Katalog der Deutschen Nationalbibliothek

Neuigkeiten

Leichte Bedienung, intuitive Suche: Die Betaversion unseres neuen Katalogs ist online! → Zur Betaversion des neuen DNB-Katalogs

 
Neuigkeiten Noch nicht die passende Literatur gefunden? → Book a Librarian
 
 
 


Ergebnis der Suche nach: "" and "RUSTIN" and "Pierre"
im Bestand: Gesamter Bestand

1 - 10 von 18
<< < > >>


Artikel 1 Lipin1 deficiency causes sarcoplasmic reticulum stress and chaperone‐responsive myopathy
Enthalten in European Molecular Biology Organization: The EMBO journal Bd. 38, 2019, Nr. 1. 21 S.
Online Ressource
Artikel 2 Succinate detection using in vivo 1H-MR spectroscopy identifies germline and somatic SDHx mutations in paragangliomas
Enthalten in European journal of nuclear medicine and molecular imaging 13.12.2019: 1-8
Online Ressource
Online Ressourcen 3 Broad AOX expression in a genetically tractable mouse model does not disturb normal physiology
Szibor, Marten. - Frankfurt am Main : Universitätsbibliothek Johann Christian Senckenberg, 2017
Online Ressource
Artikel 4 Expression of the alternative oxidase complements cytochrome c oxidase deficiency in human cells
Enthalten in European Molecular Biology Organization: EMBO molecular medicine Bd. 1, 2009, Nr. 1: 30-36. 7 S.
Online Ressource
Artikel 5 Allotopic expression of a mitochondrial alternative oxidase confers cyanide resistance to human cell respiration
Enthalten in European Molecular Biology Organization: EMBO reports Bd. 7, 2006, Nr. 3: 341-345. 5 S.
Online Ressource
Artikel 6 A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis
Enthalten in Human genetics Bd. 113, Nr. 2, date:7.2003: 118-122
Online Ressource
Artikel 7 Genotyping microsatellite DNA markers at putative disease loci in inbred/multiplex families with respiratory chain complex I deficiency allows rapid identification of a novel nonsense mutation (IVS1nt −1) in the NDUFS4 gene in Leigh syndrome
Enthalten in Human genetics Bd. 112, Nr. 5-6, date:5.2003: 563-566
Online Ressource
Artikel 8 A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency
Enthalten in Human genetics Bd. 104, Nr. 6, date:7.1999: 460-466
Online Ressource
Artikel 9 No mitochondrial cytochrome oxidase (COX) gene mutations in 18 cases of COX deficiency
Enthalten in Human genetics Bd. 101, Nr. 2, date:11.1997: 247-250
Online Ressource
Artikel 10 A homoeostatic switch causing glycerol-3-phosphate and phosphoethanolamine accumulation triggers senescence by rewiring lipid metabolism
Enthalten in Nature metabolism Bd. 6, 19.2.2024, Nr. 2, date:2.2024: 323-342
Online Ressource


1 - 10 von 18
<< < > >>


E-Mail-IconAdministration