Year |
Citation |
Score |
2020 |
Wei Y, Han X, Zhao C. PDK1 regulates the survival of the developing cortical interneurons. Molecular Brain. 13: 65. PMID 32366272 DOI: 10.1186/s13041-020-00604-6 |
0.413 |
|
2019 |
Zhang S, Zhang Y, Dong Y, Guo L, Zhang Z, Shao B, Qi J, Zhou H, Zhu W, Yan X, Hong G, Zhang L, Zhang X, Tang M, Zhao C, et al. Knockdown of Foxg1 in supporting cells increases the trans-differentiation of supporting cells into hair cells in the neonatal mouse cochlea. Cellular and Molecular Life Sciences : Cmls. PMID 31485717 DOI: 10.1007/s00018-019-03291-2 |
0.36 |
|
2019 |
Su Y, Liu J, Yu B, Ba R, Zhao C. Haploinsufficiency Impairs Dendritic Arborization and Spine Formation, Leading to Cognitive Deficits. Frontiers in Cellular Neuroscience. 13: 249. PMID 31213987 DOI: 10.3389/fncel.2019.00249 |
0.318 |
|
2018 |
Han X, Gu X, Zhang Q, Wang Q, Cheng Y, Pleasure SJ, Zhao C. FoxG1 Directly Represses Dentate Granule Cell Fate During Forebrain Development. Frontiers in Cellular Neuroscience. 12: 452. PMID 30532694 DOI: 10.3389/fncel.2018.00452 |
0.64 |
|
2018 |
He Z, Fang Q, Li H, Shao B, Zhang Y, Zhang Y, Han X, Guo R, Cheng C, Guo L, Shi L, Li A, Yu C, Kong W, Zhao C, et al. The role of FOXG1 in the postnatal development and survival of mouse cochlear hair cells. Neuropharmacology. PMID 30336149 DOI: 10.1016/j.neuropharm.2018.10.021 |
0.319 |
|
2018 |
Liu B, Xiao H, Zhao C. Forced Expression of Foxg1 in the Cortical Hem Leads to the Transformation of Cajal-Retzius Cells into Dentate Granule Neurons. Journal of Developmental Biology. 6. PMID 29949945 DOI: 10.3390/jdb6030016 |
0.425 |
|
2018 |
Shen W, Ba R, Su Y, Ni Y, Chen D, Xie W, Pleasure SJ, Zhao C. Foxg1 Regulates the Postnatal Development of Cortical Interneurons. Cerebral Cortex (New York, N.Y. : 1991). PMID 29912324 DOI: 10.1093/cercor/bhy051 |
0.607 |
|
2018 |
Xu M, Han X, Liu R, Li Y, Qi C, Yang Z, Zhao C, Gao J. PDK1 Deficit Impairs the Development of the Dentate Gyrus in Mice. Cerebral Cortex (New York, N.Y. : 1991). PMID 29420689 DOI: 10.1093/cercor/bhy024 |
0.42 |
|
2015 |
Yang Y, Shen W, Ni Y, Su Y, Yang Z, Zhao C. Impaired Interneuron Development after Foxg1 Disruption. Cerebral Cortex (New York, N.Y. : 1991). PMID 26620267 DOI: 10.1093/Cercor/Bhv297 |
0.35 |
|
2015 |
Liu R, Yang Y, Shen J, Chen H, Zhang Q, Ba R, Wei Y, Li KC, Zhang X, Zhao C. Fstl1 is involved in the regulation of radial glial scaffold development. Molecular Brain. 8: 53. PMID 26382033 DOI: 10.1186/s13041-015-0144-8 |
0.329 |
|
2014 |
Liu J, Liu B, Zhang X, Yu B, Guan W, Wang K, Yang Y, Gong Y, Wu X, Yanagawa Y, Wu S, Zhao C. Calretinin-positive L5a pyramidal neurons in the development of the paralemniscal pathway in the barrel cortex. Molecular Brain. 7: 84. PMID 25404384 DOI: 10.1186/S13041-014-0084-8 |
0.314 |
|
2012 |
Tian C, Gong Y, Yang Y, Shen W, Wang K, Liu J, Xu B, Zhao J, Zhao C. Foxg1 has an essential role in postnatal development of the dentate gyrus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 2931-49. PMID 22378868 DOI: 10.1523/JNEUROSCI.5240-11.2012 |
0.449 |
|
2011 |
Gu X, Liu B, Wu X, Yan Y, Zhang Y, Wei Y, Pleasure SJ, Zhao C. Inducible genetic lineage tracing of cortical hem derived Cajal-Retzius cells reveals novel properties. Plos One. 6: e28653. PMID 22174859 DOI: 10.1371/journal.pone.0028653 |
0.624 |
|
2011 |
Li Y, Tian C, Yang Y, Yan Y, Ni Y, Wei Y, Pleasure SJ, Zhao C. An inducible transgenic Cre mouse line for the study of hippocampal development and adult neurogenesis. Genesis (New York, N.Y. : 2000). 49: 919-26. PMID 21538809 DOI: 10.1002/dvg.20765 |
0.598 |
|
2010 |
Zhou W, Zhang Y, Li Y, Wei YS, Liu G, Liu DP, Pleasure SJ, Xie W, Zhao C. A transgenic Cre mouse line for the study of cortical and hippocampal development. Genesis (New York, N.Y. : 2000). 48: 343-50. PMID 20143346 DOI: 10.1002/dvg.20611 |
0.642 |
|
2009 |
Yang Y, Liu J, Mao H, Hu YA, Yan Y, Zhao C. The expression pattern of Follistatin-like 1 in mouse central nervous system development. Gene Expression Patterns : Gep. 9: 532-40. PMID 19595790 DOI: 10.1016/j.gep.2009.07.001 |
0.314 |
|
2009 |
Gu X, Yan Y, Li H, He D, Pleasure SJ, Zhao C. Characterization of the Frizzled10-CreER transgenic mouse: an inducible Cre line for the study of Cajal-Retzius cell development. Genesis (New York, N.Y. : 2000). 47: 210-6. PMID 19241378 DOI: 10.1002/dvg.20472 |
0.653 |
|
2008 |
Gu X, He D, Li Y, Hu C, Wei YS, Liu G, Liu D, Pleasure SJ, Xie W, Zhao C. Generation of Frizzled10-Cre transgenic mouse line: a useful tool for the study of dorsal telencephalic development. Genesis (New York, N.Y. : 2000). 46: 523-9. PMID 18802960 DOI: 10.1002/dvg.20427 |
0.631 |
|
2008 |
Hu YA, Gu X, Liu J, Yang Y, Yan Y, Zhao C. Expression pattern of Wnt inhibitor factor 1(Wif1) during the development in mouse CNS. Gene Expression Patterns : Gep. 8: 515-22. PMID 18586116 DOI: 10.1016/j.gep.2008.06.001 |
0.309 |
|
2006 |
Zhao C, Guan W, Pleasure SJ. A transgenic marker mouse line labels Cajal-Retzius cells from the cortical hem and thalamocortical axons. Brain Research. 1077: 48-53. PMID 16490185 DOI: 10.1016/j.brainres.2006.01.042 |
0.657 |
|
2005 |
Zhao C, Pleasure SJ. Frizzled9 protein is regionally expressed in the developing medial cortical wall and the cells derived from this region. Brain Research. Developmental Brain Research. 157: 93-7. PMID 15939089 DOI: 10.1016/j.devbrainres.2005.02.018 |
0.621 |
|
2005 |
Zhao C, Avilés C, Abel RA, Almli CR, McQuillen P, Pleasure SJ. Hippocampal and visuospatial learning defects in mice with a deletion of frizzled 9, a gene in the Williams syndrome deletion interval. Development (Cambridge, England). 132: 2917-27. PMID 15930120 DOI: 10.1242/Dev.01871 |
0.63 |
|
2004 |
Zhao C, Pleasure SJ. Frizzled-9 promoter drives expression of transgenes in the medial wall of the cortex and its chief derivative the hippocampus. Genesis (New York, N.Y. : 2000). 40: 32-9. PMID 15354291 DOI: 10.1002/gene.20058 |
0.617 |
|
2004 |
Zhou CJ, Zhao C, Pleasure SJ. Wnt signaling mutants have decreased dentate granule cell production and radial glial scaffolding abnormalities. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 121-6. PMID 14715945 DOI: 10.1523/JNEUROSCI.4071-03.2004 |
0.676 |
|
2001 |
Zhao C, Takita J, Tanaka Y, Setou M, Nakagawa T, Takeda S, Yang HW, Terada S, Nakata T, Takei Y, Saito M, Tsuji S, Hayashi Y, Hirokawa N. Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta. Cell. 105: 587-97. PMID 11389829 DOI: 10.1016/S0092-8674(01)00363-4 |
0.625 |
|
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