Year |
Citation |
Score |
2021 |
Krupa O, Fragola G, Hadden-Ford E, Mory JT, Liu T, Humphrey Z, Rees BW, Krishnamurthy A, Snider WD, Zylka MJ, Wu G, Xing L, Stein JL. NuMorph: Tools for cortical cellular phenotyping in tissue-cleared whole-brain images. Cell Reports. 37: 109802. PMID 34644582 DOI: 10.1016/j.celrep.2021.109802 |
0.471 |
|
2019 |
Holter MC, Hewitt LT, Koebele SV, Judd JM, Xing L, Bimonte-Nelson HA, Conrad CD, Araki T, Neel BG, Snider WD, Newbern JM. The Noonan Syndrome-linked Raf1L613V mutation drives increased glial number in the mouse cortex and enhanced learning. Plos Genetics. 15: e1008108. PMID 31017896 DOI: 10.1371/Journal.Pgen.1008108 |
0.68 |
|
2016 |
Gross C, Yao X, Engel T, Tiwari D, Xing L, Rowley S, Danielson SW, Thomas KT, Jimenez-Mateos EM, Schroeder LM, Pun RY, Danzer SC, Henshall DC, Bassell GJ. MicroRNA-Mediated Downregulation of the Potassium Channel Kv4.2 Contributes to Seizure Onset. Cell Reports. 17: 37-45. PMID 27681419 DOI: 10.1016/J.Celrep.2016.08.074 |
0.62 |
|
2016 |
Xing L, Larsen RS, Bjorklund GR, Li X, Wu Y, Philpot BD, Snider WD, Newbern JM. Layer specific and general requirements for ERK/MAPK signaling in the developing neocortex. Elife. 5. PMID 26848828 DOI: 10.7554/Elife.11123 |
0.707 |
|
2015 |
Williams KR, McAninch DS, Stefanovic S, Xing L, Allen M, Li W, Feng Y, Mihailescu MR, Bassell GJ. hnRNP-Q1 Represses Nascent Axon Growth in Cortical Neurons by Inhibiting Gap-43 mRNA Translation. Molecular Biology of the Cell. PMID 26658614 DOI: 10.1091/Mbc.E15-07-0504 |
0.615 |
|
2015 |
Xing L, Li X, Snider WD. Neurodevelopment. "RASopathic" astrocytes constrain neural plasticity. Science (New York, N.Y.). 348: 636-7. PMID 25953994 DOI: 10.1126/science.aab3738 |
0.452 |
|
2014 |
Sasaki Y, Gross C, Xing L, Goshima Y, Bassell GJ. Identification of axon-enriched microRNAs localized to growth cones of cortical neurons. Developmental Neurobiology. 74: 397-406. PMID 23897634 DOI: 10.1002/Dneu.22113 |
0.656 |
|
2013 |
Xing L, Newbern JM, Snider WD. Neuronal development: SAD kinases make happy axons. Current Biology : Cb. 23: R720-3. PMID 24028951 DOI: 10.1016/J.Cub.2013.07.073 |
0.716 |
|
2013 |
Xing L, Bassell GJ. mRNA localization: an orchestration of assembly, traffic and synthesis. Traffic (Copenhagen, Denmark). 14: 2-14. PMID 22913533 DOI: 10.1111/Tra.12004 |
0.55 |
|
2012 |
Xing L, Yao X, Williams KR, Bassell GJ. Negative regulation of RhoA translation and signaling by hnRNP-Q1 affects cellular morphogenesis. Molecular Biology of the Cell. 23: 1500-9. PMID 22357624 DOI: 10.1091/Mbc.E11-10-0867 |
0.593 |
|
2011 |
Muddashetty RS, Nalavadi VC, Gross C, Yao X, Xing L, Laur O, Warren ST, Bassell GJ. Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation, and mGluR signaling. Molecular Cell. 42: 673-88. PMID 21658607 DOI: 10.1016/J.Molcel.2011.05.006 |
0.615 |
|
2011 |
Sasaki Y, Xing L, Gross C, Goshima Y, Bassell GJ. Brain-derived neurotrophic factor regulates localization of microRNA-720 in growth cones Neuroscience Research. 71: e224-e225. DOI: 10.1016/J.Neures.2011.07.978 |
0.603 |
|
2010 |
Sasaki Y, Xing L, Gross C, Goshima Y, Bassell GJ. Profiling of microRNAs enriched in axons Neuroscience Research. 68: e354. DOI: 10.1016/J.Neures.2010.07.1570 |
0.623 |
|
2007 |
Zhang H, Xing L, Singer RH, Bassell GJ. QNQKE targeting motif for the SMN-Gemin multiprotein complexin neurons. Journal of Neuroscience Research. 85: 2657-67. PMID 17455327 DOI: 10.1002/Jnr.21308 |
0.669 |
|
2006 |
Zhang H, Xing L, Rossoll W, Wichterle H, Singer RH, Bassell GJ. Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 8622-32. PMID 16914688 DOI: 10.1523/Jneurosci.3967-05.2006 |
0.665 |
|
2005 |
Le TT, Pham LT, Butchbach ME, Zhang HL, Monani UR, Coovert DD, Gavrilina TO, Xing L, Bassell GJ, Burghes AH. SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN. Human Molecular Genetics. 14: 845-57. PMID 15703193 DOI: 10.1093/Hmg/Ddi078 |
0.561 |
|
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