Trkova M - Search Results

1

Increased sperm aneuploidy in two male carriers of germline TP53 mutations.

Paulasova P, Diblik J, Trkova M, Macek M Sr, Sedlacek Z. Paulasova P, et al. Among authors: trkova m. Cancer Genet. 2011 May;204(5):278-81. doi: 10.1016/j.cancergen.2011.03.003. Cancer Genet. 2011. PMID: 21665182

2

Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?

Trkova M, Hladikova M, Kasal P, Goetz P, Sedlacek Z. Trkova M, et al. J Hum Genet. 2002;47(8):381-6. doi: 10.1007/s100380200055. J Hum Genet. 2002. PMID: 12181637

3

A Li-Fraumeni syndrome family with retained heterozygosity for a germline TP53 mutation in two tumors.

Trkova M, Foretova L, Kodet R, Hedvicakova P, Sedlacek Z. Trkova M, et al. Cancer Genet Cytogenet. 2003 Aug;145(1):60-4. doi: 10.1016/s0165-4608(03)00031-1. Cancer Genet Cytogenet. 2003. PMID: 12885464

4

Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations.

Krutilkova V, Trkova M, Fleitz J, Gregor V, Novotna K, Krepelova A, Sumerauer D, Kodet R, Siruckova S, Plevova P, Bendova S, Hedvicakova P, Foreman NK, Sedlacek Z. Krutilkova V, et al. Among authors: trkova m. Eur J Cancer. 2005 Jul;41(11):1597-603. doi: 10.1016/j.ejca.2005.01.026. Eur J Cancer. 2005. PMID: 15925506

5

Telomere length in peripheral blood cells of germline TP53 mutation carriers is shorter than that of normal individuals of corresponding age.

Trkova M, Prochazkova K, Krutilkova V, Sumerauer D, Sedlacek Z. Trkova M, et al. Cancer. 2007 Aug 1;110(3):694-702. doi: 10.1002/cncr.22834. Cancer. 2007. PMID: 17567834 Free article.

6

[When is it useful to look for TP53 germline gene mutations in families of oncology patients?].

Trková M, Sedlácek Z. Trková M, et al. Cas Lek Cesk. 2003;142(4):220-5. Cas Lek Cesk. 2003. PMID: 12841124 Czech.

7

Analysis of genetic events in 17p13 and 9p21 regions supports predominant monoclonal origin of multifocal and recurrent bladder cancer.

Trkova M, Babjuk M, Duskova J, Benesova-Minarikova L, Soukup V, Mares J, Minarik M, Sedlacek Z. Trkova M, et al. Cancer Lett. 2006 Oct 8;242(1):68-76. doi: 10.1016/j.canlet.2005.10.036. Epub 2005 Dec 15. Cancer Lett. 2006. PMID: 16343743

8

TP53 gene mutations are rare in nondysplastic Barrett's esophagus.

Novotna K, Trkova M, Pazdro A, Smejkal M, Soukupova A, Kodetova D, Smejkal P, Sedlacek Z. Novotna K, et al. Among authors: trkova m. Dig Dis Sci. 2006 Jan;51(1):110-3. doi: 10.1007/s10620-006-3093-3. Dig Dis Sci. 2006. PMID: 16416221

9

Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres.

Hancarova M, Malikova M, Kotrova M, Drabova J, Trkova M, Sedlacek Z. Hancarova M, et al. Among authors: trkova m. Am J Med Genet A. 2018 Jun;176(6):1438-1442. doi: 10.1002/ajmg.a.38711. Epub 2018 Apr 25. Am J Med Genet A. 2018. PMID: 29696806

10

Identification of a patient with intellectual disability and de novo 3.7 Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p15.

Hancarova M, Vejvalkova S, Trkova M, Drabova J, Dleskova A, Vlckova M, Sedlacek Z. Hancarova M, et al. Among authors: trkova m. Gene. 2013 Mar 1;516(1):158-61. doi: 10.1016/j.gene.2012.12.027. Epub 2012 Dec 22. Gene. 2013. PMID: 23266801

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

46 results

Search Page

Filters