-
1
-
-
0027377580
-
FMR-1 protein: Conserved RNP family domains and selective RNA binding
-
Ashley CT, Wilkinson KD, Reines D, Warren ST (1993): FMR-1 protein: conserved RNP family domains and selective RNA binding. Science 262:563-566.
-
(1993)
Science
, vol.262
, pp. 563-566
-
-
Ashley, C.T.1
Wilkinson, K.D.2
Reines, D.3
Warren, S.T.4
-
2
-
-
0028246435
-
Fmr1 knockout mice: A model to study fragile X mental retardation
-
Bakker CE, Verheij C, Willemsen R, van der Helm R, Oerlemans F, Vermey M, Bygrave A, Hoogeveen AT, Oostra BA, Reyniers E, De Boulle K, D'Hooge R, Cras P, van Velzen D, Nagels G, Martin J-J, De Deyn PP, Darby JK, Willems PJ (1994): Fmr1 knockout mice: A model to study fragile X mental retardation. Cell 78:23-33.
-
(1994)
Cell
, vol.78
, pp. 23-33
-
-
Bakker, C.E.1
Verheij, C.2
Willemsen, R.3
Van Der Helm, R.4
Oerlemans, F.5
Vermey, M.6
Bygrave, A.7
Hoogeveen, A.T.8
Oostra, B.A.9
Reyniers, E.10
De Boulle, K.11
D'Hooge, R.12
Cras, P.13
Van Velzen, D.14
Nagels, G.15
Martin, J.-J.16
De Deyn, P.P.17
Darby, J.K.18
Willems, P.J.19
-
3
-
-
0025744743
-
Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X families
-
Cianchetti C, Sannio-Fancello G, Fratta A-L, Manconi F, Orano A, Pischedda M-P, Pruna D, Spinicci G, Archidiacono N, Filippi G (1991): Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X families. Am J Med Genet 40:234-243.
-
(1991)
Am J Med Genet
, vol.40
, pp. 234-243
-
-
Cianchetti, C.1
Sannio-Fancello, G.2
Fratta, A.-L.3
Manconi, F.4
Orano, A.5
Pischedda, M.-P.6
Pruna, D.7
Spinicci, G.8
Archidiacono, N.9
Filippi, G.10
-
4
-
-
0027509234
-
A point mutation in the FMR1 gene associated with fragile X mental retardation
-
De Boulle K, Verkerk AJMH, Reyniers E, Vits L, Hendrickx J, van Roy B, van den Bos F, de Graaff E, Oostra BA, Willems PJ (1993): A point mutation in the FMR1 gene associated with fragile X mental retardation. Nat Genet 3:31-35.
-
(1993)
Nat Genet
, vol.3
, pp. 31-35
-
-
De Boulle, K.1
Verkerk, A.J.M.H.2
Reyniers, E.3
Vits, L.4
Hendrickx, J.5
Van Roy, B.6
Van Den Bos, F.7
De Graaff, E.8
Oostra, B.A.9
Willems, P.J.10
-
5
-
-
0029955188
-
Long-term potentiation in the hippocampus of fragile X knockout mice
-
Godfraind J-M, Reyniers E, De Boulle K, D'Hooge R, Bakker CE, Oostra BA, Kooy RF, Willems PJ (1996): Long-term potentiation in the hippocampus of fragile X knockout mice. Am J Med Genet 64: 246-251.
-
(1996)
Am J Med Genet
, vol.64
, pp. 246-251
-
-
Godfraind, J.-M.1
Reyniers, E.2
De Boulle, K.3
D'Hooge, R.4
Bakker, C.E.5
Oostra, B.A.6
Kooy, R.F.7
Willems, P.J.8
-
6
-
-
0001966753
-
Physical and behavioral phenotype
-
Hagerman RJ and Silverman AC (eds): Baltimore, MD: Johns Hopkins University Press
-
Hagerman RJ (1991): Physical and behavioral phenotype. In Hagerman RJ and Silverman AC (eds): "Fragile X Syndrome: Diagnosis, Treatment, and Research," Baltimore, MD: Johns Hopkins University Press, pp. 1-68.
-
(1991)
Fragile X Syndrome: Diagnosis, Treatment, and Research
, pp. 1-68
-
-
Hagerman, R.J.1
-
8
-
-
0021173996
-
Developments of a water-maze procedure for studying spatial learning in the rat
-
Morris R (1984): Developments of a water-maze procedure for studying spatial learning in the rat. J Neurosci Methods 11:47-60.
-
(1984)
J Neurosci Methods
, vol.11
, pp. 47-60
-
-
Morris, R.1
-
9
-
-
0005535917
-
Spatial localization does not require the presence of local cues
-
Morris RGM (1981): Spatial localization does not require the presence of local cues. Learn Motiv 12:239-260.
-
(1981)
Learn Motiv
, vol.12
, pp. 239-260
-
-
Morris, R.G.M.1
-
11
-
-
0025833298
-
Absence of expression of the FMR-1 gene in fragile X syndrome
-
Pieretti M, Zhang F, Fu Y-H, Warren ST, Oostra BA, Caskey CT, Nelson DL (1991): Absence of expression of the FMR-1 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
-
12
-
-
0027327486
-
The protein product of the fragile X gene, FMR1, has characteristics of an RNA binding protein
-
Siomi H, Siomi MC, Nussbaum RL, 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
-
13
-
-
0029069223
-
FXR1, an autosomal homolog of the fragile X mental retardation gene
-
Siomi MC, Siomi H, Sauer WH, Srinivasan S, Nussbaum RL, 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
-
14
-
-
0026847039
-
Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans
-
Squire LR (1992): Memory and the hippocampus: A synthesis from findings with rats, monkeys, and humans. Psychol Rev 99:195-231.
-
(1992)
Psychol Rev
, vol.99
, pp. 195-231
-
-
Squire, L.R.1
-
15
-
-
0027236971
-
Characterization and localization of the FMR-1 gene product associated with fragile X syndrome
-
Verheij C, Bakker CE, de Graaff E, Keulemans J, Willemsen R, Verkerk AJMH, Galjaard H, Reuser AJJ, Hoogeveen AT, Oostra BA (1993): Characterization and localization of the FMR-1 gene product associated with fragile X syndrome. Nature 363:722-724.
-
(1993)
Nature
, vol.363
, pp. 722-724
-
-
Verheij, C.1
Bakker, C.E.2
De Graaff, E.3
Keulemans, J.4
Willemsen, R.5
Verkerk, A.J.M.H.6
Galjaard, H.7
Reuser, A.J.J.8
Hoogeveen, A.T.9
Oostra, B.A.10
-
16
-
-
0029063222
-
Characterization of FMR1 proteins isolated from different tissues
-
Verheij C, de Graaff E, Bakker CE, Willemsen R, Willems PJ, Meijer N, Galjaard H, Reuser AJJ, Oostra BA, Hoogeveen AT (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
-
17
-
-
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 AJMH, Pieretti M, Sutcliffe JS, Fu Y-H, Kuhl DPA, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang F, Eussen BE, van Ommen G-JB, Blonden LAJ, Riggins GJ, Chastain JL, Kunst CB, Galjaard H, Caskey CT, Nelson DL, Oostra BA, Warren ST (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..
-
18
-
-
0027996828
-
Dynamic mutations hit double figures
-
Willems PJ (1994): Dynamic mutations hit double figures. Nat Genet 8:213-215.
-
(1994)
Nat Genet
, vol.8
, pp. 213-215
-
-
Willems, P.J.1
-
20
-
-
0028971722
-
The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2
-
Zhang Y, O'Connor JP, Siomi MC, Srinivasan S, Dutra A, Nussbaum RL, Dreyfuss G (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, G.7
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