Terms: = Colorectal cancer AND NBN, AT-V2, 4683, ENSG00000104320, ATV, FLJ10155, NBS, AT-V1, MGC87362, NBS1 AND Diagnosis
4 results:
1. Co-occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome.
Ferrer-Avargues R; Castillejo MI; Dámaso E; Díez-Obrero V; Garrigos N; Molina T; Codoñer-Alejos A; Segura Á; Sánchez-Heras AB; Castillejo A; Soto JL
Cancer Commun (Lond); 2021 Mar; 41(3):218-228. PubMed ID: 33630411
[TBL] [Abstract] [Full Text] [Related]
2. Expression profile of significant immortalization genes in colon cancer.
Witkowska A; Gumprecht J; Glogowska-Ligus J; Wystrychowski G; Owczarek A; Stachowicz M; Bocianowska A; Nowakowska-Zajdel E; Mazurek U
Int J Mol Med; 2010 Mar; 25(3):321-9. PubMed ID: 20127035
[TBL] [Abstract] [Full Text] [Related]
3. cancer risk of heterozygotes with the nbn founder mutation.
Seemanová E; Jarolim P; Seeman P; Varon R; Digweed M; Swift M; Sperling K
J Natl Cancer Inst; 2007 Dec; 99(24):1875-80. PubMed ID: 18073374
[TBL] [Abstract] [Full Text] [Related]
4. Mutations of an intronic repeat induce impaired MRE11 expression in primary human cancer with microsatellite instability.
Giannini G; Rinaldi C; Ristori E; Ambrosini MI; Cerignoli F; Viel A; Bidoli E; Berni S; D'Amati G; Scambia G; Frati L; Screpanti I; Gulino A
Oncogene; 2004 Apr; 23(15):2640-7. PubMed ID: 15048091
[TBL] [Abstract] [Full Text] [Related]
