Pages that link to "Q117121"
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The following pages link to Wilson disease (Q117121):
Displaying 50 items.
- liver cirrhosis (Q147778) (← links)
- triethylenetetramine (Q418386) (← links)
- D-penicillamine (Q421239) (← links)
- Wilson's temperature syndrome (Q12238717) (← links)
- ATP7B (Q14913328) (← links)
- The Wilson disease protein ATP7B resides in the late endosomes with Rab7 and the Niemann-Pick C1 protein (Q24293217) (← links)
- The distinct functional properties of the nucleotide-binding domain of ATP7B, the human copper-transporting ATPase: analysis of the Wilson disease mutations E1064A, H1069Q, R1151H, and C1104F (Q24297174) (← links)
- Binding of copper(I) by the Wilson disease protein and its copper chaperone (Q24304146) (← links)
- Solution structure of the N-domain of Wilson disease protein: distinct nucleotide-binding environment and effects of disease mutations (Q24310820) (← links)
- The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene (Q24336948) (← links)
- Interaction of the copper chaperone HAH1 with the Wilson disease protein is essential for copper homeostasis (Q24650387) (← links)
- Molecular mechanism of copper transport in Wilson disease (Q24812338) (← links)
- Congential scoliosis in Wilson's disease: case report and review of the literature (Q27003325) (← links)
- Rapid and reliable diagnosis of Wilson disease using X-ray fluorescence (Q27338256) (← links)
- Metal Binding Domains 3 and 4 of the Wilson Disease Protein: Solution Structure and Interaction with the Copper(I) Chaperone HAH1 † ‡ (Q27650853) (← links)
- Solution structures of the actuator domain of ATP7A and ATP7B, the Menkes and Wilson disease proteins (Q27656799) (← links)
- A new hepatocytic isoform of PLZF lacking the BTB domain interacts with ATP7B, the Wilson disease protein, and positively regulates ERK signal transduction (Q28116074) (← links)
- Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant? (Q28118944) (← links)
- Treatment of Wilson disease with ammonium tetrathiomolybdate: III. Initial therapy in a total of 55 neurologically affected patients and follow-up with zinc therapy (Q28182653) (← links)
- The copper toxicosis gene product Murr1 directly interacts with the Wilson disease protein (Q28206233) (← links)
- A practice guideline on Wilson disease (Q28207512) (← links)
- Analysis of the human homologue of the canine copper toxicosis gene MURR1 in Wilson disease patients (Q28267679) (← links)
- The copper-transporting ATPases, menkes and wilson disease proteins, have distinct roles in adult and developing cerebellum (Q28301263) (← links)
- Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: genomic organization, alternative splicing, and structure/function predictions (Q28306096) (← links)
- Treatment of Wilson disease with ammonium tetrathiomolybdate: IV. Comparison of tetrathiomolybdate and trientine in a double-blind study of treatment of the neurologic presentation of Wilson disease (Q28306528) (← links)
- Increased p53 mutation load in nontumorous human liver of wilson disease and hemochromatosis: oxyradical overload diseases (Q28344887) (← links)
- Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation (Q28505378) (← links)
- Phenotype-genotype correlation in Wilson disease in a large Lebanese family: association of c.2299insC with hepatic and of p. Ala1003Thr with neurologic phenotype (Q28544874) (← links)
- Liver cell death and anemia in Wilson disease involve acid sphingomyelinase and ceramide (Q28570052) (← links)
- The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene (Q28575487) (← links)
- A novel pineal night-specific ATPase encoded by the Wilson disease gene (Q28576397) (← links)
- Defective localization of the Wilson disease protein (ATP7B) in the mammary gland of the toxic milk mouse and the effects of copper supplementation (Q28592976) (← links)
- Consequences of copper accumulation in the livers of the Atp7b-/- (Wilson disease gene) knockout mice (Q28594419) (← links)
- Two forms of Wilson disease protein produced by alternative splicing are localized in distinct cellular compartments (Q28609373) (← links)
- Wilzin (Q29006676) (← links)
- Functional characterization of new mutations in Wilson disease gene (ATP7B) using the yeast model (Q29346870) (← links)
- Treatment of Wilson Disease With Ammonium Tetrathiomolybdate (Q29396107) (← links)
- Stability and ATP binding of the nucleotide-binding domain of the Wilson disease protein: effect of the common H1069Q mutation. (Q30371296) (← links)
- Encephalopathy in Wilson disease: copper toxicity or liver failure? (Q30389756) (← links)
- Cloning and characterization of the promoter region of the Wilson disease gene (Q30634175) (← links)
- A review and current perspective on Wilson disease (Q30907824) (← links)
- Clinical correlates of cerebral water diffusion in Wilson disease (Q31032317) (← links)
- Decreased bone density, elevated serum osteoprotegerin, and beta-cross-laps in Wilson disease (Q31117495) (← links)
- Copper transport and its defect in Wilson disease: characterization of the copper-binding domain of Wilson disease ATPase (Q31388417) (← links)
- A mutation of the Wilson disease protein, ATP7B, is degraded in the proteasomes and forms protein aggregates (Q32086009) (← links)
- Neurological features and management of Wilson disease in children: an evaluation of 12 cases (Q33167081) (← links)
- Proteomic analyzes of copper metabolism in an in vitro model of Wilson disease using surface enhanced laser desorption/ionization-time of flight-mass spectrometry (Q33211033) (← links)
- Diminution of toxic copper accumulation in toxic milk mice modeling Wilson disease by embryonic hepatocyte intrasplenic transplantation (Q33217543) (← links)
- Bone mineral density of children with Wilson disease: efficacy of penicillamine and zinc therapy (Q33315628) (← links)
- Albumin dialysis: effective removal of copper in a patient with fulminant Wilson disease and successful bridging to liver transplantation: a new possibility for the elimination of protein-bound toxins (Q33330971) (← links)