-
1
-
-
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. and 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
-
2
-
-
0027475976
-
Isolation of a partial candidate gene for Menkes disease by positional cloning
-
Mercer, J.F., Livingston, J., Hall, B., Paynter, J.A., Begy, C., Chandrasekharappa, S., Lockhart, P., Grimes, A., Bhave, M., Siemieniak, D. and Glover, T.W. (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.1
Livingston, J.2
Hall, B.3
Paynter, J.A.4
Begy, C.5
Chandrasekharappa, S.6
Lockhart, P.7
Grimes, A.8
Bhave, M.9
Siemieniak, D.10
Glover, T.W.11
-
3
-
-
0027500142
-
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein
-
Chelly, J., Tumer, Z., Tonnesen, T., Petterson, A., Ishikawa Brush, Y., Tommerup, N., Horn, N. and Monaco, A.P. (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
Tumer, Z.2
Tonnesen, T.3
Petterson, A.4
Ishikawa Brush, Y.5
Tommerup, N.6
Horn, N.7
Monaco, A.P.8
-
4
-
-
0031455381
-
Expression, purification, and metal binding properties of the N-terminal domain from the Wilson disease putative copper-transporting ATPase (ATP7B)
-
DiDonato, M., Narindrasorasak, S., Forbes, J.R., Cox, D.W. and Sarkar, B. (1997) Expression, purification, and metal binding properties of the N-terminal domain from the Wilson disease putative copper-transporting ATPase (ATP7B). J. Biol. Chem., 272, 33279-33282.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 33279-33282
-
-
Didonato, M.1
Narindrasorasak, S.2
Forbes, J.R.3
Cox, D.W.4
Sarkar, B.5
-
5
-
-
0028242939
-
Wilson disease and Menkes disease: New handles on heavy-metal transport
-
Bull, P.C. and Cox, D.W. (1994) Wilson disease and Menkes disease: new handles on heavy-metal transport. Trends Genet., 10, 246-252.
-
(1994)
Trends Genet.
, vol.10
, pp. 246-252
-
-
Bull, P.C.1
Cox, D.W.2
-
6
-
-
0030898098
-
Identification and functional expression of HAH1, a novel human gene involved in copper homeostasis
-
Klomp, L.W., Lin, S.J., Yuan, D.S., Klausner, R.D., Culotta, V.C. and Gitlin, J.D. (1997) Identification and functional expression of HAH1, a novel human gene involved in copper homeostasis. J. Biol. Chem., 272, 9221-9226.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 9221-9226
-
-
Klomp, L.W.1
Lin, S.J.2
Yuan, D.S.3
Klausner, R.D.4
Culotta, V.C.5
Gitlin, J.D.6
-
7
-
-
1842366025
-
Metal ion chaperone function of the soluble Cu(I) receptor Atx1
-
Pufahl, R.A., Singer, C.P., Peariso, K.L., Lin, S., Schmidt, P.J., Fahmi, C.J., Culotta, V.C., Penner Hahn, J.E. and O'Halloran, T.V. (1997) Metal ion chaperone function of the soluble Cu(I) receptor Atx1. Science, 278, 853-856.
-
(1997)
Science
, vol.278
, pp. 853-856
-
-
Pufahl, R.A.1
Singer, C.P.2
Peariso, K.L.3
Lin, S.4
Schmidt, P.J.5
Fahmi, C.J.6
Culotta, V.C.7
Penner Hahn, J.E.8
O'Halloran, T.V.9
-
8
-
-
0031974775
-
Solution structure of the fourth metal-binding domain from the Menkes copper-transporting ATPase
-
Gitschier, J., Moffat, B., Reilly, D., Wood, W.I. and Fairbrother, W.J. (1998) Solution structure of the fourth metal-binding domain from the Menkes copper-transporting ATPase. Nature Struct. Biol., 5, 47-54.
-
(1998)
Nature Struct. Biol.
, vol.5
, pp. 47-54
-
-
Gitschier, J.1
Moffat, B.2
Reilly, D.3
Wood, W.I.4
Fairbrother, W.J.5
-
9
-
-
0032488829
-
Functional expression of the Menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases
-
Payne, A.S. and Gitlin, J.D. (1998) Functional expression of the Menkes disease protein reveals common biochemical mechanisms among the copper-transporting P-type ATPases. J. Biol. Chem., 273, 3765-3770.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 3765-3770
-
-
Payne, A.S.1
Gitlin, J.D.2
-
10
-
-
0025336606
-
Markedly reduced activity of lysyl oxidase in skin and aorta from a patient with Menkes' disease showing unusually severe connective tissue manifestations
-
Royce, P.M. and Steinmann, B. (1990) Markedly reduced activity of lysyl oxidase in skin and aorta from a patient with Menkes' disease showing unusually severe connective tissue manifestations. Pediatr. Res., 28, 137-141.
-
(1990)
Pediatr. Res.
, vol.28
, pp. 137-141
-
-
Royce, P.M.1
Steinmann, B.2
-
11
-
-
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, M.J., Mercer, J.F., Culvenor, J.G., Lockhart, P., Gleeson, P.A. and 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, 6084-6095.
-
(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
-
12
-
-
0030467256
-
Biochemical characterization and intracellular localization of the Menkes disease protein
-
Yamaguchi, Y., Heiny, M.E., Suzuki, M. and Gitlin, J.D. (1996) Biochemical characterization and intracellular localization of the Menkes disease protein. Proc. Natl Acad. Sci. USA, 93, 14030-14035.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 14030-14035
-
-
Yamaguchi, Y.1
Heiny, M.E.2
Suzuki, M.3
Gitlin, J.D.4
-
13
-
-
0031055871
-
Immunocytochemical localization of the Menkes copper transport protein (ATP7A) to the trans-Golgi network
-
Dierick, H.A., Adam, A.N., Escara Wilke, J.F. and Glover, T.W. (1997) Immunocytochemical localization of the Menkes copper transport protein (ATP7A) to the trans-Golgi network. Hum. Mol. Genet., 6, 409-416.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 409-416
-
-
Dierick, H.A.1
Adam, A.N.2
Escara Wilke, J.F.3
Glover, T.W.4
-
14
-
-
0031877944
-
A Golgi localization signal identified in the Menkes recombinant protein
-
Francis, M.J., Jones, E.E., Levy, E.R., Ponnambalam, S., Chelly, J. and Monaco, A.P. (1998) A Golgi localization signal identified in the Menkes recombinant protein. Hum. Mol. Genet., 7, 1245-1252.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1245-1252
-
-
Francis, M.J.1
Jones, E.E.2
Levy, E.R.3
Ponnambalam, S.4
Chelly, J.5
Monaco, A.P.6
-
15
-
-
0031829339
-
Functional analysis and intracellular localization of the human Menkes protein (MNK) stably expressed from a cDNA construct in Chinese hamster ovary cells (CHO-K1)
-
La Fontaine, S., Firth, S.D., Lockhart, P.J., Brooks, H., Parton, R.G., Camakaris, J. and Mercer, J.F. (1998) Functional analysis and intracellular localization of the human Menkes protein (MNK) stably expressed from a cDNA construct in Chinese hamster ovary cells (CHO-K1). Hum. Mol. Genet., 7, 1293-1300.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1293-1300
-
-
La Fontaine, S.1
Firth, S.D.2
Lockhart, P.J.3
Brooks, H.4
Parton, R.G.5
Camakaris, J.6
Mercer, J.F.7
-
16
-
-
0028972922
-
Gene amplification of the Menkes (MNK; ATP7A) P-type ATPase gene of CHO cells is associated with copper resistance and enhanced copper efflux
-
Camakaris, J., Petris, M.J., Bailey, L., Shen, P., Lockhart, P., Glover, T.W., Barcroft, C., Patton, J. and Mercer, J.F. (1995) Gene amplification of the Menkes (MNK; ATP7A) P-type ATPase gene of CHO cells is associated with copper resistance and enhanced copper efflux. Hum. Mol. Genet., 4, 2117-2123.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2117-2123
-
-
Camakaris, J.1
Petris, M.J.2
Bailey, L.3
Shen, P.4
Lockhart, P.5
Glover, T.W.6
Barcroft, C.7
Patton, J.8
Mercer, J.F.9
-
17
-
-
0344182341
-
Menkes disease: A biochemical abnormality in cultured human fibroblasts
-
Goka, T.J., Stevenson, R.E., Hefferan, P.M. and Howell, R.R. (1976) Menkes disease: a biochemical abnormality in cultured human fibroblasts. Proc. Natl Acad. Sci. USA, 73, 604-606.
-
(1976)
Proc. Natl Acad. Sci. USA
, vol.73
, pp. 604-606
-
-
Goka, T.J.1
Stevenson, R.E.2
Hefferan, P.M.3
Howell, R.R.4
-
18
-
-
0017195932
-
Copper incorporation studies on cultured cells for prenatal diagnosis of Menkes' disease
-
Horn, N. (1976) Copper incorporation studies on cultured cells for prenatal diagnosis of Menkes' disease. Lancet, i, 1156-1158.
-
(1976)
Lancet
, vol.1
, pp. 1156-1158
-
-
Horn, N.1
-
19
-
-
0018904864
-
Altered copper-metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants
-
Camakaris, J., Danks, D.M., Ackland, L., Cartwright, E., Borger, P. and Cotton, R.G. (1980) Altered copper-metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutants. Biochem. Genet., 18, 117-131.
-
(1980)
Biochem. Genet.
, vol.18
, pp. 117-131
-
-
Camakaris, J.1
Danks, D.M.2
Ackland, L.3
Cartwright, E.4
Borger, P.5
Cotton, R.G.6
-
20
-
-
0031730641
-
A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network
-
Petris, M.J., Camakaris, J., Greenough, M., La Fontaine, S. and Mercer, J.F.B. (1998) A C-terminal di-leucine is required for localization of the Menkes protein in the trans-Golgi network. Hum. Mol. Genet., 7, 2063-2071.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 2063-2071
-
-
Petris, M.J.1
Camakaris, J.2
Greenough, M.3
La Fontaine, S.4
Mercer, J.F.B.5
-
21
-
-
0031934417
-
Constitutive skipping of alternatively spliced exon 10 in the ATP7A gene abolishes Golgi localization of the Menkes protein and produces the occipital horn syndrome
-
Qi, M. and Byers, P.H. (1998) Constitutive skipping of alternatively spliced exon 10 in the ATP7A gene abolishes Golgi localization of the Menkes protein and produces the occipital horn syndrome. Hum. Mol. Genet., 7, 465-469.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 465-469
-
-
Qi, M.1
Byers, P.H.2
-
22
-
-
0032981423
-
Identification of a di-leucine motif within the C-terminus domain of the Menkes disease protein that mediates endocytosis from the plasma membrane
-
Francis, M.J., Jones, E.E., Levy, E.R., Martin, R.L., Ponnambalam, S. and Monaco, A.P. (1999) Identification of a di-leucine motif within the C-terminus domain of the Menkes disease protein that mediates endocytosis from the plasma membrane. J. Cell Sci., 112, 1721-1732.
-
(1999)
J. Cell Sci.
, vol.112
, pp. 1721-1732
-
-
Francis, M.J.1
Jones, E.E.2
Levy, E.R.3
Martin, R.L.4
Ponnambalam, S.5
Monaco, A.P.6
-
23
-
-
0020972378
-
Limited and unlimited growth of SV40-transformed cells from human diploid MRC-5 fibroblasts
-
Huschtscha, L.I. and Holliday, R. (1981) Limited and unlimited growth of SV40-transformed cells from human diploid MRC-5 fibroblasts. J. Cell Sci., 63, 77-99.
-
(1981)
J. Cell Sci.
, vol.63
, pp. 77-99
-
-
Huschtscha, L.I.1
Holliday, R.2
-
24
-
-
0032553535
-
Correction of the copper transport defect of Menkes patient fibroblasts by expression of the Menkes and Wilson ATPases
-
La Fontaine, S.L., Firth, S.D., Camakaris, J., Englezou, A., Theophilos, M.B., Petris, M.J., Howie, M., Lockhart, P.J., Greenough, M., Brooks, H., Reddel, R.R. and Mercer, J.F. (1998) Correction of the copper transport defect of Menkes patient fibroblasts by expression of the Menkes and Wilson ATPases. J. Biol. Chem., 273, 31375-31380.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 31375-31380
-
-
La Fontaine, S.L.1
Firth, S.D.2
Camakaris, J.3
Englezou, A.4
Theophilos, M.B.5
Petris, M.J.6
Howie, M.7
Lockhart, P.J.8
Greenough, M.9
Brooks, H.10
Reddel, R.R.11
Mercer, J.F.12
-
25
-
-
0032528904
-
Multiple transcripts coding for the Menkes gene: Evidence for alternative splicing of Menkes mRNA
-
Reddy, M.C. and Harris, E.D. (1998) Multiple transcripts coding for the Menkes gene: evidence for alternative splicing of Menkes mRNA. Biochem. J., 334, 71-77.
-
(1998)
Biochem. J.
, vol.334
, pp. 71-77
-
-
Reddy, M.C.1
Harris, E.D.2
-
26
-
-
0030820818
-
Restriction of copper export in Saccharomyces cerevisiae to a late Golgi or post-Golgi compartment in the secretory pathway
-
Yuan, D.S., Dancis, A. and Klausner, R.D. (1997) Restriction of copper export in Saccharomyces cerevisiae to a late Golgi or post-Golgi compartment in the secretory pathway. J. Biol. Chem., 272, 25787-25793.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 25787-25793
-
-
Yuan, D.S.1
Dancis, A.2
Klausner, R.D.3
-
27
-
-
0028916909
-
The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake
-
Yuan, D.S., Stearman, R., Dancis, A., Dunn, T., Beeler, T. and Klausner, R.D. (1995) The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake. Proc. Natl Acad. Sci. USA, 92, 2632-2636.
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 2632-2636
-
-
Yuan, D.S.1
Stearman, R.2
Dancis, A.3
Dunn, T.4
Beeler, T.5
Klausner, R.D.6
-
28
-
-
0027452091
-
The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene
-
Bull, P.C., Thomas, G.R., Rommens, J.M., Forbes, J.R. and Cox, D.W. (1993) The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene. Nature Genet., 5, 327-337.
-
(1993)
Nature 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
-
29
-
-
0027364961
-
The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
-
Tanzi, R.E., Petrukhin, K., Chernov I., Pellequer, J.L., Wasco, W., Ross, B., Romano, D.M., Parano, E., Pavone, L., Brzustowicz, L.M., Devoto, M., Peppercorn, J., Bush, A.I., Sternlieb, I., Pirastu, M., Gusella, J.F., Evgrafov, O., Penchaszadeh, G.K., Honig, B., Edelman, I.S., Soares, M.B., Scheinberg, I.H. and Gilliam, T.C. (1993) The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene. Nature Genet., 5, 344-350.
-
(1993)
Nature Genet.
, vol.5
, pp. 344-350
-
-
Tanzi, R.E.1
Petrukhin, K.2
Chernov, I.3
Pellequer, J.L.4
Wasco, W.5
Ross, B.6
Romano, D.M.7
Parano, E.8
Pavone, L.9
Brzustowicz, L.M.10
Devoto, M.11
Peppercorn, J.12
Bush, A.I.13
Sternlieb, I.14
Pirastu, M.15
Gusella, J.F.16
Evgrafov, O.17
Penchaszadeh, G.K.18
Honig, B.19
Edelman, I.S.20
Soares, M.B.21
Scheinberg, I.H.22
Gilliam, T.C.23
more..
-
30
-
-
0023203028
-
Metallothionein gene regulation in Menkes' syndrome
-
Hamer, D.H. (1987) Metallothionein gene regulation in Menkes' syndrome. Arch. Dermatol., 123, 1384a-1385a.
-
(1987)
Arch. Dermatol.
, vol.123
-
-
Hamer, D.H.1
-
31
-
-
0019448663
-
Increased copper metallothionein in Menkes cultured skin fibroblasts
-
Labadie, G.U., Hirschhorn, K., Katz, S. and Beratis, N.G. (1981) Increased copper metallothionein in Menkes cultured skin fibroblasts. Pediatr. Res., 15, 257-261.
-
(1981)
Pediatr. Res.
, vol.15
, pp. 257-261
-
-
Labadie, G.U.1
Hirschhorn, K.2
Katz, S.3
Beratis, N.G.4
-
32
-
-
0025604309
-
Metallothionein in Menkes' disease: Induction in cultured muscle cells
-
Herzberg, N.H., Wolterman, R.A., van den Berg, G.J., Barth, P.G. and Bolhuis, P.A. (1990) Metallothionein in Menkes' disease: induction in cultured muscle cells. J. Neurol. Sci., 100, 50-56.
-
(1990)
J. Neurol. Sci.
, vol.100
, pp. 50-56
-
-
Herzberg, N.H.1
Wolterman, R.A.2
Van Den Berg, G.J.3
Barth, P.G.4
Bolhuis, P.A.5
-
33
-
-
0021983077
-
Menkes' disease: Abnormal metallothionein gene regulation in response to copper
-
Leone, A., Pavlakis, G.N. and Hamer, D.H. (1985) Menkes' disease: abnormal metallothionein gene regulation in response to copper. Cell, 40, 301-309.
-
(1985)
Cell
, vol.40
, pp. 301-309
-
-
Leone, A.1
Pavlakis, G.N.2
Hamer, D.H.3
-
34
-
-
0022487744
-
Metallothionein gene regulation in Menkes' disease
-
Leone, A. (1986) Metallothionein gene regulation in Menkes' disease. Horiz. Biochem. Biophys., 8, 207-256.
-
(1986)
Horiz. Biochem. Biophys.
, vol.8
, pp. 207-256
-
-
Leone, A.1
-
35
-
-
0028007980
-
Role of membrane trafficking in plasma membrane solute transport
-
Bradbury, N.A. and Bridges, R.J. (1994) Role of membrane trafficking in plasma membrane solute transport. Am. J. Physiol., 267, C1-C24.
-
(1994)
Am. J. Physiol.
, vol.267
-
-
Bradbury, N.A.1
Bridges, R.J.2
-
36
-
-
0030729551
-
Identification and characterization of aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus with partial vasopressin response
-
Canfield, M.C., Tamarappoo, B.K., Moses, A.M., Verkman, A.S. and Holtzman, E.J. (1997) Identification and characterization of aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus with partial vasopressin response. Hum. Mol. Genet., 6, 1865-1871.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1865-1871
-
-
Canfield, M.C.1
Tamarappoo, B.K.2
Moses, A.M.3
Verkman, A.S.4
Holtzman, E.J.5
-
37
-
-
0031682122
-
Cellular mechanisms of aquaporin trafficking
-
Brown, D., Katsura, T. and Gustafson, C.E. (1998) Cellular mechanisms of aquaporin trafficking. Am. J. Physiol., 275, F328-F331.
-
(1998)
Am. J. Physiol.
, vol.275
-
-
Brown, D.1
Katsura, T.2
Gustafson, C.E.3
-
38
-
-
0030669618
-
Moving GLUT4: The biogenesis and trafficking of GLUT4 storage vesicles
-
Rea, S. and James, D.E. (1997) Moving GLUT4: the biogenesis and trafficking of GLUT4 storage vesicles. Diabetes, 46, 1667-1677.
-
(1997)
Diabetes
, vol.46
, pp. 1667-1677
-
-
Rea, S.1
James, D.E.2
-
39
-
-
0028321736
-
Insulin-stimulated GLUT4 glucose transporter recycling. A problem in membrane protein subcellular trafficking through multiple pools
-
Holman, G.D., Lo Leggio, L. and Cushman, S.W. (1994) Insulin-stimulated GLUT4 glucose transporter recycling. A problem in membrane protein subcellular trafficking through multiple pools. J. Biol. Chem., 269, 17516-17524.
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 17516-17524
-
-
Holman, G.D.1
Lo Leggio, L.2
Cushman, S.W.3
-
40
-
-
0028518842
-
Subcellular localization and trafficking of the GLUT4 glucose transporter isoform in insulin-responsive cells
-
Holman, G.D. and Cushman, S.W. (1994) Subcellular localization and trafficking of the GLUT4 glucose transporter isoform in insulin-responsive cells. Bioessays, 16, 753-759.
-
(1994)
Bioessays
, vol.16
, pp. 753-759
-
-
Holman, G.D.1
Cushman, S.W.2
-
41
-
-
0025761381
-
Immuno-localization of the insulin regulatable glucose transporter in brown adipose tissue of the rat
-
Slot, J.W., Geuze, H.J., Gigengack, S., Lienhard, G.E. and James, D.E. (1991) Immuno-localization of the insulin regulatable glucose transporter in brown adipose tissue of the rat. J. Cell Biol., 113, 123-135.
-
(1991)
J. Cell Biol.
, vol.113
, pp. 123-135
-
-
Slot, J.W.1
Geuze, H.J.2
Gigengack, S.3
Lienhard, G.E.4
James, D.E.5
-
42
-
-
0025823408
-
Translocation of the glucose transporter GLUT4 in cardiac myocytes of the rat
-
Slot, J.W., Geuze, H.J., Gigengack, S., James, D.E. and Lienhard, G.E. (1991) Translocation of the glucose transporter GLUT4 in cardiac myocytes of the rat. Proc. Natl Acad. Sci. USA, 88, 7815-7819.
-
(1991)
Proc. Natl Acad. Sci. USA
, vol.88
, pp. 7815-7819
-
-
Slot, J.W.1
Geuze, H.J.2
Gigengack, S.3
James, D.E.4
Lienhard, G.E.5
-
44
-
-
0032577524
-
Analysis of functional domains of Wilson disease protein (ATP7B) in Saccharomyces cerevisiae
-
Iida, M., Terada, K., Sambongi, Y., Wakabayashi, T., Miura, N., Koyama, K., Futai, M. and Sugiyama, T. (1998) Analysis of functional domains of Wilson disease protein (ATP7B) in Saccharomyces cerevisiae. FEBS Lett., 428, 281-285.
-
(1998)
FEBS Lett.
, vol.428
, pp. 281-285
-
-
Iida, M.1
Terada, K.2
Sambongi, Y.3
Wakabayashi, T.4
Miura, N.5
Koyama, K.6
Futai, M.7
Sugiyama, T.8
-
45
-
-
0027318045
-
Kin recognition. A model for the retention of Golgi enzymes
-
Nilsson, T., Slusarewicz, P., Hoe, M.H. and Warren, G. (1993) Kin recognition. A model for the retention of Golgi enzymes. FEBS. Lett., 330, 1-4.
-
(1993)
FEBS. Lett.
, vol.330
, pp. 1-4
-
-
Nilsson, T.1
Slusarewicz, P.2
Hoe, M.H.3
Warren, G.4
-
46
-
-
0027978637
-
Retention and retrieval in the endoplasmic reticulum and the Golgi apparatus
-
Nilsson, T. and Warren, G. (1994) Retention and retrieval in the endoplasmic reticulum and the Golgi apparatus. Curr. Opin. Cell Biol., 6, 517-521.
-
(1994)
Curr. Opin. Cell Biol.
, vol.6
, pp. 517-521
-
-
Nilsson, T.1
Warren, G.2
-
47
-
-
0030844529
-
hCTR1: A human gene for copper uptake identified by complementation in yeast
-
Zhou, B. and Gitschier, J. (1997) hCTR1: a human gene for copper uptake identified by complementation in yeast. Proc. Natl Acad. Sci. USA, 94, 7481-7486.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 7481-7486
-
-
Zhou, B.1
Gitschier, J.2
-
48
-
-
0031916833
-
HAH1 is a copper-binding protein with distinct amino acid residues mediating copper homeostasis and antioxidant defense
-
Hung, I.H., Casareno, R.L., Labesse, G., Mathews, F.S. and Gitlin, J.D. (1998) HAH1 is a copper-binding protein with distinct amino acid residues mediating copper homeostasis and antioxidant defense. J. Biol. Chem., 273, 1749-1754.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 1749-1754
-
-
Hung, I.H.1
Casareno, R.L.2
Labesse, G.3
Mathews, F.S.4
Gitlin, J.D.5
-
49
-
-
0030910597
-
A role for the Saccharomyces cerevisiae ATX1 gene in copper trafficking and iron transport
-
Lin, S.J., Pufahl, R.A., Dancis, A., O'Halloran, T.V. and Culotta, V.C. (1997) A role for the Saccharomyces cerevisiae ATX1 gene in copper trafficking and iron transport. J. Biol. Chem., 272, 9215-9220.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 9215-9220
-
-
Lin, S.J.1
Pufahl, R.A.2
Dancis, A.3
O'Halloran, T.V.4
Culotta, V.C.5
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