-
1
-
-
0027500142
-
Isolation of a candidate gene for Menkes' disease that encodes a potential heavy metal binding protein
-
Chelly, J., Turner, Z. & Tonnesen, T. (1993) Isolation of a candidate gene for Menkes' disease that encodes a potential heavy metal binding protein. Nature Genet. 3: 14-19.
-
(1993)
Nature Genet.
, vol.3
, pp. 14-19
-
-
Chelly, J.1
Turner, Z.2
Tonnesen, T.3
-
2
-
-
0024149135
-
Copper deficiency in humans
-
Danks, D. M. (1988) Copper deficiency in humans. Annu. Rev. Nutr. 8: 235-257.
-
(1988)
Annu. Rev. Nutr.
, vol.8
, pp. 235-257
-
-
Danks, D.M.1
-
3
-
-
0000386450
-
Disorders of copper transport
-
(Scriver, C. R., Baudet, A. L., Sly, W. M. & Valle, D., eds.), McGraw-Hill, New York, NY
-
Danks, D. M. (1995) Disorders of copper transport. In: The Metabolic and Molecular Basis of Inherited Disease (Scriver, C. R., Baudet, A. L., Sly, W. M. & Valle, D., eds.), pp. 2211-2235. McGraw-Hill, New York, NY.
-
(1995)
The Metabolic and Molecular Basis of Inherited Disease
, pp. 2211-2235
-
-
Danks, D.M.1
-
4
-
-
0015384074
-
Menkes' kinky hair syndrome: An inherited defect of copper absorption with widespread effects
-
Danks, D. M., Campbell, P., Stevens, B. J. & Howell, R. R. (1972) Menkes' kinky hair syndrome: an inherited defect of copper absorption with widespread effects. Pediatrics 50: 188-201.
-
(1972)
Pediatrics
, vol.50
, pp. 188-201
-
-
Danks, D.M.1
Campbell, P.2
Stevens, B.J.3
Howell, R.R.4
-
5
-
-
0015927202
-
Menkes' kinky hair disease: Further definition of the defect in copper transport
-
Washington, DC
-
Danks, D. M. & Cartwright, E. (1973) Menkes' kinky hair disease: further definition of the defect in copper transport. Science (Washington, DC) 179: 1140-1141.
-
(1973)
Science
, vol.179
, pp. 1140-1141
-
-
Danks, D.M.1
Cartwright, E.2
-
6
-
-
0025821265
-
Alterations in the levels of iron, ferritin and other trace metals in Parkinson's disease and other neurodegenerative diseases affecting the basal ganglia
-
Dexter, D. T., Carayon, A., Javoy-Agid, F., Agid, Y., Wells, F. R., Daniel, S. E., Lees, A. J., Jenner, P. & Marsden, C. D. (1991) Alterations in the levels of iron, ferritin and other trace metals in Parkinson's disease and other neurodegenerative diseases affecting the basal ganglia. Brain 114 (Part 4): 1953-1975.
-
(1991)
Brain
, vol.114
, Issue.4 PART
, pp. 1953-1975
-
-
Dexter, D.T.1
Carayon, A.2
Javoy-Agid, F.3
Agid, Y.4
Wells, F.R.5
Daniel, S.E.6
Lees, A.J.7
Jenner, P.8
Marsden, C.D.9
-
7
-
-
0024356620
-
Increased nigral iron content and alterations in other metal ions occurring in brain in Parkinson's disease
-
Dexter, D. T., Wells, F. R., Lees, A. J., Agid, F., Agid, Y., Jenner, P. & Marsden, C. D. (1989) Increased nigral iron content and alterations in other metal ions occurring in brain in Parkinson's disease. J. Neurochem. 52: 1830-1836.
-
(1989)
J. Neurochem.
, vol.52
, pp. 1830-1836
-
-
Dexter, D.T.1
Wells, F.R.2
Lees, A.J.3
Agid, F.4
Agid, Y.5
Jenner, P.6
Marsden, C.D.7
-
8
-
-
0003335867
-
Copper and disease
-
(Linder, M., ed.), Plenum Press, New York, NY
-
Goode, C. A. (1991) Copper and disease. In: Biochemistry of Copper (Linder, M., ed.), pp. 331-366. Plenum Press, New York, NY
-
(1991)
Biochemistry of Copper
, pp. 331-366
-
-
Goode, C.A.1
-
9
-
-
0026026054
-
Copper transport: An overview
-
Harris, E. D. (1991) Copper transport: an overview. Proc. Soc. Exp. Biol. Med. 196: 130-140.
-
(1991)
Proc. Soc. Exp. Biol. Med.
, vol.196
, pp. 130-140
-
-
Harris, E.D.1
-
10
-
-
0026551531
-
Deficiency of copper can cause neuronal degeneration
-
Hartmann, H. A. & Evenson, M. A. (1992) Deficiency of copper can cause neuronal degeneration. Med. Hypothesis 38: 75-85.
-
(1992)
Med. Hypothesis
, vol.38
, pp. 75-85
-
-
Hartmann, H.A.1
Evenson, M.A.2
-
11
-
-
0023108382
-
Astrocytes induce blood-brain barrier properties in endothelial cells
-
Janzer, R. C. & Raff, M. C. (1987) Astrocytes induce blood-brain barrier properties in endothelial cells. Nature (Lond.) 325: 253-257.
-
(1987)
Nature (Lond.)
, vol.325
, pp. 253-257
-
-
Janzer, R.C.1
Raff, M.C.2
-
12
-
-
0024411453
-
Role of cerebral endothelium in brain oedema
-
Joo, F. & Klatzo, I. (1989) Role of cerebral endothelium in brain oedema. Neurol. Res. 11: 67-75.
-
(1989)
Neurol. Res.
, vol.11
, pp. 67-75
-
-
Joo, F.1
Klatzo, I.2
-
13
-
-
0027236562
-
Recent development in Menkes disease
-
Kodama, H. (1993) Recent development in Menkes disease. J. Inher. Metab. Dis. 16: 791-799.
-
(1993)
J. Inher. Metab. Dis.
, vol.16
, pp. 791-799
-
-
Kodama, H.1
-
14
-
-
0027163651
-
Histochemical localization of copper in the intestine and kidney of macular mice: Light and electron microscopic study
-
Kodama, H., Abe, T., Takama, M., Takahashi, I., Kodama, M. & Nishimura, M. (1993) Histochemical localization of copper in the intestine and kidney of macular mice: light and electron microscopic study. J. Histochem. Cytochem. 41: 1529-1535.
-
(1993)
J. Histochem. Cytochem.
, vol.41
, pp. 1529-1535
-
-
Kodama, H.1
Abe, T.2
Takama, M.3
Takahashi, I.4
Kodama, M.5
Nishimura, M.6
-
15
-
-
0025936399
-
Genetic expression of Menkes disease in cultured astrocytes of the macular mouse
-
Kodama, H., Meguro, Y., Abe, T., Rayner, M. H., Suzuki, K. T., Kobayashi, S. & Nishimura, M. (1991) Genetic expression of Menkes disease in cultured astrocytes of the macular mouse. J. Inher. Metab. Dis. 14: 896-901.
-
(1991)
J. Inher. Metab. Dis.
, vol.14
, pp. 896-901
-
-
Kodama, H.1
Meguro, Y.2
Abe, T.3
Rayner, M.H.4
Suzuki, K.T.5
Kobayashi, S.6
Nishimura, M.7
-
16
-
-
0028247206
-
The mottled gene is the mouse homologue of the Menkes disease gene
-
Levinson, B., Vulpe, C., Elder, B., Martin, C., Verley, F., Packman, S. & Gitschier, J. (1994) The mottled gene is the mouse homologue of the Menkes disease gene. Nature Genet. 6: 369-373.
-
(1994)
Nature Genet.
, vol.6
, pp. 369-373
-
-
Levinson, B.1
Vulpe, C.2
Elder, B.3
Martin, C.4
Verley, F.5
Packman, S.6
Gitschier, J.7
-
17
-
-
78651124591
-
A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration
-
Menkes, J. H., Alter, M., Steigleder, G. K., Weakley, D. R. & Sung, J. H. (1962) A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration. Pediatrics 29: 764-779.
-
(1962)
Pediatrics
, vol.29
, pp. 764-779
-
-
Menkes, J.H.1
Alter, M.2
Steigleder, G.K.3
Weakley, D.R.4
Sung, J.H.5
-
18
-
-
0027475976
-
Isolation of a partial candidate gene for Menkes' disease by positional cloning
-
Mercer, J.F.B., Livingston, J. & Hall, B. (1993) Isolation of a partial candidate gene for Menkes' disease by positional cloning. Nature Genet. 3: 20-25.
-
(1993)
Nature Genet.
, vol.3
, pp. 20-25
-
-
Mercer, J.F.B.1
Livingston, J.2
Hall, B.3
-
19
-
-
0026534803
-
Localization of metallothionein in the brain of rat and mouse
-
Nishimura, N., Nishimura, H., Ghaffar, A. & Tohyama, C. (1992) Localization of metallothionein in the brain of rat and mouse. J. Histochem. Cytochem. 40: 309-315.
-
(1992)
J. Histochem. Cytochem.
, vol.40
, pp. 309-315
-
-
Nishimura, N.1
Nishimura, H.2
Ghaffar, A.3
Tohyama, C.4
-
20
-
-
0029785153
-
Coincident expression of Menkes gene with copper efflux in human placental cells
-
Cell Physiol. 39
-
Qian, Y., Majumdar, S., Reddy, M.C.M. & Harris, E. D. (1996a) Coincident expression of Menkes gene with copper efflux in human placental cells. Am. J. Physiol. 270 (Cell Physiol. 39): C1880-C1884.
-
(1996)
Am. J. Physiol.
, vol.270
-
-
Qian, Y.1
Majumdar, S.2
Reddy, M.C.M.3
Harris, E.D.4
-
21
-
-
0028804765
-
Copper transport and kinetics in cultured C6 rat glioma cells
-
Cell Physiol. 38
-
Qian, Y., Tiffany-Castiglioni, E. & Harris, E. D. (1995) Copper transport and kinetics in cultured C6 rat glioma cells. Am. J. Physiol. 269 (Cell Physiol. 38): C892-C898.
-
(1995)
Am. J. Physiol.
, vol.269
-
-
Qian, Y.1
Tiffany-Castiglioni, E.2
Harris, E.D.3
-
22
-
-
0029773626
-
Functional analysis of a genetic defect of copper transport (Menkes disease) in different cell lines
-
Cell Physiol. 40
-
Qian, Y., Tiffany-Castiglioni, E. & Harris, E. D. (1996b) Functional analysis of a genetic defect of copper transport (Menkes disease) in different cell lines. Am. J. Physiol. 271 (Cell Physiol. 40): C378-C384.
-
(1996)
Am. J. Physiol.
, vol.271
-
-
Qian, Y.1
Tiffany-Castiglioni, E.2
Harris, E.D.3
-
23
-
-
0030872355
-
A Menkes P-type ATPase involved in copper homeostasis in the central nervous system of the rat
-
Qian, Y., Tiffany-Castiglioni, E. & Harris, E. D. (1997) A Menkes P-type ATPase involved in copper homeostasis in the central nervous system of the rat. Mol. Brain Res. 48: 60-66.
-
(1997)
Mol. Brain Res.
, vol.48
, pp. 60-66
-
-
Qian, Y.1
Tiffany-Castiglioni, E.2
Harris, E.D.3
-
24
-
-
0001760677
-
Rapid isolation of total RNA from mammalian cells
-
(Sambrook, J., Fritsch, E. F. & Maniatis, T., eds.), Cold Spring Harbor, New York, NY
-
Sambrook, J., Fritsch, E. F. & Maniatis, T. (1989) Rapid isolation of total RNA from mammalian cells. In: Molecular Cloning: A Laboratory Manual (Sambrook, J., Fritsch, E. F. & Maniatis, T., eds.), pp. 7.10-7.11. Cold Spring Harbor, New York, NY.
-
(1989)
Molecular Cloning: A Laboratory Manual
, pp. 710-711
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
25
-
-
0027869687
-
Cloned mouse cerebrovascular endothelial cells that maintain their differentiation markers for factor VIII, low density lipoprotein, and angiotensin-converting enzyme
-
Sapatino, B. V., Welsh, C.J.R., Smith, C. A., Bebo, B. F. & Linthicum, D. S. (1993) Cloned mouse cerebrovascular endothelial cells that maintain their differentiation markers for factor VIII, low density lipoprotein, and angiotensin-converting enzyme. In Vitro Cell. Dev. Biol. 29A: 923-928.
-
(1993)
In Vitro Cell. Dev. Biol.
, vol.29 A
, pp. 923-928
-
-
Sapatino, B.V.1
Welsh, C.J.R.2
Smith, C.A.3
Bebo, B.F.4
Linthicum, D.S.5
-
26
-
-
0023696395
-
Copper deficiency and sideroblastic anemia associated with zinc ingestion
-
Simon, S. R., Branda, R. F., Tindle, B. F. & Burns, S. L. (1988) Copper deficiency and sideroblastic anemia associated with zinc ingestion. Am. J. Hematol. 28:181-183.
-
(1988)
Am. J. Hematol.
, vol.28
, pp. 181-183
-
-
Simon, S.R.1
Branda, R.F.2
Tindle, B.F.3
Burns, S.L.4
-
27
-
-
0026570829
-
Low copper status of rats affects polyunsaturated fatty acid composition of brain phospholipids, unrelated to neuropathology
-
Sun, S. H. & O'Dell, B. L. (1992) Low copper status of rats affects polyunsaturated fatty acid composition of brain phospholipids, unrelated to neuropathology. J. Nutr. 122: 65-73.
-
(1992)
J. Nutr.
, vol.122
, pp. 65-73
-
-
Sun, S.H.1
O'Dell, B.L.2
-
28
-
-
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. Nature Genet. 3: 7-13.
-
(1993)
Nature Genet.
, vol.3
, pp. 7-13
-
-
Vulpe, C.1
Levinson, B.2
Whitney, S.3
Packman, S.4
Gitschier, J.5
-
29
-
-
0028212288
-
Histochemical localization of copper in various organs of brindled mice
-
Yoshimura, N. (1994) Histochemical localization of copper in various organs of brindled mice. Pathol. Int. 44: 14-19.
-
(1994)
Pathol. Int.
, vol.44
, pp. 14-19
-
-
Yoshimura, N.1
-
30
-
-
0028851390
-
Histochemical localization of copper in various organs of brindled mice after copper therapy
-
Yoshimura, N., Kida, K., Usutani, S. & Nishimura, M. (1995) Histochemical localization of copper in various organs of brindled mice after copper therapy. Pathol. Int. 45: 10-18.
-
(1995)
Pathol. Int.
, vol.45
, pp. 10-18
-
-
Yoshimura, N.1
Kida, K.2
Usutani, S.3
Nishimura, M.4
|