Subcellular transcriptome alterations in a cell culture model of spinal muscular atrophy point to widespread defects in axonal growth and presynaptic differentiation

gan Saal, Lena, Briese, Michael, Kneitz, Susanne, Glinka, Michael, Sendtner, Michael
Cyhoeddwyd 2014

Whole transcriptome profiling reveals the RNA content of motor axons

gan Briese, Michael, Saal, Lena, Appenzeller, Silke, Moradi, Mehri, Baluapuri, Apoorva, Sendtner, Michael
Cyhoeddwyd yn Nucleic Acids Res (2016)

Aberrant sodium channel activity in the complex seizure disorder of Celf4 mutant mice

gan Sun, Wenzhi, Wagnon, Jacy L, Mahaffey, Connie L, Briese, Michael, Ule, Jernej, Frankel, Wayne N
Cyhoeddwyd 2013

iCLIP Predicts the Dual Splicing Effects of TIA-RNA Interactions

gan Wang, Zhen, Kayikci, Melis, Briese, Michael, Zarnack, Kathi, Luscombe, Nicholas M., Rot, Gregor, Zupan, Blaž, Curk, Tomaž, Ule, Jernej
Cyhoeddwyd 2010

CELF4 Regulates Translation and Local Abundance of a Vast Set of mRNAs, Including Genes Associated with Regulation of Synaptic Function

gan Wagnon, Jacy L., Briese, Michael, Sun, Wenzhi, Mahaffey, Connie L., Curk, Tomaž, Rot, Gregor, Ule, Jernej, Frankel, Wayne N.
Cyhoeddwyd 2012

hnRNP R and its main interactor, the noncoding RNA 7SK, coregulate the axonal transcriptome of motoneurons

gan Briese, Michael, Saal-Bauernschubert, Lena, Ji, Changhe, Moradi, Mehri, Ghanawi, Hanaa, Uhl, Michael, Appenzeller, Silke, Backofen, Rolf, Sendtner, Michael
Cyhoeddwyd yn Proc Natl Acad Sci U S A (2018)

Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan

gan Briese, Michael, Esmaeili, Behrooz, Fraboulet, Sandrine, Burt, Emma C., Christodoulou, Stefanos, Towers, Paula R., Davies, Kay E., Sattelle, David B.
Cyhoeddwyd 2009

Interaction of 7SK with the Smn complex modulates snRNP production

gan Ji, Changhe, Bader, Jakob, Ramanathan, Pradhipa, Hennlein, Luisa, Meissner, Felix, Jablonka, Sibylle, Mann, Matthias, Fischer, Utz, Sendtner, Michael, Briese, Michael
Cyhoeddwyd yn Nat Commun (2021)

Absence of Plekhg5 Results in Myelin Infoldings Corresponding to an Impaired Schwann Cell Autophagy, and a Reduced T-Cell Infiltration Into Peripheral Nerves

gan Lüningschrör, Patrick, Slotta, Carsten, Heimann, Peter, Briese, Michael, Weikert, Ulrich M., Massih, Bita, Appenzeller, Silke, Sendtner, Michael, Kaltschmidt, Christian, Kaltschmidt, Barbara
Cyhoeddwyd yn Front Cell Neurosci (2020)

Loss of Tdp-43 disrupts the axonal transcriptome of motoneurons accompanied by impaired axonal translation and mitochondria function

gan Briese, Michael, Saal-Bauernschubert, Lena, Lüningschrör, Patrick, Moradi, Mehri, Dombert, Benjamin, Surrey, Verena, Appenzeller, Silke, Deng, Chunchu, Jablonka, Sibylle, Sendtner, Michael
Cyhoeddwyd yn Acta Neuropathol Commun (2020)

Characterising the RNA targets and position-dependent splicing regulation by TDP-43; implications for neurodegenerative diseases

gan Tollervey, James R., Curk, Tomaž, Rogelj, Boris, Briese, Michael, Cereda, Matteo, Kayikci, Melis, Hortobágyi, Tibor, Nishimura, Agnes L., Župunski, Vera, Patani, Rickie, Chandran, Siddharthan, Rot, Gregor, Zupan, Blaž, Shaw, Christopher E., Ule, Jernej
Cyhoeddwyd 2011

Recursive splicing in long vertebrate genes

gan Sibley, Christopher R, Emmett, Warren, Blazquez, Lorea, Faro, Ana, Haberman, Nejc, Briese, Michael, Trabzuni, Daniah, Ryten, Mina, Weale, Michael E, Hardy, John, Modic, Miha, Curk, Tomaž, Wilson, Stephen W, Plagnol, Vincent, Ule, Jernej
Cyhoeddwyd yn Nature (2015)

R-Roscovitine Improves Motoneuron Function in Mouse Models for Spinal Muscular Atrophy

gan Tejero, Rocio, Balk, Stefanie, Franco-Espin, Julio, Ojeda, Jorge, Hennlein, Luisa, Drexl, Hans, Dombert, Benjamin, Clausen, Jan-Dierk, Torres-Benito, Laura, Saal-Bauernschubert, Lena, Blum, Robert, Briese, Michael, Appenzeller, Silke, Tabares, Lucia, Jablonka, Sibylle
Cyhoeddwyd yn iScience (2020)

A systems view of spliceosomal assembly and branchpoints with iCLIP

gan Briese, Michael, Haberman, Nejc, Sibley, Christopher R., Faraway, Rupert, Elser, Andrea S., Chakrabarti, Anob M., Wang, Zhen, König, Julian, Perera, David, Wickramasinghe, Vihandha O., Venkitaraman, Ashok R., Luscombe, Nicholas M., Saieva, Luciano, Pellizzoni, Livio, Smith, Christopher W.J., Curk, Tomaž, Ule, Jernej
Cyhoeddwyd yn Nat Struct Mol Biol (2019)

Voltage-independent GluN2A-type NMDA receptor Ca(2+) signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

gan Bertocchi, Ilaria, Eltokhi, Ahmed, Rozov, Andrey, Chi, Vivan Nguyễn, Jensen, Vidar, Bus, Thorsten, Pawlak, Verena, Serafino, Marta, Sonntag, Hannah, Yang, Boyi, Burnashev, Nail, Li, Shi-Bin, Obenhaus, Horst A., Both, Martin, Niewoehner, Burkhard, Single, Frank N., Briese, Michael, Boerner, Thomas, Gass, Peter, Rawlins, John Nick P., Köhr, Georg, Bannerman, David M., Sprengel, Rolf
Cyhoeddwyd yn Commun Biol (2021)

Author Correction: Voltage-independent GluN2A-type NMDA receptor Ca(2+) signaling promotes audiogenic seizures, attentional and cognitive deficits in mice

gan Bertocchi, Ilaria, Eltokhi, Ahmed, Rozov, Andrey, Chi, Vivan Nguyễn, Jensen, Vidar, Bus, Thorsten, Pawlak, Verena, Serafino, Marta, Sonntag, Hannah, Yang, Boyi, Burnashev, Nail, Li, Shi-Bin, Obenhaus, Horst A., Both, Martin, Niewoehner, Burkhard, Single, Frank N., Briese, Michael, Boerner, Thomas, Gass, Peter, Rawlins, John Nick P., Köhr, Georg, Bannerman, David M., Sprengel, Rolf
Cyhoeddwyd yn Commun Biol (2021)