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74 Publications
2018 | Thesis | IST-REx-ID: 10 | 
Role of genomic imprinting in cerebral cortex development
S. Laukoter, Role of Genomic Imprinting in Cerebral Cortex Development, IST Austria, 2018.
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S. Laukoter, Role of Genomic Imprinting in Cerebral Cortex Development, IST Austria, 2018.
2017 | Journal Article | IST-REx-ID: 805
The E2A splice variant E47 regulates the differentiation of projection neurons via p57(KIP2) during cortical development
S. Pfurr, Y. Chu, C. Bohrer, F. Greulich, R.J. Beattie, K. Mammadzada, M. Hils, S. Arnold, V. Taylor, K. Schachtrup, N.H. Uhlenhaut, C. Schachtrup, Development 144 (2017) 3917–3931.
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| DOI
S. Pfurr, Y. Chu, C. Bohrer, F. Greulich, R.J. Beattie, K. Mammadzada, M. Hils, S. Arnold, V. Taylor, K. Schachtrup, N.H. Uhlenhaut, C. Schachtrup, Development 144 (2017) 3917–3931.
2017 | Journal Article | IST-REx-ID: 713 |
Mapping the mouse Allelome reveals tissue specific regulation of allelic expression
D. Andergassen, C. Dotter, D. Wenzel, V. Sigl, P. Bammer, M. Muckenhuber, D. Mayer, T. Kulinski, H. Theussl, J. Penninger, C. Bock, D. Barlow, F. Pauler, Q. Hudson, ELife 6 (2017).
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D. Andergassen, C. Dotter, D. Wenzel, V. Sigl, P. Bammer, M. Muckenhuber, D. Mayer, T. Kulinski, H. Theussl, J. Penninger, C. Bock, D. Barlow, F. Pauler, Q. Hudson, ELife 6 (2017).
2017 | Journal Article | IST-REx-ID: 621 |
Mechanisms of radial glia progenitor cell lineage progression
R.J. Beattie, S. Hippenmeyer, FEBS Letters 591 (2017) 3993–4008.
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R.J. Beattie, S. Hippenmeyer, FEBS Letters 591 (2017) 3993–4008.
2017 | Journal Article | IST-REx-ID: 1016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability
M. Breuss, T. Nguyen, A. Srivatsan, I. Leca, G. Tian, T. Fritz, A.H. Hansen, D. Musaev, J. Mcevoy Venneri, J. Kiely, R. Rosti, E. Scott, U. Tan, R. Kolodner, N. Cowan, D. Keays, J. Gleeson, Human Molecular Genetics 26 (2017) 258–269.
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M. Breuss, T. Nguyen, A. Srivatsan, I. Leca, G. Tian, T. Fritz, A.H. Hansen, D. Musaev, J. Mcevoy Venneri, J. Kiely, R. Rosti, E. Scott, U. Tan, R. Kolodner, N. Cowan, D. Keays, J. Gleeson, Human Molecular Genetics 26 (2017) 258–269.