BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

468 related articles for article (PubMed ID: 26437032)

  • 1. Intron retention is a widespread mechanism of tumor-suppressor inactivation.
    Jung H; Lee D; Lee J; Park D; Kim YJ; Park WY; Hong D; Park PJ; Lee E
    Nat Genet; 2015 Nov; 47(11):1242-8. PubMed ID: 26437032
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comprehensive characterization of somatic variants associated with intronic polyadenylation in human cancers.
    Zhao Z; Xu Q; Wei R; Huang L; Wang W; Wei G; Ni T
    Nucleic Acids Res; 2021 Oct; 49(18):10369-10381. PubMed ID: 34508351
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Alternative splicing and genetic diversity: silencers are more frequently modified by SNVs associated with alternative exon/intron borders.
    de Souza JE; Ramalho RF; Galante PA; Meyer D; de Souza SJ
    Nucleic Acids Res; 2011 Jul; 39(12):4942-8. PubMed ID: 21398627
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Intron retention in mRNA: No longer nonsense: Known and putative roles of intron retention in normal and disease biology.
    Wong JJ; Au AY; Ritchie W; Rasko JE
    Bioessays; 2016 Jan; 38(1):41-9. PubMed ID: 26612485
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.
    Aretz S; Uhlhaas S; Sun Y; Pagenstecher C; Mangold E; Caspari R; Möslein G; Schulmann K; Propping P; Friedl W
    Hum Mutat; 2004 Nov; 24(5):370-80. PubMed ID: 15459959
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The allele MICB 0050204, over-represented in the Caucasian population, has an additional exon resulting from a new splice junction sequence.
    Martínez-Borra J; Rodrigo L; Rodríguez-Rodero S; Fernandez-Morera JL; Diaz-Peña R; Pruneda L; López-Vázquez A; López-Larrea C
    Hum Immunol; 2007 Aug; 68(8):705-7. PubMed ID: 17678727
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autoregulation of the human splice factor kinase CLK1 through exon skipping and intron retention.
    Uzor S; Zorzou P; Bowler E; Porazinski S; Wilson I; Ladomery M
    Gene; 2018 Sep; 670():46-54. PubMed ID: 29802995
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Why Selection Might Be Stronger When Populations Are Small: Intron Size and Density Predict within and between-Species Usage of Exonic Splice Associated cis-Motifs.
    Wu X; Hurst LD
    Mol Biol Evol; 2015 Jul; 32(7):1847-61. PubMed ID: 25771198
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Dominant optic atrophy caused by a novel OPA1 splice site mutation (IVS20+1G-->A) associated with intron retention.
    Hayashi T; Gekka T; Omoto S; Takeuchi T; Kitahara K
    Ophthalmic Res; 2005; 37(4):214-24. PubMed ID: 16006781
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical expression and new SPINK5 splicing defects in Netherton syndrome: unmasking a frequent founder synonymous mutation and unconventional intronic mutations.
    Lacroix M; Lacaze-Buzy L; Furio L; Tron E; Valari M; Van der Wier G; Bodemer C; Bygum A; Bursztejn AC; Gaitanis G; Paradisi M; Stratigos A; Weibel L; Deraison C; Hovnanian A
    J Invest Dermatol; 2012 Mar; 132(3 Pt 1):575-82. PubMed ID: 22089833
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SNPlice: variants that modulate Intron retention from RNA-sequencing data.
    Mudvari P; Movassagh M; Kowsari K; Seyfi A; Kokkinaki M; Edwards NJ; Golestaneh N; Horvath A
    Bioinformatics; 2015 Apr; 31(8):1191-8. PubMed ID: 25481010
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Alternative splicing modulated by genetic variants demonstrates accelerated evolution regulated by highly conserved proteins.
    Hsiao YH; Bahn JH; Lin X; Chan TM; Wang R; Xiao X
    Genome Res; 2016 Apr; 26(4):440-50. PubMed ID: 26888265
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inconsistency and features of single nucleotide variants detected in whole exome sequencing versus transcriptome sequencing: A case study in lung cancer.
    O'Brien TD; Jia P; Xia J; Saxena U; Jin H; Vuong H; Kim P; Wang Q; Aryee MJ; Mino-Kenudson M; Engelman JA; Le LP; Iafrate AJ; Heist RS; Pao W; Zhao Z
    Methods; 2015 Jul; 83():118-27. PubMed ID: 25913717
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. A premature termination codon within an alternative exon affecting only the metabolism of transcripts that retain this exon.
    Maillet P; Dalla Venezia N; Lorenzo F; Morinière M; Bozon M; Noël B; Delaunay J; Baklouti F
    Hum Mutat; 1999; 14(2):145-55. PubMed ID: 10425037
    [TBL] [Abstract][Full Text] [Related]  

  • 17. RegSNPs-intron: a computational framework for predicting pathogenic impact of intronic single nucleotide variants.
    Lin H; Hargreaves KA; Li R; Reiter JL; Wang Y; Mort M; Cooper DN; Zhou Y; Zhang C; Eadon MT; Dolan ME; Ipe J; Skaar TC; Liu Y
    Genome Biol; 2019 Nov; 20(1):254. PubMed ID: 31779641
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alternative splicing and nonsense-mediated mRNA decay in the regulation of a new adenomatous polyposis coli transcript.
    De Rosa M; Morelli G; Cesaro E; Duraturo F; Turano M; Rossi GB; Delrio P; Izzo P
    Gene; 2007 Jun; 395(1-2):8-14. PubMed ID: 17360132
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants.
    Pagenstecher C; Wehner M; Friedl W; Rahner N; Aretz S; Friedrichs N; Sengteller M; Henn W; Buettner R; Propping P; Mangold E
    Hum Genet; 2006 Mar; 119(1-2):9-22. PubMed ID: 16341550
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants.
    Wu H; Lin JH; Tang XY; Marenne G; Zou WB; Schutz S; Masson E; Génin E; Fichou Y; Le Gac G; Férec C; Liao Z; Chen JM
    Hum Genomics; 2024 Feb; 18(1):21. PubMed ID: 38414044
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.