| P50 | author | Yurii S. Aulchenko | Q30348344 |
| P2093 | author name string | Jan Rothuizen | |
| | Alan J Martin | |
| | Roman S Polishchuk | |
| | Bart van de Sluis | |
| | Sha Zhu | |
| | Michael J Petris | |
| | Frank G van Steenbeek | |
| | Peter A J Leegwater | |
| | Bart Spee | |
| | Ted S G A M van den Ingh | |
| | Victoria L Hodgkinson | |
| | Adrian L Watson | |
| | Hille Fieten | |
| | Paola Festa | |
| | Mafalda Concilli | |
| | Giancarlo Chesi | |
| | Yadvinder Gill | |
| | Karen Dirksen | |
| | Ellen C C P Martens | |
| | Roderick H J H Houwen | |
| P2860 | cites work | The domestic dog: man's best friend in the genomic era | Q21184025 |
| | Molecular pathogenesis of Wilson and Menkes disease: correlation of mutations with molecular defects and disease phenotypes | Q24647056 |
| | Human copper transporter 2 is localized in late endosomes and lysosomes and facilitates cellular copper uptake | Q24654300 |
| | A simple salting out procedure for extracting DNA from human nucleated cells | Q27861086 |
| | Kinetic analysis of the interaction of the copper chaperone Atox1 with the metal binding sites of the Menkes protein | Q28189009 |
| | Polymorphisms of metal transporter genes DMT1 and ATP7A in Wilson's disease | Q43655078 |
| | Nutritional management of inherited copper-associated hepatitis in the Labrador retriever | Q46944684 |
| | Further delineation of the molecular pathology of Wilson disease in the Mediterranean population | Q47815023 |
| | The toxic milk mouse is a murine model of Wilson disease | Q48059534 |
| | Wilson disease | Q56518908 |
| | Endemic Tyrolean infantile cirrhosis: an ecogenetic disorder | Q71060712 |
| | Histochemical localization of copper with rubeanic acid | Q74031967 |
| | Hepatocyte-specific localization and copper-dependent trafficking of the Wilson's disease protein in the liver | Q74590949 |
| | The canine copper toxicosis gene MURR1 is not implicated in the pathogenesis of Wilson disease | Q79991322 |
| | New mutations in the Wilson disease gene, ATP7B: implications for molecular testing | Q80974253 |
| | Distinct clinical courses according to presenting phenotypes and their correlations to ATP7B mutations in a large Wilson's disease cohort | Q84284572 |
| | Association of dietary copper and zinc levels with hepatic copper and zinc concentration in Labrador Retrievers | Q85011875 |
| | The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosis | Q28205001 |
| | Identification of a new copper metabolism gene by positional cloning in a purebred dog population | Q28216510 |
| | ImageJ for microscopy | Q28253317 |
| | Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting ATPase | Q28269082 |
| | COMMD1 (MURR1) as a candidate in patients with copper storage disease of undefined etiology | Q28281448 |
| | ATP7A-related copper transport diseases-emerging concepts and future trends | Q28302938 |
| | Conditional knockout of the Menkes disease copper transporter demonstrates its critical role in embryogenesis | Q28482175 |
| | Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation | Q28505378 |
| | Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease | Q28513437 |
| | NH2-terminal signals in ATP7B Cu-ATPase mediate its Cu-dependent anterograde traffic in polarized hepatic cells | Q28575877 |
| | GenABEL: an R library for genome-wide association analysis | Q29614587 |
| | Cardiac copper deficiency activates a systemic signaling mechanism that communicates with the copper acquisition and storage organs | Q33983956 |
| | The Wilson's disease gene and phenotypic diversity | Q34158270 |
| | Spontaneous hepatic copper accumulation in Long-Evans Cinnamon rats with hereditary hepatitis. A model of Wilson's disease | Q34190413 |
| | The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene | Q34348941 |
| | Copper biochemistry and molecular biology | Q34377161 |
| | Role of copper in Indian childhood cirrhosis | Q34468130 |
| | Cellular copper levels determine the phenotype of the Arg875 variant of ATP7B/Wilson disease protein | Q34750429 |
| | Raft-mediated trafficking of apical resident proteins occurs in both direct and transcytotic pathways in polarized hepatic cells: role of distinct lipid microdomains | Q34764402 |
| | Understanding the mechanism and function of copper P-type ATPases | Q34989947 |
| | Critical roles for the COOH terminus of the Cu-ATPase ATP7B in protein stability, trans-Golgi network retention, copper sensing, and retrograde trafficking | Q35087086 |
| | Diagnosis of copper transport disorders | Q35164918 |
| | Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analyses | Q35249090 |
| | Canine models of copper toxicosis for understanding mammalian copper metabolism | Q35745611 |
| | Cell-specific trafficking suggests a new role for renal ATP7B in the intracellular copper storage | Q36292959 |
| | Family-based association tests for genomewide association scans | Q36492206 |
| | A genetic study of Wilson's disease in the United Kingdom | Q36789573 |
| | Reduced expression of ATP7B affected by Wilson disease-causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin | Q39770874 |
| | Functional consequences of RNA interference targeting COMMD1 in a canine hepatic cell line in relation to copper toxicosis | Q40159937 |
| | Wilson disease protein ATP7B utilizes lysosomal exocytosis to maintain copper homeostasis. | Q41156563 |
| | A Simple Method for the Silver Impregnation of Reticulum | Q41944781 |
| | Affinity gradients drive copper to cellular destinations | Q42171712 |
| | Phosphorylation regulates copper-responsive trafficking of the Menkes copper transporting P-type ATPase. | Q42456407 |
| | In silico modeling of the Menkes copper-translocating P-type ATPase 3rd metal binding domain predicts that phosphorylation regulates copper-binding | Q42755592 |
| P275 | copyright license | Creative Commons Attribution 3.0 Unported | Q14947546 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 1 | |
| P921 | main subject | copper | Q753 |
| | Wilson disease | Q117121 |
| P304 | page(s) | 25-38 | |
| P577 | publication date | 2016-01-01 | |
| P1433 | published in | Disease Models & Mechanisms | Q1524006 |
| P1476 | title | The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers: a new canine model for copper-metabolism disorders | |
| P478 | volume | 9 | |