-
1
-
-
0028264422
-
A novel X gene with a widely transcribed Y homologue escapes X-inactivation in mouse and human
-
Agulnik, A. I., Mitchell, M. J., Mattei, M.-G., Borsani, G., Avner, P. R., Lerner, J. L., and Bishop, C. E. (1994). A novel X gene with a widely transcribed Y homologue escapes X-inactivation in mouse and human. Hum. Mol. Genet. 3: 879-884.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 879-884
-
-
Agulnik, A.I.1
Mitchell, M.J.2
Mattei, M.-G.3
Borsani, G.4
Avner, P.R.5
Lerner, J.L.6
Bishop, C.E.7
-
2
-
-
0024493730
-
Meeting report: Mutation at the hprt locus. Workshop on mutation at the hprt locus
-
Stockholm, May 26-28, 1988
-
Albertini, R. J., Gennett, I. N., Lambert, B., Thilly, W. G., and Vrieling, H. (1989). Meeting report: Mutation at the hprt locus. Workshop on mutation at the hprt locus, Stockholm, May 26-28, 1988. Mutat. Res. 216: 65-88.
-
(1989)
Mutat. Res.
, vol.216
, pp. 65-88
-
-
Albertini, R.J.1
Gennett, I.N.2
Lambert, B.3
Thilly, W.G.4
Vrieling, H.5
-
3
-
-
0019023345
-
Purification of mouse immunoglobulin heavy-chain messenger RNAs from total myeloma tumor RNA
-
Auffray, C., and Rougeon, F. (1980). Purification of mouse immunoglobulin heavy-chain messenger RNAs from total myeloma tumor RNA. Eur. J. Biochem. 107: 303-314.
-
(1980)
Eur. J. Biochem.
, vol.107
, pp. 303-314
-
-
Auffray, C.1
Rougeon, F.2
-
4
-
-
0023191362
-
Detailed ordering of markers localizing to the Xq26-Xqter region of the human X chromosome by the use of an interspecific Mus spretus mouse cross
-
Avner, P., Amar, L., Arnaud, D., Hanauer, A., and Cambrou, J. (1987a). Detailed ordering of markers localizing to the Xq26-Xqter region of the human X chromosome by the use of an interspecific Mus spretus mouse cross. Proc. Natl. Acad. Sci. USA 84: 1629-1633.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 1629-1633
-
-
Avner, P.1
Amar, L.2
Arnaud, D.3
Hanauer, A.4
Cambrou, J.5
-
5
-
-
0023389979
-
Characterization of a panel of somatic cell hybrids for regional mapping of the mouse X chromosome
-
Avner, P., Arnaud, D., Amar, L., Cambrou, J., Winking, H., and Russell, L. B. (1987b). Characterization of a panel of somatic cell hybrids for regional mapping of the mouse X chromosome. Proc. Natl. Acad. Sci. USA 84: 5330-5334.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 5330-5334
-
-
Avner, P.1
Arnaud, D.2
Amar, L.3
Cambrou, J.4
Winking, H.5
Russell, L.B.6
-
6
-
-
0027352581
-
The locus for pyruvate dehydrogenase E1 a subunit (Pdha-1) lies between Plp and Amg on the mouse X chromosome
-
Blair, H. J., Reed, V., Laval, S. H., and Boyd, Y. (1993). The locus for pyruvate dehydrogenase E1 a subunit (Pdha-1) lies between Plp and Amg on the mouse X chromosome. Mamm. Genome 4: 230-233.
-
(1993)
Mamm. Genome
, vol.4
, pp. 230-233
-
-
Blair, H.J.1
Reed, V.2
Laval, S.H.3
Boyd, Y.4
-
7
-
-
0021646112
-
Observations of the Menkes' and Brindled mouse phenotypes in cell hybrids
-
Brown, R. M., Camakaris, J., and Danks, D. M. (1984). Observations of the Menkes' and Brindled mouse phenotypes in cell hybrids. Som. Cell Mol. Genet. 10: 321-330.
-
(1984)
Som. Cell Mol. Genet.
, vol.10
, pp. 321-330
-
-
Brown, R.M.1
Camakaris, J.2
Danks, D.M.3
-
8
-
-
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
-
9
-
-
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
-
11
-
-
0027500142
-
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein
-
Chelly, J., Türner, Z., Tonnesen, R., 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
Türner, Z.2
Tonnesen, R.3
Petterson, A.4
Ishikawa-Brush, Y.5
Tommerup, N.6
Horn, N.7
Monaco, A.P.8
-
12
-
-
0028010889
-
Molecular characterization of a copper transport protein in S. cerevisiae: An unexpected role for copper in iron transport
-
Dancis, A., Yuan, D. S., Haile, D., Askwith, C., Eide, D., Moehle, C., Kaplan, J., and Klausner, R. D. (1994). Molecular characterization of a copper transport protein in S. cerevisiae: An unexpected role for copper in iron transport. Cell 76: 393-402.
-
(1994)
Cell
, vol.76
, pp. 393-402
-
-
Dancis, A.1
Yuan, D.S.2
Haile, D.3
Askwith, C.4
Eide, D.5
Moehle, C.6
Kaplan, J.7
Klausner, R.D.8
-
13
-
-
0001504685
-
Disorders of copper transport (in Wilson's and Menkes' diseases)
-
(J. R. Scriver, et al., Eds.), McGraw-Hill, New York
-
Danks, D. M. (1989). Disorders of copper transport (in Wilson's and Menkes' diseases). In "The Metabolic Basis Of Inherited Diseases" (J. R. Scriver, et al., Eds.), pp. 1411-1431, McGraw-Hill, New York.
-
(1989)
The Metabolic Basis of Inherited Diseases
, pp. 1411-1431
-
-
Danks, D.M.1
-
14
-
-
0021013897
-
Kinetics of Cu(II) transport and accumulation by hepatocytes from copper-deficient mice and the brindled mouse model of Menkes disease
-
Darwish, H. M., Hoke, J. E., and Ettinger, M. J. (1983). Kinetics of Cu(II) transport and accumulation by hepatocytes from copper-deficient mice and the brindled mouse model of Menkes disease. J. Biol. Chem. 258: 13621-13626.
-
(1983)
J. Biol. Chem.
, vol.258
, pp. 13621-13626
-
-
Darwish, H.M.1
Hoke, J.E.2
Ettinger, M.J.3
-
15
-
-
0027939458
-
Diverse mutations in patients with Menkes disease often lead to exon skipping
-
Das, S., Levinson, B., Whitney, S., Vulpe, C., Packman, S., and Gitschier, J. (1994). Diverse mutations in patients with Menkes disease often lead to exon skipping. Am. J. Hum. Genet. 55: 883-889.
-
(1994)
Am. J. Hum. Genet.
, vol.55
, pp. 883-889
-
-
Das, S.1
Levinson, B.2
Whitney, S.3
Vulpe, C.4
Packman, S.5
Gitschier, J.6
-
16
-
-
0001594992
-
The tortoise shell house mouse
-
Dickie, M. M. (1954). The tortoise shell house mouse. J. Hered. 45: 158-159.
-
(1954)
J. Hered.
, vol.45
, pp. 158-159
-
-
Dickie, M.M.1
-
17
-
-
0029129769
-
Molecular structure of the Menkes disease gene (ATP7A)
-
Dierick, H. A., Ambrosini, L., Spencer, J., Glover, T. W., and Mercer, J. F. B. (1995). Molecular structure of the Menkes disease gene (ATP7A). Genomics 28: 462-469.
-
(1995)
Genomics
, vol.28
, pp. 462-469
-
-
Dierick, H.A.1
Ambrosini, L.2
Spencer, J.3
Glover, T.W.4
Mercer, J.F.B.5
-
18
-
-
0025111524
-
Linkage and sequence conservation of the X linked genes DXS253E (P3) and DXS254E (GdX) in mouse and man
-
Filippi, M., Tribioli, C., and Toniolo, D. (1990). Linkage and sequence conservation of the X linked genes DXS253E (P3) and DXS254E (GdX) in mouse and man. Genomics 7: 453-457.
-
(1990)
Genomics
, vol.7
, pp. 453-457
-
-
Filippi, M.1
Tribioli, C.2
Toniolo, D.3
-
19
-
-
0001372285
-
Mottled, a sex-modified lethal in the house mouse
-
Fraser, A. S., Sobey, S., and Spicer, C. C. (1953). Mottled, a sex-modified lethal in the house mouse. J. Genet. 51: 217-221.
-
(1953)
J. Genet.
, vol.51
, pp. 217-221
-
-
Fraser, A.S.1
Sobey, S.2
Spicer, C.C.3
-
20
-
-
0027184220
-
Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: Identification of three new transcripts
-
Gecz, J., Villard, L., Lossi, A. M., Millasseau, P., Djabali, M., and Fontes, M. (1993). Physical and transcriptional mapping of DXS56-PGK1 1 Mb region: Identification of three new transcripts. Hum. Mol. Genet. 2: 1389-1396.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1389-1396
-
-
Gecz, J.1
Villard, L.2
Lossi, A.M.3
Millasseau, P.4
Djabali, M.5
Fontes, M.6
-
21
-
-
0027955773
-
Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3
-
Gecz, J., Pollard, H., Consalez, G., Villard, L., Stayton, C., Millasseau, P., Khrestchatisky, M., and Fontes, M. (1994). Cloning and expression of the murine homologue of a putative human X-linked nuclear protein gene closely linked to PGK1 in Xq13.3. Hum. Mol. Genet. 3: 39-44.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 39-44
-
-
Gecz, J.1
Pollard, H.2
Consalez, G.3
Villard, L.4
Stayton, C.5
Millasseau, P.6
Khrestchatisky, M.7
Fontes, M.8
-
22
-
-
0028086041
-
Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) mice
-
George, A. M., Reed, V., Glenister, P., Chelly, J., Tumer, Z., Horn, N., Monaco, A. P., and Boyd Y. (1994). Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) mice. Genomics 22: 27-35.
-
(1994)
Genomics
, vol.22
, pp. 27-35
-
-
George, A.M.1
Reed, V.2
Glenister, P.3
Chelly, J.4
Tumer, Z.5
Horn, N.6
Monaco, A.P.7
Boyd, Y.8
-
23
-
-
0027033477
-
One-tube versus two-step amplification of RNA transcripts using polymerase chain reaction
-
Goblet, C., Prost, E., Bockhold, K. J., and Whalen, R. G. (1992). One-tube versus two-step amplification of RNA transcripts using polymerase chain reaction. Methods Enzymol. 216: 160-168.
-
(1992)
Methods Enzymol.
, vol.216
, pp. 160-168
-
-
Goblet, C.1
Prost, E.2
Bockhold, K.J.3
Whalen, R.G.4
-
24
-
-
0023652388
-
An inverted duplication of more than 650 kb in mouse chromosome 17 mediates unequal but homologous recombination between chromosomes heterozygous for a large inversion
-
Herrmann, B. G., Barlow, D. P., and Lehrach, H. (1987). An inverted duplication of more than 650 kb in mouse chromosome 17 mediates unequal but homologous recombination between chromosomes heterozygous for a large inversion. Cell 48: 813-825.
-
(1987)
Cell
, vol.48
, pp. 813-825
-
-
Herrmann, B.G.1
Barlow, D.P.2
Lehrach, H.3
-
25
-
-
0016330759
-
Primary defect in copper transport underlies mottled mutants in the mouse
-
Hunt, D. M. (1974). Primary defect in copper transport underlies mottled mutants in the mouse. Nature 249: 852-854.
-
(1974)
Nature
, vol.249
, pp. 852-854
-
-
Hunt, D.M.1
-
28
-
-
0025897085
-
Yeast artificial chromosome libraries containing large inserts from mouse and human DNA
-
Larin, Z., Monaco, A. P., and Lehrach, H. (1991). Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. Proc. Natl. Acad. Sci. USA 88: 9628-9632.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 9628-9632
-
-
Larin, Z.1
Monaco, A.P.2
Lehrach, H.3
-
29
-
-
0016762389
-
Skeletal dysplasia, occipital horns, diarrhea and obstructive uropathy - A new hereditary syndrome
-
Lazoff, S. G., Rybak, J. J., Parker, B. R., and Luzzatti, L. (1975). Skeletal dysplasia, occipital horns, diarrhea and obstructive uropathy - A new hereditary syndrome. Birth Defects 11: 71-74.
-
(1975)
Birth Defects
, vol.11
, pp. 71-74
-
-
Lazoff, S.G.1
Rybak, J.J.2
Parker, B.R.3
Luzzatti, L.4
-
30
-
-
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., and 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
-
31
-
-
0001257719
-
A further mutation of the mottled type
-
Lyon, M. F. (1960). A further mutation of the mottled type. J. Hered. 51: 116-121.
-
(1960)
J. Hered.
, vol.51
, pp. 116-121
-
-
Lyon, M.F.1
-
32
-
-
0023946968
-
X chromosome inactivation and the location and expression of X linked genes
-
Lyon, M. F. (1988). X chromosome inactivation and the location and expression of X linked genes. Am. J. Hum. Genet. 42: 8-16.
-
(1988)
Am. J. Hum. Genet.
, vol.42
, pp. 8-16
-
-
Lyon, M.F.1
-
33
-
-
0025987763
-
cDNA cloning of the beta-subunit of the human gastric H,K-ATPase
-
Ma, J. Y., Song, Y. H., Sjostrand, D. E., Rask, L., and Mardh, S. (1991). cDNA cloning of the beta-subunit of the human gastric H,K-ATPase. Biochem. Biophys. Res. Commun. 180: 39-45.
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.180
, pp. 39-45
-
-
Ma, J.Y.1
Song, Y.H.2
Sjostrand, D.E.3
Rask, L.4
Mardh, S.5
-
34
-
-
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., and 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
-
35
-
-
0027475976
-
Isolation of a partial candidate gene for Menkes disease by positional cloning
-
Mercer, J. F. B., Livingston, J., Hall, B., Paynter, J. A., Begy, C., Chandrasekharappa, S., Lockjart, P., Grimes, A., Bhave, M., Siemieniak, C., and Glover, T. (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
Paynter, J.A.4
Begy, C.5
Chandrasekharappa, S.6
Lockjart, P.7
Grimes, A.8
Bhave, M.9
Siemieniak, C.10
Glover, T.11
-
36
-
-
0028246694
-
Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice
-
Mercer, J. F. B., Grimes, A., Ambrosini, L., Lockhart, P., Paynter, J. A., Dierick, H., and Glover, T. W. (1994). Mutations in the murine homologue of the Menkes gene in dappled and blotchy mice. Nature Genet. 6: 374-378.
-
(1994)
Nature Genet.
, vol.6
, pp. 374-378
-
-
Mercer, J.F.B.1
Grimes, A.2
Ambrosini, L.3
Lockhart, P.4
Paynter, J.A.5
Dierick, H.6
Glover, T.W.7
-
37
-
-
0020698922
-
Isolation and DNA sequence of a full-length cDNA clone for human X chromosome-encoded phosphoglycerate kinase
-
Michelson, A. M., Markham, A. F., and Orkin, S. H. (1983). Isolation and DNA sequence of a full-length cDNA clone for human X chromosome-encoded phosphoglycerate kinase. Proc. Natl. Acad. Sci. USA 80: 472-476.
-
(1983)
Proc. Natl. Acad. Sci. USA
, vol.80
, pp. 472-476
-
-
Michelson, A.M.1
Markham, A.F.2
Orkin, S.H.3
-
38
-
-
0027427695
-
Mapping, cloning and genetic characterization of the region containing the wilson disease gene
-
Petrukhin, K., Fischer, S. G., Pirastu, M., Tanzi, R. E., Chernov, I., Devoto, M., Brzutowicz, L. M., Cayanis, E., Vitale, E., Russo, J. J., Matseoane, D., Boukhgalter, B. , Wasco, W., Figus, A. L., Loudianos, J., Cao, A., Sternlieb, I., Evgrafov, O., Parano, E., Pavone, L., Warburton, D., Ott, J., Penchaszadeh, G. K., Scheinberg, I. H., and Gilliam, T. C. (1993). Mapping, cloning and genetic characterization of the region containing the Wilson disease gene. Nature Genet. 5: 338-343.
-
(1993)
Nature Genet.
, vol.5
, pp. 338-343
-
-
Petrukhin, K.1
Fischer, S.G.2
Pirastu, M.3
Tanzi, R.E.4
Chernov, I.5
Devoto, M.6
Brzutowicz, L.M.7
Cayanis, E.8
Vitale, E.9
Russo, J.J.10
Matseoane, D.11
Boukhgalter, B.12
Wasco, W.13
Figus, A.L.14
Loudianos, J.15
Cao, A.16
Sternlieb, I.17
Evgrafov, O.18
Parano, E.19
Pavone, L.20
Warburton, D.21
Ott, J.22
Penchaszadeh, G.K.23
Scheinberg, I.H.24
Gilliam, T.C.25
more..
-
39
-
-
0028040512
-
Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: Genomic organization, alternative splicing, and structure/function predictions
-
Petrukhin, K., Lutsenko, S., Chernov, I., Ross, B. M., Kaplan, J. H., and Gilliam, T. C. (1994). Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: Genomic organization, alternative splicing, and structure/function predictions. Hum. Mol. Genet. 3: 1647-1656.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1647-1656
-
-
Petrukhin, K.1
Lutsenko, S.2
Chernov, I.3
Ross, B.M.4
Kaplan, J.H.5
Gilliam, T.C.6
-
40
-
-
0011864051
-
Research news: Mutants
-
Phillips, R. J. S. (1956). Research news: Mutants. Mouse News Lett. 15: 28.
-
(1956)
Mouse News Lett.
, vol.15
, pp. 28
-
-
Phillips, R.J.S.1
-
41
-
-
0018650575
-
Primary biochemical defect in copper metabolism in mice with a recessive X-linked mutation analogous to Menkes' disease in man
-
Prins, H. W., and Van der Hamer, C. J. A. (1979). Primary biochemical defect in copper metabolism in mice with a recessive X-linked mutation analogous to Menkes' disease in man. J. Inorg. Biochem. 10: 19-27.
-
(1979)
J. Inorg. Biochem.
, vol.10
, pp. 19-27
-
-
Prins, H.W.1
Van Der Hamer, C.J.A.2
-
42
-
-
0000595941
-
Research news: Three new mottled mutations
-
Rasberry, C., and Cattanach, B. M. (1993). Research news: Three new mottled mutations. Mouse Genome 91: 851-853.
-
(1993)
Mouse Genome
, vol.91
, pp. 851-853
-
-
Rasberry, C.1
Cattanach, B.M.2
-
43
-
-
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
-
44
-
-
0025339588
-
A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones
-
Riley, J., Butler, R., Ogilvie, D., Finniear, R., Jenner, D., Powell, S., Anand, R., Smith, J. C., and Markham, A. F. (1990). A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones. Nucleic Acids Res. 18: 2887-2890.
-
(1990)
Nucleic Acids Res.
, vol.18
, pp. 2887-2890
-
-
Riley, J.1
Butler, R.2
Ogilvie, D.3
Finniear, R.4
Jenner, D.5
Powell, S.6
Anand, R.7
Smith, J.C.8
Markham, A.F.9
-
45
-
-
0030049413
-
Cloning and characterization of a murine brain specific gene Bpx and its human homologue lying within the Xic candidate region
-
Rougeulle, C., and Avner, P. (1996). Cloning and characterization of a murine brain specific gene Bpx and its human homologue lying within the Xic candidate region. Hum. Mol. Genet. 5: 41-49.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 41-49
-
-
Rougeulle, C.1
Avner, P.2
-
46
-
-
0011825547
-
Research news: Mutants
-
Russell, L. B. (1960). Research news: Mutants. Mouse News Lett. 23: 58.
-
(1960)
Mouse News Lett.
, vol.23
, pp. 58
-
-
Russell, L.B.1
-
47
-
-
0017681196
-
DNA sequencing with chain terminating inhibitors
-
Sanger, F., Nicklen, S., and Coulson, A. R. (1977). DNA sequencing with chain terminating inhibitors. Proc. Natl. Acad. Sci. USA 77: 5463-5467.
-
(1977)
Proc. Natl. Acad. Sci. USA
, vol.77
, pp. 5463-5467
-
-
Sanger, F.1
Nicklen, S.2
Coulson, A.R.3
-
48
-
-
0027989674
-
The gene responsible for LEC hepatitis, located on rat chromosome 16, is the homolog to the human Wilson disease gene
-
Sasaki, N., Hayashizaki, Y., Muramatsu, M., Matsuda, Y., Ando, Y., Kuramoto, T., Serikawa, T., Azuma, T., Naito, A., Agui, T., Yamashita, T., Miyoshi, I., Takeichi, N., and Kasai, N. (1994). The gene responsible for LEC hepatitis, located on rat chromosome 16, is the homolog to the human Wilson disease gene. Biochem. Biophys. Res. Commun. 202: 512-518.
-
(1994)
Biochem. Biophys. Res. Commun.
, vol.202
, pp. 512-518
-
-
Sasaki, N.1
Hayashizaki, Y.2
Muramatsu, M.3
Matsuda, Y.4
Ando, Y.5
Kuramoto, T.6
Serikawa, T.7
Azuma, T.8
Naito, A.9
Agui, T.10
Yamashita, T.11
Miyoshi, I.12
Takeichi, N.13
Kasai, N.14
-
49
-
-
34249923845
-
Characterization of the central region containing the X-inactivation center and terminal region of the mouse X chromosome using irradiation and fusion gene transfer hybrids
-
Sefton, L., Arnaud, D., Goodfellow, P. N., Simmler, M. C., and Avner, P. (1992). Characterization of the central region containing the X-inactivation center and terminal region of the mouse X chromosome using irradiation and fusion gene transfer hybrids. Mamm. Genome 2: 21-31.
-
(1992)
Mamm. Genome
, vol.2
, pp. 21-31
-
-
Sefton, L.1
Arnaud, D.2
Goodfellow, P.N.3
Simmler, M.C.4
Avner, P.5
-
50
-
-
0027376523
-
Human Menkes X-chromosome disease and the staphylococcal cadmium-resistance ATPase: A remarkable similarity in protein sequences
-
Silver, S., Nucifora, G., and Phung, L. T. (1993). Human Menkes X-chromosome disease and the staphylococcal cadmium-resistance ATPase: A remarkable similarity in protein sequences. Mol. Biol. 10: 7-12.
-
(1993)
Mol. Biol.
, vol.10
, pp. 7-12
-
-
Silver, S.1
Nucifora, G.2
Phung, L.T.3
-
51
-
-
0001645602
-
-
Sweet (1993). Mouse Genome 91: 862.
-
(1993)
Mouse Genome
, vol.91
, pp. 862
-
-
Sweet1
-
52
-
-
0029062630
-
Characterization of the exon structure of the Menkes disease gene using vectorette PCR
-
Turner, Z., Vural, B., Tonnesen, T., Chelly, J., Monaco, A. P., and Horn, N. (1995). Characterization of the exon structure of the Menkes disease gene using vectorette PCR. Genomics 26: 437-442.
-
(1995)
Genomics
, vol.26
, pp. 437-442
-
-
Turner, Z.1
Vural, B.2
Tonnesen, T.3
Chelly, J.4
Monaco, A.P.5
Horn, N.6
-
53
-
-
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
-
54
-
-
0028001088
-
The LEC rat has a deletion in the copper transporting ATPase gene homologous to the Wilson disease gene
-
Wu, J., Forbes, J., 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.2
Chen, H.S.3
Cox, D.W.4
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