UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Medical aspects of ketone body metabolism

Clinical and investigative medicine, 1995-06, Vol.18 (3), p.193

1995

Volltextzugriff (PDF)

Interindividual variability and parent of origin DNA methylation differences at specific human Alu elements

Human molecular genetics, 2005-08, Vol.14 (15), p.2135-2143

2005

Volltextzugriff (PDF)

Succinyl CoA: 3-oxoacid CoA transferase (SCOT) : Human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient

American journal of human genetics, 1996-09, Vol.59 (3), p.519-528

1996

Volltextzugriff (PDF)

Inborn errors of ketogenesis

Biochemical Society transactions, 1998-05, Vol.26 (2), p.136-140

1998

Volltextzugriff (PDF)

Excessive formation of hydroxyl radicals and aldehydic lipid peroxidation products in cultured skin fibroblasts from patients with complex I deficiency

The Journal of clinical investigation, 1997-06, Vol.99 (12), p.2877-2882

1997

Volltextzugriff (PDF)

Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT): Cloning of the Human SCOT Gene, Tertiary Structural Modeling of the Human SCOT Monomer, and Characterization of Three Pathogenic Mutations

Genomics (San Diego, Calif.), 2000-09, Vol.68 (2), p.144-151

2000

Volltextzugriff (PDF)

Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: Two pathogenic mutations, V133E and C456F, in Japanese siblings

Human mutation, 1998, Vol.12 (2), p.83-88

1998

Volltextzugriff (PDF)

Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): Development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency

Biochimica et biophysica acta. Molecular basis of disease, 1997-04, Vol.1360 (2), p.151-156

1997

Volltextzugriff (PDF)

Manganese Superoxide Dismutase Levels Are Elevated in a Proportion of Amyotrophic Lateral Sclerosis Patient Cell Lines

Biochemical and biophysical research communications, 2000-06, Vol.273 (1), p.359-363

2000

Volltextzugriff (PDF)

Succinyl CoA:3-Oxoacid CoA transferase (SCOT): Human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient

American journal of human genetics, 1996-01, Vol.59 (3), p.579-528

1996

Volltextzugriff (PDF)

Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency

Biochimica et biophysica acta, 1997-04, Vol.1360 (2), p.151

1997

Volltextzugriff (PDF)

Human imprinted chromosomal regions are historical hot-spots of recombination

PLoS genetics, 2006-07, Vol.2 (7), p.e101

2006

Volltextzugriff (PDF)

Reduction of Clofazimine by Mycobacterial Type 2 NADH:Quinone Oxidoreductase

The Journal of biological chemistry, 2011-03, Vol.286 (12), p.10276-10287

2011

Volltextzugriff (PDF)

Reduction of clofazimine by mycobacterial type 2 NADH:quinone oxidoreductase: a pathway for the generation of bactericidal levels of reactive oxygen species

The Journal of biological chemistry, 2011-03, Vol.286 (12), p.10276-10287

2011

Volltextzugriff (PDF)

Bach1 Modulates Heme Oxygenase-1 Expression in the Neonatal Mouse Lung

Pediatric research, 2009-02, Vol.65 (2), p.145-149

2009

Volltextzugriff (PDF)

Heme Oxygenase‐1 (HO‐1) localizes to the nucleus in hyperoxia

The FASEB journal, 2007, Vol.21 (6), p.A1143-A1144

2007

Volltextzugriff (PDF)

Human Imprinted Chromosomal Regions are Historical Hot-Spots of Recombination

PLoS genetics, 2005, Vol.preprint (2006), p.e101

2005

Volltextzugriff (PDF)

1 – 17 von 17

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(17)
Mit Volltextzugriff
(14)

Publikationsform

Artikel
(17)

Sprache

Englisch
(17)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(12)
Science & Technology
(12)
Humans
(11)
Animals
(5)
Biochemistry & Molecular Biology
(5)
Biological And Medical Sciences
(5)
Coenzyme A-Transferases - Deficiency
(5)
Genetics & Heredity
(5)
Female
(4)
Ketone Bodies - Metabolism
(4)
Medical Sciences
(4)
Sequence Analysis, Dna
(4)
Blotting, Western
(3)
Coenzyme A-Transferases - Genetics
(3)
Male
(3)
Metabolic Diseases
(3)
Amino Acid Sequence
(2)
Biophysics
(2)
Cells, Cultured
(2)
Cloning, Molecular
(2)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Medical aspects of ketone body metabolism

Interindividual variability and parent of origin DNA methylation differences at specific human Alu elements

Succinyl CoA: 3-oxoacid CoA transferase (SCOT) : Human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient

Inborn errors of ketogenesis

Excessive formation of hydroxyl radicals and aldehydic lipid peroxidation products in cultured skin fibroblasts from patients with complex I deficiency

Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT): Cloning of the Human SCOT Gene, Tertiary Structural Modeling of the Human SCOT Monomer, and Characterization of Three Pathogenic Mutations

Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: Two pathogenic mutations, V133E and C456F, in Japanese siblings

Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): Development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency

Manganese Superoxide Dismutase Levels Are Elevated in a Proportion of Amyotrophic Lateral Sclerosis Patient Cell Lines

Succinyl CoA:3-Oxoacid CoA transferase (SCOT): Human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient

Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency

Human imprinted chromosomal regions are historical hot-spots of recombination

Reduction of Clofazimine by Mycobacterial Type 2 NADH:Quinone Oxidoreductase

Reduction of clofazimine by mycobacterial type 2 NADH:quinone oxidoreductase: a pathway for the generation of bactericidal levels of reactive oxygen species

Bach1 Modulates Heme Oxygenase-1 Expression in the Neonatal Mouse Lung

Heme Oxygenase‐1 (HO‐1) localizes to the nucleus in hyperoxia

Human Imprinted Chromosomal Regions are Historical Hot-Spots of Recombination

Suchergebnisse filtern