723 related articles for article (PubMed ID: 29684050)
21. Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNA.
Tanner G; Glaus E; Barthelmes D; Ader M; Fleischhauer J; Pagani F; Berger W; Neidhardt J
Hum Mutat; 2009 Feb; 30(2):255-63. PubMed ID: 18837008
[TBL] [Abstract][Full Text] [Related]
22. Overexpression of adapted U1snRNA in patients' cells to correct a 5' splice site mutation in propionic acidemia.
Sánchez-Alcudia R; Pérez B; Pérez-Cerdá C; Ugarte M; Desviat LR
Mol Genet Metab; 2011 Feb; 102(2):134-8. PubMed ID: 21094621
[TBL] [Abstract][Full Text] [Related]
23. The phenylalanine hydroxylase c.30C>G synonymous variation (p.G10G) creates a common exonic splicing silencer.
Dobrowolski SF; Andersen HS; Doktor TK; Andresen BS
Mol Genet Metab; 2010 Aug; 100(4):316-23. PubMed ID: 20457534
[TBL] [Abstract][Full Text] [Related]
24. Characterization of the mouse phenylalanine hydroxylase mutation Pah(enu3).
Haefele MJ; White G; McDonald JD
Mol Genet Metab; 2001 Jan; 72(1):27-30. PubMed ID: 11161825
[TBL] [Abstract][Full Text] [Related]
25. The U1 snRNP protein U1C recognizes the 5' splice site in the absence of base pairing.
Du H; Rosbash M
Nature; 2002 Sep; 419(6902):86-90. PubMed ID: 12214237
[TBL] [Abstract][Full Text] [Related]
26. Principles and correction of 5'-splice site selection.
Malard F; Mackereth CD; Campagne S
RNA Biol; 2022 Jan; 19(1):943-960. PubMed ID: 35866748
[TBL] [Abstract][Full Text] [Related]
27. Identification of novel deep intronic PAH gene variants in patients diagnosed with phenylketonuria.
Jin X; Yan Y; Zhang C; Tai Y; An L; Yu X; Zhang L; Hao S; Cao X; Yin C; Ma X
Hum Mutat; 2022 Jan; 43(1):56-66. PubMed ID: 34747549
[TBL] [Abstract][Full Text] [Related]
28. Modified U1 snRNA and antisense oligonucleotides rescue splice mutations in SLC26A4 that cause hereditary hearing loss.
Lee B; Kim YR; Kim SJ; Goh SH; Kim JH; Oh SK; Baek JI; Kim UK; Lee KY
Hum Mutat; 2019 Aug; 40(8):1172-1180. PubMed ID: 31033086
[TBL] [Abstract][Full Text] [Related]
29. Exon-independent recruitment of SRSF1 is mediated by U1 snRNP stem-loop 3.
Jobbins AM; Campagne S; Weinmeister R; Lucas CM; Gosliga AR; Clery A; Chen L; Eperon LP; Hodson MJ; Hudson AJ; Allain FHT; Eperon IC
EMBO J; 2022 Jan; 41(1):e107640. PubMed ID: 34779515
[TBL] [Abstract][Full Text] [Related]
30. Cryptic splice activation but not exon skipping is observed in minigene assays of dystrophin c.9361+1G>A mutation identified by NGS.
Niba ETE; Nishida A; Tran VK; Vu DC; Matsumoto M; Awano H; Lee T; Takeshima Y; Nishio H; Matsuo M
J Hum Genet; 2017 Apr; 62(5):531-537. PubMed ID: 28100912
[TBL] [Abstract][Full Text] [Related]
31. The U1 small nuclear ribonucleoprotein/5' splice site interaction affects U2AF65 binding to the downstream 3' splice site.
Côté J; Beaudoin J; Tacke R; Chabot B
J Biol Chem; 1995 Feb; 270(8):4031-6. PubMed ID: 7876151
[TBL] [Abstract][Full Text] [Related]
32. An intron element modulating 5' splice site selection in the hnRNP A1 pre-mRNA interacts with hnRNP A1.
Chabot B; Blanchette M; Lapierre I; La Branche H
Mol Cell Biol; 1997 Apr; 17(4):1776-86. PubMed ID: 9121425
[TBL] [Abstract][Full Text] [Related]
33. Exon-Specific U1s Correct SPINK5 Exon 11 Skipping Caused by a Synonymous Substitution that Affects a Bifunctional Splicing Regulatory Element.
Dal Mas A; Fortugno P; Donadon I; Levati L; Castiglia D; Pagani F
Hum Mutat; 2015 May; 36(5):504-12. PubMed ID: 25665175
[TBL] [Abstract][Full Text] [Related]
34. A gene therapeutic approach to correct splice defects with modified U1 and U6 snRNPs.
Schmid F; Hiller T; Korner G; Glaus E; Berger W; Neidhardt J
Hum Gene Ther; 2013 Jan; 24(1):97-104. PubMed ID: 23075156
[TBL] [Abstract][Full Text] [Related]
35. HMGA1a trapping of U1 snRNP at an authentic 5' splice site induces aberrant exon skipping in sporadic Alzheimer's disease.
Ohe K; Mayeda A
Mol Cell Biol; 2010 May; 30(9):2220-8. PubMed ID: 20194618
[TBL] [Abstract][Full Text] [Related]
36. The role of overlapping U1 and U11 5' splice site sequences in a negative regulator of splicing.
Hibbert CS; Gontarek RR; Beemon KL
RNA; 1999 Mar; 5(3):333-43. PubMed ID: 10094303
[TBL] [Abstract][Full Text] [Related]
37. Base pairing at the 5' splice site with U1 small nuclear RNA promotes splicing of the upstream intron but may be dispensable for slicing of the downstream intron.
Hwang DY; Cohen JB
Mol Cell Biol; 1996 Jun; 16(6):3012-22. PubMed ID: 8649413
[TBL] [Abstract][Full Text] [Related]
38. Mouse nuclear RNAi-defective 2 promotes splicing of weak 5' splice sites.
Flemr M; Schwaiger M; Hess D; Iesmantavicius V; Ahel J; Tuck AC; Mohn F; Bühler M
RNA; 2023 Aug; 29(8):1140-1165. PubMed ID: 37137667
[TBL] [Abstract][Full Text] [Related]
39. A novel intra-U1 snRNP cross-regulation mechanism: alternative splicing switch links U1C and U1-70K expression.
Rösel-Hillgärtner TD; Hung LH; Khrameeva E; Le Querrec P; Gelfand MS; Bindereif A
PLoS Genet; 2013; 9(10):e1003856. PubMed ID: 24146627
[TBL] [Abstract][Full Text] [Related]
40. Profiling of cis- and trans-acting factors supporting noncanonical splice site activation.
Erkelenz S; Poschmann G; Ptok J; Müller L; Schaal H
RNA Biol; 2021 Jan; 18(1):118-130. PubMed ID: 32693676
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]