ℹ️
🇬🇧
Search
Search for people relevant for "pseudogene"
pseudogene
Person
Class
Person
Publication
Programmes
Export current view
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
Load more classes (7)
Publications
publication
The human rab GDI beta gene with long retroposon-rich introns maps to 10p15 and its pseudogene to 7p11-p13
1998 |
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
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
publication
Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy
2021 |
Second Faculty of Medicine
publication
Genetics of neurodevelopmental disorders
2021 |
Second Faculty of Medicine
publication
Severe paroxysmal dyskinesias without epilepsy in a RHOBTB2 mutation carrier
2020 |
First Faculty of Medicine, Second Faculty of Medicine
Load more publications (108)
Loading network view...