12 Publications

Mark all

[12]
2021 | Journal Article | IST-REx-ID: 8546 | OA
Zhang T, Liu T, Mora N, et al. Generation of excitatory and inhibitory neurons from common progenitors via Notch signaling in the cerebellum. Cell Reports. 2021;35(10). doi:10.1016/j.celrep.2021.109208
View | Files available | DOI | PubMed | Europe PMC
 
[11]
2021 | Journal Article | IST-REx-ID: 9603 | OA
Contreras X, Amberg N, Davaatseren A, et al. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. Cell Reports. 2021;35(12). doi:10.1016/j.celrep.2021.109274
View | Files available | DOI
 
[10]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter S, Pauler F, Beattie RJ, et al. Cell-type specificity of genomic imprinting in cerebral cortex. Neuron. 2020;107(6):1160-1179.e9. doi:10.1016/j.neuron.2020.06.031
View | Files available | DOI
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras X, Davaatseren A, Amberg N, et al. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. bioRxiv. 2020. doi:10.1101/2020.06.05.136192
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen AH, Hippenmeyer S. Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex. Frontiers in Cell and Developmental Biology. 2020;8(9). doi:10.3389/fcell.2020.574382
View | Files available | DOI | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie RJ, Streicher C, Amberg N, et al. Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM). Journal of Visual Experiments (JoVE). 2020;(159). doi:10.3791/61147
View | Files available | DOI
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein T, Edwards A, Přistoupilová A, Leca I, Breuss M, Pilat Carotta S, Hansen AH, Tripathy R, Traunbauer A, Hochstoeger T, Rosoklija G, Repic M, Landler L, Stránecký V, Dürnberger G, Keane T, Zuber J, Adams D, Flint J, Honzik T, Gut M, Beltran S, Mechtler K, Sherr E, Kmoch S, Gut I, Keays D. 2018. Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience. 21(2), 207–217.
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 1016
Breuss M, Nguyen T, Srivatsan A, et al. Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics. 2017;26(2):258-269. doi:10.1093/hmg/ddw383
View | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss M, Leca I, Gstrein T, Hansen AH, Keays D. Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience. 2017;84:58-67. doi:10.1016/j.mcn.2017.03.002
View | Files available | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss M, Hansen AH, Landler L, Keays D. Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research. 2017;323:47-55. doi:10.1016/j.bbr.2017.01.029
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen AH, Düllberg CF, Mieck C, Loose M, Hippenmeyer S. Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience. 2017;11. doi:10.3389/fncel.2017.00176
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie M, Breuss M, Tian G, Hansen AH, Cristofoli F, Morandell J, Kupchinsky ZA, Sifrim A, Rodriguez Rodriguez C, Dapena EP, Doonanco K, Leonard N, Tinsa F, Moortgat S, Ulucan H, Koparir E, Karaca E, Katsanis N, Marton V, Vermeesch JR, Davis EE, Cowan NJ, Keays D, Van Esch H. 2015. Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics. 97(6), 790–800.
View | DOI
 

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12 Publications

Mark all

[12]
2021 | Journal Article | IST-REx-ID: 8546 | OA
Zhang T, Liu T, Mora N, et al. Generation of excitatory and inhibitory neurons from common progenitors via Notch signaling in the cerebellum. Cell Reports. 2021;35(10). doi:10.1016/j.celrep.2021.109208
View | Files available | DOI | PubMed | Europe PMC
 
[11]
2021 | Journal Article | IST-REx-ID: 9603 | OA
Contreras X, Amberg N, Davaatseren A, et al. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. Cell Reports. 2021;35(12). doi:10.1016/j.celrep.2021.109274
View | Files available | DOI
 
[10]
2020 | Journal Article | IST-REx-ID: 8162 | OA
Laukoter S, Pauler F, Beattie RJ, et al. Cell-type specificity of genomic imprinting in cerebral cortex. Neuron. 2020;107(6):1160-1179.e9. doi:10.1016/j.neuron.2020.06.031
View | Files available | DOI
 
[9]
2020 | Preprint | IST-REx-ID: 8545 | OA
Contreras X, Davaatseren A, Amberg N, et al. A genome-wide library of MADM mice for single-cell genetic mosaic analysis. bioRxiv. 2020. doi:10.1101/2020.06.05.136192
View | DOI | Download Preprint (ext.)
 
[8]
2020 | Journal Article | IST-REx-ID: 8569 | OA
Hansen AH, Hippenmeyer S. Non-cell-autonomous mechanisms in radial projection neuron migration in the developing cerebral cortex. Frontiers in Cell and Developmental Biology. 2020;8(9). doi:10.3389/fcell.2020.574382
View | Files available | DOI | PubMed | Europe PMC
 
[7]
2020 | Journal Article | IST-REx-ID: 7815 | OA
Beattie RJ, Streicher C, Amberg N, et al. Lineage tracing and clonal analysis in developing cerebral cortex using mosaic analysis with double markers (MADM). Journal of Visual Experiments (JoVE). 2020;(159). doi:10.3791/61147
View | Files available | DOI
 
[6]
2018 | Journal Article | IST-REx-ID: 547
Gstrein T, Edwards A, Přistoupilová A, Leca I, Breuss M, Pilat Carotta S, Hansen AH, Tripathy R, Traunbauer A, Hochstoeger T, Rosoklija G, Repic M, Landler L, Stránecký V, Dürnberger G, Keane T, Zuber J, Adams D, Flint J, Honzik T, Gut M, Beltran S, Mechtler K, Sherr E, Kmoch S, Gut I, Keays D. 2018. Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans. Nature Neuroscience. 21(2), 207–217.
View | DOI
 
[5]
2017 | Journal Article | IST-REx-ID: 1016
Breuss M, Nguyen T, Srivatsan A, et al. Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability. Human Molecular Genetics. 2017;26(2):258-269. doi:10.1093/hmg/ddw383
View | DOI
 
[4]
2017 | Journal Article | IST-REx-ID: 1017 | OA
Breuss M, Leca I, Gstrein T, Hansen AH, Keays D. Tubulins and brain development: The origins of functional specification. Molecular and Cellular Neuroscience. 2017;84:58-67. doi:10.1016/j.mcn.2017.03.002
View | Files available | DOI
 
[3]
2017 | Journal Article | IST-REx-ID: 1107 | OA
Breuss M, Hansen AH, Landler L, Keays D. Brain specific knockin of the pathogenic Tubb5 E401K allele causes defects in motor coordination and prepulse inhibition. Behavioural Brain Research. 2017;323:47-55. doi:10.1016/j.bbr.2017.01.029
View | Files available | DOI
 
[2]
2017 | Journal Article | IST-REx-ID: 960 | OA
Hansen AH, Düllberg CF, Mieck C, Loose M, Hippenmeyer S. Cell polarity in cerebral cortex development - cellular architecture shaped by biochemical networks. Frontiers in Cellular Neuroscience. 2017;11. doi:10.3389/fncel.2017.00176
View | Files available | DOI
 
[1]
2015 | Journal Article | IST-REx-ID: 1106
Isrie M, Breuss M, Tian G, Hansen AH, Cristofoli F, Morandell J, Kupchinsky ZA, Sifrim A, Rodriguez Rodriguez C, Dapena EP, Doonanco K, Leonard N, Tinsa F, Moortgat S, Ulucan H, Koparir E, Karaca E, Katsanis N, Marton V, Vermeesch JR, Davis EE, Cowan NJ, Keays D, Van Esch H. 2015. Mutations in either TUBB or MAPRE2 cause circumferential skin creases Kunze type. The American Journal of Human Genetics. 97(6), 790–800.
View | DOI
 

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