNA virus-like elements. Cell Reports. 7: 898-906. PMID 24767992 DOI: 10.1016/J.Celrep.2014.03.049  0.351
2014 Walters R, Parker R. Quality control: Is there quality control of localized mRNAs? The Journal of Cell Biology. 204: 863-8. PMID 24637320 DOI: 10.1083/Jcb.201401059  0.524
2014 Walters RW, Shumilin IA, Yoon JH, Minor W, Parker R. Edc3 function in yeast and mammals is modulated by interaction with NAD-related compounds. G3 (Bethesda, Md.). 4: 613-22. PMID 24504254 DOI: 10.1534/G3.114.010470  0.508
2014 Sudhakaran IP, Hillebrand J, Dervan A, Das S, Holohan EE, Hülsmeier J, Sarov M, Parker R, VijayRaghavan K, Ramaswami M. FMRP and Ataxin-2 function together in long-term olfactory habituation and neuronal translational control. Proceedings of the National Academy of Sciences of the United States of America. 111: E99-E108. PMID 24344294 DOI: 10.1073/Pnas.1309543111  0.655
2014 Wu D, Muhlrad D, Bowler MW, Jiang S, Liu Z, Parker R, Song H. Lsm2 and Lsm3 bridge the interaction of the Lsm1-7 complex with Pat1 for decapping activation. Cell Research. 24: 233-46. PMID 24247251 DOI: 10.1038/Cr.2013.152  0.351
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  0.63
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  0.384
2013 Jain S, Parker R. The discovery and analysis of P Bodies. Advances in Experimental Medicine and Biology. 768: 23-43. PMID 23224963 DOI: 10.1007/978-1-4614-5107-5_3  0.497
2013 Mitchell SF, Jain S, She M, Parker R. Global analysis of yeast mRNPs. Nature Structural & Molecular Biology. 20: 127-33. PMID 23222640 DOI: 10.1038/Nsmb.2468  0.521
2012 Lai T, Cho H, Liu Z, Bowler MW, Piao S, Parker R, Kim YK, Song H. Structural basis of the PNRC2-mediated link between mrna surveillance and decapping. Structure (London, England : 1993). 20: 2025-37. PMID 23085078 DOI: 10.1016/J.Str.2012.09.009  0.528
2012 Luhtala N, Parker R. Structure-function analysis of Rny1 in tRNA cleavage and growth inhibition. Plos One. 7: e41111. PMID 22829915 DOI: 10.1371/Journal.Pone.0041111  0.325
2012 Parker R. RNA degradation in Saccharomyces cerevisae. Genetics. 191: 671-702. PMID 22785621 DOI: 10.1534/Genetics.111.137265  0.42
2012 Rajyaguru P, Parker R. RGG motif proteins: modulators of mRNA functional states. Cell Cycle (Georgetown, Tex.). 11: 2594-9. PMID 22767211 DOI: 10.4161/Cc.20716  0.531
2012 Decker CJ, Parker R. P-bodies and stress granules: possible roles in the control of translation and mRNA degradation. Cold Spring Harbor Perspectives in Biology. 4: a012286. PMID 22763747 DOI: 10.1101/Cshperspect.A012286  0.525
2012 Harigaya Y, Parker R. Global analysis of mRNA decay intermediates in Saccharomyces cerevisiae. Proceedings of the National Academy of Sciences of the United States of America. 109: 11764-9. PMID 22752303 DOI: 10.1073/Pnas.1119741109  0.577
2012 Rajyaguru P, She M, Parker R. Scd6 targets eIF4G to repress translation: RGG motif proteins as a class of eIF4G-binding proteins. Molecular Cell. 45: 244-54. PMID 22284680 DOI: 10.1016/J.Molcel.2011.11.026  0.49
2011 Swisher KD, Parker R. Interactions between Upf1 and the decapping factors Edc3 and Pat1 in Saccharomyces cerevisiae. Plos One. 6: e26547. PMID 22065998 DOI: 10.1371/Journal.Pone.0026547  0.452
2011 Chekulaeva M, Mathys H, Zipprich JT, Attig J, Colic M, Parker R, Filipowicz W. miRNA repression involves GW182-mediated recruitment of CCR4-NOT through conserved W-containing motifs. Nature Structural & Molecular Biology. 18: 1218-26. PMID 21984184 DOI: 10.1038/Nsmb.2166  0.422
2011 Hilliker A, Gao Z, Jankowsky E, Parker R. The DEAD-box protein Ded1 modulates translation by the formation and resolution of an eIF4F-mRNA complex. Molecular Cell. 43: 962-72. PMID 21925384 DOI: 10.1016/J.Molcel.2011.08.008  0.556
2011 McCann C, Holohan EE, Das S, Dervan A, Larkin A, Lee JA, Rodrigues V, Parker R, Ramaswami M. The Ataxin-2 protein is required for microRNA function and synapse-specific long-term olfactory habituation. Proceedings of the National Academy of Sciences of the United States of America. 108: E655-62. PMID 21795609 DOI: 10.1073/Pnas.1107198108  0.609
2011 Balagopal V, Parker R. Stm1 modulates translation after 80S formation in Saccharomyces cerevisiae. Rna (New York, N.Y.). 17: 835-42. PMID 21460238 DOI: 10.1261/Rna.2677311  0.557
2011 Buchan JR, Yoon JH, Parker R. Stress-specific composition, assembly and kinetics of stress granules in Saccharomyces cerevisiae. Journal of Cell Science. 124: 228-39. PMID 21172806 DOI: 10.1242/Jcs.078444  0.346
2010 Harigaya Y, Parker R. No-go decay: a quality control mechanism for RNA in translation. Wiley Interdisciplinary Reviews. Rna. 1: 132-41. PMID 21956910 DOI: 10.1002/Wrna.17  0.543
2010 Hillebrand J, Pan K, Kokaram A, Barbee S, Parker R, Ramaswami M. The Me31B DEAD-Box Helicase Localizes to Postsynaptic Foci and Regulates Expression of a CaMKII Reporter mRNA in Dendrites of Drosophila Olfactory Projection Neurons. Frontiers in Neural Circuits. 4: 121. PMID 21267420 DOI: 10.3389/Fncir.2010.00121  0.685
2010 Buchan JR, Nissan T, Parker R. Analyzing P-bodies and stress granules in Saccharomyces cerevisiae. Methods in Enzymology. 470: 619-40. PMID 20946828 DOI: 10.1016/S0076-6879(10)70025-2  0.791
2010 Chen L, Muhlrad D, Hauryliuk V, Cheng Z, Lim MK, Shyp V, Parker R, Song H. Structure of the Dom34-Hbs1 complex and implications for no-go decay. Nature Structural & Molecular Biology. 17: 1233-40. PMID 20890290 DOI: 10.1038/Nsmb.1922  0.385
2010 Nissan T, Rajyaguru P, She M, Song H, Parker R. Decapping activators in Saccharomyces cerevisiae act by multiple mechanisms. Molecular Cell. 39: 773-83. PMID 20832728 DOI: 10.1016/J.Molcel.2010.08.025  0.802
2010 Chekulaeva M, Parker R, Filipowicz W. The GW/WG repeats of Drosophila GW182 function as effector motifs for miRNA-mediated repression. Nucleic Acids Research. 38: 6673-83. PMID 20530530 DOI: 10.1093/Nar/Gkq501  0.455
2010 Yoon JH, Choi EJ, Parker R. Dcp2 phosphorylation by Ste20 modulates stress granule assembly and mRNA decay in Saccharomyces cerevisiae. The Journal of Cell Biology. 189: 813-27. PMID 20513766 DOI: 10.1083/Jcb.200912019  0.561
2010 Swisher KD, Parker R. Localization to, and effects of Pbp1, Pbp4, Lsm12, Dhh1, and Pab1 on stress granules in Saccharomyces cerevisiae. Plos One. 5: e10006. PMID 20368989 DOI: 10.1371/Journal.Pone.0010006  0.368
2010 Yoon JH, Parker R. Coil-in-to snRNP assembly and Cajal bodies. Nature Structural & Molecular Biology. 17: 391-3. PMID 20368721 DOI: 10.1038/Nsmb0410-391  0.307
2010 Harigaya Y, Jones BN, Muhlrad D, Gross JD, Parker R. Identification and analysis of the interaction between Edc3 and Dcp2 in Saccharomyces cerevisiae. Molecular and Cellular Biology. 30: 1446-56. PMID 20086104 DOI: 10.1128/Mcb.01305-09  0.548
2009 Buchan JR, Parker R. Eukaryotic stress granules: the ins and outs of translation. Molecular Cell. 36: 932-41. PMID 20064460 DOI: 10.1016/J.Molcel.2009.11.020  0.538
2009 Thompson DM, Parker R. Stressing out over tRNA cleavage. Cell. 138: 215-9. PMID 19632169 DOI: 10.1016/J.Cell.2009.07.001  0.339
2009 Luhtala N, Parker R. LSM1 over-expression in Saccharomyces cerevisiae depletes U6 snRNA levels. Nucleic Acids Research. 37: 5529-36. PMID 19596813 DOI: 10.1093/Nar/Gkp572  0.46
2009 Cziko AM, McCann CT, Howlett IC, Barbee SA, Duncan RP, Luedemann R, Zarnescu D, Zinsmaier KE, Parker RR, Ramaswami M. Genetic modifiers of dFMR1 encode RNA granule components in Drosophila. Genetics. 182: 1051-60. PMID 19487564 DOI: 10.1534/Genetics.109.103234  0.659
2009 Swisher KD, Parker R. Related mechanisms for mRNA and rRNA quality control. Molecular Cell. 34: 401-2. PMID 19481519 DOI: 10.1016/J.Molcel.2009.05.008  0.474
2009 Passos DO, Doma MK, Shoemaker CJ, Muhlrad D, Green R, Weissman J, Hollien J, Parker R. Analysis of Dom34 and its function in no-go decay. Molecular Biology of the Cell. 20: 3025-32. PMID 19420139 DOI: 10.1091/Mbc.E09-01-0028  0.575
2009 Balagopal V, Parker R. Polysomes, P bodies and stress granules: states and fates of eukaryotic mRNAs. Current Opinion in Cell Biology. 21: 403-8. PMID 19394210 DOI: 10.1016/J.Ceb.2009.03.005  0.581
2009 Thompson DM, Parker R. The RNase Rny1p cleaves tRNAs and promotes cell death during oxidative stress in Saccharomyces cerevisiae. The Journal of Cell Biology. 185: 43-50. PMID 19332891 DOI: 10.1083/Jcb.200811119  0.302
2009 Chekulaeva M, Filipowicz W, Parker R. Multiple independent domains of dGW182 function in miRNA-mediated repression in Drosophila. Rna (New York, N.Y.). 15: 794-803. PMID 19304924 DOI: 10.1261/Rna.1364909  0.399
2009 Rajyaguru P, Parker R. CGH-1 and the control of maternal mRNAs. Trends in Cell Biology. 19: 24-8. PMID 19062290 DOI: 10.1016/J.Tcb.2008.11.001  0.576
2009 Balagopal V, Parker R. Stm1 modulates mRNA decay and Dhh1 function in Saccharomyces cerevisiae. Genetics. 181: 93-103. PMID 19015546 DOI: 10.1534/Genetics.108.092601  0.548
2009 Cheng Z, Liu Y, Wang C, Parker R, Song H. Crystal structure of Ski8p, a WD-repeat protein with dual roles in mRNA metabolism and meiotic recombination Protein Science. 13: 2673-2684. PMID 15340168 DOI: 10.1110/Ps.04856504  0.426
2008 Nissan T, Parker R. Analyzing P-bodies in Saccharomyces cerevisiae. Methods in Enzymology. 448: 507-20. PMID 19111192 DOI: 10.1016/S0076-6879(08)02625-6  0.801
2008 Passos DO, Parker R. Analysis of cytoplasmic mRNA decay in Saccharomyces cerevisiae. Methods in Enzymology. 448: 409-27. PMID 19111187 DOI: 10.1016/S0076-6879(08)02620-7  0.571
2008 Buchan JR, Muhlrad D, Parker R. P bodies promote stress granule assembly in Saccharomyces cerevisiae. The Journal of Cell Biology. 183: 441-55. PMID 18981231 DOI: 10.1083/Jcb.200807043  0.411
2008 Hilliker A, Parker R. Stressed out? Make some modifications! Nature Cell Biology. 10: 1129-30. PMID 18830219 DOI: 10.1038/Ncb1008-1129  0.489
2008 Thompson DM, Lu C, Green PJ, Parker R. tRNA cleavage is a conserved response to oxidative stress in eukaryotes. Rna (New York, N.Y.). 14: 2095-103. PMID 18719243 DOI: 10.1261/Rna.1232808  0.357
2008 Pedro-Segura E, Vergara SV, Rodríguez-Navarro S, Parker R, Thiele DJ, Puig S. The Cth2 ARE-binding protein recruits the Dhh1 helicase to promote the decay of succinate dehydrogenase SDH4 mRNA in response to iron deficiency. The Journal of Biological Chemistry. 283: 28527-35. PMID 18715869 DOI: 10.1074/Jbc.M804910200  0.509
2008 Ling SH, Decker CJ, Walsh MA, She M, Parker R, Song H. Crystal structure of human Edc3 and its functional implications. Molecular and Cellular Biology. 28: 5965-76. PMID 18678652 DOI: 10.1128/Mcb.00761-08  0.425
2008 Nissan T, Parker R. Computational analysis of miRNA-mediated repression of translation: implications for models of translation initiation inhibition. Rna (New York, N.Y.). 14: 1480-91. PMID 18579870 DOI: 10.1261/Rna.1072808  0.738
2008 Beckham CJ, Parker R. P bodies, stress granules, and viral life cycles. Cell Host & Microbe. 3: 206-12. PMID 18407064 DOI: 10.1016/J.Chom.2008.03.004  0.508
2008 She M, Decker CJ, Svergun DI, Round A, Chen N, Muhlrad D, Parker R, Song H. Structural basis of dcp2 recognition and activation by dcp1. Molecular Cell. 29: 337-49. PMID 18280239 DOI: 10.1016/J.Molcel.2008.01.002  0.348
2008 Beckham C, Hilliker A, Cziko AM, Noueiry A, Ramaswami M, Parker R. The DEAD-box RNA helicase Ded1p affects and accumulates in Saccharomyces cerevisiae P-bodies. Molecular Biology of the Cell. 19: 984-93. PMID 18162578 DOI: 10.1091/Mbc.E07-09-0954  0.677
2008 Pilkington GR, Parker R. Pat1 contains distinct functional domains that promote P-body assembly and activation of decapping. Molecular and Cellular Biology. 28: 1298-312. PMID 18086885 DOI: 10.1128/Mcb.00936-07  0.579
2007 Buchan JR, Parker R. Molecular biology. The two faces of miRNA. Science (New York, N.Y.). 318: 1877-8. PMID 18096794 DOI: 10.1126/Science.1152623  0.368
2007 Doma MK, Parker R. RNA quality control in eukaryotes. Cell. 131: 660-8. PMID 18022361 DOI: 10.1016/J.Cell.2007.10.041  0.457
2007 Decker CJ, Teixeira D, Parker R. Edc3p and a glutamine/asparagine-rich domain of Lsm4p function in processing body assembly in Saccharomyces cerevisiae. The Journal of Cell Biology. 179: 437-49. PMID 17984320 DOI: 10.1083/Jcb.200704147  0.469
2007 Beckham CJ, Light HR, Nissan TA, Ahlquist P, Parker R, Noueiry A. Interactions between brome mosaic virus RNAs and cytoplasmic processing bodies. Journal of Virology. 81: 9759-68. PMID 17609284 DOI: 10.1128/Jvi.00844-07  0.771
2007 Brengues M, Parker R. Accumulation of polyadenylated mRNA, Pab1p, eIF4E, and eIF4G with P-bodies in Saccharomyces cerevisiae. Molecular Biology of the Cell. 18: 2592-602. PMID 17475768 DOI: 10.1091/Mbc.E06-12-1149  0.543
2007 Teixeira D, Parker R. Analysis of P-body assembly in Saccharomyces cerevisiae. Molecular Biology of the Cell. 18: 2274-87. PMID 17429074 DOI: 10.1091/Mbc.E07-03-0199  0.37
2007 Parker R, Sheth U. P bodies and the control of mRNA translation and degradation. Molecular Cell. 25: 635-46. PMID 17349952 DOI: 10.1016/J.Molcel.2007.02.011  0.55
2007 Cheng Z, Muhlrad D, Lim MK, Parker R, Song H. Structural and functional insights into the human Upf1 helicase core. The Embo Journal. 26: 253-64. PMID 17159905 DOI: 10.1038/Sj.Emboj.7601464  0.425
2007 Thompson DM, Parker R. Cytoplasmic decay of intergenic transcripts in Saccharomyces cerevisiae. Molecular and Cellular Biology. 27: 92-101. PMID 17074811 DOI: 10.1128/Mcb.01023-06  0.499
2006 Barbee SA, Estes PS, Cziko AM, Hillebrand J, Luedeman RA, Coller JM, Johnson N, Howlett IC, Geng C, Ueda R, Brand AH, Newbury SF, Wilhelm JE, Levine RB, Nakamura A, ... Parker R, et al. Staufen- and FMRP-containing neuronal RNPs are structurally and functionally related to somatic P bodies. Neuron. 52: 997-1009. PMID 17178403 DOI: 10.1016/J.Neuron.2006.10.028  0.672
2006 Doma MK, Parker R. Revenge of the NRD: preferential degradation of nonfunctional eukaryotic rRNA. Developmental Cell. 11: 757-8. PMID 17141152 DOI: 10.1016/J.Devcel.2006.11.004  0.451
2006 Hilgers V, Teixeira D, Parker R. Translation-independent inhibition of mRNA deadenylation during stress in Saccharomyces cerevisiae. Rna (New York, N.Y.). 12: 1835-45. PMID 16940550 DOI: 10.1261/Rna.241006  0.49
2006 Baker KE, Parker R. Conventional 3' end formation is not required for NMD substrate recognition in Saccharomyces cerevisiae. Rna (New York, N.Y.). 12: 1441-5. PMID 16809819 DOI: 10.1261/Rna.92706  0.622
2006 Segal SP, Dunckley T, Parker R. Sbp1p affects translational repression and decapping in Saccharomyces cerevisiae. Molecular and Cellular Biology. 26: 5120-30. PMID 16782896 DOI: 10.1128/Mcb.01913-05  0.615
2006 Sheth U, Parker R. Targeting of aberrant mRNAs to cytoplasmic processing bodies. Cell. 125: 1095-109. PMID 16777600 DOI: 10.1016/J.Cell.2006.04.037  0.535
2006 Decker CJ, Parker R. CAR-1 and trailer hitch: driving mRNP granule function at the ER? The Journal of Cell Biology. 173: 159-63. PMID 16636142 DOI: 10.1083/Jcb.200601153  0.558
2006 Doma MK, Parker R. Endonucleolytic cleavage of eukaryotic mRNAs with stalls in translation elongation. Nature. 440: 561-4. PMID 16554824 DOI: 10.1038/Nature04530  0.611
2006 Valencia-Sanchez MA, Liu J, Hannon GJ, Parker R. Control of translation and mRNA degradation by miRNAs and siRNAs. Genes & Development. 20: 515-24. PMID 16510870 DOI: 10.1101/Gad.1399806  0.539
2006 Beliakova-Bethell N, Beckham C, Giddings TH, Winey M, Parker R, Sandmeyer S. Virus-like particles of the Ty3 retrotransposon assemble in association with P-body components Rna. 12: 94-101. PMID 16373495 DOI: 10.1261/Rna.2264806  0.416
2005 Liu J, Rivas FV, Wohlschlegel J, Yates JR, Parker R, Hannon GJ. A role for the P-body component GW182 in microRNA function. Nature Cell Biology. 7: 1261-6. PMID 16284623 DOI: 10.1038/Ncb1333  0.523
2005 Coller J, Parker R. General translational repression by activators of mRNA decapping. Cell. 122: 875-86. PMID 16179257 DOI: 10.1016/J.Cell.2005.07.012  0.584
2005 Brengues M, Teixeira D, Parker R. Movement of eukaryotic mRNAs between polysomes and cytoplasmic processing bodies. Science (New York, N.Y.). 310: 486-9. PMID 16141371 DOI: 10.1126/Science.1115791  0.549
2005 Wilson MA, Meaux S, Parker R, van Hoof A. Genetic interactions between [PSI+] and nonstop mRNA decay affect phenotypic variation. Proceedings of the National Academy of Sciences of the United States of America. 102: 10244-9. PMID 16002465 DOI: 10.1073/Pnas.0504557102  0.482
2005 Cheng Z, Coller J, Parker R, Song H. Crystal structure and functional analysis of DEAD-box protein Dhh1p. Rna (New York, N.Y.). 11: 1258-70. PMID 15987810 DOI: 10.1261/Rna.2920905  0.428
2005 Liu J, Valencia-Sanchez MA, Hannon GJ, Parker R. MicroRNA-dependent localization of targeted mRNAs to mammalian P-bodies. Nature Cell Biology. 7: 719-23. PMID 15937477 DOI: 10.1038/Ncb1274  0.508
2005 Chen N, Walsh MA, Liu Y, Parker R, Song H. Crystal structures of human DcpS in ligand-free and m7GDP-bound forms suggest a dynamic mechanism for scavenger mRNA decapping. Journal of Molecular Biology. 347: 707-18. PMID 15769464 DOI: 10.1016/J.Jmb.2005.01.062  0.35
2005 Tharun S, Muhlrad D, Chowdhury A, Parker R. Mutations in the Saccharomyces cerevisiae LSM1 gene that affect mRNA decapping and 3' end protection. Genetics. 170: 33-46. PMID 15716506 DOI: 10.1534/Genetics.104.034322  0.561
2005 Muhlrad D, Parker R. The yeast EDC1 mRNA undergoes deadenylation-independent decapping stimulated by Not2p, Not4p, and Not5p The Embo Journal. 24: 1033-1045. PMID 15706350 DOI: 10.1038/Sj.Emboj.7600560  0.588
2005 Teixeira D, Sheth U, Valencia-Sanchez MA, Brengues M, Parker R. Processing bodies require RNA for assembly and contain nontranslating mRNAs Rna. 11: 371-382. PMID 15703442 DOI: 10.1261/Rna.7258505  0.484
2004 Baker KE, Coller J, Parker R. The yeast Apq12 protein affects nucleocytoplasmic mRNA transport Rna. 10: 1352-1358. PMID 15273328 DOI: 10.1261/Rna.7420504  0.581
2004 Coller J, Parker R. Eukaryotic mRNA Decapping Annual Review of Biochemistry. 73: 861-890. PMID 15189161 DOI: 10.1146/Annurev.Biochem.73.011303.074032  0.579
2004 Baker KE, Parker R. Nonsense-mediated mRNA decay: terminating erroneous gene expression. Current Opinion in Cell Biology. 16: 293-9. PMID 15145354 DOI: 10.1016/J.Ceb.2004.03.003  0.572
2004 Kshirsagar M, Parker R. Identification of Edc3p as an Enhancer of mRNA Decapping in Saccharomyces cerevisiae Genetics. 166: 729-739. PMID 15020463 DOI: 10.1534/Genetics.166.2.729  0.573
2004 She M, Decker CJ, Sundramurthy K, Liu Y, Chen N, Parker R, Song H. Crystal structure of Dcp1p and its functional implications in mRNA decapping Nature Structural and Molecular Biology. 11: 249-256. PMID 14758354 DOI: 10.1038/Nsmb730  0.403
2004 Parker R, Song H. The enzymes and control of eukaryotic mRNA turnover. Nature Structural & Molecular Biology. 11: 121-7. PMID 14749774 DOI: 10.1038/Nsmb724  0.55
2003 Hilleren PJ, Parker R. Cytoplasmic degradation of splice-defective pre-mRNAs and intermediates. Molecular Cell. 12: 1453-65. PMID 14690599 DOI: 10.1016/S1097-2765(03)00488-X  0.837
2003 Cao D, Parker R. Computational modeling and experimental analysis of nonsense-mediated decay in yeast Cell. 113: 533-545. PMID 12757713 DOI: 10.1016/S0092-8674(03)00353-2  0.562
2003 Sheth U, Parker R. Decapping and Decay of Messenger RNA Occur in Cytoplasmic Processing Bodies Science. 300: 805-808. PMID 12730603 DOI: 10.1126/Science.1082320  0.555
2003 Schwartz D, Decker CJ, Parker R. The enhancer of decapping proteins, Edc1p and Edc2p, bind RNA and stimulate the activity of the decapping enzyme Rna. 9: 239-251. PMID 12554867 DOI: 10.1261/Rna.2171203  0.496
2003 Steiger M, Carr-Schmid A, Schwartz DC, Kiledjian M, Parker R. Analysis of recombinant yeast decapping enzyme. Rna (New York, N.Y.). 9: 231-8. PMID 12554866 DOI: 10.1261/Rna.2151403  0.433
2002 Decker CJ, Parker R. mRNA decay enzymes: Decappers conserved between yeast and mammals Proceedings of the National Academy of Sciences of the United States of America. 99: 12512-12514. PMID 12271148 DOI: 10.1073/Pnas.212518099  0.544
2002 Steiger MA, Parker R. Analyzing mRNA decay in Saccharomyces cerevisiae. Methods in Enzymology. 351: 648-660. PMID 12073375 DOI: 10.1016/S0076-6879(02)51875-9  0.581
2002 van Hoof A, Parker R. Messenger RNA degradation: beginning at the end. Current Biology : Cb. 12: R285-7. PMID 11967169 DOI: 10.1016/S0960-9822(02)00802-3  0.534
2002 van Hoof A, Frischmeyer PA, Dietz HC, Parker R. Exosome-mediated recognition and degradation of mRNAs lacking a termination codon. Science (New York, N.Y.). 295: 2262-4. PMID 11910110 DOI: 10.1126/Science.1067272  0.618
2002 Frischmeyer PA, van Hoof A, O'Donnell K, Guerrerio AL, Parker R, Dietz HC. An mRNA surveillance mechanism that eliminates transcripts lacking termination codons. Science (New York, N.Y.). 295: 2258-61. PMID 11910109 DOI: 10.1126/Science.1067338  0.61
2002 Tucker M, Staples RR, Valencia-Sanchez MA, Muhlrad D, Parker R. Ccr4p is the catalytic subunit of a Ccr4p/Pop2p/Notp mRNA deadenylase complex in Saccharomyces cerevisiae. The Embo Journal. 21: 1427-36. PMID 11889048 DOI: 10.1093/Emboj/21.6.1427  0.54
2002 Wickens M, Bernstein DS, Kimble J, Parker R. A PUF family portrait: 3'UTR regulation as a way of life. Trends in Genetics : Tig. 18: 150-7. PMID 11858839 DOI: 10.1016/S0168-9525(01)02616-6  0.463
2001 Coller JM, Tucker M, Sheth U, Valencia-Sanchez MA, Parker R. The DEAD box helicase, Dhh1p, functions in mRNA decapping and interacts with both the decapping and deadenylase complexes. Rna (New York, N.Y.). 7: 1717-27. PMID 11780629 DOI: 10.1017/S135583820101994X  0.577
2001 Tharun S, Parker R. Targeting an mRNA for decapping: displacement of translation factors and association of the Lsm1p-7p complex on deadenylated yeast mRNAs. Molecular Cell. 8: 1075-83. PMID 11741542 DOI: 10.1016/S1097-2765(01)00395-1  0.56
2001 Dunckley T, Parker R. Yeast mRNA decapping enzyme. Methods in Enzymology. 342: 226-233. PMID 11586895 DOI: 10.1016/S0076-6879(01)42547-X  0.578
2001 Hilleren P, McCarthy T, Rosbash M, Parker R, Jensen TH. Quality control of mRNA 3'-end processing is linked to the nuclear exosome. Nature. 413: 538-42. PMID 11586364 DOI: 10.1038/35097110  0.844
2001 Cao D, Parker R. Computational modeling of eukaryotic mRNA turnover Rna. 7: 1192-1212. PMID 11565744 DOI: 10.1017/S1355838201010330  0.564
2001 Hilleren P, Parker R. Defects in the mRNA export factors Rat7p, Gle1p, Mex67p, and Rat8p cause hyperadenylation during 3'-end formation of nascent transcripts. Rna. 7: 753-764. PMID 11350039 DOI: 10.1017/S1355838201010147  0.829
2001 Tucker M, Valencia-Sanchez MA, Staples RR, Chen J, Denis CL, Parker R. The transcription factor associated Ccr4 and Caf1 proteins are components of the major cytoplasmic mRNA deadenylase in Saccharomyces cerevisiae. Cell. 104: 377-86. PMID 11239395 DOI: 10.1016/S0092-8674(01)00225-2  0.596
2001 Olivas W, Parker R. The Puf3 protein is a transcript-specific regulator of mRNA degradation in yeast. The Embo Journal. 19: 6602-11. PMID 11101532 DOI: 10.1093/Emboj/19.23.6602  0.587
2000 Van Hoof A, Staples RR, Baker RE, Parker R. Function of the Ski4p (Csl4p) and Ski7p proteins in 3'-to-5' degradation of mRNA Molecular and Cellular Biology. 20: 8230-8243. PMID 11027292 DOI: 10.1128/Mcb.20.21.8230-8243.2000  0.557
2000 Schwartz DC, Parker R. mRNA decapping in yeast requires dissociation of the cap binding protein, eukaryotic translation initiation factor 4E. Molecular and Cellular Biology. 20: 7933-42. PMID 11027264 DOI: 10.1128/Mcb.20.21.7933-7942.2000  0.527
2000 Tucker M, Parker R. Mechanisms And Control Of mRNA Decapping in Saccharomyces cerevisiae Annual Review of Biochemistry. 69: 571-595. PMID 10966469 DOI: 10.1146/Annurev.Biochem.69.1.571  0.578
2000 He W, Parker R. Functions of Lsm proteins in mRNA degradation and splicing. Current Opinion in Cell Biology. 12: 346-350. PMID 10801455 DOI: 10.1016/S0955-0674(00)00098-3  0.448
2000 Tharun S, He W, Mayes AE, Lennertz P, Beggs JD, Parker R. Yeast Sm-like proteins function in mRNA decapping and decay Nature. 404: 515-518. PMID 10761922 DOI: 10.1038/35006676  0.596
2000 Hoof Av, Lennertz P, Parker R. Three conserved members of the RNase D family have unique and overlapping functions in the processing of 5S, 5.8S, U4, U5, RNase MRP and RNase P RNAs in yeast. The Embo Journal. 19: 1357-1365. PMID 10716935 DOI: 10.1093/Emboj/19.6.1357  0.433
2000 Anderson JSJ, Parker R. Computational identification of cis-acting elements affecting post-transcriptional control of gene expression in Saccharomyces cerevisiae Nucleic Acids Research. 28: 1604-1617. PMID 10710427 DOI: 10.1093/Nar/28.7.1604  0.362
2000 Hoof Av, Lennertz P, Parker R. Yeast exosome mutants accumulate 3'-extended polyadenylated forms of U4 small nuclear RNA and small nucleolar RNAs. Molecular and Cellular Biology. 20: 441-452. PMID 10611222 DOI: 10.1128/Mcb.20.2.441-452.2000  0.506
2000 Schwartz DC, Parker R. 28 Interaction of mRNA Translation and mRNA Degradation in Saccharomyces cerevisiae Cold Spring Harbor Monograph Archive. 39: 807-825. DOI: 10.1101/087969618.39.807  0.566
1999 Hilleren P, Parker R. Mechanisms of mRNA surveillance in eukaryotes. Annual Review of Genetics. 33: 229-260. PMID 10690409 DOI: 10.1146/Annurev.Genet.33.1.229  0.832
1999 Muhlrad D, Parker R. Aberrant mRNAs with extended 3' UTRs are substrates for rapid degradation by mRNA surveillance. Rna. 5: 1299-1307. PMID 10573121 DOI: 10.1017/S1355838299990829  0.591
1999 Hoof Av, Parker R. The exosome: a proteasome for RNA? Cell. 99: 347-350. PMID 10571176 DOI: 10.1016/S0092-8674(00)81520-2  0.376
1999 Muhlrad D, Parker R. Recognition of yeast mRNAs as "nonsense containing" leads to both inhibition of mRNA translation and mRNA degradation: implications for the control of mRNA decapping. Molecular Biology of the Cell. 10: 3971-3978. PMID 10564284 DOI: 10.1091/Mbc.10.11.3971  0.597
1999 Dunckley T, Parker R. The DCP2 protein is required for mRNA decapping in Saccharomyces cerevisiae and contains a functional MutT motif. The Embo Journal. 18: 5411-5422. PMID 10508173 DOI: 10.1093/Emboj/18.19.5411  0.535
1999 Schwartz DC, Parker R. Mutations in translation initiation factors lead to increased rates of deadenylation and decapping of mRNAs in Saccharomyces cerevisiae. Molecular and Cellular Biology. 19: 5247-56. PMID 10409716 DOI: 10.1128/Mcb.19.8.5247  0.547
1999 Hilleren P, Parker R. mRNA surveillance in eukaryotes: Kinetic proofreading of proper translation termination as assessed by mRNP domain organization? Rna. 5: 711-719. PMID 10376871 DOI: 10.1017/S1355838299990519  0.839
1999 LaGRANDEUR T, Parker R. The cis acting sequences responsible for the differential decay of the unstable MFA2 and stable PGK1 transcripts in yeast include the context of the translational start codon. Rna. 5: 420-433. PMID 10094310 DOI: 10.1017/S1355838299981748  0.576
1999 He W, Parker R. Analysis of mRNA decay pathways in Saccharomyces cerevisiae. Methods. 17: 3-10. PMID 10075877 DOI: 10.1006/Meth.1998.0701  0.569
1999 Tharun S, Parker R. 6.13 – Turnover of mRNA in Eukaryotic Cells Rna. 6: 205-216. DOI: 10.1016/B978-0-08-091283-7.00149-1  0.497
1998 Anderson JS, Parker RP. The 3' to 5' degradation of yeast mRNAs is a general mechanism for mRNA turnover that requires the SKI2 DEVH box protein and 3' to 5' exonucleases of the exosome complex. The Embo Journal. 17: 1497-506. PMID 9482746 DOI: 10.1093/Emboj/17.5.1497  0.597
1998 LaGrandeur TE, Parker R. Isolation and characterization of Dcp1p, the yeast mRNA decapping enzyme The Embo Journal. 17: 1487-1496. PMID 9482745 DOI: 10.1093/Emboj/17.5.1487  0.534
1998 Olivas WM, Muhlrad D, Parker R. Analysis of the yeast genome: identification of new non-coding and small ORF-containing RNAs. Nucleic Acids Research. 25: 4619-25. PMID 9358174 DOI: 10.1093/Nar/25.22.4619  0.432
1996 LaGrandeur TE, Parker R. mRNA decapping activities and their biological roles Biochimie. 78: 1049-1055. PMID 9150884 DOI: 10.1016/S0300-9084(97)86729-6  0.516
1996 Caponigro G, Parker R. mRNA Turnover in Yeast Promoted by the MATα1 Instability Element Nucleic Acids Research. 24: 4304-4312. PMID 8932387 DOI: 10.1093/Nar/24.21.4304  0.569
1996 Hatfield L, Beelman CA, Stevens A, Parker R. Mutations in trans-acting factors affecting mRNA decapping in Saccharomyces cerevisiae. Molecular and Cellular Biology. 16: 5830-8. PMID 8816497 DOI: 10.1128/Mcb.16.10.5830  0.523
1996 Anderson JS, Parker R. RNA turnover: the helicase story unwinds. Current Biology : Cb. 6: 780-2. PMID 8805288 DOI: 10.1016/S0960-9822(02)00593-6  0.393
1996 Beelman CA, Stevens A, Caponigro G, LaGrandeur TE, Hatfield L, Fortner DM, Parker R. An essential component of the decapping enzyme required for normal rates of mRNA turnover. Nature. 382: 642-646. PMID 8757137 DOI: 10.1038/382642A0  0.601
1995 Mandart E, Parker R. Effects of mutations in the Saccharomyces cerevisiae RNA14, RNA15, and PAP1 genes on polyadenylation in vivo Molecular and Cellular Biology. 15: 6979-6986. PMID 8524265 DOI: 10.1128/Mcb.15.12.6979  0.482
1995 Muhlrad D, Decker CJ, Parker R. Turnover mechanisms of the stable yeast PGK1 mRNA Molecular and Cellular Biology. 15: 2145-2156. PMID 7891709 DOI: 10.1128/Mcb.15.4.2145  0.6
1995 Beelman CA, Parker R. Degradation of mRNA in eukaryotes. Cell. 81: 179-183. PMID 7736570 DOI: 10.1016/0092-8674(95)90326-7  0.574
1995 Decker CJ, Parker R. Diversity of cytoplasmic functions for the 3′ untranslated region of eukaryotic transcripts Current Opinion in Cell Biology. 7: 386-392. PMID 7662369 DOI: 10.1016/0955-0674(95)80094-8  0.539
1995 Caponigro G, Parker R. Multiple functions for the poly(A)-binding protein in mRNA decapping and deadenylation in yeast. Genes & Development. 9: 2421-2432. PMID 7557393 DOI: 10.1101/Gad.9.19.2421  0.584
1994 Muhlrad D, Parker R. Premature translational termination triggers mRNA decapping Nature. 370: 578-581. PMID 8052314 DOI: 10.1038/370578A0  0.606
1994 Decker CJ, Parker R. Mechanisms of mRNA degradation in eukaryotes Trends in Biochemical Sciences. 19: 336-340. PMID 7940679 DOI: 10.1016/0968-0004(94)90073-6  0.479
1994 Muhlrad D, Decker CJ, Parker R. Deadenylation of the unstable mRNA encoded by the yeast MFA2 gene leads to decapping followed by 5' → 3' digestion of the transcript Genes and Development. 8: 855-866. PMID 7926773 DOI: 10.1101/Gad.8.7.855  0.6
1993 Parker R, Siliciano PG. Evidence for an essential non-Watson-Crick interaction between the first and last nucleotides of a nuclear pre-mRNA intron. Nature. 361: 660-662. PMID 8437627 DOI: 10.1038/361660A0  0.825
1993 Decker CJ, Parker R. A turnover pathway for both stable and unstable mRNAs in yeast: Evidence for a requirement for deadenylation Genes and Development. 7: 1632-1643. PMID 8393418 DOI: 10.1101/Gad.7.8.1632  0.597
1993 Caponigro G, Muhlrad D, Parker R. A small segment of the MAT alpha 1 transcript promotes mRNA decay in Saccharomyces cerevisiae: a stimulatory role for rare codons. Molecular and Cellular Biology. 13: 5141-5148. PMID 8355674 DOI: 10.1128/Mcb.13.9.5141  0.435
1992 Heaton B, Decker C, Muhlrad D, Donahue J, Jacobson A, Parker R. Analysis of chimeric mRNAs derived from the STE3 mRNA identifies multiple regions within yeast mRNAs that modulate mRNA decay Nucleic Acids Research. 20: 5365-5373. PMID 1437553 DOI: 10.1093/Nar/20.20.5365  0.721
1992 Muhlrad D, Parker R. Mutations affecting stability and deadenylation of the yeast MFA2 transcript. Genes & Development. 6: 2100-2111. PMID 1427074 DOI: 10.1101/Gad.6.11.2100  0.544
1991 Parker R, Herrick D, Peltz SW, Jacobson A. Measurement of mRNA decay rates in Saccharomyces cerevisiae. Methods in Enzymology. 194: 415-23. PMID 2005800 DOI: 10.1016/0076-6879(91)94032-8  0.834
1990 Herrick D, Parker R, Jacobson A. Identification and comparison of stable and unstable mRNAs in Saccharomyces cerevisiae. Molecular and Cellular Biology. 10: 2269-84. PMID 2183028 DOI: 10.1128/Mcb.10.5.2269  0.835
1990 Parker R, Jacobson A. Translation and a 42-nucleotide segment within the coding region of the mRNA encoded by the MAT alpha 1 gene are involved in promoting rapid mRNA decay in yeast Proceedings of the National Academy of Sciences of the United States of America. 87: 2780-2784. PMID 2181450 DOI: 10.1073/Pnas.87.7.2780  0.655
1989 Parker R. Genetic methods for identification and characterization of RNA-RNA and RNA-protein interactions Methods in Enzymology. 180: 510-517. PMID 2482431 DOI: 10.1016/0076-6879(89)80120-X  0.412
1988 Parker R, Simmons T, Shuster EO, Siliciano PG, Guthrie C. Genetic analysis of small nuclear RNAs in Saccharomyces cerevisiae: viable sextuple mutant. Molecular and Cellular Biology. 8: 3150-9. PMID 2905424 DOI: 10.1128/Mcb.8.8.3150  0.811
1988 Ruohola H, Baker SM, Parker R, Platt T. Orientation-dependent function of a short CYC1 DNA fragment in directing mRNA 3' end formation in yeast Proceedings of the National Academy of Sciences of the United States of America. 85: 5041-5045. PMID 2839828 DOI: 10.1073/Pnas.85.14.5041  0.519
1987 Parker R, Siliciano PG, Guthrie C. Recognition of the TACTAAC box during mRNA splicing in yeast involves base pairing to the U2-like snRNA. Cell. 49: 229-39. PMID 3552247 DOI: 10.1016/0092-8674(87)90564-2  0.805
1987 Couto JR, Tamm J, Parker R, Guthrie C. A trans-acting suppressor restores splicing of a yeast intron with a branch point mutation. Genes & Development. 1: 445-55. PMID 2890553 DOI: 10.1101/Gad.1.5.445  0.655
1986 Cellini A, Parker R, McMahon J, Guthrie C, Rossi J. Activation of a cryptic TACTAAC box in the Saccharomyces cerevisiae actin intron. Molecular and Cellular Biology. 6: 1571-8. PMID 3023896 DOI: 10.1128/Mcb.6.5.1571  0.571
1986 Vijayraghavan U, Parker R, Tamm J, Iimura Y, Rossi J, Abelson J, Guthrie C. Mutations in conserved intron sequences affect multiple steps in the yeast splicing pathway, particularly assembly of the spliceosome. The Embo Journal. 5: 1683-95. PMID 3017708  0.585
1986 Vijayraghavan U, Parker R, Tamm J, Iimura Y, Rossi J, Abelson J, Guthrie C. Mutations in conserved intron sequences affect multiple steps in the yeast splicing pathway, particularly assembly of the spliceosome. The Embo Journal. 5: 1683-1695. DOI: 10.1002/J.1460-2075.1986.Tb04412.X  0.455
1985 Parker R, Guthrie C. A point mutation in the conserved hexanucleotide at a yeast 5' splice junction uncouples recognition, cleavage, and ligation. Cell. 41: 107-18. PMID 2986840 DOI: 10.1016/0092-8674(85)90065-0  0.601
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