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 *

Terms: = Colorectal cancer AND TGFBR2, AAT3, 7048, ENSG00000163513, P37173, TGFbeta-RII, RIIC, TAAD2, FAA3, TGFR-2, MFS2, HNPCC6 AND Diagnosis
6 results:

  • 1. Circular RNA hsa_circ_0064559 affects tumor cell growth and progression of colorectal cancer.
    Zhen Y; Sun G; Chen C; Li J; Xiao R; Xu Z
    World J Surg Oncol; 2023 Jun; 21(1):171. PubMed ID: 37280630
    [TBL] [Abstract] [Full Text] [Related]  

  • 2. Homozygous PMS2 deletion causes a severe colorectal cancer and multiple adenoma phenotype without extraintestinal cancer.
    Will O; Carvajal-Carmona LG; Gorman P; Howarth KM; Jones AM; Polanco-Echeverry GM; Chinaleong JA; Günther T; Silver A; Clark SK; Tomlinson I
    Gastroenterology; 2007 Feb; 132(2):527-30. PubMed ID: 17258725
    [TBL] [Abstract] [Full Text] [Related]  

  • 3. HNPCC-associated small bowel cancer: clinical and molecular characteristics.
    Schulmann K; Brasch FE; Kunstmann E; Engel C; Pagenstecher C; Vogelsang H; Krüger S; Vogel T; Knaebel HP; Rüschoff J; Hahn SA; Knebel-Doeberitz MV; Moeslein G; Meltzer SJ; Schackert HK; Tympner C; Mangold E; Schmiegel W;
    Gastroenterology; 2005 Mar; 128(3):590-9. PubMed ID: 15765394
    [TBL] [Abstract] [Full Text] [Related]  

  • 4. Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry-based detection of microsatellite instabilities in coding DNA sequences: a novel approach to identify DNA-mismatch repair-deficient cancer cells.
    Bonk T; Humeny A; Gebert J; Sutter C; von Knebel Doeberitz M; Becker CM
    Clin Chem; 2003 Apr; 49(4):552-61. PubMed ID: 12651806
    [TBL] [Abstract] [Full Text] [Related]  

  • 5. Germline mutation and genome instability.
    Olschwang S
    Eur J Cancer Prev; 1999 Dec; 8 Suppl 1():S33-7. PubMed ID: 10772416
    [TBL] [Abstract] [Full Text] [Related]  

  • 6. Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene.
    De Rosa M; Fasano C; Panariello L; Scarano MI; Belli G; Iannelli A; Ciciliano F; Izzo P
    Oncogene; 2000 Mar; 19(13):1719-23. PubMed ID: 10763829
    [TBL] [Abstract] [Full Text] [Related]  


    of 1.