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cell-line
Person
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Person
Publication
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prof. Ing. Zdeněk Sedláček DrSc.
Academic staff at Second Faculty of Medicine
17 classes
118 publications
Classes
class
Medical Biology I
+1
D0102337 |
Second Faculty of Medicine
class
Lékařská biologie II
+1
D0103039 |
Second Faculty of Medicine
class
Cell
+1
D1101001 |
Second Faculty of Medicine
class
Biology I.
+1
D1102338 |
Second Faculty of Medicine
class
Biology II.
+1
D1103040 |
Second Faculty of Medicine
class
Medical biology I
+1
DA0102337 |
Second Faculty of Medicine
class
Medical Biology II
+1
DA0103039 |
Second Faculty of Medicine
class
Medical biology and human genetics
D09010005 |
Second Faculty of Medicine
class
OS - Advances in Molecular Genetics
+1
DV01079 |
Second Faculty of Medicine
Load more classes (7)
Publications
publication
The expression of PAX5, p53 immunohistochemistry and p53 mutation analysis in superficial bladder carcinoma tissue. Correlation with pathological findings and clinical outcome
2003 |
Second Faculty of Medicine
publication
DNA Methylation and Neoplasia
2000 |
Second Faculty of Medicine
publication
Human and Mouse XAP-5 and XAP-5-Like (X5L) Genes: Identification of an Ancient Functional Retroposon Differentially Expressed in Testis
1999 |
Second Faculty of Medicine
publication
Tumor suppressor genes
1997 |
Second Faculty of Medicine
publication
Oncogenes and the malignancy process
1996 |
Second Faculty of Medicine
publication
A method for detection of germinal mutations in the p53 tumor suppressor gene
1996 |
Second Faculty of Medicine
publication
Highly conserved 3' UTR and expression pattern of FXR1 points to a divergent gene regulation of FXR1 and FMR1
1995 |
Second Faculty of Medicine
publication
Disruption of OVOL2 Distal Regulatory Elements as a Possible Mechanism Implicated in Corneal Endothelial Dystrophy
2024 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features
2024 |
Second Faculty of Medicine
publication
A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype-phenotype correlation
2023 |
First Faculty of Medicine, Second Faculty of Medicine
Load more publications (108)
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