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 *

439 related articles for article (PubMed ID: 35477782)

  • 21. Silent (synonymous) SNPs: should we care about them?
    Hunt R; Sauna ZE; Ambudkar SV; Gottesman MM; Kimchi-Sarfaty C
    Methods Mol Biol; 2009; 578():23-39. PubMed ID: 19768585
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Somatic mutations in single human cardiomyocytes reveal age-associated DNA damage and widespread oxidative genotoxicity.
    Choudhury S; Huang AY; Kim J; Zhou Z; Morillo K; Maury EA; Tsai JW; Miller MB; Lodato MA; Araten S; Hilal N; Lee EA; Chen MH; Walsh CA
    Nat Aging; 2022 Aug; 2(8):714-725. PubMed ID: 36051457
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genomic characterization of sarcomatoid transformation in clear cell renal cell carcinoma.
    Bi M; Zhao S; Said JW; Merino MJ; Adeniran AJ; Xie Z; Nawaf CB; Choi J; Belldegrun AS; Pantuck AJ; Kluger HM; Bilgüvar K; Lifton RP; Shuch B
    Proc Natl Acad Sci U S A; 2016 Feb; 113(8):2170-5. PubMed ID: 26864202
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Vex-seq: high-throughput identification of the impact of genetic variation on pre-mRNA splicing efficiency.
    Adamson SI; Zhan L; Graveley BR
    Genome Biol; 2018 Jun; 19(1):71. PubMed ID: 29859120
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Exon identity crisis: disease-causing mutations that disrupt the splicing code.
    Sterne-Weiler T; Sanford JR
    Genome Biol; 2014 Jan; 15(1):201. PubMed ID: 24456648
    [TBL] [Abstract][Full Text] [Related]  

  • 26. MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing.
    Mort M; Sterne-Weiler T; Li B; Ball EV; Cooper DN; Radivojac P; Sanford JR; Mooney SD
    Genome Biol; 2014 Jan; 15(1):R19. PubMed ID: 24451234
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Exposing synonymous mutations.
    Hunt RC; Simhadri VL; Iandoli M; Sauna ZE; Kimchi-Sarfaty C
    Trends Genet; 2014 Jul; 30(7):308-21. PubMed ID: 24954581
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Bicodon bias can determine the role of synonymous SNPs in human diseases.
    McCarthy C; Carrea A; Diambra L
    BMC Genomics; 2017 Mar; 18(1):227. PubMed ID: 28288557
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The Silent Sway of Splicing by Synonymous Substitutions.
    Mueller WF; Larsen LS; Garibaldi A; Hatfield GW; Hertel KJ
    J Biol Chem; 2015 Nov; 290(46):27700-11. PubMed ID: 26424794
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Germline Variants That Affect Tumor Progression.
    Chatrath A; Ratan A; Dutta A
    Trends Genet; 2021 May; 37(5):433-443. PubMed ID: 33203571
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex.
    Kim SN; Viswanadham VV; Doan RN; Dou Y; Bizzotto S; Khoshkhoo S; Huang AY; Yeh R; Chhouk B; Truong A; Chappell KM; Beaudin M; Barton A; Akula SK; Rento L; Lodato M; Ganz J; Szeto RA; Li P; Tsai JW; Hill RS; Park PJ; Walsh CA
    bioRxiv; 2023 Nov; ():. PubMed ID: 37986891
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Implication of GATA4 synonymous variants in congenital heart disease: A comprehensive in-silico approach.
    Dixit R; Kumar A; Mohapatra B
    Mutat Res; 2019 Jan; 813():31-38. PubMed ID: 30590232
    [TBL] [Abstract][Full Text] [Related]  

  • 34. In silico and in vivo splicing analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects.
    Lastella P; Surdo NC; Resta N; Guanti G; Stella A
    BMC Genomics; 2006 Sep; 7():243. PubMed ID: 16995940
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Defective pre-mRNA splicing in PKD1 due to presumed missense and synonymous mutations causing autosomal dominant polycystic disease.
    Gonzalez-Paredes FJ; Ramos-Trujillo E; Claverie-Martin F
    Gene; 2014 Aug; 546(2):243-9. PubMed ID: 24907393
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The pan-cancer landscape of prognostic germline variants in 10,582 patients.
    Chatrath A; Przanowska R; Kiran S; Su Z; Saha S; Wilson B; Tsunematsu T; Ahn JH; Lee KY; Paulsen T; Sobierajska E; Kiran M; Tang X; Li T; Kumar P; Ratan A; Dutta A
    Genome Med; 2020 Feb; 12(1):15. PubMed ID: 32066500
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor.
    Duan J; Wainwright MS; Comeron JM; Saitou N; Sanders AR; Gelernter J; Gejman PV
    Hum Mol Genet; 2003 Feb; 12(3):205-16. PubMed ID: 12554675
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Timing during translation matters: synonymous mutations in human pathologies influence protein folding and function.
    Rauscher R; Ignatova Z
    Biochem Soc Trans; 2018 Aug; 46(4):937-944. PubMed ID: 30065107
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Prevalence and architecture of posttranscriptionally impaired synonymous mutations in 8,320 genomes across 22 cancer types.
    Teng H; Wei W; Li Q; Xue M; Shi X; Li X; Mao F; Sun Z
    Nucleic Acids Res; 2020 Feb; 48(3):1192-1205. PubMed ID: 31950163
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Somatic Mutations Detected in Parkinson Disease Could Affect Genes With a Role in Synaptic and Neuronal Processes.
    Lobon I; Solís-Moruno M; Juan D; Muhaisen A; Abascal F; Esteller-Cucala P; García-Pérez R; Martí MJ; Tolosa E; Ávila J; Rahbari R; Marques-Bonet T; Casals F; Soriano E
    Front Aging; 2022; 3():851039. PubMed ID: 35821807
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 22.