-
1
-
-
0027509234
-
A point mutation in the FMR-1 gene associated with fragile X mental retardation
-
PID: 849
-
De Boulle K, Verkerk AJ, 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 FMR-1 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.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
-
2
-
-
0037188502
-
Altered synaptic plasticity in a mouse model of fragile X mental retardation
-
COI: 1:CAS:528:DC%2BD38XktlCrsLs%3D, PID: 1203
-
Huber KM, Gallagher SM, Warren ST, Bear MF (2002) Altered synaptic plasticity in a mouse model of fragile X mental retardation. Proc Natl Acad Sci U S A 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
-
3
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
COI: 1:CAS:528:DyaK38Xht1ahur4%3D, PID: 171
-
Verkerk AJ, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang FP et al (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.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.H.4
Kuhl, D.P.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.P.10
-
4
-
-
27644483475
-
Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation
-
COI: 1:CAS:528:DC%2BD2sXms1yju7c%3D, PID: 1618
-
Hessl D, Tassone F, Loesch DZ, Berry-Kravis E, Leehey MA, Gane LW, Barbato I, Rice C, Gould E, Hall DA et al (2005) Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation. Am J Med Genet B Neuropsychiatr Genet 139B:115–121
-
(2005)
Am J Med Genet B Neuropsychiatr Genet
, vol.139B
, pp. 115-121
-
-
Hessl, D.1
Tassone, F.2
Loesch, D.Z.3
Berry-Kravis, E.4
Leehey, M.A.5
Gane, L.W.6
Barbato, I.7
Rice, C.8
Gould, E.9
Hall, D.A.10
-
5
-
-
33845323746
-
Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1
-
COI: 1:CAS:528:DC%2BD2sXpslWmuw%3D%3D, PID: 1716
-
Jacquemont S, Hagerman RJ, Hagerman PJ, Leehey MA (2007) Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1. Lancet Neurol 6:45–55
-
(2007)
Lancet Neurol
, vol.6
, pp. 45-55
-
-
Jacquemont, S.1
Hagerman, R.J.2
Hagerman, P.J.3
Leehey, M.A.4
-
6
-
-
0035321892
-
Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome
-
PID: 1145
-
Bailey DB Jr, Hatton DD, Skinner M, Mesibov G (2001) Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome. J Autism Dev Disord 31:165–174
-
(2001)
J Autism Dev Disord
, vol.31
, pp. 165-174
-
-
Bailey, D.B.1
Hatton, D.D.2
Skinner, M.3
Mesibov, G.4
-
7
-
-
0036301947
-
A decade of molecular studies of fragile X syndrome
-
PID: 1205
-
O'Donnell WT, Warren ST (2002) A decade of molecular studies of fragile X syndrome. Annu Rev Neurosci 25:315–338
-
(2002)
Annu Rev Neurosci
, vol.25
, pp. 315-338
-
-
O'Donnell, W.T.1
Warren, S.T.2
-
8
-
-
0025800165
-
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
-
COI: 1:CAS:528:DyaK3MXltVOmsLc%3D, PID: 167
-
Kremer EJ, Pritchard M, Lynch M, Yu S, Holman K, Baker E, Warren ST, Schlessinger D, Sutherland GR, Richards RI (1991) Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)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
-
9
-
-
0028989063
-
Translational suppression by trinucleotide repeat expansion at FMR1
-
COI: 1:CAS:528:DyaK2MXlsVGitrk%3D, PID: 773
-
Feng Y, Zhang F, Lokey LK, Chastain JL, Lakkis L, Eberhart D, Warren ST (1995) Translational suppression by trinucleotide repeat expansion at FMR1. Science 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
Warren, S.T.7
-
10
-
-
0028979139
-
Two new cases of FMR1 deletion associated with mental impairment
-
COI: 1:CAS:528:DyaK2MXktlWrsbc%3D, PID: 782
-
Hirst M, Grewal P, Flannery A, Slatter R, Maher E, Barton D, Fryns JP, Davies K (1995) Two new cases of FMR1 deletion associated with mental impairment. Am J Hum Genet 56:67–74
-
(1995)
Am J Hum Genet
, vol.56
, pp. 67-74
-
-
Hirst, M.1
Grewal, P.2
Flannery, A.3
Slatter, R.4
Maher, E.5
Barton, D.6
Fryns, J.P.7
Davies, K.8
-
11
-
-
0028239232
-
Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region
-
COI: 1:STN:280:DyaK2M%2FivFGntA%3D%3D, PID: 794
-
Trottier Y, Imbert G, Poustka A, Fryns JP, Mandel JL (1994) Male with typical fragile X phenotype is deleted for part of the FMR1 gene and for about 100 kb of upstream region. Am J Med Genet 51:454–457
-
(1994)
Am J Med Genet
, vol.51
, pp. 454-457
-
-
Trottier, Y.1
Imbert, G.2
Poustka, A.3
Fryns, J.P.4
Mandel, J.L.5
-
12
-
-
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
-
COI: 1:CAS:528:DyaK2cXktVemsrs%3D, PID: 815
-
Siomi H, Choi M, Siomi MC, Nussbaum RL, 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
-
13
-
-
0035464960
-
Monogenic causes of X-linked mental retardation
-
COI: 1:CAS:528:DC%2BD3MXmvV2hurg%3D, PID: 1153
-
Chelly J, Mandel JL (2001) Monogenic causes of X-linked mental retardation. Nat Rev Genet 2:669–680
-
(2001)
Nat Rev Genet
, vol.2
, pp. 669-680
-
-
Chelly, J.1
Mandel, J.L.2
-
14
-
-
74249093220
-
A mouse model of the human fragile X syndrome I304N mutation
-
PID: 2001
-
Zang JB, Nosyreva ED, Spencer CM, Volk LJ, Musunuru K, Zhong R, Stone EF, Yuva-Paylor LA, Huber KM, Paylor R et al (2009) A mouse model of the human fragile X syndrome I304N mutation. PLoS Genet 5:e1000758
-
(2009)
PLoS Genet
, vol.5
, pp. 1000758
-
-
Zang, J.B.1
Nosyreva, E.D.2
Spencer, C.M.3
Volk, L.J.4
Musunuru, K.5
Zhong, R.6
Stone, E.F.7
Yuva-Paylor, L.A.8
Huber, K.M.9
Paylor, R.10
-
15
-
-
23944511133
-
Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons
-
COI: 1:CAS:528:DC%2BD2MXhtVemt73L, PID: 1609
-
Antar LN, Dictenberg JB, Plociniak M, Afroz R, Bassell GJ (2005) Localization of FMRP-associated mRNA granules and requirement of microtubules for activity-dependent trafficking in hippocampal neurons. Genes Brain Behav 4:350–359
-
(2005)
Genes Brain Behav
, vol.4
, pp. 350-359
-
-
Antar, L.N.1
Dictenberg, J.B.2
Plociniak, M.3
Afroz, R.4
Bassell, G.J.5
-
16
-
-
84886953546
-
The translation of translational control by FMRP: therapeutic targets for FXS
-
COI: 1:CAS:528:DC%2BC3sXlsl2htLY%3D, PID: 2358
-
Darnell JC, Klann E (2013) The translation of translational control by FMRP: therapeutic targets for FXS. Nat Neurosci 16:1530–1536
-
(2013)
Nat Neurosci
, vol.16
, pp. 1530-1536
-
-
Darnell, J.C.1
Klann, E.2
-
17
-
-
79960779323
-
FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism
-
COI: 1:CAS:528:DC%2BC3MXptleksbo%3D, PID: 2178
-
Darnell JC, Van Driesche SJ, Zhang C, Hung KY, Mele A, Fraser CE, Stone EF, Chen C, Fak JJ, Chi SW et al (2011) FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism. Cell 146:247–261
-
(2011)
Cell
, vol.146
, pp. 247-261
-
-
Darnell, J.C.1
Van Driesche, S.J.2
Zhang, C.3
Hung, K.Y.4
Mele, A.5
Fraser, C.E.6
Stone, E.F.7
Chen, C.8
Fak, J.J.9
Chi, S.W.10
-
18
-
-
76649121578
-
Fragile X mental retardation protein in learning-related synaptic plasticity
-
COI: 1:CAS:528:DC%2BC3cXisV2nsg%3D%3D, PID: 2004
-
Mercaldo V, Descalzi G, Zhuo M (2009) Fragile X mental retardation protein in learning-related synaptic plasticity. Mol Cells 28:501–507
-
(2009)
Mol Cells
, vol.28
, pp. 501-507
-
-
Mercaldo, V.1
Descalzi, G.2
Zhuo, M.3
-
19
-
-
84875850679
-
Fragile X mental retardation protein and synaptic plasticity
-
COI: 1:CAS:528:DC%2BC3sXotFCntbk%3D, PID: 2356
-
Sidorov MS, Auerbach BD, Bear MF (2013) Fragile X mental retardation protein and synaptic plasticity. Mol Brain 6:15
-
(2013)
Mol Brain
, vol.6
, pp. 15
-
-
Sidorov, M.S.1
Auerbach, B.D.2
Bear, M.F.3
-
20
-
-
0027377580
-
FMR1 protein: conserved RNP family domains and selective RNA binding
-
COI: 1:CAS:528:DyaK3sXms1Cqtr0%3D, PID: 769
-
Ashley CT Jr, Wilkinson KD, Reines D, Warren ST (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.1
Wilkinson, K.D.2
Reines, D.3
Warren, S.T.4
-
21
-
-
77952539696
-
Arginines of the RGG box regulate FMRP association with polyribosomes and mRNA
-
COI: 1:CAS:528:DC%2BC3cXjs1Gksrk%3D, PID: 2006
-
Blackwell E, Zhang X, Ceman S (2010) Arginines of the RGG box regulate FMRP association with polyribosomes and mRNA. Hum Mol Genet 19:1314–1323
-
(2010)
Hum Mol Genet
, vol.19
, pp. 1314-1323
-
-
Blackwell, E.1
Zhang, X.2
Ceman, S.3
-
22
-
-
0029816723
-
The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals
-
COI: 1:CAS:528:DyaK28XkslSrtbs%3D, PID: 884
-
Eberhart DE, Malter HE, Feng Y, Warren ST (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
-
23
-
-
0031046778
-
Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes
-
COI: 1:CAS:528:DyaK2sXhtlOmsrw%3D, PID: 903
-
Feng Y, Gutekunst CA, Eberhart DE, Yi H, Warren ST, Hersch SM (1997) Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes. J Neurosci 17:1539–1547
-
(1997)
J Neurosci
, vol.17
, pp. 1539-1547
-
-
Feng, Y.1
Gutekunst, C.A.2
Eberhart, D.E.3
Yi, H.4
Warren, S.T.5
Hersch, S.M.6
-
24
-
-
0027236971
-
Characterization and localization of the FMR-1 gene product associated with fragile X syndrome
-
COI: 1:CAS:528:DyaK3sXltFCrurs%3D, PID: 851
-
Verheij C, Bakker CE, de Graaff E, Keulemans J, Willemsen R, Verkerk AJ, Galjaard H, Reuser AJ, 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.6
Galjaard, H.7
Reuser, A.J.8
Hoogeveen, A.T.9
Oostra, B.A.10
-
25
-
-
23044512658
-
Two members of the Fxr gene family, Fmr1 and Fxr1, are differentially expressed in Xenopus tropicalis
-
COI: 1:CAS:528:DC%2BD2MXpsFeksb8%3D, PID: 1596
-
Blonden L, van’t Padje S, Severijnen LA, Destree O, Oostra BA, Willemsen R (2005) Two members of the Fxr gene family, Fmr1 and Fxr1, are differentially expressed in Xenopus tropicalis. Int J Dev Biol 49:437–441
-
(2005)
Int J Dev Biol
, vol.49
, pp. 437-441
-
-
Blonden, L.1
van’t Padje, S.2
Severijnen, L.A.3
Destree, O.4
Oostra, B.A.5
Willemsen, R.6
-
26
-
-
33749064907
-
Identification of messenger RNAs and microRNAs associated with fragile X mental retardation protein
-
COI: 1:CAS:528:DC%2BD28XksFSntLs%3D, PID: 1695
-
Duan R, Jin P (2006) Identification of messenger RNAs and microRNAs associated with fragile X mental retardation protein. Methods Mol Biol 342:267–276
-
(2006)
Methods Mol Biol
, vol.342
, pp. 267-276
-
-
Duan, R.1
Jin, P.2
-
27
-
-
1642540373
-
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway
-
COI: 1:CAS:528:DC%2BD2cXmvVGmtA%3D%3D, PID: 1470
-
Jin P, Zarnescu DC, Ceman S, Nakamoto M, Mowrey J, Jongens TA, Nelson DL, Moses K, Warren ST (2004) Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. Nat Neurosci 7:113–117
-
(2004)
Nat Neurosci
, vol.7
, pp. 113-117
-
-
Jin, P.1
Zarnescu, D.C.2
Ceman, S.3
Nakamoto, M.4
Mowrey, J.5
Jongens, T.A.6
Nelson, D.L.7
Moses, K.8
Warren, S.T.9
-
28
-
-
75949101467
-
Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132
-
COI: 1:CAS:528:DC%2BC3cXlt1Kmt70%3D, PID: 2015
-
Edbauer D, Neilson JR, Foster KA, Wang CF, Seeburg DP, Batterton MN, Tada T, Dolan BM, Sharp PA, Sheng M (2010) Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132. Neuron 65:373–384
-
(2010)
Neuron
, vol.65
, pp. 373-384
-
-
Edbauer, D.1
Neilson, J.R.2
Foster, K.A.3
Wang, C.F.4
Seeburg, D.P.5
Batterton, M.N.6
Tada, T.7
Dolan, B.M.8
Sharp, P.A.9
Sheng, M.10
-
29
-
-
44949231424
-
Analyzing real-time PCR data by the comparative C(T) method
-
COI: 1:CAS:528:DC%2BD1cXmvVemt7c%3D, PID: 1854
-
Schmittgen TD, Livak KJ (2008) Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc 3:1101–1108
-
(2008)
Nat Protoc
, vol.3
, pp. 1101-1108
-
-
Schmittgen, T.D.1
Livak, K.J.2
-
30
-
-
77953312769
-
Joint genome-wide profiling of miRNA and mRNA expression in Alzheimer's disease cortex reveals altered miRNA regulation
-
PID: 2012
-
Nunez-Iglesias J, Liu CC, Morgan TE, Finch CE, Zhou XJ (2010) Joint genome-wide profiling of miRNA and mRNA expression in Alzheimer's disease cortex reveals altered miRNA regulation. PLoS One 5:e8898
-
(2010)
PLoS One
, vol.5
, pp. 8898
-
-
Nunez-Iglesias, J.1
Liu, C.C.2
Morgan, T.E.3
Finch, C.E.4
Zhou, X.J.5
-
31
-
-
22244467087
-
MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells
-
COI: 1:CAS:528:DC%2BD2MXmt1eht7c%3D, PID: 1602
-
Chan JA, Krichevsky AM, Kosik KS (2005) MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells. Cancer Res 65:6029–6033
-
(2005)
Cancer Res
, vol.65
, pp. 6029-6033
-
-
Chan, J.A.1
Krichevsky, A.M.2
Kosik, K.S.3
-
32
-
-
84861572492
-
Prognostic value of a microRNA signature in nasopharyngeal carcinoma: a microRNA expression analysis
-
COI: 1:CAS:528:DC%2BC38XnvFOntbY%3D, PID: 2256
-
Liu N, Chen NY, Cui RX, Li WF, Li Y, Wei RR, Zhang MY, Sun Y, Huang BJ, Chen M et al (2012) Prognostic value of a microRNA signature in nasopharyngeal carcinoma: a microRNA expression analysis. Lancet Oncol 13:633–641
-
(2012)
Lancet Oncol
, vol.13
, pp. 633-641
-
-
Liu, N.1
Chen, N.Y.2
Cui, R.X.3
Li, W.F.4
Li, Y.5
Wei, R.R.6
Zhang, M.Y.7
Sun, Y.8
Huang, B.J.9
Chen, M.10
-
33
-
-
2342642197
-
A high-throughput method to monitor the expression of microRNA precursors
-
PID: 1498
-
Schmittgen TD, Jiang J, Liu Q, Yang L (2004) A high-throughput method to monitor the expression of microRNA precursors. Nucleic Acids Res 32:e43
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 43
-
-
Schmittgen, T.D.1
Jiang, J.2
Liu, Q.3
Yang, L.4
-
34
-
-
0346094457
-
Prediction of mammalian microRNA targets
-
COI: 1:CAS:528:DC%2BD2cXhsFCnsw%3D%3D, PID: 1469
-
Lewis BP, Shih IH, Jones-Rhoades MW, Bartel DP, Burge CB (2003) Prediction of mammalian microRNA targets. Cell 115:787–798
-
(2003)
Cell
, vol.115
, pp. 787-798
-
-
Lewis, B.P.1
Shih, I.H.2
Jones-Rhoades, M.W.3
Bartel, D.P.4
Burge, C.B.5
-
35
-
-
14044251458
-
Human microRNA targets
-
PID: 1550
-
John B, Enright AJ, Aravin A, Tuschl T, Sander C, Marks DS (2004) Human microRNA targets. PLoS Biol 2:e363
-
(2004)
PLoS Biol
, vol.2
, pp. 363
-
-
John, B.1
Enright, A.J.2
Aravin, A.3
Tuschl, T.4
Sander, C.5
Marks, D.S.6
-
36
-
-
20944450160
-
Combinatorial microRNA target predictions
-
COI: 1:CAS:528:DC%2BD2MXjsF2ksrw%3D, PID: 1580
-
Krek A, Grun D, Poy MN, Wolf R, Rosenberg L, Epstein EJ, MacMenamin P, da Piedade I, Gunsalus KC, Stoffel M et al (2005) Combinatorial microRNA target predictions. Nat Genet 37:495–500
-
(2005)
Nat Genet
, vol.37
, pp. 495-500
-
-
Krek, A.1
Grun, D.2
Poy, M.N.3
Wolf, R.4
Rosenberg, L.5
Epstein, E.J.6
MacMenamin, P.7
da Piedade, I.8
Gunsalus, K.C.9
Stoffel, M.10
-
37
-
-
33846078622
-
The UCSC genome browser database: update 2007
-
COI: 1:CAS:528:DC%2BD2sXivFKgsg%3D%3D, PID: 1714
-
Kuhn RM, Karolchik D, Zweig AS, Trumbower H, Thomas DJ, Thakkapallayil A, Sugnet CW, Stanke M, Smith KE, Siepel A et al (2007) The UCSC genome browser database: update 2007. Nucleic Acids Res 35:D668–D673
-
(2007)
Nucleic Acids Res
, vol.35
, pp. 668-673
-
-
Kuhn, R.M.1
Karolchik, D.2
Zweig, A.S.3
Trumbower, H.4
Thomas, D.J.5
Thakkapallayil, A.6
Sugnet, C.W.7
Stanke, M.8
Smith, K.E.9
Siepel, A.10
-
38
-
-
34547840224
-
Information theory applied to the sparse gene ontology annotation network to predict novel gene function
-
COI: 1:CAS:528:DC%2BD2sXos1yrsLc%3D, PID: 1764
-
Tao Y, Sam L, Li J, Friedman C, Lussier YA (2007) Information theory applied to the sparse gene ontology annotation network to predict novel gene function. Bioinformatics 23:i529–i538
-
(2007)
Bioinformatics
, vol.23
, pp. 529-538
-
-
Tao, Y.1
Sam, L.2
Li, J.3
Friedman, C.4
Lussier, Y.A.5
-
39
-
-
6344276563
-
The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development
-
COI: 1:CAS:528:DC%2BD2cXpsVSgtL8%3D, PID: 1547
-
Lu R, Wang H, Liang Z, Ku L, O'Donnell WT, Li W, Warren ST, Feng Y (2004) The fragile X protein controls microtubule-associated protein 1B translation and microtubule stability in brain neuron development. Proc Natl Acad Sci U S A 101:15201–15206
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 15201-15206
-
-
Lu, R.1
Wang, H.2
Liang, Z.3
Ku, L.4
O'Donnell, W.T.5
Li, W.6
Warren, S.T.7
Feng, Y.8
-
40
-
-
3042735950
-
Defective neuronal development in the mushroom bodies of Drosophila fragile X mental retardation 1 mutants
-
PID: 1521
-
Michel CI, Kraft R, Restifo LL (2004) Defective neuronal development in the mushroom bodies of Drosophila fragile X mental retardation 1 mutants. J Neurosci 24:5798–5809
-
(2004)
J Neurosci
, vol.24
, pp. 5798-5809
-
-
Michel, C.I.1
Kraft, R.2
Restifo, L.L.3
-
41
-
-
0027257348
-
On the role of the hippocampus in learning and memory in the rat
-
COI: 1:STN:280:DyaK2c%2FivFymtg%3D%3D, PID: 821
-
Jarrard LE (1993) On the role of the hippocampus in learning and memory in the rat. Behav Neural Biol 60:9–26
-
(1993)
Behav Neural Biol
, vol.60
, pp. 9-26
-
-
Jarrard, L.E.1
-
42
-
-
0022500985
-
The neurobiology of learning and memory
-
COI: 1:STN:280:DyaL283ovFCgtw%3D%3D, PID: 373
-
Thompson RF (1986) The neurobiology of learning and memory. Science 233:941–947
-
(1986)
Science
, vol.233
, pp. 941-947
-
-
Thompson, R.F.1
-
43
-
-
79955682738
-
Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning
-
COI: 1:CAS:528:DC%2BC3MXltFyqtrg%3D, PID: 2151
-
Guo W, Allan AM, Zong R, Zhang L, Johnson EB, Schaller EG, Murthy AC, Goggin SL, Eisch AJ, Oostra BA et al (2011) Ablation of Fmrp in adult neural stem cells disrupts hippocampus-dependent learning. Nat Med 17:559–565
-
(2011)
Nat Med
, vol.17
, pp. 559-565
-
-
Guo, W.1
Allan, A.M.2
Zong, R.3
Zhang, L.4
Johnson, E.B.5
Schaller, E.G.6
Murthy, A.C.7
Goggin, S.L.8
Eisch, A.J.9
Oostra, B.A.10
-
44
-
-
0033802736
-
FMRP involvement in formation of synapses among cultured hippocampal neurons
-
COI: 1:STN:280:DC%2BD3M%2FgvV2lsA%3D%3D, PID: 1100
-
Braun K, Segal M (2000) FMRP involvement in formation of synapses among cultured hippocampal neurons. Cereb Cortex 10:1045–1052
-
(2000)
Cereb Cortex
, vol.10
, pp. 1045-1052
-
-
Braun, K.1
Segal, M.2
-
45
-
-
0025734533
-
At what age is the developing cerebral cortex of the rat comparable to that of the full-term newborn human baby?
-
COI: 1:STN:280:DyaK38%2Fgslelsw%3D%3D, PID: 191
-
Romijn HJ, Hofman MA, Gramsbergen A (1991) At what age is the developing cerebral cortex of the rat comparable to that of the full-term newborn human baby? Early Hum Dev 26:61–67
-
(1991)
Early Hum Dev
, vol.26
, pp. 61-67
-
-
Romijn, H.J.1
Hofman, M.A.2
Gramsbergen, A.3
-
46
-
-
62149089881
-
Minocycline promotes dendritic spine maturation and improves behavioural performance in the fragile X mouse model
-
COI: 1:CAS:528:DC%2BD1MXktVygsbc%3D, PID: 1883
-
Bilousova TV, Dansie L, Ngo M, Aye J, Charles JR, Ethell DW, Ethell IM (2009) Minocycline promotes dendritic spine maturation and improves behavioural performance in the fragile X mouse model. J Med Genet 46:94–102
-
(2009)
J Med Genet
, vol.46
, pp. 94-102
-
-
Bilousova, T.V.1
Dansie, L.2
Ngo, M.3
Aye, J.4
Charles, J.R.5
Ethell, D.W.6
Ethell, I.M.7
-
47
-
-
0029818460
-
A nuclear role for the fragile X mental retardation protein
-
COI: 1:CAS:528:DyaK28XmsVehsro%3D, PID: 889
-
Fridell RA, Benson RE, Hua J, Bogerd HP, Cullen BR (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
-
48
-
-
33746852731
-
Dicer-derived microRNAs are utilized by the fragile X mental retardation protein for assembly on target RNAs
-
PID: 1705
-
Plante I, Davidovic L, Ouellet DL, Gobeil LA, Tremblay S, Khandjian EW, Provost P (2006) Dicer-derived microRNAs are utilized by the fragile X mental retardation protein for assembly on target RNAs. J Biomed Biotechnol 2006:64347
-
(2006)
J Biomed Biotechnol
, vol.2006
, pp. 64347
-
-
Plante, I.1
Davidovic, L.2
Ouellet, D.L.3
Gobeil, L.A.4
Tremblay, S.5
Khandjian, E.W.6
Provost, P.7
-
49
-
-
60849094795
-
Phosphorylation of FMRP inhibits association with Dicer
-
COI: 1:CAS:528:DC%2BD1MXis1agsbo%3D, PID: 1915
-
Cheever A, Ceman S (2009) Phosphorylation of FMRP inhibits association with Dicer. RNA 15:362–366
-
(2009)
RNA
, vol.15
, pp. 362-366
-
-
Cheever, A.1
Ceman, S.2
-
50
-
-
59649103076
-
A distinct class of small RNAs arises from pre-miRNA-proximal regions in a simple chordate
-
COI: 1:CAS:528:DC%2BD1MXntFKjtg%3D%3D, PID: 1915
-
Shi W, Hendrix D, Levine M, Haley B (2009) A distinct class of small RNAs arises from pre-miRNA-proximal regions in a simple chordate. Nat Struct Mol Biol 16:183–189
-
(2009)
Nat Struct Mol Biol
, vol.16
, pp. 183-189
-
-
Shi, W.1
Hendrix, D.2
Levine, M.3
Haley, B.4
-
51
-
-
70849093653
-
A high-resolution structure of the pre-microRNA nuclear export machinery
-
COI: 1:CAS:528:DC%2BD1MXhsVKhtbfK, PID: 1996
-
Okada C, Yamashita E, Lee SJ, Shibata S, Katahira J, Nakagawa A, Yoneda Y, Tsukihara T (2009) A high-resolution structure of the pre-microRNA nuclear export machinery. Science 326:1275–1279
-
(2009)
Science
, vol.326
, pp. 1275-1279
-
-
Okada, C.1
Yamashita, E.2
Lee, S.J.3
Shibata, S.4
Katahira, J.5
Nakagawa, A.6
Yoneda, Y.7
Tsukihara, T.8
-
52
-
-
84871413198
-
FMRP targets distinct mRNA sequence elements to regulate protein expression
-
COI: 1:CAS:528:DC%2BC38XhvVajur7N, PID: 2323
-
Ascano M Jr, Mukherjee N, Bandaru P, Miller JB, Nusbaum JD, Corcoran DL, Langlois C, Munschauer M, Dewell S, Hafner M et al (2012) FMRP targets distinct mRNA sequence elements to regulate protein expression. Nature 492:382–386
-
(2012)
Nature
, vol.492
, pp. 382-386
-
-
Ascano, M.1
Mukherjee, N.2
Bandaru, P.3
Miller, J.B.4
Nusbaum, J.D.5
Corcoran, D.L.6
Langlois, C.7
Munschauer, M.8
Dewell, S.9
Hafner, M.10
-
53
-
-
18044379515
-
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome
-
COI: 1:CAS:528:DC%2BD3MXovVCnsL4%3D, PID: 1171
-
Brown V, Jin P, Ceman S, Darnell JC, O'Donnell WT, Tenenbaum SA, Jin X, Feng Y, Wilkinson KD, Keene JD et al (2001) Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome. Cell 107:477–487
-
(2001)
Cell
, vol.107
, pp. 477-487
-
-
Brown, V.1
Jin, P.2
Ceman, S.3
Darnell, J.C.4
O'Donnell, W.T.5
Tenenbaum, S.A.6
Jin, X.7
Feng, Y.8
Wilkinson, K.D.9
Keene, J.D.10
-
54
-
-
11844278458
-
Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets
-
COI: 1:CAS:528:DC%2BD2MXot1ChsA%3D%3D, PID: 1565
-
Lewis BP, Burge CB, Bartel DP (2005) Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell 120:15–20
-
(2005)
Cell
, vol.120
, pp. 15-20
-
-
Lewis, B.P.1
Burge, C.B.2
Bartel, D.P.3
-
55
-
-
57749110627
-
MicroRNAs impair MET-mediated invasive growth
-
COI: 1:CAS:528:DC%2BD1cXhsV2it7fP, PID: 1907
-
Migliore C, Petrelli A, Ghiso E, Corso S, Capparuccia L, Eramo A, Comoglio PM, Giordano S (2008) MicroRNAs impair MET-mediated invasive growth. Cancer Res 68:10128–10136
-
(2008)
Cancer Res
, vol.68
, pp. 10128-10136
-
-
Migliore, C.1
Petrelli, A.2
Ghiso, E.3
Corso, S.4
Capparuccia, L.5
Eramo, A.6
Comoglio, P.M.7
Giordano, S.8
-
56
-
-
64549151568
-
Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain
-
COI: 1:CAS:528:DC%2BD1MXktFGmtLs%3D, PID: 1922
-
Judson MC, Bergman MY, Campbell DB, Eagleson KL, Levitt P (2009) Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain. J Comp Neurol 513:511–531
-
(2009)
J Comp Neurol
, vol.513
, pp. 511-531
-
-
Judson, M.C.1
Bergman, M.Y.2
Campbell, D.B.3
Eagleson, K.L.4
Levitt, P.5
-
57
-
-
79851508020
-
Genetic disruption of Met signaling impairs GABAergic striatal development and cognition
-
COI: 1:CAS:528:DC%2BC3MXhvFKjs74%3D, PID: 2119
-
Martins GJ, Shahrokh M, Powell EM (2011) Genetic disruption of Met signaling impairs GABAergic striatal development and cognition. Neuroscience 176:199–209
-
(2011)
Neuroscience
, vol.176
, pp. 199-209
-
-
Martins, G.J.1
Shahrokh, M.2
Powell, E.M.3
|