11 Publications

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[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie, Robert J., et al. “Lineage Tracing and Clonal Analysis in Developing Cerebral Cortex Using Mosaic Analysis with Double Markers (MADM).” Journal of Visual Experiments (JoVE), no. 159, e61147, 2020, doi:10.3791/61147.
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Zhang, Tingting, et al. “Generation of Neuronal Diversity from Common Progenitors via Notch Signaling in the Cerebellum.” BioRxiv, Cold Spring Harbor Laboratory, doi:10.1101/2020.03.18.997205.
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras, Ximena, et al. “A Genome-Wide Library of MADM Mice for Single-Cell Genetic Mosaic Analysis.” BioRxiv, Cold Spring Harbor Laboratory, 2020, doi:10.1101/2020.06.05.136192.
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen, Andi H., and Simon Hippenmeyer. “Non-Cell-Autonomous Mechanisms in Radial Projection Neuron Migration in the Developing Cerebral Cortex.” Frontiers in Cell and Developmental Biology, vol. 8, no. 9, 574382, Frontiers, 2020, doi:10.3389/fcell.2020.574382.
View | Files available | DOI | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter, Susanne, et al. “Cell-Type Specificity of Genomic Imprinting in Cerebral Cortex.” Neuron, vol. 107, no. 6, Elsevier, 2020, p. 1160–1179.e9, doi:10.1016/j.neuron.2020.06.031.
View | Files available | DOI
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein, Thomas, et al. “Mutations in Vps15 Perturb Neuronal Migration in Mice and Are Associated with Neurodevelopmental Disease in Humans.” Nature Neuroscience, vol. 21, no. 2, Nature Publishing Group, 2018, pp. 207–17, doi:10.1038/s41593-017-0053-5.
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen, Andi H., et al. “Cell Polarity in Cerebral Cortex Development - Cellular Architecture Shaped by Biochemical Networks.” Frontiers in Cellular Neuroscience, vol. 11, 176, Frontiers Research Foundation, 2017, doi:10.3389/fncel.2017.00176.
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss, Martin, et al. “Uner Tan Syndrome Caused by a Homozygous TUBB2B Mutation Affecting Microtubule Stability.” Human Molecular Genetics, vol. 26, no. 2, Oxford University Press, 2017, pp. 258–69, doi:10.1093/hmg/ddw383.
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss, Martin, et al. “Tubulins and Brain Development: The Origins of Functional Specification.” Molecular and Cellular Neuroscience, vol. 84, Academic Press, 2017, pp. 58–67, doi:10.1016/j.mcn.2017.03.002.
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss, Martin, et al. “Brain Specific Knockin of the Pathogenic Tubb5 E401K Allele Causes Defects in Motor Coordination and Prepulse Inhibition.” Behavioural Brain Research, vol. 323, Elsevier, 2017, pp. 47–55, doi:10.1016/j.bbr.2017.01.029.
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie, Mala, et al. “Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.” The American Journal of Human Genetics, vol. 97, no. 6, Cell Press, 2015, pp. 790–800, doi:10.1016/j.ajhg.2015.10.014.
View | DOI
 

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11 Publications

Mark all

[11]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie, Robert J., et al. “Lineage Tracing and Clonal Analysis in Developing Cerebral Cortex Using Mosaic Analysis with Double Markers (MADM).” Journal of Visual Experiments (JoVE), no. 159, e61147, 2020, doi:10.3791/61147.
View | Files available | DOI
 
[10]
2020 | Preprint | IST-REx-ID: 8546 | OA
Zhang, Tingting, et al. “Generation of Neuronal Diversity from Common Progenitors via Notch Signaling in the Cerebellum.” BioRxiv, Cold Spring Harbor Laboratory, doi:10.1101/2020.03.18.997205.
View | DOI | Download Preprint (ext.)
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras, Ximena, et al. “A Genome-Wide Library of MADM Mice for Single-Cell Genetic Mosaic Analysis.” BioRxiv, Cold Spring Harbor Laboratory, 2020, doi:10.1101/2020.06.05.136192.
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen, Andi H., and Simon Hippenmeyer. “Non-Cell-Autonomous Mechanisms in Radial Projection Neuron Migration in the Developing Cerebral Cortex.” Frontiers in Cell and Developmental Biology, vol. 8, no. 9, 574382, Frontiers, 2020, doi:10.3389/fcell.2020.574382.
View | Files available | DOI | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter, Susanne, et al. “Cell-Type Specificity of Genomic Imprinting in Cerebral Cortex.” Neuron, vol. 107, no. 6, Elsevier, 2020, p. 1160–1179.e9, doi:10.1016/j.neuron.2020.06.031.
View | Files available | DOI
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein, Thomas, et al. “Mutations in Vps15 Perturb Neuronal Migration in Mice and Are Associated with Neurodevelopmental Disease in Humans.” Nature Neuroscience, vol. 21, no. 2, Nature Publishing Group, 2018, pp. 207–17, doi:10.1038/s41593-017-0053-5.
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen, Andi H., et al. “Cell Polarity in Cerebral Cortex Development - Cellular Architecture Shaped by Biochemical Networks.” Frontiers in Cellular Neuroscience, vol. 11, 176, Frontiers Research Foundation, 2017, doi:10.3389/fncel.2017.00176.
View | Files available | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1016
Breuss, Martin, et al. “Uner Tan Syndrome Caused by a Homozygous TUBB2B Mutation Affecting Microtubule Stability.” Human Molecular Genetics, vol. 26, no. 2, Oxford University Press, 2017, pp. 258–69, doi:10.1093/hmg/ddw383.
View | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss, Martin, et al. “Tubulins and Brain Development: The Origins of Functional Specification.” Molecular and Cellular Neuroscience, vol. 84, Academic Press, 2017, pp. 58–67, doi:10.1016/j.mcn.2017.03.002.
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss, Martin, et al. “Brain Specific Knockin of the Pathogenic Tubb5 E401K Allele Causes Defects in Motor Coordination and Prepulse Inhibition.” Behavioural Brain Research, vol. 323, Elsevier, 2017, pp. 47–55, doi:10.1016/j.bbr.2017.01.029.
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie, Mala, et al. “Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type.” The American Journal of Human Genetics, vol. 97, no. 6, Cell Press, 2015, pp. 790–800, doi:10.1016/j.ajhg.2015.10.014.
View | DOI
 

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