138 related articles for article (PubMed ID: 37021934)
21. Finding exonic islands in a sea of non-coding sequence: splicing related constraints on protein composition and evolution are common in intron-rich genomes.
Warnecke T; Parmley JL; Hurst LD
Genome Biol; 2008; 9(2):R29. PubMed ID: 18257921
[TBL] [Abstract][Full Text] [Related]
22. A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes.
Liu HX; Cartegni L; Zhang MQ; Krainer AR
Nat Genet; 2001 Jan; 27(1):55-8. PubMed ID: 11137998
[TBL] [Abstract][Full Text] [Related]
23. In vitro splicing analysis showed that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G-->A mutations in introns of the dystrophin gene.
Habara Y; Takeshima Y; Awano H; Okizuka Y; Zhang Z; Saiki K; Yagi M; Matsuo M
J Med Genet; 2009 Aug; 46(8):542-7. PubMed ID: 19001018
[TBL] [Abstract][Full Text] [Related]
24. The intronic GABRG2 mutation, IVS6+2T->G, associated with childhood absence epilepsy altered subunit mRNA intron splicing, activated nonsense-mediated decay, and produced a stable truncated γ2 subunit.
Tian M; Macdonald RL
J Neurosci; 2012 Apr; 32(17):5937-52. PubMed ID: 22539854
[TBL] [Abstract][Full Text] [Related]
25. An intron splicing enhancer containing a G-rich repeat facilitates inclusion of a vertebrate micro-exon.
Carlo T; Sterner DA; Berget SM
RNA; 1996 Apr; 2(4):342-53. PubMed ID: 8634915
[TBL] [Abstract][Full Text] [Related]
26. BAP1 missense mutation c.2054 A>T (p.E685V) completely disrupts normal splicing through creation of a novel 5' splice site in a human mesothelioma cell line.
Morrison A; Chekaluk Y; Bacares R; Ladanyi M; Zhang L
PLoS One; 2015; 10(4):e0119224. PubMed ID: 25830670
[TBL] [Abstract][Full Text] [Related]
27. Rules and tools to predict the splicing effects of exonic and intronic mutations.
Ohno K; Takeda JI; Masuda A
Wiley Interdiscip Rev RNA; 2018 Jan; 9(1):. PubMed ID: 28949076
[TBL] [Abstract][Full Text] [Related]
28. Identification of intron and exon sequences involved in alternative splicing of insulin receptor pre-mRNA.
Kosaki A; Nelson J; Webster NJ
J Biol Chem; 1998 Apr; 273(17):10331-7. PubMed ID: 9553088
[TBL] [Abstract][Full Text] [Related]
29. Sequence of the polypyrimidine tract of the 3'-terminal 3' splicing signal can affect intron-dependent pre-mRNA processing in vivo.
Liu X; Mertz JE
Nucleic Acids Res; 1996 May; 24(9):1765-73. PubMed ID: 8649998
[TBL] [Abstract][Full Text] [Related]
30. Splicing in action: assessing disease causing sequence changes.
Baralle D; Baralle M
J Med Genet; 2005 Oct; 42(10):737-48. PubMed ID: 16199547
[TBL] [Abstract][Full Text] [Related]
31. Multiple splicing defects in an intronic false exon.
Sun H; Chasin LA
Mol Cell Biol; 2000 Sep; 20(17):6414-25. PubMed ID: 10938119
[TBL] [Abstract][Full Text] [Related]
32. Identification and characterization of aberrant GAA pre-mRNA splicing in pompe disease using a generic approach.
Bergsma AJ; Kroos M; Hoogeveen-Westerveld M; Halley D; van der Ploeg AT; Pijnappel WW
Hum Mutat; 2015 Jan; 36(1):57-68. PubMed ID: 25243733
[TBL] [Abstract][Full Text] [Related]
33. Splicing of 5' introns dictates alternative splice selection of acetylcholinesterase pre-mRNA and specific expression during myogenesis.
Luo ZD; Camp S; Mutero A; Taylor P
J Biol Chem; 1998 Oct; 273(43):28486-95. PubMed ID: 9774478
[TBL] [Abstract][Full Text] [Related]
34. Self-splicing of a group II intron in yeast mitochondria: dependence on 5' exon sequences.
van der Veen R; Arnberg AC; Grivell LA
EMBO J; 1987 Apr; 6(4):1079-84. PubMed ID: 3297671
[TBL] [Abstract][Full Text] [Related]
35. Splicing analysis disclosed a determinant single nucleotide for exon skipping caused by a novel intraexonic four-nucleotide deletion in the dystrophin gene.
Tran VK; Takeshima Y; Zhang Z; Yagi M; Nishiyama A; Habara Y; Matsuo M
J Med Genet; 2006 Dec; 43(12):924-30. PubMed ID: 16738009
[TBL] [Abstract][Full Text] [Related]
36. Nonsense but not missense mutations can decrease the abundance of nuclear mRNA for the mouse major urinary protein, while both types of mutations can facilitate exon skipping.
Belgrader P; Maquat LE
Mol Cell Biol; 1994 Sep; 14(9):6326-36. PubMed ID: 8065364
[TBL] [Abstract][Full Text] [Related]
37. Identical G+1 to A mutations in three different introns of the type III procollagen gene (COL3A1) produce different patterns of RNA splicing in three variants of Ehlers-Danlos syndrome. IV. An explanation for exon skipping some mutations and not others.
Kuivaniemi H; Kontusaari S; Tromp G; Zhao MJ; Sabol C; Prockop DJ
J Biol Chem; 1990 Jul; 265(20):12067-74. PubMed ID: 2365710
[TBL] [Abstract][Full Text] [Related]
38. Trans splicing in Oenothera mitochondria: nad1 mRNAs are edited in exon and trans-splicing group II intron sequences.
Wissinger B; Schuster W; Brennicke A
Cell; 1991 May; 65(3):473-82. PubMed ID: 1850322
[TBL] [Abstract][Full Text] [Related]
39. Understanding human DNA variants affecting pre-mRNA splicing in the NGS era.
Dufner-Almeida LG; do Carmo RT; Masotti C; Haddad LA
Adv Genet; 2019; 103():39-90. PubMed ID: 30904096
[TBL] [Abstract][Full Text] [Related]
40. The self-splicing intron in the Neurospora apocytochrome b gene contains a long reading frame in frame with the upstream exon.
Collins RA; Reynolds CA; Olive J
Nucleic Acids Res; 1988 Feb; 16(3):1125-34. PubMed ID: 2963999
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
