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1. Mercer, JFB
   The molecular basis of copper-transport diseases
   TRENDS IN MOLECULAR MEDICINE
   
   J.F.B. Mercer, "The molecular basis of copper-transport diseases", TRENDS MO M, 7(2), 2001, pp. 64-69
2. Hall, MA; Moshkov, IE; Novikova, GV; Mur, LAJ; Smith, AR
   Ethylene signal perception and transduction: multiple paradigms?
   BIOLOGICAL REVIEWS
   
   M.A. Hall et al., "Ethylene signal perception and transduction: multiple paradigms?", BIOL REV, 76(1), 2001, pp. 103-128
3. Linder, MC
   Copper and genomic stability in mammals
   MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
   
   M.C. Linder, "Copper and genomic stability in mammals", MUT RES-F M, 475(1-2), 2001, pp. 141-152
4. Jung, CG; Miyamoto, T; Tsumagari, T; Agui, T
   Genetic association between low expression phenotype of CD62L (L-selectin)in peripheral CD4(+) T cells and the thid (T-helper immunodeficiency) phenotype in the LEC rat
   EXPERIMENTAL ANIMALS
   
   C.G. Jung et al., "Genetic association between low expression phenotype of CD62L (L-selectin)in peripheral CD4(+) T cells and the thid (T-helper immunodeficiency) phenotype in the LEC rat", EXP ANIM, 50(4), 2001, pp. 337-340
5. Yamamoto, H; Watanabe, T; Mizuno, H; Endo, K; Fukushige, J; Hosokawa, T; Kazusaka, A; Fujita, S
   The antioxidant effect of DL-alpha-lipoic acid on copper-induced acute hepatitis in Long-Evans Cinnamon (LEC) rats
   FREE RADICAL RESEARCH
   
   H. Yamamoto et al., "The antioxidant effect of DL-alpha-lipoic acid on copper-induced acute hepatitis in Long-Evans Cinnamon (LEC) rats", FREE RAD RE, 34(1), 2001, pp. 69-80
6. Palsson, R; Jonasson, JG; Kristjansson, M; Bodvarsson, A; Goldin, RD; Cox, DW; Olafsson, S
   Genotype-phenotype interactions in Wilson's disease: insight from an Icelandic mutation
   EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
   
   R. Palsson et al., "Genotype-phenotype interactions in Wilson's disease: insight from an Icelandic mutation", EUR J GASTR, 13(4), 2001, pp. 433-436
7. Nanji, M; Coronado, VA; Cox, DW
   ATP6H, a subunit of vacuolar ATPase involved in metal transport: evaluation in canine copper toxicosis
   MAMMALIAN GENOME
   
   M. Nanji et al., "ATP6H, a subunit of vacuolar ATPase involved in metal transport: evaluation in canine copper toxicosis", MAMM GENOME, 12(8), 2001, pp. 617-621
8. Coronado, V; Nanji, M; Cox, DW
   The Jackson toxic milk mouse as a model for copper loading
   MAMMALIAN GENOME
   
   V. Coronado et al., "The Jackson toxic milk mouse as a model for copper loading", MAMM GENOME, 12(10), 2001, pp. 793-795
9. Portala, K; Westermark, K; Ekselius, L; von Knorring, L
   Personality traits in treated Wilson's disease determined by means of the Karolinska Scales of Personality (KSP)
   EUROPEAN PSYCHIATRY
   
   K. Portala et al., "Personality traits in treated Wilson's disease determined by means of the Karolinska Scales of Personality (KSP)", EUR PSYCHIA, 16(6), 2001, pp. 362-371
10. Hayashi, M; Kuge, T; Endoh, D; Nakayama, K; Arikawa, J; Takazawa, A; Okui, T
    No significant differences were observed in the amounts of DNA strand breaks produced by copper between male and female liver cells of Long-Evans Cinnamon (LEC) strain rats
    JOURNAL OF VETERINARY MEDICAL SCIENCE
    
    M. Hayashi et al., "No significant differences were observed in the amounts of DNA strand breaks produced by copper between male and female liver cells of Long-Evans Cinnamon (LEC) strain rats", J VET MED S, 63(10), 2001, pp. 1109-1113
11. Ishikawa, S; Nomoto, S; Yoshida, K; Tokuda, T; Ikeda, S
    Trientine increases fecal copper excretion in Wilson's disease: A case report
    JOURNAL OF TRACE ELEMENTS IN EXPERIMENTAL MEDICINE
    
    S. Ishikawa et al., "Trientine increases fecal copper excretion in Wilson's disease: A case report", J TR EL EXP, 14(4), 2001, pp. 405-407
12. Brewer, GJ
    Commentary: Landmark articles on copper in the field of human health
    JOURNAL OF TRACE ELEMENTS IN EXPERIMENTAL MEDICINE
    
    G.J. Brewer, "Commentary: Landmark articles on copper in the field of human health", J TR EL EXP, 14(2), 2001, pp. 191-194
13. Pourahmad, J; Ross, S; O'Brien, PJ
    Lysosomal involvement in hepatocyte cytotoxicity induced by Cu2+ but not Cd2+
    FREE RADICAL BIOLOGY AND MEDICINE
    
    J. Pourahmad et al., "Lysosomal involvement in hepatocyte cytotoxicity induced by Cu2+ but not Cd2+", FREE RAD B, 30(1), 2001, pp. 89-97
14. Svetel, M; Kozic, D; Stefanova, E; Semnic, R; Dragasevic, N; Kostic, VS
    Dystonia in Wilson's disease
    MOVEMENT DISORDERS
    
    M. Svetel et al., "Dystonia in Wilson's disease", MOVEMENT D, 16(4), 2001, pp. 719-723
15. Strausak, D; Mercer, JFB; Dieter, HH; Stremmel, W; Multhaup, G
    Copper in disorders with neurological symptoms: Alzheimer's, Menkes, and Wilson diseases
    BRAIN RESEARCH BULLETIN
    
    D. Strausak et al., "Copper in disorders with neurological symptoms: Alzheimer's, Menkes, and Wilson diseases", BRAIN RES B, 55(2), 2001, pp. 175-185
16. Watt, NT; Hooper, NM
    The response of neurones and glial cells to elevated copper
    BRAIN RESEARCH BULLETIN
    
    N.T. Watt e N.M. Hooper, "The response of neurones and glial cells to elevated copper", BRAIN RES B, 55(2), 2001, pp. 219-224
17. Barthel, H; Sorger, D; Kuhn, HJ; Wagner, A; Kluge, R; Hermann, W
    Differential alteration of the nigrostriatal dopaminergic system in Wilson's disease investigated with [I-123]beta-CIT and high-resolution SPET
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE
    
    H. Barthel et al., "Differential alteration of the nigrostriatal dopaminergic system in Wilson's disease investigated with [I-123]beta-CIT and high-resolution SPET", EUR J NUCL, 28(11), 2001, pp. 1656-1663
18. Furman, B; Bashiri, A; Wiznitzer, A; Erez, O; Holcberg, G; Mazor, M
    Wilson's disease in pregnancy: five successful consecutive pregnancies of the same woman
    EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY
    
    B. Furman et al., "Wilson's disease in pregnancy: five successful consecutive pregnancies of the same woman", EUR J OB GY, 96(2), 2001, pp. 232-234
19. van Mil, SWC; Klomp, LWJ; Bull, LN; Houwen, RHJ
    FIC1 disease: A spectrum of intrahepatic cholestatic disorders
    SEMINARS IN LIVER DISEASE
    
    S.W.C. van Mil et al., "FIC1 disease: A spectrum of intrahepatic cholestatic disorders", SEM LIV DIS, 21(4), 2001, pp. 535-544
20. Michel, M; Lafaurie, M; Noel, V; Pico, L; Bastie, A; Godeau, B; Schaeffer, A
    Acute hemolytic anemia as the first manifestation of Wilson's disease: report of two cases.
    REVUE DE MEDECINE INTERNE
    
    M. Michel et al., "Acute hemolytic anemia as the first manifestation of Wilson's disease: report of two cases.", REV MED IN, 22(3), 2001, pp. 280-283
21. Jonas, L; Fulda, G; Salameh, T; Schmidt, W; Kroning, GE; Hopt, UT; Nizze, H
    Electron microscopic detection of copper in the liver of two patients withmorbus Wilson by EELS and EDX
    ULTRASTRUCTURAL PATHOLOGY
    
    L. Jonas et al., "Electron microscopic detection of copper in the liver of two patients withmorbus Wilson by EELS and EDX", ULTRA PATH, 25(2), 2001, pp. 111-118
22. Kobayashi, S; Ochiai, T; Hori, S; Suzuki, T; Shimizu, T; Gunji, Y; Shimada, H; Yamamoto, S; Ogawa, A; Kohno, Y; Sunaga, A; Shimazu, A; Tanaka, K
    Copper metabolism after living donor liver transplantation for hepatic failure of Wilson's disease from a gene mutated donor
    HEPATO-GASTROENTEROLOGY
    
    S. Kobayashi et al., "Copper metabolism after living donor liver transplantation for hepatic failure of Wilson's disease from a gene mutated donor", HEP-GASTRO, 48(41), 2001, pp. 1259-1261
23. Reich, DE; Lander, ES
    On the allelic spectrum of human disease
    TRENDS IN GENETICS
    
    D.E. Reich e E.S. Lander, "On the allelic spectrum of human disease", TRENDS GEN, 17(9), 2001, pp. 502-510
24. Caca, K; Ferenci, P; Kuhn, HJ; Polli, C; Willgerodt, H; Kunath, B; Hermann, W; Mossner, J; Berr, F
    High prevalence of the H1069Q mutation in East German patients with Wilsondisease: rapid detection of mutations by limited sequencing and phenotype-genotype analysis
    JOURNAL OF HEPATOLOGY
    
    K. Caca et al., "High prevalence of the H1069Q mutation in East German patients with Wilsondisease: rapid detection of mutations by limited sequencing and phenotype-genotype analysis", J HEPATOL, 35(5), 2001, pp. 575-581
25. Najda, J; Stella-Holowiecka, B; Machalski, M
    Low-dose zinc administration as an effective Wilson's disease treatment
    BIOLOGICAL TRACE ELEMENT RESEARCH
    
    J. Najda et al., "Low-dose zinc administration as an effective Wilson's disease treatment", BIOL TR EL, 80(3), 2001, pp. 281-284
26. Morita, A; Abdireyim, D; Kimura, M; Itokawa, Y
    The effect of aging on the mineral status of female SAMP1 and SAMR1
    BIOLOGICAL TRACE ELEMENT RESEARCH
    
    A. Morita et al., "The effect of aging on the mineral status of female SAMP1 and SAMR1", BIOL TR EL, 80(1), 2001, pp. 53-65
27. Orth, M; Schapira, AHV
    Mitochondria and degenerative disorders
    AMERICAN JOURNAL OF MEDICAL GENETICS
    
    M. Orth e A.H.V. Schapira, "Mitochondria and degenerative disorders", AM J MED G, 106(1), 2001, pp. 27-36
28. Firneisz, G; Woller, J; Ferenci, P; Szalay, F
    Postcremation diagnosis from an electric shaver
    LANCET
    
    G. Firneisz et al., "Postcremation diagnosis from an electric shaver", LANCET, 358(9275), 2001, pp. 34-34
29. Huffman, DL; O'Halloran, TV
    Function, structure, and mechanism of intracellular copper trafficking proteins
    ANNUAL REVIEW OF BIOCHEMISTRY
    
    D.L. Huffman e T.V. O'Halloran, "Function, structure, and mechanism of intracellular copper trafficking proteins", ANN R BIOCH, 70, 2001, pp. 677-701
30. Karabanov, AV; Ovchinnikov, IV; Illarioshkin, SN; Poleschuk, VV; Slominsky, PA; Markova, ED; Rebrova, OY; Limborskaya, SA; Ivanova-Smolenskaya, IA
    Analysis of mutations in ATP7B gene and experience of the direct DNA-diagnosis in hepatolenticular degeneration
    ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA
    
    A.V. Karabanov et al., "Analysis of mutations in ATP7B gene and experience of the direct DNA-diagnosis in hepatolenticular degeneration", ZH NEVR PS, 101(4), 2001, pp. 44-47
31. Axelsen, KB; Palmgren, MG
    Inventory of the superfamily of P-type ion pumps in Arabidopsis
    PLANT PHYSIOLOGY
    
    K.B. Axelsen e M.G. Palmgren, "Inventory of the superfamily of P-type ion pumps in Arabidopsis", PLANT PHYSL, 126(2), 2001, pp. 696-706
32. Andrews, NC
    Mining copper transport genes
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    
    N.C. Andrews, "Mining copper transport genes", P NAS US, 98(12), 2001, pp. 6543-6545
33. Kuo, YM; Zhou, B; Cosco, D; Gitschier, J
    The copper transporter CTR1 provides an essential function in mammalian embryonic development
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    
    Y.M. Kuo et al., "The copper transporter CTR1 provides an essential function in mammalian embryonic development", P NAS US, 98(12), 2001, pp. 6836-6841
34. Lee, LW; Prohaska, JR; Thiele, DJ
    Essential role for mammalian copper transporter Ctr1 in copper homeostasisand embryonic development
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    
    L.W. Lee et al., "Essential role for mammalian copper transporter Ctr1 in copper homeostasisand embryonic development", P NAS US, 98(12), 2001, pp. 6842-6847
35. Perretti, A; Pellecchia, MT; Lanzillo, B; Campanella, G; Santoro, L
    Excitatory and inhibitory mechanisms in Wilson's disease: investigation with magnetic motor cortex stimulation
    JOURNAL OF THE NEUROLOGICAL SCIENCES
    
    A. Perretti et al., "Excitatory and inhibitory mechanisms in Wilson's disease: investigation with magnetic motor cortex stimulation", J NEUR SCI, 192(1-2), 2001, pp. 35-40
36. Narayanan, VS; Fitch, CA; Levenson, CW
    Tumor suppressor protein p53 mRNA and subcellular localization are alteredby changes in cellular copper in human Hep G2 cells
    JOURNAL OF NUTRITION
    
    V.S. Narayanan et al., "Tumor suppressor protein p53 mRNA and subcellular localization are alteredby changes in cellular copper in human Hep G2 cells", J NUTR, 131(5), 2001, pp. 1427-1432
37. Tagawa, A; Ono, S; Shibata, M; Imai, T; Suzuki, M; Shimizu, N
    A new neurological entity manifesting as involuntary movements and dysarthria with possible abnormal copper metabolism
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    
    A. Tagawa et al., "A new neurological entity manifesting as involuntary movements and dysarthria with possible abnormal copper metabolism", J NE NE PSY, 71(6), 2001, pp. 780-783
38. Nicholl, DJ; Ferenci, P; Polli, C; Burdon, MB; Pall, HS
    Wilson's disease presenting in a family with an apparent dominant history of tremor
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    
    D.J. Nicholl et al., "Wilson's disease presenting in a family with an apparent dominant history of tremor", J NE NE PSY, 70(4), 2001, pp. 514-516
39. Jordan, IK; Natale, DA; Koonin, EV; Galperin, MY
    Independent evolution of heavy metal-associated domains in copper chaperones and copper-transporting ATPases
    JOURNAL OF MOLECULAR EVOLUTION
    
    I.K. Jordan et al., "Independent evolution of heavy metal-associated domains in copper chaperones and copper-transporting ATPases", J MOL EVOL, 53(6), 2001, pp. 622-633
40. Wang, A; Cortas, N; Edelman, IS
    Mg-dependent, Zn-ATPase: Enzymatic characteristics, ion specificities and tissue distribution
    JOURNAL OF MEMBRANE BIOLOGY
    
    A. Wang et al., "Mg-dependent, Zn-ATPase: Enzymatic characteristics, ion specificities and tissue distribution", J MEMBR BIO, 181(1), 2001, pp. 11-20
41. Arnesano, F; Banci, L; Bertini, I; Cantini, F; Ciofi-Baffoni, S; Huffman, DL; O'Halloran, TV
    Characterization of the binding interface between the copper chaperone Atx1 and the first cytosolic domain of Ccc2 ATPase
    JOURNAL OF BIOLOGICAL CHEMISTRY
    
    F. Arnesano et al., "Characterization of the binding interface between the copper chaperone Atx1 and the first cytosolic domain of Ccc2 ATPase", J BIOL CHEM, 276(44), 2001, pp. 41365-41376
42. Voskoboinik, I; Mar, J; Strausak, D; Camakaris, J
    The regulation of catalytic activity of the menkes copper-translocating P-type ATPase - Role of high affinity copper-binding sites
    JOURNAL OF BIOLOGICAL CHEMISTRY
    
    I. Voskoboinik et al., "The regulation of catalytic activity of the menkes copper-translocating P-type ATPase - Role of high affinity copper-binding sites", J BIOL CHEM, 276(30), 2001, pp. 28620-28627
43. Banci, L; Bertini, I; Ciofi-Baffoni, S; Huffman, DL; O'Halloran, TV
    Solution structure of the yeast copper transporter domain Ccc2a in the apoand Cu(I)-loaded states
    JOURNAL OF BIOLOGICAL CHEMISTRY
    
    L. Banci et al., "Solution structure of the yeast copper transporter domain Ccc2a in the apoand Cu(I)-loaded states", J BIOL CHEM, 276(11), 2001, pp. 8415-8426
44. Durand, F; Bernuau, J; Giostra, E; Mentha, G; Shouval, D; Degott, C; Benhamou, JP; Valla, D
    Wilson's disease with severe hepatic insufficiency: beneficial effects of early administration of D-penicillamine
    GUT
    
    F. Durand et al., "Wilson's disease with severe hepatic insufficiency: beneficial effects of early administration of D-penicillamine", GUT, 48(6), 2001, pp. 849-852
45. Bal, N; Mintz, E; Guillain, F; Catty, P
    A possible regulatory role for the metal-binding domain of CadA, the Listeria monocytogenes Cd2+-ATPase
    FEBS LETTERS
    
    N. Bal et al., "A possible regulatory role for the metal-binding domain of CadA, the Listeria monocytogenes Cd2+-ATPase", FEBS LETTER, 506(3), 2001, pp. 249-252
46. Bain, BJ
    The spherocytic haemolytic anaemias
    BRITISH JOURNAL OF HAEMATOLOGY
    
    B.J. Bain, "The spherocytic haemolytic anaemias", BR J HAEM, 115(1), 2001, pp. 229-230
47. Prella, M; Baccala, R; Horisberger, JD; Belin, D; Di Raimondo, F; Invernizzi, R; Garozzo, R; Schapira, M
    Haemolytic onset of Wilson disease in a patient with homozygous truncationof ATP7B at Arg1319
    BRITISH JOURNAL OF HAEMATOLOGY
    
    M. Prella et al., "Haemolytic onset of Wilson disease in a patient with homozygous truncationof ATP7B at Arg1319", BR J HAEM, 114(1), 2001, pp. 230-232
48. Kawano, H; Takeuchi, Y; Yoshimoto, K; Matsumoto, K; Sugimoto, T
    Histological changes in monoaminergic neurons of Long-Evans Cinnamon rats
    BRAIN RESEARCH
    
    H. Kawano et al., "Histological changes in monoaminergic neurons of Long-Evans Cinnamon rats", BRAIN RES, 915(1), 2001, pp. 25-31
49. Mitra, B; Sharma, R
    The cysteine-rich amino-terminal domain of ZntA, a Pb(II)/Zn(II)/Cd(II)-translocating ATPase from Escherichia coli, is not essential for its function
    BIOCHEMISTRY
    
    B. Mitra e R. Sharma, "The cysteine-rich amino-terminal domain of ZntA, a Pb(II)/Zn(II)/Cd(II)-translocating ATPase from Escherichia coli, is not essential for its function", BIOCHEM, 40(25), 2001, pp. 7694-7699
50. Fan, B; Grass, G; Rensing, C; Rosen, BP
    Escherichia coli CopA N-terminal Cys(X)(2)Cys motifs are not required for copper resistance or transport
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    
    B. Fan et al., "Escherichia coli CopA N-terminal Cys(X)(2)Cys motifs are not required for copper resistance or transport", BIOC BIOP R, 286(2), 2001, pp. 414-418
51. Voskoboinik, I; Greenough, M; La Fontaine, S; Mercer, JFB; Camakaris, J
    Functional studies on the Wilson copper P-type ATPase and toxic milk mousemutant
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    
    I. Voskoboinik et al., "Functional studies on the Wilson copper P-type ATPase and toxic milk mousemutant", BIOC BIOP R, 281(4), 2001, pp. 966-970
52. Sayer, JA; Pearce, SHS
    Diagnosis and clinical biochemistry of inherited tubulopathies
    ANNALS OF CLINICAL BIOCHEMISTRY
    
    J.A. Sayer e S.H.S. Pearce, "Diagnosis and clinical biochemistry of inherited tubulopathies", ANN CLIN BI, 38, 2001, pp. 459-470
53. Shishido, N; Nakayama, K; Takazawa, A; Ohyama, T; Nakamura, M
    Cu-metallothioneins (Cu(I)(8)-MTs) in LEC rat livers 13 weeks after birth still act as antioxidants
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
    
    N. Shishido et al., "Cu-metallothioneins (Cu(I)(8)-MTs) in LEC rat livers 13 weeks after birth still act as antioxidants", ARCH BIOCH, 387(2), 2001, pp. 216-222
54. Aburto, EM; Cribb, AE; Fuentealba, C
    Effect of chronic exposure to excess dietary copper and dietary selenium supplementation on liver specimens from rats
    AMERICAN JOURNAL OF VETERINARY RESEARCH
    
    E.M. Aburto et al., "Effect of chronic exposure to excess dietary copper and dietary selenium supplementation on liver specimens from rats", AM J VET RE, 62(9), 2001, pp. 1423-1427
55. Rosenzweig, AC
    Copper delivery by metallochaperone proteins
    ACCOUNTS OF CHEMICAL RESEARCH
    
    A.C. Rosenzweig, "Copper delivery by metallochaperone proteins", ACC CHEM RE, 34(2), 2001, pp. 119-128
56. Balint, G; Szebenyi, B
    Hereditary disorders mimicking and/or causing premature osteoarthritis
    BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY
    
    G. Balint e B. Szebenyi, "Hereditary disorders mimicking and/or causing premature osteoarthritis", BEST PR R C, 14(2), 2000, pp. 219-250
57. Lee, CC; Wu, JY; Tsai, FJ; Kodama, H; Abe, T; Yang, CF; Tsai, CH
    Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association
    JOURNAL OF HUMAN GENETICS
    
    C.C. Lee et al., "Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation association", J HUM GENET, 45(5), 2000, pp. 275-279
58. Kusuda, Y; Hamaguchi, K; Mori, T; Shin, R; Seike, M; Sakata, T
    Novel mutations of the ATP7B gene in Japanese patients with Wilson disease
    JOURNAL OF HUMAN GENETICS
    
    Y. Kusuda et al., "Novel mutations of the ATP7B gene in Japanese patients with Wilson disease", J HUM GENET, 45(2), 2000, pp. 86-91
59. Ba, Y; Tonoki, H; Tada, M; Nakata, D; Hamada, J; Moriuchi, T
    Transcriptional slippage of p53 gene enhanced by cellular damage in rat liver: monitoring the slippage by a yeast functional assay
    MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
    
    Y. Ba et al., "Transcriptional slippage of p53 gene enhanced by cellular damage in rat liver: monitoring the slippage by a yeast functional assay", MUT RES-F M, 447(2), 2000, pp. 209-220
60. Rodo, M; Czonkowska, A; Pulawska, M; Swiderska, M; Tarnacka, B; Wehr, H
    The level of serum lipids, vitamin E and low density lipoprotein oxidationin Wilson's disease patients
    EUROPEAN JOURNAL OF NEUROLOGY
    
    M. Rodo et al., "The level of serum lipids, vitamin E and low density lipoprotein oxidationin Wilson's disease patients", EUR J NEUR, 7(5), 2000, pp. 491-494
61. Tarnacka, B; Gromadzka, G; Rodo, M; Mierzejewski, P; Czloonkowska, A
    Frequency of His1069Gln and Gly1267Lys mutations in Polish Wilson's disease population
    EUROPEAN JOURNAL OF NEUROLOGY
    
    B. Tarnacka et al., "Frequency of His1069Gln and Gly1267Lys mutations in Polish Wilson's disease population", EUR J NEUR, 7(5), 2000, pp. 495-498
62. Muramatsu, Y; Yamada, T; Moralejo, DH; Mochizuki, H; Sogawa, K; Matsumoto, K
    Increased polyploid incidence is associated with abnormal copper accumulation in the liver of LEC mutant rat
    RESEARCH COMMUNICATIONS IN MOLECULAR PATHOLOGY AND PHARMACOLOGY
    
    Y. Muramatsu et al., "Increased polyploid incidence is associated with abnormal copper accumulation in the liver of LEC mutant rat", RES COM M P, 107(1-2), 2000, pp. 129-136
63. Wernimont, AK; Huffman, DL; Lamb, AL; O'Halloran, TV; Rosenzweig, AC
    Structural basis for copper transfer by the metallochaperone for the Menkes/Wilson disease proteins
    NATURE STRUCTURAL BIOLOGY
    
    A.K. Wernimont et al., "Structural basis for copper transfer by the metallochaperone for the Menkes/Wilson disease proteins", NAT ST BIOL, 7(9), 2000, pp. 766-771
64. Okada, T; Shiono, Y; Hayashi, H; Satoh, H; Sawada, T; Suzuki, A; Takeda, Y; Yano, M; Michitaka, K; Onji, M; Mabuchi, H
    Mutational analysis of ATP7B and genotype - Phenotype correlation in Japanese with Wilson's disease
    HUMAN MUTATION
    
    T. Okada et al., "Mutational analysis of ATP7B and genotype - Phenotype correlation in Japanese with Wilson's disease", HUM MUTAT, 15(5), 2000, pp. 454-462
65. Woeste, KE; Kieber, JJ
    A strong loss-of-function mutation in RAN1 results in constitutive activation of the ethylene response pathway as well as a rosette-lethal phenotype
    PLANT CELL
    
    K.E. Woeste e J.J. Kieber, "A strong loss-of-function mutation in RAN1 results in constitutive activation of the ethylene response pathway as well as a rosette-lethal phenotype", PL CELL, 12(3), 2000, pp. 443-455
66. Olsson, C; Waldenstrom, E; Westermark, K; Landegren, U; Syvanen, AC
    Determination of the frequencies of ten allelic variants of the Wilson disease gene (ATP7B), in pooled DNA samples
    EUROPEAN JOURNAL OF HUMAN GENETICS
    
    C. Olsson et al., "Determination of the frequencies of ten allelic variants of the Wilson disease gene (ATP7B), in pooled DNA samples", EUR J HUM G, 8(12), 2000, pp. 933-938
67. Rinaldi, AC
    Meeting report - Copper research at the top
    BIOMETALS
    
    A.C. Rinaldi, "Meeting report - Copper research at the top", BIOMETALS, 13(1), 2000, pp. 9-13
68. Agui, T; Miyamoto, T; Jung, CG; Tsumagari, T; Masuda, K; Manabe, T
    Genetic linkage analysis of X-ray hypersensitivity in the LEC mutant rat
    MAMMALIAN GENOME
    
    T. Agui et al., "Genetic linkage analysis of X-ray hypersensitivity in the LEC mutant rat", MAMM GENOME, 11(10), 2000, pp. 862-865
69. Brewer, GJ
    Raulin Award Lecture: Wilson's disease therapy with zinc and tetrathiomolybdate
    JOURNAL OF TRACE ELEMENTS IN EXPERIMENTAL MEDICINE
    
    G.J. Brewer, "Raulin Award Lecture: Wilson's disease therapy with zinc and tetrathiomolybdate", J TR EL EXP, 13(1), 2000, pp. 51-61
70. Milkiewicz, P; Saksena, S; Hubscher, SG; Elias, E
    Wilson's disease with superimposed autoimmune features: Report of two cases and review
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
    
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90. Cauza, E; Ulrich-Pur, H; Polli, C; Gangl, A; Ferenci, P
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