-
1
-
-
0027300283
-
Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain
-
Abitbol, M., Menini, C., Delezoide, A. L., Rhyner, T., Vekemans, M., & Mallet, J. (1993) Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain. Nature Genet. 4, 147-153.
-
(1993)
Nature Genet.
, vol.4
, pp. 147-153
-
-
Abitbol, M.1
Menini, C.2
Delezoide, A.L.3
Rhyner, T.4
Vekemans, M.5
Mallet, J.6
-
2
-
-
0027377580
-
FMR1 protein: Conserved RNP family domains and selective RNA binding
-
Ashley, C. T., Jr., Wilkinson, K. D., Reines, D., & Warren, S. T. (1993) FMR1 protein: Conserved RNP family domains and selective RNA binding. Science 262, 563-566.
-
(1993)
Science
, vol.262
, pp. 563-566
-
-
Ashley C.T., Jr.1
Wilkinson, K.D.2
Reines, D.3
Warren, S.T.4
-
3
-
-
0027176361
-
The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation
-
Devys, D., Lutz, Y., Rouyer, N., Bellocq, J. P., & Mandel, J. L. (1993) The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation. Nature Genet. 4, 335-340.
-
(1993)
Nature Genet.
, vol.4
, pp. 335-340
-
-
Devys, D.1
Lutz, Y.2
Rouyer, N.3
Bellocq, J.P.4
Mandel, J.L.5
-
4
-
-
0029816723
-
The Fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals
-
Eberhart, D. E., Malter, H. E., Feng, Y., & Warren, S. T. (1996) The Fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals. Hum. Mol. Genet. 5, 1083-1091.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1083-1091
-
-
Eberhart, D.E.1
Malter, H.E.2
Feng, Y.3
Warren, S.T.4
-
5
-
-
0027209517
-
Fine structure of the human FMR1 gene
-
Eichler, E. E., Richards, S., Gibbs, R. A., & Nelson, D. L. (1993) Fine structure of the human FMR1 gene. Hum. Mol. Genet. 2, 1147-1153.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1147-1153
-
-
Eichler, E.E.1
Richards, S.2
Gibbs, R.A.3
Nelson, D.L.4
-
6
-
-
0029130169
-
The HIV-1 Rev activation domain is a nuclear export signal that accesses an export pathway used by specific cellular RNAs
-
Fischer, U., Huber, J., Boelens, W. C., Mattaj, I. W., & Lührmann, R. (1995) The HIV-1 Rev activation domain is a nuclear export signal that accesses an export pathway used by specific cellular RNAs. Cell 82, 475-483.
-
(1995)
Cell
, vol.82
, pp. 475-483
-
-
Fischer, U.1
Huber, J.2
Boelens, W.C.3
Mattaj, I.W.4
Lührmann, R.5
-
7
-
-
0029818460
-
A nuclear role for the Fragile X mental retardation protein
-
Fridell, R. A., Benson, R. E., Hua, J., Bogerd, H. P., & Cullen, B. R. (1996) A nuclear role for the Fragile X mental retardation protein. EMBO J. 15, 5408-5414.
-
(1996)
EMBO J.
, vol.15
, pp. 5408-5414
-
-
Fridell, R.A.1
Benson, R.E.2
Hua, J.3
Bogerd, H.P.4
Cullen, B.R.5
-
8
-
-
0029121296
-
Nuclear transport signals and the fast track to the cytoplasm
-
Gerace, L. (1995) Nuclear transport signals and the fast track to the cytoplasm. Cell 82, 341-344.
-
(1995)
Cell
, vol.82
, pp. 341-344
-
-
Gerace, L.1
-
9
-
-
0027397928
-
Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome
-
Hinds, H. L., Ashley, C. T., Sutcliffe, J. S., Nelson, D. L., Warren, S. T., Housman, D. E., & Schalling, M. (1993) Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome. Nature Genet. 3, 36-43.
-
(1993)
Nature Genet.
, vol.3
, pp. 36-43
-
-
Hinds, H.L.1
Ashley, C.T.2
Sutcliffe, J.S.3
Nelson, D.L.4
Warren, S.T.5
Housman, D.E.6
Schalling, M.7
-
10
-
-
0026751769
-
Intracellular distribution of the U1A protein depends on active transport and nuclear binding to U1 snRNA
-
Kambach, C., & Mattaj, I. W. (1992) Intracellular distribution of the U1A protein depends on active transport and nuclear binding to U1 snRNA. J. Cell Biol. 118, 11-21.
-
(1992)
J. Cell Biol.
, vol.118
, pp. 11-21
-
-
Kambach, C.1
Mattaj, I.W.2
-
11
-
-
0026583943
-
Structure, localization and transcriptional properties of two classes of retinoic acid receptor alpha fusion proteins in acute promyelocytic leukemia (APL): Structural similarities with a new family of oncoproteins
-
Kastner, P., Perez, A., Lutz, Y., Rochette-Egly, C., Gaub, M. P., Durand, B., Lanotte, M., Berger, R., & Chambon, P. (1992) Structure, localization and transcriptional properties of two classes of retinoic acid receptor alpha fusion proteins in acute promyelocytic leukemia (APL): Structural similarities with a new family of oncoproteins. EMBO J. 11, 629-642.
-
(1992)
EMBO J.
, vol.11
, pp. 629-642
-
-
Kastner, P.1
Perez, A.2
Lutz, Y.3
Rochette-Egly, C.4
Gaub, M.P.5
Durand, B.6
Lanotte, M.7
Berger, R.8
Chambon, P.9
-
12
-
-
0029042740
-
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture
-
Khandjian, E. W., Fortin, A., Thibodeau, A., Tremblay, S., Côté, F., Devys, D., Mandel, J. L., & Rousseau, F. (1995) A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture. Hum. Mol. Genet. 4, 783-789.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 783-789
-
-
Khandjian, E.W.1
Fortin, A.2
Thibodeau, A.3
Tremblay, S.4
Côté, F.5
Devys, D.6
Mandel, J.L.7
Rousseau, F.8
-
13
-
-
0030059545
-
The fragile X mental retardation protein is associated with ribosomes
-
Khandjian, E. W., Corbin, F., Woerly, S., & Rousseau, F. (1996) The fragile X mental retardation protein is associated with ribosomes. Nature Genet. 12, 91-93.
-
(1996)
Nature Genet.
, vol.12
, pp. 91-93
-
-
Khandjian, E.W.1
Corbin, F.2
Woerly, S.3
Rousseau, F.4
-
14
-
-
0025800165
-
Mapping of DNA instability at the Fragile X to a trinucleotide repeat sequence (pCCG)n
-
Kremer, E. J., Pritchard, M., Lynch, M., Yu, S., Holman, K., Baker, E., Warren, S. T., Schlessinger, D., Sutherland, G. R., & Richards, R. I. (1991) Mapping of DNA instability at the Fragile X to a trinucleotide repeat sequence (pCCG)n. Science 252, 1711-1714.
-
(1991)
Science
, vol.252
, pp. 1711-1714
-
-
Kremer, E.J.1
Pritchard, M.2
Lynch, M.3
Yu, S.4
Holman, K.5
Baker, E.6
Warren, S.T.7
Schlessinger, D.8
Sutherland, G.R.9
Richards, R.I.10
-
15
-
-
0028040020
-
Cytoplasmic retention of Xenopus nuclear factor 7 before the mid blastula transition uses a unique anchoring mechanism involving a retention domain and several phosphorylation sites
-
Li, X., Shou, W., Kloc, M., Reddy, B. A., & Etkin, L. D. (1994) Cytoplasmic retention of Xenopus nuclear factor 7 before the mid blastula transition uses a unique anchoring mechanism involving a retention domain and several phosphorylation sites. J. Cell Biol. 124, 7-17.
-
(1994)
J. Cell Biol.
, vol.124
, pp. 7-17
-
-
Li, X.1
Shou, W.2
Kloc, M.3
Reddy, B.A.4
Etkin, L.D.5
-
16
-
-
0026339303
-
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
-
Oberlé, I., Rousseau, F., Heitz, D., Kretz, C., Devys, D., Hanauer, A., Boue, J., Bertheas, M. F., & Mandel, J. L. (1991) Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome. Science 252, 1097-1102.
-
(1991)
Science
, vol.252
, pp. 1097-1102
-
-
Oberlé, I.1
Rousseau, F.2
Heitz, D.3
Kretz, C.4
Devys, D.5
Hanauer, A.6
Boue, J.7
Bertheas, M.F.8
Mandel, J.L.9
-
17
-
-
0025833298
-
Absence of expression of the FMR1 gene in fragile X syndrome
-
Pieretti, M., Zhang, F., Fu, Y-H., Warren, S. T., Oostra, B. A., Caskey, C. T., & Nelson, D. L. (1991) Absence of expression of the FMR1 gene in fragile X syndrome. Cell 66, 817-822.
-
(1991)
Cell
, vol.66
, pp. 817-822
-
-
Pieretti, M.1
Zhang, F.2
Fu, Y.-H.3
Warren, S.T.4
Oostra, B.A.5
Caskey, C.T.6
Nelson, D.L.7
-
18
-
-
0027933911
-
The differential localization of human cyclins A and B is due to a cytoplasmic retention signal in cyclin B
-
Pines, J., & Hunter, T. (1994) The differential localization of human cyclins A and B is due to a cytoplasmic retention signal in cyclin B. EMBO J. 13, 3772-3781.
-
(1994)
EMBO J.
, vol.13
, pp. 3772-3781
-
-
Pines, J.1
Hunter, T.2
-
19
-
-
0030595342
-
A novel receptor-mediated nuclear protein import pathway
-
Pollard, V. W., Michael, W. M., Nakielny, S., Siomi, M. C., Wang, F., & Dreyfuss, G. (1996) A novel receptor-mediated nuclear protein import pathway. Cell 86, 985-994.
-
(1996)
Cell
, vol.86
, pp. 985-994
-
-
Pollard, V.W.1
Michael, W.M.2
Nakielny, S.3
Siomi, M.C.4
Wang, F.5
Dreyfuss, G.6
-
20
-
-
0023669094
-
The effect of protein context on nuclear location signal function
-
Roberts, B. L., Richardson, W. D., & Smith, A. E. (1987) The effect of protein context on nuclear location signal function. Cell 50, 465-475.
-
(1987)
Cell
, vol.50
, pp. 465-475
-
-
Roberts, B.L.1
Richardson, W.D.2
Smith, A.E.3
-
21
-
-
0026022910
-
How proteins enter the nucleus
-
Silver, P. A. (1991) How proteins enter the nucleus. Cell 64, 489-497.
-
(1991)
Cell
, vol.64
, pp. 489-497
-
-
Silver, P.A.1
-
22
-
-
0027327486
-
The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein
-
Siomi, H., Siomi, M. C., Nussbaum, R. L., & Dreyfuss, G. (1993) The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein. Cell 74, 291-298.
-
(1993)
Cell
, vol.74
, pp. 291-298
-
-
Siomi, H.1
Siomi, M.C.2
Nussbaum, R.L.3
Dreyfuss, G.4
-
23
-
-
0028236525
-
Essential role for KH domains in RNA binding: Impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome
-
Siomi, H., Choi, M., Siomi, M. C., Nussbaum, R. L., & Dreyfuss, G. (1994) Essential role for KH domains in RNA binding: Impaired RNA binding by a mutation in the KH domain of FMR1 that causes fragile X syndrome. Cell 77, 33-39.
-
(1994)
Cell
, vol.77
, pp. 33-39
-
-
Siomi, H.1
Choi, M.2
Siomi, M.C.3
Nussbaum, R.L.4
Dreyfuss, G.5
-
24
-
-
0029069223
-
FXR1, an autosomal homolog of the fragile X mental retardation gene
-
Siomi, M. C., Siomi, H., Sauer, W. H., Srinivasan, S., Nussbaum, R. L., & Dreyfuss, G. (1995) FXR1, an autosomal homolog of the fragile X mental retardation gene. EMBO J. 14, 2401-2408.
-
(1995)
EMBO J.
, vol.14
, pp. 2401-2408
-
-
Siomi, M.C.1
Siomi, H.2
Sauer, W.H.3
Srinivasan, S.4
Nussbaum, R.L.5
Dreyfuss, G.6
-
25
-
-
0029972935
-
Specific sequences in the fragile X syndrome protein FMR1 and FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them
-
Siomi, M. C., Zhang, Y., Siomi, H., & Dreyfuss, G. (1996) Specific sequences in the fragile X syndrome protein FMR1 and FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them. Mol. Cell. Biol. 16, 3825-3832.
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 3825-3832
-
-
Siomi, M.C.1
Zhang, Y.2
Siomi, H.3
Dreyfuss, G.4
-
26
-
-
0030051618
-
Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms
-
Sittler, A., Devys, D., Weber, C., & Mandel, J. L. (1996) Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms. Hum. Mol. Genet. 5, 95-102.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 95-102
-
-
Sittler, A.1
Devys, D.2
Weber, C.3
Mandel, J.L.4
-
27
-
-
0026922707
-
DNA methylation represses FMR-1 transcription in fragile X syndrome
-
Sutcliffe, J. S., Nelson, D. L., Zhang, F., Pieretti, M., Caskey, C. T., Saxe, D., & Warren, S. T. (1992) DNA methylation represses FMR-1 transcription in fragile X syndrome. Hum. Mol. Genet. 1, 397-400.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 397-400
-
-
Sutcliffe, J.S.1
Nelson, D.L.2
Zhang, F.3
Pieretti, M.4
Caskey, C.T.5
Saxe, D.6
Warren, S.T.7
-
28
-
-
0029894592
-
FMRP is associated to the ribosomes via RNA
-
Tamanini, F., Meijer, N., Verheij, C., Willems, P. J., Galjaard, H., Oostra, B. A., & Hoogeveen, A. T. (1996) FMRP is associated to the ribosomes via RNA. Hum. Mol. Genet. 5, 809-813.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 809-813
-
-
Tamanini, F.1
Meijer, N.2
Verheij, C.3
Willems, P.J.4
Galjaard, H.5
Oostra, B.A.6
Hoogeveen, A.T.7
-
29
-
-
0029063222
-
Characterization of FMR1 proteins isolated from different tissues
-
Verheij, C., de Graaff, E., Bakker, C. E., Willemsen, R., Willems, P. J., Meijer, N., Galjaard, H., Reuser, A. J. J., Oostra, B. A., & Hoogeveen, A. T. (1995) Characterization of FMR1 proteins isolated from different tissues. Hum. Mol. Genet. 4, 895-901.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 895-901
-
-
Verheij, C.1
De Graaff, E.2
Bakker, C.E.3
Willemsen, R.4
Willems, P.J.5
Meijer, N.6
Galjaard, H.7
Reuser, A.J.J.8
Oostra, B.A.9
Hoogeveen, A.T.10
-
30
-
-
0027409764
-
Alternative splicing in the fragile X gene FMR1
-
Verkerk, A. J., de Graaff, E., De Boulle, K., Eichler, E. E., Konecki, D. S., Reyniers, E., Manca, A., Poustka, A., Willems, P. J., Nelson, D. L., & Oostra, B. A. (1993) Alternative splicing in the fragile X gene FMR1. Hum. Mol. Genet. 2, 399-404.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 399-404
-
-
Verkerk, A.J.1
De Graaff, E.2
De Boulle, K.3
Eichler, E.E.4
Konecki, D.S.5
Reyniers, E.6
Manca, A.7
Poustka, A.8
Willems, P.J.9
Nelson, D.L.10
Oostra, B.A.11
-
31
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk, A. J. M. H., Pieretti, M., Sutcliffe, J. S., Fu, Y. H., Kuhl, D. P. A., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F., Eussen, B. E., Van Ommen, G. J. B., Blonden, L. A. J., Riggins, G. J., Chastain, J. L., Kunst, C. B., Galjaard, H., Caskey, C. T., Nelson, D. L., Oostra, B. A., & Warren, S. T. (1991) Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65, 905-914.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.H.4
Kuhl, D.P.A.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.10
Eussen, B.E.11
Van Ommen, G.J.B.12
Blonden, L.A.J.13
Riggins, G.J.14
Chastain, J.L.15
Kunst, C.B.16
Galjaard, H.17
Caskey, C.T.18
Nelson, D.L.19
Oostra, B.A.20
Warren, S.T.21
more..
-
32
-
-
0029130168
-
Identification of a signal for rapid export of proteins from the nucleus
-
Wen, W., Meinkoth, J. L., Tsien, R. Y., & Taylor, S. S. (1995) Identification of a signal for rapid export of proteins from the nucleus. Cell 82, 463-473.
-
(1995)
Cell
, vol.82
, pp. 463-473
-
-
Wen, W.1
Meinkoth, J.L.2
Tsien, R.Y.3
Taylor, S.S.4
-
33
-
-
0028971722
-
The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2
-
Zhang, Y., O'Connor, J. P., Siomi, M. C., Srinivasan, S., Dutra, A., Nussbaum, R. L., & Dreyfuss, R. (1995) The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2. EMBO J. 14, 5358-5366.
-
(1995)
EMBO J.
, vol.14
, pp. 5358-5366
-
-
Zhang, Y.1
O'Connor, J.P.2
Siomi, M.C.3
Srinivasan, S.4
Dutra, A.5
Nussbaum, R.L.6
Dreyfuss, R.7
|