edoc

Items where Author is "Kovac, Michal"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Date | Item Type | Refereed
Jump to: 2019 | 2014 | 2012 | 2011 | 2010 | 2008
Number of items: 10.

2019

Lackner, Carolin and Quagliata, Luca and Cross, William and Ribi, Sebastian and Heinimann, Karl and Paradiso, Viola and Quintavalle, Cristina and Kovacova, Monika and Baumhoer, Daniel and Piscuoglio, Salvatore and Terracciano, Luigi and Kovac, Michal. (2019) Convergent Evolution of Copy Number Alterations in Multi-Centric Hepatocellular Carcinoma. Scientific reports, 9 (1). p. 4611.

2014

Kishore, Shivendra and Piscuoglio, Salvatore and Kovac, Michal and Gylling, Annette and Wenzel, Friedel and Trapani, Francesca and Altermatt, Hans Joerg and Mele, Valentina and Marra, Giancarlo and Peltomäki, Päivi and Terracciano, Luigi and Zavolan, Mihaela and Heinimann, Karl. (2014) 3'UTR poly(T/U) tract deletions and altered expression of EWSR1 are a hallmark of mismatch repair deficient cancers. Cancer research, 74 (1). pp. 224-234.

Quagliata, Luca and Matter, Matthias S. and Piscuoglio, Salvatore and Arabi, Leila and Ruiz, Christian and Procino, Alfredo and Kovac, Michal and Moretti, Francesca and Makowska, Zuzanna and Boldanova, Tujana and Andersen, Jesper B. and Hammerle, Monika and Tornillo, Luigi and Heim, Markus H. and Diederichs, Sven and Cillo, Clemente and Terracciano, Luigi M.. (2014) Long noncoding RNA HOTTIP/HOXA13 expression is associated with disease progression and predicts outcome in hepatocellular carcinoma patients. Hepatology, 59 (3). pp. 911-923.

Quagliata, Luca and Andreozzi, Mariacarla and Kovac, Michal and Tornillo, Luigi and Makowska, Zuzanna and Moretti, Francesca and Heim, Markus H. and Heinimann, Karl and Piscuoglio, Salvatore and Terracciano, Luigi Maria. (2014) SH2D4A is frequently downregulated in hepatocellular carcinoma and cirrhotic nodules. European Journal of Cancer, 50 (4). pp. 731-738.

2012

Buerki, Nicole and Gautier, Lucienne and Kovac, Michal and Marra, Giancarlo and Buser, Mauro and Mueller, Hansjakob and Heinimann, Karl. (2012) Evidence for breast cancer as an integral part of Lynch syndrome. Genes, chromosomes & cancer, Vol. 51. pp. 83-91.

2011

Necker, Judith and Kovac, Michal and Attenhofer, Michèle and Reichlin, Bruno and Heinimann, Karl. (2011) Detection of APC germ line mosaicism in patients with de novo familial adenomatous polyposis : a plea for the protein truncation test. Journal of medical genetics, Vol. 48, H. 8. pp. 526-529.

Kovac, Michal and Laczko, Endre and Haider, Ritva and Jiricny, Josef and Mueller, Hansjakob and Heinimann, Karl and Marra, Giancarlo. (2011) Familial colorectal cancer: eleven years of data from a registry program in Switzerland. Familial cancer, Vol. 10, H. 3. pp. 605-616.

2010

Burger, Bettina and Hershkovitz, Dov and Indelman, Margarita and Kovac, Michal and Galambos, Jörg and Haeusermann, Peter and Sprecher, Eli and Itin, Peter H.. (2010) Buschke-Ollendorff syndrome in a three-generation family: influence of a novel LEMD3 mutation to tropoelastin expression. European journal of dermatology : EJD, 20 (6). pp. 693-697.

Zlobec, Inti and Kovac, Michal and Erzberger, Priska and Molinari, Francesca and Bihl, Michel P. and Rufle, Alexander and Foerster, Anja and Frattini, Milo and Terracciano, Luigi and Heinimann, Karl and Lugli, Alessandro. (2010) Combined analysis of specific KRAS mutation, BRAF and microsatellite instability identifies prognostic subgroups of sporadic and hereditary colorectal cancer. International journal of cancer, Vol. 127, H. 11. pp. 2569-2575.

2008

Bujalkova, Maria and Zavodna, Katarina and Krivulcik, Tomas and Ilencikova, Denisa and Wolf, Brigitte and Kovac, Michal and Karner-Hanusch, Judith and Heinimann, Karl and Marra, Giancarlo and Jiricny, Josef and Bartosova, Zdena. (2008) Multiplex SNaPshot genotyping for detecting loss of heterozygosity in the mismatch-repair genes MLH1 and MSH2 in microsatellite-unstable tumors. Clinical chemistry, 54 (11). pp. 1844-1854.

This list was generated on Thu Mar 28 10:10:00 2024 CET.