-
1
-
-
0020569082
-
Toxic milk: A new mutation affecting copper metabolism in the mouse
-
Rauch, H. (1983) Toxic milk: a new mutation affecting copper metabolism in the mouse. J. Hered., 74, 141-144.
-
(1983)
J. Hered.
, vol.74
, pp. 141-144
-
-
Rauch, H.1
-
2
-
-
0025892297
-
Spontaneous hepatic copper accumulation in Long-Evans Cinnamon rats with hereditary hepatitis: A model for Wilson's disease
-
Li, Y., Togashi, Y., Sato, S., Emoto, T., Kang, J.-H., Takeichi, N., Kobayashi, H., Kojima, Y., Une, Y. and Uchino, J. (1991) Spontaneous hepatic copper accumulation in Long-Evans Cinnamon rats with hereditary hepatitis: a model for Wilson's disease. J. Clin. Invest., 87, 1858-1861.
-
(1991)
J. Clin. Invest.
, vol.87
, pp. 1858-1861
-
-
Li, Y.1
Togashi, Y.2
Sato, S.3
Emoto, T.4
Kang, J.-H.5
Takeichi, N.6
Kobayashi, H.7
Kojima, Y.8
Une, Y.9
Uchino, J.10
-
3
-
-
0020183916
-
A comparison of copper-loading disease in Bedlington terriers and Wilson's disease in humans
-
Su, L.C., Ravanshad, S., Owen, C.A. Jr, McCall, J.T., Zollman, P.E. and Hardy, R.M. (1982) A comparison of copper-loading disease in Bedlington terriers and Wilson's disease in humans. Am. J. Physiol., 243, G226-G230.
-
(1982)
Am. J. Physiol.
, vol.243
-
-
Su, L.C.1
Ravanshad, S.2
Owen C.A., Jr.3
McCall, J.T.4
Zollman, P.E.5
Hardy, R.M.6
-
4
-
-
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
-
5
-
-
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., Brzustowitz, L.M., Devoto, M., Peppercorn, J., Bush, A.I., Sternlieb, I., Piratsu, 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
Brzustowitz, L.M.10
Devoto, M.11
Peppercorn, J.12
Bush, A.I.13
Sternlieb, I.14
Piratsu, 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..
-
6
-
-
0029799960
-
The toxic milk mouse is a murine model of Wilson disease
-
Theophilos, M.B., Cox. D.W. and Mercer, J.F.B. (1996) The toxic milk mouse is a murine model of Wilson disease. Hum. Mol. Genet., 5, 1619-1624.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1619-1624
-
-
Theophilos, M.B.1
Cox, D.W.2
Mercer, J.F.B.3
-
7
-
-
0028001088
-
The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene
-
Wu, J., Forbes, J.R., Chen, H.S. and Cox, D.W. (1994) The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene. Nature Genet., 7, 541-545.
-
(1994)
Nature Genet.
, vol.7
, pp. 541-545
-
-
Wu, J.1
Forbes, J.R.2
Chen, H.S.3
Cox, D.W.4
-
8
-
-
0026800853
-
Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene
-
Scheffer, H., Houwen, R.H.J., te Meerman, G.J., Loessner, J., Bachmann, B., Kunert, E., Verlind, E. and Buys, C.H.C.M. (1992) Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene. Hum. Genet., 89, 607-611.
-
(1992)
Hum. Genet.
, vol.89
, pp. 607-611
-
-
Scheffer, H.1
Houwen, R.H.J.2
Te Meerman, G.J.3
Loessner, J.4
Bachmann, B.5
Kunert, E.6
Verlind, E.7
Buys, C.H.C.M.8
-
9
-
-
0029101109
-
Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8
-
Reed, V., Williamson, P., Bull, P.C., Cox, D.W. and Boyd, Y. (1995) Mapping of the mouse homologue of the Wilson disease gene to mouse chromosome 8. Genomics, 28, 573-575.
-
(1995)
Genomics
, vol.28
, pp. 573-575
-
-
Reed, V.1
Williamson, P.2
Bull, P.C.3
Cox, D.W.4
Boyd, Y.5
-
10
-
-
0027537299
-
Linkage studies of the esterase D and retinoblastoma genes to canine copper toxicosis: A model for Wilson disease
-
Yuzbasiyan-Gurkan, V., Wagnitz, S., Halloran Blanton, S. and Brewer, G.J. (1993) Linkage studies of the esterase D and retinoblastoma genes to canine copper toxicosis: a model for Wilson disease. Genomics, 15, 86-90.
-
(1993)
Genomics
, vol.15
, pp. 86-90
-
-
Yuzbasiyan-Gurkan, V.1
Wagnitz, S.2
Halloran Blanton, S.3
Brewer, G.J.4
-
11
-
-
0027493788
-
Absence of linkage between the retinonoblastoma gene and hts gene in the LEC rat: A model of Wilson's disease
-
Sasaki, N., Hayashizaki, Y. and Kasai, N. (1993) Absence of linkage between the retinonoblastoma gene and hts gene in the LEC rat: a model of Wilson's disease. Jpn. J. Cancer Res., 84, 1019-1022.
-
(1993)
Jpn. J. Cancer Res.
, vol.84
, pp. 1019-1022
-
-
Sasaki, N.1
Hayashizaki, Y.2
Kasai, N.3
-
12
-
-
0018706646
-
Clinical, morphologic and chemical studies on copper toxicosis of Bedlington Terriers
-
Twedt, D.C., Sternlieb, I. and Gilbertson, S.R. (1979) Clinical, morphologic and chemical studies on copper toxicosis of Bedlington Terriers. J. Am. Vet. Med. Assoc., 175, 269-275.
-
(1979)
J. Am. Vet. Med. Assoc.
, vol.175
, pp. 269-275
-
-
Twedt, D.C.1
Sternlieb, I.2
Gilbertson, S.R.3
-
13
-
-
0022487199
-
A study of the role of metallothionein in the inherited copper toxicosis of dogs
-
Hunt, D.M., Wake, S.A., Mercer, J.F. and Danks, D.M. (1986) A study of the role of metallothionein in the inherited copper toxicosis of dogs. Biochem. J., 236, 409-415.
-
(1986)
Biochem. J.
, vol.236
, pp. 409-415
-
-
Hunt, D.M.1
Wake, S.A.2
Mercer, J.F.3
Danks, D.M.4
-
14
-
-
0028923703
-
Genes of the copper pathway
-
Cox, D.W. (1995) Genes of the copper pathway. Am. J. Hum. Genet., 56, 828-834.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 828-834
-
-
Cox, D.W.1
-
15
-
-
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
-
16
-
-
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
-
17
-
-
0030638285
-
Linkage of a microsatellite marker to the canine copper toxicosis locus in Bedlington terriers
-
Yuzbasiyan-Gurkan, V., Halloran Blanton, S., Cao, Y., Ferguson, P., Li, J., Venta, P.J. and Brewer, G.J. (1997) Linkage of a microsatellite marker to the canine copper toxicosis locus in Bedlington terriers. Am. J. Vet. Res., 58, 23-27.
-
(1997)
Am. J. Vet. Res.
, vol.58
, pp. 23-27
-
-
Yuzbasiyan-Gurkan, V.1
Halloran Blanton, S.2
Cao, Y.3
Ferguson, P.4
Li, J.5
Venta, P.J.6
Brewer, G.J.7
-
18
-
-
0345129652
-
Preparation and characterization of an eightfold redundant BAC library of the dog genome
-
Li, R., Zhao, B., Osoegawa, K., Catanese, J., Henthorn, P., Patterson, D.A., Ostrander, E. A., van Oost, B., Mignot, E. and de Jong, P.J. (1997) Preparation and characterization of an eightfold redundant BAC library of the dog genome. In CSH Genome Mapping and Sequencing, p. 132.
-
(1997)
CSH Genome Mapping and Sequencing
, pp. 132
-
-
Li, R.1
Zhao, B.2
Osoegawa, K.3
Catanese, J.4
Henthorn, P.5
Patterson, D.A.6
Ostrander, E.A.7
Van Oost, B.8
Mignot, E.9
De Jong, P.J.10
-
20
-
-
0029678394
-
The application of FISH techniques for physical mapping in the dog (Canis familiaris)
-
Fischer, P.E., Holmes, N.G., Dickens, H.F., Thomas, R., Binns, M.M. and Nacheva, E.P. (1996) The application of FISH techniques for physical mapping in the dog (Canis familiaris). Mamm. Genome, 7, 37-41.
-
(1996)
Mamm. Genome
, vol.7
, pp. 37-41
-
-
Fischer, P.E.1
Holmes, N.G.2
Dickens, H.F.3
Thomas, R.4
Binns, M.M.5
Nacheva, E.P.6
-
21
-
-
0029835132
-
Gene localization and syntenic mapping by FISH in the dog
-
Dutra, A.S., Mignot, E. and Puck, J.M. (1996) Gene localization and syntenic mapping by FISH in the dog. Cytogenet. Cell Genet., 74, 113-117.
-
(1996)
Cytogenet. Cell Genet.
, vol.74
, pp. 113-117
-
-
Dutra, A.S.1
Mignot, E.2
Puck, J.M.3
-
22
-
-
0026683521
-
YAC mapping by FISH using Alu-PCR generated probes
-
Breen, M., Arveiler, B., Murray, I., Gosden, J.R. and Porteous, D.J. (1992) YAC mapping by FISH using Alu-PCR generated probes. Genomics, 13, 726-730.
-
(1992)
Genomics
, vol.13
, pp. 726-730
-
-
Breen, M.1
Arveiler, B.2
Murray, I.3
Gosden, J.R.4
Porteous, D.J.5
-
23
-
-
0029888541
-
An extended nomenclature of the canine karyotype
-
Reimann, N., Bartnitzke, S., Bullerdiek, J., Schmitz, U., Rogalla, P., Nolte, I. and Ronne, M. (1996) An extended nomenclature of the canine karyotype. Cytogenet. Cell Genet., 731, 140-144.
-
(1996)
Cytogenet. Cell Genet.
, vol.731
, pp. 140-144
-
-
Reimann, N.1
Bartnitzke, S.2
Bullerdiek, J.3
Schmitz, U.4
Rogalla, P.5
Nolte, I.6
Ronne, M.7
-
24
-
-
0031216309
-
Molecular cloning of a canine metallothionein cDNA
-
Kobayashi, K., Shimada, A., Yamano, Y. and Umemura, T. (1997) Molecular cloning of a canine metallothionein cDNA. J. Vet. Med. Sci., 59, 819-823.
-
(1997)
J. Vet. Med. Sci.
, vol.59
, pp. 819-823
-
-
Kobayashi, K.1
Shimada, A.2
Yamano, Y.3
Umemura, T.4
-
25
-
-
0029983769
-
Endemic Tyrolean infantile cirrhosis: An ecogenetic disorder
-
Müller, T., Feichtinger, H., Berger, H. and Müller, W. (1996) Endemic Tyrolean infantile cirrhosis: an ecogenetic disorder. Lancet, 347, 877-880.
-
(1996)
Lancet
, vol.347
, pp. 877-880
-
-
Müller, T.1
Feichtinger, H.2
Berger, H.3
Müller, W.4
-
26
-
-
13044292638
-
Endemic Tyrolean Infantile Cirrhosis (ETIC) is not an allelic variant of Wilson's disease
-
Wijmenga, C., Müller T., Murli, I.S., Brunt, T., Feichtiger, H., Schonitzer, D., Houwen, R.H.J., Müller, W., Sandkuijl, L.A. and Pearson, P.L. (1998) Endemic Tyrolean Infantile Cirrhosis (ETIC) is not an allelic variant of Wilson's disease. Eur. J. Hum. Genet., 6, 624-628.
-
(1998)
Eur. J. Hum. Genet.
, vol.6
, pp. 624-628
-
-
Wijmenga, C.1
Müller, T.2
Murli, I.S.3
Brunt, T.4
Feichtiger, H.5
Schonitzer, D.6
Houwen, R.H.J.7
Müller, W.8
Sandkuijl, L.A.9
Pearson, P.L.10
-
27
-
-
0031573856
-
A linkage map of the canine genome
-
Mellersh, C.S., Langston, A.A., Acland, G.M., Fleming, M.A., Ray, K., Wiegand, N.A., Francisco, L.V., Gibbs, M., Aguirre, G.D. and Ostrander, E.A. (1997) A linkage map of the canine genome. Genomics, 46, 326-336.
-
(1997)
Genomics
, vol.46
, pp. 326-336
-
-
Mellersh, C.S.1
Langston, A.A.2
Acland, G.M.3
Fleming, M.A.4
Ray, K.5
Wiegand, N.A.6
Francisco, L.V.7
Gibbs, M.8
Aguirre, G.D.9
Ostrander, E.A.10
-
28
-
-
0031573913
-
Construction of a panel of canine-rodent hybrid cell lines for use in partitioning of the canine genome
-
Langston, A.A., Mellersh, C.S., Neal, C.L., Ray, K., Acland, G.M., Gibbs, M., Aguirre, G.D., Fournier, R.E.K. and Ostrander, E.A. (1997) Construction of a panel of canine-rodent hybrid cell lines for use in partitioning of the canine genome. Genomics, 46, 317-325.
-
(1997)
Genomics
, vol.46
, pp. 317-325
-
-
Langston, A.A.1
Mellersh, C.S.2
Neal, C.L.3
Ray, K.4
Acland, G.M.5
Gibbs, M.6
Aguirre, G.D.7
Fournier, R.E.K.8
Ostrander, E.A.9
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