BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

Terms: = Brain cancer AND MUTYH, MYH, 4595, ENSG00000132781, hMYH, MGC4416, MYHbeta
28 results:

  • 1. First report of medulloblastoma in a patient with mutyh-associated polyposis.
    Villy MC; Warcoin M; Filser M; Buecher B; Golmard L; Suybeng V; Schwartz M; Bieche I; Vacher S; Laurence V; Bourdeaut F; Bernier M; Gutman T; Stoppa-Lyonnet D; Masliah-Planchon J; Colas C
    Neuropathol Appl Neurobiol; 2023 Aug; 49(4):e12929. PubMed ID: 37524406
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. Germline mutyh mutations and high-grade gliomas: Novel evidence for a potential association.
    Bedics G; Kotmayer L; Zajta E; Hegyi LL; Brückner EÁ; Rajnai H; Reiniger L; Bödör C; Garami M; Scheich B
    Genes Chromosomes Cancer; 2022 Oct; 61(10):622-628. PubMed ID: 35545820
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. Mismatch repair deficiency and mutyh variants in small intestine-neuroendocrine tumors.
    Helderman NC; Elsayed FA; van Wezel T; Terlouw D; Langers AMJ; van Egmond D; Kilinç G; Hristova H; Farina Sarasqueta A; Morreau H; Nielsen M; Suerink M;
    Hum Pathol; 2022 Jul; 125():11-17. PubMed ID: 35417733
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. Application of Multigene Panel Testing in Patients With High Risk for Hereditary Colorectal cancer: A Descriptive Report Focused on Genotype-Phenotype Correlation.
    Park JS; Park JW; Shin S; Lee ST; Shin SJ; Min BS; Park SJ; Park JJ; Cheon JH; Kim WH; Kim TI
    Dis Colon Rectum; 2022 Jun; 65(6):793-803. PubMed ID: 34897210
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Survey of germline variants in cancer-associated genes in young adults with colorectal cancer.
    Mikaeel RR; Young JP; Li Y; Smith E; Horsnell M; Uylaki W; Tapia Rico G; Poplawski NK; Hardingham JE; Tomita Y; Townsend AR; Feng J; Zibat A; Kaulfuß S; Müller C; Yigit G; Wollnik B; Price TJ
    Genes Chromosomes Cancer; 2022 Feb; 61(2):105-113. PubMed ID: 34761457
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.
    Boulouard F; Kasper E; Buisine MP; Lienard G; Vasseur S; Manase S; Bahuau M; Barouk Simonet E; Bubien V; Coulet F; Cusin V; Dhooge M; Golmard L; Goussot V; Hamzaoui N; Lacaze E; Lejeune S; Mauillon J; Beaumont MP; Pinson S; Tlemsani C; Toulas C; Rey JM; Uhrhammer N; Bougeard G; Frebourg T; Houdayer C; Baert-Desurmont S
    Clin Genet; 2021 May; 99(5):662-672. PubMed ID: 33454955
    [TBL] [Abstract] [Full Text] [Related]  

  • 7. Identification of Prognostic Signatures of Alternative Splicing in Glioma.
    Zeng Y; Zhang P; Wang X; Wang K; Zhou M; Long H; Lin J; Wu Z; Gao L; Song Y
    J Mol Neurosci; 2020 Oct; 70(10):1484-1492. PubMed ID: 32602029
    [TBL] [Abstract] [Full Text] [Related]  

  • 8. Constitutional Mismatch Repair Gene Defect Syndrome Presenting With Adenomatous Polyposis and Cafe au Lait Spots: A Case Report.
    Sağ E; Erkut M; Saygin İ; Çebi AH; Bahadir A; Erduran E; Saruhan H; Cakir M
    J Pediatr Hematol Oncol; 2020 Oct; 42(7):e689-e691. PubMed ID: 31599855
    [TBL] [Abstract] [Full Text] [Related]  

  • 9. Atypical central neurocytoma with novel EWSR1-ATF1 fusion and mutyh mutation detected by next-generation sequencing.
    Aghajan Y; Malicki DM; Levy ML; Crawford JR
    BMJ Case Rep; 2019 Jan; 12(1):. PubMed ID: 30642852
    [TBL] [Abstract] [Full Text] [Related]  

  • 10. Reduced expression of DNA repair genes and chemosensitivity in 1p19q codeleted lower-grade gliomas.
    Tang L; Deng L; Bai HX; Sun J; Neale N; Wu J; Wang Y; Chang K; Huang RY; Zhang PJ; Li X; Xiao B; Cao Y; Tao Y; Yang L
    J Neurooncol; 2018 Sep; 139(3):563-571. PubMed ID: 29923053
    [TBL] [Abstract] [Full Text] [Related]  

  • 11. Aberrant base excision repair pathway of oxidatively damaged DNA: Implications for degenerative diseases.
    Talhaoui I; Matkarimov BT; Tchenio T; Zharkov DO; Saparbaev MK
    Free Radic Biol Med; 2017 Jun; 107():266-277. PubMed ID: 27890638
    [TBL] [Abstract] [Full Text] [Related]  

  • 12. Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis.
    Adam R; Spier I; Zhao B; Kloth M; Marquez J; Hinrichsen I; Kirfel J; Tafazzoli A; Horpaopan S; Uhlhaas S; Stienen D; Friedrichs N; Altmüller J; Laner A; Holzapfel S; Peters S; Kayser K; Thiele H; Holinski-Feder E; Marra G; Kristiansen G; Nöthen MM; Büttner R; Möslein G; Betz RC; Brieger A; Lifton RP; Aretz S
    Am J Hum Genet; 2016 Aug; 99(2):337-51. PubMed ID: 27476653
    [TBL] [Abstract] [Full Text] [Related]  

  • 13. Risk of extracolonic cancers for people with biallelic and monoallelic mutations in mutyh.
    Win AK; Reece JC; Dowty JG; Buchanan DD; Clendenning M; Rosty C; Southey MC; Young JP; Cleary SP; Kim H; Cotterchio M; Macrae FA; Tucker KM; Baron JA; Burnett T; Le Marchand L; Casey G; Haile RW; Newcomb PA; Thibodeau SN; Hopper JL; Gallinger S; Winship IM; Lindor NM; Jenkins MA
    Int J Cancer; 2016 Oct; 139(7):1557-63. PubMed ID: 27194394
    [TBL] [Abstract] [Full Text] [Related]  

  • 14. Colorectal adenomatous polyposis syndromes: Genetic determinism, clinical presentation and recommendations for care.
    Buecher B
    Bull Cancer; 2016 Feb; 103(2):199-209. PubMed ID: 26805944
    [TBL] [Abstract] [Full Text] [Related]  

  • 15. Disruption of the APC gene by t(5;7) translocation in a Turcot family.
    Sahnane N; Bernasconi B; Carnevali I; Furlan D; Viel A; Sessa F; Tibiletti MG
    Cancer Genet; 2016 Mar; 209(3):107-11. PubMed ID: 26797314
    [TBL] [Abstract] [Full Text] [Related]  

  • 16. Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis.
    Spier I; Kerick M; Drichel D; Horpaopan S; Altmüller J; Laner A; Holzapfel S; Peters S; Adam R; Zhao B; Becker T; Lifton RP; Holinski-Feder E; Perner S; Thiele H; Nöthen MM; Hoffmann P; Timmermann B; Schweiger MR; Aretz S
    Fam Cancer; 2016 Apr; 15(2):281-8. PubMed ID: 26780541
    [TBL] [Abstract] [Full Text] [Related]  

  • 17. Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases.
    Spier I; Drichel D; Kerick M; Kirfel J; Horpaopan S; Laner A; Holzapfel S; Peters S; Adam R; Zhao B; Becker T; Lifton RP; Perner S; Hoffmann P; Kristiansen G; Timmermann B; Nöthen MM; Holinski-Feder E; Schweiger MR; Aretz S
    J Med Genet; 2016 Mar; 53(3):172-9. PubMed ID: 26613750
    [TBL] [Abstract] [Full Text] [Related]  

  • 18. Inhibition of DNA-repair genes Ercc1 and Mgmt enhances temozolomide efficacy in gliomas treatment: a pre-clinical study.
    Boccard SG; Marand SV; Geraci S; Pycroft L; Berger FR; Pelletier LA
    Oncotarget; 2015 Oct; 6(30):29456-68. PubMed ID: 26336131
    [TBL] [Abstract] [Full Text] [Related]  

  • 19. High Prevalence of Hereditary cancer Syndromes in Adolescents and Young Adults With Colorectal cancer.
    Mork ME; You YN; Ying J; Bannon SA; Lynch PM; Rodriguez-Bigas MA; Vilar E
    J Clin Oncol; 2015 Nov; 33(31):3544-9. PubMed ID: 26195711
    [TBL] [Abstract] [Full Text] [Related]  

  • 20. Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas.
    Spier I; Holzapfel S; Altmüller J; Zhao B; Horpaopan S; Vogt S; Chen S; Morak M; Raeder S; Kayser K; Stienen D; Adam R; Nürnberg P; Plotz G; Holinski-Feder E; Lifton RP; Thiele H; Hoffmann P; Steinke V; Aretz S
    Int J Cancer; 2015 Jul; 137(2):320-31. PubMed ID: 25529843
    [TBL] [Abstract] [Full Text] [Related]  


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