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tumour suppressor genes
Person
Class
Person
Publication
Programmes
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
Medical biology and human genetics
D09010005 |
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
OS - Advances in Molecular Genetics
+1
DV01079 |
Second Faculty of Medicine
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Publications
publication
Li-Fraumeni Syndrome
2003 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
Significance of TP53 gene identification in tumour affected families
2003 |
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
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
publication
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities
2021 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Missense variants in DPYSL5 cause a neurodevelopmental disorder with corpus callosum agenesis and cerebellar abnormalities
2021 |
Second Faculty of Medicine
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