These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

440 related articles for article (PubMed ID: 35477782)

  • 1. Synonymous Variants: Necessary Nuance in Our Understanding of Cancer Drivers and Treatment Outcomes.
    Kaissarian NM; Meyer D; Kimchi-Sarfaty C
    J Natl Cancer Inst; 2022 Aug; 114(8):1072-1094. PubMed ID: 35477782
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inferring Potential Cancer Driving Synonymous Variants.
    Zeng Z; Bromberg Y
    Genes (Basel); 2022 Apr; 13(5):. PubMed ID: 35627162
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synonymous variants in holoprosencephaly alter codon usage and impact the Sonic Hedgehog protein.
    Kim A; Le Douce J; Diab F; Ferovova M; Dubourg C; Odent S; Dupé V; David V; Diambra L; Watrin E; de Tayrac M
    Brain; 2020 Jul; 143(7):2027-2038. PubMed ID: 32542401
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Synonymous ADAMTS13 variants impact molecular characteristics and contribute to variability in active protein abundance.
    Jankowska KI; Meyer D; Holcomb DD; Kames J; Hamasaki-Katagiri N; Katneni UK; Hunt RC; Ibla JC; Kimchi-Sarfaty C
    Blood Adv; 2022 Sep; 6(18):5364-5378. PubMed ID: 35667091
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Computational identification of deleterious synonymous variants in human genomes using a feature-based approach.
    Shi F; Yao Y; Bin Y; Zheng CH; Xia J
    BMC Med Genomics; 2019 Jan; 12(Suppl 1):12. PubMed ID: 30704475
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An Ensemble Approach to Predict the Pathogenicity of Synonymous Variants.
    Ranganathan Ganakammal S; Alexov E
    Genes (Basel); 2020 Sep; 11(9):. PubMed ID: 32967157
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Synonymous Somatic Variants in Human Cancer Are Not Infamous: A Plea for Full Disclosure in Databases and Publications.
    Soussi T; Taschner PE; Samuels Y
    Hum Mutat; 2017 Apr; 38(4):339-342. PubMed ID: 28026089
    [TBL] [Abstract][Full Text] [Related]  

  • 8. regSNPs-splicing: a tool for prioritizing synonymous single-nucleotide substitution.
    Zhang X; Li M; Lin H; Rao X; Feng W; Yang Y; Mort M; Cooper DN; Wang Y; Wang Y; Wells C; Zhou Y; Liu Y
    Hum Genet; 2017 Sep; 136(9):1279-1289. PubMed ID: 28391525
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Broken silence: 22,841 predicted deleterious synonymous variants identified in the human exome through computational analysis.
    Mello AC; Leao D; Dias L; Colombelli F; Recamonde-Mendoza M; Turchetto-Zolet AC; Matte U
    Genet Mol Biol; 2024; 46(3 Suppl 1):e20230125. PubMed ID: 38259032
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synonymous variants that disrupt messenger RNA structure are significantly constrained in the human population.
    Gaither JBS; Lammi GE; Li JL; Gordon DM; Kuck HC; Kelly BJ; Fitch JR; White P
    Gigascience; 2021 Apr; 10(4):. PubMed ID: 33822938
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Decoding the effects of synonymous variants.
    Zeng Z; Aptekmann AA; Bromberg Y
    Nucleic Acids Res; 2021 Dec; 49(22):12673-12691. PubMed ID: 34850938
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detecting somatic point mutations in cancer genome sequencing data: a comparison of mutation callers.
    Wang Q; Jia P; Li F; Chen H; Ji H; Hucks D; Dahlman KB; Pao W; Zhao Z
    Genome Med; 2013; 5(10):91. PubMed ID: 24112718
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Assessment of somatic single-nucleotide variation in brain tissue of cases with schizophrenia.
    Fullard JF; Charney AW; Voloudakis G; Uzilov AV; Haroutunian V; Roussos P
    Transl Psychiatry; 2019 Jan; 9(1):21. PubMed ID: 30655504
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Codon bias and the folding dynamics of the cystic fibrosis transmembrane conductance regulator.
    Bartoszewski R; Króliczewski J; Piotrowski A; Jasiecka AJ; Bartoszewska S; Vecchio-Pagan B; Fu L; Sobolewska A; Matalon S; Cutting GR; Rowe SM; Collawn JF
    Cell Mol Biol Lett; 2016; 21():23. PubMed ID: 28536625
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The functional relevance of somatic synonymous mutations in melanoma and other cancers.
    Gotea V; Gartner JJ; Qutob N; Elnitski L; Samuels Y
    Pigment Cell Melanoma Res; 2015 Nov; 28(6):673-84. PubMed ID: 26300548
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Decoding mechanisms by which silent codon changes influence protein biogenesis and function.
    Bali V; Bebok Z
    Int J Biochem Cell Biol; 2015 Jul; 64():58-74. PubMed ID: 25817479
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A pan-cancer analysis of synonymous mutations.
    Sharma Y; Miladi M; Dukare S; Boulay K; Caudron-Herger M; Groß M; Backofen R; Diederichs S
    Nat Commun; 2019 Jun; 10(1):2569. PubMed ID: 31189880
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Code inside the codon: The role of synonymous mutations in regulating splicing machinery and its impact on disease.
    Sarkar A; Panati K; Narala VR
    Mutat Res Rev Mutat Res; 2022; 790():108444. PubMed ID: 36307006
    [TBL] [Abstract][Full Text] [Related]  

  • 19. In silico methods for predicting functional synonymous variants.
    Lin BC; Katneni U; Jankowska KI; Meyer D; Kimchi-Sarfaty C
    Genome Biol; 2023 May; 24(1):126. PubMed ID: 37217943
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cancer-Associated Perturbations in Alternative Pre-messenger RNA Splicing.
    Shkreta L; Bell B; Revil T; Venables JP; Prinos P; Elela SA; Chabot B
    Cancer Treat Res; 2013; 158():41-94. PubMed ID: 24222354
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.