Peng Jin - Publications

Affiliations: 
Emory School of Medicine 
Area:
Repeat instability, fragile X-related disorders, neuroepigenetics

74 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
2025 Qiu W, Hazard C, Li Y, Jin P, Zhou H. High-Sensitivity Fluorescence-Based Detection of Reverse Transcriptase Read-Through of GC-Rich Short Tandem Repeat RNA. Analytical Chemistry. PMID 39945490 DOI: 10.1021/acs.analchem.4c06236  0.466
2023 Ye J, Huang Z, Li Q, Li Z, Lan Y, Wang Z, Ni C, Wu X, Jiang T, Li Y, Yang Q, Lim J, Ren CY, Jiang M, Li S, ... Jin P, et al. Transition of allele-specific DNA hydroxymethylation at regulatory loci is associated with phenotypic variation in monozygotic twins discordant for psychiatric disorders. Bmc Medicine. 21: 491. PMID 38082312 DOI: 10.1186/s12916-023-03177-y  0.453
2023 Mei Z, Liu J, Schroeder JP, Weinshenker D, Duong DM, Seyfried NT, Li Y, Jin P, Wingo AP, Wingo TS. Lowering Hippocampal miR-29a Expression Slows Cognitive Decline and Reduces Beta-Amyloid Deposition in 5×FAD Mice. Molecular Neurobiology. PMID 37989983 DOI: 10.1007/s12035-023-03791-0  0.421
2023 Mei Z, Liu J, Schroeder JP, Weinshenker D, Duong DM, Seyfried NT, Li Y, Jin P, Wingo AP, Wingo TS. Lowering hippocampal miR-29a expression slows cognitive decline and reduces beta-amyloid deposition in 5xFAD mice. Research Square. PMID 37645711 DOI: 10.21203/rs.3.rs-3235257/v1  0.428
2023 Lin L, Liu X, Cheng X, Li Y, Gearing M, Levey A, Huang X, Li Y, Jin P, Li X. MicroRNA-650 Regulates the Pathogenesis of Alzheimer's Disease Through Targeting Cyclin-Dependent Kinase 5. Molecular Neurobiology. PMID 36656459 DOI: 10.1007/s12035-023-03224-y  0.43
2022 Liu Q, Zhang K, Kang Y, Li Y, Deng P, Li Y, Tian Y, Sun Q, Tang Y, Xu K, Zhou Y, Wang JL, Guo J, Li JD, Xia K, ... ... Jin P, et al. Expression of expanded GGC repeats within causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease. Science Advances. 8: eadd6391. PMID 36417528 DOI: 10.1126/sciadv.add6391  0.522
2022 Jin Y, Su K, Kong HE, Ma W, Wang Z, Li Y, Li R, Allen EG, Wu H, Jin P. Cell-type specific DNA methylome signatures reveal epigenetic mechanisms for neuronal diversity and neurodevelopmental disorder. Human Molecular Genetics. PMID 35947991 DOI: 10.1093/hmg/ddac189  0.488
2022 Albizua I, Charen K, Shubeck L, Talboy A, Berry-Kravis E, Kaufmann WE, Stallworth JL, Drazba KT, Erickson CA, Sweeney JA, Tartaglia N, Warren SF, Hagerman R, Sherman SL, Warren ST, ... Jin P, et al. Descriptive analysis of seizures and comorbidities associated with fragile X syndrome. Molecular Genetics & Genomic Medicine. e2001. PMID 35852003 DOI: 10.1002/mgg3.2001  0.487
2022 Min S, Xu Q, Qin L, Li Y, Li Z, Chen C, Wu H, Han J, Zhu X, Jin P, Tang B. Altered Hydroxymethylome in the substantia Nigra of Parkinson's disease. Human Molecular Genetics. PMID 35661211 DOI: 10.1093/hmg/ddac122  0.438
2022 Reyes Diaz JV, Jin Y, Garber K, Cossen KM, Li Y, Jin P, Li H, Ham JN. A homozygous exonic variant leading to exon skipping in ABCC8 as the cause of severe congenital hyperinsulinism. American Journal of Medical Genetics. Part A. PMID 35621279 DOI: 10.1002/ajmg.a.62843  0.481
2022 Kong HE, Lim J, Linsalata A, Kang Y, Malik I, Allen EG, Cao Y, Shubeck L, Johnston R, Huang Y, Gu Y, Guo X, Zwick ME, Qin Z, Wingo TS, ... ... Jin P, et al. Identification of as a genetic modifier of fragile X-associated tremor/ataxia syndrome. Proceedings of the National Academy of Sciences of the United States of America. 119: e2118124119. PMID 35617426 DOI: 10.1073/pnas.2118124119  0.536
2021 Kang Y, Zhou Y, Li Y, Han Y, Xu J, Niu W, Li Z, Liu S, Feng H, Huang W, Duan R, Xu T, Raj N, Zhang F, Dou J, ... ... Jin P, et al. A human forebrain organoid model of fragile X syndrome exhibits altered neurogenesis and highlights new treatment strategies. Nature Neuroscience. PMID 34413513 DOI: 10.1038/s41593-021-00913-6  0.687
2021 Meng C, Gu L, Li Y, Li R, Cao Y, Li Z, Allen EG, Zhu D, Jin P. Ten-eleven translocation 2 modulates allergic inflammation by 5-hydroxymethylcytosine remodeling of immunologic pathways. Human Molecular Genetics. PMID 34165552 DOI: 10.1093/hmg/ddab167  0.484
2021 Xu K, Li Y, Allen EG, Jin P. Therapeutic Development for CGG Repeat Expansion-Associated Neurodegeneration. Frontiers in Cellular Neuroscience. 15: 655568. PMID 34054431 DOI: 10.3389/fncel.2021.655568  0.527
2021 Trevino CE, Rounds JC, Charen K, Shubeck L, Hipp HS, Spencer JB, Johnston HR, Cutler DJ, Zwick ME, Epstein MP, Murray A, Macpherson JN, Mila M, Rodriguez-Revenga L, Berry-Kravis E, ... ... Jin P, et al. Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation. Fertility and Sterility. PMID 34016428 DOI: 10.1016/j.fertnstert.2021.04.021  0.492
2021 Kim H, Kang Y, Li Y, Chen L, Lin L, Johnson ND, Zhu D, Robinson MH, McSwain L, Barwick BG, Yuan X, Liao X, Zhao J, Zhang Z, Shu Q, ... ... Jin P, et al. Ten-eleven translocation protein 1 modulates medulloblastoma progression. Genome Biology. 22: 125. PMID 33926529 DOI: 10.1186/s13059-021-02352-9  0.483
2021 Raj N, McEachin ZT, Harousseau W, Zhou Y, Zhang F, Merritt-Garza ME, Taliaferro JM, Kalinowska M, Marro SG, Hales CM, Berry-Kravis E, Wolf-Ochoa MW, Martinez-Cerdeño V, Wernig M, Chen L, ... ... Jin P, et al. Cell-type-specific profiling of human cellular models of fragile X syndrome reveal PI3K-dependent defects in translation and neurogenesis. Cell Reports. 35: 108991. PMID 33852833 DOI: 10.1016/j.celrep.2021.108991  0.564
2020 Lin Y, Xue J, Deng J, He H, Luo S, Chen J, Li J, Yu L, Zhao J, Chen J, Allen EG, Jin P, Duan R. Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating Sima. Neurobiology of Disease. 105013. PMID 32653676 DOI: 10.1016/j.nbd.2020.105013  0.303
2019 Qin L, Xu Q, Li Z, Chen L, Li Y, Yang N, Liu Z, Guo J, Shen L, Allen EG, Chen C, Ma C, Wu H, Zhu X, Jin P, et al. Ethnicity-specific and overlapping alterations of brain hydroxymethylome in Alzheimer's disease. Human Molecular Genetics. PMID 31814020 DOI: 10.1093/Hmg/Ddz273  0.481
2019 Tian Y, Wang JL, Huang W, Zeng S, Jiao B, Liu Z, Chen Z, Li Y, Wang Y, Min HX, Wang XJ, You Y, Zhang RX, Chen XY, Yi F, ... ... Jin P, et al. Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders. American Journal of Human Genetics. PMID 31178126 DOI: 10.1016/j.ajhg.2019.05.013  0.457
2018 Cheng Y, Sun M, Chen L, Li Y, Lin L, Yao B, Li Z, Wang Z, Chen J, Miao Z, Xin N, Huang L, Allen EG, Wu H, Xu X, ... Jin P, et al. Ten-Eleven Translocation Proteins Modulate the Response to Environmental Stress in Mice. Cell Reports. 25: 3194-3203.e4. PMID 30540950 DOI: 10.1016/J.Celrep.2018.11.061  0.447
2018 Cheng Y, Wang ZM, Tan W, Wang X, Li Y, Bai B, Li Y, Zhang SF, Yan HL, Chen ZL, Liu CM, Mi TW, Xia S, Zhou Z, Liu A, ... ... Jin P, et al. Partial loss of psychiatric risk gene Mir137 in mice causes repetitive behavior and impairs sociability and learning via increased Pde10a. Nature Neuroscience. PMID 30397325 DOI: 10.1038/S41593-018-0261-7  0.438
2018 Zhang F, Kang Y, Wang M, Li Y, Xu T, Yang W, Song H, Wu H, Shu Q, Jin P. Fragile X mental retardation protein modulates the stability of its m6A-marked messenger RNA targets. Human Molecular Genetics. PMID 30107516 DOI: 10.1093/Hmg/Ddy292  0.53
2018 Yao B, Li Y, Wang Z, Chen L, Poidevin M, Zhang C, Lin L, Wang F, Bao H, Jiao B, Lim J, Cheng Y, Huang L, Phillips BL, Xu T, ... ... Jin P, et al. Active N-Methyladenine Demethylation by DMAD Regulates Gene Expression by Coordinating with Polycomb Protein in Neurons. Molecular Cell. PMID 30078725 DOI: 10.1016/J.Molcel.2018.07.005  0.508
2018 Guo J, Cui Y, Liu Q, Yang Y, Li Y, Weng L, Tang B, Jin P, Li XJ, Yang S, Li S. Piperine ameliorates SCA17 neuropathology by reducing ER stress. Molecular Neurodegeneration. 13: 4. PMID 29378605 DOI: 10.1186/S13024-018-0236-X  0.48
2017 Yao B, Cheng Y, Wang Z, Li Y, Chen L, Huang L, Zhang W, Chen D, Wu H, Tang B, Jin P. DNA N6-methyladenine is dynamically regulated in the mouse brain following environmental stress. Nature Communications. 8: 1122. PMID 29066820 DOI: 10.1038/S41467-017-01195-Y  0.484
2017 Li X, Yao B, Chen L, Kang Y, Li Y, Cheng Y, Li L, Lin L, Wang Z, Wang M, Pan F, Dai Q, Zhang W, Wu H, Shu Q, ... ... Jin P, et al. Ten-eleven translocation 2 interacts with forkhead box O3 and regulates adult neurogenesis. Nature Communications. 8: 15903. PMID 28660881 DOI: 10.1038/Ncomms15903  0.493
2017 Kong HE, Zhao J, Xu S, Jin P, Jin Y. Fragile X-Associated Tremor/Ataxia Syndrome: From Molecular Pathogenesis to Development of Therapeutics. Frontiers in Cellular Neuroscience. 11: 128. PMID 28529475 DOI: 10.3389/fncel.2017.00128  0.301
2016 Zhang F, Hammack C, Ogden SC, Cheng Y, Lee EM, Wen Z, Qian X, Nguyen HN, Li Y, Yao B, Xu M, Xu T, Chen L, Wang Z, Feng H, ... ... Jin P, et al. Molecular signatures associated with ZIKV exposure in human cortical neural progenitors. Nucleic Acids Research. PMID 27580721 DOI: 10.1093/Nar/Gkw765  0.449
2016 Papale LA, Li S, Madrid A, Zhang Q, Chen L, Chopra P, Jin P, Keleş S, Alisch RS. Sex-specific hippocampal 5-hydroxymethylcytosine is disrupted in response to acute stress. Neurobiology of Disease. PMID 27576189 DOI: 10.1016/J.Nbd.2016.08.014  0.637
2016 Qian X, Nguyen HN, Song MM, Hadiono C, Ogden SC, Hammack C, Yao B, Hamersky GR, Jacob F, Zhong C, Yoon KJ, Jeang W, Lin L, Li Y, Thakor J, ... ... Jin P, et al. Brain-Region-Specific Organoids Using Mini-bioreactors for Modeling ZIKV Exposure. Cell. PMID 27118425 DOI: 10.1016/J.Cell.2016.04.032  0.451
2016 Bernstein AI, Lin Y, Street RC, Lin L, Dai Q, Yu L, Bao H, Gearing M, Lah JJ, Nelson PT, He C, Levey AI, Mullé JG, Duan R, Jin P. 5-hydroxymethylation-associated epigenetic modifiers of Alzheimer's disease modulate Tau-induced neurotoxicity. Human Molecular Genetics. PMID 27060332 DOI: 10.1093/Hmg/Ddw109  0.574
2016 Tang H, Hammack C, Ogden SC, Wen Z, Qian X, Li Y, Yao B, Shin J, Zhang F, Lee EM, Christian KM, Didier RA, Jin P, Song H, Ming GL. Zika Virus Infects Human Cortical Neural Progenitors and Attenuates Their Growth. Cell Stem Cell. PMID 26952870 DOI: 10.1016/J.Stem.2016.02.016  0.44
2016 Wingo AP, Almli LM, Stevens JS, Klengel T, Uddin M, Li Y, Bustamante AC, Lori A, Koen N, Stein DJ, Smith AK, Aiello AE, Koenen KC, Wildman DE, Galea S, ... ... Jin P, et al. Corrigendum: DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression. Nature Communications. 7: 10958. PMID 26936533 DOI: 10.1038/Ncomms10958  0.406
2016 Cugusi S, Li Y, Jin P, Lucchesi JC. The Drosophila Helicase MLE Targets Hairpin Structures in Genomic Transcripts. Plos Genetics. 12: e1005761. PMID 26752049 DOI: 10.1371/journal.pgen.1005761  0.487
2015 Wingo AP, Almli LM, Stevens JJ, Klengel T, Uddin M, Li Y, Bustamante AC, Lori A, Koen N, Stein DJ, Smith AK, Aiello AE, Koenen KC, Wildman DE, Galea S, ... ... Jin P, et al. DICER1 and microRNA regulation in post-traumatic stress disorder with comorbid depression. Nature Communications. 6: 10106. PMID 26632874 DOI: 10.1038/Ncomms10106  0.482
2015 Li S, Papale LA, Zhang Q, Madrid A, Chen L, Chopra P, Keleş S, Jin P, Alisch RS. Genome-wide alterations in hippocampal 5-hydroxymethylcytosine links plasticity genes to acute stress. Neurobiology of Disease. PMID 26598390 DOI: 10.1016/J.Nbd.2015.11.010  0.651
2015 Zeng J, Mi R, Wang Y, Li Y, Lin L, Yao B, Song L, Van Die I, Chapman AB, Cummings RD, Jin P, Ju T. Promoters of human Cosmc and T-synthase are similar in structure, yet different in epigenetic regulation. The Journal of Biological Chemistry. PMID 26063800 DOI: 10.1074/Jbc.M115.654244  0.485
2015 Feng J, Shao N, Szulwach KE, Vialou V, Huynh J, Zhong C, Le T, Ferguson D, Cahill ME, Li Y, Koo JW, Ribeiro E, Labonte B, Laitman BM, Estey D, ... ... Jin P, et al. Role of Tet1 and 5-hydroxymethylcytosine in cocaine action. Nature Neuroscience. 18: 536-44. PMID 25774451 DOI: 10.1038/Nn.3976  0.426
2015 Myrick LK, Deng PY, Hashimoto H, Oh YM, Cho Y, Poidevin MJ, Suhl JA, Visootsak J, Cavalli V, Jin P, Cheng X, Warren ST, Klyachko VA. Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures. Proceedings of the National Academy of Sciences of the United States of America. 112: 949-56. PMID 25561520 DOI: 10.1073/Pnas.1423094112  0.734
2014 Guo JU, Szulwach KE, Su Y, Li Y, Yao B, Xu Z, Shin JH, Xie B, Gao Y, Ming GL, Jin P, Song H. Genome-wide antagonism between 5-hydroxymethylcytosine and DNA methylation in the adult mouse brain. Frontiers in Biology. 9: 66-74. PMID 25568643 DOI: 10.1007/S11515-014-1295-1  0.473
2014 Huang H, Li Y, Szulwach KE, Zhang G, Jin P, Chen D. AGO3 Slicer activity regulates mitochondria-nuage localization of Armitage and piRNA amplification. The Journal of Cell Biology. 206: 217-30. PMID 25049272 DOI: 10.1083/jcb.201401002  0.49
2014 Galloway JN, Shaw C, Yu P, Parghi D, Poidevin M, Jin P, Nelson DL. CGG repeats in RNA modulate expression of TDP-43 in mouse and fly models of fragile X tremor ataxia syndrome. Human Molecular Genetics. 23: 5906-15. PMID 24986919 DOI: 10.1093/Hmg/Ddu314  0.326
2014 Zhang W, Cheng Y, Li Y, Chen Z, Jin P, Chen D. A feed-forward mechanism involving Drosophila fragile X mental retardation protein triggers a replication stress-induced DNA damage response. Human Molecular Genetics. 23: 5188-96. PMID 24833720 DOI: 10.1093/hmg/ddu241  0.518
2014 Leung D, Du T, Wagner U, Xie W, Lee AY, Goyal P, Li Y, Szulwach KE, Jin P, Lorincz MC, Ren B. Regulation of DNA methylation turnover at LTR retrotransposons and imprinted loci by the histone methyltransferase Setdb1. Proceedings of the National Academy of Sciences of the United States of America. 111: 6690-5. PMID 24757056 DOI: 10.1073/Pnas.1322273111  0.441
2014 Zhu G, Li Y, Zhu F, Wang T, Jin W, Mu W, Lin W, Tan W, Li W, Street RC, Peng S, Zhang J, Feng Y, Warren ST, Sun Q, ... Jin P, et al. Coordination of engineered factors with TET1/2 promotes early-stage epigenetic modification during somatic cell reprogramming. Stem Cell Reports. 2: 253-61. PMID 24672749 DOI: 10.1016/J.Stemcr.2014.01.012  0.672
2014 Yao B, Lin L, Street RC, Zalewski ZA, Galloway JN, Wu H, Nelson DL, Jin P. Genome-wide alteration of 5-hydroxymethylcytosine in a mouse model of fragile X-associated tremor/ataxia syndrome. Human Molecular Genetics. 23: 1095-107. PMID 24108107 DOI: 10.1093/Hmg/Ddt504  0.308
2013 Wang T, Warren ST, Jin P. Toward pluripotency by reprogramming: mechanisms and application. Protein & Cell. 4: 820-32. PMID 24078387 DOI: 10.1007/S13238-013-3074-1  0.544
2013 Li Y, Ji P, Jin P. Probing the microRNA pathway with small molecules. Bioorganic & Medicinal Chemistry. 21: 6119-23. PMID 23791866 DOI: 10.1016/j.bmc.2013.05.030  0.479
2013 Wang T, Wu H, Li Y, Szulwach KE, Lin L, Li X, Chen IP, Goldlust IS, Chamberlain SJ, Dodd A, Gong H, Ananiev G, Han JW, Yoon YS, Rudd MK, ... ... Jin P, et al. Subtelomeric hotspots of aberrant 5-hydroxymethylcytosine-mediated epigenetic modifications during reprogramming to pluripotency. Nature Cell Biology. 15: 700-11. PMID 23685628 DOI: 10.1038/Ncb2748  0.715
2013 Song CX, Szulwach KE, Dai Q, Fu Y, Mao SQ, Lin L, Street C, Li Y, Poidevin M, Wu H, Gao J, Liu P, Li L, Xu GL, Jin P, et al. Genome-wide profiling of 5-formylcytosine reveals its roles in epigenetic priming. Cell. 153: 678-91. PMID 23602153 DOI: 10.1016/J.Cell.2013.04.001  0.461
2013 Xu Z, Poidevin M, Li X, Li Y, Shu L, Nelson DL, Li H, Hales CM, Gearing M, Wingo TS, Jin P. Expanded GGGGCC repeat RNA associated with amyotrophic lateral sclerosis and frontotemporal dementia causes neurodegeneration. Proceedings of the National Academy of Sciences of the United States of America. 110: 7778-83. PMID 23553836 DOI: 10.1073/Pnas.1219643110  0.513
2012 Li Y, Song CX, He C, Jin P. Selective capture of 5-hydroxymethylcytosine from genomic DNA. Journal of Visualized Experiments : Jove. PMID 23070273 DOI: 10.3791/4441  0.456
2012 Wang T, Pan Q, Lin L, Szulwach KE, Song CX, He C, Wu H, Warren ST, Jin P, Duan R, Li X. Genome-wide DNA hydroxymethylation changes are associated with neurodevelopmental genes in the developing human cerebellum. Human Molecular Genetics. 21: 5500-10. PMID 23042784 DOI: 10.1093/Hmg/Dds394  0.581
2012 Li Y, Lin L, Li Z, Ye X, Xiong K, Aryal B, Xu Z, Paroo Z, Liu Q, He C, Jin P. Iron homeostasis regulates the activity of the microRNA pathway through poly(C)-binding protein 2. Cell Metabolism. 15: 895-904. PMID 22633452 DOI: 10.1016/J.Cmet.2012.04.021  0.452
2012 Li Y, Jin P. RNA-mediated neurodegeneration in fragile X-associated tremor/ataxia syndrome Brain Research. 1462: 112-117. PMID 22459047 DOI: 10.1016/j.brainres.2012.02.057  0.529
2011 Szulwach KE, Li X, Li Y, Song CX, Wu H, Dai Q, Irier H, Upadhyay AK, Gearing M, Levey AI, Vasanthakumar A, Godley LA, Chang Q, Cheng X, He C, ... Jin P, et al. 5-hmC-mediated epigenetic dynamics during postnatal neurodevelopment and aging. Nature Neuroscience. 14: 1607-16. PMID 22037496 DOI: 10.1038/Nn.2959  0.498
2011 Szulwach KE, Li X, Li Y, Song CX, Han JW, Kim S, Namburi S, Hermetz K, Kim JJ, Rudd MK, Yoon YS, Ren B, He C, Jin P. Integrating 5-hydroxymethylcytosine into the epigenomic landscape of human embryonic stem cells. Plos Genetics. 7: e1002154. PMID 21731508 DOI: 10.1371/Journal.Pgen.1002154  0.488
2011 Song CX, Szulwach KE, Fu Y, Dai Q, Yi C, Li X, Li Y, Chen CH, Zhang W, Jian X, Wang J, Zhang L, Looney TJ, Zhang B, Godley LA, ... ... Jin P, et al. Selective chemical labeling reveals the genome-wide distribution of 5-hydroxymethylcytosine. Nature Biotechnology. 29: 68-72. PMID 21151123 DOI: 10.1038/Nbt.1732  0.469
2010 Li Y, He C, Jin P. Emergence of Chemical Biology Approaches to the RNAi/miRNA Pathway Chemistry & Biology. 17: 584-589. PMID 20609408 DOI: 10.1016/J.Chembiol.2010.05.014  0.475
2010 Szulwach KE, Li X, Smrt RD, Li Y, Luo Y, Lin L, Santistevan NJ, Li W, Zhao X, Jin P. Cross talk between microRNA and epigenetic regulation in adult neurogenesis. The Journal of Cell Biology. 189: 127-41. PMID 20368621 DOI: 10.1083/Jcb.200908151  0.473
2009 Chang S, Wen S, Chen D, Jin P. Small regulatory RNAs in neurodevelopmental disorders. Human Molecular Genetics. 18: R18-26. PMID 19297398 DOI: 10.1093/hmg/ddp072  0.559
2008 Li Y, Lin L, Jin P. The microRNA pathway and fragile X mental retardation protein. Biochimica Et Biophysica Acta. 1779: 702-5. PMID 18687414 DOI: 10.1016/j.bbagrm.2008.07.003  0.515
2008 Shan G, Li Y, Zhang J, Li W, Szulwach KE, Duan R, Faghihi MA, Khalil AM, Lu L, Paroo Z, Chan AW, Shi Z, Liu Q, Wahlestedt C, He C, ... Jin P, et al. A small molecule enhances RNA interference and promotes microRNA processing. Nature Biotechnology. 26: 933-40. PMID 18641635 DOI: 10.1038/Nbt.1481  0.515
2008 Chang S, Bray SM, Li Z, Zarnescu DC, He C, Jin P, Warren ST. Identification of small molecules rescuing fragile X syndrome phenotypes in Drosophila. Nature Chemical Biology. 4: 256-63. PMID 18327252 DOI: 10.1038/Nchembio.78  0.725
2007 Alisch RS, Jin P, Epstein M, Caspary T, Warren ST. Argonaute2 is essential for mammalian gastrulation and proper mesoderm formation. Plos Genetics. 3: e227. PMID 18166081 DOI: 10.1371/Journal.Pgen.0030227  0.716
2007 Zhao X, Pak C, Smrt RD, Jin P. Epigenetics and Neural developmental disorders: Washington DC, September 18 and 19, 2006. Epigenetics. 2: 126-34. PMID 17965627 DOI: 10.4161/Epi.2.2.4236  0.305
2007 Jin P, Duan R, Qurashi A, Qin Y, Tian D, Rosser TC, Liu H, Feng Y, Warren ST. Pur α Binds to rCGG Repeats and Modulates Repeat-Mediated Neurodegeneration in a Drosophila Model of Fragile X Tremor/Ataxia Syndrome Neuron. 55: 556-564. PMID 17698009 DOI: 10.1016/J.Neuron.2007.07.020  0.767
2005 Nakamoto M, Jin P, O'Donnell WT, Warren ST. Physiological identification of human transcripts translationally regulated by a specific microRNA. Human Molecular Genetics. 14: 3813-21. PMID 16239240 DOI: 10.1093/Hmg/Ddi397  0.755
2005 Zarnescu DC, Jin P, Betschinger J, Nakamoto M, Wang Y, Dockendorff TC, Feng Y, Jongens TA, Sisson JC, Knoblich JA, Warren ST, Moses K. Fragile X protein functions with lgl and the par complex in flies and mice. Developmental Cell. 8: 43-52. PMID 15621528 DOI: 10.1016/J.Devcel.2004.10.020  0.639
2004 Jin P, Alisch RS, Warren ST. RNA and microRNAs in fragile X mental retardation Nature Cell Biology. 6: 1048-1053. PMID 15516998 DOI: 10.1038/Ncb1104-1048  0.742
2004 Jin P, Zarnescu DC, Ceman S, Nakamoto M, Mowrey J, Jongens TA, Nelson DL, Moses K, Warren ST. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. Nature Neuroscience. 7: 113-7. PMID 14703574 DOI: 10.1038/Nn1174  0.766
2003 Jin P, Zarnescu DC, Zhang F, Pearson CE, Lucchesi JC, Moses K, Warren ST. RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila. Neuron. 39: 739-47. PMID 12948442 DOI: 10.1016/S0896-6273(03)00533-6  0.577
2003 Jin P, Warren ST. New insights into fragile X syndrome: From molecules to neurobehaviors Trends in Biochemical Sciences. 28: 152-158. PMID 12633995 DOI: 10.1016/S0968-0004(03)00033-1  0.574
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