J. Mercer

发表

Rat ceruloplasmin. Molecular cloning and gene expression in liver, choroid plexus, yolk sac, placenta, and testis.

A. Aldred, G. Schreiber, A. Grimes, 1987, The Journal of biological chemistry.

Copper-transporting P-type ATPase, ATP7A, confers multidrug resistance and its expression is related to resistance to SN-38 in clinical colon cancer.

S. Owatari, K. Tsujikawa, T. Aikou, 2007, Cancer research.

Copper levels are increased in the cerebral cortex and liver of APP and APLP2 knockout mice

C. Masters, A. Bush, G. Multhaup, 1999, Brain Research.

Copper metabolism of astrocytes

R. Dringen, J. Mercer, Ivo F Scheiber, 2013, Front. Aging Neurosci..

Clusterin and COMMD1 Independently Regulate Degradation of the Mammalian Copper ATPases ATP7A and ATP7B*

L. Klomp, J. Mercer, S. Materia, 2011, The Journal of Biological Chemistry.

Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease.

P. Lockhart, D. Newgreen, A. Grimes, 1997, Human molecular genetics.

Copper-regulated Trafficking of the Menkes Disease Copper ATPase Is Associated with Formation of a Phosphorylated Catalytic Intermediate*

I. Voskoboinik, J. Camakaris, Byung-Eun Kim, 2002, The Journal of Biological Chemistry.

Correction of a mouse model of Menkes disease by the human Menkes gene.

J. Mercer, Bi-Xia Ke, R. Llanos, 2006, Biochimica et biophysica acta.

Two apparent molecular weight forms of human and monkey phenylalanine hydroxylase are due to phosphorylation.

R. Cotton, B. Kemp, J. Mercer, 1984, The Journal of biological chemistry.

Mammalian copper-transporting P-type ATPases, ATP7A and ATP7B: emerging roles.

J. Mercer, M Leigh Ackland, Sharon La Fontaine, 2010, The international journal of biochemistry & cell biology.

Role of Glutaredoxin1 and Glutathione in Regulating the Activity of the Copper-transporting P-type ATPases, ATP7A and ATP7B*

D. Richardson, Yu Yu, J. Mercer, 2010, The Journal of Biological Chemistry.

Copper transport during lactation in transgenic mice expressing the human ATP7A protein.

M. Linder, D. Freestone, J. Mercer, 2008, Biochemical and biophysical research communications.

ATP7B Expression in Human Breast Epithelial Cells Is Mediated by Lactational Hormones

J. Camakaris, M. Linder, D. Freestone, 2008, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Copper dyshomoeostasis in Parkinson's disease: implications for pathogenesis and indications for novel therapeutics.

K. Double, Katherine M. Davies, J. Mercer, 2016, Clinical science.

Oral Treatment with CuII(atsm) Increases Mutant SOD1 In Vivo but Protects Motor Neurons and Improves the Phenotype of a Transgenic Mouse Model of Amyotrophic Lateral Sclerosis

Blaine R. Roberts, James L. Hickey, C. Masters, 2014, The Journal of Neuroscience.

Oral Treatment with Cu [ superscript II ] ( atsm ) Increases Mutant SOD 1 In Vivo but Protects Motor Neurons and Improves the Phenotype of a Transgenic Mouse Model of Amyotrophic Lateral Sclerosis

James L. Hickey, C. Masters, A. Bush, 2014 .

Defective localization of the Wilson disease protein (ATP7B) in the mammary gland of the toxic milk mouse and the effects of copper supplementation.

K. Allen, J. Mercer, A. Michalczyk, 2000, The Biochemical journal.

Localization of copper and copper transporters in the human brain.

K. Double, G. Halliday, D. Hare, 2013, Metallomics : integrated biometal science.

Investigating copper‐regulated protein expression in Menkes fibroblasts using antibody microarrays

C. Masters, A. Bush, R. Cherny, 2008, Proteomics.

Cloning and expression analysis of the sheep ceruloplasmin cDNA.

P. Lockhart, J. Mercer, 1999, Gene.

Functional analysis of the sheep Wilson disease protein (sATP7B) in CHO cells.

P. Lockhart, J. Mercer, 2001, European journal of cell biology.

Expression, localisation and hormone regulation of the human copper transporter hCTR1 in placenta and choriocarcinoma Jeg-3 cells.

Y. Kuo, E. Wallace, J. Mercer, 2006, Placenta.

Differential expression of ATP7A, ATP7B and CTR1 in adult rat dorsal root ganglion tissue

M. McKeage, J. Mercer, Johnson J. Liu, 2010, Molecular pain.

Isolation of a human ceruloplasmin cDNA clone that includes the N‐terminal leader sequence

A. Grimes, J. Mercer, 1986, FEBS letters.

Selection of a cDNA clone which contains the complete coding sequence for the mature form of ornithine transcarbamylase from rat liver: expression of the cloned protein in Escherichia coli. Molecular cloning of rat ornithine transcarbamylase.

P. Hudson, M. G. Peterson, J. Mercer, 1984, European journal of biochemistry.

A phosphoglycerate mutase brain isoform (PGAM 1) pseudogene is localized within the human Menkes disease gene (ATP7 A).

T. Glover, J. Mercer, H. Dierick, 1997, Gene.

Chronological changes in tissue copper, zinc and iron in the toxic milk mouse and effects of copper loading

K. Allen, N. Buck, J. Mercer, 2006, Biometals.

Copper Transporter ATP7A Protects Against Endothelial Dysfunction in Type 1 Diabetic Mice by Regulating Extracellular Superoxide Dismutase

M. Ushio-Fukai, N. Urao, T. Fukai, 2013, Diabetes.

DB121228 3839..3850

M. Ushio-Fukai, N. Urao, T. Fukai, 2013 .

Stability of protein and mRNA in human postmortem liver--analysis by two-dimensional gel electrophoresis.

R. Cotton, D. Danks, J. Mercer, 1987, Clinica chimica acta; international journal of clinical chemistry.

Copper-induced trafficking of the Cu-ATPases: A key mechanism for copper homeostasis

J. Mercer, Natalie L Barnes, R. Llanos, 2003, Biometals.

Differential expression of four linked sheep metallothionein genes.

M. G. Peterson, J. Mercer, M. Peterson, 1988, European journal of biochemistry.

Cloning, mapping and expression analysis of the sheep Wilson disease gene homologue.

P. Lockhart, J. Mercer, H. Dahl, 2000, Biochimica et biophysica acta.

Antithrombin III mRNA in adult rat liver and kidney and in rat liver during development.

J. Mercer, S. E. D'Souza, 1987, Biochemical and biophysical research communications.

Isolation and sequence of a cDNA clone which contains the complete coding region of rat phenylalanine hydroxylase. Structural homology with tyrosine hydroxylase, glucocorticoid regulation, and use of alternate polyadenylation sites.

H. Dahl, J. Mercer, 1986, The Journal of biological chemistry.

Biochemical and Molecular Roles of Nutrients Hepatic MetallothioneÃ¬n Gene Expression in Toxic Milk Mice1

J. Mercer, A. Rauch, C. Mackinnon, 1992 .

Developmental variation in copper, zinc and metallothionein mRNA in brindled mutant and nutritionally copper deficient mice.

D. Danks, J. Camakaris, J. Mercer, 1991, Biochimica et biophysica acta.

Phenylalanine hydroxylase gene haplotypes in Polynesians: evolutionary origins and absence of alleles associated with severe phenylketonuria.

H. Dahl, R. Trent, J. Mercer, 1989, American journal of human genetics.

Eukaryotic expression vectors that replicate to low copy number in bacteria: transient expression of the Menkes protein.

P. Lockhart, J. Mercer, S. Firth, 1998, Plasmid.

Neuronal expression of copper transporter 1 in rat dorsal root ganglia: association with platinum neurotoxicity

M. McKeage, S. Jamieson, J. Mercer, 2009, Cancer Chemotherapy and Pharmacology.

Menkes syndrome and animal models.

J. Mercer, 1998, The American journal of clinical nutrition.

Contributions of rat Ctr1 to the uptake and toxicity of copper and platinum anticancer drugs in dorsal root ganglion neurons.

Q. Ding, M. McKeage, J. Mercer, 2013, Biochemical pharmacology.

Author ' s personal copy Contributions of rat Ctr 1 to the uptake and toxicity of copper and platinum anticancer drugs in dorsal root ganglion neurons

M. McKeage, J. Mercer, Nancy N. Jong, 2013 .

A total extract dot blot hybridization procedure for mRNA quantitation in small samples of tissues or cultured cells.

A. Grimes, J. Mercer, H. McArdle, 1988, Analytical biochemistry.

The effect of D-penicillamine on metallothionein mRNA levels and copper distribution in mouse hepatocytes.

D. Danks, H. Mcardle, P. Kyriakou, 1990, Chemico-biological interactions.

A comparison of the chromatographic properties of various polyadenylate binding materials.

J. Mercer, H. Naora, 1975, Journal of chromatography.

Copper: effects of deficiency and overload.

R. Dringen, J. Mercer, Ivo F Scheiber, 2013, Metal ions in life sciences.

Identification of the copper chaperone SAH in Ovis aries: expression analysis and in vitro interaction of SAH with ATP7B.

P. Lockhart, J. Mercer, Julian F. B. Mercer, 2000, Biochimica et biophysica acta.

Correction of the Copper Transport Defect of Menkes Patient Fibroblasts by Expression of the Menkes and Wilson ATPases*

P. Lockhart, R. Reddel, A. Englezou, 1998, The Journal of Biological Chemistry.

Expression of the Menkes gene homologue in mouse tissues lack of effect of copper on the mRNA levels

P. Lockhart, A. Grimes, J. Mercer, 1994, FEBS letters.

Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice

P. Lockhart, T. Glover, A. Grimes, 1994, Nature Genetics.

Zinc, Copper and Metallothionein mRNA in Sheep Liver during Development

D. Danks, A. Grimes, J. Mercer, 1988 .

Structure and regulation of the sheep metallothionein-Ia gene.

J. Mercer, M. Peterson, 1986, European journal of biochemistry.

Variation in the amounts of hepatic copper, zinc and metallothionein mRNA during development in the rat.

A. Grimes, J. Mercer, 1986, The Biochemical journal.

The molecular basis of copper-transport diseases.

J. Mercer, Julian F. B. Mercer, 2001, Trends in molecular medicine.

Trafficking of the copper-ATPases, ATP7A and ATP7B: role in copper homeostasis.

J. Mercer, S. La Fontaine, 2007, Archives of biochemistry and biophysics.

The Role of GMXCXXC Metal Binding Sites in the Copper-induced Redistribution of the Menkes Protein*

P. Lockhart, J. Mercer, S. Firth, 1999, The Journal of Biological Chemistry.

Copper in disorders with neurological symptoms: Alzheimer’s, Menkes, and Wilson diseases

G. Multhaup, W. Stremmel, H. Dieter, 2001, Brain Research Bulletin.

Effect of the toxic milk mutation (tx) on the function and intracellular localization of Wnd, the murine homologue of the Wilson copper ATPase.

R. Parton, R. Gould, J. Mercer, 2001, Human molecular genetics.

Gene amplification of the Menkes (MNK; ATP7A) P-type ATPase gene of CHO cells is associated with copper resistance and enhanced copper efflux.

P. Lockhart, T. Glover, P. Shen, 1995, Human molecular genetics.

Effects of cellular copper content on copper uptake and metallothionein and ceruloplasmin mRNA levels in mouse hepatocytes.

D. Danks, H. Mcardle, J. Mercer, 1990, The Journal of nutrition.

The Menkes copper transporter is required for the activation of tyrosinase.

J. Mercer, M. Petris, J F Mercer, 2000, Human molecular genetics.

Two new sulphur-containing amino acids in man.

R. Cotton, D. Danks, J. Hammond, 1981, Biomedical mass spectrometry.

Effects of ATP7A overexpression in mice on copper transport and metabolism in lactation and gestation

M. Linder, J. Mercer, Yuanyuan Chu, 2014, Physiological reports.

Alteration of copper physiology in mice overexpressing the human Menkes protein ATP7A.

J. Mercer, R. Llanos, Magali Wright, 2006, American journal of physiology. Regulatory, integrative and comparative physiology.

Copper Transport and Its Disorders

J. Mercer, A. Leone, 1999, Advances in Experimental Medicine and Biology.

Cloning and characterization of cutE, a gene involved in copper transport in Escherichia coli

J. Camakaris, M. Bhave, J. Mercer, 1991, Journal of bacteriology.

The development of phenylalanine hydroxylase in rat liver; in vivo, and in vitro studies utilizing fetal hepatocyte cultures.

E. Edkins, H. Dahl, G. Yeoh, 1988, Differentiation; research in biological diversity.

Isolation of a partial candidate gene for Menkes disease by positional cloning

Thomas W. Glover, Paul Lockhart, P. Lockhart, 1993, Nature Genetics.

The toxic milk mouse is a murine model of Wilson disease.

D W Cox, D. Cox, J. Mercer, 1996, Human molecular genetics.

Nonsense-mediated mRNA decay of collagen –emerging complexity in RNA surveillance mechanisms

Yiwen Fang, J. Bateman, J. Mercer, 2013, Journal of Cell Science.

Metabolism and functions of copper in brain

R. Dringen, J. Mercer, Ivo F Scheiber, 2014, Progress in Neurobiology.

Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy.

T. Ferguson, T. Bird, S. Kaler, 2010, American journal of human genetics.

The sheep metallothionein gene family. Structure, sequence and evolutionary relationship of five linked genes.

F. Hannan, J. Mercer, M. Peterson, 1988, European journal of biochemistry.

beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformations.

G. Brown, R. Cotton, D. Danks, 1982, Pediatrics.

A Single PDZ Domain Protein Interacts with the Menkes Copper ATPase, ATP7A

J. Mercer, Sarah E M Stephenson, S. La Fontaine, 2005, Journal of Biological Chemistry.

Functional analysis of the Menkes protein (MNK) expressed from a cDNA construct.

P. Lockhart, J. Camakaris, J. Mercer, 1999, Advances in experimental medicine and biology.

Copper pathology in vulnerable brain regions in Parkinson's disease

R. Ortega, K. Double, G. Halliday, 2014, Neurobiology of Aging.

Conditionally immortalized mouse hepatocytes for use in liver gene therapy

R. Whitehead, J. Mercer, R. Williamson, 2000, Journal of gastroenterology and hepatology.

Copper accumulation by cultured astrocytes

R. Dringen, J. Mercer, Ivo F Scheiber, 2010, Neurochemistry International.

Liver cell transplantation leads to repopulation and functional correction in a mouse model of Wilson's disease

K. Allen, J. Mercer, P. Wright, 2004, Journal of gastroenterology and hepatology.

A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network.

J. Camakaris, J. Mercer, M. Petris, 1998, Human molecular genetics.

Copper Transporting P-Type ATPases in the Brain

J. Camakaris, J. Mercer, S. Fontaine, 2012 .

Regulation of 5-aminolevulinate synthase mRNA in different rat tissues.

C. Elferink, J. Mercer, B. May, 1988, The Journal of biological chemistry.

Molecular Basis of Diseases of Copper Homeostasis

J. Camakaris, J. Mercer, D. R. Kramer, 2002 .

Animal models of Menkes disease.

S. Horton, A. Grimes, J. Mercer, 1999, Advances in experimental medicine and biology.

Menkes’ and Wilson’s Diseases: Genetic Disorders of Copper Transport

J. Camakaris, J. Mercer, 1998 .

An analysis of the rate of metallothionein mRNA poly(A)-shortening using RNA blot hybridization.

J. Mercer, S. Wake, 1985, Nucleic acids research.

Poly(A) sequences in plant polysomal RNA.

T. Higgins, J. Mercer, P. Goodwin, 1973, Nature: New biology.

ATP7B mediates vesicular sequestration of copper: insight into biliary copper excretion.

J. Mercer, M. Cater, S. La Fontaine, 2006, Gastroenterology.

Characterizing the molecular phenotype of an Atp7a(T985I) conditional knock in mouse model for X-linked distal hereditary motor neuropathy (dHMNX).

S. Züchner, C. Speck-Martins, G. Nicholson, 2016, Metallomics : integrated biometal science.

Copper comes of age in Melbourne.

J. Camakaris, J. Mercer, 2016, Metallomics : integrated biometal science.

Clusterin (Apolipoprotein J), a Molecular Chaperone That Facilitates Degradation of the Copper-ATPases ATP7A and ATP7B*

L. Klomp, J. Mercer, S. Materia, 2011, The Journal of Biological Chemistry.

Intracellular copper deficiency increases amyloid-beta secretion by diverse mechanisms.

A. Bush, Qiao-Xin Li, I. Volitakis, 2008, The Biochemical journal.

ATP7A transgenic and nontransgenic mice are resistant to high copper exposure.

J. Mercer, R. Llanos, Bi-xia Ke, 2008, The Journal of nutrition.

ATP 7 A Transgenic and Nontransgenic Mice Are Resistant to High Copper Exposure 1 – 3

J. Mercer, R. Llanos, Bi-xia Ke, 2008 .

Copper binding to the N-terminal metal-binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B).

J. Mercer, M. Cater, S. La Fontaine, 2007, The Biochemical journal.

Copper-dependent interaction of glutaredoxin with the N termini of the copper-ATPases (ATP7A and ATP7B) defective in Menkes and Wilson diseases.

J. Mercer, M. Cater, S. La Fontaine, 2006, Biochemical and biophysical research communications.

Copper-dependent Interaction of Dynactin Subunit p62 with the N Terminus of ATP7B but Not ATP7A*

J. Mercer, M. Cater, S. La Fontaine, 2006, Journal of Biological Chemistry.

Expression and localization of menkes and Wilson copper transporting ATPases in human placenta.

E. Wallace, J. Mercer, U. Manuelpillai, 2004, Placenta.

Intracellular trafficking of the human Wilson protein: the role of the six N-terminal metal-binding sites.

D. Cox, J. Forbes, J. Mercer, 2004, The Biochemical journal.

The Menkes protein (ATP7A; MNK) cycles via the plasma membrane both in basal and elevated extracellular copper using a C-terminal di-leucine endocytic signal.

J. Mercer, M. Petris, 1999, Human molecular genetics.

Expression of Menkes disease gene in mammary carcinoma cells.

E. J. Cornish, A. Grimes, J. Mercer, 1997, The Biochemical journal.

The molecular basis of copper homeostasis copper-related disorders.

J. Mercer, R. Llanos, 2002, DNA and cell biology.

Cloning and sequencing of a sheep metallothionein cDNA.

D. Danks, J. Mercer, I. Lazdins, 1984, European journal of biochemistry.

Hormonal regulation of the Menkes and Wilson copper-transporting ATPases in human placental Jeg-3 cells.

J. Camakaris, J. Mercer, A. Michalczyk, 2007, The Biochemical journal.

Understanding the mechanism and function of copper P-type ATPases.

I. Voskoboinik, J. Camakaris, J. Mercer, 2002, Advances in protein chemistry.

Functional Analysis of the N-terminal CXXC Metal-binding Motifs in the Human Menkes Copper-transporting P-type ATPase Expressed in Cultured Mammalian Cells*

I. Voskoboinik, J. Camakaris, J. Mercer, 1999, The Journal of Biological Chemistry.

The Potential of Bone Marrow Stem Cells to Correct Liver Dysfunction in a Mouse Model of Wilson's Disease

J. Vadolas, P. Ioannou, K. Allen, 2004, Cell Transplantation.

Purification and membrane reconstitution of catalytically active Menkes copper-transporting P-type ATPase (MNK; ATP7A).

Ya Hui Hung, M. Layton, I. Voskoboinik, 2007, The Biochemical journal.

Endosomal trafficking of the Menkes copper ATPase ATP7A is mediated by vesicles containing the Rab7 and Rab5 GTPase proteins.

C. Bucci, M. Torrisi, O. Moltedo, 2003, Experimental cell research.

Lack of ceruloplasmin expression alters aspects of copper transport to the fetus and newborn, as determined in mice

M. Linder, J. Mercer, Y. Chu, 2011, BioMetals.

Altered intracellular localization and valosin-containing protein (p97 VCP) interaction underlie ATP7A-related distal motor neuropathy.

S. Kaler, J. Garbern, M. Kennerson, 2012, Human molecular genetics.

Copper in mammals: mechanisms of homeostasis and pathophysiology

J. Mercer, M. Cater, 2005 .

Kinetic Analysis of the Interaction of the Copper Chaperone Atox1 with the Metal Binding Sites of the Menkes Protein*

G. Multhaup, R. Pipkorn, Gerd Multhaup, 2003, Journal of Biological Chemistry.

A highly basic N‐terminal extension of the mitochondrial matrix enzyme ornithine transcarbamylase from rat liver

P. Hudson, J. Mercer, N. Hoogenraad, 1984, FEBS letters.

Decreased carbonic anhydrase III levels in the liver of the mouse mutant 'toxic milk' (tx) due to copper accumulation.

M. Bhave, A. Grimes, J. Mercer, 1997, Biochemical Journal.

Hepatic ceruloplasmin gene expression is unaltered in the toxic milk mouse.

D. Danks, A. Grimes, J. Mercer, 1991, The Journal of nutrition.

The primary structure of the imported mitochondrial protein, ornithine transcarbamylase from rat liver: mRNA levels during ontogeny.

P. Hudson, J. Mercer, N. Hoogenraad, 1985, DNA.

Lack of ceruloplasmin expression alters aspects of copper transport to the fetus and newborn, as determined in mice

M. Linder, J. Mercer, Y. Chu, 2012, BioMetals.

Heterozygous tx mice have an increased sensitivity to copper loading: Implications for Wilson’s disease carriers

C. Chow, K. Allen, N. Buck, 2007, BioMetals.

Molecular and cellular aspects of copper transport in developing mammals.

J. Mercer, R. Llanos, 2003, The Journal of nutrition.

The pathology and trace element status of the toxic milk mutant mouse.

J. Mercer, J. M. Howell, 1994, Journal of comparative pathology.

The murine mutation, lethal milk, results in production of zinc-deficient milk.

J. Mercer, M. Ackland, 1992, The Journal of nutrition.

Copper transport and its disorders : molecular and cellular aspects

J. Mercer, A. Leone, 1999 .

Copper induction of translatable metallothionein messenger RNA

D. Danks, J. Camakaris, J. Mercer, 1981, Bioscience reports.

Mutational Analysis of the Copper ATpase Affected in Menkes Disease

J. Mercer, D. Strausak, L. Ambrosini, 1999 .

Copper exposure induces trafficking of the menkes protein in intestinal epithelium of ATP7A transgenic mice.

J. Mercer, R. Llanos, D. R. Kramer, 2005, The Journal of nutrition.

Defective copper-induced trafficking and localization of the Menkes protein in patients with mild and copper-treated classical Menkes disease.

J. Mercer, L. Ambrosini, Julian F. B. Mercer, 1999, Human molecular genetics.

Intracellular Localization and Loss of Copper Responsiveness of Mnk, the Murine Homologue of the Menkes Protein, in Cells from Blotchy (Moblo) and Brindled (Mobr) Mouse Mutants

P. Lockhart, J. Camakaris, J. Mercer, 1999 .

Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutants.

P. Lockhart, J. Camakaris, J. Mercer, 1999, Human molecular genetics.

The cell biology of the Menkes disease protein.

J. Camakaris, J. Mercer, M. Petris, 1999, Advances in experimental medicine and biology.

Molecular structure of the Menkes disease gene (ATP7A).

T. Glover, J. Spencer, J. Mercer, 1995, Genomics.

Expression of the Human Menkes ATPase in Xenopus laevis Oocytes

K. Bissig, M. Solioz, J. Mercer, 2001, Biological chemistry.

The effect of streptozotocin-induced diabetes on phenylalanine hydroxylase expression in rat liver.

M. J. Fisher, A. K. Green, H. Dahl, 1989, The Biochemical journal.

Molecular mechanisms of copper homeostasis.

I. Voskoboinik, J. Camakaris, J. Mercer, 1999, Biochemical and biophysical research communications.

Copper metabolism of astrocytes

R. Dringen, J. Mercer, Ivo F Scheiber, 2013, Front. Aging Neurosci..

A 37‐year‐old Menkes disease patient—Residual ATP7A activity and early copper administration as key factors in beneficial treatment

Z. Tümer, L. Møller, S. Bilz, 2017, Clinical genetics.

Cloning of metallothionein cDNA from neonatal rat liver

P. Hudson, J. Mercer, 1982, Bioscience reports.

The W and L allelic forms of phenylalanine hydroxylase in the rat differ by a threonine to isoleucine substitution.

J. Mercer, I. Walker, W. Mcadam, 1986, The Biochemical journal.

Induction of metallothionein mRNA in rat liver and kidney after copper chloride injection.

J. Mercer, S. Wake, 1985, The Biochemical journal.

Hepatic metallothionein gene expression in toxic milk mice.

A. Grimes, J. Mercer, H. Rauch, 1992, The Journal of nutrition.

Molecular biology of phenylalanine hydroxylase

R. Cotton, D. Danks, I. Jennings, 1986, Journal of Inherited Metabolic Disease.

Intracellular copper deficiency increases amyloid-beta secretion by diverse mechanisms.

A. Bush, Qiao-Xin Li, I. Volitakis, 2008, The Biochemical journal.