(Q34559789)

3 August 2017

1 reference

title

Mechanisms of liver injury relevant to pediatric hepatology (English)

1 reference

3 August 2017

Tanner MS

1

1 reference

3 August 2017

publication date

1 February 2002

1 reference

Critical Reviews in Clinical Laboratory Sciences

3 August 2017

published in

1 reference

3 August 2017

volume

39

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3 August 2017

issue

1

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3 August 2017

page(s)

1-61

1 reference

Venoocclusive liver disease (VOD) as a complication of Wilms' tumour management in the series of consecutive 206 patients.

3 August 2017

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Alagille syndrome. The widening spectrum of arteriohepatic dysplasia

21 January 2018

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Biology of hepatic stellate cells and their possible relevance in the pathogenesis of portal hypertension in cirrhosis

21 January 2018

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Carbon monoxide: an endogenous modulator of sinusoidal tone in the perfused rat liver

21 January 2018

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Carbon monoxide as a regulator of bile canalicular contractility in cultured rat hepatocytes

21 January 2018

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Zonation of parenchymal and nonparenchymal metabolism in liver

21 January 2018

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https://api.crossref.org/works/10.1080%2F10408360290795439

Oxygen: modulator of metabolic zonation and disease of the liver

21 January 2018

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https://api.crossref.org/works/10.1080%2F10408360290795439

Apoptosis in diseases of the liver

21 January 2018

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Apoptosis and liver diseases: recent concepts of mechanism and significance

21 January 2018

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https://api.crossref.org/works/10.1080%2F10408360290795439

Lethal effect of the anti-Fas antibody in mice

21 January 2018

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https://api.crossref.org/works/10.1080%2F10408360290795439

The hepatic stellate (Ito) cell: its role in human liver disease

21 January 2018

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https://api.crossref.org/works/10.1080%2F10408360290795439

Hepatic stellate (ITO) cells: expanding roles for a liver-specific pericyte

21 January 2018

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https://api.crossref.org/works/10.1080%2F10408360290795439

Na+/H+ exchange and growth factor-induced cytosolic pH changes. Role in cellular proliferation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Rat liver myofibroblasts and hepatic stellate cells: different cell populations of the fibroblast lineage with fibrogenic potential

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Nitric oxide in liver injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Mechanisms of nitric oxide-dependent apoptosis: involvement of mitochondrial mediators

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Nitric oxide induces apoptosis via triggering mitochondrial permeability transition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The TNF receptor superfamily of cellular and viral proteins: activation, costimulation, and death

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The mitochondrial permeability transition is required for tumor necrosis factor alpha-mediated apoptosis and cytochrome c release

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Dissection of TNF receptor 1 effector functions: JNK activation is not linked to apoptosis while NF-kappaB activation prevents cell death

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Reactive oxygen and mechanisms of inflammatory liver injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Liver complications of pediatric parenteral nutrition--epidemiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The hepatic microvascular responses to sepsis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The role of chemokines in the immunopathology of the liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Pathophysiological roles of interleukin-18 in inflammatory liver diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The liver as a crucial organ in the first line of host defense: the roles of Kupffer cells, natural killer (NK) cells and NK1.1 Ag+ T cells in T helper 1 immune responses

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Early-onset liver disease complicated with acute liver failure in Alstrom syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Nonalcoholic Steatohepatitis in Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Prospective evaluation of alcohol abuse and alcoholic liver injury in men as predictors of development of cirrhosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Obesity increases sensitivity to endotoxin liver injury: implications for the pathogenesis of steatohepatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Mitochondrial abnormalities in non-alcoholic steatohepatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Nonalcoholic steatohepatitis: association of insulin resistance and mitochondrial abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Free fatty acid effects on mitochondrial permeability: an overview

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Palmitic acid opens a novel cyclosporin A-insensitive pore in the inner mitochondrial membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

A pilot study of a thiazolidinedione, troglitazone, in nonalcoholic steatohepatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Severe cholestatic hepatitis from troglitazone in a patient with nonalcoholic steatohepatitis and diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Metabolic and nutritional considerations in nonalcoholic fatty liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Aflatoxin excretion in children with kwashiorkor or marasmic kwashiorkor--a clinical investigation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Aflatoxin Exposure and its Relationship to Kwashiorkor in African Children

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Susceptibility to autoimmune chronic active hepatitis: human leukocyte antigens DR4 and A1-B8-DR3 are independent risk factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Autoimmune chronic active hepatitis in a family

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Inadequate antibody response to hBAg or suppressor T-cell defect in development of active chronic hepatitis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Autoimmune hepatitis type 2 induced by HCV and persisting after viral clearance

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Epstein-Barr virus as a trigger for autoimmune hepatitis in susceptible individuals

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Autoantibodies in liver disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

International Autoimmune Hepatitis Group Report: review of criteria for diagnosis of autoimmune hepatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Plasma membrane cytochromes P450 as neoantigens and autoimmune targets in drug-induced hepatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Liver/kidney microsomal antibody type 1 targets CYP2D6 on hepatocyte plasma membrane.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Recognition of uridine diphosphate glucuronosyl transferases by LKM-3 antibodies in chronic hepatitis D.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Identification of target antigen for SLA/LP autoantibodies in autoimmune hepatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Soluble liver antigen: isolation of a 35-kd recombinant protein (SLA-p35) specifically recognizing sera from patients with autoimmune hepatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Autoantibodies against a serine tRNA-protein complex implicated in cotranslational selenocysteine insertion

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

A bioinformatical approach suggests the function of the autoimmune hepatitis target antigen soluble liver antigen/liver pancreas

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Direct ex vivo analysis of hepatitis B virus-specific CD8(+) T cells associated with the control of infection

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

H-2(d) mice born to and reared by HBeAg-transgenic mothers do not develop T cell tolerance toward the hepatitis B virus core gene products

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Pathogenesis of chronic hepatitis C: immunological features of hepatic injury and viral persistence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Cellular immune responses persist and humoral responses decrease two decades after recovery from a single-source outbreak of hepatitis C

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Hepatitis C virus in multiple episodes of acute hepatitis in polytransfused thalassaemic children

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Prevalence of non-organ-specific autoantibodies and chronic liver disease in the general population: a nested case-control study of the Dionysos cohort

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The outcome of acute hepatitis C predicted by the evolution of the viral quasispecies

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Analysis of a successful immune response against hepatitis C virus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Analysis of successful immune responses in persons infected with hepatitis C virus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

LKM-1 autoantibodies recognize a short linear sequence in P450IID6, a cytochrome P-450 monooxygenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Cytochromes P450 and uridine triphosphate-glucuronosyltransferases: model autoantigens to study drug-induced, virus-induced, and autoimmune liver disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

N-acetyltransferases: pharmacogenetics and clinical consequences of polymorphic drug metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Role of biotransformation in conceptal toxicity of drugs and other chemicals

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Normal thymic architecture and negative selection are associated with Aire expression, the gene defective in the autoimmune-polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Mutations in the AIRE gene: effects on subcellular location and transactivation function of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Isolation and characterization of the mouse Aire gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The APECED polyglandular autoimmune syndrome protein, AIRE-1, contains the SAND domain and is probably a transcription factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The autoimmune regulator protein has transcriptional transactivating properties and interacts with the common coactivator CREB-binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Lafora disease: a progressive myoclonus epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Lafora's disease: towards a clinical, pathologic, and molecular synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Heteropolymerization of S, I, and Z alpha1-antitrypsin and liver cirrhosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Protein misfolding and degradation in genetic diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

A lag in intracellular degradation of mutant alpha 1-antitrypsin correlates with the liver disease phenotype in homozygous PiZZ alpha 1-antitrypsin deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The Niemann-Pick C lesion and its relationship to the intracellular distribution and utilization of LDL cholesterol

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Cessation of rapid late endosomal tubulovesicular trafficking in Niemann-Pick type C1 disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Dynamic movements of organelles containing Niemann-Pick C1 protein: NPC1 involvement in late endocytic events

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Genotype-phenotype relationship of Niemann-Pick disease type C: a possible correlation between clinical onset and levels of NPC1 protein in isolated skin fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Evidence for a Niemann-pick C (NPC) gene family: identification and characterization of NPC1L1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Type 1 hereditary tyrosinemia. Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patient

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Genetic control of morphogenetic and biochemical differentiation: Lethal albino deletions in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

In vivo suppressor mutations correct a murine model of hereditary tyrosinemia type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Hepatocyte injury in tyrosinemia type 1 is induced by fumarylacetoacetate and is inhibited by caspase inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Deficient DNA-ligase activity in the metabolic disease tyrosinemia type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Tyrosinaemia type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione).

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Different clinical forms of hereditary tyrosinemia (type I) in patients with identical genotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Purified hematopoietic stem cells can differentiate into hepatocytes in vivo.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Komrower Lecture. Galactosaemia today: the enigma and the challenge.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Galactose metabolism in mice with galactose-1-phosphate uridyltransferase deficiency: sucklings and 7-week-old animals fed a high-galactose diet

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Metabolic depletion of ATP by fructose inversely controls CD95- and tumor necrosis factor receptor 1-mediated hepatic apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Neonatal screening for hereditary fructose intolerance: frequency of the most common mutant aldolase B allele (A149P) in the British population

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Hereditary fructose intolerance

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Mitochondrial respiratory chain disorders and the liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Valproic acid hepatic fatalities. III. U.S. experience since 1986.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Valproate-induced liver failure in one of two siblings with Alpers disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Inappropriate liver transplantation in a child with Alpers-Huttenlocher syndrome misdiagnosed as valproate-induced acute liver failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Orthotopic liver transplantation with poor neurologic outcome in valproate-associated liver failure: a need for critical risk-benefit appraisal in the use of valproate

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Fatal liver failure associated with valproate therapy in a patient with Friedreich's disease: review of valproate hepatotoxicity in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Medium chain acyl-CoA dehydrogenase deficiency and fatal valproate toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Alpers progressive infantile neuronal poliodystrophy: an acute neonatal form with findings of the fetal akinesia syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Fatal deterioration of neurological disease after orthotopic liver transplantation for valproic acid-induced liver damage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Depletion of mitochondrial DNA associated with infantile cholestasis and progressive liver fibrosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Secondary respiratory chain defect in a boy with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: possible diagnostic pitfalls

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Liver disease in pregnancy and fetal fatty acid oxidation defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

A broad spectrum of clinical presentations in congenital disorders of glycosylation I: a series of 26 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Phosphomannose isomerase deficiency: a carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Structure and chemistry of the copper chaperone proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The copper chaperone Atox1 in canine copper toxicosis in Bedlington terriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Interaction of the copper chaperone HAH1 with the Wilson disease protein is essential for copper homeostasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Structure, expression, and chromosomal localization of the mouse Atox1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The copper chaperone for superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The copper chaperone CCS directly interacts with copper/zinc superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The copper chaperone CCS is abundant in neurons and astrocytes in human and rodent brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Molecular cloning and characterization of a copper chaperone for copper/zinc superoxide dismutase from the rat

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The mitochondrial copper metallochaperone Cox17 exists as an oligomeric, polycopper complex.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Isolation of a cDNA encoding the human homolog of COX17, a yeast gene essential for mitochondrial copper recruitment

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Copper-dependent trafficking of Wilson disease mutant ATP7B proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Fulminant hepatic failure resulting from coexistent Wilson's disease and hepatitis E

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Toxic milk, a new mutation affecting cooper metabolism in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The toxic milk mouse is a murine model of Wilson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Functional studies on the Wilson copper P-type ATPase and toxic milk mouse mutant

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The Long-Evans cinnamon (LEC) rat and copper metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Correction of liver disease following transplantation of normal rat hepatocytes into Long-Evans Cinnamon rats modeling Wilson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Long term survival in Indian childhood cirrhosis treated with D-penicillamine

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The prevention of Indian childhood cirrhosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

First description of "Indian childhood cirrhosis" in a non-Indian infant in Europe

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Copper associated childhood cirrhosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Normal metallothionein synthesis in fibroblasts obtained from children with Indian childhood cirrhosis or copper-associated childhood cirrhosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Hepatic iron storage in very low birthweight infants after multiple blood transfusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Neonatal hemochromatosis: outcomes of pharmacologic and surgical therapies

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Rapid development of hepatocellular siderosis after liver transplantation for neonatal hemochromatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Progressive familial intrahepatic cholestasis. Genetic basis and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Intrahepatic cholestasis: order out of chaos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Identification of a new inborn error in bile acid synthesis: mutation of the oxysterol 7alpha-hydroxylase gene causes severe neonatal liver disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Familial giant cell hepatitis associated with synthesis of 3 beta, 7 alpha-dihydroxy-and 3 beta,7 alpha, 12 alpha-trihydroxy-5-cholenoic acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Lack of 3 beta-hydroxy-delta 5-C27-steroid dehydrogenase/isomerase in fibroblasts from a child with urinary excretion of 3 beta-hydroxy-delta 5-bile acids. A new inborn error of metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The bile acid synthetic gene 3beta-hydroxy-Delta(5)-C(27)-steroid oxidoreductase is mutated in progressive intrahepatic cholestasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Delta 4-3-oxosteroid 5 beta-reductase deficiency described in identical twins with neonatal hepatitis. A new inborn error in bile acid synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Cloning and expression of cDNA of human delta 4-3-oxosteroid 5 beta-reductase and substrate specificity of the expressed enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Clinical and biochemical findings in progressive familial intrahepatic cholestasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Genetic basis of progressive familial intrahepatic cholestasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

A gene encoding a liver-specific ABC transporter is mutated in progressive familial intrahepatic cholestasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Mutations in the MDR3 gene cause progressive familial intrahepatic cholestasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Identification of a locus for progressive familial intrahepatic cholestasis PFIC2 on chromosome 2q24

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease [PFIC-1] and Byler syndrome): evidence for heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Mapping of a locus for progressive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, the benign recurrent intrahepatic cholestasis region

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

The wide spectrum of multidrug resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Heterozygous MDR3 missense mutation associated with intrahepatic cholestasis of pregnancy: evidence for a defect in protein trafficking

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Bile acid-induced rat hepatocyte apoptosis is inhibited by antioxidants and blockers of the mitochondrial permeability transition

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Ursodeoxycholic acid prevents cytochrome c release in apoptosis by inhibiting mitochondrial membrane depolarization and channel formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Progressive infantile poliodystrophy (Alpers' disease) with a defect in citric acid cycle activity in liver and fibroblasts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Copper Storage Disease of the Liver and Chronic Dietary Copper Intoxication in Two Further German Infants Mimicking Indian Childhood Cirrhosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Polymorphism in the Human Complement C4 Genes and Genetic Susceptibility to Autoimmune Hepatitis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

A Kinetic Mechanism for the Polymerization of α1-Antitrypsin

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

Pathogenic α1-Antitrypsin Polymers Are Formed by Reactive Loop-β-Sheet A Linkage

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10408360290795439

10.1080/10408360290795439

21 January 2018

Identifiers

DOI

1 reference

3 August 2017

1 reference