-
1
-
-
28744442194
-
Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells
-
Arocena D.G., Iwahashi C.K., Won N., Beilina A., Ludwig A.L., Tassone F., Schwartz P.H., Hagerman P.J. Induction of inclusion formation and disruption of lamin A/C structure by premutation CGG-repeat RNA in human cultured neural cells. Hum. Mol. Genet. 2005, 14:3661-3671.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3661-3671
-
-
Arocena, D.G.1
Iwahashi, C.K.2
Won, N.3
Beilina, A.4
Ludwig, A.L.5
Tassone, F.6
Schwartz, P.H.7
Hagerman, P.J.8
-
2
-
-
84859179041
-
A pathogenic mechanism in Huntington''s disease involves small CAG-repeated RNAs with neurotoxic activity
-
Bañez-Coronel M., Porta S., Kagerbauer B., Mateu-Huertas E., Pantano L., Ferrer I., Guzmán M., Estivill X., Martí E. A pathogenic mechanism in Huntington''s disease involves small CAG-repeated RNAs with neurotoxic activity. PLoS Genet. 2012, 8:e1002481.
-
(2012)
PLoS Genet.
, vol.8
-
-
Bañez-Coronel, M.1
Porta, S.2
Kagerbauer, B.3
Mateu-Huertas, E.4
Pantano, L.5
Ferrer, I.6
Guzmán, M.7
Estivill, X.8
Martí, E.9
-
3
-
-
77649301567
-
Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration
-
Chen Y., Tassone F., Berman R.F., Hagerman P.J., Hagerman R.J., Willemsen R., Pessah I.N. Murine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration. Hum. Mol. Genet. 2010, 19:196-208.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 196-208
-
-
Chen, Y.1
Tassone, F.2
Berman, R.F.3
Hagerman, P.J.4
Hagerman, R.J.5
Willemsen, R.6
Pessah, I.N.7
-
4
-
-
43749120042
-
Conditional loss of Dicer disrupts cellular and tissue morphogenesis in the cortex and hippocampus
-
Davis T.H., Cuellar T.L., Koch S.M., Barker A.J., Harfe B.D., McManus M.T., Ullian E.M. Conditional loss of Dicer disrupts cellular and tissue morphogenesis in the cortex and hippocampus. J. Neurosci. 2008, 28:4322-4330.
-
(2008)
J. Neurosci.
, vol.28
, pp. 4322-4330
-
-
Davis, T.H.1
Cuellar, T.L.2
Koch, S.M.3
Barker, A.J.4
Harfe, B.D.5
McManus, M.T.6
Ullian, E.M.7
-
5
-
-
80054832080
-
Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS
-
DeJesus-Hernandez M., Mackenzie I.R., Boeve B.F., Boxer A.L., Baker M., Rutherford N.J., Nicholson A.M., Finch N.A., Flynn H., Adamson J., et al. Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS. Neuron 2011, 72:245-256.
-
(2011)
Neuron
, vol.72
, pp. 245-256
-
-
DeJesus-Hernandez, M.1
Mackenzie, I.R.2
Boeve, B.F.3
Boxer, A.L.4
Baker, M.5
Rutherford, N.J.6
Nicholson, A.M.7
Finch, N.A.8
Flynn, H.9
Adamson, J.10
-
6
-
-
9144224451
-
Processing of primary microRNAs by the Microprocessor complex
-
Denli A.M., Tops B.B., Plasterk R.H., Ketting R.F., Hannon G.J. Processing of primary microRNAs by the Microprocessor complex. Nature 2004, 432:231-235.
-
(2004)
Nature
, vol.432
, pp. 231-235
-
-
Denli, A.M.1
Tops, B.B.2
Plasterk, R.H.3
Ketting, R.F.4
Hannon, G.J.5
-
7
-
-
59749089928
-
MiRNAs are essential for survival and differentiation of newborn neurons but not for expansion of neural progenitors during early neurogenesis in the mouse embryonic neocortex
-
De Pietri Tonelli D., Pulvers J.N., Haffner C., Murchison E.P., Hannon G.J., Huttner W.B. miRNAs are essential for survival and differentiation of newborn neurons but not for expansion of neural progenitors during early neurogenesis in the mouse embryonic neocortex. Development 2008, 135:3911-3921.
-
(2008)
Development
, vol.135
, pp. 3911-3921
-
-
De Pietri Tonelli, D.1
Pulvers, J.N.2
Haffner, C.3
Murchison, E.P.4
Hannon, G.J.5
Huttner, W.B.6
-
8
-
-
0021100690
-
Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei
-
Dignam J.D., Lebovitz R.M., Roeder R.G. Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei. Nucleic Acids Res. 1983, 11:1475-1489.
-
(1983)
Nucleic Acids Res.
, vol.11
, pp. 1475-1489
-
-
Dignam, J.D.1
Lebovitz, R.M.2
Roeder, R.G.3
-
9
-
-
84867769481
-
A small molecule that targets r(CGG)(exp) and improves defects in fragile X-associated tremor ataxia syndrome
-
Disney M.D., Liu B., Yang W.Y., Sellier C., Tran T., Charlet-Berguerand N., Childs-Disney J.L. A small molecule that targets r(CGG)(exp) and improves defects in fragile X-associated tremor ataxia syndrome. ACS Chem. Biol. 2012, 7:1711-1718.
-
(2012)
ACS Chem. Biol.
, vol.7
, pp. 1711-1718
-
-
Disney, M.D.1
Liu, B.2
Yang, W.Y.3
Sellier, C.4
Tran, T.5
Charlet-Berguerand, N.6
Childs-Disney, J.L.7
-
10
-
-
34247637636
-
Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model
-
Entezam A., Biacsi R., Orrison B., Saha T., Hoffman G.E., Grabczyk E., Nussbaum R.L., Usdin K. Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model. Gene 2007, 395:125-134.
-
(2007)
Gene
, vol.395
, pp. 125-134
-
-
Entezam, A.1
Biacsi, R.2
Orrison, B.3
Saha, T.4
Hoffman, G.E.5
Grabczyk, E.6
Nussbaum, R.L.7
Usdin, K.8
-
11
-
-
79952733634
-
Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex
-
Fénelon K., Mukai J., Xu B., Hsu P.K., Drew L.J., Karayiorgou M., Fischbach G.D., Macdermott A.B., Gogos J.A. Deficiency of Dgcr8, a gene disrupted by the 22q11.2 microdeletion, results in altered short-term plasticity in the prefrontal cortex. Proc. Natl. Acad. Sci. USA 2011, 108:4447-4452.
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 4447-4452
-
-
Fénelon, K.1
Mukai, J.2
Xu, B.3
Hsu, P.K.4
Drew, L.J.5
Karayiorgou, M.6
Fischbach, G.D.7
Macdermott, A.B.8
Gogos, J.A.9
-
12
-
-
0036345801
-
Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers
-
Greco C.M., Hagerman R.J., Tassone F., Chudley A.E., Del Bigio M.R., Jacquemont S., Leehey M., Hagerman P.J. Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers. Brain 2002, 125:1760-1771.
-
(2002)
Brain
, vol.125
, pp. 1760-1771
-
-
Greco, C.M.1
Hagerman, R.J.2
Tassone, F.3
Chudley, A.E.4
Del Bigio, M.R.5
Jacquemont, S.6
Leehey, M.7
Hagerman, P.J.8
-
13
-
-
30344473617
-
Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS)
-
Greco C.M., Berman R.F., Martin R.M., Tassone F., Schwartz P.H., Chang A., Trapp B.D., Iwahashi C., Brunberg J., Grigsby J., et al. Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS). Brain 2006, 129:243-255.
-
(2006)
Brain
, vol.129
, pp. 243-255
-
-
Greco, C.M.1
Berman, R.F.2
Martin, R.M.3
Tassone, F.4
Schwartz, P.H.5
Chang, A.6
Trapp, B.D.7
Iwahashi, C.8
Brunberg, J.9
Grigsby, J.10
-
14
-
-
9144225636
-
The Microprocessor complex mediates the genesis of microRNAs
-
Gregory R.I., Yan K.P., Amuthan G., Chendrimada T., Doratotaj B., Cooch N., Shiekhattar R. The Microprocessor complex mediates the genesis of microRNAs. Nature 2004, 432:235-240.
-
(2004)
Nature
, vol.432
, pp. 235-240
-
-
Gregory, R.I.1
Yan, K.P.2
Amuthan, G.3
Chendrimada, T.4
Doratotaj, B.5
Cooch, N.6
Shiekhattar, R.7
-
15
-
-
0035838379
-
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
-
Hagerman R.J., Leehey M., Heinrichs W., Tassone F., Wilson R., Hills J., Grigsby J., Gage B., Hagerman P.J. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology 2001, 57:127-130.
-
(2001)
Neurology
, vol.57
, pp. 127-130
-
-
Hagerman, R.J.1
Leehey, M.2
Heinrichs, W.3
Tassone, F.4
Wilson, R.5
Hills, J.6
Grigsby, J.7
Gage, B.8
Hagerman, P.J.9
-
16
-
-
10644234841
-
The Drosha-DGCR8 complex in primary microRNA processing
-
Han J., Lee Y., Yeom K.H., Kim Y.K., Jin H., Kim V.N. The Drosha-DGCR8 complex in primary microRNA processing. Genes Dev. 2004, 18:3016-3027.
-
(2004)
Genes Dev.
, vol.18
, pp. 3016-3027
-
-
Han, J.1
Lee, Y.2
Yeom, K.H.3
Kim, Y.K.4
Jin, H.5
Kim, V.N.6
-
17
-
-
33744520104
-
Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex
-
Han J., Lee Y., Yeom K.H., Nam J.W., Heo I., Rhee J.K., Sohn S.Y., Cho Y., Zhang B.T., Kim V.N. Molecular basis for the recognition of primary microRNAs by the Drosha-DGCR8 complex. Cell 2006, 125:887-901.
-
(2006)
Cell
, vol.125
, pp. 887-901
-
-
Han, J.1
Lee, Y.2
Yeom, K.H.3
Nam, J.W.4
Heo, I.5
Rhee, J.K.6
Sohn, S.Y.7
Cho, Y.8
Zhang, B.T.9
Kim, V.N.10
-
18
-
-
0344442391
-
The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer
-
Handa V., Saha T., Usdin K. The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer. Nucleic Acids Res. 2003, 31:6243-6248.
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 6243-6248
-
-
Handa, V.1
Saha, T.2
Usdin, K.3
-
19
-
-
77955599311
-
MiRNA malfunction causes spinal motor neuron disease
-
Haramati S., Chapnik E., Sztainberg Y., Eilam R., Zwang R., Gershoni N., McGlinn E., Heiser P.W., Wills A.M., Wirguin I., et al. miRNA malfunction causes spinal motor neuron disease. Proc. Natl. Acad. Sci. USA 2010, 107:13111-13116.
-
(2010)
Proc. Natl. Acad. Sci. USA
, vol.107
, pp. 13111-13116
-
-
Haramati, S.1
Chapnik, E.2
Sztainberg, Y.3
Eilam, R.4
Zwang, R.5
Gershoni, N.6
McGlinn, E.7
Heiser, P.W.8
Wills, A.M.9
Wirguin, I.10
-
20
-
-
67249150481
-
Ectopic expression of CGG containing mRNA is neurotoxic in mammals
-
Hashem V., Galloway J.N., Mori M., Willemsen R., Oostra B.A., Paylor R., Nelson D.L. Ectopic expression of CGG containing mRNA is neurotoxic in mammals. Hum. Mol. Genet. 2009, 18:2443-2451.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 2443-2451
-
-
Hashem, V.1
Galloway, J.N.2
Mori, M.3
Willemsen, R.4
Oostra, B.A.5
Paylor, R.6
Nelson, D.L.7
-
21
-
-
77957735016
-
Genetic ablation of Dicer in adult forebrain neurons results in abnormal tau hyperphosphorylation and neurodegeneration
-
Hébert S.S., Papadopoulou A.S., Smith P., Galas M.C., Planel E., Silahtaroglu A.N., Sergeant N., Buée L., De Strooper B. Genetic ablation of Dicer in adult forebrain neurons results in abnormal tau hyperphosphorylation and neurodegeneration. Hum. Mol. Genet. 2010, 19:3959-3969.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 3959-3969
-
-
Hébert, S.S.1
Papadopoulou, A.S.2
Smith, P.3
Galas, M.C.4
Planel, E.5
Silahtaroglu, A.N.6
Sergeant, N.7
Buée, L.8
De Strooper, B.9
-
22
-
-
79955987951
-
CGG-repeat length threshold for FMR1 RNA pathogenesis in a cellular model for FXTAS
-
Hoem G., Raske C.R., Garcia-Arocena D., Tassone F., Sanchez E., Ludwig A.L., Iwahashi C.K., Kumar M., Yang J.E., Hagerman P.J. CGG-repeat length threshold for FMR1 RNA pathogenesis in a cellular model for FXTAS. Hum. Mol. Genet. 2011, 20:2161-2170.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 2161-2170
-
-
Hoem, G.1
Raske, C.R.2
Garcia-Arocena, D.3
Tassone, F.4
Sanchez, E.5
Ludwig, A.L.6
Iwahashi, C.K.7
Kumar, M.8
Yang, J.E.9
Hagerman, P.J.10
-
23
-
-
77955944561
-
Wnt1-cre-mediated conditional loss of Dicer results in malformation of the midbrain and cerebellum and failure of neural crest and dopaminergic differentiation in mice
-
Huang T., Liu Y., Huang M., Zhao X., Cheng L. Wnt1-cre-mediated conditional loss of Dicer results in malformation of the midbrain and cerebellum and failure of neural crest and dopaminergic differentiation in mice. J. Mol. Cell. Biol. 2010, 2:152-163.
-
(2010)
J. Mol. Cell. Biol.
, vol.2
, pp. 152-163
-
-
Huang, T.1
Liu, Y.2
Huang, M.3
Zhao, X.4
Cheng, L.5
-
24
-
-
30344441794
-
Protein composition of the intranuclear inclusions of FXTAS
-
Iwahashi C.K., Yasui D.H., An H.J., Greco C.M., Tassone F., Nannen K., Babineau B., Lebrilla C.B., Hagerman R.J., Hagerman P.J. Protein composition of the intranuclear inclusions of FXTAS. Brain 2006, 129:256-271.
-
(2006)
Brain
, vol.129
, pp. 256-271
-
-
Iwahashi, C.K.1
Yasui, D.H.2
An, H.J.3
Greco, C.M.4
Tassone, F.5
Nannen, K.6
Babineau, B.7
Lebrilla, C.B.8
Hagerman, R.J.9
Hagerman, P.J.10
-
25
-
-
0037384643
-
Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates
-
Jacquemont S., Hagerman R.J., Leehey M., Grigsby J., Zhang L., Brunberg J.A., Greco C., Des Portes V., Jardini T., Levine R., et al. Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. Am. J. Hum. Genet. 2003, 72:869-878.
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 869-878
-
-
Jacquemont, S.1
Hagerman, R.J.2
Leehey, M.3
Grigsby, J.4
Zhang, L.5
Brunberg, J.A.6
Greco, C.7
Des Portes, V.8
Jardini, T.9
Levine, R.10
-
26
-
-
0041880131
-
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila
-
Jin P., Zarnescu D.C., Zhang F., Pearson C.E., Lucchesi J.C., Moses K., Warren S.T. RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in Drosophila. Neuron 2003, 39:739-747.
-
(2003)
Neuron
, vol.39
, pp. 739-747
-
-
Jin, P.1
Zarnescu, D.C.2
Zhang, F.3
Pearson, C.E.4
Lucchesi, J.C.5
Moses, K.6
Warren, S.T.7
-
27
-
-
34547681603
-
Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome
-
Jin P., Duan R., Qurashi A., Qin Y., Tian D., Rosser T.C., Liu H., Feng Y., Warren S.T. Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome. Neuron 2007, 55:556-564.
-
(2007)
Neuron
, vol.55
, pp. 556-564
-
-
Jin, P.1
Duan, R.2
Qurashi, A.3
Qin, Y.4
Tian, D.5
Rosser, T.C.6
Liu, H.7
Feng, Y.8
Warren, S.T.9
-
28
-
-
67651162116
-
Structural insights into CUG repeats containing the ''stretched U-U wobble'': implications for myotonic dystrophy
-
Kiliszek A., Kierzek R., Krzyzosiak W.J., Rypniewski W. Structural insights into CUG repeats containing the ''stretched U-U wobble'': implications for myotonic dystrophy. Nucleic Acids Res. 2009, 37:4149-4156.
-
(2009)
Nucleic Acids Res.
, vol.37
, pp. 4149-4156
-
-
Kiliszek, A.1
Kierzek, R.2
Krzyzosiak, W.J.3
Rypniewski, W.4
-
29
-
-
80052481911
-
Crystal structures of CGG RNA repeats with implications for fragile X-associated tremor ataxia syndrome
-
Kiliszek A., Kierzek R., Krzyzosiak W.J., Rypniewski W. Crystal structures of CGG RNA repeats with implications for fragile X-associated tremor ataxia syndrome. Nucleic Acids Res. 2011, 39:7308-7315.
-
(2011)
Nucleic Acids Res.
, vol.39
, pp. 7308-7315
-
-
Kiliszek, A.1
Kierzek, R.2
Krzyzosiak, W.J.3
Rypniewski, W.4
-
30
-
-
33847077134
-
Ribonuclease dicer cleaves triplet repeat hairpins into shorter repeats that silence specific targets
-
Krol J., Fiszer A., Mykowska A., Sobczak K., de Mezer M., Krzyzosiak W.J. Ribonuclease dicer cleaves triplet repeat hairpins into shorter repeats that silence specific targets. Mol. Cell 2007, 25:575-586.
-
(2007)
Mol. Cell
, vol.25
, pp. 575-586
-
-
Krol, J.1
Fiszer, A.2
Mykowska, A.3
Sobczak, K.4
de Mezer, M.5
Krzyzosiak, W.J.6
-
31
-
-
80052730505
-
A crystal structure of a model of the repeating r(CGG) transcript found in fragile X syndrome
-
Kumar A., Fang P., Park H., Guo M., Nettles K.W., Disney M.D. A crystal structure of a model of the repeating r(CGG) transcript found in fragile X syndrome. ChemBioChem 2011, 12:2140-2142.
-
(2011)
ChemBioChem
, vol.12
, pp. 2140-2142
-
-
Kumar, A.1
Fang, P.2
Park, H.3
Guo, M.4
Nettles, K.W.5
Disney, M.D.6
-
32
-
-
10344248903
-
The human DiGeorge syndrome critical region gene 8 and Its D. melanogaster homolog are required for miRNA biogenesis
-
Landthaler M., Yalcin A., Tuschl T. The human DiGeorge syndrome critical region gene 8 and Its D. melanogaster homolog are required for miRNA biogenesis. Curr. Biol. 2004, 14:2162-2167.
-
(2004)
Curr. Biol.
, vol.14
, pp. 2162-2167
-
-
Landthaler, M.1
Yalcin, A.2
Tuschl, T.3
-
33
-
-
0141843656
-
The nuclear RNase III Drosha initiates microRNA processing
-
Lee Y., Ahn C., Han J., Choi H., Kim J., Yim J., Lee J., Provost P., Rådmark O., Kim S., Kim V.N. The nuclear RNase III Drosha initiates microRNA processing. Nature 2003, 425:415-419.
-
(2003)
Nature
, vol.425
, pp. 415-419
-
-
Lee, Y.1
Ahn, C.2
Han, J.3
Choi, H.4
Kim, J.5
Yim, J.6
Lee, J.7
Provost, P.8
Rådmark, O.9
Kim, S.10
Kim, V.N.11
-
34
-
-
28044432118
-
The structural basis of myotonic dystrophy from the crystal structure of CUG repeats
-
Mooers B.H., Logue J.S., Berglund J.A. The structural basis of myotonic dystrophy from the crystal structure of CUG repeats. Proc. Natl. Acad. Sci. USA 2005, 102:16626-16631.
-
(2005)
Proc. Natl. Acad. Sci. USA
, vol.102
, pp. 16626-16631
-
-
Mooers, B.H.1
Logue, J.S.2
Berglund, J.A.3
-
35
-
-
34447107760
-
The mirtron pathway generates microRNA-class regulatory RNAs in Drosophila
-
Okamura K., Hagen J.W., Duan H., Tyler D.M., Lai E.C. The mirtron pathway generates microRNA-class regulatory RNAs in Drosophila. Cell 2007, 130:89-100.
-
(2007)
Cell
, vol.130
, pp. 89-100
-
-
Okamura, K.1
Hagen, J.W.2
Duan, H.3
Tyler, D.M.4
Lai, E.C.5
-
36
-
-
34447097693
-
Intronic microRNA precursors that bypass Drosha processing
-
Ruby J.G., Jan C.H., Bartel D.P. Intronic microRNA precursors that bypass Drosha processing. Nature 2007, 448:83-86.
-
(2007)
Nature
, vol.448
, pp. 83-86
-
-
Ruby, J.G.1
Jan, C.H.2
Bartel, D.P.3
-
37
-
-
34447261382
-
Cerebellar neurodegeneration in the absence of microRNAs
-
Schaefer A., O'Carroll D., Tan C.L., Hillman D., Sugimori M., Llinas R., Greengard P. Cerebellar neurodegeneration in the absence of microRNAs. J. Exp. Med. 2007, 204:1553-1558.
-
(2007)
J. Exp. Med.
, vol.204
, pp. 1553-1558
-
-
Schaefer, A.1
O'Carroll, D.2
Tan, C.L.3
Hillman, D.4
Sugimori, M.5
Llinas, R.6
Greengard, P.7
-
38
-
-
79953278448
-
Monoallelic deletion of the microRNA biogenesis gene Dgcr8 produces deficits in the development of excitatory synaptic transmission in the prefrontal cortex
-
Schofield C.M., Hsu R., Barker A.J., Gertz C.C., Blelloch R., Ullian E.M. Monoallelic deletion of the microRNA biogenesis gene Dgcr8 produces deficits in the development of excitatory synaptic transmission in the prefrontal cortex. Neural Dev. 2011, 6:11.
-
(2011)
Neural Dev.
, vol.6
, pp. 11
-
-
Schofield, C.M.1
Hsu, R.2
Barker, A.J.3
Gertz, C.C.4
Blelloch, R.5
Ullian, E.M.6
-
39
-
-
77950529507
-
Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients
-
Sellier C., Rau F., Liu Y., Tassone F., Hukema R.K., Gattoni R., Schneider A., Richard S., Willemsen R., Elliott D.J., et al. Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients. EMBO J. 2010, 29:1248-1261.
-
(2010)
EMBO J.
, vol.29
, pp. 1248-1261
-
-
Sellier, C.1
Rau, F.2
Liu, Y.3
Tassone, F.4
Hukema, R.K.5
Gattoni, R.6
Schneider, A.7
Richard, S.8
Willemsen, R.9
Elliott, D.J.10
-
40
-
-
0142009656
-
RNA structure of trinucleotide repeats associated with human neurological diseases
-
Sobczak K., de Mezer M., Michlewski G., Krol J., Krzyzosiak W.J. RNA structure of trinucleotide repeats associated with human neurological diseases. Nucleic Acids Res. 2003, 31:5469-5482.
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 5469-5482
-
-
Sobczak, K.1
de Mezer, M.2
Michlewski, G.3
Krol, J.4
Krzyzosiak, W.J.5
-
41
-
-
34547697173
-
RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS
-
Sofola O.A., Jin P., Qin Y., Duan R., Liu H., de Haro M., Nelson D.L., Botas J. RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS. Neuron 2007, 55:565-571.
-
(2007)
Neuron
, vol.55
, pp. 565-571
-
-
Sofola, O.A.1
Jin, P.2
Qin, Y.3
Duan, R.4
Liu, H.5
de Haro, M.6
Nelson, D.L.7
Botas, J.8
-
42
-
-
43949124669
-
Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model
-
Stark K.L., Xu B., Bagchi A., Lai W.S., Liu H., Hsu R., Wan X., Pavlidis P., Mills A.A., Karayiorgou M., Gogos J.A. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model. Nat. Genet. 2008, 40:751-760.
-
(2008)
Nat. Genet.
, vol.40
, pp. 751-760
-
-
Stark, K.L.1
Xu, B.2
Bagchi, A.3
Lai, W.S.4
Liu, H.5
Hsu, R.6
Wan, X.7
Pavlidis, P.8
Mills, A.A.9
Karayiorgou, M.10
Gogos, J.A.11
-
43
-
-
84863694093
-
MicroRNA-277 modulates the neurodegeneration caused by Fragile X premutation rCGG repeats
-
Tan H., Poidevin M., Li H., Chen D., Jin P. MicroRNA-277 modulates the neurodegeneration caused by Fragile X premutation rCGG repeats. PLoS Genet. 2012, 8:e1002681.
-
(2012)
PLoS Genet.
, vol.8
-
-
Tan, H.1
Poidevin, M.2
Li, H.3
Chen, D.4
Jin, P.5
-
44
-
-
0034684031
-
Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA
-
Tassone F., Hagerman R.J., Loesch D.Z., Lachiewicz A., Taylor A.K., Hagerman P.J. Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA. Am. J. Med. Genet. 2000, 94:232-236.
-
(2000)
Am. J. Med. Genet.
, vol.94
, pp. 232-236
-
-
Tassone, F.1
Hagerman, R.J.2
Loesch, D.Z.3
Lachiewicz, A.4
Taylor, A.K.5
Hagerman, P.J.6
-
45
-
-
23944431645
-
FMR1 RNA within the intranuclear inclusions of fragile X-associated tremor/ataxia syndrome (FXTAS)
-
Tassone F., Iwahashi C., Hagerman P.J. FMR1 RNA within the intranuclear inclusions of fragile X-associated tremor/ataxia syndrome (FXTAS). RNA Biol. 2004, 1:103-105.
-
(2004)
RNA Biol.
, vol.1
, pp. 103-105
-
-
Tassone, F.1
Iwahashi, C.2
Hagerman, P.J.3
-
46
-
-
34250869612
-
CGG repeat length correlates with age of onset of motor signs of the fragile X-associated tremor/ataxia syndrome (FXTAS)
-
Tassone F., Adams J., Berry-Kravis E.M., Cohen S.S., Brusco A., Leehey M.A., Li L., Hagerman R.J., Hagerman P.J. CGG repeat length correlates with age of onset of motor signs of the fragile X-associated tremor/ataxia syndrome (FXTAS). Am. J. Med. Genet. B Neuropsychiatr. Genet. 2007, 144B:566-569.
-
(2007)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.144 B
, pp. 566-569
-
-
Tassone, F.1
Adams, J.2
Berry-Kravis, E.M.3
Cohen, S.S.4
Brusco, A.5
Leehey, M.A.6
Li, L.7
Hagerman, R.J.8
Hagerman, P.J.9
-
47
-
-
33847323881
-
DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal
-
Wang Y., Medvid R., Melton C., Jaenisch R., Blelloch R. DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal. Nat. Genet. 2007, 39:380-385.
-
(2007)
Nat. Genet.
, vol.39
, pp. 380-385
-
-
Wang, Y.1
Medvid, R.2
Melton, C.3
Jaenisch, R.4
Blelloch, R.5
-
48
-
-
0038025990
-
The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome
-
Willemsen R., Hoogeveen-Westerveld M., Reis S., Holstege J., Severijnen L.A., Nieuwenhuizen I.M., Schrier M., van Unen L., Tassone F., Hoogeveen A.T., et al. The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome. Hum. Mol. Genet. 2003, 12:949-959.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 949-959
-
-
Willemsen, R.1
Hoogeveen-Westerveld, M.2
Reis, S.3
Holstege, J.4
Severijnen, L.A.5
Nieuwenhuizen, I.M.6
Schrier, M.7
van Unen, L.8
Tassone, F.9
Hoogeveen, A.T.10
-
49
-
-
23044502585
-
Efficient processing of primary microRNA hairpins by Drosha requires flanking nonstructured RNA sequences
-
Zeng Y., Cullen B.R. Efficient processing of primary microRNA hairpins by Drosha requires flanking nonstructured RNA sequences. J. Biol. Chem. 2005, 280:27595-27603.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 27595-27603
-
-
Zeng, Y.1
Cullen, B.R.2
-
50
-
-
36249002312
-
Secondary structure and dynamics of the r(CGG) repeat in the mRNA of the fragile X mental retardation 1 (FMR1) gene
-
Zumwalt M., Ludwig A., Hagerman P.J., Dieckmann T. Secondary structure and dynamics of the r(CGG) repeat in the mRNA of the fragile X mental retardation 1 (FMR1) gene. RNA Biol. 2007, 4:93-100.
-
(2007)
RNA Biol.
, vol.4
, pp. 93-100
-
-
Zumwalt, M.1
Ludwig, A.2
Hagerman, P.J.3
Dieckmann, T.4
|