UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 228

Sortiert nach

Interactions in the Metabolism of Glutamate and the Branched-Chain Amino Acids and Ketoacids in the CNS

Neurochemical research, 2017-01, Vol.42 (1), p.10-18

Yudkoff, Marc

2017

Volltextzugriff (PDF)

Beyond aerobic glycolysis: Transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis

Proceedings of the National Academy of Sciences - PNAS, 2007-12, Vol.104 (49), p.19345-19350

2007

Volltextzugriff (PDF)

Myc Regulates a Transcriptional Program That Stimulates Mitochondrial Glutaminolysis and Leads to Glutamine Addiction

Proceedings of the National Academy of Sciences - PNAS, 2008-12, Vol.105 (48), p.18782-18787

2008

Volltextzugriff (PDF)

A role for bacterial urease in gut dysbiosis and Crohn's disease

Science translational medicine, 2017-11, Vol.9 (416)

2017

Volltextzugriff (PDF)

Inborn error of metabolism patients after liver transplantation: Outcomes of 35 patients over 27 years in one pediatric quaternary hospital

American journal of medical genetics. Part A, 2022-05, Vol.188 (5), p.1443-1447

2022

Volltextzugriff (PDF)

Ketosis and brain handling of glutamate, glutamine, and GABA

Epilepsia (Copenhagen), 2008-11, Vol.49 (s8), p.73-75

2008

Volltextzugriff (PDF)

ASL expression in ALDH1A1+ neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype

Human genetics, 2021-10, Vol.140 (10), p.1471-1485

2021

Volltextzugriff (PDF)

Compartmentation of Brain Glutamate Metabolism in Neurons and Glia

The Journal of nutrition, 2000-04, Vol.130 (4), p.1026S-1031S

2000

Volltextzugriff (PDF)

The Molecular and Metabolic Influence of Long Term Agmatine Consumption

The Journal of biological chemistry, 2014-04, Vol.289 (14), p.9710-9729

2014

Volltextzugriff (PDF)

Brain metabolism of branched-chain amino acids

Glia, 1997-09, Vol.21 (1), p.92-98

Yudkoff, Marc

1997

Volltextzugriff (PDF)

Inflammation-induced preterm birth alters neuronal morphology in the mouse fetal brain

Journal of neuroscience research, 2010-07, Vol.88 (9), p.1872-1881

2010

Volltextzugriff (PDF)

Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy

Orphanet journal of rare diseases, 2019-08, Vol.14 (1), p.198-198, Article 198

2019

Volltextzugriff (PDF)

Augmenting Ureagenesis in Patients with Partial Carbamyl Phosphate Synthetase 1 Deficiency with N-carbamyl- l -glutamate

The Journal of pediatrics, 2014-08, Vol.165 (2), p.401-403.e3

2014

Volltextzugriff (PDF)

Phenotypes of undiagnosed adults with actionable OTC and GLA variants

HGG advances, 2023-10, Vol.4 (4), p.100226-100226, Article 100226

2023

Volltextzugriff (PDF)

Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease

PLoS genetics, 2008-04, Vol.4 (4), p.e1000061-e1000061

2008

Volltextzugriff (PDF)

Ifosfamide-induced nephrotoxicity: mechanism and prevention

Cancer research (Chicago, Ill.), 2006-08, Vol.66 (15), p.7824-7831

2006

Volltextzugriff (PDF)

N-carbamylglutamate enhancement of ureagenesis leads to discovery of a novel deleterious mutation in a newly defined enhancer of the NAGS gene and to effective therapy

Human mutation, 2011-10, Vol.32 (10), p.1153-1160

2011

Volltextzugriff (PDF)

A Signaling Role of Glutamine in Insulin Secretion

The Journal of biological chemistry, 2004-04, Vol.279 (14), p.13393-13401

2004

Volltextzugriff (PDF)

Very Long-Chain Acyl-CoA Dehydrogenase Deficiency in a Patient with Normal Newborn Screening by Tandem Mass Spectrometry

The Journal of pediatrics, 2010-03, Vol.156 (3), p.492-494

2010

Volltextzugriff (PDF)

Regulation of Leucine-stimulated Insulin Secretion and Glutamine Metabolism in Isolated Rat Islets

The Journal of biological chemistry, 2003-01, Vol.278 (5), p.2853-2858

2003

Volltextzugriff (PDF)

Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium

Molecular genetics and metabolism, 2010, Vol.100 (Suppl 1), p.S97-S105

2010

Volltextzugriff (PDF)

Proteolytic Degradation of Tyrosine Nitrated Proteins

Archives of biochemistry and biophysics, 2000-08, Vol.380 (2), p.360-366

2000

Volltextzugriff (PDF)

Muscle oxidative phosphorylation quantitation using creatine chemical exchange saturation transfer (CrCEST) MRI in mitochondrial disorders

JCI insight, 2016-11, Vol.1 (18), p.e88207-e88207

2016

Volltextzugriff (PDF)

Manifestations of OXCT1 heterozygosity

Molecular genetics and metabolism, 2024-04, Vol.141 (4), p.108343, Article 108343

2024

Volltextzugriff (PDF)

Ketogenic diet, amino acid metabolism, and seizure control

Journal of neuroscience research, 2001-12, Vol.66 (5), p.931-940

2001

Volltextzugriff (PDF)

1 – 25 von 228

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(221)
Mit Volltextzugriff
(212)

Publikationsform

Artikel
(225)
Buchkapitel
(3)

Sprache

Englisch
(228)
Japanisch
(29)

Erscheinungsjahr

n.n

Thema

Science & Technology
(139)
Life Sciences & Biomedicine
(133)
Humans
(95)
Animals
(82)
Male
(72)
Biological And Medical Sciences
(51)
Female
(46)
Biochemistry & Molecular Biology
(44)
Rats
(40)
Neurosciences & Neurology
(39)
Neurosciences
(35)
Child
(30)
Fundamental And Applied Biological Sciences. Psychology
(30)
Adult
(29)
Genetics & Heredity
(29)
Pediatrics
(28)
Medical Sciences
(25)
Infant
(24)
Medicine, Research & Experimental
(24)
Nitrogen Isotopes
(24)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Interactions in the Metabolism of Glutamate and the Branched-Chain Amino Acids and Ketoacids in the CNS

Beyond aerobic glycolysis: Transformed cells can engage in glutamine metabolism that exceeds the requirement for protein and nucleotide synthesis

Myc Regulates a Transcriptional Program That Stimulates Mitochondrial Glutaminolysis and Leads to Glutamine Addiction

A role for bacterial urease in gut dysbiosis and Crohn's disease

Inborn error of metabolism patients after liver transplantation: Outcomes of 35 patients over 27 years in one pediatric quaternary hospital

Ketosis and brain handling of glutamate, glutamine, and GABA

ASL expression in ALDH1A1+ neurons in the substantia nigra metabolically contributes to neurodegenerative phenotype

Compartmentation of Brain Glutamate Metabolism in Neurons and Glia

The Molecular and Metabolic Influence of Long Term Agmatine Consumption

Brain metabolism of branched-chain amino acids

Inflammation-induced preterm birth alters neuronal morphology in the mouse fetal brain

Early diagnosis of infantile-onset lysosomal acid lipase deficiency in the advent of available enzyme replacement therapy

Augmenting Ureagenesis in Patients with Partial Carbamyl Phosphate Synthetase 1 Deficiency with N-carbamyl- l -glutamate

Phenotypes of undiagnosed adults with actionable OTC and GLA variants

Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease

Ifosfamide-induced nephrotoxicity: mechanism and prevention

N-carbamylglutamate enhancement of ureagenesis leads to discovery of a novel deleterious mutation in a newly defined enhancer of the NAGS gene and to effective therapy

A Signaling Role of Glutamine in Insulin Secretion

Very Long-Chain Acyl-CoA Dehydrogenase Deficiency in a Patient with Normal Newborn Screening by Tandem Mass Spectrometry

Regulation of Leucine-stimulated Insulin Secretion and Glutamine Metabolism in Isolated Rat Islets

Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium

Proteolytic Degradation of Tyrosine Nitrated Proteins

Muscle oxidative phosphorylation quantitation using creatine chemical exchange saturation transfer (CrCEST) MRI in mitochondrial disorders

Manifestations of OXCT1 heterozygosity

Ketogenic diet, amino acid metabolism, and seizure control

Suchergebnisse filtern