All Relations between neuroglial cell and isocortex

Reference Sentence Publish Date Extraction Date Species
Lei Wang, Jun Young Park, Fengming Liu, Kris M Olesen, Shirui Hou, Jamy C Peng, Jordan Infield, Anna C Levesque, Yong-Dong Wang, Hongjian Jin, Yiping Fan, Patrick J Connelly, Shondra M Pruett-Miller, Miaofen G Hu, Philip W Hinds, Young-Goo Ha. A kinase-independent function of cyclin-dependent kinase 6 promotes outer radial glia expansion and neocortical folding. Proceedings of the National Academy of Sciences of the United States of America vol 119 issue 38 2022 36095192 outer radial glia (orgs), npcs that are abundant in gyrencephalic species but rare in lissencephalic species, are thought to play key roles in the expansion and folding of the neocortex. 2022-09-12 2022-09-14 Not clear
Anneline Pinson, Lei Xing, Takashi Namba, Nereo Kalebic, Jula Peters, Christina Eugster Oegema, Sofia Traikov, Katrin Reppe, Stephan Riesenberg, Tomislav Maricic, Razvan Derihaci, Pauline Wimberger, Svante P\\xc3\\xa4\\xc3\\xa4bo, Wieland B Huttne. Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals. Science (New York, N.Y.) vol 377 issue 6611 2022 36074851 using overexpression in developing mouse and ferret neocortex, knockout in fetal human neocortical tissue, and genome-edited cerebral organoids, we found that the modern human variant, htktl1, but not the neanderthal variant, increases the abundance of basal radial glia (brg) but not that of intermediate progenitors (bips). 2022-09-08 2022-09-14 Not clear
Simone Mader, Lior Brimberg, An Vo, Joshua J Strohl, James M Crawford, Alexandre Bonnin, Joseph Carri\\xc3\\xb3n, Delcora Campbell, Tom\\xc3\\xa1s S Huerta, Andrea La Bella, Roseann Berlin, Stephen L Dewey, Matthew Hellman, David Eidelberg, Irena Dujmovic, Jelena Drulovic, Jeffrey L Bennett, Bruce T Volpe, Patricio T Huerta, Betty Diamon. In utero exposure to maternal anti-aquaporin-4 antibodies alters brain vasculature and neural dynamics in male mouse offspring. Science translational medicine vol 14 issue 641 2022 35442708 we found that embryonic radial glia cells in neocortex express aqp4. 2022-04-20 2022-04-25 Not clear
Zhongfu Shen, Yang Lin, Jiajun Yang, David J J\\xc3\\xb6rg, Yuwei Peng, Xiuli Zhang, Yifan Xu, Luisirene Hernandez, Jian Ma, Benjamin D Simons, Song-Hai Sh. Distinct progenitor behavior underlying neocortical gliogenesis related to tumorigenesis. Cell reports vol 34 issue 11 2021 33730566 radial glial progenitors (rgps) give rise to the vast majority of neurons and glia in the neocortex. 2022-01-26 2022-01-13 Not clear
Xiangbin Ruan, Gaoao Liu, Jiafeng Zhou, Pan Chen, Changjie Sun, Wei Liu, Chao Wu, Lin Hou, Bin Yin, Boqin Qiang, Pengcheng Shu, Xiaozhong Pen. Zbed3 Is Indispensable for Wnt Signaling Regulation of Cortical Layers Formation in Developing Brain. Cerebral cortex (New York, N.Y. : 1991) vol 31 issue 9 2021 33822906 here, we report that zbed3, which is a positive regulator of wnt/\xce\xb2-catenin signaling, colocalizes with \xce\xb2-catenin at the endfeet of radial glia in the ventricular zone of embryo mouse neocortex. 2021-11-30 2022-01-14 Not clear
Zhongfu Shen, Yang Lin, Jiajun Yang, David J J\\xc3\\xb6rg, Yuwei Peng, Xiuli Zhang, Yifan Xu, Luisirene Hernandez, Jian Ma, Benjamin D Simons, Song-Hai Sh. Distinct progenitor behavior underlying neocortical gliogenesis related to tumorigenesis. Cell reports vol 34 issue 11 2021 33730566 radial glial progenitors (rgps) give rise to the vast majority of neurons and glia in the neocortex. 2021-10-22 2022-01-13 Not clear
Jiafeng Zhou, Gaoao Liu, Xiaoling Zhang, Chao Wu, Mengjie Ma, Jiarui Wu, Lin Hou, Bin Yin, Boqin Qiang, Pengcheng Shu, Xiaozhong Pen. Comparison of the Spatiotemporal Expression Patterns of Three Cre Lines, Emx1IRES-Cre, D6-Cre and hGFAP-Cre, Commonly Used in Neocortical Development Research. Cerebral cortex (New York, N.Y. : 1991) vol issue 2021 34550336 meanwhile, we used the three cre lines to mediate dicer knockout and observed inconsistent phenotypes, including discrepancies in radial glial cell number, survival and neurogenesis in the neocortex and hippocampus. 2021-09-22 2022-01-13 Not clear
Zhen Li, William A Tyler, Ella Zeldich, Gabriel Santpere Bar\\xc3\\xb3, Mayumi Okamoto, Tianliuyun Gao, Mingfeng Li, Nenad Sestan, Tarik F Hayda. Transcriptional priming as a conserved mechanism of lineage diversification in the developing mouse and human neocortex. Science advances vol 6 issue 45 2021 33158872 using single-cell rna-sequencing and in vivo confirmation, we uncover previously unrecognized neural stem and progenitor cell diversity within the fetal mouse and human neocortex, including multiple types of radial glia and intermediate progenitors. 2021-09-18 2022-01-13 Not clear
Shirui Hou, Wan-Ling Ho, Lei Wang, Bryan Kuo, Jun Young Park, Young-Goo Ha. Biphasic Roles of Hedgehog Signaling in the Production and Self-Renewal of Outer Radial Glia in the Ferret Cerebral Cortex. Cerebral cortex (New York, N.Y. : 1991) vol 31 issue 10 2021 34002221 the expansion of outer radial glia (orgs) and intermediate progenitor cells (ipcs) plays key roles in the expansion and consequential folding of the neocortex. 2021-09-15 2022-01-13 Not clear
Li He, Jennifer Jones, Weiguo He, Bryan C Bjork, Jiayu Wen, Qi Da. PRDM16 regulates a temporal transcriptional program to promote progression of cortical neural progenitors. Development (Cambridge, England) vol 148 issue 6 2021 33597191 radial glia (rg) in the neocortex sequentially generate distinct subtypes of projection neurons, accounting for the diversity and complex assembly of cortical neural circuits. 2021-09-13 2022-01-13 Not clear
Jan A Kullmann, Sophie Meyer, Fabrizia Pipicelli, Christina Kyrousi, Felix Schneider, Nora Bartels, Silvia Cappello, Marco B Rus. Profilin1-Dependent F-Actin Assembly Controls Division of Apical Radial Glia and Neocortex Development. Cerebral cortex (New York, N.Y. : 1991) vol 30 issue 6 2021 31867667 profilin1-dependent f-actin assembly controls division of apical radial glia and neocortex development. 2021-05-04 2022-01-13 Not clear
Jan A Kullmann, Sophie Meyer, Fabrizia Pipicelli, Christina Kyrousi, Felix Schneider, Nora Bartels, Silvia Cappello, Marco B Rus. Profilin1-Dependent F-Actin Assembly Controls Division of Apical Radial Glia and Neocortex Development. Cerebral cortex (New York, N.Y. : 1991) vol 30 issue 6 2021 31867667 however, proliferative activity at basal positions was doubled in the mutant neocortex during mid-neurogenesis, with a drastic and specific increase in basal pax6+ cells indicative for elevated numbers of basal radial glia (brg). 2021-05-04 2022-01-13 Not clear
Caroline Alayne Pearson, Destaye M Moore, Haley O Tucker, Joseph D Dekker, Hui Hu, Amaya Miquelaj\\xc3\\xa1uregui, Bennett G Novitc. Foxp1 Regulates Neural Stem Cell Self-Renewal and Bias Toward Deep Layer Cortical Fates. Cell reports vol 30 issue 6 2021 32049024 the laminar architecture of the mammalian neocortex depends on the orderly generation of distinct neuronal subtypes by apical radial glia (arg) during embryogenesis. 2021-03-08 2022-01-13 Not clear
Sebastian R\\xc3\\xb6mer, Hannah Bender, Wolfgang Knabe, Elke Zimmermann, Rudolf R\\xc3\\xbcbsamen, Johannes Seeger, Simone A Fiet. Neural Progenitors in the Developing Neocortex of the Northern Tree Shrew ( Frontiers in neuroanatomy vol 12 issue 2020 29725291 previous studies revealed that the svz thickness as well as the abundance and distribution of npcs, especially that of basal radial glia (brg), differ markedly between the lissencephalic rodent and gyrencephalic primate neocortex. 2020-09-30 2022-01-13 Not clear
Young-Goo Ha. Sonic hedgehog signaling: A conserved mechanism for the expansion of outer radial glia and intermediate progenitor cells and for the growth and folding of the neocortex. Neurogenesis (Austin, Tex.) vol 3 issue 1 2020 28255571 sonic hedgehog signaling: a conserved mechanism for the expansion of outer radial glia and intermediate progenitor cells and for the growth and folding of the neocortex. 2020-09-30 2022-01-13 Not clear
Young-Goo Ha. Sonic hedgehog signaling: A conserved mechanism for the expansion of outer radial glia and intermediate progenitor cells and for the growth and folding of the neocortex. Neurogenesis (Austin, Tex.) vol 3 issue 1 2020 28255571 the expansion of outer radial glia (orgs, also called basal rgs) and intermediate progenitor cells (ipcs) has played a key role in the evolutionary expansion and folding of the neocortex, resulting in superior sensorimotor and cognitive abilities. 2020-09-30 2022-01-13 Not clear
Lenin Veeraval, Conor J O'Leary, Helen M Coope. Adherens Junctions: Guardians of Cortical Development. Frontiers in cell and developmental biology vol 8 issue 2020 32117958 apical radial glia comprise the pseudostratified neuroepithelium lining the embryonic lateral ventricles and give rise to the extensive repertoire of pyramidal neuronal subtypes of the neocortex. 2020-09-28 2022-01-13 Not clear
Valentina Castiglioni, Andrea Faedo, Marco Onorati, Vittoria Dickinson Bocchi, Zhen Li, Raffaele Iennaco, Romina Vuono, Gaetano P Bulfamante, Luca Muzio, Gianvito Martino, Nenad Sestan, Roger A Barker, Elena Cattane. Dynamic and Cell-Specific DACH1 Expression in Human Neocortical and Striatal Development. Cerebral cortex (New York, N.Y. : 1991) vol 29 issue 5 2020 29688344 single-cell global transcriptional analysis revealed that dach1 is specifically enriched in neuroepithelial and ventricular radial glia cells of the developing human neocortex. 2020-07-16 2022-01-13 Not clear
Christopher A Blackwoo. Jagged1 is Essential for Radial Glial Maintenance in the Cortical Proliferative Zone. Neuroscience vol 413 issue 2020 31202705 together, these data support a role for jagged1 in radial glia maintenance in the neocortex. 2020-03-09 2022-01-13 Not clear
Stefania Tavano, Elena Taverna, Nereo Kalebic, Christiane Haffner, Takashi Namba, Andreas Dahl, Michaela Wilsch-Br\\xc3\\xa4uninger, Judith T M L Paridaen, Wieland B Huttne. Insm1 Induces Neural Progenitor Delamination in Developing Neocortex via Downregulation of the Adherens Junction Belt-Specific Protein Plekha7. Neuron vol 97 issue 6 2019 29503187 forced insm1 expression in embryonic mouse neocortex causes npc delamination, converting apical to basal radial glia. 2019-07-15 2022-01-13 Not clear
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