- Variabilní oční fenotypy u zadní polymorfní dystrofie rohovky způsobené mutacemi v genu ZEB12010 | 1. lékařská fakulta
- Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles2021 | 1. lékařská fakulta
- Identification of Six Novel Mutations in ZEB1 and Description of the Associated Phenotypes in Patients with Posterior Polymorphous Corneal Dystrophy 32015 | 1. lékařská fakulta
- Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 32016 | 1. lékařská fakulta, 2. lékařská fakulta
- Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy2007 | 1. lékařská fakulta
- Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy2007 | Fakulta tělesné výchovy a sportu
- Further Genetic and Clinical Insights of Posterior Polymorphous Corneal Dystrophy 32013 | 1. lékařská fakulta
- Expression of circular RNAs in myelodysplastic neoplasms and their association with mutations in the splicing factor gene SF3B12023 | Přírodovědecká fakulta, Ústřední knihovna
- Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophy2022 | 1. lékařská fakulta
- CUGC for posterior polymorphous corneal dystrophy (PPCD)2020 | 1. lékařská fakulta
- The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis2019 | 1. lékařská fakulta, 3. lékařská fakulta
- Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 42018 | 1. lékařská fakulta, 3. lékařská fakulta
- Coincidental Occurrence of Schnyder Corneal Dystrophy and Posterior Polymorphous Corneal Dystrophy Type 32019 | 1. lékařská fakulta
- Active transforming growth factor-beta 2 in the aqueous humor of posterior polymorphous corneal dystrophy patients2017 | 1. lékařská fakulta
- MicroRNAs in Pancreatic Cancer: Involvement in Carcinogenesis and Potential Use for Diagnosis and Prognosis2015 | 1. lékařská fakulta
- Upregulation of ZEB1-Derived Circular RNAs Is Associated with SF3B1-Mutated Myelodysplastic NeoplasmsPublikace bez příslušnosti k fakultě
- Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy2023 | 1. lékařská fakulta, 3. lékařská fakulta
- SF3B1 mutations and their impact on cellular bioenergetics in myelodysplastic syndromesPublikace bez příslušnosti k fakultě
- Unravelling heterogeneous effects of cancer-associated fibroblasts on poor prognosis markers in breast cancer EM-G3 cell line: In vitro-targeted treatment (anti-IL-6, anti-VEGF-A, anti-MFGE8) based on transcriptomic profiling2024 | 1. lékařská fakulta, 3. lékařská fakulta
- Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL22016 | 1. lékařská fakulta
- Attenuated cell cycle and DNA damage response transcriptome signatures and overrepresented cell adhesion processes imply accelerated progression in patients with lower-risk myelodysplastic neoplasms2024 | 1. lékařská fakulta, Fakulta tělesné výchovy a sportu, Přírodovědecká fakulta
- Low-grade spindle cell proliferation in clear cell renal cell carcinoma is unlikely to be an initial step in sarcomatoid differentiation2018 | Lékařská fakulta v Plzni