about
Endothelial quality of pre-cut posterior corneal lamellae for Descemet membrane endothelial keratoplasty with a stromal rim (DMEK-S): two-year outcome of manual preparation in an ocular tissue bank.The Bank of Biological Material (BBM) of the First Faculty of Medicine of Charles University in Prague, Czech Republic.Active transforming growth factor-β2 in the aqueous humor of posterior polymorphous corneal dystrophy patients.Large proteoglycan complexes and disturbed collagen architecture in the corneal extracellular matrix of mucopolysaccharidosis type VII (Sly syndrome).Macular corneal dystrophy and associated corneal thinning.High prevalence of posterior polymorphous corneal dystrophy in the Czech Republic; linkage disequilibrium mapping and dating an ancestral mutation.A simple alkaline method for decellularizing human amniotic membrane for cell culture.Validation of rs2956540:G>C and rs3735520:G>A association with keratoconus in a population of European descent.Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2Variable ocular phenotypes of posterior polymorphous corneal dystrophy caused by mutations in the ZEB1 gene.The impairment of lysyl oxidase in keratoconus and in keratoconus-associated disorders.The OV-TL 12/30 clone of anti-cytokeratin 7 antibody as a new marker of corneal conjunctivalization in patients with limbal stem cell deficiency.Amniotic membrane in ophthalmology: properties, preparation, storage and indications for grafting-a review.Descemet membrane endothelial keratoplasty with a stromal rim in the treatment of posterior polymorphous corneal dystrophy.Regulatory Impact of Amniotic Membrane Transplantation on Presence of Adhesion/Growth-Regulatory Galectins-1 and -7 in Corneal Explants from Acanthamoeba Keratitis Patients: Clinical Note.Rapid cooling of the amniotic membrane as a model system for the vitrification of posterior corneal lamellae.Cytokeratin 8 is expressed in human corneoconjunctival epithelium, particularly in limbal epithelial cells.Using corneal confocal microscopy to track changes in the corneal layers of dry eye patients after autologous serum treatment.The effect of culture medium and carrier on explant culture of human limbal epithelium: A comparison of ultrastructure, keratin profile and gene expression.The assessment of pathogenic prions in the brains of eye tissue donors: 2-years experience in the Czech Republic.Comparison of impact of two decontamination solutions on the viability of the cells in human amnion.Detailed assessment of renal function in a proband with Harboyan syndrome caused by a novel homozygous SLC4A11 nonsense mutation.Novel TGFBI mutation p.(Leu558Arg) in a lattice corneal dystrophy patient.Molecular and biochemical expression of TLRs in human amniotic membrane: a comparative study of fresh and cryopreserved specimens.Mucolipidosis IV: report of a case with ocular restricted phenotype caused by leaky splice mutation.Posterior Polymorphous Corneal Dystrophy in Czech Families Maps to Chromosome 20 and Excludes theVSX1GeneIdentification of Six Novel Mutations inZEB1and Description of the Associated Phenotypes in Patients with Posterior Polymorphous Corneal Dystrophy 3Recurrence of posterior polymorphous corneal dystrophy is caused by the overgrowth of the original diseased host endotheliumIs copper imbalance an environmental factor influencing keratoconus development?Changes in lysyl oxidase (LOX) distribution and its decreased activity in keratoconus corneasDescemet membrane endothelial keratoplasty with a stromal rim (DMEK-S)Role of matrix metalloproteinases in recurrent corneal meltingChanges in the localization of collagens IV and VIII in corneas obtained from patients with posterior polymorphous corneal dystrophySequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutationImmunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patientsExpression, Epigenetic and Genetic Changes of HNF1B in Endometrial LesionsInterleukin-13 maintains the stemness of conjunctival epithelial cell cultures prepared from human limbal explantsCold jet: a method to obtain pure Schwann cell cultures without the need for cytotoxic, apoptosis-inducing drug treatmentNeurotoxicity of tetraphenylporphinesulfonate (TPPS4) and a hematoporphyrin derivative (Photosan) in organotypic cultures of chick embryonic dorsal root gangliaNitric oxide synthase induction and cytotoxic nitrogen-related oxidant formation in conjunctival epithelium of dry eye (Sjögren's syndrome)
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
@nl
հետազոտող
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name
Katerina Jirsova
@ast
Katerina Jirsova
@en
Katerina Jirsova
@es
Katerina Jirsova
@nl
Katerina Jirsova
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type
label
Katerina Jirsova
@ast
Katerina Jirsova
@en
Katerina Jirsova
@es
Katerina Jirsova
@nl
Katerina Jirsova
@sl
prefLabel
Katerina Jirsova
@ast
Katerina Jirsova
@en
Katerina Jirsova
@es
Katerina Jirsova
@nl
Katerina Jirsova
@sl
P106
P1153
12773057900
P21
P31
P496
0000-0002-4625-6701