메뉴 건너뛰기




Volumn 18, Issue 1, 2012, Pages

Early intervention with psychostimulants or antidepressants to increase methyl-CpG-binding protein 2 (MeCP2) expressions: A potential therapy for Rett syndrome

Author keywords

Antidepressants; Methyl CpG binding protein 2 (MeCP2); Psychostimulants; Rett syndrome; Treatment; X chromosome inactivation

Indexed keywords

COCAINE; DESIPRAMINE; FLUOXETINE; METHYL CPG BINDING PROTEIN 2;

EID: 84855292340     PISSN: 12341010     EISSN: 16433750     Source Type: Journal    
DOI: 10.12659/MSM.882183     Document Type: Article
Times cited : (4)

References (19)
  • 1
    • 0032830639 scopus 로고    scopus 로고
    • Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    • Amir RE, Van den Veyver IB, Wan M et al: Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet, 1999; 23: 185-88
    • (1999) Nat Genet , vol.23 , pp. 185-188
    • Amir, R.E.1    van den Veyver, I.B.2    Wan, M.3
  • 3
    • 0035194413 scopus 로고    scopus 로고
    • Pathophysiology of Rett syndrome from the standpoint of clinical characteristics
    • Segawa M: Pathophysiology of Rett syndrome from the standpoint of clinical characteristics. Brain Dev, 2001; 23(Suppl.1): S94-98
    • (2001) Brain Dev , vol.23 , Issue.1 SUPPL.
    • Segawa, M.1
  • 4
    • 79956280638 scopus 로고    scopus 로고
    • Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brain
    • Panayotis N, Ghata A, Villard L, Roux JC: Biogenic amines and their metabolites are differentially affected in the Mecp2-deficient mouse brain. BMC Neurosci, 2011; 12: 47
    • (2011) BMC Neurosci , vol.12 , pp. 47
    • Panayotis, N.1    Ghata, A.2    Villard, L.3    Roux, J.C.4
  • 5
    • 27144431761 scopus 로고    scopus 로고
    • Natural history of Rett syndrome
    • Nomura Y, Segawa M: Natural history of Rett syndrome. J Child Neurol, 2005; 20: 764-68
    • (2005) J Child Neurol , vol.20 , pp. 764-768
    • Nomura, Y.1    Segawa, M.2
  • 6
    • 33847266846 scopus 로고    scopus 로고
    • Reversal of neurological defects in a mouse model of Rett syndrome
    • Guy J, Gan J, Selfridge J et al: Reversal of neurological defects in a mouse model of Rett syndrome. Science, 2007; 315: 1143-47
    • (2007) Science , vol.315 , pp. 1143-1147
    • Guy, J.1    Gan, J.2    Selfridge, J.3
  • 7
    • 0035094767 scopus 로고    scopus 로고
    • A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
    • Guy J, Hendrich B, Holmes M et al: A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Nat Genet, 2001; 27: 322-26
    • (2001) Nat Genet , vol.27 , pp. 322-326
    • Guy, J.1    Hendrich, B.2    Holmes, M.3
  • 8
    • 0035853013 scopus 로고    scopus 로고
    • MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features
    • Auranen M, Vanhala R, Vosman M et al: MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features. Neurology, 2001; 56: 611-17
    • (2001) Neurology , vol.56 , pp. 611-617
    • Auranen, M.1    Vanhala, R.2    Vosman, M.3
  • 9
    • 35648978121 scopus 로고    scopus 로고
    • The story of Rett syndrome: From clinic to neurobiology
    • Chahrour M, Zoghbi HY: The story of Rett syndrome: from clinic to neurobiology. Neuron, 2007; 56: 422-37
    • (2007) Neuron , vol.56 , pp. 422-437
    • Chahrour, M.1    Zoghbi, H.Y.2
  • 10
    • 0042893900 scopus 로고    scopus 로고
    • Rett syndrome in adolescent and adult females: Clinical and molecular genetic findings
    • Smeets E, Schollen E, Moog U et al: Rett syndrome in adolescent and adult females: clinical and molecular genetic findings. Am J Med Genet A, 2003; 122A: 227-33
    • (2003) Am J Med Genet A , vol.122 A , pp. 227-233
    • Smeets, E.1    Schollen, E.2    Moog, U.3
  • 11
    • 0036273943 scopus 로고    scopus 로고
    • Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype
    • Hoffbuhr KC, Moses LM, Jerdonek MA et al: Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype. Ment Retard Dev Disabil Res Rev, 2002; 8: 99-105
    • (2002) Ment Retard Dev Disabil Res Rev , vol.8 , pp. 99-105
    • Hoffbuhr, K.C.1    Moses, L.M.2    Jerdonek, M.A.3
  • 12
    • 1542344372 scopus 로고    scopus 로고
    • X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome
    • Young JI, Zoghbi HY: X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome. Am J Hum Genet, 2004; 74: 511-20
    • (2004) Am J Hum Genet , vol.74 , pp. 511-520
    • Young, J.I.1    Zoghbi, H.Y.2
  • 13
    • 33746256453 scopus 로고    scopus 로고
    • Fluoxetine and cocaine in- duce the epigenetic factors MeCP2 and MBD1 in adult rat brain
    • Cassel S, Carouge D, Gensburger C et al: Fluoxetine and cocaine in- duce the epigenetic factors MeCP2 and MBD1 in adult rat brain. Mol Pharmacol, 2006; 70: 487-92
    • (2006) Mol Pharmacol , vol.70 , pp. 487-492
    • Cassel, S.1    Carouge, D.2    Gensburger, C.3
  • 14
    • 33745466540 scopus 로고    scopus 로고
    • Lithium and antidepressants: Potential agents for the treatment of Rett syndrome
    • Tsai SJ: Lithium and antidepressants: Potential agents for the treatment of Rett syndrome. Med Hypotheses, 2006; 67: 626-29
    • (2006) Med Hypotheses , vol.67 , pp. 626-629
    • Tsai, S.J.1
  • 15
    • 80054037873 scopus 로고    scopus 로고
    • Serotonin reuptake inhibitor antidepressants (SSRIs) against atherosclerosis
    • Wozniak G, Toska A, Saridi M, Mouzas O: Serotonin reuptake inhibitor antidepressants (SSRIs) against atherosclerosis. Med Sci Monit, 2011; 17(9): 205-14
    • (2011) Med Sci Monit , vol.17 , Issue.9 , pp. 205-214
    • Wozniak, G.1    Toska, A.2    Saridi, M.3    Mouzas, O.4
  • 16
    • 36849075300 scopus 로고    scopus 로고
    • Oral treatment with desipra- mine improves breathing and life span in Rett syndrome mouse model
    • Zanella S, Mebarek S, Lajard AM et al: Oral treatment with desipra- mine improves breathing and life span in Rett syndrome mouse model. Respir Physiol Neurobiol, 2008; 160: 116-21
    • (2008) Respir Physiol Neurobiol , vol.160 , pp. 116-121
    • Zanella, S.1    Mebarek, S.2    Lajard, A.M.3
  • 17
    • 34147198993 scopus 로고    scopus 로고
    • Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome
    • Roux JC, Dura E, Moncla A et al: Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome. Eur J Neurosci, 2007; 25: 1915-22
    • (2007) Eur J Neurosci , vol.25 , pp. 1915-1922
    • Roux, J.C.1    Dura, E.2    Moncla, A.3
  • 18
    • 0023582259 scopus 로고
    • The hands, and the mind, pre- and post-regression, in Rett syndrome
    • Kerr AM, Montague J, Stephenson JB: The hands, and the mind, pre- and post-regression, in Rett syndrome. Brain Dev, 1987; 9: 487-90
    • (1987) Brain Dev , vol.9 , pp. 487-490
    • Kerr, A.M.1    Montague, J.2    Stephenson, J.B.3
  • 19
    • 0031900414 scopus 로고    scopus 로고
    • X chromosome-inactivation patterns in patients with Rett syndrome
    • Krepischi AC, Kok F, Otto PG: X chromosome-inactivation patterns in patients with Rett syndrome. Hum Genet, 1998; 102: 319-21
    • (1998) Hum Genet , vol.102 , pp. 319-321
    • Krepischi, A.C.1    Kok, F.2    Otto, P.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.