受强制性开放获取政策约束的文章 - Eirene Markenscoff-Papadimitriou了解详情
可在其他位置公开访问的文章：17 篇
Widespread transcription at neuronal activity-regulated enhancers
TK Kim, M Hemberg, JM Gray, AM Costa, DM Bear, J Wu, DA Harmin, ...
Nature 465 (7295), 182-187, 2010
强制性开放获取政策： US National Institutes of Health
Genome-wide analysis of MEF2 transcriptional program reveals synaptic target genes and neuronal activity-dependent polyadenylation site selection
SW Flavell, TK Kim, JM Gray, DA Harmin, M Hemberg, EJ Hong, ...
Neuron 60 (6), 1022-1038, 2008
强制性开放获取政策： US National Institutes of Health
The psychencode project
S Akbarian, C Liu, JA Knowles, FM Vaccarino, PJ Farnham, GE Crawford, ...
Nature neuroscience 18 (12), 1707-1712, 2015
强制性开放获取政策： US National Institutes of Health, US Department of Veterans Affairs
Nuclear aggregation of olfactory receptor genes governs their monogenic expression
EJ Clowney, MA LeGros, CP Mosley, FG Clowney, ...
Cell 151 (4), 724-737, 2012
强制性开放获取政策： US National Institutes of Health
An epigenetic signature for monoallelic olfactory receptor expression
A Magklara, A Yen, BM Colquitt, EJ Clowney, W Allen, ...
Cell 145 (4), 555-570, 2011
强制性开放获取政策： US National Institutes of Health
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder
JY An, K Lin, L Zhu, DM Werling, S Dong, H Brand, HZ Wang, X Zhao, ...
Science 362 (6420), eaat6576, 2018
强制性开放获取政策： US National Institutes of Health
An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder
DM Werling, H Brand, JY An, MR Stone, L Zhu, JT Glessner, RL Collins, ...
Nature genetics 50 (5), 727-736, 2018
强制性开放获取政策： US National Institutes of Health, Autism Science Foundation, USA
Enhancer interaction networks as a means for singular olfactory receptor expression
E Markenscoff-Papadimitriou, WE Allen, BM Colquitt, T Goh, KK Murphy, ...
Cell 159 (3), 543-557, 2014
强制性开放获取政策： US National Institutes of Health
Soft X-ray tomography reveals gradual chromatin compaction and reorganization during neurogenesis in vivo
MA Le Gros, EJ Clowney, A Magklara, A Yen, ...
Cell reports 17 (8), 2125-2136, 2016
强制性开放获取政策： US Department of Energy, US National Institutes of Health
A chromatin accessibility atlas of the developing human telencephalon
E Markenscoff-Papadimitriou, S Whalen, P Przytycki, R Thomas, ...
Cell 182 (3), 754-769. e18, 2020
强制性开放获取政策： US National Institutes of Health
Machine learning dissection of human accelerated regions in primate neurodevelopment
S Whalen, F Inoue, H Ryu, T Fair, E Markenscoff-Papadimitriou, K Keough, ...
Neuron 111 (6), 857-873. e8, 2023
强制性开放获取政策： US National Institutes of Health, Chan Zuckerberg Initiative
Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes
E Markenscoff-Papadimitriou, F Binyameen, S Whalen, J Price, K Lim, ...
Cell reports 37 (10), 2021
强制性开放获取政策： US National Institutes of Health
Dnmt3a regulates global gene expression in olfactory sensory neurons and enables odorant-induced transcription
BM Colquitt, E Markenscoff-Papadimitriou, R Duffié, S Lomvardas
Neuron 83 (4), 823-838, 2014
强制性开放获取政策： US National Institutes of Health
Genomic views of transcriptional enhancers: essential determinants of cellular identity and activity-dependent responses in the CNS
JM Gray, TK Kim, AE West, AS Nord, E Markenscoff-Papadimitriou, ...
Journal of Neuroscience 35 (41), 13819-13826, 2015
强制性开放获取政策： US National Institutes of Health
Altered hippocampal-prefrontal communication during anxiety-related avoidance in mice deficient for the autism-associated gene Pogz
MM Cunniff, E Markenscoff-Papadimitriou, J Ostrowski, JLR Rubenstein, ...
Elife 9, e54835, 2020
强制性开放获取政策： US National Institutes of Health
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
Y Chen, R Dawes, HC Kim, A Ljungdahl, SL Stenton, S Walker, J Lord, ...
Nature 632 (8026), 832-840, 2024
强制性开放获取政策： National Health and Medical Research Council, Australia, Fonds de recherche …
De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders
Y Chen, R Dawes, HC Kim, SL Stenton, S Walker, A Ljungdahl, J Lord, ...
medRxiv, 2024
强制性开放获取政策： National Health and Medical Research Council, Australia, Fonds de recherche …
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