| Year |
Citation |
Score |
| 2023 |
Li WK, Zhang SQ, Peng WL, Shi YH, Yuan B, Yuan YT, Xue ZY, Wang JC, Han WJ, Chen ZF, Shan SF, Xue BQ, Chen JL, Zhang C, Zhu SJ, ... ... Qiu ZL, et al. Whole-brain in vivo base editing reverses behavioral changes in Mef2c-mutant mice. Nature Neuroscience. PMID 38012399 DOI: 10.1038/s41593-023-01499-x |
0.501 |
|
| 2023 |
Wang J, Li W, Li Z, Xue Z, Zhang Y, Yuan Y, Shi Y, Shan S, Han W, Li F, Qiu Z. Taok1 haploinsufficiency leads to autistic-like behaviors in mice via the dorsal raphe nucleus. Cell Reports. 42: 113078. PMID 37656623 DOI: 10.1016/j.celrep.2023.113078 |
0.505 |
|
| 2023 |
Wang J, Yu J, Wang M, Zhang L, Yang K, Du X, Wu J, Wang X, Li F, Qiu Z. Discovery and validation of novel genes in a large Chinese ASD cohort. Biological Psychiatry. PMID 37393044 DOI: 10.1016/j.biopsych.2023.06.025 |
0.484 |
|
| 2023 |
Wu SH, Li X, Qin DD, Zhang LH, Cheng TL, Chen ZF, Nie BB, Ren XF, Wu J, Wang WC, Hu YZ, Gu YL, Lv LB, Yin Y, Hu XT, ... Qiu ZL, et al. Corrigendum to "Induction of core symptoms of autism spectrum disorders by in vivo CRISPR/Cas9-based gene editing in the brain of adolescent rhesus monkeys" [Sci. Bull. 66(9) (2021) 937-946. Science Bulletin. PMID 36842864 DOI: 10.1016/j.scib.2023.02.025 |
0.734 |
|
| 2023 |
Zhang S, Song L, Yuan B, Zhang C, Cao J, Chen J, Qiu J, Tai Y, Chen J, Qiu Z, Zhao XM, Cheng TL. TadA reprogramming to generate potent miniature base editors with high precision. Nature Communications. 14: 413. PMID 36702845 DOI: 10.1038/s41467-023-36004-2 |
0.729 |
|
| 2023 |
Zhang S, Yuan B, Cao J, Song L, Chen J, Qiu J, Qiu Z, Zhao XM, Chen J, Cheng TL. TadA orthologs enable both cytosine and adenine editing of base editors. Nature Communications. 14: 414. PMID 36702837 DOI: 10.1038/s41467-023-36003-3 |
0.726 |
|
| 2022 |
Qin Y, Du Y, Chen L, Liu Y, Xu W, Liu Y, Li Y, Leng J, Wang Y, Zhang XY, Feng J, Zhang F, Jin L, Qiu Z, Gong X, et al. A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling. Molecular Psychiatry. PMID 35388181 DOI: 10.1038/s41380-022-01539-1 |
0.323 |
|
| 2021 |
Yang K, Shi Y, Du X, Wang J, Zhang Y, Shan S, Yuan Y, Wang R, Zhou C, Liu Y, Cai Z, Wang Y, Fan L, Xu H, Yu J, ... ... Qiu Z, et al. SENP1 in the retrosplenial agranular cortex regulates core autistic-like symptoms in mice. Cell Reports. 37: 109939. PMID 34731627 DOI: 10.1016/j.celrep.2021.109939 |
0.525 |
|
| 2021 |
Zhang R, He H, Yuan B, Wu Z, Wang X, Du Y, Chen Y, Qiu Z. An Intronic Variant of CHD7 Identified in Autism Patients Interferes with Neuronal Differentiation and Development. Neuroscience Bulletin. PMID 33948885 DOI: 10.1007/s12264-021-00685-w |
0.314 |
|
| 2020 |
Sun L, Chen R, Li L, Yuan B, Song K, Pan N, Cheng TL, Chang S, Lin K, He X, Wu Q, Xu F, Qiu Z, Wang X. Visualization and correction of social abnormalities-associated neural ensembles in adult MECP2 duplication mice. Science Bulletin. 65: 1192-1202. PMID 36659149 DOI: 10.1016/j.scib.2020.03.026 |
0.735 |
|
| 2020 |
Wu SH, Li X, Qin DD, Zhang LH, Cheng TL, Chen ZF, Nie BB, Ren XF, Wu J, Wang WC, Hu YZ, Gu YL, Lv LB, Yin Y, Hu XT, ... Qiu ZL, et al. Induction of core symptoms of autism spectrum disorder by in vivo CRISPR/Cas9-based gene editing in the brain of adolescent rhesus monkeys. Science Bulletin. 66: 937-946. PMID 36654241 DOI: 10.1016/j.scib.2020.12.017 |
0.757 |
|
| 2020 |
Li S, Yuan B, Cao J, Chen J, Chen J, Qiu J, Zhao XM, Wang X, Qiu Z, Cheng TL. Docking sites inside Cas9 for adenine base editing diversification and RNA off-target elimination. Nature Communications. 11: 5827. PMID 33203850 DOI: 10.1038/s41467-020-19730-9 |
0.713 |
|
| 2020 |
Cai DC, Wang Z, Bo T, Yan S, Liu Y, Liu Z, Zeljic K, Chen X, Zhan Y, Xu X, Du Y, Wang Y, Cang J, Wang GZ, Zhang J, ... ... Qiu Z, et al. duplication causes aberrant GABA pathways, circuits and behaviors in transgenic monkeys: neural mappings to patients with autismMapping from transgenic monkeys to autism patients. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 32269107 DOI: 10.1523/Jneurosci.2727-19.2020 |
0.394 |
|
| 2020 |
He X, Chen W, Liu Z, Yu G, Chen Y, Cai YJ, Sun L, Xu W, Zhong L, Gao C, Chen J, Zhang M, Yang S, Yao Y, Zhang Z, ... ... Qiu Z, et al. Efficient and risk-reduced genome editing using double nicks enhanced by bacterial recombination factors in multiple species. Nucleic Acids Research. PMID 32232370 DOI: 10.1093/nar/gkaa195 |
0.735 |
|
| 2020 |
Yu B, Yuan B, Dai JK, Cheng TL, Xia SN, He LJ, Yuan YT, Zhang YF, Xu HT, Xu FQ, Liang ZF, Qiu ZL. Reversal of Social Recognition Deficit in Adult Mice with MECP2 Duplication via Normalization of MeCP2 in the Medial Prefrontal Cortex. Neuroscience Bulletin. PMID 32144612 DOI: 10.1007/S12264-020-00467-W |
0.755 |
|
| 2020 |
Li S, Hu Y, Li Y, Hu M, Wang W, Ma Y, Cai Y, Wei M, Yao Y, Wang Y, Dong K, Gu Y, Zhao H, Bao J, Qiu Z, et al. Generation of nonhuman primate retinitis pigmentosa model by in situ knockout of RHO in rhesus macaque retina Chinese Science Bulletin. DOI: 10.1016/J.Scib.2020.09.008 |
0.307 |
|
| 2020 |
Sun L, Chen R, Li L, Yuan B, Song K, Pan N, Cheng T, Chang S, Lin K, He X, Wu Q, Xu F, Qiu Z, Wang X. Visualization and correction of social abnormalities-associated neural ensembles in adult MECP2 duplication mice Science Bulletin. 65: 1192-1202. DOI: 10.1016/J.Scib.2020.03.026 |
0.36 |
|
| 2019 |
Qiu Z, Yuan B. Towards the Framework of Understanding Autism Spectrum Disorders. Neuroscience Bulletin. PMID 31707712 DOI: 10.1007/s12264-019-00443-z |
0.319 |
|
| 2019 |
Cheng TL, Li S, Yuan B, Wang X, Zhou W, Qiu Z. Expanding C-T base editing toolkit with diversified cytidine deaminases. Nature Communications. 10: 3612. PMID 31399578 DOI: 10.1038/s41467-019-11562-6 |
0.71 |
|
| 2019 |
Yu X, Yang L, Li J, Li W, Li D, Wang R, Wu K, Chen W, Zhang Y, Qiu Z, Zhou W. De Novo and Inherited SETD1A Variants in Early-onset Epilepsy. Neuroscience Bulletin. PMID 31197650 DOI: 10.1007/s12264-019-00400-w |
0.379 |
|
| 2019 |
Tong DL, Chen RG, Lu YL, Li WK, Zhang YF, Lin JK, He LJ, Dang T, Shan SF, Xu XH, Zhang Y, Zhang C, Du YS, Zhou WH, Wang X, ... Qiu Z, et al. The critical role of ASD-related gene CNTNAP3 in regulating synaptic development and social behavior in mice. Neurobiology of Disease. 104486. PMID 31150793 DOI: 10.1016/J.Nbd.2019.104486 |
0.419 |
|
| 2019 |
Cai Y, Cheng T, Yao Y, Li X, Ma Y, Li L, Zhao H, Bao J, Zhang M, Qiu Z, Xue T. In vivo genome editing rescues photoreceptor degeneration via a Cas9/RecA-mediated homology-directed repair pathway. Science Advances. 5: eaav3335. PMID 31001583 DOI: 10.1126/Sciadv.Aav3335 |
0.343 |
|
| 2019 |
Cheng C, Yang K, Wu X, Zhang Y, Shan S, Gitler A, Ghosh A, Qiu Z. Loss of CREST leads to neuroinflammatory responses and ALS-like motor defects in mice. Translational Neurodegeneration. 8: 13. PMID 30976389 DOI: 10.1186/S40035-019-0152-1 |
0.595 |
|
| 2018 |
Yu X, Hu L, Liu X, Zhan G, Mei M, Wang H, Zhang X, Qiu Z, Zhou W, Yang L. A Novel MYCN Variant Associated with Intellectual Disability Regulates Neuronal Development. Neuroscience Bulletin. PMID 29786759 DOI: 10.1007/s12264-018-0236-4 |
0.322 |
|
| 2017 |
Li X, Yu B, Sun Q, Zhang Y, Ren M, Zhang X, Li A, Yuan J, Madisen L, Luo Q, Zeng H, Gong H, Qiu Z. Generation of a whole-brain atlas for the cholinergic system and mesoscopic projectome analysis of basal forebrain cholinergic neurons. Proceedings of the National Academy of Sciences of the United States of America. PMID 29259118 DOI: 10.1073/Pnas.1703601115 |
0.304 |
|
| 2017 |
Xu X, Li C, Gao X, Xia K, Guo H, Li Y, Hao Z, Zhang L, Gao D, Xu C, Xu H, Xiong ZQ, Qiu Z, Mei L, Xie X, et al. Excessive UBE3A dosage impairs retinoic acid signaling and synaptic plasticity in autism spectrum disorders. Cell Research. PMID 29076503 DOI: 10.1038/Cr.2017.132 |
0.365 |
|
| 2017 |
Qiu Z. Deciphering MECP2-associated disorders: disrupted circuits and the hope for repair. Current Opinion in Neurobiology. 48: 30-36. PMID 28961504 DOI: 10.1016/j.conb.2017.09.004 |
0.424 |
|
| 2017 |
Tian Y, Yang C, Shang S, Cai Y, Deng X, Zhang J, Shao F, Zhu D, Liu Y, Chen G, Liang J, Sun Q, Qiu Z, Zhang C. Loss of FMRP Impaired Hippocampal Long-Term Plasticity and Spatial Learning in Rats. Frontiers in Molecular Neuroscience. 10: 269. PMID 28894415 DOI: 10.3389/fnmol.2017.00269 |
0.33 |
|
| 2017 |
Cheng TL, Qiu Z. Long non-coding RNA tagging and expression manipulation via CRISPR/Cas9-mediated targeted insertion. Protein & Cell. PMID 28875452 DOI: 10.1007/s13238-017-0464-9 |
0.722 |
|
| 2017 |
Wen Z, Cheng TL, Li GZ, Sun SB, Yu SY, Zhang Y, Du YS, Qiu Z. Identification of autism-related MECP2 mutations by whole-exome sequencing and functional validation. Molecular Autism. 8: 43. PMID 28785396 DOI: 10.1186/s13229-017-0157-5 |
0.761 |
|
| 2017 |
Zhang D, Yu B, Liu J, Jiang W, Xie T, Zhang R, Tong D, Qiu Z, Yao H. Altered visual cortical processing in a mouse model of MECP2 duplication syndrome. Scientific Reports. 7: 6468. PMID 28743991 DOI: 10.1038/S41598-017-06916-3 |
0.39 |
|
| 2017 |
Yu X, Qiu Z, Zhang D. Recent Research Progress in Autism Spectrum Disorder. Neuroscience Bulletin. PMID 28285467 DOI: 10.1007/s12264-017-0117-2 |
0.306 |
|
| 2017 |
Wen Z, Cheng TL, Yin DZ, Sun SB, Wang Z, Yu SY, Zhang Y, Qiu Z, Du YS. Identification of the Genetic Cause for Childhood Disintegrative Disorder by Whole-Exome Sequencing. Neuroscience Bulletin. PMID 28283807 DOI: 10.1007/S12264-017-0119-0 |
0.728 |
|
| 2017 |
Wang M, Li H, Takumi T, Qiu Z, Xu X, Yu X, Bian WJ. Distinct Defects in Spine Formation or Pruning in Two Gene Duplication Mouse Models of Autism. Neuroscience Bulletin. PMID 28258509 DOI: 10.1007/S12264-017-0111-8 |
0.43 |
|
| 2017 |
Qiu Z, Li X. Non-human Primate Models for Brain Disorders - Towards Genetic Manipulations via Innovative Technology. Neuroscience Bulletin. PMID 28251519 DOI: 10.1007/s12264-017-0115-4 |
0.344 |
|
| 2017 |
Cheng TL, Chen J, Wan H, Tang B, Tian W, Liao L, Qiu Z. Regulation of mRNA splicing by MeCP2 via epigenetic modifications in the brain. Scientific Reports. 7: 42790. PMID 28211484 DOI: 10.1038/srep42790 |
0.769 |
|
| 2017 |
Chen Z, Li X, Zhou J, Yuan B, Yu B, Tong D, Cheng C, Shao Y, Xia S, Zhang R, Lyu J, Yu X, Dong C, Zhou WH, Qiu Z. Accumulated quiescent neural stem cells in adult hippocampus of the mouse model for the MECP2 duplication syndrome. Scientific Reports. 7: 41701. PMID 28139724 DOI: 10.1038/Srep41701 |
0.341 |
|
| 2017 |
Ma S, Sun R, Jiang B, Gao J, Deng W, Liu P, He R, Cui J, Ji M, Yi W, Yang P, Wu X, Xiong Y, Qiu Z, Ye D, et al. L2hgdh deficiency accumulates L-2-hydroxyglutarate with progressive leukoencephalopathy and neurodegeneration. Molecular and Cellular Biology. PMID 28137912 DOI: 10.1128/Mcb.00492-16 |
0.309 |
|
| 2016 |
Yuan B, Cheng TL, Yang K, Zhang X, Qiu Z. Autism-related protein MeCP2 regulates FGF13 expression and emotional behaviors. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 27916441 DOI: 10.1016/j.jgg.2016.10.004 |
0.731 |
|
| 2016 |
Liu X, Han D, Somel M, Jiang X, Hu H, Guijarro P, Zhang N, Mitchell A, Halene T, Ely JJ, Sherwood CC, Hof PR, Qiu Z, Pääbo S, Akbarian S, et al. Disruption of an Evolutionarily Novel Synaptic Expression Pattern in Autism. Plos Biology. 14: e1002558. PMID 27685936 DOI: 10.1371/Journal.Pbio.1002558 |
0.409 |
|
| 2016 |
Jennings CG, Landman R, Zhou Y, Sharma J, Hyman J, Movshon JA, Qiu Z, Roberts AC, Roe AW, Wang X, Zhou H, Wang L, Zhang F, Desimone R, Feng G. Opportunities and challenges in modeling human brain disorders in transgenic primates. Nature Neuroscience. 19: 1123-1130. PMID 27571191 DOI: 10.1038/Nn.4362 |
0.323 |
|
| 2016 |
Li H, Zhao P, Xu Q, Shan S, Hu C, Qiu Z, Xu X. The autism-related gene SNRPN regulates cortical and spine development via controlling nuclear receptor Nr4a1. Scientific Reports. 6: 29878. PMID 27430727 DOI: 10.1038/srep29878 |
0.438 |
|
| 2016 |
Zhang Y, Chen M, Qiu Z, Hu K, McGee W, Chen X, Liu J, Zhu L, Wu JY. MiR-130a regulates neurite outgrowth and dendritic spine density by targeting MeCP2. Protein & Cell. PMID 27245166 DOI: 10.1007/S13238-016-0272-7 |
0.327 |
|
| 2016 |
Lyu JW, Yuan B, Cheng TL, Qiu ZL, Zhou WH. Reciprocal regulation of autism-related genes MeCP2 and PTEN via microRNAs. Scientific Reports. 6: 20392. PMID 26843422 DOI: 10.1038/srep20392 |
0.776 |
|
| 2016 |
Liu Z, Li X, Zhang JT, Cai YJ, Cheng TL, Cheng C, Wang Y, Zhang CC, Nie YH, Chen ZF, Bian WJ, Zhang L, Xiao J, Lu B, Zhang YF, ... ... Qiu Z, et al. Autism-like behaviours and germline transmission in transgenic monkeys overexpressing MeCP2. Nature. PMID 26808898 DOI: 10.1038/Nature16533 |
0.764 |
|
| 2015 |
Bian WJ, Miao WY, He SJ, Qiu Z, Yu X. Coordinated Spine Pruning and Maturation Mediated by Inter-Spine Competition for Cadherin/Catenin Complexes. Cell. 162: 808-22. PMID 26255771 DOI: 10.1016/J.Cell.2015.07.018 |
0.339 |
|
| 2015 |
Zhao PP, Yao MJ, Chang SY, Gou LT, Liu MF, Qiu ZL, Yuan XB. Novel function of PIWIL1 in neuronal polarization and migration via regulation of microtubule-associated proteins. Molecular Brain. 8: 39. PMID 26104391 DOI: 10.1186/s13041-015-0131-0 |
0.344 |
|
| 2015 |
Lyu J, Yu X, He L, Cheng T, Zhou J, Cheng C, Chen Z, Cheng G, Qiu Z, Zhou W. The protein phosphatase activity of PTEN is essential for regulating neural stem cell differentiation. Molecular Brain. 8: 26. PMID 25927309 DOI: 10.1186/S13041-015-0114-1 |
0.375 |
|
| 2015 |
Ma SM, Chen LX, Lin YF, Yan H, Lv JW, Xiong M, Li J, Cheng GQ, Yang Y, Qiu ZL, Zhou WH. Periostin Promotes Neural Stem Cell Proliferation and Differentiation following Hypoxic-Ischemic Injury. Plos One. 10: e0123585. PMID 25894199 DOI: 10.1371/journal.pone.0123585 |
0.309 |
|
| 2015 |
Zhang R, Huang M, Cao Z, Qi J, Qiu Z, Chiang LY. MeCP2 plays an analgesic role in pain transmission through regulating CREB / miR-132 pathway. Molecular Pain. 11: 19. PMID 25885346 DOI: 10.1186/s12990-015-0015-4 |
0.315 |
|
| 2015 |
Xin YJ, Yuan B, Yu B, Wang YQ, Wu JJ, Zhou WH, Qiu Z. Tet1-mediated DNA demethylation regulates neuronal cell death induced by oxidative stress. Scientific Reports. 5: 7645. PMID 25561289 DOI: 10.1038/srep07645 |
0.308 |
|
| 2014 |
He LJ, Liu N, Cheng TL, Chen XJ, Li YD, Shu YS, Qiu ZL, Zhang XH. Conditional deletion of Mecp2 in parvalbumin-expressing GABAergic cells results in the absence of critical period plasticity. Nature Communications. 5: 5036. PMID 25297674 DOI: 10.1038/Ncomms6036 |
0.761 |
|
| 2014 |
Cheng TL, Qiu Z. MeCP2: multifaceted roles in gene regulation and neural development. Neuroscience Bulletin. 30: 601-9. PMID 25082535 DOI: 10.1007/s12264-014-1452-6 |
0.78 |
|
| 2014 |
Liu Z, Zhou X, Zhu Y, Chen ZF, Yu B, Wang Y, Zhang CC, Nie YH, Sang X, Cai YJ, Zhang YF, Zhang C, Zhou WH, Sun Q, Qiu Z. Generation of a monkey with MECP2 mutations by TALEN-based gene targeting. Neuroscience Bulletin. 30: 381-6. PMID 24838303 DOI: 10.1007/s12264-014-1434-8 |
0.377 |
|
| 2014 |
Yang L, Shen C, Mei M, Zhan G, Zhao Y, Wang H, Huang G, Qiu Z, Lu W, Zhou W. De novo GLI3 mutation in esophageal atresia: reproducing the phenotypic spectrum of Gli3 defects in murine models. Biochimica Et Biophysica Acta. 1842: 1755-61. PMID 24819706 DOI: 10.1016/j.bbadis.2014.05.001 |
0.33 |
|
| 2014 |
Cheng TL, Wang Z, Liao Q, Zhu Y, Zhou WH, Xu W, Qiu Z. MeCP2 suppresses nuclear microRNA processing and dendritic growth by regulating the DGCR8/Drosha complex. Developmental Cell. 28: 547-60. PMID 24636259 DOI: 10.1016/j.devcel.2014.01.032 |
0.772 |
|
| 2014 |
Cheng J, Huang M, Zhu Y, Xin YJ, Zhao YK, Huang J, Yu JX, Zhou WH, Qiu Z. SUMOylation of MeCP2 is essential for transcriptional repression and hippocampal synapse development. Journal of Neurochemistry. 128: 798-806. PMID 24188180 DOI: 10.1111/jnc.12523 |
0.451 |
|
| 2013 |
Lv JW, Cheng TL, Qiu ZL, Zhou WH. Role of the PTEN signaling pathway in autism spectrum disorder. Neuroscience Bulletin. 29: 773-8. PMID 24136242 DOI: 10.1007/s12264-013-1382-3 |
0.757 |
|
| 2013 |
Lv J, Xin Y, Zhou W, Qiu Z. The epigenetic switches for neural development and psychiatric disorders. Journal of Genetics and Genomics = Yi Chuan Xue Bao. 40: 339-46. PMID 23876774 DOI: 10.1016/j.jgg.2013.04.007 |
0.403 |
|
| 2012 |
Xu X, Xu Q, Zhang Y, Zhang X, Cheng T, Wu B, Ding Y, Lu P, Zheng J, Zhang M, Qiu Z, Yu X. A case report of Chinese brothers with inherited MECP2-containing duplication: autism and intellectual disability, but not seizures or respiratory infections. Bmc Medical Genetics. 13: 75. PMID 22909152 DOI: 10.1186/1471-2350-13-75 |
0.342 |
|
| 2012 |
Gong X, Jiang YW, Zhang X, An Y, Zhang J, Wu Y, Wang J, Sun Y, Liu Y, Gao X, Shen Y, Wu X, Qiu Z, Jin L, Wu BL, et al. High proportion of 22q13 deletions and SHANK3 mutations in Chinese patients with intellectual disability. Plos One. 7: e34739. PMID 22509352 DOI: 10.1371/Journal.Pone.0034739 |
0.318 |
|
| 2012 |
Wilke SA, Hall BJ, Antonios JK, Denardo LA, Otto S, Yuan B, Chen F, Robbins EM, Tiglio K, Williams ME, Qiu Z, Biederer T, Ghosh A. NeuroD2 regulates the development of hippocampal mossy fiber synapses. Neural Development. 7: 9. PMID 22369234 DOI: 10.1186/1749-8104-7-9 |
0.749 |
|
| 2012 |
Liu X, Somel M, Tang L, Yan Z, Jiang X, Guo S, Yuan Y, He L, Oleksiak A, Zhang Y, Li N, Hu Y, Chen W, Qiu Z, Pääbo S, et al. Extension of cortical synaptic development distinguishes humans from chimpanzees and macaques. Genome Research. 22: 611-22. PMID 22300767 DOI: 10.1101/Gr.127324.111 |
0.351 |
|
| 2012 |
Qiu Z, Sylwestrak EL, Lieberman DN, Zhang Y, Liu XY, Ghosh A. The Rett syndrome protein MeCP2 regulates synaptic scaling. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 989-94. PMID 22262897 DOI: 10.1523/Jneurosci.0175-11.2012 |
0.763 |
|
| 2010 |
Qiu Z, Cheng J. The role of calcium-dependent gene expression in autism spectrum disorders: lessons from MeCP2, Ube3a and beyond. Neuro-Signals. 18: 72-81. PMID 20956852 DOI: 10.1159/000320970 |
0.451 |
|
| 2009 |
Qiu Z. Histone modifier, the gatekeeper of good memory. Cell Research. 19: 920-1. PMID 19648947 DOI: 10.1038/cr.2009.93 |
0.317 |
|
| 2009 |
Yuan SH, Qiu Z, Ghosh A. TOX3 regulates calcium-dependent transcription in neurons. Proceedings of the National Academy of Sciences of the United States of America. 106: 2909-14. PMID 19196971 DOI: 10.1073/pnas.0805555106 |
0.605 |
|
| 2008 |
Qiu Z, Ghosh A. A calcium-dependent switch in a CREST-BRG1 complex regulates activity-dependent gene expression. Neuron. 60: 775-87. PMID 19081374 DOI: 10.1016/j.neuron.2008.09.040 |
0.62 |
|
| 2008 |
Qiu Z, Ghosh A. A brief history of neuronal gene expression: regulatory mechanisms and cellular consequences. Neuron. 60: 449-55. PMID 18995819 DOI: 10.1016/j.neuron.2008.10.039 |
0.637 |
|
| 2007 |
Wu JI, Lessard J, Olave IA, Qiu Z, Ghosh A, Graef IA, Crabtree GR. Regulation of dendritic development by neuron-specific chromatin remodeling complexes. Neuron. 56: 94-108. PMID 17920018 DOI: 10.1016/J.Neuron.2007.08.021 |
0.63 |
|
| 2006 |
Kashani AH, Qiu Z, Jurata L, Lee SK, Pfaff S, Goebbels S, Nave KA, Ghosh A. Calcium activation of the LMO4 transcription complex and its role in the patterning of thalamocortical connections. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 8398-408. PMID 16899735 DOI: 10.1523/Jneurosci.0618-06.2006 |
0.72 |
|
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