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Volumn 204, Issue 1, 2005, Pages 8-20

Non-syndromic X-linked mental retardation: From a molecular to a clinical point of view

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; CARRIER PROTEIN; GUANOSINE TRIPHOSPHATASE; LONG CHAIN FATTY ACID COENZYME A LIGASE; POSTSYNAPTIC DENSITY PROTEIN 95; PROTEIN ACSL4; PROTEIN AT2; PROTEIN SLC6A8; RAB PROTEIN; RHO GUANINE NUCLEOTIDE BINDING PROTEIN; SYNAPSE ASSOCIATED PROTEIN 102; UNCLASSIFIED DRUG;

EID: 20144381139     PISSN: 00219541     EISSN: None     Source Type: Journal    
DOI: 10.1002/jcp.20296     Document Type: Review
Times cited : (30)

References (101)
  • 3
    • 0033646967 scopus 로고    scopus 로고
    • Rett syndrome: Methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations
    • Amir RE, Zoghbi HY. 2000. Rett syndrome: Methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations. Am J Med Genet 97(2):147-152.
    • (2000) Am J Med Genet , vol.97 , Issue.2 , pp. 147-152
    • Amir, R.E.1    Zoghbi, H.Y.2
  • 4
    • 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, Tran CQ, Francke U, Zoghbi HY. 1999. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet 23(2):185-188.
    • (1999) Nat Genet , vol.23 , Issue.2 , 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
  • 6
    • 0038377518 scopus 로고    scopus 로고
    • IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosis
    • Bahi N, Friocourt G, Carrie A, Graham ME, Weiss JL, Chafey P, Fauchereau F, Burgoyne RD, Chelly J. 2003. IL1 receptor accessory protein like, a protein involved in X-linked mental retardation, interacts with Neuronal Calcium Sensor-1 and regulates exocytosis. Hum Mol Genet 12(12):1415-1425.
    • (2003) Hum Mol Genet , vol.12 , Issue.12 , pp. 1415-1425
    • Bahi, N.1    Friocourt, G.2    Carrie, A.3    Graham, M.E.4    Weiss, J.L.5    Chafey, P.6    Fauchereau, F.7    Burgoyne, R.D.8    Chelly, J.9
  • 7
    • 0036626596 scopus 로고    scopus 로고
    • MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain
    • Balmer D, Arredondo J, Samaco RC, LaSalle JM. 2002. MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain. Hum Genet 110(6):545-552.
    • (2002) Hum Genet , vol.110 , Issue.6 , pp. 545-552
    • Balmer, D.1    Arredondo, J.2    Samaco, R.C.3    LaSalle, J.M.4
  • 8
    • 0042306314 scopus 로고    scopus 로고
    • Diagnostic evaluation of developmental delay/mental retardation: An overview
    • Battaglia A, Carey JC. 2003. Diagnostic evaluation of developmental delay/mental retardation: An overview. Am J Med Genet 117C(1):3-14.
    • (2003) Am J Med Genet , vol.117 C , Issue.1 , pp. 3-14
    • Battaglia, A.1    Carey, J.C.2
  • 9
    • 0038495879 scopus 로고    scopus 로고
    • Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia
    • Bergmann C, Zerres K, Senderek J, Rudnik-Schoneborn S, Eggermann T, Hausler M, Mull M, Ramaekers VT. 2003. Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasia. Brain 126(Pt 7):1537-1544.
    • (2003) Brain , vol.126 , Issue.PART 7 , pp. 1537-1544
    • Bergmann, C.1    Zerres, K.2    Senderek, J.3    Rudnik-Schoneborn, S.4    Eggermann, T.5    Hausler, M.6    Mull, M.7    Ramaekers, V.T.8
  • 12
    • 0035156560 scopus 로고    scopus 로고
    • The neuronal calcium sensor family of Ca2+-binding proteins
    • Burgoyne R, Weiss J. 2001. The neuronal calcium sensor family of Ca2+-binding proteins. Biochem J 353:1-12.
    • (2001) Biochem J , vol.353 , pp. 1-12
    • Burgoyne, R.1    Weiss, J.2
  • 13
    • 0032522157 scopus 로고    scopus 로고
    • Cloning, expression, and chromosomal localization of human long-chain fatty acid-CoA ligase 4 (FACL4)
    • Cao Y, Traer E, Zimmerman GA, McIntyre TM, Prescott SM. 1998. Cloning, expression, and chromosomal localization of human long-chain fatty acid-CoA ligase 4 (FACL4). Genomics 49:327-330.
    • (1998) Genomics , vol.49 , pp. 327-330
    • Cao, Y.1    Traer, E.2    Zimmerman, G.A.3    McIntyre, T.M.4    Prescott, S.M.5
  • 15
    • 0141455375 scopus 로고    scopus 로고
    • Is mental retardation a defect of synapse structure and function?
    • Chechlacz M, Gleeson JG. 2003. Is mental retardation a defect of synapse structure and function? Pediatr Neurol 29(1):11-17.
    • (2003) Pediatr Neurol , vol.29 , Issue.1 , pp. 11-17
    • Chechlacz, M.1    Gleeson, J.G.2
  • 16
    • 0035464960 scopus 로고    scopus 로고
    • Monogenic causes of X-linked mental retardation
    • Chelly J, Mandel J. 2001. Monogenic causes of X-linked mental retardation. Nat Rev Genet 2(9):669-680.
    • (2001) Nat Rev Genet , vol.2 , Issue.9 , pp. 669-680
    • Chelly, J.1    Mandel, J.2
  • 21
    • 0036719449 scopus 로고    scopus 로고
    • Breaking the neuronal sphere: Regulation of the actin cytoskeleton in neuritogenesis
    • da Silva JS, Dotti CG. 2002. Breaking the neuronal sphere: Regulation of the actin cytoskeleton in neuritogenesis. Nat Rev Neurosci 3(9):694-704.
    • (2002) Nat Rev Neurosci , vol.3 , Issue.9 , pp. 694-704
    • Da Silva, J.S.1    Dotti, C.G.2
  • 22
    • 0033199655 scopus 로고    scopus 로고
    • p21-activated protein kinase: A crucial component of morphological signaling?
    • Daniels RH, Bokoch GM. 1999. p21-activated protein kinase: A crucial component of morphological signaling? Trends Biochem Sci 24(9):350-355.
    • (1999) Trends Biochem Sci , vol.24 , Issue.9 , pp. 350-355
    • Daniels, R.H.1    Bokoch, G.M.2
  • 25
    • 0035253071 scopus 로고    scopus 로고
    • Rho GTPases in growth cone guidance
    • Dickson BJ. 2001. Rho GTPases in growth cone guidance. Curr Opin Neurobiol 11(1):103-110.
    • (2001) Curr Opin Neurobiol , vol.11 , Issue.1 , pp. 103-110
    • Dickson, B.J.1
  • 26
    • 0037413674 scopus 로고    scopus 로고
    • Molecular phylogenetics of the RrmJ/fibrillarin superfamily of ribose 2′-O-methyltransferases
    • Feder M, Pas J, Wyrwicz LS, Bujnicki JM. 2003. Molecular phylogenetics of the RrmJ/fibrillarin superfamily of ribose 2′-O-methyltransferases. Gene 302(1-2):129-138.
    • (2003) Gene , vol.302 , Issue.1-2 , pp. 129-138
    • Feder, M.1    Pas, J.2    Wyrwicz, L.S.3    Bujnicki, J.M.4
  • 28
    • 0036948994 scopus 로고    scopus 로고
    • X-linked mental retardation: Vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms
    • Frints SG, Froyen G, Marynen P, Fryns JP. 2002. X-linked mental retardation: Vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms. Clin Genet 62(6):423-432.
    • (2002) Clin Genet , vol.62 , Issue.6 , pp. 423-432
    • Frints, S.G.1    Froyen, G.2    Marynen, P.3    Fryns, J.P.4
  • 30
    • 0030137717 scopus 로고    scopus 로고
    • Identification of the gene FMR2, associated with FRAXE mental retardation
    • Gecz J, Gedeon A, Sutherland G, Mulley J. 1996. Identification of the gene FMR2, associated with FRAXE mental retardation. Nat Genet 13(1):105-108.
    • (1996) Nat Genet , vol.13 , Issue.1 , pp. 105-108
    • Gecz, J.1    Gedeon, A.2    Sutherland, G.3    Mulley, J.4
  • 31
    • 0033237655 scopus 로고    scopus 로고
    • Signals from the AT2 (angiotensin type 2) receptor of angiotensin II inhibit p21 ras and activate MAPK (mitogen activated protein kinase) to induce morphological neuronal differentiation in NG108-15 cells
    • Gendron L, Laflamme L, Rivard N, Asselin C, Payet M, Gallo-Payet N. 1999. Signals from the AT2 (angiotensin type 2) receptor of angiotensin II inhibit p21 ras and activate MAPK (mitogen activated protein kinase) to induce morphological neuronal differentiation in NG108-15 cells. Mol Endocrinol 13:1615-1626.
    • (1999) Mol Endocrinol , vol.13 , pp. 1615-1626
    • Gendron, L.1    Laflamme, L.2    Rivard, N.3    Asselin, C.4    Payet, M.5    Gallo-Payet, N.6
  • 32
    • 0030138905 scopus 로고    scopus 로고
    • Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island
    • Gu Y, Shen Y, Gibbs R, Nelson D. 1996. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island. Nat Genet 13(1):109-113.
    • (1996) Nat Genet , vol.13 , Issue.1 , pp. 109-113
    • Gu, Y.1    Shen, Y.2    Gibbs, R.3    Nelson, D.4
  • 33
    • 0032559362 scopus 로고    scopus 로고
    • Rho GTPases and the actin cytoskeleton
    • Hall A. 1998. Rho GTPases and the actin cytoskeleton. Science 279(5350):509-514.
    • (1998) Science , vol.279 , Issue.5350 , pp. 509-514
    • Hall, A.1
  • 34
    • 0035047263 scopus 로고    scopus 로고
    • Fragile XE-associated familial mental retardation protein 2 (FMR2) acts as a potent transcription activator
    • Hillman MA, Gecz J. 2001. Fragile XE-associated familial mental retardation protein 2 (FMR2) acts as a potent transcription activator. J Hum Genet 46(5): 251-259.
    • (2001) J Hum Genet , vol.46 , Issue.5 , pp. 251-259
    • Hillman, M.A.1    Gecz, J.2
  • 37
    • 0032488855 scopus 로고    scopus 로고
    • Eukaryotic transcription: An interlaced network of transcription factors and chromatin-modifying machines
    • Kadonaga JT. 1998. Eukaryotic transcription: An interlaced network of transcription factors and chromatin-modifying machines. Cell 92(3):307-313.
    • (1998) Cell , vol.92 , Issue.3 , pp. 307-313
    • Kadonaga, J.T.1
  • 40
    • 0029963657 scopus 로고    scopus 로고
    • Synaptic activity and the construction of cortical circuits
    • Katz LC, Shatz CJ. 1996. Synaptic activity and the construction of cortical circuits. Science 274(5290):1133-1138.
    • (1996) Science , vol.274 , Issue.5290 , pp. 1133-1138
    • Katz, L.C.1    Shatz, C.J.2
  • 44
    • 12144288873 scopus 로고    scopus 로고
    • Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly
    • Lenski C, Abidi F, Meindl A, Gibson A, Platzer M, Frank Kooy R, Lubs HA, Stevenson RE, Ramser J, Schwartz CE. 2004. Novel truncating mutations in the polyglutamine tract binding protein 1 gene (PQBP1) cause Renpenning syndrome and X-linked mental retardation in another family with microcephaly. Am J Hum Genet 74(4):777-780.
    • (2004) Am J Hum Genet , vol.74 , Issue.4 , pp. 777-780
    • Lenski, C.1    Abidi, F.2    Meindl, A.3    Gibson, A.4    Platzer, M.5    Frank Kooy, R.6    Lubs, H.A.7    Stevenson, R.E.8    Ramser, J.9    Schwartz, C.E.10
  • 45
    • 0037238316 scopus 로고    scopus 로고
    • A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: Proposal of a rapid enzymatic assay for screening mentally retarded patients
    • Longo I, Frints SG, Fryns JP, Meloni I, Pescucci C, Ariani F, Borghgraef M, Raynaud M, Marynen P, Schwartz C, Renieri A, Froyen G. 2003. A third MRX family (MRX68) is the result of mutation in the long chain fatty acid-CoA ligase 4 (FACL4) gene: Proposal of a rapid enzymatic assay for screening mentally retarded patients. J Med Genet 40(1):11-17.
    • (2003) J Med Genet , vol.40 , Issue.1 , pp. 11-17
    • Longo, I.1    Frints, S.G.2    Fryns, J.P.3    Meloni, I.4    Pescucci, C.5    Ariani, F.6    Borghgraef, M.7    Raynaud, M.8    Marynen, P.9    Schwartz, C.10    Renieri, A.11    Froyen, G.12
  • 46
    • 0032541392 scopus 로고    scopus 로고
    • The angiotensin II type 2 (AT2) receptor promotes axonal regeneration in the optic nerve of adult rats
    • Lucius R, Gallinat S, Rosenstiel P, Herdegen T, Sievers J, Unger T. 1998. The angiotensin II type 2 (AT2) receptor promotes axonal regeneration in the optic nerve of adult rats. J Exp Med 188(4):661-670.
    • (1998) J Exp Med , vol.188 , Issue.4 , pp. 661-670
    • Lucius, R.1    Gallinat, S.2    Rosenstiel, P.3    Herdegen, T.4    Sievers, J.5    Unger, T.6
  • 47
    • 0034574572 scopus 로고    scopus 로고
    • Rho GTPases in neuronal morphogenesis
    • Luo L. 2000. Rho GTPases in neuronal morphogenesis. Nat Rev Neurosci 1(3): 173-180.
    • (2000) Nat Rev Neurosci , vol.1 , Issue.3 , pp. 173-180
    • Luo, L.1
  • 50
    • 0034721711 scopus 로고    scopus 로고
    • Actin-based plasticity in dendritic spines
    • Matus A. 2000. Actin-based plasticity in dendritic spines. Science 290(5492):754-758.
    • (2000) Science , vol.290 , Issue.5492 , pp. 754-758
    • Matus, A.1
  • 55
    • 0034813107 scopus 로고    scopus 로고
    • Mitogen-regulated RSK2-CBP interaction controls their kinase and acetylase activities
    • Merienne K, Pannetier S, Harel-Bellan A, Sassone-Corsi P. 2001. Mitogen-regulated RSK2-CBP interaction controls their kinase and acetylase activities. Mol Cell Biol 21(20):7089-7096.
    • (2001) Mol Cell Biol , vol.21 , Issue.20 , pp. 7089-7096
    • Merienne, K.1    Pannetier, S.2    Harel-Bellan, A.3    Sassone-Corsi, P.4
  • 57
    • 0026683988 scopus 로고
    • Nomenclature guidelines for X-linked mental retardation
    • Mulley JC, Kerr B, Stevenson R, Lubs H. 1992. Nomenclature guidelines for X-linked mental retardation. Am J Med Genet 43(1-2):383-391.
    • (1992) Am J Med Genet , vol.43 , Issue.1-2 , pp. 383-391
    • Mulley, J.C.1    Kerr, B.2    Stevenson, R.3    Lubs, H.4
  • 58
    • 0032616816 scopus 로고    scopus 로고
    • X-linked mental retardation
    • Neri G, Chiurazzi P. 1999. X-linked mental retardation. Adv Genet 41:55-94.
    • (1999) Adv Genet , vol.41 , pp. 55-94
    • Neri, G.1    Chiurazzi, P.2
  • 59
    • 0030860083 scopus 로고    scopus 로고
    • The diversity of Rab proteins in vesicle transport
    • Novick P, Zerial M. 1997. The diversity of Rab proteins in vesicle transport. Curr Opin Cell Biol 9(4):496-504.
    • (1997) Curr Opin Cell Biol , vol.9 , Issue.4 , pp. 496-504
    • Novick, P.1    Zerial, M.2
  • 61
    • 0035504082 scopus 로고    scopus 로고
    • PQBP-1 (Np/PQ): A polyglutamine tract-binding and nuclear inclusion-forming protein
    • Okazawa H, Sudol M, Rich T. 2001. PQBP-1 (Np/PQ): A polyglutamine tract-binding and nuclear inclusion-forming protein. Brain Res Bull 56(3-4):273-280.
    • (2001) Brain Res Bull , vol.56 , Issue.3-4 , pp. 273-280
    • Okazawa, H.1    Sudol, M.2    Rich, T.3
  • 64
  • 65
    • 0016251748 scopus 로고
    • Dendritic spine "dysgenesis" and mental retardation
    • Purpura DP. 1974. Dendritic spine "dysgenesis" and mental retardation. Science 186(4169):1126-1128.
    • (1974) Science , vol.186 , Issue.4169 , pp. 1126-1128
    • Purpura, D.P.1
  • 66
    • 0036543312 scopus 로고    scopus 로고
    • Rho proteins, mental retardation and the cellular basis of cognition
    • Ramakers GJ. 2002. Rho proteins, mental retardation and the cellular basis of cognition. Trends Neurosci 25(4):191-199.
    • (2002) Trends Neurosci , vol.25 , Issue.4 , pp. 191-199
    • Ramakers, G.J.1
  • 67
    • 4444382164 scopus 로고    scopus 로고
    • A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9)
    • Ramser J, Winnepenninckx B, Lenski C, Errijgers V, Platzer M, Schwartz CE, Meindl A, Kooy RF. 2004. A splice site mutation in the methyltransferase gene FTSJ1 in Xp11.23 is associated with non-syndromic mental retardation in a large Belgian family (MRX9). J Med Genet 41(9):679-683.
    • (2004) J Med Genet , vol.41 , Issue.9 , pp. 679-683
    • Ramser, J.1    Winnepenninckx, B.2    Lenski, C.3    Errijgers, V.4    Platzer, M.5    Schwartz, C.E.6    Meindl, A.7    Kooy, R.F.8
  • 68
  • 69
    • 0032768843 scopus 로고    scopus 로고
    • Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41
    • Rosati M, Franze A, Matarazzo MR, Grimaldi G. 1999. Coding region intron/exon organization, alternative splicing, and X-chromosome inactivation of the KRAB/FPB-domain-containing human zinc finger gene ZNF41. Cytogenet Cell Genet 85(3-4):291-296.
    • (1999) Cytogenet Cell Genet , vol.85 , Issue.3-4 , pp. 291-296
    • Rosati, M.1    Franze, A.2    Matarazzo, M.R.3    Grimaldi, G.4
  • 71
    • 0036009738 scopus 로고    scopus 로고
    • Angiotensin AT2 receptor ligands: Do they have potential as future treatments for neurological disease?
    • Rosenstiel P, Gallinat S, Arlt A, Unger T, Sievers J, Lucius R. 2002. Angiotensin AT2 receptor ligands: Do they have potential as future treatments for neurological disease? CNS Drugs 16:145-153.
    • (2002) CNS Drugs , vol.16 , pp. 145-153
    • Rosenstiel, P.1    Gallinat, S.2    Arlt, A.3    Unger, T.4    Sievers, J.5    Lucius, R.6
  • 74
    • 0037523396 scopus 로고    scopus 로고
    • CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein
    • Schenck A, Bardoni B, Langmann C, Harden N, Mandel JL, Giangrande A. 2003. CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein. Neuron 38(6):887-898.
    • (2003) Neuron , vol.38 , Issue.6 , pp. 887-898
    • Schenck, A.1    Bardoni, B.2    Langmann, C.3    Harden, N.4    Mandel, J.L.5    Giangrande, A.6
  • 75
    • 0035118229 scopus 로고    scopus 로고
    • Targeting histone deacetylase complexes via KRAB-zinc finger proteins: The PHD and bromodomains of KAP-1 form a cooperative unit that recruits a novel isoform of the Mi-2alpha subunit of NuRD
    • Schultz DC, Friedman JR, Rauscher FJ IIIrd. 2001. Targeting histone deacetylase complexes via KRAB-zinc finger proteins: The PHD and bromodomains of KAP-1 form a cooperative unit that recruits a novel isoform of the Mi-2alpha subunit of NuRD. Genes Dev 15(4):428-443.
    • (2001) Genes Dev , vol.15 , Issue.4 , pp. 428-443
    • Schultz, D.C.1    Friedman, J.R.2    Rauscher III, F.J.3
  • 76
    • 0031763366 scopus 로고    scopus 로고
    • Factors regulating the transcriptional elongation activity of RNA polymerase II
    • Shilatifard A. 1998. Factors regulating the transcriptional elongation activity of RNA polymerase II. Faseb J 12(14):1437-1446.
    • (1998) Faseb J , vol.12 , Issue.14 , pp. 1437-1446
    • Shilatifard, A.1
  • 81
    • 2542433290 scopus 로고    scopus 로고
    • Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations
    • Traynor J, Agarwal P, Lazzeroni L, Francke U. 2002. Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations. BMC Med Genet 3(1):12.
    • (2002) BMC Med Genet , vol.3 , Issue.1 , pp. 12
    • Traynor, J.1    Agarwal, P.2    Lazzeroni, L.3    Francke, U.4
  • 83
    • 0037180492 scopus 로고    scopus 로고
    • Transcriptional profiling of a mouse model for Rett syndrome reveals subtle transcriptional changes in the brain
    • Tudor M, Akbarian S, Chen RZ, 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(24):15536-15541.
    • (2002) Proc Natl Acad Sci USA , vol.99 , Issue.24 , pp. 15536-15541
    • Tudor, M.1    Akbarian, S.2    Chen, R.Z.3    Jaenisch, R.4
  • 84
    • 0016248119 scopus 로고
    • X-linked mental retardation
    • Turner G, Turner B. 1974. X-linked mental retardation. J Med Genet 11(2):109-113.
    • (1974) J Med Genet , vol.11 , Issue.2 , pp. 109-113
    • Turner, G.1    Turner, B.2
  • 85
    • 0035876746 scopus 로고    scopus 로고
    • Genetic deletion of angiotensin AT2 receptor leads to increased cell numbers in different brain structures
    • Van Bohlen O, Walther T, Bader M, Albrecht D. 2001. Genetic deletion of angiotensin AT2 receptor leads to increased cell numbers in different brain structures. Regul Pept 99:209-216.
    • (2001) Regul Pept , vol.99 , pp. 209-216
    • Van Bohlen, O.1    Walther, T.2    Bader, M.3    Albrecht, D.4
  • 86
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
    • Verkerk A, Piretti M, Sutcliffe J, Fu Y, Kuhl D, Pizzuti A, Reiner O. 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.1    Piretti, M.2    Sutcliffe, J.3    Fu, Y.4    Kuhl, D.5    Pizzuti, A.6    Reiner, O.7
  • 88
    • 0036078163 scopus 로고    scopus 로고
    • Alpha-thalassemia/mental retardation syndrome, X-linked (ATR-X, MIM#301040, ATR-X/XNP/XH2 gene MIM#300032)
    • Villard L, Fontes M. 2002. Alpha-thalassemia/mental retardation syndrome, X-linked (ATR-X, MIM#301040, ATR-X/XNP/XH2 gene MIM#300032). Eur J Hum Genet 10:223-225.
    • (2002) Eur J Hum Genet , vol.10 , pp. 223-225
    • Villard, L.1    Fontes, M.2
  • 89
    • 0028017704 scopus 로고
    • Creatine kinase in non-muscle tissues and cells
    • Wallimann T, Hemmer W. 1994. Creatine kinase in non-muscle tissues and cells. Mol Cell Biochem 133(134):193-220.
    • (1994) Mol Cell Biochem , vol.133 , Issue.134 , pp. 193-220
    • Wallimann, T.1    Hemmer, W.2
  • 90
    • 0034142085 scopus 로고    scopus 로고
    • Is CREB a key to neuronal survival?
    • Walton M, Dragunow M. 2000. Is CREB a key to neuronal survival? Trends Neurosci 23:48-53.
    • (2000) Trends Neurosci , vol.23 , pp. 48-53
    • Walton, M.1    Dragunow, M.2
  • 91
    • 0031916187 scopus 로고    scopus 로고
    • Arginine kinase expression and localization in growth cone migration
    • Wang YE, Esbensen P, Bentley D. 1998. Arginine kinase expression and localization in growth cone migration. J Neurosci 18(3):987-998.
    • (1998) J Neurosci , vol.18 , Issue.3 , pp. 987-998
    • Wang, Y.E.1    Esbensen, P.2    Bentley, D.3
  • 93
    • 0035097553 scopus 로고    scopus 로고
    • Lilliputian: An AF4/FMR2-related protein that controls cell identity and cell growth
    • Wittwer F, van der Straten A, Keleman K, Dickson BJ, Hafen E. 2001. Lilliputian: An AF4/FMR2-related protein that controls cell identity and cell growth. Development 128(5):791-800.
    • (2001) Development , vol.128 , Issue.5 , pp. 791-800
    • Wittwer, F.1    Van Der Straten, A.2    Keleman, K.3    Dickson, B.J.4    Hafen, E.5
  • 94
    • 0030446448 scopus 로고    scopus 로고
    • Structural insights into the function of the Rab GDI superfamily
    • Wu SK, Zeng K, Wilson IA, Balch WE. 1996. Structural insights into the function of the Rab GDI superfamily. Trends Biochem Sci 21(12):472-476.
    • (1996) Trends Biochem Sci , vol.21 , Issue.12 , pp. 472-476
    • Wu, S.K.1    Zeng, K.2    Wilson, I.A.3    Balch, W.E.4
  • 95
    • 0141703327 scopus 로고    scopus 로고
    • The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies
    • Xue Y, Gibbons R, Yan Z, Yang D, McDowell TL, Sechi S, Qin J, Zhou S, Higgs D, Wang W. 2003. The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies. Proc Natl Acad Sci USA 100(19): 10635-10640.
    • (2003) Proc Natl Acad Sci USA , vol.100 , Issue.19 , pp. 10635-10640
    • Xue, Y.1    Gibbons, R.2    Yan, Z.3    Yang, D.4    McDowell, T.L.5    Sechi, S.6    Qin, J.7    Zhou, S.8    Higgs, D.9    Wang, W.10
  • 96
    • 2142809686 scopus 로고    scopus 로고
    • Acetylation of nuclear factor-kappaB in rat amygdala improves long-term but not short-term retention of fear memory
    • Yeh SH, Lin CH, Gean PW. 2004. Acetylation of nuclear factor-kappaB in rat amygdala improves long-term but not short-term retention of fear memory. Mol Pharmacol 65(5):1286-1292.
    • (2004) Mol Pharmacol , vol.65 , Issue.5 , pp. 1286-1292
    • Yeh, S.H.1    Lin, C.H.2    Gean, P.W.3
  • 100
    • 0035577350 scopus 로고    scopus 로고
    • A high density of X-linked genes for general cognitive ability: A run-away process shaping human evolution?
    • Zechner U, Wilda M, Kehre-Sawatzki H, Vogel W, Fundele R, Hameister H. 2001. A high density of X-linked genes for general cognitive ability: A run-away process shaping human evolution? TRENDS in Genetics 17(12):697-701.
    • (2001) TRENDS in Genetics , vol.17 , Issue.12 , pp. 697-701
    • Zechner, U.1    Wilda, M.2    Kehre-Sawatzki, H.3    Vogel, W.4    Fundele, R.5    Hameister, H.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.