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ZEB1
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Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in the ZEB1 gene
2010 |
First Faculty of Medicine
publication
Non-Penetrance for Ocular Phenotype in Two Individuals Carrying Heterozygous Loss-of-Function ZEB1 Alleles
2021 |
First Faculty of Medicine
publication
Identification of Six Novel Mutations in ZEB1 and Description of the Associated Phenotypes in Patients with Posterior Polymorphous Corneal Dystrophy 3
2015 |
First Faculty of Medicine
publication
Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3
2016 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy
2007 |
First Faculty of Medicine
publication
Novel mutations in the ZEB1 gene identified in Czech and British patients with posterior polymorphous corneal dystrophy
2007 |
Faculty of Physical Education and Sport
publication
Further Genetic and Clinical Insights of Posterior Polymorphous Corneal Dystrophy 3
2013 |
First Faculty of Medicine
publication
Expression of circular RNAs in myelodysplastic neoplasms and their association with mutations in the splicing factor gene SF3B1
2023 |
Faculty of Science, Central Library of Charles University
publication
Posterior corneal vesicles are not associated with the genetic variants that cause posterior polymorphous corneal dystrophy
2022 |
First Faculty of Medicine
publication
CUGC for posterior polymorphous corneal dystrophy (PPCD)
2020 |
First Faculty of Medicine
publication
The utility of massively parallel sequencing for posterior polymorphous corneal dystrophy type 3 molecular diagnosis
2019 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Ectopic GRHL2 Expression Due to Non-coding Mutations Promotes Cell State Transition and Causes Posterior Polymorphous Corneal Dystrophy 4
2018 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Coincidental Occurrence of Schnyder Corneal Dystrophy and Posterior Polymorphous Corneal Dystrophy Type 3
2019 |
First Faculty of Medicine
publication
Active transforming growth factor-beta 2 in the aqueous humor of posterior polymorphous corneal dystrophy patients
2017 |
First Faculty of Medicine
publication
MicroRNAs in Pancreatic Cancer: Involvement in Carcinogenesis and Potential Use for Diagnosis and Prognosis
2015 |
First Faculty of Medicine
publication
Upregulation of ZEB1-Derived Circular RNAs Is Associated with SF3B1-Mutated Myelodysplastic Neoplasms
Publication without faculty affiliation
publication
Phenotype and genotype of concurrent keratoconus and Fuchs endothelial corneal dystrophy
2023 |
First Faculty of Medicine, Third Faculty of Medicine
publication
SF3B1 mutations and their impact on cellular bioenergetics in myelodysplastic syndromes
Publication without faculty affiliation
publication
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 profiling
2024 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2
2016 |
First Faculty of Medicine
publication
Attenuated cell cycle and DNA damage response transcriptome signatures and overrepresented cell adhesion processes imply accelerated progression in patients with lower-risk myelodysplastic neoplasms
2024 |
First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Science
publication
Low-grade spindle cell proliferation in clear cell renal cell carcinoma is unlikely to be an initial step in sarcomatoid differentiation
2018 |
Faculty of Medicine in Pilsen