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Přesná shoda Sémantické

4 záznamů v Medvik

Abstrakt

Genetic deffects of human mitochondrial ATP synthase

Houštěk, Josef, 1947-
Autor Autorita ORCID Institute of Physiology, Academy of Sciences of the Czech Republic, Prague
Klement, Petr
Autor Klement, Petr Institute of Physiology, Academy of Sciences of the Czech Republic, Prague
Floryk, Daniel
Autor Autorita Institute of Physiology, Academy of Sciences of the Czech Republic, Prague
Antonická, Hana
Autor Autorita ORCID Institute of Physiology, Academy of Sciences of the Czech Republic, Prague
Heřmanská, Jana
Autor Heřmanská, Jana Institute of Physiology, Academy of Sciences of the Czech Republic, Prague
Kalous, Martin, 1957-
Autor Autorita Institute of Physiology, Academy of Sciences of the Czech Republic, Prague
Hansíková, Hana
Autor Autorita ORCID Department of Pediatrics, Institute for Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University, Prague
Houšťková, Hana
Autor Houšťková, Hana Department of Pediatrics, Institute for Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University, Prague
Chowdhury, Subir
Autor Chowdhury, Subir Institute of Physiology, Academy of Sciences of the Czech Republic, Prague
Kmoch, Stanislav, 1963-
Autor Autorita ORCID Department of Pediatrics, Institute for Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University, Prague

Chemické listy. 2000 ; 94 (8) : 620-621.

Chem. Listy
ISSN 0009-2770
Medvik
Zdroj

Publikační typ
abstrakt z konference MeSH

Abstrakt

RNA binding proteins specific for mitochondrial ATP synthase β-subunit

Chemické listy. 2000 ; 94 (8) : 621-622.

Chem. Listy
ISSN 0009-2770
Medvik
Zdroj

Publikační typ
abstrakt z konference MeSH

Článek online

A novel deficiency of mitochondrial ATPase of nuclear origin

Human molecular genetics. 1999 ; Roč. 8 (č. 11) : s. 1967-1974.

ISSN 0964-6906
Medvik
Zdroj

MeSH
buněčné jádro genetika MeSH
fibroblasty enzymologie patologie MeSH
kojenec MeSH
lidé MeSH
mitochondrie enzymologie patologie MeSH
mnohočetné abnormality enzymologie etiologie MeSH
novorozenec MeSH
vrozené poruchy metabolismu enzymologie genetika komplikace MeSH
Check Tag
kojenec MeSH
lidé MeSH
novorozenec MeSH
Publikační typ
kazuistiky MeSH

Článek online

Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy with ragged-red fibres ('MERRF') at position

Biochemical journal (London. 1984). 1999 ; Roč. 342 (č. 3) : s. 537-544.

ISSN 0264-6021
Medvik
Zdroj

MeSH
fibroblasty enzymologie patofyziologie MeSH
kinetika MeSH
lidé MeSH
membránové potenciály MeSH
mitochondrie enzymologie genetika patofyziologie MeSH
respirační komplex IV analýza fyziologie MeSH
syndrom MERRF enzymologie genetika MeSH
Check Tag
lidé MeSH