EmPr Julian Mercer

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

Z Tümer, M Petris, S Zhu, J Mercer, J Bukrinski, S Bilz, K Baerlocher, N Horn, L Møller

(2017), Vol. 92, pp. 548-553, Clinical Genetics, London, Eng., C1

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

K Davies, J Mercer, N Chen, K Double

(2016), Vol. 130, pp. 565-574, Clinical science, London, Eng., C1

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

G Perez-Siles, A Grant, M Ellis, C Ly, A Kidambi, M Khalil, R Llanos, S Fontaine, A Strickland, S Züchner, S Bermeo, E Neist, T Brennan-Speranza, R Takata, C Speck-Martins, J Mercer, G Nicholson, M Kennerson

(2016), Vol. 8, pp. 981-992, Metallomics, England, C1

Copper pathology in vulnerable brain regions in Parkinson's disease

K Davies, S Bohic, A Carmona, R Ortega, V Cottam, D Hare, J Finberg, S Reyes, G Halliday, J Mercer, K Double

(2014), Vol. 36, pp. 858-866, Neurobiology of aging, Amsterdam, The Netherlands, C1

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

J Wadwa, Y Chu, N Nguyen, T Henson, A Figueroa, R Llanos, M Ackland, A Michalczyk, H Fullriede, G Brennan, J Mercer, M Linder

(2014), Vol. 2, pp. 1-11, Physiological Reports, Oxford, United Kingdom, C1

Oral treatment with Cu(II)(atsm) increases mutant SOD1 in vivo but protects motor neurons and improves the phenotype of a transgenic mouse model of amyotrophic lateral sclerosis

B Roberts, N Lim, E McAllum, P Donnelly, D Hare, P Doble, B Turner, K Price, S Lim, B Paterson, J Hickey, T Rhoads, J Williams, K Kanninen, L Hung, J Liddell, A Grubman, J Monty, R Llanos, D Kramer, J Mercer, A Bush, C Masters, J Duce, Q Li, J Beckman, K Barnham, A White, P Crouch

(2014), Vol. 34, pp. 8021-8031, Journal of neuroscience, Washington, D.C., C1

Metabolism and functions of copper in brain

I Scheiber, J Mercer, R Dringen

(2014), Vol. 116, pp. 33-57, Progress in neurobiology, London, Eng., C1

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

J Liu, Y Kim, F Yan, Q Ding, V Ip, N Jong, J Mercer, M McKeage

(2013), Vol. 85, pp. 207-215, Biochemical pharmacology, Amsterdam, The Netherlands, C1

Localization of copper and copper transporters in the human brain

K Davies, D Hare, V Cottam, N Chen, L Hilgers, G Halliday, J Mercer, K Double

(2013), Vol. 5, pp. 43-51, Metallomics, Cambridge, England, C1

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

Y Fang, J Bateman, J Mercer, S Lamande

(2013), Vol. 126, pp. 2551-2560, Journal of cell science, Cambridge, England, C1

Copper metabolism of astrocytes

R Dringen, I Scheiber, J Mercer

(2013), Vol. 5, pp. 1-4, Frontiers in aging neuroscience, Lausanne, Switzerland, C1

Copper transporter ATP7A protects against endothelial dysfunction in type 1 diabetic mice by regulating extracellular superoxide dismutase

V Sudhahar, N Urao, J Oshikawa, R McKinney, R Llanos, J Mercer, M Ushio-Fukai, T Fukai

(2013), Vol. 62, pp. 3839-3850, Diabetes, Alexandria, Va., C1-1

Clusterin and COMMD1 independently regulate degradation of the mammalian copper ATPases ATP7A and ATP7B

S Materia, M Cater, L Klomp, J Mercer, S La Fontaine

(2012), Vol. 287, pp. 2485-2499, Journal of biological chemistry, Bethesda, Md., C1

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

L Yi, A Donsante, M Kennerson, J Mercer, J Garbern, S Kaler

(2012), Vol. 21, pp. 1794-1807, Human molecular genetics, Oxford, England, C1

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

Y Chu, E Sauble, A Cabrera, A Roth, M Ackland, J Mercer, M Linder

(2012), Vol. 25, pp. 373-382, BioMetals, Dordrecht, The Netherlands, C1

Clusterin (APOJ) : a molecular chaperone that facilitates degradation of the copper-ATPases ATP7A and ATP7B

S Materia, M Cater, L Klomp, J Mercer, S La Fontaine

(2011), Vol. 286, pp. 10073-10083, Journal of biological chemistry, Bethesda, Md., C1

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

S La Fontaine, M Ackland, J Mercer

(2010), Vol. 42, pp. 206-209, International journal of biochemistry & cell biology, Oxford, England, C1

Role of glutaredoxin1 and glutathione in regulating the activity of the copper-transporting P-type ATPases, ATP7A and ATP7B

W Singleton, K McInnes, M Cater, W Winnall, R McKirdy, Y Yu, P Taylor, B Ke, D Richardson, J Mercer, S La Fontaine

(2010), Vol. 285, pp. 27111-27121, Journal of biological chemistry, Bethesda, Md., C1

Copper accumulation by cultured astrocytes

I Scheiber, J Mercer, R Dringen

(2010), Vol. 56, pp. 451-460, Neurochemistry International, Oxford, England, C1

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

V Ip, J Liu, J Mercer, M McKeage

(2010), Vol. 6, pp. 1-10, Molecular pain, London, England, C1

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

M Kennerson, G Nicholson, S Kaler, B Kowalski, J Mercer, J Tang, R Llanos, S Chu, R Takata, C Speck-Martins, J Baets, L Almeida-Souza, D Fischer, V Timmerman, P Taylor, S Scherer, T Ferguson, T Bird, P De Jonghe, S Feely, M Shy, J Garbern

(2010), Vol. 86, pp. 342-352, American journal of human genetics, Cambridge, Mass., C1-1

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

J Liu, S Jamieson, J Subramaniam, V Ip, N Jong, J Mercer, M McKeage

(2009), Vol. 64, pp. 847-856, Cancer chemotherapy and pharmacology, Berlin, Germany, C1-1

Leptin: Back and Forward

Julian Mercer

(2009), Vol. 21, pp. 1063-1064, JOURNAL OF NEUROENDOCRINOLOGY, United States, C1-1

ATP7B expression in human breast epithelial cells is mediated by lactational hormones

A Michalczyk, E Bastow, M Greenough, J Camakaris, D Freestone, P Taylor, M Linder, J Mercer, M Ackland

(2008), Vol. 56, pp. 389-399, Journal of histochemistry and cytochemistry, Seattle, Wash., C1

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

R Llanos, A Michalczyk, D Freestone, S Currie, M Linder, M Ackland, J Mercer

(2008), Vol. 372, pp. 613-617, Biochemical and biophysical research communications, San Diego, Calif., C1

Intracellular copper deficiency increases amyloid-beta secretion by diverse mechanisms

M Cater, K McInnes, Q Li, I Volitalis, S La Fontaine, J Mercer, A Bush

(2008), Vol. 412, pp. 141-152, Biochemical journal, London, England, C1-1

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

T Du, S La Fontaine, M Abdo, S Bellingham, M Greenough, I Volitakis, R Cherny, A Bush, P Hudson, J Camakaris, J Mercer, P Crouch, C Masters, V Perreau, A White

(2008), Vol. 8, pp. 1819-1831, Proteomics, Weinheim, Germany, C1-1

ATP7A transgenic and nontransgenic mice are resistant to high copper exposure

B Ke, R Llanos, J Mercer

(2008), Vol. 138, pp. 693-697, Journal of nutrition, Bethesda, Md., C1-1

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)

M Cater, S La Fontaine, J Mercer

(2007), Vol. 401, pp. 143-153, Biochemical journal, London, England, C1

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, S Akune, M Komatsu, R Ikeda, S Firth, X Che, M Yamamoto, K Tsujikawa, M Kitazono, T Ishizawa, T Takeuchi, T Aikou, J Mercer, S Akiyama, T Furukawa

(2007), Vol. 67, pp. 4860-4868, Cancer research, Philadelphia, Pa., C1

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

B Hardman, A Michalczyk, M Greenough, J Camakaris, J Mercer, L Ackland

(2007), Vol. 402, pp. 241-250, Biochemical journal, London, England, C1

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

Y Hung, M Layton, I Voskoboinik, J Mercer, J Camakaris

(2007), Vol. 401, pp. 569-579, Biochemical journal, London, England, C1

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

S La Fontaine, J Mercer

(2007), Vol. 463, pp. 149-167, Archives of biochemistry and biophysics, Amsterdam, The Netherlands, C1

Heterozygous tx mice have an increased sensitivity to copper loading: implications for Wilson's Disease carriers

D Cheah, Y Deal, P Wright, N Buck, C Chow, J Mercer, K Allen

(2007), Vol. 20, pp. 751-757, BioMetals, Amsterdam, The Netherlands, C1

Distinct functional roles for the Menkes and Wilson copper translocating P-type ATPases in Human Placental Cells

B Hardman, A Michalczyk, M Greenough, J Camakaris, J Mercer, L Ackland

(2007), Vol. 20, pp. 1073-1084, Cellular physiology and biochemistry, Basel, Switzerland, C1

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

R Llanos, B Ke, M Wright, Y Deal, F Monty, D Kramer, J Mercer

(2006), Vol. 1762, pp. 485-493, Biochimica et biophysica acta (BBA) - molecular basis of disease, Amsterdam, The Netherlands, C1

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

B Hardman, U Manuelpillai, E Wallace, J Monty, D Kramer, Y Kuo, J Mercer, L Ackland

(2006), Vol. 27, pp. 968-977, Placenta, London, England, C1

Copper-dependent interaction of dynactin subunit p62 with the N terminus of ATP7B but not ATP7A

C Lim, M Cater, J Mercer, S La Fontaine

(2006), Vol. 281, pp. 14006-14014, Journal of biological chemistry, Bethesda, Md, C1

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

C Lim, M Cater, J Mercer, S La Fontaine

(2006), Vol. 348, pp. 428-436, Biochemical and biophysical research communications, Amsterdam, The Netherlands, C1

Alteration of copper physiology in mice overexpressing the human menkes protein ATP7A

B Ke, R Llanos, M Wright, Y Deal, J Mercer

(2006), Vol. 290, pp. 1460-1467, American journal of physiology : regulatory, interative comparative physiology, Bethesda, Md., C1

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

M Cater, S La Fontaine, K Shield, Y Deal, J Mercer

(2006), Vol. 130, pp. 493-506, Gastroenterology, Amsterdam, Nertherlands, C1

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

K Allen, N Buck, D Cheah, S Gazeas, P Bhathal, J Mercer

(2006), Vol. 19, pp. 555-564, BioMetals, Amsterdam, The Netherlands, C1

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

J Monty, R Llanos, J Mercer, D Kramer

(2005), Vol. 135, pp. 2762-2766, Journal of nutrition, Bethesda, Md., C1

A single PDZ domain protein interacts with the menkes copper ATPase, ATP7A : a new protein implicated in copper homeostasis

S Stephenson, D Dubach, C Lim, J Mercer, S La Fontaine

(2005), Vol. 280, pp. 33270-33279, Journal of biological chemistry, Baltimore, Md, C1-1

Expression and localization of Menkes and Wilson copper transporting ATPases in human placenta

B Hardman, U Manuelpillai, E Wallace, S van de Waasenburg, M Cater, J Mercer, L Ackland

(2004), Vol. 25, pp. 512-517, Placenta, Amsterdam, Netherlands, C1

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

M Cater, J Forbes, S La Fontaine, D Cox, J Mercer

(2004), Vol. 380, pp. 805-813, Biochemical journal, London, England, C1

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

K Allen, D Cheah, P Wright, S Gazeas, N Pettigrew-Buck, Y Deal, J Mercer, R Williamson

(2004), Vol. 19, pp. 1283-1290, Journal of gastroenterology and hepatology, New York, NY., C1

The potential of bone marrow stem cells to correct liver dysfunction in a mouse model of Wilson's disease

K Allen, D Cheah, L Xiao, N Pettigrew-Buck, J Vadolas, J Mercer, P Ioannou, R Williamson

(2004), Vol. 13, pp. 765-773, Cell Transplantation, United States, C1-1

Molecular and cellular aspects of copper transport in developing mammals

J Mercer, R Llanos

(2003), Vol. 133, Journal of nutrition, Bethesda, Md., C1

Copper-induced trafficking of the Cu-ATPase: a key mechanism for copper homeostasis

J Mercer, N Barnes, J Stevenson, D Strausak, R Llanos

(2003), Vol. 16, pp. 175-184, BioMetals, Amsterdam, The Netherlands, C1

Kinetic analysis of the interaction of the copper chaperone Atox1 with the metal binding sites of the Menkes protein

D Strausak, M Howie, S Firth, A Schlicksupp, R Pipkorn, G Multhaup, J Mercer

(2003), Vol. 278, pp. 20821-20827, Journal of biological chemistry, Baltimore, Md., C1

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

M Pascale, S Franceschelli, O Moltedo, F Belleudi, M Torrisi, C Bucci, S La Fontaine, J Mercer, A Leone

(2003), Vol. 291, pp. 377-385, Experimental cell research, San Diego, Calif, C1

Correction of the copper transport defect of Menkes patient fibroblasts by expression of two forms of the sheep Wilson ATPase

P Lockhart, S La Fontaine, S Firth, M Greenough, J Camakaris, J Mercer

(2002), Vol. 1588, pp. 189-194, Biochimica et biophysica acta (BBA) - molecular basis of disease, Netherlands, C1

The molecular basis of copper homeostasis and copper-related disorders

R Llanos, J Mercer

(2002), Vol. 21, pp. 259-270, DNA and cell biology, New York, N.Y., C1

Copper-regulated trafficking of the Menkes disease copper ATPase associated with formation of a phosphorylated catalytic intermediate

M Petris, I Voskoboinik, M Cater, K Smith, B Kim, R Llanos, D Strausak, J Camakaris, J Mercer

(2002), Vol. 277, pp. 46736-46742, Journal of biological chemistry, Baltimore, Md., C1

The molecular basis of copper-transport diseases

J Mercer

(2001), Vol. 7, pp. 64-69, Trends in molecular medicine, New York, N.Y., C1

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

P Lockhart, J Mercer

(2001), Vol. 80, pp. 349-357, European journal of cell biology, Amsterdam, The Netherlands, C1

Copper in disorders with neurological symptoms: Alzheimer`s, Menkes, and Wilson Diseases

D Strausak, J Mercer, H Dieter, W Stremmel, G Multhaup

(2001), Vol. 55, pp. 175-185, Brain research bulletin, New York, NY, C1

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

S La Fontaine, M Theophilos, S Firth, R Gould, R Parton, J Mercer

(2001), Vol. 10, pp. 361-370, Human molecular genetics, Oxford, England, C1

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

I Voskoboinik, M Greenough, S La Fontaine, J Mercer, J Camakaris

(2001), Vol. 281, pp. 966-970, Biochemical and biophysical research communications, San Diego, Calif, C1

Expression of the human Menkes ATPase in Xenopus laevis oocytes

K Bissig, S La Fontaine, J Mercer, M Solioz

(2001), Vol. 382, pp. 711-714, Biological chemistry, Berlin, Germany, C1-1

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

A Michalczyk, J Rieger, K Allen, J Mercer, M Ackland

(2000), Vol. 352, pp. 565-571, Biochemical journal, London, Eng., C1-1

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

P Lockhart, J Mercer

(2000), Vol. 1490, pp. 11-20, Biochimica et Biophysica Acta - Gene Structure and Expression, Netherlands, C1-1

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

P Lockhart, S Wilcox, H Dahl, J Mercer

(2000), Vol. 1491, pp. 229-239, Biochimica et Biophysica Acta - Gene Structure and Expression, Netherlands, C1-1

The Menkes copper transporter is required for the activation of tyrosinase

M Petris, D Strausak, J Mercer

(2000), Vol. 9, pp. 2845-2851, Human Molecular Genetics, England, C1-1

Conditionally immortalized mouse hepatocytes use in liver gene therapy

K Allen, R Reyes, K Demmler, J Mercer, R Williamson, R Whitehead

(2000), Vol. 15, pp. 1325-1332, Journal of Gastroenterology and Hepatology (Australia), Australia, C1-1

Expression of Menkes copper-transporting ATPase, MNK, in the lactating human breast: possible role in copper transport into milk

M Ackland, P Anikijenko, A Michalczyk, J Mercer

(1999), Vol. 47, pp. 1553-1562, Journal of Histochemistry and Cytochemistry, Thousand Oaks, Calif., C1-1

The role of GMXCXXC metal binding sites in the copper-induced redistribution of the Menkes protein

D Strausak, S La Fontaine, J Hill, S Firth, P Lockhart, J Mercer

(1999), Vol. 274, pp. 11170-11177, Journal of Biological Chemistry, Bethesda, Md., C1-1

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

S La Fontaine, S Firth, P Lockhart, H Brooks, J Camakaris, J Mercer

(1999), Vol. 8, pp. 1069-1075, Human Molecular Genetics, Oxford, Eng., C1-1

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

A White, R Reyes, J Mercer, J Camakaris, H Zheng, A Bush, G Multhaup, K Beyreuther, C Masters, R Cappai

(1999), Vol. 842, pp. 439-444, Brain Research, Netherlands, C1-1

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

M Petris, J Mercer

(1999), Vol. 8, pp. 2107-2115, Human Molecular Genetics, England, C1-1

Molecular mechanisms of copper homeostasis

J Camakaris, I Voskoboinik, J Mercer

(1999), Vol. 261, pp. 225-232, Biochemical and Biophysical Research Communications, United States, C1-1

Cloning and expression analysis of the sheep ceruloplasmin cDNA

P Lockhart, J Mercer

(1999), Vol. 236, pp. 251-257, Gene, Netherlands, C1-1

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

L Ambrosini, J Mercer

(1999), Vol. 8, pp. 1547-1555, Human Molecular Genetics, England, C1-1

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, D Strausak, M Greenough, H Brooks, M Petris, S Smith, J Mercer, J Camakaris

(1999), Vol. 274, pp. 22008-22012, Journal of Biological Chemistry, United States, C1-1

Correction of the copper transport defect of Menkes patient fibroblasts by expression of the Menkes and Wilson ATPases

S La Fontaine, S Firth, J Camakaris, A Englezou, M Theophilos, M Petris, M Howie, P Lockhart, M Greenough, H Brooks, R Reddel, J Mercer

(1998), Vol. 273, pp. 31375-31380, Journal of biological chemistry, Rockville, Md., C1-1

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

M Petris, J Camakaris, M Greenough, S LaFontaine, J Mercer

(1998), Vol. 7, pp. 2063-2071, Human molecular genetics, Oxford, Eng., C1-1

Analysis of the distribution of Cu, Fe and Zn and other elements in brindled mouse kidney using a scanning proton microprobe

B Kirby, D Danks, G Legge, J Mercer

(1998), Vol. 71, pp. 189-197, Journal of Inorganic Biochemistry, United States, C1-1

Expression of Menkes disease gene in mammary carcinoma cells

M Ackland, E Cornish, A Paynter, A Grimes, A Michalczyk, F Mercer

(1997), Vol. 328, pp. 237-243, Biochemical journal, London, Eng., C1-1

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

H Dierick, J Mercer, T Glover

(1997), Vol. 198, pp. 37-41, Gene, Netherlands, C1-1

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

A Grimes, J Paynter, I Walker, M Bhave, J Mercer

(1997), Vol. 321, pp. 341-345, Biochemical Journal, England, C1-1

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

A Grimes, C Hearn, P Lockhart, D Newgreen, J Mercer

(1997), Vol. 6, pp. 1037-1042, Human Molecular Genetics, England, C1-1

Ligand-regulated transport of the Menkes copper P-type ATPase efflux pump from the Golgi apparatus to the plasma membrane: A novel mechanism of regulated trafficking

M Petris, J Mercer, J Culvenor, P Lockhart, P Gleeson, J Camakaris

(1996), Vol. 15, pp. 6084-6095, EMBO Journal, England, C1-1

The toxic milk mouse is a murine model of Wilson disease

M Theophilos, D Cox, J Mercer

(1996), Vol. 5, pp. 1619-1624, Human Molecular Genetics, England, C1-1

Molecular structure of the menkes disease gene (ATP7A)

H Dierick, L Ambrosini, J Spencer, T Glover, J Mercer

(1995), Vol. 28, pp. 462-469, Genomics, United States, C1-1

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

J Camakaris, M Petris, L Bailey, P Shen, P Lockhart, T Glover, C Barcroft, J Patton, J Mercer

(1995), Vol. 4, pp. 2117-2123, Human Molecular Genetics, England, C1-1

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

J Mercer, A Grimes, L Ambrosini, P Lockhart, J Paynter, H Dierick, T Glover

(1994), Vol. 6, pp. 374-378, Nature Genetics, United States, C1-1

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

J Howell, J Mercer

(1994), Vol. 110, pp. 37-47, Journal of Comparative Pathology, England, C1-1

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

J Paynter, A Grimes, P Lockhart, J Mercer

(1994), Vol. 351, pp. 186-190, FEBS Letters, England, C1-1

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

J Mercer, J Livingston, B Hall, J Paynter, C Begy, S Chandrasekharappa, P Lockhart, A Grimes, M Bhave, D Siemieniak, T Glover

(1993), Vol. 3, pp. 20-25, Nature Genetics, United States, C1-1

Hepatic metallothionein gene expression in toxic milk mice

J Mercer, A Grimes, H Rauch

(1992), Vol. 122, pp. 1254-1259, Journal of Nutrition, United States, C1-1

Hepatic ceruloplasmin gene expression is unaltered in the toxic milk mouse

J Mercer, A Grimes, D Danks, H Rauch

(1991), Vol. 121, pp. 894-899, Journal of Nutrition, United States, C1-1

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

S Rogers, M Bhave, J Mercer, J Camakaris, B Lee

(1991), Vol. 173, pp. 6742-6748, Journal of Bacteriology, United States, C1-1

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

J Mercer, T Stevenson, S Wake, G Mitropoulos, J Camakaris, D Danks

(1991), Vol. 1097, pp. 205-211, BBA - Molecular Basis of Disease, Netherlands, C1-1

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

H McArdle, J Mercer, A Sargeson, D Danks

(1990), Vol. 120, pp. 1370-1375, Journal of Nutrition, United States, C1-1

Analysis of hepatic copper, zinc, metallothionein and metallothionein‐Ia mRNA in developing sheep

J PAYNTER, J CAMAKARIS, J MERCER

(1990), Vol. 190, pp. 149-154, European Journal of Biochemistry, England, C1-1

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

H McArdle, P Kyriakou, A Grimes, J Mercer, D Danks

(1990), Vol. 75, pp. 315-324, Chemico-Biological Interactions, Ireland, C1-1

Cloning and organization of bovine metallothionein genes

X Shen, W Yang, H Peng, M Peterson, J Mercer, S Woo

(1989), Vol. 34, pp. 953-956, Kexue tongbao, Scientia, C1-1

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

M Hertzberg, K Jahromi, V Ferguson, H Dahl, J Mercer, K Mickleson, R Trent

(1989), Vol. 44, pp. 382-387, American Journal of Human Genetics, United States, C1-1

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

D Taylor, H Dahl, J Mercer, A Green, M Fisher

(1989), Vol. 264, pp. 185-190, Biochemical Journal, England, C1-1

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

M PETERSON, F HANNAN, J MERCER

(1988), Vol. 174, pp. 417-424, European Journal of Biochemistry, England, C1-1

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

A Grimes, H McArdle, J Mercer

(1988), Vol. 172, pp. 436-443, Analytical Biochemistry, United States, C1-1

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

G Yeoh, E Edkins, K Mackenzie, S Fuller, J Mercer, H Dahl

(1988), Vol. 38, pp. 42-48, Differentiation, England, C1-1

Differential expression of four linked sheep metallothionein genes

M PETERSON, J MERCER

(1988), Vol. 174, pp. 425-429, European Journal of Biochemistry, England, C1-1

Regulation of 5-aminolevulinate synthase mRNA in different rat tissues

G Srivastava, I Borthwick, D Maguire, C Elferink, M Bawden, J Mercer, B May

(1988), Vol. 263, pp. 5202-5209, Journal of Biological Chemistry, United States, C1-1

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

S D'Souza, J Mercer

(1987), Vol. 142, pp. 417-421, Biochemical and Biophysical Research Communications, United States, C1-1

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

A Aldred, A Grimes, G Schreiber, J Mercer

(1987), Vol. 262, pp. 2875-2878, Journal of Biological Chemistry, United States, C1-1

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

J Finger, J Mercer, R Cotton, D Danks

(1987), Vol. 170, pp. 209-218, Clinica Chimica Acta, Netherlands, C1-1

Structure and regulation of the sheep metallothionein‐Ia gene

M PETERSON, J MERCER

(1986), Vol. 160, pp. 579-585, European Journal of Biochemistry, England, C1-1

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

J Mercer, A Grimes

(1986), Vol. 238, pp. 23-27, Biochemical Journal, England, C1-1

A study of the role of metallothionein in the inherited copper toxicosis of dogs

D Hunt, S Wake, J Mercer, D Danks

(1986), Vol. 236, pp. 409-415, Biochemical Journal, England, C1-1

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

J Mercer, W McAdam, G Chambers, I Walker

(1986), Vol. 236, pp. 679-683, Biochemical Journal, England, C1-1

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), Vol. 261, pp. 4148-4153, Journal of Biological Chemistry, United States, C1-1

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

J Mercer, A Grimes

(1986), Vol. 203, pp. 185-190, FEBS Letters, England, C1-1

The Primary Structure of the Imported Mitochondrial Protein, Ornithine Transcarbamylase from Rat Liver: mRNA Levels During Ontogeny

P Mcintyre, L Graf, J Mercer, S Wake, P Hudson, N Hoogenraad

(1985), Vol. 4, pp. 147-156, DNA, United States, C1-1

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

J Mercer, S Wake

(1985), Vol. 13, pp. 7929-7943, Nucleic Acids Research, England, C1-1

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

S Wake, J Mercer

(1985), Vol. 228, pp. 425-432, Biochemical Journal, England, C1-1

Cloning and sequencing of a sheep metallothionein cDNA

M PETERSON, I LAZDINS, D DANKS, J MERCER

(1984), Vol. 143, pp. 507-511, European Journal of Biochemistry, England, C1-1

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

S Smith, B Kemp, W McAdam, J Mercer, R Cotton

(1984), Vol. 259, pp. 11284-11289, Journal of Biological Chemistry, United States, C1-1

Identification of two molecular-mass forms of phenylalanine hydroxylase that segregate independently in rats. Specific association of each form with certain rat strains

J Mercer, A Grimes, I Jennings, R Cotton

(1984), Vol. 219, pp. 891-898, Biochemical Journal, England, C1-1

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

P Mclntyre, L Graf, J Mercer, G Peterson, P Hudson, N Hoogenraad

(1984), Vol. 177, pp. 41-46, FEBS Letters, England, C1-1

The two molecular weight forms of rat phenylalanine hydroxylase are encoded by different messenger RNAs

J Mercer, S Hunt, R Cotton

(1983), Vol. 258, pp. 5854-5857, Journal of Biological Chemistry, United States, C1-1

Cloning of metallothionein cDNA from neonatal rat liver

J Mercer, P Hudson

(1982), Vol. 2, pp. 761-768, Bioscience Reports, England, C1-1

β-Hydroxyisobutyryl coenzyme A deacylase deficiency: A defect in valine metabolism associated with physical malformations

G Brown, S Hunt, R Scholem, K Fowler, A Grimes, J Mercer, R Truscott, R Cotton, J Rogers, D Danks

(1982), Vol. 70, pp. 532-538, Pediatrics, United States, C1-1

Two new sulphur‐containing amino acids in man

R Truscott, D Malegan, E McCairns, B Halpern, J Hammond, R Cotton, J Mercer, S Hunt, J Rogers, D Danks

(1981), Vol. 8, pp. 99-104, Biological Mass Spectrometry, England, C1-1

Copper induction of translatable metallothionein messenger RNA

J Mercer, I Lazdins, T Stevenson, J Camakaris, D Danks

(1981), Vol. 1, pp. 793-800, Bioscience Reports, England, C1-1

POLY(A) SEQUENCES IN PLANT POLYSOMAL RNA

T HIGGINS, J MERCER, P GOODWIN

(1973), Vol. 246, pp. 68-70, NATURE-NEW BIOLOGY, England, C1-1

PEPTIDYL-DONOR SUBSTRATES FOR RIBOSOMAL PEPTIDYL TRANSFERASE - CHEMICAL SYNTHESIS AND BIOLOGICAL-ACTIVITY OF N-ACETYL AMINOACYL DI-NUCLEOTIDES AND TRI-NUCLEOTIDES

J MERCER, R SYMONS

(1972), Vol. 28, pp. 38-&, EUROPEAN JOURNAL OF BIOCHEMISTRY, England, C1-1

USE OF N-ETHOXYCARBONYL-2-ETHOXY-1,2-DIHYDROQUINOLINE IN SELECTIVE N4-ACYLATION OF CYTIDINE AND ITS DERIVATIVES

J MERCER, R SYMONS

(1971), Vol. 238, pp. 27-&, BIOCHIMICA ET BIOPHYSICA ACTA, Netherlands, C1-1