-
2
-
-
0036800592
-
A genetic view of iron homeostasis
-
Andrews NC. 2002. A genetic view of iron homeostasis. Semin Hematol. 39:227-34
-
(2002)
Semin Hematol
, vol.39
, pp. 227-234
-
-
Andrews, N.C.1
-
4
-
-
0030846021
-
Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin
-
Babcock M, de Silva D, Oaks R, Davis-Kaplan S, Jiralerspong S, et al. 1997. Regulation of mitochondrial iron accumulation by Yfh1p, a putative homolog of frataxin. Science 276:1709-12
-
(1997)
Science
, vol.276
, pp. 1709-1712
-
-
Babcock, M.1
de Silva, D.2
Oaks, R.3
Davis-Kaplan, S.4
Jiralerspong, S.5
-
5
-
-
33746889803
-
Copper homeostasis in eukaryotes: Teetering on a tightrope
-
Balamurugan K, Schaffner W. 2006. Copper homeostasis in eukaryotes: teetering on a tightrope. Biochim.. Biophys. Acta 1763:737-46
-
(2006)
Biochim.. Biophys. Acta
, vol.1763
, pp. 737-746
-
-
Balamurugan, K.1
Schaffner, W.2
-
7
-
-
0030739637
-
Transport of iron in the blood-brain-cerebrospinal fluid system
-
Bradbury MW. 1997. Transport of iron in the blood-brain-cerebrospinal fluid system. J. Neurochem. 69:443-54
-
(1997)
J. Neurochem
, vol.69
, pp. 443-454
-
-
Bradbury, M.W.1
-
8
-
-
0031444294
-
The cellular prion protein binds copper in vivo
-
Brown DR, Qin K, Herms JW, Madlung A, Manson J, et al. 1997. The cellular prion protein binds copper in vivo. Nature 390:684-87
-
(1997)
Nature
, vol.390
, pp. 684-687
-
-
Brown, D.R.1
Qin, K.2
Herms, J.W.3
Madlung, A.4
Manson, J.5
-
9
-
-
0027452091
-
The Wilson disease gene is a putative copper transporting P-type Atpase similar to the Menkes gene
-
Bull PC, Thomas GR, Rommens JM, Forbes JR, Cox DW. 1993. The Wilson disease gene is a putative copper transporting P-type Atpase similar to the Menkes gene. Nat. Genet. 5:327-37
-
(1993)
Nat. Genet
, vol.5
, pp. 327-337
-
-
Bull, P.C.1
Thomas, G.R.2
Rommens, J.M.3
Forbes, J.R.4
Cox, D.W.5
-
10
-
-
0034035616
-
Metals and neuroscience
-
Bush AI. 2000. Metals and neuroscience. Cum. Opin. Chem. Biol. 4:184-91
-
(2000)
Cum. Opin. Chem. Biol
, vol.4
, pp. 184-191
-
-
Bush, A.I.1
-
11
-
-
33747047271
-
NMDA receptor-nitric oxide transmission mediates neuronal iron homeostasis via the GTPase dexrasl
-
Cheah JH, Kim SF, Hester LD, Clancy KW, Patterson SE, et al. 2006. NMDA receptor-nitric oxide transmission mediates neuronal iron homeostasis via the GTPase dexrasl. Neuron 51:431-40
-
(2006)
Neuron
, vol.51
, pp. 431-440
-
-
Cheah, J.H.1
Kim, S.F.2
Hester, L.D.3
Clancy, K.W.4
Patterson, S.E.5
-
12
-
-
0027500142
-
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein
-
Chelly J, Turner Z, Tonnesen T, Petterson A, Ishikawa-Brush Y, et al. 1993. Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein. Nat. Genet. 3:14-19
-
(1993)
Nat. Genet
, vol.3
, pp. 14-19
-
-
Chelly, J.1
Turner, Z.2
Tonnesen, T.3
Petterson, A.4
Ishikawa-Brush, Y.5
-
13
-
-
33845899114
-
Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation
-
Chinnery PF, Crompton DE, Birchall D, Jackson MJ, Coulthard A, et al. 2007. Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation. Brain 130:110-19
-
(2007)
Brain
, vol.130
, pp. 110-119
-
-
Chinnery, P.F.1
Crompton, D.E.2
Birchall, D.3
Jackson, M.J.4
Coulthard, A.5
-
14
-
-
0032485513
-
Early treatment of Menkes disease with parenteral copper-histidine: Long-term follow-up of four treated patients
-
Christodoulou J, Danks DM, Sarkar B, Baerlocher KE, Casey R, et al. 1998. Early treatment of Menkes disease with parenteral copper-histidine: long-term follow-up of four treated patients. Am. J. Med. Genet. 76:154-64
-
(1998)
Am. J. Med. Genet
, vol.76
, pp. 154-164
-
-
Christodoulou, J.1
Danks, D.M.2
Sarkar, B.3
Baerlocher, K.E.4
Casey, R.5
-
15
-
-
0011938460
-
Tissue distribution and clearance kinetics of non-transferrin-bound iron in the hypotransferrinemic mouse: A rodent model for hemochromatosis
-
Craven CM, Alexander J, Eldridge M, Kushner JP, Bernstein S, Kaplan J. 1987. Tissue distribution and clearance kinetics of non-transferrin-bound iron in the hypotransferrinemic mouse: a rodent model for hemochromatosis. Proc. Natl. Acad. Sci. USA 84:3457-61
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 3457-3461
-
-
Craven, C.M.1
Alexander, J.2
Eldridge, M.3
Kushner, J.P.4
Bernstein, S.5
Kaplan, J.6
-
16
-
-
0000471415
-
Disorders of copper transport
-
ed. CR Scriver, AL Beaudet, WS Sly, D Valle, pp, New York: McGraw-Hill
-
Culotta VC, Gitlin JD. 2001. Disorders of copper transport. In The Molecular and Metabolic Basis of Inherited Disease, ed. CR Scriver, AL Beaudet, WS Sly, D Valle, pp. 3105-36. New York: McGraw-Hill
-
(2001)
The Molecular and Metabolic Basis of Inherited Disease
, pp. 3105-3136
-
-
Culotta, V.C.1
Gitlin, J.D.2
-
17
-
-
33746932518
-
Activation of superoxide dismutases: Putting the metal to the pedal
-
Culotta VC, Yang M, O'Halloran TV. 2006. Activation of superoxide dismutases: putting the metal to the pedal. Biochim. Biophys. Acta 1763:747-58
-
(2006)
Biochim. Biophys. Acta
, vol.1763
, pp. 747-758
-
-
Culotta, V.C.1
Yang, M.2
O'Halloran, T.V.3
-
18
-
-
0034941118
-
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
-
Curtis AR, Fey C, Morris CM, Bindoff LA, Ince PG, et al. 2001. Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. Nat. Genet. 28:350-54
-
(2001)
Nat. Genet
, vol.28
, pp. 350-354
-
-
Curtis, A.R.1
Fey, C.2
Morris, C.M.3
Bindoff, L.A.4
Ince, P.G.5
-
19
-
-
27744573043
-
Deletion of peptide amidation enzymatic activity leads to edema and embryonic lethality in the mouse
-
Czyzyk TA, Ning Y, Hsu MS, Peng B, Mains RE, et al. 2005. Deletion of peptide amidation enzymatic activity leads to edema and embryonic lethality in the mouse. Dev. Biol. 287:301-13
-
(2005)
Dev. Biol
, vol.287
, pp. 301-313
-
-
Czyzyk, T.A.1
Ning, Y.2
Hsu, M.S.3
Peng, B.4
Mains, R.E.5
-
21
-
-
0025896008
-
The neuropsychiatry of Wilson's disease: A review
-
Dening TR. 1991. The neuropsychiatry of Wilson's disease: a review. Int. J. Psychiatr. Med. 21:135-48
-
(1991)
Int. J. Psychiatr. Med
, vol.21
, pp. 135-148
-
-
Dening, T.R.1
-
22
-
-
2942729775
-
Metals in our minds: Therapeutic implications for neurodegenerative disorders
-
Doraiswamy PM, Fineffock AE. 2004. Metals in our minds: therapeutic implications for neurodegenerative disorders. Lancet Neurol. 3:431-34
-
(2004)
Lancet Neurol
, vol.3
, pp. 431-434
-
-
Doraiswamy, P.M.1
Fineffock, A.E.2
-
23
-
-
0031464954
-
Suppression of long-term potentiation in hippocampal slices by copper
-
Doreulee N, Yanovsky Y, Haas HL. 1997. Suppression of long-term potentiation in hippocampal slices by copper. Hippocampus 7:666-69
-
(1997)
Hippocampus
, vol.7
, pp. 666-669
-
-
Doreulee, N.1
Yanovsky, Y.2
Haas, H.L.3
-
24
-
-
0029821176
-
Clinical and genetic abnormalities in patients with Friedreich's ataxia
-
Durr A, Cossee M, Agid Y, Campuzano V, Mignard C, et al. 1996. Clinical and genetic abnormalities in patients with Friedreich's ataxia. N. Engl. J. Med. 335:1169-75
-
(1996)
N. Engl. J. Med
, vol.335
, pp. 1169-1175
-
-
Durr, A.1
Cossee, M.2
Agid, Y.3
Campuzano, V.4
Mignard, C.5
-
25
-
-
24144458246
-
The developmentally regulated expression of Menkes protein Atp7A suggests a role in axon extension and synaptogenesis
-
El Meskini R, Cline LB, Eipper BA, Ronnett GV. 2005. The developmentally regulated expression of Menkes protein Atp7A suggests a role in axon extension and synaptogenesis. Dev. Neurosci. 27:333-48
-
(2005)
Dev. Neurosci
, vol.27
, pp. 333-348
-
-
El Meskini, R.1
Cline, L.B.2
Eipper, B.A.3
Ronnett, G.V.4
-
26
-
-
0035886108
-
Orthotopic liver transplantation for Wilson's disease: A single-center experience
-
Emre S, Atillasoy EO, Ozdemir S, Schilsky M, Rathna Vanna CV, et al. 2001. Orthotopic liver transplantation for Wilson's disease: a single-center experience. Transplantation 72:1232-36
-
(2001)
Transplantation
, vol.72
, pp. 1232-1236
-
-
Emre, S.1
Atillasoy, E.O.2
Ozdemir, S.3
Schilsky, M.4
Rathna Vanna, C.V.5
-
27
-
-
5444271161
-
Pathophysiology and clinical features of Wilson disease
-
Ferenci P. 2004. Pathophysiology and clinical features of Wilson disease. Metab. Brain Dis. 19:229-39
-
(2004)
Metab. Brain Dis
, vol.19
, pp. 229-239
-
-
Ferenci, P.1
-
28
-
-
29044438902
-
The crucial role of metal ions in neurodegeneration: The basis for a promising therapeutic strategy
-
Gaeta A, Hider RC. 2005. The crucial role of metal ions in neurodegeneration: the basis for a promising therapeutic strategy. Br. J. Pharmacol. 146:1041-59
-
(2005)
Br. J. Pharmacol
, vol.146
, pp. 1041-1059
-
-
Gaeta, A.1
Hider, R.C.2
-
29
-
-
0030712294
-
Early neuroradiologic evidence of degeneration in Menkes' disease
-
Geller TJ, Pan Y, Martin DS. 1997. Early neuroradiologic evidence of degeneration in Menkes' disease. Pediatr. Neurol. 17:255-58
-
(1997)
Pediatr. Neurol
, vol.17
, pp. 255-258
-
-
Geller, T.J.1
Pan, Y.2
Martin, D.S.3
-
30
-
-
0031816970
-
Aceruloplasminemia
-
Gitlin JD. 1998. Aceruloplasminemia. Pediatr. Res. 44:271-76
-
(1998)
Pediatr. Res
, vol.44
, pp. 271-276
-
-
Gitlin, J.D.1
-
31
-
-
0345059398
-
Wilson disease
-
Gitlin JD. 2003. Wilson disease. Gastroenterology 125:1868-77
-
(2003)
Gastroenterology
, vol.125
, pp. 1868-1877
-
-
Gitlin, J.D.1
-
32
-
-
0015535059
-
Studies on the nature and excretion of biliary copper in man
-
Gollan JL, Deller DJ. 1973. Studies on the nature and excretion of biliary copper in man. Clin. Sci. 44:9-15
-
(1973)
Clin. Sci
, vol.44
, pp. 9-15
-
-
Gollan, J.L.1
Deller, D.J.2
-
33
-
-
0031982247
-
Wilson disease in 1998: Genetic, diagnostic and therapeutic aspects
-
Gollan JL, Gollan TJ. 1998. Wilson disease in 1998: genetic, diagnostic and therapeutic aspects. J. Hepatol. 28(Suppl. 1):28-36
-
(1998)
J. Hepatol
, vol.28
, Issue.SUPPL. 1
, pp. 28-36
-
-
Gollan, J.L.1
Gollan, T.J.2
-
34
-
-
30944445397
-
Neurodegeneration with brain iron accumulation
-
Gregory A, Hayflick SJ. 2005. Neurodegeneration with brain iron accumulation. Folia Neuropathol. 43:286-96
-
(2005)
Folia Neuropathol
, vol.43
, pp. 286-296
-
-
Gregory, A.1
Hayflick, S.J.2
-
35
-
-
13944261999
-
Imaging iron stores in the brain using magnetic resonance imaging
-
Haacke EM, Cheng NY, House MJ, Liu Q, Neelavalli J, et al. 2005. Imaging iron stores in the brain using magnetic resonance imaging. Magn. Reson. Imaging 23:1-25
-
(2005)
Magn. Reson. Imaging
, vol.23
, pp. 1-25
-
-
Haacke, E.M.1
Cheng, N.Y.2
House, M.J.3
Liu, Q.4
Neelavalli, J.5
-
36
-
-
0035811058
-
The metallochaperone Atox1 plays a critical role in perinatal copper homeostasis
-
Hamza I, Faisst A, Prohaska J, Chen J, Gruss P, Gitlin JD. 2001. The metallochaperone Atox1 plays a critical role in perinatal copper homeostasis. Proc. Natl. Acad. Sci. USA 98:6848-52
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 6848-6852
-
-
Hamza, I.1
Faisst, A.2
Prohaska, J.3
Chen, J.4
Gruss, P.5
Gitlin, J.D.6
-
37
-
-
0036820458
-
Copper chaperones for cytochrome c oxidase and human disease
-
Hamza I, Gitlin JD. 2002. Copper chaperones for cytochrome c oxidase and human disease. J. Bioenerg. Biomembr. 34:381-88
-
(2002)
J. Bioenerg. Biomembr
, vol.34
, pp. 381-388
-
-
Hamza, I.1
Gitlin, J.D.2
-
38
-
-
0037417798
-
Essential role for Atox1 in the copper-mediated intracellular trafficking of the Menkes Atpase
-
Hamza I, Prohaska J, Gitlin JD. 2003. Essential role for Atox1 in the copper-mediated intracellular trafficking of the Menkes Atpase. Proc. Natl. Acad. Sci. USA 100:1215-20
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 1215-1220
-
-
Hamza, I.1
Prohaska, J.2
Gitlin, J.D.3
-
39
-
-
0037301661
-
The Yin and Yang of NMDA receptor signalling
-
Hardingham GE, Bading H. 2003. The Yin and Yang of NMDA receptor signalling. Trends Neurosci. 26:81-89
-
(2003)
Trends Neurosci
, vol.26
, pp. 81-89
-
-
Hardingham, G.E.1
Bading, H.2
-
40
-
-
0032875387
-
Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux
-
Harris ZL, Durley AP, Man TK, Gidin JD. 1999. Targeted gene disruption reveals an essential role for ceruloplasmin in cellular iron efflux. Proc. Natl. Acad. Sci. USA 96:10812-17
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 10812-10817
-
-
Harris, Z.L.1
Durley, A.P.2
Man, T.K.3
Gidin, J.D.4
-
41
-
-
0031981976
-
Aceruloplasminemia: An inherited neurodegenerative disease with impairment of iron homeostasis
-
Harris ZL, Klonip LW, Gidin JD. 1998. Aceruloplasminemia: an inherited neurodegenerative disease with impairment of iron homeostasis. Am. J. Clin. Nutr. 67:972S-77
-
(1998)
Am. J. Clin. Nutr
, vol.67
-
-
Harris, Z.L.1
Klonip, L.W.2
Gidin, J.D.3
-
42
-
-
0028903259
-
Aceruloplasminemia: Molecular characterization of this disorder of iron metabolism
-
Harris ZL, Takahashi Y, Miyajima H, Serizawa M, MacGillivray RT, Gitlin JD. 1995. Aceruloplasminemia: molecular characterization of this disorder of iron metabolism. Proc. Natl. Acad. Sci. USA 92:2539-43
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 2539-2543
-
-
Harris, Z.L.1
Takahashi, Y.2
Miyajima, H.3
Serizawa, M.4
MacGillivray, R.T.5
Gitlin, J.D.6
-
43
-
-
0023748491
-
Evidence for release of copper in the brain: Depolarization-induced release of newly taken-up 67copper
-
Hartter DE, Barnea A. 1988. Evidence for release of copper in the brain: depolarization-induced release of newly taken-up 67copper. Synapse 2:412-15
-
(1988)
Synapse
, vol.2
, pp. 412-415
-
-
Hartter, D.E.1
Barnea, A.2
-
44
-
-
0037413484
-
Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome
-
Hayflick SJ, Westaway SK, Levinson B, Zhou B, Johnson MA, et al. 2003. Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome. N. Engl. J. Med. 348:33-40
-
(2003)
N. Engl. J. Med
, vol.348
, pp. 33-40
-
-
Hayflick, S.J.1
Westaway, S.K.2
Levinson, B.3
Zhou, B.4
Johnson, M.A.5
-
45
-
-
0036400025
-
Ceruloplasmin metabolism and function
-
Hellman NE, Gitlin JD. 2002. Ceruloplasmin metabolism and function. Annu. Rev. Nutr. 22:439-58
-
(2002)
Annu. Rev. Nutr
, vol.22
, pp. 439-458
-
-
Hellman, N.E.1
Gitlin, J.D.2
-
46
-
-
2042546096
-
Balancing acts: Molecular control of mammalian iron metabolism
-
Hentze MW, Muckenthaler MU, Andrews NC. 2004. Balancing acts: molecular control of mammalian iron metabolism. Cell 117:285-97
-
(2004)
Cell
, vol.117
, pp. 285-297
-
-
Hentze, M.W.1
Muckenthaler, M.U.2
Andrews, N.C.3
-
47
-
-
0032571387
-
Reduced fertility in female mice lacking copper-zinc superoxide dismutase
-
Ho YS, Gargano M, Cao J, Bronson RT, Heimler I, Hutz RJ. 1998. Reduced fertility in female mice lacking copper-zinc superoxide dismutase. J. Biol. Chem. 273:7765-69
-
(1998)
J. Biol. Chem
, vol.273
, pp. 7765-7769
-
-
Ho, Y.S.1
Gargano, M.2
Cao, J.3
Bronson, R.T.4
Heimler, I.5
Hutz, R.J.6
-
48
-
-
0038529805
-
Lysyl oxidase is required for vascular and diaphragmatic development in mice
-
Hornstra IK, Birge S, Starcher B, Bailey AJ, Mecham RP, Shapiro SD. 2003. Lysyl oxidase is required for vascular and diaphragmatic development in mice. J. Biol. Chem. 278:14387-93
-
(2003)
J. Biol. Chem
, vol.278
, pp. 14387-14393
-
-
Hornstra, I.K.1
Birge, S.2
Starcher, B.3
Bailey, A.J.4
Mecham, R.P.5
Shapiro, S.D.6
-
49
-
-
0038711587
-
Glycosylphosphatidylinositol-anchored ceruloplasmin is required for iron efflux from cells in the central nervous system
-
Jeong SY, David S. 2003. Glycosylphosphatidylinositol-anchored ceruloplasmin is required for iron efflux from cells in the central nervous system. J. Biol. Chem. 278:27144-48
-
(2003)
J. Biol. Chem
, vol.278
, pp. 27144-27148
-
-
Jeong, S.Y.1
David, S.2
-
50
-
-
33748889489
-
Age-related changes in iron homeostasis and cell death in the cerebellum of ceruloplasmin-deficient mice
-
Jeong SY, David S. 2006. Age-related changes in iron homeostasis and cell death in the cerebellum of ceruloplasmin-deficient mice. J. Neurosci. 26:9810-19
-
(2006)
J. Neurosci
, vol.26
, pp. 9810-9819
-
-
Jeong, S.Y.1
David, S.2
-
51
-
-
1842504252
-
Mitochondrial localization of human PANK2 and hypotheses of secondary iron accumulation in pantothenate kinase-associated neurodegeneration
-
Johnson MA, Kuo YM, Westaway SK, Parker SM, Ching KH, et al. 2004. Mitochondrial localization of human PANK2 and hypotheses of secondary iron accumulation in pantothenate kinase-associated neurodegeneration. Ann. N.Y. Acad. Sci. 1012:282-98
-
(2004)
Ann. N.Y. Acad. Sci
, vol.1012
, pp. 282-298
-
-
Johnson, M.A.1
Kuo, Y.M.2
Westaway, S.K.3
Parker, S.M.4
Ching, K.H.5
-
52
-
-
0031598230
-
Metabolic and molecular bases of Menkes disease and occipital horn syndrome
-
Kaler SG. 1998. Metabolic and molecular bases of Menkes disease and occipital horn syndrome. Pediatr. Dev. Pathol. 1:85-98
-
(1998)
Pediatr. Dev. Pathol
, vol.1
, pp. 85-98
-
-
Kaler, S.G.1
-
53
-
-
0029616291
-
Early copper therapy in classic Menkes disease patients with a novel splicing mutation
-
Kaler SG, Buist NR, Holmes CS, Goldstein DS, Miller RC, Gahl WA. 1995. Early copper therapy in classic Menkes disease patients with a novel splicing mutation. Ann. Neurol. 38:921-28
-
(1995)
Ann. Neurol
, vol.38
, pp. 921-928
-
-
Kaler, S.G.1
Buist, N.R.2
Holmes, C.S.3
Goldstein, D.S.4
Miller, R.C.5
Gahl, W.A.6
-
54
-
-
0036898075
-
Astrocytic deformity and globular structures are characteristic of the brains of patients with aceruloplasminemia
-
Kaneko K, Yoshida K, Arima K, Ohara S, Miyajima H, et al. 2002. Astrocytic deformity and globular structures are characteristic of the brains of patients with aceruloplasminemia. J. Neuropathol. Exp. Neurol. 61:1069-77
-
(2002)
J. Neuropathol. Exp. Neurol
, vol.61
, pp. 1069-1077
-
-
Kaneko, K.1
Yoshida, K.2
Arima, K.3
Ohara, S.4
Miyajima, H.5
-
55
-
-
0024362166
-
Nerve endings from rat brain tissue release copper upon depolarization. A possible role in regulating neuronal excitability
-
Kardos J, Kovacs I, Hajos F, Kalman M, Simonyi M. 1989. Nerve endings from rat brain tissue release copper upon depolarization. A possible role in regulating neuronal excitability. Neurosci. Lett. 103:139-44
-
(1989)
Neurosci. Lett
, vol.103
, pp. 139-144
-
-
Kardos, J.1
Kovacs, I.2
Hajos, F.3
Kalman, M.4
Simonyi, M.5
-
56
-
-
0031981647
-
Effect of copper deficiency on prenatal development and pregnancy outcome
-
Keen CL, Uriu-Hare JY, Hawk SN, Jankowski MA, Daston GP, et al. 1998. Effect of copper deficiency on prenatal development and pregnancy outcome. Am.. J. Clin. Nutr. 67:1003S-11
-
(1998)
Am.. J. Clin. Nutr
, vol.67
-
-
Keen, C.L.1
Uriu-Hare, J.Y.2
Hawk, S.N.3
Jankowski, M.A.4
Daston, G.P.5
-
57
-
-
0029948054
-
Amurine model of Menkes disease reveals a physiological function of metallothionein
-
Kelly EJ, Palmiter RD. 1996. Amurine model of Menkes disease reveals a physiological function of metallothionein. Nat. Genet. 13:219-22
-
(1996)
Nat. Genet
, vol.13
, pp. 219-222
-
-
Kelly, E.J.1
Palmiter, R.D.2
-
59
-
-
0029800745
-
Expression of the ceruloplasmin gene in the human retina and brain: Implications for a pathogenic model in aceruloplasminemia
-
Klomp LW, Gidin JD. 1996. Expression of the ceruloplasmin gene in the human retina and brain: implications for a pathogenic model in aceruloplasminemia. Hum. Mol. Genet. 5:1989-96
-
(1996)
Hum. Mol. Genet
, vol.5
, pp. 1989-1996
-
-
Klomp, L.W.1
Gidin, J.D.2
-
60
-
-
0032783060
-
Clinical manifestations and treatment of Menkes disease and its variants
-
Kodama H, Murata Y, Kobayashi M. 1999. Clinical manifestations and treatment of Menkes disease and its variants. Pediatr. Int. 41:423-29
-
(1999)
Pediatr. Int
, vol.41
, pp. 423-429
-
-
Kodama, H.1
Murata, Y.2
Kobayashi, M.3
-
61
-
-
33745870402
-
Molecular and pathological basis of aceruloplasminemia
-
Kono S, Miyajima H. 2006. Molecular and pathological basis of aceruloplasminemia. Biol. Res. 39:15-23
-
(2006)
Biol. Res
, vol.39
, pp. 15-23
-
-
Kono, S.1
Miyajima, H.2
-
62
-
-
3142674792
-
New insights into erythropoiesis: The roles of folate, vitamin B12, and iron
-
Koury MJ, Ponka P. 2004. New insights into erythropoiesis: the roles of folate, vitamin B12, and iron. Annu. Rev. Nutr. 24:105-31
-
(2004)
Annu. Rev. Nutr
, vol.24
, pp. 105-131
-
-
Koury, M.J.1
Ponka, P.2
-
63
-
-
0019857598
-
Histochemical detection of zinc and copper in various neurons of the central nervous system
-
Kozma M, Szerdahelyi P, Kasa P. 1981. Histochemical detection of zinc and copper in various neurons of the central nervous system. Acta Histochem. 69:12-17
-
(1981)
Acta Histochem
, vol.69
, pp. 12-17
-
-
Kozma, M.1
Szerdahelyi, P.2
Kasa, P.3
-
64
-
-
3242718536
-
Copper deficiency myelopathy produces a clinical picture like subacute combined degeneration
-
Kumar N, Gross JBJ, Ahlskog JE. 2004. Copper deficiency myelopathy produces a clinical picture like subacute combined degeneration. Neurology 63:33-39
-
(2004)
Neurology
, vol.63
, pp. 33-39
-
-
Kumar, N.1
Gross, J.B.J.2
Ahlskog, J.E.3
-
65
-
-
31544454133
-
2 006. Copper transport protein (Ctrl) levels in mice are tissue specific and dependent on copper status
-
Kuo YM, Gybina AA, Pyatskowit JW, Gitschier J, Prohaska JR. 2 006. Copper transport protein (Ctrl) levels in mice are tissue specific and dependent on copper status. J. Nutr. 136:21-26
-
J. Nutr
, vol.136
, pp. 21-26
-
-
Kuo, Y.M.1
Gybina, A.A.2
Pyatskowit, J.W.3
Gitschier, J.4
Prohaska, J.R.5
-
66
-
-
0035811069
-
The copper transporter CTR1 provides an essential function in mammalian embryonic development
-
Kuo YM, Zhou B, Cosco D, Gitschier J. 2001. The copper transporter CTR1 provides an essential function in mammalian embryonic development. Proc. Natl. Acad. Sci. USA 98:6836-41
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 6836-6841
-
-
Kuo, Y.M.1
Zhou, B.2
Cosco, D.3
Gitschier, J.4
-
67
-
-
0035138456
-
Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in mice
-
LaVaute T, Smith S, Cooperman S, Iwai K, Land W, et al. 2001. Targeted deletion of the gene encoding iron regulatory protein-2 causes misregulation of iron metabolism and neurodegenerative disease in mice. Nat. Genet. 27:209-14
-
(2001)
Nat. Genet
, vol.27
, pp. 209-214
-
-
LaVaute, T.1
Smith, S.2
Cooperman, S.3
Iwai, K.4
Land, W.5
-
68
-
-
33845596232
-
The human cytochrome c oxidase assembly factors SCO1 and SCO2 have regulatory roles in the maintenance of cellular copper homeostasis
-
Leary SC, Cobine PA, Kaufman BA, Guercin GH, Mattman A, et al. 2007. The human cytochrome c oxidase assembly factors SCO1 and SCO2 have regulatory roles in the maintenance of cellular copper homeostasis. Cell Metab. 5:9-20
-
(2007)
Cell Metab
, vol.5
, pp. 9-20
-
-
Leary, S.C.1
Cobine, P.A.2
Kaufman, B.A.3
Guercin, G.H.4
Mattman, A.5
-
69
-
-
33645326193
-
Iron dysregulation and neurodegeneration: The molecular connection
-
Lee DW, Andersen JK, Kaur D. 2006. Iron dysregulation and neurodegeneration: the molecular connection. Mol. Interv. 6:89-97
-
(2006)
Mol. Interv
, vol.6
, pp. 89-97
-
-
Lee, D.W.1
Andersen, J.K.2
Kaur, D.3
-
70
-
-
0035811053
-
Essential role for mammalian copper transporter Ctrl in copper homeostasis and embryonic development
-
Lee J, Prohaska JR, Thiele DJ. 2001. Essential role for mammalian copper transporter Ctrl in copper homeostasis and embryonic development. Proc. Natl. Acad. Sci. USA 98:6842-47
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 6842-6847
-
-
Lee, J.1
Prohaska, J.R.2
Thiele, D.J.3
-
72
-
-
14544294357
-
Neuroferritinopathy: A neurodegenerative disorder associated with L-ferritin mutation
-
Levi S, Cozzi A, Arosio P. 2005. Neuroferritinopathy: a neurodegenerative disorder associated with L-ferritin mutation. Best. Pract. Res. Clin. Haematol. 18:265-76
-
(2005)
Best. Pract. Res. Clin. Haematol
, vol.18
, pp. 265-276
-
-
Levi, S.1
Cozzi, A.2
Arosio, P.3
-
73
-
-
33751177803
-
Iron-sulfur protein biogenesis in eukaryotes: Components and mechanisms
-
Lill R, Mühlenhoff U. 2006. Iron-sulfur protein biogenesis in eukaryotes: components and mechanisms. Annu. Rev. Cell Dev. Biol. 22:457-86
-
(2006)
Annu. Rev. Cell Dev. Biol
, vol.22
, pp. 457-486
-
-
Lill, R.1
Mühlenhoff, U.2
-
74
-
-
0028090209
-
Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus
-
Logan JI, Harveyson KB, Wisdom GB, Hughes AE, Archbold GP. 1994. Hereditary caeruloplasmin deficiency, dementia and diabetes mellitus. Q. J. Med. 87:663-70
-
(1994)
Q. J. Med
, vol.87
, pp. 663-670
-
-
Logan, J.I.1
Harveyson, K.B.2
Wisdom, G.B.3
Hughes, A.E.4
Archbold, G.P.5
-
75
-
-
33745502924
-
Long-lasting neural and behavioral effects of iron deficiency in infancy
-
discussion S72-91
-
Lozoff B, Beard J, Connor J, Barbara F, Georgieff M, Schallert T. 2006. Long-lasting neural and behavioral effects of iron deficiency in infancy. Nutr. Rev. 64:S34-43; discussion S72-91
-
(2006)
Nutr. Rev
, vol.64
-
-
Lozoff, B.1
Beard, J.2
Connor, J.3
Barbara, F.4
Georgieff, M.5
Schallert, T.6
-
76
-
-
0035132869
-
Activation of synaptic NMDA receptors induces membrane insertion of new AMPA receptors and LTP in cultured hippocampal neurons
-
Lu W, Man H, Ju W, Trimble WS, MacDonald JF, Wang YT. 2001. Activation of synaptic NMDA receptors induces membrane insertion of new AMPA receptors and LTP in cultured hippocampal neurons. Neuron 29:243-54
-
(2001)
Neuron
, vol.29
, pp. 243-254
-
-
Lu, W.1
Man, H.2
Ju, W.3
Trimble, W.S.4
MacDonald, J.F.5
Wang, Y.T.6
-
77
-
-
0037802583
-
Function and regulation of the mammalian copper-transporting Atpases: Insights from biochemical and cell biological approaches
-
Lutsenko S, Petris MJ. 2003. Function and regulation of the mammalian copper-transporting Atpases: insights from biochemical and cell biological approaches. J. Membr. Biol. 191:1-12
-
(2003)
J. Membr. Biol
, vol.191
, pp. 1-12
-
-
Lutsenko, S.1
Petris, M.J.2
-
78
-
-
23844553465
-
Neuroferritinopathy: Missense mutation in FTL causing early-onset bilateral pallidal involvement
-
Maciel P, Cruz VT, Constante M, Iniesta I, Costa MC, et al. 2005. Neuroferritinopathy: missense mutation in FTL causing early-onset bilateral pallidal involvement. Neurology 65:603-5
-
(2005)
Neurology
, vol.65
, pp. 603-605
-
-
Maciel, P.1
Cruz, V.T.2
Constante, M.3
Iniesta, I.4
Costa, M.C.5
-
79
-
-
16844363930
-
Hereditary ferritinopathy: A novel mutation, its cellular pathology, and pathogenetic insights
-
Mancuso M, Davidzon G, Kurlan RM, Tawil R, Bonilla E, et al. 2005. Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights. J. Neuropathol. Exp. Neurol. 64:280-94
-
(2005)
J. Neuropathol. Exp. Neurol
, vol.64
, pp. 280-294
-
-
Mancuso, M.1
Davidzon, G.2
Kurlan, R.M.3
Tawil, R.4
Bonilla, E.5
-
80
-
-
33746558633
-
Atp7a determines a hierarchy of copper metabolism essential for notochord development
-
Mendelsohn BA, Yin C, Johnson SL, Wilm TP, Solnica-Krezel L, Gitlin JD. 2006. Atp7a determines a hierarchy of copper metabolism essential for notochord development. Cell Metab. 4:155-62
-
(2006)
Cell Metab
, vol.4
, pp. 155-162
-
-
Mendelsohn, B.A.1
Yin, C.2
Johnson, S.L.3
Wilm, T.P.4
Solnica-Krezel, L.5
Gitlin, J.D.6
-
81
-
-
0031971144
-
Menkes syndrome and animal models
-
Mercer JF. 1998. Menkes syndrome and animal models. Am. J. Clin. Nutr. 67:1022S-28
-
(1998)
Am. J. Clin. Nutr
, vol.67
-
-
Mercer, J.F.1
-
82
-
-
0027475976
-
Isolation of a partial candidate gene for Menkes disease by positional cloning
-
Mercer JF, Livingston J, Hall B, Paynter JA, Begy C, et al. 1993. Isolation of a partial candidate gene for Menkes disease by positional cloning. Nat. Genet. 3:20-25
-
(1993)
Nat. Genet
, vol.3
, pp. 20-25
-
-
Mercer, J.F.1
Livingston, J.2
Hall, B.3
Paynter, J.A.4
Begy, C.5
-
83
-
-
0023240051
-
Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration
-
Miyajima H, Nishimura Y, Mizoguchi K, Sakamoto M, Shimizu T, Honda N. 1987. Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration. Neurology 37:761-67
-
(1987)
Neurology
, vol.37
, pp. 761-767
-
-
Miyajima, H.1
Nishimura, Y.2
Mizoguchi, K.3
Sakamoto, M.4
Shimizu, T.5
Honda, N.6
-
84
-
-
0000241356
-
Similar splice-site mutations of the Atp7A gene lead to different phenotypes: Classical Menkes disease or occipital horn syndrome
-
Moller LB, Tumer Z, Lund C, Petersen C, Cole T, et al. 2000. Similar splice-site mutations of the Atp7A gene lead to different phenotypes: classical Menkes disease or occipital horn syndrome. Am. J. Hum. Genet. 66:1211-20
-
(2000)
Am. J. Hum. Genet
, vol.66
, pp. 1211-1220
-
-
Moller, L.B.1
Tumer, Z.2
Lund, C.3
Petersen, C.4
Cole, T.5
-
85
-
-
1842504357
-
The metabolism of neuronal iron and its pathogenic role in neurological disease: Review
-
Moos T, Morgan EH. 2004. The metabolism of neuronal iron and its pathogenic role in neurological disease: review. Ann. N.Y.Acad. Sci. 1012:14-26
-
(2004)
Ann. N.Y.Acad. Sci
, vol.1012
, pp. 14-26
-
-
Moos, T.1
Morgan, E.H.2
-
86
-
-
33748090285
-
Brain capillary endothelial cells mediate iron transport into the brain by segregating iron from transferrin without the involvement of divalent metal transporter 1
-
Moos T, Skjoerringe T, Gosk S, Morgan EH. 2006. Brain capillary endothelial cells mediate iron transport into the brain by segregating iron from transferrin without the involvement of divalent metal transporter 1. J. Neurochem. 98:1946-58
-
(2006)
J. Neurochem
, vol.98
, pp. 1946-1958
-
-
Moos, T.1
Skjoerringe, T.2
Gosk, S.3
Morgan, E.H.4
-
87
-
-
33745553895
-
PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron
-
Morgan NV, Westaway SK, Morton JE, Gregory A, Gissen P, et al. 2006. PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron. Nat. Genet. 38:752-54
-
(2006)
Nat. Genet
, vol.38
, pp. 752-754
-
-
Morgan, N.V.1
Westaway, S.K.2
Morton, J.E.3
Gregory, A.4
Gissen, P.5
-
88
-
-
0029007765
-
Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a Japanese family
-
Morita H, Ikeda S, Yamamoto K, Morita S, Yoshida K, et al. 1995. Hereditary ceruloplasmin deficiency with hemosiderosis: a clinicopathological study of a Japanese family. Ann. Neurol. 37:646-56
-
(1995)
Ann. Neurol
, vol.37
, pp. 646-656
-
-
Morita, H.1
Ikeda, S.2
Yamamoto, K.3
Morita, S.4
Yoshida, K.5
-
89
-
-
33750133047
-
Regulation of iron metabolism by hepcidin
-
Nemeth E, Ganz T. 2006. Regulation of iron metabolism by hepcidin. Annu. Rev. Nutr. 26:323-42
-
(2006)
Annu. Rev. Nutr
, vol.26
, pp. 323-342
-
-
Nemeth, E.1
Ganz, T.2
-
90
-
-
10844258104
-
Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization
-
Nemeth E, Tuttle MS, Powelson J, Vaughn MB, Donovan A, et al. 2004. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization. Science 306:2090-93
-
(2004)
Science
, vol.306
, pp. 2090-2093
-
-
Nemeth, E.1
Tuttle, M.S.2
Powelson, J.3
Vaughn, M.B.4
Donovan, A.5
-
91
-
-
0036800145
-
The copper-iron connection: Hereditary aceruloplasminemia
-
Nittis T, Gidin JD. 2002. The copper-iron connection: hereditary aceruloplasminemia. Semin. Hematol. 39:282-89
-
(2002)
Semin. Hematol
, vol.39
, pp. 282-289
-
-
Nittis, T.1
Gidin, J.D.2
-
92
-
-
33747849534
-
Ctr1 drives intestinal copper absorption and is essential for growth, iron metabolism, and neonatal cardiac function
-
Nose Y, Kim BE, Thiele DJ. 2006. Ctr1 drives intestinal copper absorption and is essential for growth, iron metabolism, and neonatal cardiac function. Cell Metab. 4:235-44
-
(2006)
Cell Metab
, vol.4
, pp. 235-244
-
-
Nose, Y.1
Kim, B.E.2
Thiele, D.J.3
-
93
-
-
0034682776
-
Metallochaperones, an intracellular shuttle service for metal ions
-
O'Halloran TV, Culotta VC. 2000. Metallochaperones, an intracellular shuttle service for metal ions. J. Biol. Chem. 275:25057-60
-
(2000)
J. Biol. Chem
, vol.275
, pp. 25057-25060
-
-
O'Halloran, T.V.1
Culotta, V.C.2
-
94
-
-
0025739298
-
Neurological and neuropsychiatric spectrum of Wilson's disease: A prospective study of 45 cases
-
Oder W, Grimm G, Kollegger H, Ferenci P, Schneider B, Deecke L. 1991. Neurological and neuropsychiatric spectrum of Wilson's disease: a prospective study of 45 cases. J. Neurol. 238:281-87
-
(1991)
J. Neurol
, vol.238
, pp. 281-287
-
-
Oder, W.1
Grimm, G.2
Kollegger, H.3
Ferenci, P.4
Schneider, B.5
Deecke, L.6
-
95
-
-
33644944155
-
Iron overload and antioxidative role of perivascular astrocytes in aceruloplasminemia
-
Oide T, Yoshida K, Kaneko K, Ohta M, Arima K. 2006. Iron overload and antioxidative role of perivascular astrocytes in aceruloplasminemia. Neuropathol. Appl. Neurobiol. 32:170-76
-
(2006)
Neuropathol. Appl. Neurobiol
, vol.32
, pp. 170-176
-
-
Oide, T.1
Yoshida, K.2
Kaneko, K.3
Ohta, M.4
Arima, K.5
-
96
-
-
0026026324
-
Menkes' kinky hair disease: Morphological and immunohistochemical comparison of two autopsied patients
-
Okeda R, Gei S, Chen I, Okaniwa M, Shinomiya M, Matsubara O. 1991. Menkes' kinky hair disease: morphological and immunohistochemical comparison of two autopsied patients. Acta Neuropathol. (Berl.) 81:450-57
-
(1991)
Acta Neuropathol. (Berl.)
, vol.81
, pp. 450-457
-
-
Okeda, R.1
Gei, S.2
Chen, I.3
Okaniwa, M.4
Shinomiya, M.5
Matsubara, O.6
-
97
-
-
0034635402
-
Alternative RNA splicing generates a glycosylphosphatidylinositol-anchored form of ceruloplasmin in mammalian brain
-
Patel BN, Dunn RJ, David S. 2000. Alternative RNA splicing generates a glycosylphosphatidylinositol-anchored form of ceruloplasmin in mammalian brain. J. Biol. Chem.. 275:4305-10
-
(2000)
J. Biol. Chem
, vol.275
, pp. 4305-4310
-
-
Patel, B.N.1
Dunn, R.J.2
David, S.3
-
98
-
-
0036703490
-
Ceruloplasmin regulates iron levels in the CNS and prevents free radical injury
-
Patel BN, Dunn RJ, Jeong SY, Zhu Q, Julien JP, David S. 2002. Ceruloplasmin regulates iron levels in the CNS and prevents free radical injury. J. Neurosci. 22:6578-86
-
(2002)
J. Neurosci
, vol.22
, pp. 6578-6586
-
-
Patel, B.N.1
Dunn, R.J.2
Jeong, S.Y.3
Zhu, Q.4
Julien, J.P.5
David, S.6
-
99
-
-
0037477740
-
A delicate balance: Homeostatic control of copper uptake and distribution
-
Pena MM, Lee J, Thiele DJ. 1999. A delicate balance: homeostatic control of copper uptake and distribution. J. Nutr. 129:1251-60
-
(1999)
J. Nutr
, vol.129
, pp. 1251-1260
-
-
Pena, M.M.1
Lee, J.2
Thiele, D.J.3
-
100
-
-
0029909937
-
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
-
Petris MJ, Mercer JF, Culvenor JG, Lockhart P, Gleeson PA, Camakaris J. 1996. 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. EMBO J. 15:6084-95
-
(1996)
EMBO J
, vol.15
, pp. 6084-6095
-
-
Petris, M.J.1
Mercer, J.F.2
Culvenor, J.G.3
Lockhart, P.4
Gleeson, P.A.5
Camakaris, J.6
-
101
-
-
33750095012
-
Hereditary hemochromatosis
-
Pietrangelo A. 2006a. Hereditary hemochromatosis. Annu. Rev. Nutr. 26:251-70
-
(2006)
Annu. Rev. Nutr
, vol.26
, pp. 251-270
-
-
Pietrangelo, A.1
-
102
-
-
33746868342
-
Hereditary hemochromatosis
-
Pietrangelo A. 2006b. Hereditary hemochromatosis. Biochim. Biophys. Acta 1763:700-10
-
(2006)
Biochim. Biophys. Acta
, vol.1763
, pp. 700-710
-
-
Pietrangelo, A.1
-
103
-
-
0032964289
-
Cellular iron metabolism
-
Ponka P. 1999. Cellular iron metabolism. Kidney Int. 69(Suppl.):S2-11
-
(1999)
Kidney Int
, vol.69
, Issue.SUPPL.
-
-
Ponka, P.1
-
104
-
-
1842608738
-
Hereditary causes of disturbed iron homeostasis in the central nervous system
-
Ponka P. 2004. Hereditary causes of disturbed iron homeostasis in the central nervous system. Ann. N.Y. Acad. Sci. 1012:267-81
-
(2004)
Ann. N.Y. Acad. Sci
, vol.1012
, pp. 267-281
-
-
Ponka, P.1
-
106
-
-
0036792121
-
The timing of perinatal copper deficiency in mice influences offspring survival
-
Prohaska JR, Brokate B. 2002. The timing of perinatal copper deficiency in mice influences offspring survival. J. Nutr. 132:3142-45
-
(2002)
J. Nutr
, vol.132
, pp. 3142-3145
-
-
Prohaska, J.R.1
Brokate, B.2
-
107
-
-
0035138072
-
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits
-
Puccio H, Simon D, Cossee M, Criqui-Filipe P, Tiziano F, et al. 2001. Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits. Nat. Genet. 27:181-86
-
(2001)
Nat. Genet
, vol.27
, pp. 181-186
-
-
Puccio, H.1
Simon, D.2
Cossee, M.3
Criqui-Filipe, P.4
Tiziano, F.5
-
108
-
-
0033617578
-
Undetectable intracellular free copper: The requirement of a copper chaperone for superoxide dismutase
-
Rae TD, Schmidt PJ, Pufahl RA, Culotta VC, O'Halloran TV. 1999. Undetectable intracellular free copper: the requirement of a copper chaperone for superoxide dismutase. Science 284:805-8
-
(1999)
Science
, vol.284
, pp. 805-808
-
-
Rae, T.D.1
Schmidt, P.J.2
Pufahl, R.A.3
Culotta, V.C.4
O'Halloran, T.V.5
-
109
-
-
33746361251
-
The role of iron regulatory proteins in mammalian iron homeostasis and disease
-
Rouault TA. 2006. The role of iron regulatory proteins in mammalian iron homeostasis and disease. Nat. Chem. Biol. 2:406-14
-
(2006)
Nat. Chem. Biol
, vol.2
, pp. 406-414
-
-
Rouault, T.A.1
-
110
-
-
17144378216
-
Iron-sulphur cluster biogenesis and mitochondrial iron homeostasis
-
Rouault TA, Tong WH. 2005. Iron-sulphur cluster biogenesis and mitochondrial iron homeostasis. Nat. Rev. Mol. Cell. Biol. 6:345-51
-
(2005)
Nat. Rev. Mol. Cell. Biol
, vol.6
, pp. 345-351
-
-
Rouault, T.A.1
Tong, W.H.2
-
111
-
-
0027968067
-
Localization of copper to afferent terminals in rat locus ceruleus, in contrast to mitochondrial copper in cerebellum
-
Sato M, Ohtomo K, Daimon T, Sugiyama T, Iijima K. 1994. Localization of copper to afferent terminals in rat locus ceruleus, in contrast to mitochondrial copper in cerebellum. J. Histochem. Cytochem. 42:1585-91
-
(1994)
J. Histochem. Cytochem
, vol.42
, pp. 1585-1591
-
-
Sato, M.1
Ohtomo, K.2
Daimon, T.3
Sugiyama, T.4
Iijima, K.5
-
112
-
-
0032932229
-
Genetic disorders of membrane transport. IV Wilson's disease and Menkes disease
-
Schaefer M, Gidin JD. 1999. Genetic disorders of membrane transport. IV Wilson's disease and Menkes disease. Am. J. Physiol. 276:G311-14
-
(1999)
Am. J. Physiol
, vol.276
-
-
Schaefer, M.1
Gidin, J.D.2
-
113
-
-
33749534285
-
Role of the Menkes copper transporting Atpase in NMDA receptor-mediated neuronal toxicity
-
Schlief M, West T, Craig A, Holtzman D, Gitlin J. 2006. Role of the Menkes copper transporting Atpase in NMDA receptor-mediated neuronal toxicity. Proc. Natl. Acad. Sci. USA 103:14919-24
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 14919-14924
-
-
Schlief, M.1
West, T.2
Craig, A.3
Holtzman, D.4
Gitlin, J.5
-
114
-
-
12144257164
-
NMDA receptor activation mediates copper homeostasis in hippocampal neurons
-
Schlief ML, Craig AM, Gidin JD. 2005. NMDA receptor activation mediates copper homeostasis in hippocampal neurons. J. Neurosci. 25:239-46
-
(2005)
J. Neurosci
, vol.25
, pp. 239-246
-
-
Schlief, M.L.1
Craig, A.M.2
Gidin, J.D.3
-
115
-
-
33646856612
-
Copper homeostasis in the CNS: A novel link between the NMDA receptor and copper homeostasis in the hippocampus
-
Schlief ML, Gitlin JD. 2006. Copper homeostasis in the CNS: a novel link between the NMDA receptor and copper homeostasis in the hippocampus. Mol. Neurobiol. 33:81-90
-
(2006)
Mol. Neurobiol
, vol.33
, pp. 81-90
-
-
Schlief, M.L.1
Gitlin, J.D.2
-
116
-
-
0035082414
-
Liver transplantation in neurologic Wilson's disease
-
Schumacher G, Platz KP, Mueller AR, Neuhaus R, Luck W, et al. 2001. Liver transplantation in neurologic Wilson's disease. Transplant. Proc. 33:1518-19
-
(2001)
Transplant. Proc
, vol.33
, pp. 1518-1519
-
-
Schumacher, G.1
Platz, K.P.2
Mueller, A.R.3
Neuhaus, R.4
Luck, W.5
-
117
-
-
33644748145
-
Mitoferrin is essential for erythroid iron assimilation
-
Shaw GC, Cope JJ, Li L, Corson K, Hersey C, et al. 2006. Mitoferrin is essential for erythroid iron assimilation. Nature 440:96-100
-
(2006)
Nature
, vol.440
, pp. 96-100
-
-
Shaw, G.C.1
Cope, J.J.2
Li, L.3
Corson, K.4
Hersey, C.5
-
118
-
-
0141702360
-
Trace amounts of copper in water induce beta-amyloid plaques and learning deficits in a rabbit model of Alzheimer's disease
-
Sparks DL, Schreurs BG. 2003. Trace amounts of copper in water induce beta-amyloid plaques and learning deficits in a rabbit model of Alzheimer's disease. Proc. Natl. Acad. Sci. USA 100:11065-69
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 11065-11069
-
-
Sparks, D.L.1
Schreurs, B.G.2
-
119
-
-
0027364961
-
The Wilson disease gene is a copper transporting Atpase with homology to the Menkes disease gene
-
Tanzi RE, Petrukhin K, Chernov I, Pellequer JL, Wasco W, et al. 1993. The Wilson disease gene is a copper transporting Atpase with homology to the Menkes disease gene. Nat. Genet. 5:344-50
-
(1993)
Nat. Genet
, vol.5
, pp. 344-350
-
-
Tanzi, R.E.1
Petrukhin, K.2
Chernov, I.3
Pellequer, J.L.4
Wasco, W.5
-
120
-
-
0038241789
-
Hepatic copper metabolism: Insights from genetic disease
-
Tao TY, Gitlin JD. 2003. Hepatic copper metabolism: insights from genetic disease. Hepatology 37:1241-47
-
(2003)
Hepatology
, vol.37
, pp. 1241-1247
-
-
Tao, T.Y.1
Gitlin, J.D.2
-
121
-
-
4043144143
-
Neurodegenerative disease and iron storage in the brain
-
Thomas M, Jankovic J. 2004. Neurodegenerative disease and iron storage in the brain. Curr. Opin. Neurol. 17:437-42
-
(2004)
Curr. Opin. Neurol
, vol.17
, pp. 437-442
-
-
Thomas, M.1
Jankovic, J.2
-
122
-
-
0029910647
-
Differential modulation by zinc and copper of amino acid receptors from rat olfactory bulb neurons
-
Trombley PQ, Shepherd GM. 1996. Differential modulation by zinc and copper of amino acid receptors from rat olfactory bulb neurons. J. Neurophysiol. 76:2536-46
-
(1996)
J. Neurophysiol
, vol.76
, pp. 2536-2546
-
-
Trombley, P.Q.1
Shepherd, G.M.2
-
123
-
-
12144288949
-
Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene
-
Vidal R, Ghetti B, Takao M, Brefel-Courbon C, Uro-Coste E, et al. 2004. Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene. J. Neuropathol. Exp. Neurol. 63:363-80
-
(2004)
J. Neuropathol. Exp. Neurol
, vol.63
, pp. 363-380
-
-
Vidal, R.1
Ghetti, B.2
Takao, M.3
Brefel-Courbon, C.4
Uro-Coste, E.5
-
124
-
-
0029964789
-
Copper modulation of NMDA responses in mouse and rat cultured hippocampal neurons
-
Vlachova V, Zemkova H, Vyklicky LJ. 1996. Copper modulation of NMDA responses in mouse and rat cultured hippocampal neurons. Eur. J. Neurosci. 8:2257-64
-
(1996)
Eur. J. Neurosci
, vol.8
, pp. 2257-2264
-
-
Vlachova, V.1
Zemkova, H.2
Vyklicky, L.J.3
-
125
-
-
1542350111
-
Friedreich ataxia-update on pathogenesis and possible therapies
-
Voncken M, Ioannou P, Delatycki MB. 2004. Friedreich ataxia-update on pathogenesis and possible therapies. Neurogenetics 5:1-8
-
(2004)
Neurogenetics
, vol.5
, pp. 1-8
-
-
Voncken, M.1
Ioannou, P.2
Delatycki, M.B.3
-
126
-
-
0027446365
-
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting Atpase
-
Vulpe C, Levinson B, Whitney S, Packman S, Gitschier J. 1993. Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper-transporting Atpase. Nat. Genet. 3:7-13
-
(1993)
Nat. Genet
, vol.3
, pp. 7-13
-
-
Vulpe, C.1
Levinson, B.2
Whitney, S.3
Packman, S.4
Gitschier, J.5
-
127
-
-
0032909207
-
Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse
-
Vulpe CD, Kuo YM, Murphy TL, Cowley L, Askwith C, et al. 1999. Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse. Nat. Genet. 21:195-99
-
(1999)
Nat. Genet
, vol.21
, pp. 195-199
-
-
Vulpe, C.D.1
Kuo, Y.M.2
Murphy, T.L.3
Cowley, L.4
Askwith, C.5
-
129
-
-
0030566645
-
The effects of copper ions on glutamate receptors in cultured rat cortical neurons
-
Weiser T, Wienrich M. 1996. The effects of copper ions on glutamate receptors in cultured rat cortical neurons. Brain Res. 742:211-18
-
(1996)
Brain Res
, vol.742
, pp. 211-218
-
-
Weiser, T.1
Wienrich, M.2
-
130
-
-
0034646410
-
Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase
-
Wong PC, Waggoner D, Subramaniam JR, Tessarollo L, Bartnikas TB, et al. 2000. Copper chaperone for superoxide dismutase is essential to activate mammalian Cu/Zn superoxide dismutase. Proc. Natl. Acad. Sci. USA 97:2886-91
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 2886-2891
-
-
Wong, P.C.1
Waggoner, D.2
Subramaniam, J.R.3
Tessarollo, L.4
Bartnikas, T.B.5
-
131
-
-
10744219518
-
Expression of the iron transporter ferroportin in synaptic vesicles and the blood-brain barrier
-
Wu LJ, Leenders AG, Cooperman S, Meyron-Holtz E, Smith S, et al. 2004. Expression of the iron transporter ferroportin in synaptic vesicles and the blood-brain barrier. Brain Res. 1001:108-17
-
(2004)
Brain Res
, vol.1001
, pp. 108-117
-
-
Wu, L.J.1
Leenders, A.G.2
Cooperman, S.3
Meyron-Holtz, E.4
Smith, S.5
-
132
-
-
0027431996
-
Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease
-
Yamaguchi Y, Heiny ME, Gitlin JD. 1993. Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease. Biochem. Biophys. Res. Commun. 197:271-77
-
(1993)
Biochem. Biophys. Res. Commun
, vol.197
, pp. 271-277
-
-
Yamaguchi, Y.1
Heiny, M.E.2
Gitlin, J.D.3
-
133
-
-
0028895749
-
A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans
-
Yoshida K, Furihata K, Takeda S, Nakamura A, Yamamoto K, et al. 1995. A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans. Nat. Genet. 9:267-72
-
(1995)
Nat. Genet
, vol.9
, pp. 267-272
-
-
Yoshida, K.1
Furihata, K.2
Takeda, S.3
Nakamura, A.4
Yamamoto, K.5
-
134
-
-
8344265251
-
Iron, brain ageing and neurodegenerative disorders
-
Zecca L, Youdim MB, Riederer P, Connor JR, Crichton RR. 2004. Iron, brain ageing and neurodegenerative disorders. Nat. Rev. Neurosci. 5:863-73
-
(2004)
Nat. Rev. Neurosci
, vol.5
, pp. 863-873
-
-
Zecca, L.1
Youdim, M.B.2
Riederer, P.3
Connor, J.R.4
Crichton, R.R.5
-
135
-
-
0034935036
-
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome
-
Zhou B, Westaway SK, Levinson B, Johnson MA, Gitschier J, Hayflick SJ. 2001. A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome. Nat. Genet. 28:345-49
-
(2001)
Nat. Genet
, vol.28
, pp. 345-349
-
-
Zhou, B.1
Westaway, S.K.2
Levinson, B.3
Johnson, M.A.4
Gitschier, J.5
Hayflick, S.J.6
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