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 *

129 related articles for article (PubMed ID: 38564685)

  • 1. Solving Missing Heritability in Patients With Familial Adenomatous Polyposis With DNA-RNA Paired Testing.
    Young CC; Horton C; Grzybowski J; Abualkheir N; Ramirez Castano J; Molparia B; Karam R; Chao E; Richardson ME
    JCO Precis Oncol; 2024 Mar; 8():e2300404. PubMed ID: 38564685
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Germline mutations of the adenomatous polyposis coli (APC) gene in Algerian familial adenomatous polyposis cohort: first report.
    Khider F; Cherbal F; Boumehdi AL; Layaida K; Mahfouf H; Zebboudj F; Maaoui M
    Mol Biol Rep; 2022 May; 49(5):3823-3837. PubMed ID: 35142982
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial adenomatous polyposis.
    Half E; Bercovich D; Rozen P
    Orphanet J Rare Dis; 2009 Oct; 4():22. PubMed ID: 19822006
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.
    Nielsen M; Hes FJ; Nagengast FM; Weiss MM; Mathus-Vliegen EM; Morreau H; Breuning MH; Wijnen JT; Tops CM; Vasen HF
    Clin Genet; 2007 May; 71(5):427-33. PubMed ID: 17489848
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Targeted next-generation sequencing approach for molecular genetic diagnosis of hereditary colorectal cancer: Identification of a novel single nucleotide germline insertion in adenomatous polyposis coli gene causes familial adenomatous polyposis.
    Wang D; Liang S; Zhang X; Dey SK; Li Y; Xu C; Yu Y; Li M; Zhao G; Zhang Z
    Mol Genet Genomic Med; 2019 Jan; 7(1):e00505. PubMed ID: 30523670
    [TBL] [Abstract][Full Text] [Related]  

  • 6. APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.
    Filipe B; Baltazar C; Albuquerque C; Fragoso S; Lage P; Vitoriano I; Mão de Ferro S; Claro I; Rodrigues P; Fidalgo P; Chaves P; Cravo M; Nobre Leitão C
    Clin Genet; 2009 Sep; 76(3):242-55. PubMed ID: 19793053
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel pathogenic splice acceptor site germline mutation in intron 14 of the APC gene in a Chinese family with familial adenomatous polyposis.
    Wang D; Liang S; Zhang Z; Zhao G; Hu Y; Liang S; Zhang X; Banerjee S
    Oncotarget; 2017 Mar; 8(13):21327-21335. PubMed ID: 28423518
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Germline hypermethylation of the APC promoter is not a frequent cause of familial adenomatous polyposis in APC/MUTYH mutation negative families.
    Romero-Giménez J; Dopeso H; Blanco I; Guerra-Moreno A; Gonzalez S; Vogt S; Aretz S; Schwartz S; Capella G; Arango D
    Int J Cancer; 2008 Mar; 122(6):1422-5. PubMed ID: 18027849
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Colon cancer prevention by detection of APC gene mutation in a family with attenuated familial adenomatous polyposis.
    Poovorawan K; Suksawatamnuay S; Sahakitrungruang C; Treeprasertsuk S; Wisedopas N; Komolmit P; Poovorawan Y
    Asian Pac J Cancer Prev; 2012; 13(10):5101-4. PubMed ID: 23244118
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pseudoexons provide a mechanism for allele-specific expression of APC in familial adenomatous polyposis.
    Nieminen TT; Pavicic W; Porkka N; Kankainen M; Järvinen HJ; Lepistö A; Peltomäki P
    Oncotarget; 2016 Oct; 7(43):70685-70698. PubMed ID: 27683109
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Paired Somatic-Germline Testing of 15 Polyposis and Colorectal Cancer-Predisposing Genes Highlights the Role of APC Mosaicism in de Novo Familial Adenomatous Polyposis.
    Rofes P; González S; Navarro M; Moreno-Cabrera JM; Solanes A; Darder E; Carrasco E; Iglesias S; Salinas M; Gómez C; Velasco À; Tuset N; Varela M; Llort G; Ramon Y Cajal T; Grau È; Dueñas N; de la Ossa Merlano N; Matías-Guiu X; Rivera B; Balmaña J; Pineda M; Brunet J; Capellá G; Del Valle J; Lázaro C
    J Mol Diagn; 2021 Nov; 23(11):1452-1459. PubMed ID: 34454113
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The genetics of familial adenomatous polyposis (FAP) and MutYH-associated polyposis (MAP).
    Claes K; Dahan K; Tejpar S; De Paepe A; Bonduelle M; Abramowicz M; Verellen C; Franchimont D; Van Cutsem E; Kartheuser A
    Acta Gastroenterol Belg; 2011 Sep; 74(3):421-6. PubMed ID: 22103048
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel and reported APC germline mutations in Chinese patients with familial adenomatous polyposis.
    Zhang S; Qin H; Lv W; Luo S; Wang J; Fu C; Ma R; Shen Y; Chen S; Wu L
    Gene; 2016 Feb; 577(2):187-92. PubMed ID: 26625971
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Synonymous mutation adenomatous polyposis coliΔ486s affects exon splicing and may predispose patients to adenomatous polyposis coli/mutY DNA glycosylase mutation‑negative familial adenomatous polyposis.
    Liu WQ; Dong J; Peng YX; Li WL; Yang J
    Mol Med Rep; 2018 Dec; 18(6):4931-4939. PubMed ID: 30272267
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of a child with an APC pathogenic mutation, aberrant expression of splice variants and positive family history of FAP.
    Taki K; Sato Y; Sato Y; Ashihara Y; Chino A; Igarashi M; Sato K; Kitagawa T; Maetani I; Nemoto C; Nasuno K; Sekine T; Arai M
    Jpn J Clin Oncol; 2014 Jun; 44(6):602-6. PubMed ID: 24823678
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Novel germline APC mutations in Swedish patients with familial adenomatous polyposis and Gardner syndrome.
    Nilbert M; Fernebro J; Kristoffersson U
    Scand J Gastroenterol; 2000 Nov; 35(11):1200-3. PubMed ID: 11145293
    [TBL] [Abstract][Full Text] [Related]  

  • 17. APC haploinsufficiency, but not CTNNB1 or CDH1 gene mutations, accounts for a fraction of familial adenomatous polyposis patients without APC truncating mutations.
    Venesio T; Balsamo A; Rondo-Spaudo M; Varesco L; Risio M; Ranzani GN
    Lab Invest; 2003 Dec; 83(12):1859-66. PubMed ID: 14691304
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Appropriate Management of Attenuated Familial Adenomatous Polyposis: Report of a Case and Review of the Literature.
    Sokic-Milutinovic A
    Dig Dis; 2019; 37(5):400-405. PubMed ID: 30836352
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Intron 4 mutation in APC gene results in splice defect and attenuated FAP phenotype.
    Neklason DW; Solomon CH; Dalton AL; Kuwada SK; Burt RW
    Fam Cancer; 2004; 3(1):35-40. PubMed ID: 15131404
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A neoepitope derived from a novel human germline APC gene mutation in familial adenomatous polyposis shows selective immunogenicity.
    Majumder S; Shah R; Elias J; Mistry Y; Coral K; Shah P; Maurya AK; Mittal B; D'Silva JK; Murugan S; Mahadevan L; Sathian R; Ramprasad VL; Chakraborty P; Gupta R; Chaudhuri A; Khanna-Gupta A
    PLoS One; 2018; 13(9):e0203845. PubMed ID: 30256815
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.