Katalog der Deutschen Nationalbibliothek

Gesamter Bestand

Musikarchiv

Buchmuseum

Suchformular zurücksetzen

Expertensuche ?

Noch nicht die passende Literatur gefunden? → Book a Librarian

Bitte beachten Sie unsere geänderten Servicezeiten ab dem 1. November 2024.

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

1 - 10 von 22

	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.
	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
	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
	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.
	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.
	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
	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
	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
	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
	10	Clinical presentations and laboratory investigations in respiratory chain deficiency Enthalten in Zeitschrift für Kinderheilkunde Bd. 155, Nr. 4, date:4.1996: 262-274

1 - 10 von 22

Alle Materialarten

Alle Standorte > Leipzig (22)

Aktionen