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pDESTsplice Citations (7)

Originally described in: Rapid generation of splicing reporters with pSpliceExpress.
Kishore S, Khanna A, Stamm S Gene. 2008 Dec 31;427(1-2):104-10. Epub 2008 Oct 1.
PubMed Journal

Articles Citing pDESTsplice

Articles
N6-methyladenosine demethylase FTO targets pre-mRNAs and regulates alternative splicing and 3'-end processing. Bartosovic M, Molares HC, Gregorova P, Hrossova D, Kudla G, Vanacova S. Nucleic Acids Res. 2017 Nov 2;45(19):11356-11370. doi: 10.1093/nar/gkx778. PubMed
Synonymous variants associated with Alzheimer disease in multiplex families. Tang M, Alaniz ME, Felsky D, Vardarajan B, Reyes-Dumeyer D, Lantigua R, Medrano M, Bennett DA, de Jager PL, Mayeux R, Santa-Maria I, Reitz C. Neurol Genet. 2020 Jun 8;6(4):e450. doi: 10.1212/NXG.0000000000000450. eCollection 2020 Aug. PubMed
Principles and Practical Considerations for the Analysis of Disease-Associated Alternative Splicing Events Using the Gateway Cloning-Based Minigene Vectors pDESTsplice and pSpliceExpress. Putscher E, Hecker M, Fitzner B, Lorenz P, Zettl UK. Int J Mol Sci. 2021 May 13;22(10). pii: ijms22105154. doi: 10.3390/ijms22105154. PubMed
Abnormal Pre-mRNA Splicing in Exonic Fabry Disease-Causing GLA Mutations. Alfen F, Putscher E, Hecker M, Zettl UK, Hermann A, Lukas J. Int J Mol Sci. 2022 Dec 3;23(23):15261. doi: 10.3390/ijms232315261. PubMed
DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia. Dicke AK, Pilatz A, Wyrwoll MJ, Punab M, Ruckert C, Nagirnaja L, Aston KI, Conrad DF, Di Persio S, Neuhaus N, Fietz D, Laan M, Stallmeyer B, Tuttelmann F. Commun Biol. 2023 Mar 31;6(1):350. doi: 10.1038/s42003-023-04714-4. PubMed
Long-read sequencing and profiling of RNA-binding proteins reveals the pathogenic mechanism of aberrant splicing of an SCN1A poison exon in epilepsy. Happ HC, Schneider PN, Hong JH, Goes E, Bandouil M, Biar CG, Ramamurthy A, Reese F, Engel K, Weckhuysen S, Scheffer IE, Mefford HC, Calhoun JD, Carvill GL. bioRxiv. 2023 May 4:2023.05.04.538282. doi: 10.1101/2023.05.04.538282. Preprint. PubMed
Combined Bioinformatic and Splicing Analysis of Likely Benign Intronic and Synonymous Variants Reveals Evidence for Pathogenicity. Hirschi OR, Felker SA, Rednam SP, Vallance KL, Parsons DW, Roy A, Cooper GM, Plon SE. medRxiv [Preprint]. 2023 Nov 1:2023.10.30.23297632. doi: 10.1101/2023.10.30.23297632. PubMed

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