-
1
-
-
0035675794
-
The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders
-
Rogers S.J., Wehner D.E., Hagerman R. The behavioral phenotype in fragile X: symptoms of autism in very young children with fragile X syndrome, idiopathic autism, and other developmental disorders. J Dev Behav Pediatr 2001, 22:409-417.
-
(2001)
J Dev Behav Pediatr
, vol.22
, pp. 409-417
-
-
Rogers, S.J.1
Wehner, D.E.2
Hagerman, R.3
-
2
-
-
0028989063
-
Translational suppression by trinucleotide repeat expansion at FMR1
-
Feng Y., Zhang F., Lokey L.K., Chastain J.L., Lakkis L., Eberhart D., et al. Translational suppression by trinucleotide repeat expansion at FMR1. Science 1995, 268:731-734.
-
(1995)
Science
, vol.268
, pp. 731-734
-
-
Feng, Y.1
Zhang, F.2
Lokey, L.K.3
Chastain, J.L.4
Lakkis, L.5
Eberhart, D.6
-
3
-
-
84876449659
-
The unstable repeats - three evolving faces of neurological disease
-
Nelson D.L., Orr H.T., Warren S.T. The unstable repeats - three evolving faces of neurological disease. Neuron 2013, 77:825-843.
-
(2013)
Neuron
, vol.77
, pp. 825-843
-
-
Nelson, D.L.1
Orr, H.T.2
Warren, S.T.3
-
4
-
-
78650693402
-
Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome
-
Todd P.K., Oh S.Y., Krans A., Pandey U.B., Di Prospero N.A., Min K.T., et al. Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome. PLoS Genet 2010, 6:e1001240.
-
(2010)
PLoS Genet
, vol.6
-
-
Todd, P.K.1
Oh, S.Y.2
Krans, A.3
Pandey, U.B.4
Di Prospero, N.A.5
Min, K.T.6
-
5
-
-
33750283784
-
Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation
-
Farzin F., Perry H., Hessl D., Loesch D., Cohen J., Bacalman S., et al. Autism spectrum disorders and attention-deficit/hyperactivity disorder in boys with the fragile X premutation. J Dev Behav Pediatr 2006, 27:S137-S144.
-
(2006)
J Dev Behav Pediatr
, vol.27
-
-
Farzin, F.1
Perry, H.2
Hessl, D.3
Loesch, D.4
Cohen, J.5
Bacalman, S.6
-
6
-
-
84874535035
-
Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice
-
Iliff A.J., Renoux A.J., Krans A., Usdin K., Sutton M.A., Todd P.K. Impaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation mice. Hum Mol Genet 2013, 22:1180-1192.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 1180-1192
-
-
Iliff, A.J.1
Renoux, A.J.2
Krans, A.3
Usdin, K.4
Sutton, M.A.5
Todd, P.K.6
-
7
-
-
84897370853
-
CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size
-
Ludwig A.L., Espinal G.M., Pretto D., Jamal A.L., Arque G., Tassone F., et al. CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size. Hum Mol Genet 2014.
-
(2014)
Hum Mol Genet
-
-
Ludwig, A.L.1
Espinal, G.M.2
Pretto, D.3
Jamal, A.L.4
Arque, G.5
Tassone, F.6
-
8
-
-
84893788051
-
Reduced excitatory amino acid transporter 1 and metabotropic glutamate receptor 5 expression in the cerebellum of fragile X mental retardation gene 1 premutation carriers with fragile X-associated tremor/ataxia syndrome
-
Pretto D.I., Kumar M., Cao Z., Cunningham C.L., Durbin-Johnson B., Qi L., et al. Reduced excitatory amino acid transporter 1 and metabotropic glutamate receptor 5 expression in the cerebellum of fragile X mental retardation gene 1 premutation carriers with fragile X-associated tremor/ataxia syndrome. Neurobiol Aging 2014, 35:1189-1197.
-
(2014)
Neurobiol Aging
, vol.35
, pp. 1189-1197
-
-
Pretto, D.I.1
Kumar, M.2
Cao, Z.3
Cunningham, C.L.4
Durbin-Johnson, B.5
Qi, L.6
-
9
-
-
34147129139
-
Autism spectrum phenotype in males and females with fragile X full mutation and premutation
-
Clifford S., Dissanayake C., Bui Q.M., Huggins R., Taylor A.K., Loesch D.Z. Autism spectrum phenotype in males and females with fragile X full mutation and premutation. J Autism Dev Disord 2007, 37:738-747.
-
(2007)
J Autism Dev Disord
, vol.37
, pp. 738-747
-
-
Clifford, S.1
Dissanayake, C.2
Bui, Q.M.3
Huggins, R.4
Taylor, A.K.5
Loesch, D.Z.6
-
10
-
-
84864152357
-
Genetic models of sensorimotor gating: relevance to neuropsychiatric disorders
-
Powell S.B., Weber M., Geyer M.A. Genetic models of sensorimotor gating: relevance to neuropsychiatric disorders. Curr Top Behav Neurosci 2012, 12:251-318.
-
(2012)
Curr Top Behav Neurosci
, vol.12
, pp. 251-318
-
-
Powell, S.B.1
Weber, M.2
Geyer, M.A.3
-
11
-
-
66649136789
-
Prepulse inhibition in fragile X syndrome: feasibility, reliability, and implications for treatment
-
Hessl D., Berry-Kravis E., Cordeiro L., Yuhas J., Ornitz E.M., Campbell A., et al. Prepulse inhibition in fragile X syndrome: feasibility, reliability, and implications for treatment. Am J Med Genet B: Neuropsychiatr Genet 2009, 150B:545-553.
-
(2009)
Am J Med Genet B: Neuropsychiatr Genet
, vol.150 B
, pp. 545-553
-
-
Hessl, D.1
Berry-Kravis, E.2
Cordeiro, L.3
Yuhas, J.4
Ornitz, E.M.5
Campbell, A.6
-
12
-
-
44949125523
-
Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice
-
de Vrij F.M., Levenga J., van der Linde H.C., Koekkoek S.K., De Zeeuw C.I., Nelson D.L., et al. Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice. Neurobiol Dis 2008, 31:127-132.
-
(2008)
Neurobiol Dis
, vol.31
, pp. 127-132
-
-
de Vrij, F.M.1
Levenga, J.2
van der Linde, H.C.3
Koekkoek, S.K.4
De Zeeuw, C.I.5
Nelson, D.L.6
-
13
-
-
57049188895
-
Reversal of sensorimotor gating abnormalities in Fmr1 knockout mice carrying a human Fmr1 transgene
-
Paylor R., Yuva-Paylor L.A., Nelson D.L., Spencer C.M. Reversal of sensorimotor gating abnormalities in Fmr1 knockout mice carrying a human Fmr1 transgene. Behav Neurosci 2008, 122:1371-1377.
-
(2008)
Behav Neurosci
, vol.122
, pp. 1371-1377
-
-
Paylor, R.1
Yuva-Paylor, L.A.2
Nelson, D.L.3
Spencer, C.M.4
-
14
-
-
83655164085
-
Genetic reduction of muscarinic M4 receptor modulates analgesic response and acoustic startle response in a mouse model of fragile X syndrome (FXS)
-
Veeraragavan S., Graham D., Bui N., Yuva-Paylor L.A., Wess J., Paylor R. Genetic reduction of muscarinic M4 receptor modulates analgesic response and acoustic startle response in a mouse model of fragile X syndrome (FXS). Behav Brain Res 2012, 228:1-8.
-
(2012)
Behav Brain Res
, vol.228
, pp. 1-8
-
-
Veeraragavan, S.1
Graham, D.2
Bui, N.3
Yuva-Paylor, L.A.4
Wess, J.5
Paylor, R.6
-
15
-
-
77955139512
-
Male and female Fmr1 knockout mice on C57 albino background exhibit spatial learning and memory impairments
-
Baker K.B., Wray S.P., Ritter R., Mason S., Lanthorn T.H., Savelieva K.V. Male and female Fmr1 knockout mice on C57 albino background exhibit spatial learning and memory impairments. Genes Brain Behav 2010, 9:562-574.
-
(2010)
Genes Brain Behav
, vol.9
, pp. 562-574
-
-
Baker, K.B.1
Wray, S.P.2
Ritter, R.3
Mason, S.4
Lanthorn, T.H.5
Savelieva, K.V.6
-
16
-
-
0035804765
-
Fragile X mice develop sensory hyperreactivity to auditory stimuli
-
Chen L., Toth M. Fragile X mice develop sensory hyperreactivity to auditory stimuli. Neuroscience 2001, 103:1043-1050.
-
(2001)
Neuroscience
, vol.103
, pp. 1043-1050
-
-
Chen, L.1
Toth, M.2
-
17
-
-
2042473496
-
Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice
-
Frankland P.W., Wang Y., Rosner B., Shimizu T., Balleine B.W., Dykens E.M., et al. Sensorimotor gating abnormalities in young males with fragile X syndrome and Fmr1-knockout mice. Mol Psychiatry 2004, 9:417-425.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 417-425
-
-
Frankland, P.W.1
Wang, Y.2
Rosner, B.3
Shimizu, T.4
Balleine, B.W.5
Dykens, E.M.6
-
18
-
-
0037039527
-
Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndrome
-
Nielsen D.M., Derber W.J., McClellan D.A., Crnic L.S. Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndrome. Brain Res 2002, 927:8-17.
-
(2002)
Brain Res
, vol.927
, pp. 8-17
-
-
Nielsen, D.M.1
Derber, W.J.2
McClellan, D.A.3
Crnic, L.S.4
-
19
-
-
84859499358
-
Prepulse inhibition in patients with fragile X-associated tremor ataxia syndrome
-
Schneider A., Ballinger E., Chavez A., Tassone F., Hagerman R.J., Hessl D. Prepulse inhibition in patients with fragile X-associated tremor ataxia syndrome. Neurobiol Aging 2012, 33:1045-1053.
-
(2012)
Neurobiol Aging
, vol.33
, pp. 1045-1053
-
-
Schneider, A.1
Ballinger, E.2
Chavez, A.3
Tassone, F.4
Hagerman, R.J.5
Hessl, D.6
-
20
-
-
0028246435
-
Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium
-
Fmr1 knockout mice: a model to study fragile X mental retardation. The Dutch-Belgian Fragile X Consortium. Cell 1994, 78:23-33.
-
(1994)
Cell
, vol.78
, pp. 23-33
-
-
-
21
-
-
16644365348
-
Response properties of single auditory nerve fibers in the mouse
-
Taberner A.M., Liberman M.C. Response properties of single auditory nerve fibers in the mouse. J Neurophysiol 2005, 93:557-569.
-
(2005)
J Neurophysiol
, vol.93
, pp. 557-569
-
-
Taberner, A.M.1
Liberman, M.C.2
-
22
-
-
34848830061
-
Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice
-
Karolyi I.J., Dootz G.A., Halsey K., Beyer L., Probst F.J., Johnson K.R., et al. Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice. Mamm Genome 2007, 18:596-608.
-
(2007)
Mamm Genome
, vol.18
, pp. 596-608
-
-
Karolyi, I.J.1
Dootz, G.A.2
Halsey, K.3
Beyer, L.4
Probst, F.J.5
Johnson, K.R.6
-
23
-
-
0031469713
-
A major gene affecting age-related hearing loss in C57BL/6J mice
-
Johnson K.R., Erway L.C., Cook S.A., Willott J.F., Zheng Q.Y. A major gene affecting age-related hearing loss in C57BL/6J mice. Hear Res 1997, 114:83-92.
-
(1997)
Hear Res
, vol.114
, pp. 83-92
-
-
Johnson, K.R.1
Erway, L.C.2
Cook, S.A.3
Willott, J.F.4
Zheng, Q.Y.5
-
25
-
-
35848931692
-
Age-related hearing loss in C57BL/6J mice has both frequency-specific and non-frequency-specific components that produce a hyperacusis-like exaggeration of the acoustic startle reflex
-
Ison J.R., Allen P.D., O'Neill W.E. Age-related hearing loss in C57BL/6J mice has both frequency-specific and non-frequency-specific components that produce a hyperacusis-like exaggeration of the acoustic startle reflex. J Assoc Res Otolaryngol 2007, 8:539-550.
-
(2007)
J Assoc Res Otolaryngol
, vol.8
, pp. 539-550
-
-
Ison, J.R.1
Allen, P.D.2
O'Neill, W.E.3
-
26
-
-
79751535827
-
A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis
-
Qin M., Entezam A., Usdin K., Huang T., Liu Z.H., Hoffman G.E., et al. A mouse model of the fragile X premutation: effects on behavior, dendrite morphology, and regional rates of cerebral protein synthesis. Neurobiol Dis 2011, 42:85-98.
-
(2011)
Neurobiol Dis
, vol.42
, pp. 85-98
-
-
Qin, M.1
Entezam, A.2
Usdin, K.3
Huang, T.4
Liu, Z.H.5
Hoffman, G.E.6
-
27
-
-
0028108218
-
Prepulse inhibition of the startle response in mice: relationship to hearing loss and auditory system plasticity
-
Willott J.F., Carlson S., Chen H. Prepulse inhibition of the startle response in mice: relationship to hearing loss and auditory system plasticity. Behav Neurosci 1994, 108:703-713.
-
(1994)
Behav Neurosci
, vol.108
, pp. 703-713
-
-
Willott, J.F.1
Carlson, S.2
Chen, H.3
-
28
-
-
0037188502
-
Altered synaptic plasticity in a mouse model of fragile X mental retardation
-
Huber K.M., Gallagher S.M., Warren S.T., Bear M.F. Altered synaptic plasticity in a mouse model of fragile X mental retardation. Proc Natl Acad Sci U S A 2002, 99:7746-7750.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 7746-7750
-
-
Huber, K.M.1
Gallagher, S.M.2
Warren, S.T.3
Bear, M.F.4
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