-
1
-
-
0027377580
-
FMR1 protein: Conserved RNP family domains and selective RNA binding
-
Ashley C.T. Jr., Wilkinson K.D., Reines D., Warren S.T. FMR1 protein. conserved RNP family domains and selective RNA binding Science. 262:1993;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
-
2
-
-
0026554288
-
A 33kDa polypeptide with homology to the laminin receptor: Component of translation machinery
-
Auth D., Brawerman G. A 33kDa polypeptide with homology to the laminin receptor. component of translation machinery Proc. Natl. Acad. Sci. USA. 89:1992;4368-4372.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 4368-4372
-
-
Auth, D.1
Brawerman, G.2
-
3
-
-
0031445652
-
Analysis of domains affecting intracellular localization of the FMRP protein
-
Bardoni B., Sittler A., Shen Y., Mandel J.L. Analysis of domains affecting intracellular localization of the FMRP protein. Neurobiol. Dis. 4:1997;329-336.
-
(1997)
Neurobiol. Dis.
, vol.4
, pp. 329-336
-
-
Bardoni, B.1
Sittler, A.2
Shen, Y.3
Mandel, J.L.4
-
4
-
-
0032758839
-
A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein
-
Bardoni B., Schenck A., Mandel J.L. A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein. Hum. Mol. Genet. 8:1999;2557-2566.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 2557-2566
-
-
Bardoni, B.1
Schenck, A.2
Mandel, J.L.3
-
5
-
-
0032546976
-
Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein
-
Brown V., Small K., Lakkis L., Feng Y., Gunter C., Wilkinson K.D., Warren S.T. Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein. J. Biol. Chem. 273:1998;15521-15527.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 15521-15527
-
-
Brown, V.1
Small, K.2
Lakkis, L.3
Feng, Y.4
Gunter, C.5
Wilkinson, K.D.6
Warren, S.T.7
-
6
-
-
18044379515
-
Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome
-
Brown V., Jin P., Ceman S., Darnell J.C., O'Donnell W.T., Tenenbaum S.A., Jin X., Feng Y., Wilkinson K.D., Keene J.D.et al. Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome. Cell. 107:2001;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
-
8
-
-
0033499661
-
Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex
-
Ceman S., Brown V., Warren S.T. Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex. Mol. Cell. Biol. 19:1999;7925-7932.
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 7925-7932
-
-
Ceman, S.1
Brown, V.2
Warren, S.T.3
-
9
-
-
0034731497
-
Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle
-
Ceman S., Nelson R., Warren S.T. Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle. Biochem. Biophys. Res. Commun. 279:2000;904-908.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.279
, pp. 904-908
-
-
Ceman, S.1
Nelson, R.2
Warren, S.T.3
-
10
-
-
0035830310
-
An autosomal genomic screen for autism
-
An autosomal genomic screen for autism. Am. J. Med. Genet. 105:2001;609-615.
-
(2001)
Am. J. Med. Genet.
, vol.105
, pp. 609-615
-
-
-
11
-
-
0030986183
-
Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits
-
Comery T.A., Harris J.B., Willems P.J., Oostra B.A., Irwin S.A., Weiler I.J., Greenough W.T. Abnormal dendritic spines in fragile X knockout mice. maturation and pruning deficits Proc. Natl. Acad. Sci. USA. 94:1997;5401-5404.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 5401-5404
-
-
Comery, T.A.1
Harris, J.B.2
Willems, P.J.3
Oostra, B.A.4
Irwin, S.A.5
Weiler, I.J.6
Greenough, W.T.7
-
12
-
-
0030760613
-
The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes
-
Corbin F., Bouillon M., Fortin A., Morin S., Rousseau F., Khandjian E.W. The fragile X mental retardation protein is associated with poly(A)+ mRNA in actively translating polyribosomes. Hum. Mol. Genet. 6:1997;1465-1472.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1465-1472
-
-
Corbin, F.1
Bouillon, M.2
Fortin, A.3
Morin, S.4
Rousseau, F.5
Khandjian, E.W.6
-
13
-
-
0035900649
-
Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function
-
Darnell J.C., Jensen K.B., Jin P., Brown V., Warren S.T., Darnell R.B. Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function. Cell. 107:2001;489-499.
-
(2001)
Cell
, vol.107
, pp. 489-499
-
-
Darnell, J.C.1
Jensen, K.B.2
Jin, P.3
Brown, V.4
Warren, S.T.5
Darnell, R.B.6
-
14
-
-
0037192842
-
Gankyrin is an ankyrin-repeat oncoprotein that interacts with CDK4 kinase and the S6ATPase of the 26S proteasome
-
Dawson S., Apcher S., Mee M., Higashitsuji H., Baker R., Uhle S., Dubiel W., Fujita J., Mayer R. Gankyrin is an ankyrin-repeat oncoprotein that interacts with CDK4 kinase and the S6ATPase of the 26S proteasome. J. Biol. Chem. 277:2002;10893-10902.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 10893-10902
-
-
Dawson, S.1
Apcher, S.2
Mee, M.3
Higashitsuji, H.4
Baker, R.5
Uhle, S.6
Dubiel, W.7
Fujita, J.8
Mayer, R.9
-
15
-
-
0027509234
-
A point mutation in the FMR-1 gene associated with fragile X mental retardation
-
De Boulle K., Verkerk A.J., Reyniers E., Vits L., Hendrickx J., Van Roy B., Van den Bos F., de Graaff E., Oostra B.A., Willems P.J. A point mutation in the FMR-1 gene associated with fragile X mental retardation. Nat. Genet. 3:1993;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
-
16
-
-
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. The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation. Nat. Genet. 4:1993;335-340.
-
(1993)
Nat. Genet.
, vol.4
, pp. 335-340
-
-
Devys, D.1
Lutz, Y.2
Rouyer, N.3
Bellocq, J.P.4
Mandel, J.L.5
-
17
-
-
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 Cell. 78:1994;23-33.
-
(1994)
Cell
, vol.78
, pp. 23-33
-
-
-
18
-
-
0002986754
-
Medical conditions associated with autism
-
Ed. Second, D.J. Cohen, & F.R. Volkmar. New York: Wiley. 388-410.pp
-
Dykens E., Volkmar F.R. Medical conditions associated with autism. Second Ed., Cohen D.J., Volkmar F.R. Handbook of Autism and Pervasive Developmental Disorders. 1997;Wiley, New York. 388-410.pp.
-
(1997)
Handbook of Autism and Pervasive Developmental Disorders
-
-
Dykens, E.1
Volkmar, F.R.2
-
19
-
-
0035503566
-
MRNA expression analysis of tissue sections and single cells
-
Eberwine J., Kacharmina J.E., Andrews C., Miyashiro K., McIntosh T., Becker K., Barrett T., Hinkle D., Dent G., Marciano P. mRNA expression analysis of tissue sections and single cells. J. Neurosci. 21:2001;8310-8314.
-
(2001)
J. Neurosci.
, vol.21
, pp. 8310-8314
-
-
Eberwine, J.1
Kacharmina, J.E.2
Andrews, C.3
Miyashiro, K.4
McIntosh, T.5
Becker, K.6
Barrett, T.7
Hinkle, D.8
Dent, G.9
Marciano, P.10
-
20
-
-
0032461803
-
Autism: The point of view from fragile X studies
-
Feinstein C., Reiss A.L. Autism. the point of view from fragile X studies J. Autism Dev. Disord. 28:1998;395-402.
-
(1998)
J. Autism Dev. Disord.
, vol.28
, pp. 395-402
-
-
Feinstein, C.1
Reiss, A.L.2
-
22
-
-
0036809998
-
Cortisol and behavior in fragile X syndrome
-
Hessl D., Glaser B., Dyer-Friedman J., Blasey C., Hastie T., Gunnar M., Reiss A. Cortisol and behavior in fragile X syndrome. Psychoneuroendocrinology. 27:2002;855-872.
-
(2002)
Psychoneuroendocrinology
, vol.27
, pp. 855-872
-
-
Hessl, D.1
Glaser, B.2
Dyer-Friedman, J.3
Blasey, C.4
Hastie, T.5
Gunnar, M.6
Reiss, A.7
-
23
-
-
0034883367
-
A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
-
International Molecular Genetic Study of Autism Consortium A genomewide screen for autism. strong evidence for linkage to chromosomes 2q, 7q, and 16p Am. J. Hum. Genet. 69:2001;570-581.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 570-581
-
-
-
24
-
-
0034222555
-
Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation
-
Irwin S.A., Swain R.A., Christmon C.A., Chakravarti A., Weiler I.J., Greenough W.T. Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation. Neurobiol. Learn. Mem. 74:2000;87-93.
-
(2000)
Neurobiol. Learn. Mem.
, vol.74
, pp. 87-93
-
-
Irwin, S.A.1
Swain, R.A.2
Christmon, C.A.3
Chakravarti, A.4
Weiler, I.J.5
Greenough, W.T.6
-
25
-
-
0034898520
-
Corticosteroid actions in the hippocampus
-
Joels M.J. Corticosteroid actions in the hippocampus. J. Neuroendocrinol. 13:2001;657-669.
-
(2001)
J. Neuroendocrinol.
, vol.13
, pp. 657-669
-
-
Joels, M.J.1
-
26
-
-
0035912793
-
Ribonucleoprotein infrastructure regulating the flow of genetic information between the genome and the proteome
-
Keene J.D. Ribonucleoprotein infrastructure regulating the flow of genetic information between the genome and the proteome. Proc. Natl. Acad. Sci. USA. 98:2001;7018-7024.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 7018-7024
-
-
Keene, J.D.1
-
27
-
-
0035864826
-
Evidence that fragile X mental retardation protein is a negative regulator of translation
-
Laggerbauer B., Ostareck D., Keidel E.M., Ostareck-Lederer A., Fischer U. Evidence that fragile X mental retardation protein is a negative regulator of translation. Hum. Mol. Genet. 10:2001;329-338.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 329-338
-
-
Laggerbauer, B.1
Ostareck, D.2
Keidel, E.M.3
Ostareck-Lederer, A.4
Fischer, U.5
-
28
-
-
0035368955
-
The fragile X mental retardation protein inhibits translation via interacting with mRNA
-
Li Z., Zhang Y., Ku L., Wilkinson K.D., Warren S.T., Feng Y. The fragile X mental retardation protein inhibits translation via interacting with mRNA. Nucleic Acids Res. 29:2001;2276-2283.
-
(2001)
Nucleic Acids Res.
, vol.29
, pp. 2276-2283
-
-
Li, Z.1
Zhang, Y.2
Ku, L.3
Wilkinson, K.D.4
Warren, S.T.5
Feng, Y.6
-
29
-
-
0037071888
-
Drosophila fragile X protein, dFXR, regulates neuronal morphology and function in the brain
-
Morales J., Hiesinger P.R., Schroeder A.J., Kume K., Verstreken P., Jackson F.R., Nelson D.L., Hassan B.A. Drosophila fragile X protein, dFXR, regulates neuronal morphology and function in the brain. Neuron. 34:2002;961-972.
-
(2002)
Neuron
, vol.34
, pp. 961-972
-
-
Morales, J.1
Hiesinger, P.R.2
Schroeder, A.J.3
Kume, K.4
Verstreken, P.5
Jackson, F.R.6
Nelson, D.L.7
Hassan, B.A.8
-
30
-
-
0026339303
-
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome
-
Oberle I., Rousseau F., Heitz D., Kretz C., Devys D., Hanauer A., Boue J., Bertheas M.F., Mandel J.L. Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome. Science. 252:1991;1097-1102.
-
(1991)
Science
, vol.252
, pp. 1097-1102
-
-
Oberle, 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
-
31
-
-
0032945941
-
Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study
-
Philippe A., Martinez M., Guilloud-Bataille M., Gillberg C., Rastam M., Sponheim E., Coleman M., Zappella M., Aschauer H., Van Maldergem L.et al. Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study. Hum. Mol. Genet. 8:1999;805-812.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 805-812
-
-
Philippe, A.1
Martinez, M.2
Guilloud-Bataille, M.3
Gillberg, C.4
Rastam, M.5
Sponheim, E.6
Coleman, M.7
Zappella, M.8
Aschauer, H.9
Van Maldergem, L.10
-
33
-
-
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. 22:2001;409-417.
-
(2001)
J. Dev. Behav. Pediatr.
, vol.22
, pp. 409-417
-
-
Rogers, S.J.1
Wehner, D.E.2
Hagerman, R.3
-
34
-
-
0034164416
-
1999 Curt P. Richter award: Glucocorticoids and the regulation of memory consolidation
-
Roozendaal B. 1999 Curt P. Richter award. glucocorticoids and the regulation of memory consolidation Psychoneuroendocrinology. 25:2000;213-238.
-
(2000)
Psychoneuroendocrinology
, vol.25
, pp. 213-238
-
-
Roozendaal, B.1
-
35
-
-
0021837533
-
Adult fragile X syndrome. Clinico-neuropathologic findings
-
Rudelli R.D., Brown W.T., Wisniewski K., Jenkins E.C., Laure-Kamionowska M., Connell F., Wisniewski H.M. Adult fragile X syndrome. Clinico-neuropathologic findings. Acta Neuropathol. (Berl). 67:1985;289-295.
-
(1985)
Acta Neuropathol. (Berl)
, vol.67
, pp. 289-295
-
-
Rudelli, R.D.1
Brown, W.T.2
Wisniewski, K.3
Jenkins, E.C.4
Laure-Kamionowska, M.5
Connell, F.6
Wisniewski, H.M.7
-
36
-
-
0035801393
-
The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif
-
Schaeffer C., Bardoni B., Mandel J.L., Ehresmann B., Ehresmann C., Moine H. The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif. EMBO J. 20:2001;4803-4813.
-
(2001)
EMBO J.
, vol.20
, pp. 4803-4813
-
-
Schaeffer, C.1
Bardoni, B.2
Mandel, J.L.3
Ehresmann, B.4
Ehresmann, C.5
Moine, H.6
-
37
-
-
0035902466
-
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P
-
Schenck A., Bardoni B., Moro A., Bagni C., Mandel J.L. A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P. Proc. Natl. Acad. Sci. USA. 98:2001;8844-8849.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 8844-8849
-
-
Schenck, A.1
Bardoni, B.2
Moro, A.3
Bagni, C.4
Mandel, J.L.5
-
38
-
-
37649026213
-
Genomic screen and follow-up analysis for autistic disorder
-
Shao Y., Wolpert C.M., Raiford K.L., Menold M.M., Donnelly S.L., Ravan S.A., Bass M.P., McClain C., von Wendt L., Vance J.M.et al. Genomic screen and follow-up analysis for autistic disorder. Am. J. Med. Genet. 114:2002;99-105.
-
(2002)
Am. J. Med. Genet.
, vol.114
, pp. 99-105
-
-
Shao, Y.1
Wolpert, C.M.2
Raiford, K.L.3
Menold, M.M.4
Donnelly, S.L.5
Ravan, S.A.6
Bass, M.P.7
McClain, C.8
Von Wendt, L.9
Vance, J.M.10
-
39
-
-
0029972935
-
Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them
-
Siomi M.C., Zhang Y., Siomi H., Dreyfuss G. Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them. Mol. Cell. Biol. 16:1996;3825-3832.
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 3825-3832
-
-
Siomi, M.C.1
Zhang, Y.2
Siomi, H.3
Dreyfuss, G.4
-
40
-
-
0030051618
-
Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms
-
Sittler A., Devys D., Weber C., Mandel J.L. Alternative splicing of exon 14 determines nuclear or cytoplasmic localisation of fmr1 protein isoforms. Hum. Mol. Genet. 5:1996;95-102.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 95-102
-
-
Sittler, A.1
Devys, D.2
Weber, C.3
Mandel, J.L.4
-
41
-
-
0028981873
-
Glycogen synthase kinase-3 beta phosphorylates tau protein at multiple sites in intact cells
-
Sperber B.R., Leight S., Goedert M., Lee V.M. Glycogen synthase kinase-3 beta phosphorylates tau protein at multiple sites in intact cells. Neurosci. Lett. 197:1995;149-153.
-
(1995)
Neurosci. Lett.
, vol.197
, pp. 149-153
-
-
Sperber, B.R.1
Leight, S.2
Goedert, M.3
Lee, V.M.4
-
42
-
-
0032536361
-
No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome
-
Steward O., Bakker C.E., Willems P.J., Oostra B.A. No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome. Neuroreport. 9:1998;477-481.
-
(1998)
Neuroreport
, vol.9
, pp. 477-481
-
-
Steward, O.1
Bakker, C.E.2
Willems, P.J.3
Oostra, B.A.4
-
43
-
-
0035885312
-
Annexin-1 is abnormally expressed in fragile X syndrome: Two-dimensional electrophoresis study in lymphocytes
-
Sun H.T., Cohen S., Kaufmann W.E. Annexin-1 is abnormally expressed in fragile X syndrome. two-dimensional electrophoresis study in lymphocytes Am. J. Med. Genet. 103:2001;81-90.
-
(2001)
Am. J. Med. Genet.
, vol.103
, pp. 81-90
-
-
Sun, H.T.1
Cohen, S.2
Kaufmann, W.E.3
-
44
-
-
0034618767
-
RNAs that interact with the fragile X syndrome RNA binding protein FMRP
-
Sung Y.J., Conti J., Currie J.R., Brown W.T., Denman R.B. RNAs that interact with the fragile X syndrome RNA binding protein FMRP. Biochem. Biophys. Res. Commun. 275:2000;973-980.
-
(2000)
Biochem. Biophys. Res. Commun.
, vol.275
, pp. 973-980
-
-
Sung, Y.J.1
Conti, J.2
Currie, J.R.3
Brown, W.T.4
Denman, R.B.5
-
45
-
-
0030753950
-
Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis
-
Tamanini F., Willemsen R., van Unen L., Bontekoe C., Galjaard H., Oostra B.A., Hoogeveen A.T. Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis. Hum. Mol. Genet. 6:1997;1315-1322.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1315-1322
-
-
Tamanini, F.1
Willemsen, R.2
Van Unen, L.3
Bontekoe, C.4
Galjaard, H.5
Oostra, B.A.6
Hoogeveen, A.T.7
-
46
-
-
0033231022
-
Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P
-
Tamanini F., Van Unen L., Bakker C., Sacchi N., Galjaard H., Oostra B.A., Hoogeveen A.T. Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P. Biochem. J. 343:1999;517-523.
-
(1999)
Biochem. J.
, vol.343
, pp. 517-523
-
-
Tamanini, F.1
Van Unen, L.2
Bakker, C.3
Sacchi, N.4
Galjaard, H.5
Oostra, B.A.6
Hoogeveen, A.T.7
-
47
-
-
0023690861
-
In situ transcription: Specific synthesis of complementary DNA in fixed tissue sections
-
Tecott L.H., Barchas J.D., Eberwine J.H. In situ transcription. specific synthesis of complementary DNA in fixed tissue sections Science. 240:1988;661-664.
-
(1988)
Science
, vol.240
, pp. 661-664
-
-
Tecott, L.H.1
Barchas, J.D.2
Eberwine, J.H.3
-
48
-
-
0034687794
-
Identifying mRNA subsets in messenger ribonucleoprotein complexes by using cDNA arrays
-
Tenenbaum S.A., Carson C.C., Lager P.J., Keene J.D. Identifying mRNA subsets in messenger ribonucleoprotein complexes by using cDNA arrays. Proc. Natl. Acad. Sci. USA. 97:2000;14085-14090.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 14085-14090
-
-
Tenenbaum, S.A.1
Carson, C.C.2
Lager, P.J.3
Keene, J.D.4
-
49
-
-
0032877216
-
Finding the right RNA: Identification of cellular mRNA substrates for RNA-binding proteins
-
Trifillis P., Day N., Kiledjian M. Finding the right RNA. identification of cellular mRNA substrates for RNA-binding proteins RNA. 5:1999;1071-1082.
-
(1999)
RNA
, vol.5
, pp. 1071-1082
-
-
Trifillis, P.1
Day, N.2
Kiledjian, M.3
-
51
-
-
84942947953
-
Advances in molecular analysis of fragile X syndrome
-
Warren S.T., Nelson D.L. Advances in molecular analysis of fragile X syndrome. JAMA. 271:1994;536-542.
-
(1994)
JAMA
, vol.271
, pp. 536-542
-
-
Warren, S.T.1
Nelson, D.L.2
-
52
-
-
0345528532
-
Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation
-
Weiler I.J., Irwin S.A., Klintsova A.Y., Spencer C.M., Brazelton A.D., Miyashiro K., Comery T.A., Patel B., Eberwine J., Greenough W.T. Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation. Proc. Natl. Acad. Sci. USA. 94:1997;5395-5400.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 5395-5400
-
-
Weiler, I.J.1
Irwin, S.A.2
Klintsova, A.Y.3
Spencer, C.M.4
Brazelton, A.D.5
Miyashiro, K.6
Comery, T.A.7
Patel, B.8
Eberwine, J.9
Greenough, W.T.10
-
53
-
-
0034251867
-
Cortisol and social stressors in children with fragile X: A pilot study
-
Wisbeck J.M., Huffman L.C., Freund L., Gunnar M.R., Davis E.P., Reiss A.L. Cortisol and social stressors in children with fragile X. a pilot study J. Dev. Behav. Pediatr. 21:2000;278-282.
-
(2000)
J. Dev. Behav. Pediatr.
, vol.21
, pp. 278-282
-
-
Wisbeck, J.M.1
Huffman, L.C.2
Freund, L.3
Gunnar, M.R.4
Davis, E.P.5
Reiss, A.L.6
-
54
-
-
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 G. The fragile X mental retardation syndrome protein interacts with novel homologs FXR1 and FXR2. EMBO J. 14:1995;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
-
55
-
-
0035977134
-
Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function
-
a
-
Zhang Y.Q., Bailey A.M., Matthies H.J., Renden R.B., Smith M.A., Speese S.D., Rubin G.M., Broadie K. Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function. Cell. 107:2001;591-603. a.
-
(2001)
Cell
, vol.107
, pp. 591-603
-
-
Zhang, Y.Q.1
Bailey, A.M.2
Matthies, H.J.3
Renden, R.B.4
Smith, M.A.5
Speese, S.D.6
Rubin, G.M.7
Broadie, K.8
-
56
-
-
0035826719
-
Protein quantification from complex protein mixtures using a proteomics methodology with single-cell resolution
-
b
-
Zhang H.T., Kacharmina J.E., Miyashiro K., Greene M.I., Eberwine J. Protein quantification from complex protein mixtures using a proteomics methodology with single-cell resolution. Proc. Natl. Acad. Sci. USA. 98:2001;5497-5502. b.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 5497-5502
-
-
Zhang, H.T.1
Kacharmina, J.E.2
Miyashiro, K.3
Greene, M.I.4
Eberwine, J.5
|