ERS2544731 SAMEA4724593 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:58Z External Id SAMEA4724593 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:58Z INSDC status public Submitter Id RNASeq_primaryNeurons1 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons1 scientific_name Mus musculus tissue type Primary neuronal cultures ERS2544732 SAMEA4724594 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:59Z External Id SAMEA4724594 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:59Z INSDC status public Submitter Id RNASeq_primaryNeurons2 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons2 scientific_name Mus musculus tissue type Primary neuronal cultures ERS2544733 SAMEA4724595 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:59Z External Id SAMEA4724595 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:59Z INSDC status public Submitter Id RNASeq_primaryNeurons3 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons3 scientific_name Mus musculus tissue type Primary neuronal cultures ERS2544734 SAMEA4724596 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:59Z External Id SAMEA4724596 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:59Z INSDC status public Submitter Id RNASeq_primaryNeurons4 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons4 scientific_name Mus musculus tissue type Primary neuronal cultures ERS2544735 SAMEA4724597 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:59Z External Id SAMEA4724597 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:59Z INSDC status public Submitter Id RNASeq_primaryNeurons5 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons5 scientific_name Mus musculus tissue type Primary neuronal cultures ERS2544736 SAMEA4724598 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:59Z External Id SAMEA4724598 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:59Z INSDC status public Submitter Id RNASeq_primaryNeurons6 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons6 scientific_name Mus musculus tissue type Primary neuronal cultures ERS2544737 SAMEA4724599 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:59Z External Id SAMEA4724599 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:59Z INSDC status public Submitter Id RNASeq_primaryNeurons7 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons7 scientific_name Mus musculus tissue type Primary neuronal cultures ERS2544738 SAMEA4724600 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:59Z External Id SAMEA4724600 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:59Z INSDC status public Submitter Id RNASeq_primaryNeurons8 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons8 scientific_name Mus musculus tissue type Primary neuronal cultures ERS2544739 SAMEA4724601 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:59Z External Id SAMEA4724601 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:59Z INSDC status public Submitter Id RNASeq_primaryNeurons9 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons9 scientific_name Mus musculus tissue type Primary neuronal cultures ERS2544740 SAMEA4724602 10090 Mus musculus Primary neuronal cultures were established from mouse embryos at embryonic day 11.5. Each embryo isolate was split into two wells of a 6-well dish coated with poly-D-lysine. Neuronal cells were subsequently cultured in neurobasal A medium (supplemented with B27, penicillin, streptomycin, gentamycin and L-glutamine) for 2 weeks. To prevent outgrowth of dividing cells, Cytosine β-D-arabinofuranoside (Ara-C) (Sigma Aldrich, MO) was added to 1 µM after 48 h. After 96 h the concentration was raised to 5 µM. For splicing inhibition, cells were treated with meayamycin at a concentration of 15 nM or DMSO as control. ENA-FIRST-PUBLIC 2019-07-24T04:04:17Z ENA-LAST-UPDATE 2018-06-12T12:45:59Z External Id SAMEA4724602 INSDC center name UNIVERSITY OF VIENNA INSDC first public 2019-07-24T04:04:17Z INSDC last update 2018-06-12T12:45:59Z INSDC status public Submitter Id RNASeq_primaryNeurons10 common name house mouse dev stage embryonic day 11.5 sample name RNASeq_primaryNeurons10 scientific_name Mus musculus tissue type Primary neuronal cultures