Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

94 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Germline mutation in the TP53 gene in uveal melanoma.
Hajkova N, Hojny J, Nemejcova K, Dundr P, Ulrych J, Jirsova K, Glezgova J, Ticha I. Hajkova N, et al. Among authors: jirsova k. Sci Rep. 2018 May 16;8(1):7618. doi: 10.1038/s41598-018-26040-0. Sci Rep. 2018. PMID: 29769598 Free PMC article.
Expression, Epigenetic and Genetic Changes of HNF1B in Endometrial Lesions.
Němejcová K, Tichá I, Kleiblová P, Bártů M, Cibula D, Jirsová K, Dundr P. Němejcová K, et al. Among authors: jirsova k. Pathol Oncol Res. 2016 Jul;22(3):523-30. doi: 10.1007/s12253-015-0037-2. Epub 2015 Dec 19. Pathol Oncol Res. 2016. PMID: 26685938 Free article.
Novel TGFBI mutation p.(Leu558Arg) in a lattice corneal dystrophy patient.
Dudakova L, Palos M, Jirsova K, Skalicka P, Dundr P, Liskova P. Dudakova L, et al. Among authors: jirsova k. Ophthalmic Genet. 2016 Dec;37(4):473-474. doi: 10.3109/13816810.2015.1126615. Epub 2016 Mar 30. Ophthalmic Genet. 2016. PMID: 27028151 No abstract available.
HNF1B, EZH2 and ECI2 in prostate carcinoma. Molecular, immunohistochemical and clinico-pathological study.
Dundr P, Bártů M, Hojný J, Michálková R, Hájková N, Stružinská I, Krkavcová E, Hadravský L, Kleissnerová L, Kopejsková J, Hiep BQ, Němejcová K, Jakša R, Čapoun O, Řezáč J, Jirsová K, Franková V. Dundr P, et al. Among authors: jirsova k. Sci Rep. 2020 Sep 1;10(1):14365. doi: 10.1038/s41598-020-71427-7. Sci Rep. 2020. PMID: 32873863 Free PMC article.
Familial Limbal Stem Cell Deficiency: Clinical, Cytological and Genetic Characterization.
Dudakova L, Cheong SS, Merjava SR, Skalicka P, Michalickova M, Palos M, Mahelkova G, Krizova D, Hlozanek M, Trkova M, Chojnowski JL, Hrdlickova E, Pontikos N, Plagnol V, Veselá V, Jirsova K, Hardcastle AJ, Filipec M, Lauderdale JD, Liskova P. Dudakova L, et al. Among authors: jirsova k. Stem Cell Rev Rep. 2018 Feb;14(1):148-151. doi: 10.1007/s12015-017-9780-y. Stem Cell Rev Rep. 2018. PMID: 29134474 No abstract available.
High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.
Liskova P, Gwilliam R, Filipec M, Jirsova K, Reinstein Merjava S, Deloukas P, Webb TR, Bhattacharya SS, Ebenezer ND, Morris AG, Hardcastle AJ. Liskova P, et al. Among authors: jirsova k. PLoS One. 2012;7(9):e45495. doi: 10.1371/journal.pone.0045495. Epub 2012 Sep 25. PLoS One. 2012. PMID: 23049806 Free PMC article.
Macular corneal dystrophy and associated corneal thinning.
Dudakova L, Palos M, Svobodova M, Bydzovsky J, Huna L, Jirsova K, Hardcastle AJ, Tuft SJ, Liskova P. Dudakova L, et al. Among authors: jirsova k. Eye (Lond). 2014 Oct;28(10):1201-5. doi: 10.1038/eye.2014.164. Epub 2014 Aug 1. Eye (Lond). 2014. PMID: 25081284 Free PMC article.
94 results