FISH
WT + MO1-prpf4
Human Disease modelled by WT + MO1-prpf4
| Disease | Conditions | Citation |
|---|---|---|
| retinitis pigmentosa | standard conditions | Linder et al., 2011 |
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RNA Expression
| Expressed Gene | Structure | Conditions | Figures |
|---|---|---|---|
| myf5 | standard conditions | Fig. 5 from Linder et al., 2011 | |
| myod1 | standard conditions | Fig. 5 from Linder et al., 2011 | |
| pax2a | standard conditions | Fig. 5 from Linder et al., 2011 | |
| pcna | standard conditions | Fig. 5 from Linder et al., 2011 | |
| rho | standard conditions | Fig. 5 from Linder et al., 2011 |
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Protein Expression
Reporter Gene Expression
- Linder, B., Hirmer, A., Gal, A., Rüther, K., Bolz, H.J., Winkler, C., Laggerbauer, B., Fischer, U. (2014) Identification of a PRPF4 Loss-of-Function Variant That Abrogates U4/U6.U5 Tri-snRNP Integration and Is Associated with Retinitis Pigmentosa. PLoS One. 9:e111754
- Linder, B., Dill, H., Hirmer, A., Brocher, J., Lee, G.P., Mathavan, S., Bolz, H.J., Winkler, C., Laggerbauer, B., and Fischer, U. (2011) Systemic splicing factor deficiency causes tissue-specific defects: A zebrafish model for Retinitis pigmentosa. Human molecular genetics. 20(2):368-377
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