-
1
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada, A.R., Wilson, E.M., Lubahn, D.B., Harding, A.E. and Fischbeck. K.H. (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature, 352, 77-79.
-
(1991)
Nature
, vol.352
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
2
-
-
0027023516
-
Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy
-
La Spada, A.R., Roling, D.B., Harding, A.E., Warner, C.L., Spiegel, R., Hausmanowa Petrusewicz. I., Yee, W.C. and Fischbeck, K.H. (1992) Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. Nature Genet., 2, 301-304.
-
(1992)
Nature Genet.
, vol.2
, pp. 301-304
-
-
La Spada, A.R.1
Roling, D.B.2
Harding, A.E.3
Warner, C.L.4
Spiegel, R.5
Hausmanowa Petrusewicz, I.6
Yee, W.C.7
Fischbeck, K.H.8
-
3
-
-
0026894334
-
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy
-
Biancalana, V., Serville, F., Pommier, J., Julien, J., Hanauer, A. and Mandel, J.L. (1992) Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy. Hum. Mol. Genet., 1, 255-258.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 255-258
-
-
Biancalana, V.1
Serville, F.2
Pommier, J.3
Julien, J.4
Hanauer, A.5
Mandel, J.L.6
-
4
-
-
0028925739
-
CAG repeat length variation in sperm from a patient with Kennedy's disease
-
Zhang, L., Fischbeck, K.H. and Arnheim, N. (1995) CAG repeat length variation in sperm from a patient with Kennedy's disease. Hum. Mol. Genet., 4, 303-305.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 303-305
-
-
Zhang, L.1
Fischbeck, K.H.2
Arnheim, N.3
-
5
-
-
16944364511
-
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
-
David,G., Abbas, N., Stevanin,G., Durr, A.,Yvert, G., Cancel.G.,Weber.C., Imbert, G., Saudou, F., Antoniou, E., Drabkin, H., Gemmill, R., Giunti. P., Benomar, A., Wood, N., Ruberg, M., Agid, Y., Mandel, J.L. and Brice, A. (1997) Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nature Genet., 17, 65-70.
-
(1997)
Nature Genet.
, vol.17
, pp. 65-70
-
-
David, G.1
Abbas, N.2
Stevanin, G.3
Durr, A.4
Yvert, G.5
Cancel, G.6
Weber, C.7
Imbert, G.8
Saudou, F.9
Antoniou, E.10
Drabkin, H.11
Gemmill, R.12
Giunti, P.13
Benomar, A.14
Wood, N.15
Ruberg, M.16
Agid, Y.17
Mandel, J.L.18
Brice, A.19
-
6
-
-
0030700891
-
Rethinking genotype and phenotype correlations in polyglutamine expansion disorders
-
Andrew, S.E., Goldberg, Y.P. and Hayden, M.R. (1997) Rethinking genotype and phenotype correlations in polyglutamine expansion disorders. Hum. Mol. Genet., 6, 2005-2010.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2005-2010
-
-
Andrew, S.E.1
Goldberg, Y.P.2
Hayden, M.R.3
-
7
-
-
0030793199
-
Trinucleotide repeat instability: Genetic features and molecular mechanisms
-
La Spada, A.R. (1997) Trinucleotide repeat instability: genetic features and molecular mechanisms. Brain Pathol., 7, 943-963.
-
(1997)
Brain Pathol.
, vol.7
, pp. 943-963
-
-
La Spada, A.R.1
-
8
-
-
0028242797
-
Simple repeat DNA is not replicated simply
-
Richards, R.I. and Sutherland, G.R. (1994) Simple repeat DNA is not replicated simply. Nature Genet., 6. 114-116.
-
(1994)
Nature Genet.
, vol.6
, pp. 114-116
-
-
Richards, R.I.1
Sutherland, G.R.2
-
10
-
-
0028857157
-
Mechanisms of DNA expansion
-
McMurray, C.T. (1995) Mechanisms of DNA expansion. Chromosoma, 104, 2-13.
-
(1995)
Chromosoma
, vol.104
, pp. 2-13
-
-
McMurray, C.T.1
-
11
-
-
0028878844
-
Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice
-
Bingham, P.M., Scott, M.O., Wang, S., McPhaul, M.J., Wilson, E.M., Garbern, J.Y., Merry, D.E. and Fischbeck, K.H. (1995) Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice. Nature Genet., 9, 191-196.
-
(1995)
Nature Genet.
, vol.9
, pp. 191-196
-
-
Bingham, P.M.1
Scott, M.O.2
Wang, S.3
McPhaul, M.J.4
Wilson, E.M.5
Garbern, J.Y.6
Merry, D.E.7
Fischbeck, K.H.8
-
12
-
-
0029163222
-
SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat
-
Burright, E.N.,Clark, H.B., Servadio, A., Matilla, T.,Feddersen. R.M., Yunis. W.S., Duvick, L.A, Zoghbi, H.Y. and Orr, H.T. (1995) SCA1 transgenic mice: a model for neurodegeneration caused by an expanded CAG trinucleotide repeat. Cell, 82, 937-948.
-
(1995)
Cell
, vol.82
, pp. 937-948
-
-
Burright, E.N.1
Clark, H.B.2
Servadio, A.3
Matilla, T.4
Feddersen, R.M.5
Yunis, W.S.6
Duvick, L.A.7
Zoghbi, H.Y.8
Orr, H.T.9
-
13
-
-
9044229711
-
Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript
-
Goldberg, Y.P., Kalchman, M.A., Metzler, M., Nasir, J., Zeisler. J., Graham, R., Koide, H.B., O'Kusky. J., Sharp, A.H., Ross, C.A., Jirik, F. and Hayden, M.R. (1996) Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript. Hum. Mol. Genet., 5, 177-185.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 177-185
-
-
Goldberg, Y.P.1
Kalchman, M.A.2
Metzler, M.3
Nasir, J.4
Zeisler, J.5
Graham, R.6
Koide, H.B.7
O'Kusky, J.8
Sharp, A.H.9
Ross, C.A.10
Jirik, F.11
Hayden, M.R.12
-
14
-
-
0030058208
-
Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in n'vo
-
Ikeda, H., Yamaguchi, M., Sugai, S., Aze, Y., Narumiya, S. and Kakizuka, A. (1996) Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in n'vo. Nature Genet., 13, 196-202.
-
(1996)
Nature Genet.
, vol.13
, pp. 196-202
-
-
Ikeda, H.1
Yamaguchi, M.2
Sugai, S.3
Aze, Y.4
Narumiya, S.5
Kakizuka, A.6
-
15
-
-
0001610768
-
Toward a mouse model for spinal and bulbar muscular atrophy: Effect of neuronal expression of androgen receptor in transgenic mice
-
abstract
-
Merry, D.E., McCampbell. A., Taye, A.A., Winston, R.L. and Fischbeck, K.H. (1996) Toward a mouse model for spinal and bulbar muscular atrophy: effect of neuronal expression of androgen receptor in transgenic mice. Am. J. Hum. Genet., 59. A271 (abstract).
-
(1996)
Am. J. Hum. Genet.
, vol.59
-
-
Merry, D.E.1
McCampbell, A.2
Taye, A.A.3
Winston, R.L.4
Fischbeck, K.H.5
-
16
-
-
0031038809
-
Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice
-
Gourdon, G., Radvanyi, F., Lia, A.S., Duros, C., Blanche, M., Abitbol, M., Junien, C. and Hofmann Radvanyi. H. (1997) Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice. Nature Genet., 15, 190-192.
-
(1997)
Nature Genet.
, vol.15
, pp. 190-192
-
-
Gourdon, G.1
Radvanyi, F.2
Lia, A.S.3
Duros, C.4
Blanche, M.5
Abitbol, M.6
Junien, C.7
Hofmann Radvanyi, H.8
-
17
-
-
0031056685
-
Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation
-
Mangiarini, L., Sathasivam, K., Mahal, A., Mott. R., Seller, M. and Bates, G.P. (1997) Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation. Nature Genet., 15, 197-200.
-
(1997)
Nature Genet.
, vol.15
, pp. 197-200
-
-
Mangiarini, L.1
Sathasivam, K.2
Mahal, A.3
Mott, R.4
Seller, M.5
Bates, G.P.6
-
18
-
-
0031054076
-
Hypermutable myotonic dystrophy CTG repeats in transgenic mice
-
Monckton, D.G., Coolbaugh, M.I., Ashizawa. K.T., Siciliano. M.J. and Caskey, C.T. (1997) Hypermutable myotonic dystrophy CTG repeats in transgenic mice. Nature Genet., 15, 193-196.
-
(1997)
Nature Genet.
, vol.15
, pp. 193-196
-
-
Monckton, D.G.1
Coolbaugh, M.I.2
Ashizawa, K.T.3
Siciliano, M.J.4
Caskey, C.T.5
-
19
-
-
0030700381
-
Increased trinucleotide repeat instability with advanced maternal age
-
Kaytor, M.D., Burright, E.N., Duvick, LA., Zoghbi, H.Y. and Orr, H.T. (1997) Increased trinucleotide repeat instability with advanced maternal age. Hum. Mol. Genet., 6, 2135-2139.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2135-2139
-
-
Kaytor, M.D.1
Burright, E.N.2
Duvick, L.A.3
Zoghbi, H.Y.4
Orr, H.T.5
-
20
-
-
0042115272
-
Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: Evidence from single sperm analyses
-
Chong, S., Almqvist, E., Telenius, H., LaTray, L., Nichol. K., Bourdelat-Parks. B., Goldberg, Y, Haddad, B., Richards, F., Sillence, D., Greenberg, C., Ives, E., van den Engh, G., Hughes, M. and Hayden, M. (1997) Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses, Hum. Mol. Genet., 6, 301-309.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 301-309
-
-
Chong, S.1
Almqvist, E.2
Telenius, H.3
LaTray, L.4
Nichol, K.5
Bourdelat-Parks, B.6
Goldberg, Y.7
Haddad, B.8
Richards, F.9
Sillence, D.10
Greenberg, C.11
Ives, E.12
Van Den Engh, G.13
Hughes, M.14
Hayden, M.15
-
21
-
-
0027829543
-
Transgenic mice containing a 248-kilobase human beta locus yeast artificial chromosome display proper developmental control of human globin genes
-
Peterson, K.R., Clegg, C.H., Huxley, C., Josephson, B.M., Haugen, H.S., Furukawa, T. and Stamatoyannopoulos, G. (1993) Transgenic mice containing a 248-kilobase human beta locus yeast artificial chromosome display proper developmental control of human globin genes. Trans. Ass. Am. Physicians, 106, 101-109.
-
(1993)
Trans. Ass. Am. Physicians
, vol.106
, pp. 101-109
-
-
Peterson, K.R.1
Clegg, C.H.2
Huxley, C.3
Josephson, B.M.4
Haugen, H.S.5
Furukawa, T.6
Stamatoyannopoulos, G.7
-
22
-
-
0029035710
-
Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1
-
Chong, S.S., McCall, A.E., Cota. J., Subramony, S.H., Orr, H.T., Hughes, M.R. and Zoghbi, H.Y. (1995) Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1. Nature Genet., 10, 344-350.
-
(1995)
Nature Genet.
, vol.10
, pp. 344-350
-
-
Chong, S.S.1
McCall, A.E.2
Cota, J.3
Subramony, S.H.4
Orr, H.T.5
Hughes, M.R.6
Zoghbi, H.Y.7
-
23
-
-
0028339385
-
Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm
-
Telenius, H., Kremer, B., Goldberg, Y.P., Theilmann, J., Andrew, S.E., Zeisler, J., Adam, S., Greenberg, C., Ives, E.J., Clarkee, L.A. and Hayden, M.R. (1994) Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm. Nature Genet., 6, 409-414.
-
(1994)
Nature Genet.
, vol.6
, pp. 409-414
-
-
Telenius, H.1
Kremer, B.2
Goldberg, Y.P.3
Theilmann, J.4
Andrew, S.E.5
Zeisler, J.6
Adam, S.7
Greenberg, C.8
Ives, E.J.9
Clarkee, L.A.10
Hayden, M.R.11
-
24
-
-
0028873248
-
Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: Small pool PCR analyses
-
Monckton, D.G., Wong, L.J., Ashizawa, T. and Caskey, C.T. (1995) Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses. Hum. Mol. Genet., 4, 1-8.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1-8
-
-
Monckton, D.G.1
Wong, L.J.2
Ashizawa, T.3
Caskey, C.T.4
-
25
-
-
16044373842
-
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
-
Mangiarini, L., Sathasivam, K., Seller, M., Cozens, B., Harper, A., Hetherington, C., Lawton, M., Trottier, Y, Lehrach, H., Davies, S.W. and Bates, O.P. (1996) Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell, 87, 493-506.
-
(1996)
Cell
, vol.87
, pp. 493-506
-
-
Mangiarini, L.1
Sathasivam, K.2
Seller, M.3
Cozens, B.4
Harper, A.5
Hetherington, C.6
Lawton, M.7
Trottier, Y.8
Lehrach, H.9
Davies, S.W.10
Bates, O.P.11
-
26
-
-
0027495515
-
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I
-
Chung, M. Y., Ranum, L.P., Duvick, L.A., Servadio, A., Zoghbi, H.Y. and Orr, H.T. (1993) Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I. Nature Genet., 5, 254-258.
-
(1993)
Nature Genet.
, vol.5
, pp. 254-258
-
-
Chung, M.Y.1
Ranum, L.P.2
Duvick, L.A.3
Servadio, A.4
Zoghbi, H.Y.5
Orr, H.T.6
-
27
-
-
0030292488
-
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
-
Pulst, S.M., Nechiporuk, A., Nechiporuk, T., Gispert. S., Chen, X.N., Lopes Cendes, I., Pearlman, S., Starkman. S., Orozco Diaz, G., Lunkes. A., DeJong, P., Rouleau, G.A., Auburger, G., Korenberg, J.R., Figueroa, C. and Sahba, S. (1996) Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genet., 14, 269-276.
-
(1996)
Nature Genet.
, vol.14
, pp. 269-276
-
-
Pulst, S.M.1
Nechiporuk, A.2
Nechiporuk, T.3
Gispert, S.4
Chen, X.N.5
Lopes Cendes, I.6
Pearlman, S.7
Starkman, S.8
Orozco Diaz, G.9
Lunkes, A.10
DeJong, P.11
Rouleau, G.A.12
Auburger, G.13
Korenberg, J.R.14
Figueroa, C.15
Sahba, S.16
-
28
-
-
2442761245
-
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: Implications for the molecular mechanisms of the instability of the CAG repeat
-
Igarashi, S., Takiyama. Y., Cancel, G., Rogaeva, E.A., Sasaki, H., Wakisaka, A., Zhou, Y.X., Takano, H., Endo, K., Sanpei, K., Oyake, M., Tanaka, H., Stevanin, G., Abbas, N., Durr. A., Rogaev, E.I., Sherrington, R., Tsuda, T., Ikeda, M., Cassa, E., Nishizawa, M., Benomar, A., Julien, J., Weissenbach, J., Wang, G.-X., Agid, Y., St George-Hyslop, P.H., Brice, A. and Tsuji, S. (1996) Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat, Hum. Mol. Genet., 5, 923-932.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 923-932
-
-
Igarashi, S.1
Takiyama, Y.2
Cancel, G.3
Rogaeva, E.A.4
Sasaki, H.5
Wakisaka, A.6
Zhou, Y.X.7
Takano, H.8
Endo, K.9
Sanpei, K.10
Oyake, M.11
Tanaka, H.12
Stevanin, G.13
Abbas, N.14
Durr, A.15
Rogaev, E.I.16
Sherrington, R.17
Tsuda, T.18
Ikeda, M.19
Cassa, E.20
Nishizawa, M.21
Benomar, A.22
Julien, J.23
Weissenbach, J.24
Wang, G.-X.25
Agid, Y.26
St George-Hyslop, P.H.27
Brice, A.28
Tsuji, S.29
more..
-
29
-
-
0029009456
-
Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease
-
Takiyama, Y., Igarashi, S., Rogaeva, E.A., Endo, K., Rogaev, E.I.,Tanaka, H., Sherrington, R., Sanpei, K., Liang, Y., Saito, M., Tsuda, T., Takano, H., Ikeda, M., Lin, C., Chi, H., Kennedy, J.L., Lang. A.E., Wherrett, J.R., Segawa. M., Nomura, Y. Yuasa, T., Weissenbach, J., Yoshida, M., Nishizawa, M., Kidd, K.K., Tsuji, S. and St George-Hyslop. P.H. (1995) Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease, Hum. Mol. Genet., 4. 1137-1146.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1137-1146
-
-
Takiyama, Y.1
Igarashi, S.2
Rogaeva, E.A.3
Endo, K.4
Rogaev, E.I.5
Tanaka, H.6
Sherrington, R.7
Sanpei, K.8
Liang, Y.9
Saito, M.10
Tsuda, T.11
Takano, H.12
Ikeda, M.13
Lin, C.14
Chi, H.15
Kennedy, J.L.16
Lang, A.E.17
Wherrett, J.R.18
Segawa, M.19
Nomura, Y.20
Yuasa, T.21
Weissenbach, J.22
Yoshida, M.23
Nishizawa, M.24
Kidd, K.K.25
Tsuji, S.26
St George-Hyslop, P.H.27
more..
-
30
-
-
0028882509
-
Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population
-
Goldberg, Y.P., McMurray, C.T.. Zeisler, J., Almqvist, E., Sillence, D., Richards, F., Gacy, A.M., Buchanan, J., Telenius, H. and Hayden, M.R. (1995) Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population. Hum. Mol. Genet., 4, 1911-1918.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1911-1918
-
-
Goldberg, Y.P.1
McMurray, C.T.2
Zeisler, J.3
Almqvist, E.4
Sillence, D.5
Richards, F.6
Gacy, A.M.7
Buchanan, J.8
Telenius, H.9
Hayden, M.R.10
-
32
-
-
0031439034
-
A CAG/CTG expansion in the normal population
-
Nakamoto, M., Takebayashi, H., Kawaguchi, Y., Narumiya, S., Taniwaki, M., Nakamura, Y., Ishikawa, Y., Akiguchi, I., Kimura, J. and Kakizuka, A. (1997) A CAG/CTG expansion in the normal population. Nature Genet., 17, 385-386.
-
(1997)
Nature Genet.
, vol.17
, pp. 385-386
-
-
Nakamoto, M.1
Takebayashi, H.2
Kawaguchi, Y.3
Narumiya, S.4
Taniwaki, M.5
Nakamura, Y.6
Ishikawa, Y.7
Akiguchi, I.8
Kimura, J.9
Kakizuka, A.10
-
33
-
-
0030058075
-
Molecular basis of genetic instability of triplet repeats
-
Wells, R.D. (1996) Molecular basis of genetic instability of triplet repeats. J. Biol. Chem., 271, 2875-2878.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 2875-2878
-
-
Wells, R.D.1
-
34
-
-
0029951497
-
Somatic stability of the expanded CAG trinucleotide repeat in X-linked spinal and bulbar muscular atrophy
-
Spiegel, R., La Spada, A.R., Kress, W., Fischbeck, K.H. and Schmid, W. (1996) Somatic stability of the expanded CAG trinucleotide repeat in X-linked spinal and bulbar muscular atrophy. Hum. Mutat., 8, 32-37.
-
(1996)
Hum. Mutat.
, vol.8
, pp. 32-37
-
-
Spiegel, R.1
La Spada, A.R.2
Kress, W.3
Fischbeck, K.H.4
Schmid, W.5
-
35
-
-
0030044128
-
Differential pattern in tissue-specific somatic mosaicism of expanded CAG trinucleotide repeat in dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and X-linked recessive spinal and bulbar muscular atrophy
-
Tanaka, F., Sobue, G., Doyu, M., Ito. Y, Yamamoto, M., Shimada, N., Yamamoto, K., Riku, S., Hshizume, Y and Mitsuma, T. (1996) Differential pattern in tissue-specific somatic mosaicism of expanded CAG trinucleotide repeat in dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and X-linked recessive spinal and bulbar muscular atrophy. J. Neurol. Sci., 135, 43-50.
-
(1996)
J. Neurol. Sci.
, vol.135
, pp. 43-50
-
-
Tanaka, F.1
Sobue, G.2
Doyu, M.3
Ito, Y.4
Yamamoto, M.5
Shimada, N.6
Yamamoto, K.7
Riku, S.8
Hshizume, Y.9
Mitsuma, T.10
-
36
-
-
0024306555
-
Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity
-
Lubahn, D.B., Brown, T.R., Simental, J.A., Higgs, H.N., Migeon, C.J., Wilson, E.M. and French. F.S. (1989) Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity. Proc. Natl Acad. Sci. USA, 86, 9534-9538.
-
(1989)
Proc. Natl Acad. Sci. USA
, vol.86
, pp. 9534-9538
-
-
Lubahn, D.B.1
Brown, T.R.2
Simental, J.A.3
Higgs, H.N.4
Migeon, C.J.5
Wilson, E.M.6
French, F.S.7
-
37
-
-
0001029139
-
Fluorescence in situ hybridization
-
Birren, B., Green, E., Hieter, P. and Myers, R. (eds), Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, in press
-
Trask, B.J. (1998) Fluorescence in situ hybridization. In Birren, B., Green, E., Hieter, P. and Myers, R. (eds), Genome Analysis: A Laboratory Manual. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, in press.
-
(1998)
Genome Analysis: A Laboratory Manual
-
-
Trask, B.J.1
-
38
-
-
0031051305
-
Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family
-
Wise, C.A., Clines, G.A., Massa, H., Trask, B.J. and Lovett, M. (1997) Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family. Genome Res., 7, 10-16.
-
(1997)
Genome Res.
, vol.7
, pp. 10-16
-
-
Wise, C.A.1
Clines, G.A.2
Massa, H.3
Trask, B.J.4
Lovett, M.5
-
39
-
-
0026752336
-
Targeted integration of neomycin into yeast artificial chromosomes (YACs) for transfection into mammalian cells
-
Riley, J.H., Morten, J.E. and Anand, R. (1992) Targeted integration of neomycin into yeast artificial chromosomes (YACs) for transfection into mammalian cells. Nucleic Acids Res., 20, 2971-2976.
-
(1992)
Nucleic Acids Res.
, vol.20
, pp. 2971-2976
-
-
Riley, J.H.1
Morten, J.E.2
Anand, R.3
-
40
-
-
0025981879
-
The human HPRT gene on a yeast artificial chromosome is functional when transferred to mouse cells by cell fusion
-
Huxley, C., Hagino, Y., Schlessinger, D. and Olson, M.V. (1991) The human HPRT gene on a yeast artificial chromosome is functional when transferred to mouse cells by cell fusion. Genomics, 9, 742-750.
-
(1991)
Genomics
, vol.9
, pp. 742-750
-
-
Huxley, C.1
Hagino, Y.2
Schlessinger, D.3
Olson, M.V.4
-
41
-
-
0004136246
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Sambrook, J., Fritsch, E.F. and Maniatis, T (1989) Molecular Cloning: A Laboratory Manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
(1989)
Molecular Cloning: A Laboratory Manual, 2nd Edn.
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
42
-
-
0029075809
-
Construction of a panel of transgenic mice containing a containing 2-Mb set of YAC/P1 clones from human chromosome 21q22.2
-
Smith, D.J., Zhu, Y, Zhang, J., Cheng, J.F. and Rubin, E.M. (1995) Construction of a panel of transgenic mice containing a containing 2-Mb set of YAC/P1 clones from human chromosome 21q22.2. Genomics, 27, 425-434.
-
(1995)
Genomics
, vol.27
, pp. 425-434
-
-
Smith, D.J.1
Zhu, Y.2
Zhang, J.3
Cheng, J.F.4
Rubin, E.M.5
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