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cytochrome-c
Person
Class
Person
Publication
Programmes
prof. MUDr. Jiří Zeman DrSc.
Academic staff at First Faculty of Medicine
5 classes
661 publications
Classes
class
Paediatrics for Students of Stomatology
+1
B00137 |
First Faculty of Medicine
class
Intesive Care in Paediatrics 1
B01566 |
First Faculty of Medicine
class
Intensive care in paediatrics 2
B01579 |
First Faculty of Medicine
class
Intensive care in paediatrics and neonatology
B02961 |
First Faculty of Medicine
Publications
publication
High-resolution melting analysis of 15 genes in 60 patients with cytochrome-c oxidase deficiency
2012 |
First Faculty of Medicine
publication
YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferation
2012 |
First Faculty of Medicine
publication
Myoclonic Epilepsy and Deafness in Siblings with the 7512T>C Mutation in the Mitochondrial Encoded tRNA(Ser(UCN)) Gene - Case Reports
2010 |
First Faculty of Medicine, Faculty of Science, Faculty of Physical Education and Sport, Faculty of Medicine in Hradec Králové
publication
Myoclonic Epilepsy and Deafness in Siblings with the 7512T > C Mutation in the Mitochondrial Encoded tRNA(Ser(UCN)) Gene - Case Reports
2010 |
First Faculty of Medicine
publication
Mitochondrial DNA content and expression of genes involved in mtDNA transcription, regulation and maintenance during human fetal development
2010 |
First Faculty of Medicine
publication
Sco2 Protein Deficiency-Based Mitochondrial Encephalomyopathy with the SMA-like Picture of Neurogenic Muscle Atrophy - Case Reports
2010 |
First Faculty of Medicine
publication
Assembly factors and ATP- dependent proteases in cytochrome c oxidase biogenesis
2010 |
First Faculty of Medicine
publication
Ultrastructural and functional abnormalities of mitochondria in cultivated fibroblasts from alpha-mannosidosis patients
2009 |
First Faculty of Medicine
publication
Cytochrome C oxidase deficiency in childhood
2009 |
First Faculty of Medicine
publication
SURF1 missense mutations promote a mild Leigh phenotype
2009 |
First Faculty of Medicine
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