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 *

474 related articles for article (PubMed ID: 21195604)

  • 1. First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
    Morak M; Massdorf T; Sykora H; Kerscher M; Holinski-Feder E
    Eur J Cancer; 2011 May; 47(7):1046-55. PubMed ID: 21195604
    [TBL] [Abstract][Full Text] [Related]  

  • 2. MUTYH-associated polyposis - variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations.
    Morak M; Laner A; Bacher U; Keiling C; Holinski-Feder E
    Clin Genet; 2010 Oct; 78(4):353-63. PubMed ID: 20618354
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
    Lejeune S; Guillemot F; Triboulet JP; Cattan S; Mouton C; ; Porchet N; Manouvrier S; Buisine MP
    Hum Mutat; 2006 Oct; 27(10):1064. PubMed ID: 16941501
    [TBL] [Abstract][Full Text] [Related]  

  • 4. No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients.
    Steinke V; Rahner N; Morak M; Keller G; Schackert HK; Görgens H; Schmiegel W; Royer-Pokora B; Dietmaier W; Kloor M; Engel C; Propping P; Aretz S;
    Eur J Hum Genet; 2008 May; 16(5):587-92. PubMed ID: 18301448
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Alterations of the base excision repair gene MUTYH in sporadic colorectal cancer.
    Kuno T; Matsubara N; Tsuda S; Kobayashi M; Hamanaka M; Yamagishi D; Tsukamoto K; Yamano T; Noda M; Ikeuchi H; Kim S; Tamura K; Tomita N
    Oncol Rep; 2012 Aug; 28(2):473-80. PubMed ID: 22641385
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MUTYH hotspot mutations in unselected colonoscopy patients.
    Casper M; Plotz G; Juengling B; Zeuzem S; Lammert F; Raedle J
    Colorectal Dis; 2012 May; 14(5):e238-44. PubMed ID: 22469480
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Germline MUTYH (MYH) mutations in Portuguese individuals with multiple colorectal adenomas.
    Isidro G; Laranjeira F; Pires A; Leite J; Regateiro F; Castro e Sousa F; Soares J; Castro C; Giria J; Brito MJ; Medeira A; Teixeira R; Morna H; Gaspar I; Marinho C; Jorge R; Brehm A; Ramos JS; Boavida MG
    Hum Mutat; 2004 Oct; 24(4):353-4. PubMed ID: 15366000
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair.
    Boardman LA; Schmidt S; Lindor NM; Burgart LJ; Cunningham JM; Price-Troska T; Snow K; Ahlquist DA; Thibodeau SN
    Genes Chromosomes Cancer; 2001 Feb; 30(2):181-6. PubMed ID: 11135435
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MutYH (MYH) and colorectal cancer.
    Sampson JR; Jones S; Dolwani S; Cheadle JP
    Biochem Soc Trans; 2005 Aug; 33(Pt 4):679-83. PubMed ID: 16042573
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The first mutations in the MYH gene reported in Moroccan colon cancer patients.
    Laarabi FZ; Cherkaoui Jaouad I; Baert-Desurmont S; Ouldim K; Ibrahimi A; Kanouni N; Frebourg T; Sefiani A
    Gene; 2012 Mar; 496(1):55-8. PubMed ID: 22266422
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutational analysis of OGG1, MYH, MTH1 in FAP, HNPCC and sporadic colorectal cancer patients: R154H OGG1 polymorphism is associated with sporadic colorectal cancer patients.
    Kim IJ; Ku JL; Kang HC; Park JH; Yoon KA; Shin Y; Park HW; Jang SG; Lim SK; Han SY; Shin YK; Lee MR; Jeong SY; Shin HR; Lee JS; Kim WH; Park JG
    Hum Genet; 2004 Nov; 115(6):498-503. PubMed ID: 15449173
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Germline variation in the oxidative DNA repair genes NUDT1 and OGG1 is not associated with hereditary colorectal cancer or polyposis.
    Mur P; Jemth AS; Bevc L; Amaral N; Navarro M; Valdés-Mas R; Pons T; Aiza G; Urioste M; Valencia A; Lázaro C; Moreno V; Puente XS; Stenmark P; Warpman-Berglund U; Capellá G; Helleday T; Valle L
    Hum Mutat; 2018 Sep; 39(9):1214-1225. PubMed ID: 29900613
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MUTYH-associated polyposis--from defect in base excision repair to clinical genetic testing.
    Cheadle JP; Sampson JR
    DNA Repair (Amst); 2007 Mar; 6(3):274-9. PubMed ID: 17161978
    [TBL] [Abstract][Full Text] [Related]  

  • 15. An in-frame exon-skipping MUTYH mutation is associated with early-onset colorectal cancer.
    Fostira F; Papademitriou C; Efremidis A; Yannoukakos D
    Dis Colon Rectum; 2010 Aug; 53(8):1197-201. PubMed ID: 20628285
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MUTYH-associated polyposis (MAP).
    Nielsen M; Morreau H; Vasen HF; Hes FJ
    Crit Rev Oncol Hematol; 2011 Jul; 79(1):1-16. PubMed ID: 20663686
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [From gene to disease; MutYH-associated polyposis coli (MAP)].
    Nielsen M; Weiss MM; Vasen HF; Hes FJ
    Ned Tijdschr Geneeskd; 2005 Dec; 149(53):2970-2. PubMed ID: 16425850
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Cells with pathogenic biallelic mutations in the human MUTYH gene are defective in DNA damage binding and repair.
    Parker AR; Sieber OM; Shi C; Hua L; Takao M; Tomlinson IP; Eshleman JR
    Carcinogenesis; 2005 Nov; 26(11):2010-8. PubMed ID: 15987719
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC families.
    Johnson V; Lipton LR; Cummings C; Eftekhar Sadat AT; Izatt L; Hodgson SV; Talbot IC; Thomas HJ; Silver AJ; Tomlinson IP
    J Med Genet; 2005 Oct; 42(10):756-62. PubMed ID: 15788729
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.