FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor.

Autor: Cannon-Albright LA; Division of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT, USA.; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA., Teerlink CC; Division of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT, USA., Stevens J; Division of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT, USA., Snow AK; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA., Thompson BA; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.; Department of Pathology, Royal Melbourne Hospital, Melbourne, Australia., Bell R; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA., Nguyen KN; Division of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT, USA., Sargent NR; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA., Kohlmann WK; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA., Neklason DW; Division of Epidemiology, Department of Internal Medicine, University of Utah School of Medicine, Salt Lake City, UT, USA.; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA., Tavtigian SV; Huntsman Cancer Institute, University of Utah, Salt Lake City, UT, USA.; Department of Oncological Sciences, University of Utah School of Medicine, Salt Lake City, UT, USA.

Publikováno v: Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2020 Dec; Vol. 8 (12), pp. e1532. Date of Electronic Publication: 2020 Oct 29.

Activating mutation in MET oncogene in familial colorectal cancer.

Autor: Neklason DW; Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA. deb.neklason@hci.utah.edu, Done MW, Sargent NR, Schwartz AG, Anton-Culver H, Griffin CA, Ahnen DJ, Schildkraut JM, Tomlinson GE, Strong LC, Miller AR, Stopfer JE, Burt RW

Publikováno v: BMC cancer [BMC Cancer] 2011 Oct 04; Vol. 11, pp. 424. Date of Electronic Publication: 2011 Oct 04.

Evaluation of MET T1010I and MET rs40239 single-nucleotide polymorphisms in triple-negative breast cancer: a case–control study.

Autor: Kalapanida, Despoina (AUTHOR), Zagouri, Flora (AUTHOR), Gazouli, Maria (AUTHOR), Tsiakou, Andriani (AUTHOR), Zografos, Eleni (AUTHOR), Dimitrakakis, Constantine (AUTHOR), Marinopoulos, Spyridon (AUTHOR), Giannos, Aris (AUTHOR), Sergentanis, Theodoros N (AUTHOR), Kastritis, Efstathios (AUTHOR), Terpos, Evangelos (AUTHOR), Dimopoulos, Meletios-Athanassios (AUTHOR)

Publikováno v: OncoTargets & Therapy. May2019, Vol. 12, p4195-4202. 8p.

Constitutional chromothripsis of the APC locus as a cause of genetic predisposition to colon cancer.

Autor: Scharf, Florentine, Leal Silva, Rafaela Magalhaes, Morak, Monika, Hastie, Alex, Pickl, Julia M. A., Sendelbach, Kai, Gebhard, Christian, Locher, Melanie, Laner, Andreas, Steinke-Lange, Verena, Koehler, Udo, Holinski-Feder, Elke, Wolf, Dieter A.

Publikováno v: Journal of Medical Genetics; Oct2022, Vol. 59 Issue 10, p976-983, 8p

MET Gene Copy Number Alterations and Expression of MET and Hepatocyte Growth Factor Are Potential Biomarkers in Angiosarcomas and Undifferentiated Pleomorphic Sarcomas.

Autor: Schmitz, Katja^1,2, Koeppen, Hartmut³, Binot, Elke¹, Fassunke, Jana¹, Künstlinger, Helen¹, Ihle, Michaela A.¹, Heydt, Carina¹, Wardelmann, Eva^1,4, Büttner, Reinhard¹, Merkelbach-Bruse, Sabine¹, Rüschoff, Josef⁵, Schildhaus, Hans-Ulrich^1,2 hans-ulrich.schildhaus@med.uni-goettingen.de

Publikováno v: PLoS ONE. Apr2015, Vol. 10 Issue 4, p1-18. 18p.