Wilson disease and Menkes disease: new handles on heavy-metal transport.

scientific article

Wilson disease and Menkes disease: new handles on heavy-metal transport. is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1016/0168-9525(94)90172-4
P698PubMed publication ID8091505

P50authorPeter C. BullQ47502958
P2093author name stringD W Cox
P433issue7
P921main subjectWilson diseaseQ117121
Menkes diseaseQ639203
P304page(s)246-252
P577publication date1994-07-01
P1433published inTrends in GeneticsQ2451468
P1476titleWilson disease and Menkes disease: new handles on heavy-metal transport
P478volume10

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cites work (P2860)
Q574056787 Menkes and Wilson Diseases
Q41366843A Multicopper oxidase (Cj1516) and a CopA homologue (Cj1161) are major components of the copper homeostasis system of Campylobacter jejuni.
Q91908276A Smart Nanotherapeutic Agent for in vitro and in vivo Reversal of Heavy-Metal-Induced Causality: Key Information from Optical Spectroscopy
Q36806242A chromosomal locus required for copper resistance, competitive fitness, and cytochrome c biogenesis in Pseudomonas fluorescens
Q34181273A combined zinc/cadmium sensor and zinc/cadmium export regulator in a heavy metal pump.
Q79209622A comparison of the mutation spectra of Menkes disease and Wilson disease
Q52546644A copper-responsive transcription factor, CRF1, mediates copper and cadmium resistance in Yarrowia lipolytica.
Q47902129A copper-sensing transcription factor regulates iron uptake genes in Schizosaccharomyces pombe.
Q54151896A mercuric ion uptake role for the integral inner membrane protein, MerC, involved in bacterial mercuric ion resistance.
Q39680275A novel histidine-rich CPx-ATPase from the filamentous cyanobacterium Oscillatoria brevis related to multiple-heavy-metal cotolerance
Q28576397A novel pineal night-specific ATPase encoded by the Wilson disease gene
Q28567311A pineal regulatory element (PIRE) mediates transactivation by the pineal/retina-specific transcription factor CRX
Q42673846ActP controls copper homeostasis in Rhizobium leguminosarum bv. viciae and Sinorhizobium meliloti preventing low pH-induced copper toxicity
Q24300450Alteration of copper physiology in mice overexpressing the human Menkes protein ATP7A
Q41545482An update of hair shaft disorders
Q48537055Analyses of apoptosis and DNA damage in bovine cumulus cells after in vitro maturation with different copper concentrations: consequences on early embryo development.
Q47881123Analysis of functional domains of Wilson disease protein (ATP7B) in Saccharomyces cerevisiae
Q24560198Arabidopsis HMA2, a divalent heavy metal-transporting P(IB)-type ATPase, is involved in cytoplasmic Zn2+ homeostasis
Q33350381Arabidopsis NPCC6/NaKR1 is a phloem mobile metal binding protein necessary for phloem function and root meristem maintenance
Q35966527Bacterial infection as assessed by in vivo gene expression
Q34209269Bacterial mercury resistance from atoms to ecosystems
Q40536101Bacterial resistance mechanisms for heavy metals of environmental concern
Q24323546Biochemical characterization and intracellular localization of the Menkes disease protein
Q24534124Biochemical characterization and subcellular localization of human copper transporter 1 (hCTR1)
Q53648009Cell cycle‐ and age‐dependent activation of Sod1p drives the formation of stress resistant cell subpopulations within clonal yeast cultures
Q27646537Characterization and Structure of a Zn2+ and [2Fe-2S]-containing Copper Chaperone from Archaeoglobus fulgidus
Q36338282Characterization of a cobalt-specific P(1B)-ATPase
Q43029611Characterization of a thermophilic P-type Ag+/Cu+-ATPase from the extremophile Archaeoglobus fulgidus
Q40942795Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization
Q28245045Cloning and characterization of a mammalian proton-coupled metal-ion transporter
Q39505004Cloning and functional analysis of the pbr lead resistance determinant of Ralstonia metallidurans CH34.
Q36790012Cloning and membrane topology of a P type ATPase from Helicobacter pylori
Q48049639Cloning of a cDNA encoding a putative metal-transporting P-type ATPase from Arabidopsis thaliana
Q44124968Cofactors of mitochondrial enzymes attenuate copper-induced death in vitro and in vivo
Q42505747Comparison between copper and cisplatin transport mediated by human copper transporter 1 (hCTR1).
Q42692935Complete sequence of the IncP-9 TOL plasmid pWW0 from Pseudomonas putida
Q38557041Computational gene discovery and human disease
Q27679487Conformations of the apo-, substrate-bound and phosphate-bound ATP-binding domain of the Cu(II) ATPase CopB illustrate coupling of domain movement to the catalytic cycle
Q42479770Cooperative binding of copper(I) to the metal binding domains in Menkes disease protein
Q34214009Copper and genomic stability in mammals
Q40871230Copper deficiency and heart disease: molecular basis, recent advances and current concepts
Q34989940Copper metalloregulation of gene expression
Q41583323Copper-binding motifs in catalysis, transport, detoxification and signaling
Q73726369Copper-regulatory domain involved in gene expression
Q44128397Copper-transporting P-type adenosine triphosphatase (ATP7B) as a cisplatin based chemoresistance marker in ovarian carcinoma: comparative analysis with expression of MDR1, MRP1, MRP2, LRP and BCRP.
Q43861419Copper-transporting P-type adenosine triphosphatase (ATP7B) is expressed in human breast carcinoma
Q53949644Copper-transporting P-type adenosine triphosphatase (ATP7B) is expressed in human gastric carcinoma.
Q27619033Crystal structure of the Atx1 metallochaperone protein at 1.02 A resolution
Q50026458Cu+-specific CopB transporter: Revising P1B-type ATPase classification.
Q33734674Diagnosis of inherited metabolic disorders affecting the nervous system
Q77632386Differential expression of proteins associated with liver transplantation in Wilson's disease patients
Q33992452Diversity of the metal-transporting P1B-type ATPases
Q33786450Dynamic regulation of copper uptake and detoxification genes in Saccharomyces cerevisiae
Q92537828Effect of Dietary Copper on Intestinal Microbiota and Antimicrobial Resistance Profiles of Escherichia coli in Weaned Piglets
Q44100726Evidence for Cu(I)-thiolate ligation and prediction of a putative copper-binding site in the Escherichia coli NADH dehydrogenase-2.
Q36186589Expression Profiling of Solute Carrier Gene Families at the Blood-CSF Barrier
Q78740213Expression of copper-transporting P-type adenosine triphosphatase (ATP7B) as a chemoresistance marker in human oral squamous cell carcinoma treated with cisplatin
Q42683711Full-genome identification and characterization of NBS-encoding disease resistance genes in wheat
Q48261472Functional analysis of mutations in the ATP loop of the Wilson disease copper transporter, ATP7B.
Q28118944Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant?
Q42951282Genes of the copper pathway.
Q95841117Heavy Metal Stress-Associated Proteins in Rice and Arabidopsis: Genome-Wide Identification, Phylogenetics, Duplication, and Expression Profiles Analysis
Q33677490High frequency of two mutations in codon 778 in exon 8 of the ATP7B gene in Taiwanese families with Wilson disease
Q49607298How tapeworm infection and consumption of a Cd and Zn hyperaccumulating plant may affect Cu, Fe, and Mn concentrations in an animal-a plant consumer and tapeworm host.
Q42430117Identification of a hemerythrin-like domain in a P1B-type transport ATPase
Q24671725Identification of cutC and cutF (nlpE) genes involved in copper tolerance in Escherichia coli
Q44703982Identification of ion-selectivity determinants in heavy-metal transport P1B-type ATPases.
Q28681074Insights from the architecture of the bacterial transcription apparatus
Q42123099Intermediate phosphorylation reactions in the mechanism of ATP utilization by the copper ATPase (CopA) of Thermotoga maritima
Q74310623Intracellular distribution of the Wilson's disease gene product (ATPase7B) after in vitro and in vivo exogenous expression in hepatocytes from the LEC rat, an animal model of Wilson's disease
Q78145844Intracellular localization of the Menkes and Wilson's disease proteins and their role in intracellular copper transport
Q74009931Inventory of the superfamily of P-type ion pumps in Arabidopsis
Q40536095Ion efflux systems involved in bacterial metal resistances
Q42030956Iron promotes protein insolubility and aging in C. elegans
Q52165503Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutant.
Q37824297Mass spectrometry as test bench for medicinal chemistry studies
Q73596025Membrane permeability. The diversity of transmembrane transport processes
Q28568699Menkes Copper ATPase (Atp7a) is a novel metal-responsive gene in rat duodenum, and immunoreactive protein is present on brush-border and basolateral membrane domains
Q33678640Menkes disease: recent advances and new aspects
Q41056676Menkes disease: recent advances and new insights into copper metabolism.
Q27650853Metal Binding Domains 3 and 4 of the Wilson Disease Protein: Solution Structure and Interaction with the Copper(I) Chaperone HAH1 † ‡
Q37589510Metal Selectivity of a Cd-, Co-, and Zn-Transporting P1B-type ATPase
Q33902264Metallochaperones, an intracellular shuttle service for metal ions
Q46915826Mitochondrial structure and function in the untreated Jackson toxic milk (tx-j) mouse, a model for Wilson disease
Q41155037Molecular biology of iron acquisition in Saccharomyces cerevisiae
Q42679774Molecular genetics of a chromosomal locus involved in copper tolerance in Escherichia coli K-12.
Q74127971Mutations of ATP7B gene in Wilson disease in Japan: identification of nine mutations and lack of clear founder effect in a Japanese population
Q33407018MytiBase: a knowledgebase of mussel (M. galloprovincialis) transcribed sequences
Q43685909Participation of manganese-superoxide dismutase in the neuroprotection exerted by copper sulfate against 1-methyl 4-phenylpyridinium neurotoxicity
Q33798087Pipes and wiring: the regulation of copper uptake and distribution in yeast.
Q38598305Possible role of trace elements in epilepsy and febrile seizures: a meta-analysis
Q33710864Protein Biochemistry and Expression Regulation of Cadmium/Zinc Pumping ATPases in the Hyperaccumulator Plants Arabidopsis halleri and Noccaea caerulescens.
Q42173716Reaction cycle of Thermotoga maritima copper ATPase and conformational characterization of catalytically deficient mutants
Q43128903Role of N-terminal His-rich domain of Oscillatoria brevis Bxa1 in both Ag(I)/Cu(I) and Cd(II)/Zn(II) tolerance
Q30901949Role of a Candida albicans P1-type ATPase in resistance to copper and silver ion toxicity
Q46802639Sequence variation in the ATP-binding domain of the Wilson disease transporter, ATP7B, affects copper transport in a yeast model system
Q44473349Severe reduction of superoxide dismutase activity in the yeast Saccharomyces cerevisae with the deletion or overexpression of GTS1.
Q64057956Single-Piece Solid Contact Cu-Selective Electrodes Based on a Synthesized Macrocyclic Calix[4]arene Derivative as a Neutral Carrier Ionophore
Q73666078Soluble P-type ATPase from an archaeon, Methanococcus jannaschii
Q54458800Solution structure and intermolecular interactions of the third metal-binding domain of ATP7A, the Menkes disease protein.
Q40610761Structural basis of pathogen recognition by an integrated HMA domain in a plant NLR immune receptor.
Q33878323Structure and chemistry of the copper chaperone proteins
Q34595930Structure of human Wilson protein domains 5 and 6 and their interplay with domain 4 and the copper chaperone HAH1 in copper uptake
Q46958204Structure of the ATP binding domain from the Archaeoglobus fulgidus Cu+-ATPase
Q77754835Structure-function analyses of the ATX1 metallochaperone
Q28575487The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene
Q27935957The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake
Q40875658The N-terminal degenerated metal-binding domain is involved in the heavy metal transport activity of TaHMA2.
Q48075338The Wilson disease gene: spectrum of mutations and their consequences
Q34158270The Wilson's disease gene and phenotypic diversity
Q32064295The catalytic domain of the P-type ATPase has the haloacid dehalogenase fold
Q28366364The copper transporter CTR1 provides an essential function in mammalian embryonic development
Q35546736The many highways for intracellular trafficking of metals
Q28211287The ubiquitously expressed MURR1 protein is absent in canine copper toxicosis
Q41959227Thiamine supplementation attenuated hepatocellular carcinoma in the Atp7b mouse model of Wilson's disease.
Q36432934Toward a molecular understanding of metal transport by P(1B)-type ATPases
Q39496734Toxicity of copper, cobalt, and nickel salts is dependent on histidine metabolism in the yeast Saccharomyces cerevisiae
Q35598944Trace elements in human physiology and pathology. Copper
Q64057698Transcriptome Analysis Reveals Cotton () Genes That Are Differentially Expressed in Cadmium Stress Tolerance
Q24812330Transport of toxic metals by molecular mimicry
Q33728768Transposon Tn21, flagship of the floating genome
Q28609373Two forms of Wilson disease protein produced by alternative splicing are localized in distinct cellular compartments
Q44193580Valproic acid increases biliary copper excretion in the rat.
Q55670524Whispering dysphonia in an Australian family (DYT4): a clinical and genetic reappraisal
Q77814544Wilson's disease: presymptomatic patients and Kayser-Fleischer rings
Q50946053Wilson's disease: presymptomatic patients and Kayser-Fleischer rings.
Q34506792Yeast superoxide dismutase mutants reveal a pro-oxidant action of weak organic acid food preservatives
Q30333096Zn(II) metabolism in prokaryotes.

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