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...

Chronic hepatitis without hepatic steatosis caused by citrin deficiency in a child

Hepatology research, 2016-04, Vol.46 (4), p.357-362

2016

Volltextzugriff (PDF)

Adult-onset type II citrullinemia manifested as hepatosteatosis or steatohepatitis: A report of three Chinese cases

Journal of digestive diseases, 2022-04, Vol.23 (4), p.240-245

2022

Volltextzugriff (PDF)

Deficiency of the mitochondrial transporter of aspartate/glutamate aralar/AGC1 causes hypomyelination and neuronal defects unrelated to myelin deficits in mouse brain

Journal of neuroscience research, 2011-12, Vol.89 (12), p.2008-2017

2011

Volltextzugriff (PDF)

Low levels of citrin (SLC25A13) expression in adult mouse brain restricted to neuronal clusters

Journal of neuroscience research, 2010-04, Vol.88 (5), p.1009-1016

2010

Volltextzugriff (PDF)

AGC1‐malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway

Journal of neurochemistry, 2013-02, Vol.124 (3), p.347-362

2013

Volltextzugriff (PDF)

Role of aralar, the mitochondrial transporter of aspartate-glutamate, in brain N-acetylaspartate formation and Ca2+ signaling in neuronal mitochondria

Journal of neuroscience research, 2007-11, Vol.85 (15), p.3359-3366

2007

Volltextzugriff (PDF)

Metabolic derangements in deficiency of citrin, a liver-type mitochondrial aspartate–glutamate carrier

Hepatology research, 2005-10, Vol.33 (2), p.181-184

2005

Volltextzugriff (PDF)

Histological findings in the livers of patients with neonatal intrahepatic cholestasis caused by citrin deficiency

Hepatology research, 2010-03, Vol.40 (3), p.295-303

2010

Volltextzugriff (PDF)

Effectiveness of carbohydrate-restricted diet and arginine granules therapy for adult-onset type II citrullinemia: a case report of siblings showing homozygous SLC25A13 mutation with and without the disease

Hepatology research, 2003-05, Vol.26 (1), p.68-72

2003

Volltextzugriff (PDF)

Adult‐onset type II citrullinemia manifested as hepatosteatosis or steatohepatitis: A report of three Chinese cases

Journal of digestive diseases, 2022-04, Vol.23 (4), p.240-245

2022

Volltextzugriff (PDF)

A possible mechanism of neonatal intrahepatic cholestasis caused by citrin deficiency

Hepatology research, 2005-03, Vol.31 (3), p.168-171

2005

Volltextzugriff (PDF)

Role of aralar, the mitochondrial transporter of aspartate-glutamate, in brain N-acetylaspartate formation and Ca(2+) signaling in neuronal mitochondria

Journal of neuroscience research, 2007-11, Vol.85 (15), p.3359-3366

2007

Volltextzugriff (PDF)

Long-chain fatty acids suppress the induction of urea cycle enzyme genes by glucocorticoid action

FEBS letters, 1996-12, Vol.399 (3), p.310-312

1996

Volltextzugriff (PDF)

Orthotopic liver transplantation for urea cycle enzyme deficiency

Hepatology (Baltimore, Md.), 1992-03, Vol.15 (3), p.419-422

1992

Volltextzugriff (PDF)

AGC 1‐malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway

Journal of neurochemistry, 2013-02, Vol.124 (3), p.347-362

2013

Volltextzugriff (PDF)

Pancreatic secretory trypsin inhibitor gene is highly expressed in the liver of adult-onset type II citrullinemia

FEBS letters, 1995-09, Vol.372 (1), p.69-73

1995

Volltextzugriff (PDF)

Pyruvate dehydrogenase kinase 4 mRNA is increased in the hypertrophied ventricles of carnitine-deficient juvenile visceral steatosis (JVS) mice

BioFactors (Oxford), 1999, Vol.10 (2-3), p.301-309

1999

Volltextzugriff (PDF)

Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations

Human mutation, 2002-02, Vol.19 (2), p.122-130

2002

Volltextzugriff (PDF)

Immunocytochemical localization of argininosuccinate synthetase in the rat brain

Journal of comparative neurology (1911), 1991-10, Vol.312 (4), p.652-679

1991

Volltextzugriff (PDF)

Molecular cloning and expression of human caldecrin

FEBS letters, 1996-05, Vol.386 (1), p.26-28

1996

Volltextzugriff (PDF)

Ten novel mutations of the ornithine transcarbamylase (OTC) gene in OTC deficiency

Human mutation, 1998, Vol.11 (S1), p.S5-S7

1998

Volltextzugriff (PDF)

Adult-onset type II citrullinemia associated with idopathic hypertriglyceridemia as a preceding feature

Journal of gastroenterology and hepatology, 2006-10, Vol.21 (10), p.1634-1635

2006

Volltextzugriff (PDF)

Role of aralar, the mitochondrial transporter of aspartate‐glutamate, in brain N‐acetylaspartate formation and Ca 2+ signaling in neuronal mitochondria

Journal of neuroscience research, 2007-11, Vol.85 (15), p.3359-3366

2007

Volltextzugriff (PDF)

Feasibility of auxiliary partial orthotopic liver transplantation from living donors for patients with adult‐onset type II citrullinemia

Liver transplantation, 2004-04, Vol.10 (4), p.550-554

2004

Volltextzugriff (PDF)

1 – 25 von 50

Suche als RSS-Feed

Aktive Filter

KollektionWiley Online Library Full Collection 2018

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(45)
Mit Volltextzugriff
(45)

Publikationsform

Artikel
(45)
Berichte
(5)

Sprache

Englisch
(50)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

Wiley Online Library Journals Frontfile Complete
(50)
Journals@Ovid Complete
(49)
MEDLINE
(32)
Ingenta
(24)
Free E-Journal (出版社公開部分のみ）
(19)
Elsevier ScienceDirect Journals Complete
(14)
IngentaConnect Journals
(3)
JSTOR
(1)
SAGE Complete
(1)

4 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Chronic hepatitis without hepatic steatosis caused by citrin deficiency in a child

Adult-onset type II citrullinemia manifested as hepatosteatosis or steatohepatitis: A report of three Chinese cases

Deficiency of the mitochondrial transporter of aspartate/glutamate aralar/AGC1 causes hypomyelination and neuronal defects unrelated to myelin deficits in mouse brain

Low levels of citrin (SLC25A13) expression in adult mouse brain restricted to neuronal clusters

AGC1‐malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway

Role of aralar, the mitochondrial transporter of aspartate-glutamate, in brain N-acetylaspartate formation and Ca2+ signaling in neuronal mitochondria

Metabolic derangements in deficiency of citrin, a liver-type mitochondrial aspartate–glutamate carrier

Histological findings in the livers of patients with neonatal intrahepatic cholestasis caused by citrin deficiency

Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients

Effectiveness of carbohydrate-restricted diet and arginine granules therapy for adult-onset type II citrullinemia: a case report of siblings showing homozygous SLC25A13 mutation with and without the disease

Adult‐onset type II citrullinemia manifested as hepatosteatosis or steatohepatitis: A report of three Chinese cases

A possible mechanism of neonatal intrahepatic cholestasis caused by citrin deficiency

Role of aralar, the mitochondrial transporter of aspartate-glutamate, in brain N-acetylaspartate formation and Ca(2+) signaling in neuronal mitochondria

Long-chain fatty acids suppress the induction of urea cycle enzyme genes by glucocorticoid action

Orthotopic liver transplantation for urea cycle enzyme deficiency

AGC 1‐malate aspartate shuttle activity is critical for dopamine handling in the nigrostriatal pathway

Pancreatic secretory trypsin inhibitor gene is highly expressed in the liver of adult-onset type II citrullinemia

Pyruvate dehydrogenase kinase 4 mRNA is increased in the hypertrophied ventricles of carnitine-deficient juvenile visceral steatosis (JVS) mice

Screening of SLC25A13 mutations in early and late onset patients with citrin deficiency and in the Japanese population: Identification of two novel mutations and establishment of multiple DNA diagnosis methods for nine mutations

Immunocytochemical localization of argininosuccinate synthetase in the rat brain

Molecular cloning and expression of human caldecrin

Ten novel mutations of the ornithine transcarbamylase (OTC) gene in OTC deficiency

Adult-onset type II citrullinemia associated with idopathic hypertriglyceridemia as a preceding feature

Role of aralar, the mitochondrial transporter of aspartate‐glutamate, in brain N‐acetylaspartate formation and Ca 2+ signaling in neuronal mitochondria

Feasibility of auxiliary partial orthotopic liver transplantation from living donors for patients with adult‐onset type II citrullinemia

Aktive Filter

Suchergebnisse filtern