BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

315 related articles for article (PubMed ID: 27683109)

  • 1. 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]  

  • 2. Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis.
    Spier I; Horpaopan S; Vogt S; Uhlhaas S; Morak M; Stienen D; Draaken M; Ludwig M; Holinski-Feder E; Nöthen MM; Hoffmann P; Aretz S
    Hum Mutat; 2012 Jul; 33(7):1045-50. PubMed ID: 22431159
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis.
    Pavicic W; Nieminen TT; Gylling A; Pursiheimo JP; Laiho A; Gyenesei A; Järvinen HJ; Peltomäki P
    Genes Chromosomes Cancer; 2014 Oct; 53(10):857-64. PubMed ID: 24946964
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary.
    Papp J; Kovacs ME; Matrai Z; Orosz E; Kásler M; Børresen-Dale AL; Olah E
    Fam Cancer; 2016 Jan; 15(1):85-97. PubMed ID: 26446593
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Presence of c.3956delC mutation in familial adenomatous polyposis patients from Brazil.
    Moreira-Nunes CA; Alcântara Dd; Lima-Júnior SF; Cavalléro SR; Rey JA; Pinto GR; de Assumpção PP; Burbano RR
    World J Gastroenterol; 2015 Aug; 21(31):9413-9. PubMed ID: 26309368
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Allele-specific expression of APC in adenomatous polyposis families.
    Castellsagué E; González S; Guinó E; Stevens KN; Borràs E; Raymond VM; Lázaro C; Blanco I; Gruber SB; Capellá G
    Gastroenterology; 2010 Aug; 139(2):439-47, 447.e1. PubMed ID: 20434453
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel pathogenic germline mutation in the adenomatous polyposis coli gene in a Chinese family with familial adenomatous coli.
    Jiang SS; Li JJ; Li Y; He LJ; Wang QJ; Weng DS; Pan K; Liu Q; Zhao JJ; Pan QZ; Zhang XF; Tang Y; Chen CL; Zhang HX; Xu GL; Zeng YX; Xia JC
    Oncotarget; 2015 Sep; 6(29):27267-74. PubMed ID: 26311738
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Correlation between mutations and mRNA expression of APC and MUTYH genes: new insight into hereditary colorectal polyposis predisposition.
    Aceto GM; Fantini F; De Iure S; Di Nicola M; Palka G; Valanzano R; Di Gregorio P; Stigliano V; Genuardi M; Battista P; Cama A; Curia MC
    J Exp Clin Cancer Res; 2015 Oct; 34():131. PubMed ID: 26511139
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP).
    Ghadamyari F; Heidari MM; Zeinali S; Khatami M; Merat S; Bagherian H; Rejali L; Ghasemi F
    J Clin Lab Anal; 2021 May; 35(5):e23768. PubMed ID: 33769591
    [TBL] [Abstract][Full Text] [Related]  

  • 12. APC promoter 1B deletion in familial polyposis--implications for mutation-negative families.
    Kadiyska TK; Todorov TP; Bichev SN; Vazharova RV; Nossikoff AV; Savov AS; Mitev VI
    Clin Genet; 2014 May; 85(5):452-7. PubMed ID: 23725351
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Reduced expression of APC-1B but not APC-1A by the deletion of promoter 1B is responsible for familial adenomatous polyposis.
    Yamaguchi K; Nagayama S; Shimizu E; Komura M; Yamaguchi R; Shibuya T; Arai M; Hatakeyama S; Ikenoue T; Ueno M; Miyano S; Imoto S; Furukawa Y
    Sci Rep; 2016 May; 6():26011. PubMed ID: 27217144
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Adenomatous polyposis families that screen APC mutation-negative by conventional methods are genetically heterogeneous.
    Renkonen ET; Nieminen P; Abdel-Rahman WM; Moisio AL; Järvelä I; Arte S; Järvinen HJ; Peltomäki P
    J Clin Oncol; 2005 Aug; 23(24):5651-9. PubMed ID: 16110024
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant.
    Li J; Woods SL; Healey S; Beesley J; Chen X; Lee JS; Sivakumaran H; Wayte N; Nones K; Waterfall JJ; Pearson J; Patch AM; Senz J; Ferreira MA; Kaurah P; Mackenzie R; Heravi-Moussavi A; Hansford S; Lannagan TRM; Spurdle AB; Simpson PT; da Silva L; Lakhani SR; Clouston AD; Bettington M; Grimpen F; Busuttil RA; Di Costanzo N; Boussioutas A; Jeanjean M; Chong G; Fabre A; Olschwang S; Faulkner GJ; Bellos E; Coin L; Rioux K; Bathe OF; Wen X; Martin HC; Neklason DW; Davis SR; Walker RL; Calzone KA; Avital I; Heller T; Koh C; Pineda M; Rudloff U; Quezado M; Pichurin PN; Hulick PJ; Weissman SM; Newlin A; Rubinstein WS; Sampson JE; Hamman K; Goldgar D; Poplawski N; Phillips K; Schofield L; Armstrong J; Kiraly-Borri C; Suthers GK; Huntsman DG; Foulkes WD; Carneiro F; Lindor NM; Edwards SL; French JD; Waddell N; Meltzer PS; Worthley DL; Schrader KA; Chenevix-Trench G
    Am J Hum Genet; 2016 May; 98(5):830-842. PubMed ID: 27087319
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.