-
1
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir, R.E., Van den Veyver, I.B., Wan, M., Tran, C.Q., Francke, U. and Zoghbi, H.Y. (1999) Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat. Genet., 23 185-188.
-
(1999)
Nat. Genet.
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van den Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
Zoghbi, H.Y.6
-
2
-
-
0020507697
-
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: Report of 35 cases
-
Hagberg, B., Aicardi, J., Dias, K. and Ramos, O. (1983) A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: RettRs syndrome: report of 35 cases. Ann. Neurol., 14 471-479.
-
(1983)
Ann. Neurol.
, vol.14
, pp. 471-479
-
-
Hagberg, B.1
Aicardi, J.2
Dias, K.3
Ramos, O.4
-
3
-
-
0014011176
-
Uber ein eigenartiges hirnatrophisches Syndrom bei Hyperammonamie im Kindesalter
-
Rett, V.A. (1966) Uber ein eigenartiges hirnatrophisches Syndrom bei Hyperammonamie im Kindesalter. Weiner Medizinische Wochenschrift, 37, 723-726.
-
(1966)
Weiner Medizinische Wochenschrift
, vol.37
, pp. 723-726
-
-
Rett, V.A.1
-
4
-
-
0035094767
-
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
-
Guy, J., Hendrich, B., Holmes, M., Martin, J.E. and Bird, A. (2001) A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat. Genet., 27, 322-326.
-
(2001)
Nat. Genet.
, vol.27
, pp. 322-326
-
-
Guy, J.1
Hendrich, B.2
Holmes, M.3
Martin, J.E.4
Bird, A.5
-
5
-
-
0035093830
-
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
-
Chen, R.Z., Akbarian, S., Tudor, M. and Jaenisch, R. (2001) Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice. Nat. Genet., 27, 327-331.
-
(2001)
Nat. Genet.
, vol.27
, pp. 327-331
-
-
Chen, R.Z.1
Akbarian, S.2
Tudor, M.3
Jaenisch, R.4
-
6
-
-
0037130455
-
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3
-
Shahbazian, M., Young, J., Yuva-Paylor, L., Spencer, C., Antalffy, B., Noebels, J., Armstrong, D., Paylor, R. and Zoghbi, H. (2002) Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron, 35, 243-254.
-
(2002)
Neuron
, vol.35
, pp. 243-254
-
-
Shahbazian, M.1
Young, J.2
Yuva-Paylor, L.3
Spencer, C.4
Antalffy, B.5
Noebels, J.6
Armstrong, D.7
Paylor, R.8
Zoghbi, H.9
-
7
-
-
0037081840
-
Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation
-
Shahbazian, M.D., Antalffy, B., Armstrong, D.L. and Zoghbi, H.Y. (2002) Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation. Hum. Mol. Genet., 11, 115-124.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 115-124
-
-
Shahbazian, M.D.1
Antalffy, B.2
Armstrong, D.L.3
Zoghbi, H.Y.4
-
8
-
-
7244243971
-
MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions
-
Kishi, N. and Macklis, J.D. (2004) MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions. Mol. Cell. Neurosci., 27, 306-321.
-
(2004)
Mol. Cell. Neurosci.
, vol.27
, pp. 306-321
-
-
Kishi, N.1
Macklis, J.D.2
-
9
-
-
1942533500
-
Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice
-
Luikenhuis, S., Giacometti, E., Beard, C.F. and Jaenisch, R (2004) Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice. Proc. Natl Acad. Sci. USA, 101, 6033-6038.
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 6033-6038
-
-
Luikenhuis, S.1
Giacometti, E.2
Beard, C.F.3
Jaenisch, R.4
-
10
-
-
0031837109
-
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
-
Jones, P.L., Veenstra, G.J., Wade, P.A., Vermaak, D., Kass, S.U., Landsberger, N., Strouboulis, J. and Wolffe, A.P. (1998) Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. Nat. Genet., 19, 187-191.
-
(1998)
Nat. Genet.
, vol.19
, pp. 187-191
-
-
Jones, P.L.1
Veenstra, G.J.2
Wade, P.A.3
Vermaak, D.4
Kass, S.U.5
Landsberger, N.6
Strouboulis, J.7
Wolffe, A.P.8
-
11
-
-
0026747761
-
Purification, sequence and cellular localisation of a novel chromosomal protein that binds to methylated DNA
-
Lewis, J.D., Meehan, R.R., Henzel, W.J., Maurer-Fogy, I., Jeppesen, P., Klein, F. and Bird, A. (1992) Purification, sequence and cellular localisation of a novel chromosomal protein that binds to methylated DNA. Cell, 69, 905-914.
-
(1992)
Cell
, vol.69
, pp. 905-914
-
-
Lewis, J.D.1
Meehan, R.R.2
Henzel, W.J.3
Maurer-Fogy, I.4
Jeppesen, P.5
Klein, F.6
Bird, A.7
-
12
-
-
0342437491
-
MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin
-
Nan, X., Campoy, J. and Bird, A. (1997) MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin. Cell, 88, 471-481.
-
(1997)
Cell
, vol.88
, pp. 471-481
-
-
Nan, X.1
Campoy, J.2
Bird, A.3
-
13
-
-
0032574977
-
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
-
Nan, X., Ng, H.-H., Johnson, C.A., Laherty, C.D., Turner, B.M., Eisenman, R.N. and Bird, A. (1998) Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex. Nature, 393, 386-389.
-
(1998)
Nature
, vol.393
, pp. 386-389
-
-
Nan, X.1
Ng, H.-H.2
Johnson, C.A.3
Laherty, C.D.4
Turner, B.M.5
Eisenman, R.N.6
Bird, A.7
-
14
-
-
0037180492
-
Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain
-
Tudor, M., Akbarian, S., Chen, R.Z. and Jaenisch, R. (2002) Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain. Proc. Natl Acad. Sci. USA, 99, 15 536-15 541.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 15536-15541
-
-
Tudor, M.1
Akbarian, S.2
Chen, R.Z.3
Jaenisch, R.4
-
15
-
-
0242332183
-
Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2
-
Chen, W.G., Chang, Q., Lin, Y., Meissner, A., West, A.E., Griffith, E.C., Jaenisch, R. and Greenberg, M.E. (2003) Derepression of BDNF transcription involves calcium-dependent phosphorylation of MeCP2. Science, 302, 885-889.
-
(2003)
Science
, vol.302
, pp. 885-889
-
-
Chen, W.G.1
Chang, Q.2
Lin, Y.3
Meissner, A.4
West, A.E.5
Griffith, E.C.6
Jaenisch, R.7
Greenberg, M.E.8
-
16
-
-
0242300612
-
DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation
-
Martinowich, K., Hattori, D., Wu, H., Fouse, S., He, F., Hu, Y., Fan, G. and Sun, Y.E. (2003) DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation. Science, 302, 890-893.
-
(2003)
Science
, vol.302
, pp. 890-893
-
-
Martinowich, K.1
Hattori, D.2
Wu, H.3
Fouse, S.4
He, F.5
Hu, Y.6
Fan, G.7
Sun, Y.E.8
-
17
-
-
14044252235
-
Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3
-
Samaco, R.C., Hogart, A. and LaSalle, J.M. (2005) Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Hum. Mol. Genet., 14 483-492.
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 483-492
-
-
Samaco, R.C.1
Hogart, A.2
LaSalle, J.M.3
-
18
-
-
11244328520
-
Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome
-
Horike, S., Cai, S., Miyano, M., Cheng, J.F. and Kohwi-Shigematsu, T. (2005) Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome. Nat. Genet., 37, 31-40.
-
(2005)
Nat. Genet.
, vol.37
, pp. 31-40
-
-
Horike, S.1
Cai, S.2
Miyano, M.3
Cheng, J.F.4
Kohwi-Shigematsu, T.5
-
19
-
-
0032567143
-
Glucocorticoid signalling - Multiple variations of a common theme
-
Reichardt, H.M. and Schutz, G. (1998) Glucocorticoid signalling - multiple variations of a common theme. Mol. Cell. Endocrinol., 146, 1-6.
-
(1998)
Mol. Cell. Endocrinol.
, vol.146
, pp. 1-6
-
-
Reichardt, H.M.1
Schutz, G.2
-
20
-
-
0034937430
-
Transcriptional regulation of rat hepatic aryl sulfotransferase (SULT1A1) gene expression by glucocorticoids
-
Duanmu, Z., Kocarek, T.A. and Runge-Morris, M. (2001) Transcriptional regulation of rat hepatic aryl sulfotransferase (SULT1A1) gene expression by glucocorticoids. Drug Metab. Dispos., 29, 1130-1135.
-
(2001)
Drug Metab. Dispos.
, vol.29
, pp. 1130-1135
-
-
Duanmu, Z.1
Kocarek, T.A.2
Runge-Morris, M.3
-
21
-
-
0035856598
-
Regulation and physiological roles of serum- and glucocorticoid-induced protein kinase isoforms
-
Lang, F. and Cohen, P. (2001) Regulation and physiological roles of serum- and glucocorticoid-induced protein kinase isoforms. Sci. STKE 2001, RE17.
-
(2001)
Sci. STKE
, vol.2001
-
-
Lang, F.1
Cohen, P.2
-
22
-
-
0034907647
-
Inhibition of heat shock transcription factor by GR
-
Wadekar, S.A., Li, D., Periyasamy, S. and Sanchez, E.R. (2001) Inhibition of heat shock transcription factor by GR. Mol. Endocrinol. 15, 1396-1410.
-
(2001)
Mol. Endocrinol.
, vol.15
, pp. 1396-1410
-
-
Wadekar, S.A.1
Li, D.2
Periyasamy, S.3
Sanchez, E.R.4
-
23
-
-
2342427775
-
Oxygen-regulated expression of the RNA-binding proteins RBM3 and CIRP by a HIF-1-independent mechanism
-
Wellmann, S., Buhrer, C., Moderegger, E., Zelmer, A., Kirschner, R., Koehne, P., Fujita, J. and Seeger, K. (2004) Oxygen-regulated expression of the RNA-binding proteins RBM3 and CIRP by a HIF-1-independent mechanism. J. Cell Sci., 117, 1785-1794.
-
(2004)
J. Cell Sci.
, vol.117
, pp. 1785-1794
-
-
Wellmann, S.1
Buhrer, C.2
Moderegger, E.3
Zelmer, A.4
Kirschner, R.5
Koehne, P.6
Fujita, J.7
Seeger, K.8
-
24
-
-
0033018628
-
Glucocorticoid resistance in the squirrel monkey is associated with overexpression of the immunophilin FKBP51
-
Reynolds, P.D., Ruan, Y., Smith, D.F. and Scammell, J.G. (1999) Glucocorticoid resistance in the squirrel monkey is associated with overexpression of the immunophilin FKBP51. J. Clin. Endocrinol. Metab., 84, 663-669.
-
(1999)
J. Clin. Endocrinol. Metab.
, vol.84
, pp. 663-669
-
-
Reynolds, P.D.1
Ruan, Y.2
Smith, D.F.3
Scammell, J.G.4
-
25
-
-
9644252785
-
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment
-
Binder, E.B., Salyakina, D., Lichtner, P., Wochnik, G.M., Ising, M., Putz, B., Papiol, S., Seaman, S., Lucae, S., Kohli, M.A. et al. (2004) Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nat. Genet., 36, 1319-1325.
-
(2004)
Nat. Genet.
, vol.36
, pp. 1319-1325
-
-
Binder, E.B.1
Salyakina, D.2
Lichtner, P.3
Wochnik, G.M.4
Ising, M.5
Putz, B.6
Papiol, S.7
Seaman, S.8
Lucae, S.9
Kohli, M.A.10
-
26
-
-
0023712315
-
Stress, glucocorticoids and development
-
De Kloet, E.R., Rosenfeld, P., Van Eekelen, J.A., Sutanto, W. and Levine, S. (1988) Stress, glucocorticoids and development. Prog. Brain Res., 73, 101-120.
-
(1988)
Prog. Brain Res.
, vol.73
, pp. 101-120
-
-
De Kloet, E.R.1
Rosenfeld, P.2
Van Eekelen, J.A.3
Sutanto, W.4
Levine, S.5
-
27
-
-
0035836457
-
Prenatal glucocorticoid programming of brain corticosteroid receptors and corticotrophin-releasing hormone: Possible implications for behaviour
-
Welberg, L.A., Seckl, J.R. and Holmes, M.C. (2001) Prenatal glucocorticoid programming of brain corticosteroid receptors and corticotrophin-releasing hormone: Possible implications for behaviour. Neuroscience, 104, 71-79.
-
(2001)
Neuroscience
, vol.104
, pp. 71-79
-
-
Welberg, L.A.1
Seckl, J.R.2
Holmes, M.C.3
-
28
-
-
1642290227
-
Outcomes at school age after postnatal dexamethasone therapy for lung disease of prematurity
-
Yeh, T.F., Lin, Y.J., Lin, H.C., Huang, C.C., Hsieh, W.S., Lin, C.H. and Tsai, C.H. (2004) Outcomes at school age after postnatal dexamethasone therapy for lung disease of prematurity. N. Engl. J. Med., 350 1304-1313.
-
(2004)
N. Engl. J. Med.
, vol.350
, pp. 1304-1313
-
-
Yeh, T.F.1
Lin, Y.J.2
Lin, H.C.3
Huang, C.C.4
Hsieh, W.S.5
Lin, C.H.6
Tsai, C.H.7
-
29
-
-
0018838792
-
Cerebellar granule cell genesis in the hydrocortisone-treated rats
-
Bohn, M.C. and Lauder, J.M. (1980) Cerebellar granule cell genesis in the hydrocortisone-treated rats. Dev. Neurosci., 3, 81-89.
-
(1980)
Dev. Neurosci.
, vol.3
, pp. 81-89
-
-
Bohn, M.C.1
Lauder, J.M.2
-
31
-
-
0035201347
-
Bone histomorphometry in three females with Rett syndrome
-
Budden, S.S. and Gunness, M.E. (2001) Bone histomorphometry in three females with Rett syndrome. Brain Dev., 23 (Suppl. 1), S133-S137.
-
(2001)
Brain Dev.
, vol.23
, Issue.SUPPL. 1
-
-
Budden, S.S.1
Gunness, M.E.2
-
32
-
-
0030734344
-
Osteopenia in Rett syndrome
-
Haas, R.H., Dixon, S.D., Sartoris, D.J. and Hennessy, M.J. (1997) Osteopenia in Rett syndrome. J. Pediatr., 131, 771-774.
-
(1997)
J. Pediatr.
, vol.131
, pp. 771-774
-
-
Haas, R.H.1
Dixon, S.D.2
Sartoris, D.J.3
Hennessy, M.J.4
-
33
-
-
0032940559
-
A population-based approach to the investigation of osteopenia in Rett syndrome
-
Leonard, H., Thomson, M.R., Glasson, E.J., Fyfe, S., Leonard, S., Bower, C., Christodoulou, J. and Ellaway, C. (1999) A population-based approach to the investigation of osteopenia in Rett syndrome. Dev. Med. Child Neurol., 41, 323-328.
-
(1999)
Dev. Med. Child Neurol.
, vol.41
, pp. 323-328
-
-
Leonard, H.1
Thomson, M.R.2
Glasson, E.J.3
Fyfe, S.4
Leonard, S.5
Bower, C.6
Christodoulou, J.7
Ellaway, C.8
-
34
-
-
0035889662
-
Dendritic reorganization in pyramidal neurons in medial prefrontal cortex after chronic corticosterone administration
-
Wellman, C.L. (2001) Dendritic reorganization in pyramidal neurons in medial prefrontal cortex after chronic corticosterone administration. J. Neurobiol., 49, 245-253.
-
(2001)
J. Neurobiol.
, vol.49
, pp. 245-253
-
-
Wellman, C.L.1
-
35
-
-
0030905665
-
Dysregulation of diurnal rhythms of serotonin 5-HT2C and corticosteroid receptor gene expression in the hippocampus with food restriction and glucocorticoids
-
Holmes, M.C., French, K.L. and Seekl, J.R. (1997) Dysregulation of diurnal rhythms of serotonin 5-HT2C and corticosteroid receptor gene expression in the hippocampus with food restriction and glucocorticoids. J. Neurosci., 17, 4056-4065.
-
(1997)
J. Neurosci.
, vol.17
, pp. 4056-4065
-
-
Holmes, M.C.1
French, K.L.2
Seekl, J.R.3
-
36
-
-
3042794155
-
Gene expression changes in the course of neural progenitor cell differentiation
-
Gurok, U., Steinhoff, C., Lipkowitz, B., Ropers, H.H., Scharff, C. and Nuber, U.A. (2004) Gene expression changes in the course of neural progenitor cell differentiation. J. Neurosci., 24, 5982-6002.
-
(2004)
J. Neurosci.
, vol.24
, pp. 5982-6002
-
-
Gurok, U.1
Steinhoff, C.2
Lipkowitz, B.3
Ropers, H.H.4
Scharff, C.5
Nuber, U.A.6
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