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Volumn 122, Issue 11, 1999, Pages 2015-2031

The genetic basis of cognition

Author keywords

Cognition; Genetics; Learning; Memory; Mental retardation

Indexed keywords

BEHAVIOR; CHROMOSOME ABERRATION; COGNITION; COGNITIVE DEFECT; DYSLEXIA; GENE FUNCTION; GENE MUTATION; GENETIC DISORDER; GENETIC ENGINEERING; GENETICS; HUMAN; INTELLIGENCE QUOTIENT; LANGUAGE DISABILITY; LEARNING; MEMORY; MENTAL DEFICIENCY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; REVIEW; SIGNAL TRANSDUCTION;

EID: 0032721892     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/122.11.2015     Document Type: Review
Times cited : (60)

References (196)
  • 1
    • 0032535968 scopus 로고    scopus 로고
    • Memory suppressor genes: Inhibitory constraints on the storage of long-term memory
    • Abel T, Martin KC, Bartsch D, Kandel ER. Memory suppressor genes: inhibitory constraints on the storage of long-term memory. [Review]. Science 1998; 279: 338-41.
    • (1998) Science , vol.279 , pp. 338-341
    • Abel, T.1    Martin, K.C.2    Bartsch, D.3    Kandel, E.R.4
  • 4
    • 0023937052 scopus 로고
    • Serial position memory of boys with Duchenne muscular dystrophy
    • Anderson SW, Routh DK, Ionasescu VV. Serial position memory of boys with Duchenne muscular dystrophy. Dev Med Child Neurol 1988; 30: 328-33.
    • (1988) Dev Med Child Neurol , vol.30 , pp. 328-333
    • Anderson, S.W.1    Routh, D.K.2    Ionasescu, V.V.3
  • 5
    • 0027538548 scopus 로고
    • Structural changes accompanying memory storage
    • Bailey CH, Kandel ER. Structural changes accompanying memory storage. [Review]. Annu Rev Physiol 1993; 55: 397-426.
    • (1993) Annu Rev Physiol , vol.55 , pp. 397-426
    • Bailey, C.H.1    Kandel, E.R.2
  • 6
    • 0030450763 scopus 로고    scopus 로고
    • Toward a molecular definition of long-term memory storage
    • Bailey CH, Bartsch D, Kandel ER. Toward a molecular definition of long-term memory storage. [Review]. Proc Natl Acad Sci USA 1996; 93: 13445-52.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 13445-13452
    • Bailey, C.H.1    Bartsch, D.2    Kandel, E.R.3
  • 7
    • 0032538271 scopus 로고    scopus 로고
    • CREB1 encodes a nuclear activator, a represser, and a cytoplasmic modulator that form a regulatory unit critical for long-term facilitation
    • Bartsch D, Casadio A, Karl KA, Serodio P, Kandel ER. CREB1 encodes a nuclear activator, a represser, and a cytoplasmic modulator that form a regulatory unit critical for long-term facilitation. Cell 1998; 95: 211-23.
    • (1998) Cell , vol.95 , pp. 211-223
    • Bartsch, D.1    Casadio, A.2    Karl, K.A.3    Serodio, P.4    Kandel, E.R.5
  • 8
    • 0025137740 scopus 로고
    • Neuropsychological, neurological, and neuroanatomical profile of Williams syndrome
    • Bellugi U, Bihrle A, Jernigan T, Trauner D, Doherty S. Neuropsychological, neurological, and neuroanatomical profile of Williams syndrome. Am J Med Genet 1990; Suppl 6: 115-25.
    • (1990) Am J Med Genet , Issue.6 SUPPL. , pp. 115-125
    • Bellugi, U.1    Bihrle, A.2    Jernigan, T.3    Trauner, D.4    Doherty, S.5
  • 9
    • 0027095821 scopus 로고
    • Cognitive functions in Duchenne muscular dystrophy: A reappraisal and comparison with spinal muscular atrophy
    • Billard C, Gillet P, Signoret JL, Uicaut E, Bertrand P, Fardeau M, et al. Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophy. Neuromusc Disord 1992; 2: 371-8.
    • (1992) Neuromusc Disord , vol.2 , pp. 371-378
    • Billard, C.1    Gillet, P.2    Signoret, J.L.3    Uicaut, E.4    Bertrand, P.5    Fardeau, M.6
  • 10
    • 0031974681 scopus 로고    scopus 로고
    • Reading ability and processing in Duchenne muscular dystrophy and spinal muscular atrophy
    • Billard C, Gillet P, Barthez MA, Hommet C, Bertrand P. Reading ability and processing in Duchenne muscular dystrophy and spinal muscular atrophy. Dev Med Child Neurol 1998; 40: 12-20.
    • (1998) Dev Med Child Neurol , vol.40 , pp. 12-20
    • Billard, C.1    Gillet, P.2    Barthez, M.A.3    Hommet, C.4    Bertrand, P.5
  • 11
    • 0032580161 scopus 로고    scopus 로고
    • Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation
    • Billuart P, Bienvenu T, Ronce N, des Portes V, Vinet MC, Zemni R, et al. Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation. Nature 1998; 392: 923-6.
    • (1998) Nature , vol.392 , pp. 923-926
    • Billuart, P.1    Bienvenu, T.2    Ronce, N.3    Des Portes, V.4    Vinet, M.C.5    Zemni, R.6
  • 12
    • 0028872434 scopus 로고
    • Genetic basis of specific language impairment: Evidence from a twin study
    • Bishop DV, North T, Donlan C. Genetic basis of specific language impairment: evidence from a twin study. Dev Med Child Neurol 1995; 37: 56-71.
    • (1995) Dev Med Child Neurol , vol.37 , pp. 56-71
    • Bishop, D.V.1    North, T.2    Donlan, C.3
  • 13
    • 0029980672 scopus 로고    scopus 로고
    • Targeting of the CREB gene leads to up-regulation of a novel CREB mRNA isoform
    • Blendy JA, Kaestner KH, Schmid W, Gass P, Schutz G. Targeting of the CREB gene leads to up-regulation of a novel CREB mRNA isoform. EMBO J 1996; 15: 1098-106.
    • (1996) EMBO J , vol.15 , pp. 1098-1106
    • Blendy, J.A.1    Kaestner, K.H.2    Schmid, W.3    Gass, P.4    Schutz, G.5
  • 14
    • 0027476024 scopus 로고
    • A synaptic model of memory: Long-term potentiation in the hippocampus
    • Bliss TV, Collingridge GL. A synaptic model of memory: long-term potentiation in the hippocampus. [Review]. Nature 1993; 361: 31-9.
    • (1993) Nature , vol.361 , pp. 31-39
    • Bliss, T.V.1    Collingridge, G.L.2
  • 15
    • 2642611921 scopus 로고    scopus 로고
    • Genetic and environmental influences on adult intelligence and special mental abilities
    • Bouchard TJ Jr. Genetic and environmental influences on adult intelligence and special mental abilities. [Review], Hum Biol 1998; 70: 257-79.
    • (1998) Hum Biol , vol.70 , pp. 257-279
    • Bouchard T.J., Jr.1
  • 16
    • 0028071507 scopus 로고
    • Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein
    • Bourtchuladze R, Frenguelli B, Blendy J, Cioffi D, Schutz G, Silva AJ. Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein. Cell 1994; 79: 59-68.
    • (1994) Cell , vol.79 , pp. 59-68
    • Bourtchuladze, R.1    Frenguelli, B.2    Blendy, J.3    Cioffi, D.4    Schutz, G.5    Silva, A.J.6
  • 17
    • 0002193261 scopus 로고
    • Theoretical links among naming speed, precise timing mechanisms and orthographic skill in dyslexia
    • Bowers PG, Wolf M. Theoretical links among naming speed, precise timing mechanisms and orthographic skill in dyslexia. Reading Writing 1993; 5: 69-85.
    • (1993) Reading Writing , vol.5 , pp. 69-85
    • Bowers, P.G.1    Wolf, M.2
  • 18
    • 0020700815 scopus 로고
    • Categorizing sounds and learning to read -a causal connection
    • Bradley L, Bryant PE. Categorizing sounds and learning to read -a causal connection. Nature 1983; 301: 419-21.
    • (1983) Nature , vol.301 , pp. 419-421
    • Bradley, L.1    Bryant, P.E.2
  • 20
    • 0026846986 scopus 로고
    • The CREB family of transcription activators
    • Brindle PK, Montminy MR. The CREB family of transcription activators. Curr Opin Genet Dev 1992; 2: 199-204.
    • (1992) Curr Opin Genet Dev , vol.2 , pp. 199-204
    • Brindle, P.K.1    Montminy, M.R.2
  • 21
    • 0030756674 scopus 로고    scopus 로고
    • Progress in the autosomal segmental aneusomy syndromes (SASs): Single or multi-locus disorders?
    • Budarf ML, Emanuel BS. Progress in the autosomal segmental aneusomy syndromes (SASs): single or multi-locus disorders? [Review]. Hum Mol Genet 1997; 6: 1657-65.
    • (1997) Hum Mol Genet , vol.6 , pp. 1657-1665
    • Budarf, M.L.1    Emanuel, B.S.2
  • 22
    • 0022521057 scopus 로고
    • Williams syndrome
    • Burn J. Williams syndrome. [Review]. J Med Genet 1986; 23: 389-95.
    • (1986) J Med Genet , vol.23 , pp. 389-395
    • Burn, J.1
  • 24
    • 0030065380 scopus 로고    scopus 로고
    • Presynaptic facilitation revisited: State and time dependence
    • Byrne JH, Kandel ER. Presynaptic facilitation revisited: state and time dependence. J Neurosci 1996; 16: 425-35.
    • (1996) J Neurosci , vol.16 , pp. 425-435
    • Byrne, J.H.1    Kandel, E.R.2
  • 26
    • 0029076876 scopus 로고
    • Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, DeFries JC. Quantitative trait locus for reading disability on chromosome 6 [see comments]. Science 1994; 266: 276-9. Comment in: Science 1995; 268: 786-8.
    • (1995) Science , vol.268 , pp. 786-788
  • 27
    • 0032568517 scopus 로고    scopus 로고
    • Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human Huntington disease gene
    • Cha J-H, Kosinski CM, Kerner JA, Alsdorf SA, Mangiarini L, Davies SW, et al. Altered brain neurotransmitter receptors in transgenic mice expressing a portion of an abnormal human Huntington disease gene. Proc Natl Acad Sci USA 1998; 95: 6480-5.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 6480-6485
    • Cha, J.-H.1    Kosinski, C.M.2    Kerner, J.A.3    Alsdorf, S.A.4    Mangiarini, L.5    Davies, S.W.6
  • 28
    • 0028114735 scopus 로고
    • Abnormal fear response and aggressive behavior in mutant mice deficient for alpha-calcium-calmodulin kinase II
    • Chen C, Rainnie DG, Greene RW, Tonegawa S. Abnormal fear response and aggressive behavior in mutant mice deficient for alpha-calcium-calmodulin kinase II [see comments]. Science 1994; 266: 291-4. Comment in: Science 1995; 267: 437.
    • (1994) Science , vol.266 , pp. 291-294
    • Chen, C.1    Rainnie, D.G.2    Greene, R.W.3    Tonegawa, S.4
  • 29
    • 0028908519 scopus 로고
    • Chen C, Rainnie DG, Greene RW, Tonegawa S. Abnormal fear response and aggressive behavior in mutant mice deficient for alpha-calcium-calmodulin kinase II [see comments]. Science 1994; 266: 291-4. Comment in: Science 1995; 267: 437.
    • (1995) Science , vol.267 , pp. 437
  • 30
    • 0009703087 scopus 로고    scopus 로고
    • Behavioral phenotypes of inbred mouse strains: Implications and recommendations for molecular studies
    • Berl
    • Crawley JN, Belknap JK, Collins A, Crabbe JC, Frankel W, Henderson N, et al. Behavioral phenotypes of inbred mouse strains: implications and recommendations for molecular studies. [Review]. Psychopharmacology (Berl) 1997; 132: 107-24.
    • (1997) Psychopharmacology , vol.132 , pp. 107-124
    • Crawley, J.N.1    Belknap, J.K.2    Collins, A.3    Crabbe, J.C.4    Frankel, W.5    Henderson, N.6
  • 31
  • 32
    • 17344369362 scopus 로고    scopus 로고
    • Mutations in GDI1 are responsible for X-linked non-specific mental retardation
    • published erratum appears in Nat Genet 1998; 19: 303
    • D'Adamo P, Menegon A, Lo Nigro C, Grasso M, Gulisano M, Tamanini F, et al. Mutations in GDI1 are responsible for X-linked non-specific mental retardation [see comments] [published erratum appears in Nat Genet 1998; 19: 303]. Nat Genet 1998; 19: 4-139. Comment in: Nat Genet 1998; 19: 106-8.
    • (1998) Nat Genet , vol.19 , pp. 4-139
    • D'Adamo, P.1    Menegon, A.2    Lo Nigro, C.3    Grasso, M.4    Gulisano, M.5    Tamanini, F.6
  • 33
    • 0031865393 scopus 로고    scopus 로고
    • D'Adamo P, Menegon A, Lo Nigro C, Grasso M, Gulisano M, Tamanini F, et al. Mutations in GDI1 are responsible for X-linked non-specific mental retardation [see comments] [published erratum appears in Nat Genet 1998; 19: 303]. Nat Genet 1998; 19: 4-139. Comment in: Nat Genet 1998; 19: 106-8.
    • (1998) Nat Genet , vol.19 , pp. 106-108
  • 34
    • 18544410106 scopus 로고    scopus 로고
    • Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
    • Davies SW, Turmaine M, Cozens BA, DiFiglia M, Shar AH, Ross CA, et al. Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation. Cell 1997; 90: 537-48.
    • (1997) Cell , vol.90 , pp. 537-548
    • Davies, S.W.1    Turmaine, M.2    Cozens, B.A.3    DiFiglia, M.4    Shar, A.H.5    Ross, C.A.6
  • 35
    • 0025896771 scopus 로고
    • The Drosophila dunce locus: Learning and memory genes in the fly
    • Davis RL, Dauwalder B. The Drosophila dunce locus: learning and memory genes in the fly. [Review], Trends Genet 1991; 7: 224-9.
    • (1991) Trends Genet , vol.7 , pp. 224-229
    • Davis, R.L.1    Dauwalder, B.2
  • 36
    • 0029815737 scopus 로고    scopus 로고
    • Expression of Drosophila mushroom body mutations in alternative genetic backgrounds: A case study of the mushroom body miniature gene (mbm)
    • de Belle JS, Heisenberg M. Expression of Drosophila mushroom body mutations in alternative genetic backgrounds: a case study of the mushroom body miniature gene (mbm). Proc Natl Acad Sci USA 1996; 93: 9875-80.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 9875-9880
    • De Belle, J.S.1    Heisenberg, M.2
  • 37
    • 0030855087 scopus 로고    scopus 로고
    • The heritability of IQ
    • Devlin B, Daniels M, Roeder K. The heritability of IQ [see comments]. Nature 1997; 388: 468-71. Comment in: Nature 1997; 388: 417-8.
    • (1997) Nature , vol.388 , pp. 468-471
    • Devlin, B.1    Daniels, M.2    Roeder, K.3
  • 38
    • 0030752338 scopus 로고    scopus 로고
    • Devlin B, Daniels M, Roeder K. The heritability of IQ [see comments]. Nature 1997; 388: 468-71. Comment in: Nature 1997; 388: 417-8.
    • (1997) Nature , vol.388 , pp. 417-418
  • 39
    • 0023918408 scopus 로고
    • Language and learning disorders of older boys with Duchenne muscular dystrophy
    • Dorman C, Hurley AD, D'Avignon J. Language and learning disorders of older boys with Duchenne muscular dystrophy. Dev Med Child Neurol 1988; 30: 316-27.
    • (1988) Dev Med Child Neurol , vol.30 , pp. 316-327
    • Dorman, C.1    Hurley, A.D.2    D'Avignon, J.3
  • 40
    • 0028246435 scopus 로고
    • Dutch-Belgian Fragile X Consortium. Fmr1 knockout mice: A model to study fragile X mental retardation
    • Dutch-Belgian Fragile X Consortium. Fmr1 knockout mice: a model to study fragile X mental retardation. Cell 1994; 78: 23-33.
    • (1994) Cell , vol.78 , pp. 23-33
  • 42
    • 0028879267 scopus 로고
    • Spatial learning. The LTP memory connection
    • Eichenbaum H. Spatial learning. The LTP memory connection [news]. Nature 1995; 378: 131-2.
    • (1995) Nature , vol.378 , pp. 131-132
    • Eichenbaum, H.1
  • 43
    • 0030738460 scopus 로고    scopus 로고
    • Behavioral and emotional disturbance in individuals with Williams syndrome
    • Einfeld SL, Tonge BJ, FIorio T. Behavioral and emotional disturbance in individuals with Williams syndrome. Am J Ment Retard 1997; 102: 45-53.
    • (1997) Am J Ment Retard , vol.102 , pp. 45-53
    • Einfeld, S.L.1    Tonge, B.J.2    Fiorio, T.3
  • 44
    • 0027185655 scopus 로고
    • Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
    • Ewart AK, Morris CA, Atkinson D, Jin W, Sternes K, Spallone P, et al. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nat Genet 1993; 5: 11-6.
    • (1993) Nat Genet , vol.5 , pp. 11-16
    • Ewart, A.K.1    Morris, C.A.2    Atkinson, D.3    Jin, W.4    Sternes, K.5    Spallone, P.6
  • 45
    • 0031310667 scopus 로고    scopus 로고
    • FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association
    • Feng Y, Absher D, Eberhart DE, Brown V, Malter HE, Warren ST. FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association. Mol Cell 1997a; 1: 109-18.
    • (1997) Mol Cell , vol.1 , pp. 109-118
    • Feng, Y.1    Absher, D.2    Eberhart, D.E.3    Brown, V.4    Malter, H.E.5    Warren, S.T.6
  • 46
    • 0031046778 scopus 로고    scopus 로고
    • Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes
    • Feng Y, Gutekunst CA, Eberhart DE, Yi H, Warren ST, Hersch SM. Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes. J Neurosci 1997b; 17: 1539-47.
    • (1997) J Neurosci , vol.17 , pp. 1539-1547
    • Feng, Y.1    Gutekunst, C.A.2    Eberhart, D.E.3    Yi, H.4    Warren, S.T.5    Hersch, S.M.6
  • 47
    • 0033366739 scopus 로고    scopus 로고
    • A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia
    • W
    • Fisher SE, Marlow AJ, Lamb J, Maestrini E, Williams DF, W, Richardson AJ, et al. A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia. Am J Hum Genet 1999; 64: 146-56.
    • (1999) Am J Hum Genet , vol.64 , pp. 146-156
    • Fisher, S.E.1    Marlow, A.J.2    Lamb, J.3    Maestrini, E.4    Williams, D.F.5    Richardson, A.J.6
  • 48
    • 0029991349 scopus 로고    scopus 로고
    • Annotation: Behavioural phenotypes: A window onto the biology of behaviour
    • Flint J. Annotation: behavioural phenotypes: a window onto the biology of behaviour. [Review]. J Child Psychol Psychiatry 1996; 37: 355-67.
    • (1996) J Child Psychol Psychiatry , vol.37 , pp. 355-367
    • Flint, J.1
  • 52
    • 0030137717 scopus 로고    scopus 로고
    • Identification of the gene FMR2, associated with FRAXE mental retardation
    • Gecz J. Gedeon AK, Sutherland GR, Mulley JC. Identification of the gene FMR2, associated with FRAXE mental retardation. Nat Genet 1996; 13: 105-8.
    • (1996) Nat Genet , vol.13 , pp. 105-108
    • Gecz, J.1    Gedeon, A.K.2    Sutherland, G.R.3    Mulley, J.C.4
  • 53
    • 0031239275 scopus 로고    scopus 로고
    • Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators
    • Gecz J, Bielby S, Sutherland GR, Mulley JC. Gene structure and subcellular localization of FMR2, a member of a new family of putative transcription activators. Genomics 1997a; 44: 201-13.
    • (1997) Genomics , vol.44 , pp. 201-213
    • Gecz, J.1    Bielby, S.2    Sutherland, G.R.3    Mulley, J.C.4
  • 57
    • 0028939603 scopus 로고
    • Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)
    • Gibbons RJ, Picketts DJ, Villard L, Higgs DR. Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome). Cell 1995; 80: 837-45.
    • (1995) Cell , vol.80 , pp. 837-845
    • Gibbons, R.J.1    Picketts, D.J.2    Villard, L.3    Higgs, D.R.4
  • 58
    • 0028893812 scopus 로고
    • Longitudinal neuropsychological and genetic linkage analysis of persons at risk for Huntington's disease
    • Giordani B, Berent S, Boivin MJ, Penney JB, Lehtinen S, Markel DS, et al. Longitudinal neuropsychological and genetic linkage analysis of persons at risk for Huntington's disease. Arch Neurol 1995; 52: 59-64.
    • (1995) Arch Neurol , vol.52 , pp. 59-64
    • Giordani, B.1    Berent, S.2    Boivin, M.J.3    Penney, J.B.4    Lehtinen, S.5    Markel, D.S.6
  • 59
    • 0026088977 scopus 로고
    • Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
    • Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, et al. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease [see comments]. Nature 1991; 349: 704-6. Comment in: Nature 1991; 348: 653-4, Comment in: Nature 1991; 350: 564.
    • (1991) Nature , vol.349 , pp. 704-706
    • Goate, A.1    Chartier-Harlin, M.C.2    Mullan, M.3    Brown, J.4    Crawford, F.5    Fidani, L.6
  • 60
    • 0026088977 scopus 로고
    • Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, et al. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease [see comments]. Nature 1991; 349: 704-6. Comment in: Nature 1991; 348: 653-4, Comment in: Nature 1991; 350: 564.
    • (1991) Nature , vol.348 , pp. 653-654
  • 61
    • 0025853053 scopus 로고
    • Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, et al. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease [see comments]. Nature 1991; 349: 704-6. Comment in: Nature 1991; 348: 653-4, Comment in: Nature 1991; 350: 564.
    • (1991) Nature , vol.350 , pp. 564
  • 62
    • 0025343411 scopus 로고
    • Feature-blind grammar and dysphagia
    • Gopnik M. Feature-blind grammar and dysphagia [letter] [see comments]. Nature 1990; 344: 715. Comment in: Nature 1990; 346: 226.
    • (1990) Nature , vol.344 , pp. 715
    • Gopnik, M.1
  • 63
    • 0025307440 scopus 로고
    • Gopnik M. Feature-blind grammar and dysphagia [letter] [see comments]. Nature 1990; 344: 715. Comment in: Nature 1990; 346: 226.
    • (1990) Nature , vol.346 , pp. 226
  • 64
    • 0026145984 scopus 로고
    • Familial aggregation of a developmental language disorder
    • Gopnik M, Crago MB. Familial aggregation of a developmental language disorder. Cognition 1991; 39: 1-50.
    • (1991) Cognition , vol.39 , pp. 1-50
    • Gopnik, M.1    Crago, M.B.2
  • 65
    • 0027092647 scopus 로고
    • Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice
    • Grant SG, O'Dell TJ, Karl KA, Stein PL, Soriano P, Kandel ER. Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice [see comments]. Science 1992; 258: 1903-10. Comment in: Science 1992; 262: 760-3.
    • (1992) Science , vol.258 , pp. 1903-1910
    • Grant, S.G.1    O'Dell, T.J.2    Karl, K.A.3    Stein, P.L.4    Soriano, P.5    Kandel, E.R.6
  • 66
    • 0027092647 scopus 로고
    • Grant SG, O'Dell TJ, Karl KA, Stein PL, Soriano P, Kandel ER. Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice [see comments]. Science 1992; 258: 1903-10. Comment in: Science 1992; 262: 760-3.
    • (1992) Science , vol.262 , pp. 760-763
  • 68
    • 0031027824 scopus 로고    scopus 로고
    • Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15
    • Grigorenko EL, Wood FB, Meyer MS, Hart LA, Speed WC, Shuster A, et al. Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15 [see comments]. Am J Hum Genet 1997; 60: 27-39. Comment in: Am J Hum Genet 1997; 60: 13-6.
    • (1997) Am J Hum Genet , vol.60 , pp. 27-39
    • Grigorenko, E.L.1    Wood, F.B.2    Meyer, M.S.3    Hart, L.A.4    Speed, W.C.5    Shuster, A.6
  • 69
    • 0031027824 scopus 로고    scopus 로고
    • Grigorenko EL, Wood FB, Meyer MS, Hart LA, Speed WC, Shuster A, et al. Susceptibility loci for distinct components of developmental dyslexia on chromosomes 6 and 15 [see comments]. Am J Hum Genet 1997; 60: 27-39. Comment in: Am J Hum Genet 1997; 60: 13-6.
    • (1997) Am J Hum Genet , vol.60 , pp. 13-16
  • 70
    • 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 RA, Nelson DL. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island. Nat Genet 1996; 13: 109-13.
    • (1996) Nat Genet , vol.13 , pp. 109-113
    • Gu, Y.1    Shen, Y.2    Gibbs, R.A.3    Nelson, D.L.4
  • 71
    • 0031052381 scopus 로고    scopus 로고
    • Amyloid, the presenilins and Alzheimer's disease
    • Hardy J. Amyloid, the presenilins and Alzheimer's disease [see comments]. Trends Neurosci 1997; 20: 154-9. Comment in: Trends Neurosci 1997; 20: 558-9.
    • (1997) Trends Neurosci , vol.20 , pp. 154-159
    • Hardy, J.1
  • 72
    • 0030710114 scopus 로고    scopus 로고
    • Hardy J. Amyloid, the presenilins and Alzheimer's disease [see comments]. Trends Neurosci 1997; 20: 154-9. Comment in: Trends Neurosci 1997; 20: 558-9.
    • (1997) Trends Neurosci , vol.20 , pp. 558-559
  • 73
    • 0032150877 scopus 로고    scopus 로고
    • Genetic dissection of Alzheimer's disease and related dementias: Amyloid and its relationship to tau
    • Hardy J, Duf K, Hardy KG, Perez-Tur J, Hutton M. Genetic dissection of Alzheimer's disease and related dementias: amyloid and its relationship to tau. Nat Neurosci 1998; 1: 355-8.
    • (1998) Nat Neurosci , vol.1 , pp. 355-358
    • Hardy, J.1    Duf, K.2    Hardy, K.G.3    Perez-Tur, J.4    Hutton, M.5
  • 74
    • 0031817020 scopus 로고    scopus 로고
    • A multivariate genetic analysis of correlations between intelligence and personality
    • Harris JA, Vernon PA, Jang KL. A multivariate genetic analysis of correlations between intelligence and personality. Dev Neuropsychol 1998; 14: 127-42.
    • (1998) Dev Neuropsychol , vol.14 , pp. 127-142
    • Harris, J.A.1    Vernon, P.A.2    Jang, K.L.3
  • 75
    • 0023614188 scopus 로고
    • Dystrophin: The protein product of the Duchenne muscular dystrophy locus
    • Hoffman EP, Brown RH Jr, Kunkel LM. Dystrophin: the protein product of the Duchenne muscular dystrophy locus. Cell 1987; 51: 919-28.
    • (1987) Cell , vol.51 , pp. 919-928
    • Hoffman, E.P.1    Brown R.H., Jr.2    Kunkel, L.M.3
  • 76
    • 0032555155 scopus 로고    scopus 로고
    • Functional connectivity of the angular gyrus in normal reading and dyslexia
    • Horwitz B, Rumsey JM, Donohue BC. Functional connectivity of the angular gyrus in normal reading and dyslexia. Proc Natl Acad Sci USA 1998; 95: 8939-44.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 8939-8944
    • Horwitz, B.1    Rumsey, J.M.2    Donohue, B.C.3
  • 77
    • 0031825008 scopus 로고    scopus 로고
    • An epidemiological and aetiological study of children with intellectual disability in Taiwan
    • Hou J-W, Wang TR, Chuang S-M. An epidemiological and aetiological study of children with intellectual disability in Taiwan. J Intellect Disabil Res 1998; 42: 137-43.
    • (1998) J Intellect Disabil Res , vol.42 , pp. 137-143
    • Hou, J.-W.1    Wang, T.R.2    Chuang, S.-M.3
  • 78
    • 0028968143 scopus 로고
    • Practitioner review: Verbal working memory development and its disorders
    • Hulme C, Roodenrys S. Practitioner review: verbal working memory development and its disorders. [Review]. J Child Psychol Psychiatry 1995; 36: 373-98.
    • (1995) J Child Psychol Psychiatry , vol.36 , pp. 373-398
    • Hulme, C.1    Roodenrys, S.2
  • 79
    • 0028238472 scopus 로고
    • Targeted mutation of the CREB gene: Compensation within the CREB/ATF family of transcription factors
    • Hummler E, Cole TJ, Blendy JA, Ganss R, Aguzzi A, Schmid W, et al. Targeted mutation of the CREB gene: compensation within the CREB/ATF family of transcription factors. Proc Natl Acad Sci USA 1994; 91: 5647-51.
    • (1994) Proc Natl Acad Sci USA , vol.91 , pp. 5647-5651
    • Hummler, E.1    Cole, T.J.2    Blendy, J.A.3    Ganss, R.4    Aguzzi, A.5    Schmid, W.6
  • 80
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
    • Huntington Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes [see comments]. Cell 1993; 72: 971-83. Comment in: Cell 1993; 72: 817-8.
    • (1993) Cell , vol.72 , pp. 971-983
  • 81
    • 0027480255 scopus 로고
    • Huntington Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes [see comments]. Cell 1993; 72: 971-83. Comment in: Cell 1993; 72: 817-8.
    • (1993) Cell , vol.72 , pp. 817-818
  • 83
    • 0032543684 scopus 로고    scopus 로고
    • Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17
    • Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, et al. Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature 1998; 393: 702-5.
    • (1998) Nature , vol.393 , pp. 702-705
    • Hutton, M.1    Lendon, C.L.2    Rizzu, P.3    Baker, M.4    Froelich, S.5    Houlden, H.6
  • 84
    • 0031895069 scopus 로고    scopus 로고
    • Verbal and nonverbal abilities in the Williams syndrome phenotype: Evidence for diverging developmental trajectories
    • Jarrold C, Baddeley AD, Hewes AK. Verbal and nonverbal abilities in the Williams syndrome phenotype: evidence for diverging developmental trajectories. J Child Psychol Psychiatry 1998; 39: 511-23.
    • (1998) J Child Psychol Psychiatry , vol.39 , pp. 511-523
    • Jarrold, C.1    Baddeley, A.D.2    Hewes, A.K.3
  • 85
    • 0030882268 scopus 로고    scopus 로고
    • Cognitive manifestations of Huntington disease in relation to genetic structure and clinical onset
    • Jason GW, Suchowersky O, Pajurkova EM, Graham L, Klimek ML, Garber AT, et al. Cognitive manifestations of Huntington disease in relation to genetic structure and clinical onset. Arch Neurol 1997; 54: 1081-8.
    • (1997) Arch Neurol , vol.54 , pp. 1081-1088
    • Jason, G.W.1    Suchowersky, O.2    Pajurkova, E.M.3    Graham, L.4    Klimek, M.L.5    Garber, A.T.6
  • 86
    • 0019917243 scopus 로고
    • Molecular biology of learning: Modulation of transmitter release
    • Kandel ER, Schwartz JH. Molecular biology of learning: modulation of transmitter release. Science 1982; 218: 433-43.
    • (1982) Science , vol.218 , pp. 433-443
    • Kandel, E.R.1    Schwartz, J.H.2
  • 90
    • 0032568888 scopus 로고    scopus 로고
    • Abolition of long-term stability of new hippocampal place cell maps by NMDA receptor blockade
    • Kentros C, Hargreaves E, Hawkins RD, Kandel ER, Shapiron M, Muller RV. Abolition of long-term stability of new hippocampal place cell maps by NMDA receptor blockade. Science 1998; 280: 2121-6.
    • (1998) Science , vol.280 , pp. 2121-2126
    • Kentros, C.1    Hargreaves, E.2    Hawkins, R.D.3    Kandel, E.R.4    Shapiron, M.5    Muller, R.V.6
  • 91
    • 0030059545 scopus 로고    scopus 로고
    • The fragile X mental retardation protein is associated with ribosomes
    • Khandjian EW, Corbin F, Woerly S, Rousseau F. The fragile X mental retardation protein is associated with ribosomes, Nat Genet 1996; 12: 91-3.
    • (1996) Nat Genet , vol.12 , pp. 91-93
    • Khandjian, E.W.1    Corbin, F.2    Woerly, S.3    Rousseau, F.4
  • 92
    • 0031012849 scopus 로고    scopus 로고
    • UBE3A/E6-AP mutations cause Angelman syndrome
    • published erratum appears in Nat Genet 1997; 15: 411
    • Kishino T, Lalande M, Wagstaff J. UBE3A/E6-AP mutations cause Angelman syndrome [published erratum appears in Nat Genet 1997; 15: 411]. Nat Genet 1997; 15: 70-3.
    • (1997) Nat Genet , vol.15 , pp. 70-73
    • Kishino, T.1    Lalande, M.2    Wagstaff, J.3
  • 93
    • 0032475941 scopus 로고    scopus 로고
    • Ataxin-1 nuclear localization and aggregation: Role in polyglutamine-induced disease in SCA1 transgenic mice
    • Klement IA, Skinner PJ, Kaytor MD, Yi H, Hersch SM, Clark HB, et al. Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice [see comments]. Cell 1998; 95: 41-53. Comment in: Cell 1998; 95: 1-4.
    • (1998) Cell , vol.95 , pp. 41-53
    • Klement, I.A.1    Skinner, P.J.2    Kaytor, M.D.3    Yi, H.4    Hersch, S.M.5    Clark, H.B.6
  • 94
    • 0032475941 scopus 로고    scopus 로고
    • Klement IA, Skinner PJ, Kaytor MD, Yi H, Hersch SM, Clark HB, et al. Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice [see comments]. Cell 1998; 95: 41-53. Comment in: Cell 1998; 95: 1-4.
    • (1998) Cell , vol.95 , pp. 1-4
  • 95
    • 0019390636 scopus 로고
    • Intellect and behaviour in Duchenne muscular dystrophy
    • Leibowitz D, Dubowitz V. Intellect and behaviour in Duchenne muscular dystrophy. Dev Med Child Neurol 1981; 23: 577-90.
    • (1981) Dev Med Child Neurol , vol.23 , pp. 577-590
    • Leibowitz, D.1    Dubowitz, V.2
  • 96
    • 0026567423 scopus 로고
    • The Drosophila learning and memory gene rutabaga encodes a Ca2+/calmodulin-responsive adenylyl cyclase
    • Levin LR, Han P-L, Hwang PM, Feinstein PG, Davis RL, Reed RR. The Drosophila learning and memory gene rutabaga encodes a Ca2+/calmodulin-responsive adenylyl cyclase. Cell 1992; 68: 479-89.
    • (1992) Cell , vol.68 , pp. 479-489
    • Levin, L.R.1    Han, P.-L.2    Hwang, P.M.3    Feinstein, P.G.4    Davis, R.L.5    Reed, R.R.6
  • 97
    • 0029087026 scopus 로고
    • Candidate gene for the chromosome-1 familial Alzheimer's disease locus
    • Levy-Lahad E, Wasco W, Poorkaj P, Romano DM, Oshima J, Pettingell WH, et al. Candidate gene for the chromosome-1 familial Alzheimer's disease locus [see comments]. Science 1995a; 269: 973-7. Comment in: Science 1995; 269: 917-8.
    • (1995) Science , vol.269 , pp. 973-977
    • Levy-Lahad, E.1    Wasco, W.2    Poorkaj, P.3    Romano, D.M.4    Oshima, J.5    Pettingell, W.H.6
  • 98
    • 0029087026 scopus 로고
    • Levy-Lahad E, Wasco W, Poorkaj P, Romano DM, Oshima J, Pettingell WH, et al. Candidate gene for the chromosome-1 familial Alzheimer's disease locus [see comments]. Science 1995a; 269: 973-7. Comment in: Science 1995; 269: 917-8.
    • (1995) , vol.269 , pp. 917-918
  • 100
    • 0029126319 scopus 로고
    • Comment in: Science 1995b; 269: 917-8.
    • (1995) Comment In: Science , vol.269 , pp. 917-918
  • 101
    • 0030866899 scopus 로고    scopus 로고
    • Social interaction and sensorimotor gating abnormalities in mice lacking Dv11
    • Lijam N, Paylor R, McDonald MP, Crawley JN, Deng C-X, Herrup K, et al. Social interaction and sensorimotor gating abnormalities in mice lacking Dv11. Cell 1997; 90: 895-905.
    • (1997) Cell , vol.90 , pp. 895-905
    • Lijam, N.1    Paylor, R.2    McDonald, M.P.3    Crawley, J.N.4    Deng, C.-X.5    Herrup, K.6
  • 102
    • 0029764770 scopus 로고    scopus 로고
    • Reduction of morphine abstinence in mice with a mutation in the gene encoding CREB
    • Maldonado R, Blendy JA, Tzavara E, Gass P, Roques BP, Hanoune J, et al. Reduction of morphine abstinence in mice with a mutation in the gene encoding CREB [see comments]. Science 1996; 273: 657-9. Comment in: Science 1996; 273: 611-2.
    • (1996) Science , vol.273 , pp. 657-659
    • Maldonado, R.1    Blendy, J.A.2    Tzavara, E.3    Gass, P.4    Roques, B.P.5    Hanoune, J.6
  • 103
    • 0029785148 scopus 로고    scopus 로고
    • Maldonado R, Blendy JA, Tzavara E, Gass P, Roques BP, Hanoune J, et al. Reduction of morphine abstinence in mice with a mutation in the gene encoding CREB [see comments]. Science 1996; 273: 657-9. Comment in: Science 1996; 273: 611-2.
    • (1996) Science , vol.273 , pp. 611-612
  • 104
    • 0021260566 scopus 로고
    • Idiopathic infantile hypercalcaemia - A continuing enigma
    • Martin ND, Snodgrass GJ, Cohen RD. Idiopathic infantile hypercalcaemia - a continuing enigma. Arch Dis Child 1984; 59: 605-13.
    • (1984) Arch Dis Child , vol.59 , pp. 605-613
    • Martin, N.D.1    Snodgrass, G.J.2    Cohen, R.D.3
  • 105
    • 0031879558 scopus 로고    scopus 로고
    • A process approach to describing mathematics difficulties in girls with Turner syndrome
    • Mazzocco MM. A process approach to describing mathematics difficulties in girls with Turner syndrome. Pediatrics 1998; 102: 492-6.
    • (1998) Pediatrics , vol.102 , pp. 492-496
    • Mazzocco, M.M.1
  • 106
    • 0030976148 scopus 로고    scopus 로고
    • Substantial genetic influence on cognitive abilities in twins 80 or more years old
    • McClearn GE, Johansson B, Berg S, Pedersen NL, Ahern F, Petrill SA, et al. Substantial genetic influence on cognitive abilities in twins 80 or more years old [see comments]. Science 1997; 276: 1560-3. Comment in: Science 1997; 276: 1522-3, Comment in: Science 1997; 278: 1383-4; discussion 1386-7.
    • (1997) Science , vol.276 , pp. 1560-1563
    • McClearn, G.E.1    Johansson, B.2    Berg, S.3    Pedersen, N.L.4    Ahern, F.5    Petrill, S.A.6
  • 107
    • 0030906941 scopus 로고    scopus 로고
    • McClearn GE, Johansson B, Berg S, Pedersen NL, Ahern F, Petrill SA, et al. Substantial genetic influence on cognitive abilities in twins 80 or more years old [see comments]. Science 1997; 276: 1560-3. Comment in: Science 1997; 276: 1522-3, Comment in: Science 1997; 278: 1383-4; discussion 1386-7.
    • (1997) Science , vol.276 , pp. 1522-1523
  • 108
    • 0030698431 scopus 로고    scopus 로고
    • discussion 1386-7
    • McClearn GE, Johansson B, Berg S, Pedersen NL, Ahern F, Petrill SA, et al. Substantial genetic influence on cognitive abilities in twins 80 or more years old [see comments]. Science 1997; 276: 1560-3. Comment in: Science 1997; 276: 1522-3, Comment in: Science 1997; 278: 1383-4; discussion 1386-7.
    • (1997) Science , vol.278 , pp. 1383-1384
  • 109
    • 0030475008 scopus 로고    scopus 로고
    • Impaired hippocampal representation of space in CA1-specific NMDAR1 knockout mice
    • McHugh TJ, Blum KI, Tsien JZ, Tonegawa S, Wilson MA. Impaired hippocampal representation of space in CA1-specific NMDAR1 knockout mice [see comments]. Cell 1996; 87: 1339-49. Comment in: Cell 1996; 87: 1147-8.
    • (1996) Cell , vol.87 , pp. 1339-1349
    • McHugh, T.J.1    Blum, K.I.2    Tsien, J.Z.3    Tonegawa, S.4    Wilson, M.A.5
  • 110
    • 0030465053 scopus 로고    scopus 로고
    • McHugh TJ, Blum KI, Tsien JZ, Tonegawa S, Wilson MA. Impaired hippocampal representation of space in CA1-specific NMDAR1 knockout mice [see comments]. Cell 1996; 87: 1339-49. Comment in: Cell 1996; 87: 1147-8.
    • (1996) Cell , vol.87 , pp. 1147-1148
  • 111
    • 0031441897 scopus 로고    scopus 로고
    • Fear conditioning induces a lasting potentiation of synaptic currents in vitro
    • McKernan MG, Shinnick-Gallagher P. Fear conditioning induces a lasting potentiation of synaptic currents in vitro [see comments]. Nature 1997; 390: 607-11. Comment in: Nature 1997; 390: 552-3.
    • (1997) Nature , vol.390 , pp. 607-611
    • McKernan, M.G.1    Shinnick-Gallagher, P.2
  • 112
    • 0031565083 scopus 로고    scopus 로고
    • McKernan MG, Shinnick-Gallagher P. Fear conditioning induces a lasting potentiation of synaptic currents in vitro [see comments]. Nature 1997; 390: 607-11. Comment in: Nature 1997; 390: 552-3.
    • (1997) Nature , vol.390 , pp. 552-553
  • 113
    • 0027561783 scopus 로고
    • Specific neuro-cognitive impairments associated with Turner (45,XXY) and Klinefelter (47,XXY) syndromes: A review
    • Money J. Specific neuro-cognitive impairments associated with Turner (45,XXY) and Klinefelter (47,XXY) syndromes: a review. [Review]. Soc Biol 1993; 40: 147-51.
    • (1993) Soc Biol , vol.40 , pp. 147-151
    • Money, J.1
  • 114
    • 0014731182 scopus 로고
    • Lack of personality pathology in Turner's syndrome: Relation to cytogenetics, hormones and physique
    • Money J, Mittenthal S. Lack of personality pathology in Turner's syndrome: relation to cytogenetics, hormones and physique. Behav Genet 1970; 1:43-56.
    • (1970) Behav Genet , vol.1 , pp. 43-56
    • Money, J.1    Mittenthal, S.2
  • 116
    • 0027480948 scopus 로고
    • Association between brain temperature and dentate field potentials in exploring and swimming rats
    • Moser E, Mathiesen I, Andersen P. Association between brain temperature and dentate field potentials in exploring and swimming rats. Science 1993; 259: 1324-6.
    • (1993) Science , vol.259 , pp. 1324-1326
    • Moser, E.1    Mathiesen, I.2    Andersen, P.3
  • 118
    • 0020198529 scopus 로고
    • Atypical hemispheric lateralization in Turner syndrome subjects
    • Netley C, Rovet J. Atypical hemispheric lateralization in Turner syndrome subjects. Cortex 1982; 18: 377-84.
    • (1982) Cortex , vol.18 , pp. 377-384
    • Netley, C.1    Rovet, J.2
  • 119
    • 0032076307 scopus 로고    scopus 로고
    • Imprinting in Prader-Willi and Angelman syndromes
    • Nicholls RD, Saitoh S, Horsthemke B. Imprinting in Prader-Willi and Angelman syndromes. [Review]. Trends Genet 1998; 14: 194-200.
    • (1998) Trends Genet , vol.14 , pp. 194-200
    • Nicholls, R.D.1    Saitoh, S.2    Horsthemke, B.3
  • 120
    • 0028961293 scopus 로고
    • Rho, rac and cdc42 GTPases regulate the assembly of multimolecular focal complexes associated with actin stress fibers, lamellipodia and filopodia
    • Nobes CD, Hall A. Rho, rac and cdc42 GTPases regulate the assembly of multimolecular focal complexes associated with actin stress fibers, lamellipodia and filopodia. Cell 1995; 81: 53-62.
    • (1995) Cell , vol.81 , pp. 53-62
    • Nobes, C.D.1    Hall, A.2
  • 121
    • 0017090744 scopus 로고
    • Behavior in the Lesch-Nyhan syndrome
    • Nyhan WL. Behavior in the Lesch-Nyhan syndrome. J Autism Child Schizophr 1976; 6: 235-52.
    • (1976) J Autism Child Schizophr , vol.6 , pp. 235-252
    • Nyhan, W.L.1
  • 122
    • 0027752699 scopus 로고
    • Hippocampus, theta, and spatial memory
    • O'Keefe J. Hippocampus, theta, and spatial memory. [Review]. Curr Opin Neurobiol 1993; 3: 917-24.
    • (1993) Curr Opin Neurobiol , vol.3 , pp. 917-924
    • O'Keefe, J.1
  • 126
    • 0026953405 scopus 로고
    • The external validity of age-versus IQ-discrepancy definitions of reading disability: Lessons from a twin study
    • Pennington BF, Gilger JW, Olson RK, DeFries JC. The external validity of age-versus IQ-discrepancy definitions of reading disability: lessons from a twin study. J Learn Disabil 1992; 25: 562-73.
    • (1992) J Learn Disabil , vol.25 , pp. 562-573
    • Pennington, B.F.1    Gilger, J.W.2    Olson, R.K.3    DeFries, J.C.4
  • 127
    • 0003637433 scopus 로고
    • New York: Oxford University Press
    • Perfetti CA. Reading ability. New York: Oxford University Press; 1985.
    • (1985) Reading Ability
    • Perfetti, C.A.1
  • 128
    • 0029022770 scopus 로고
    • Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP
    • Petrij F, Giles RH, Dauwerse HG, Saris JJ, Hennekam RC, Masuno M, et al. Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP [see comments]. Nature 1995; 376: 348-51. Comment in: Nature 1995; 376: 292-3.
    • (1995) Nature , vol.376 , pp. 348-351
    • Petrij, F.1    Giles, R.H.2    Dauwerse, H.G.3    Saris, J.J.4    Hennekam, R.C.5    Masuno, M.6
  • 129
    • 0029653034 scopus 로고
    • Petrij F, Giles RH, Dauwerse HG, Saris JJ, Hennekam RC, Masuno M, et al. Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP [see comments]. Nature 1995; 376: 348-51. Comment in: Nature 1995; 376: 292-3.
    • (1995) Nature , vol.376 , pp. 292-293
  • 130
    • 8244257351 scopus 로고    scopus 로고
    • No association between general cognitive ability and the A1 allele of the D2 dopamine receptor gene
    • Petrill SA, Plomin R, McClearn GE, Smith DL, Vignetti S, Chorney MJ, et al. No association between general cognitive ability and the A1 allele of the D2 dopamine receptor gene. Behav Genet 1997; 27: 29-31.
    • (1997) Behav Genet , vol.27 , pp. 29-31
    • Petrill, S.A.1    Plomin, R.2    McClearn, G.E.3    Smith, D.L.4    Vignetti, S.5    Chorney, M.J.6
  • 131
    • 0032167859 scopus 로고    scopus 로고
    • Genetic lesions in Drosophila behavioural mutants
    • Pflugfelder GO. Genetic lesions in Drosophila behavioural mutants. [Review]. Behav Brain Res 1998; 95: 3-15.
    • (1998) Behav Brain Res , vol.95 , pp. 3-15
    • Pflugfelder, G.O.1
  • 134
    • 0028353167 scopus 로고
    • DNA markers associated with high versus low IQ: The IQ quantitative trait loci (QTL) project
    • Plomin R, McClearn GE, Smith DL, Vignetti, Chorney MJ, Chorney K, et al. DNA markers associated with high versus low IQ: the IQ quantitative trait loci (QTL) project [see comments]. Behav Genet 1994; 24: 107-18. Comment in: Behav Genet 1995; 25: 197-8.
    • (1994) Behav Genet , vol.24 , pp. 107-118
    • Plomin, R.1    McClearn, G.E.2    Smith, D.L.3    Chorney, M.J.4    Chorney, K.5
  • 135
    • 0029265818 scopus 로고
    • Plomin R, McClearn GE, Smith DL, Vignetti, Chorney MJ, Chorney K, et al. DNA markers associated with high versus low IQ: the IQ quantitative trait loci (QTL) project [see comments]. Behav Genet 1994; 24: 107-18. Comment in: Behav Genet 1995; 25: 197-8.
    • (1995) Behav Genet , vol.25 , pp. 197-198
  • 136
    • 16944365777 scopus 로고    scopus 로고
    • Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22
    • Quaderi NA, Schweiger S, Gaudenz K, Franco B, Rugarli EI, Berger W, et al. Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22. Nat Genet 1997; 17: 285-91.
    • (1997) Nat Genet , vol.17 , pp. 285-291
    • Quaderi, N.A.1    Schweiger, S.2    Gaudenz, K.3    Franco, B.4    Rugarli, E.I.5    Berger, W.6
  • 137
    • 0002129364 scopus 로고
    • The nonword reading deficit in developmental dyslexia: A review
    • Rack JP, Snowling MJ, Olson RK. The nonword reading deficit in developmental dyslexia: a review. Reading Res Quart 1992; 27: 28-55.
    • (1992) Reading Res Quart , vol.27 , pp. 28-55
    • Rack, J.P.1    Snowling, M.J.2    Olson, R.K.3
  • 138
    • 0026338937 scopus 로고
    • Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy
    • Rapaport D, Passos-Bueno MR, Brandao L, Love D, Vainzof M, Zatz M. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy. Am J Med Genet 1991; 39: 437-41.
    • (1991) Am J Med Genet , vol.39 , pp. 437-441
    • Rapaport, D.1    Passos-Bueno, M.R.2    Brandao, L.3    Love, D.4    Vainzof, M.5    Zatz, M.6
  • 139
    • 0343877356 scopus 로고    scopus 로고
    • NMDA receptors, synaptic plasticity and learning and memory
    • Conti F, Hicks TP, editors. Cambridge (MA): MIT Press
    • Rawlins JNP. NMDA receptors, synaptic plasticity and learning and memory. In: Conti F, Hicks TP, editors. Excitatory amino acids and the cerebral cortex. Cambridge (MA): MIT Press; 1996. p. 275-84.
    • (1996) Excitatory Amino Acids and the Cerebral Cortex , pp. 275-284
    • Rawlins, J.N.P.1
  • 140
    • 0029114706 scopus 로고
    • A mouse model for Down syndrome exhibits learning and behavior deficits
    • Reeves RH, Irving NG, Moran TH, Wohn A, Kitt C, Sisodia SS, et al. A mouse model for Down syndrome exhibits learning and behavior deficits [see comments]. Nat Genet 1995; 11: 177-84. Comment in: Nat Genet 1995; 11: 109-11.
    • (1995) Nat Genet , vol.11 , pp. 177-184
    • Reeves, R.H.1    Irving, N.G.2    Moran, T.H.3    Wohn, A.4    Kitt, C.5    Sisodia, S.S.6
  • 141
    • 0029392822 scopus 로고
    • Reeves RH, Irving NG, Moran TH, Wohn A, Kitt C, Sisodia SS, et al. A mouse model for Down syndrome exhibits learning and behavior deficits [see comments]. Nat Genet 1995; 11: 177-84. Comment in: Nat Genet 1995; 11: 109-11.
    • (1995) Nat Genet , vol.11 , pp. 109-111
  • 142
    • 0027174513 scopus 로고
    • The effects of X monosomy on brain development: Monozygotic twins discordant for Turner's syndrome
    • Reiss AL, Freund L, Plotnick L, Baumgardner T, Green K, Sozer AC, et al. The effects of X monosomy on brain development: monozygotic twins discordant for Turner's syndrome. Ann Neurology 1993; 34: 95-107.
    • (1993) Ann Neurology , vol.34 , pp. 95-107
    • Reiss, A.L.1    Freund, L.2    Plotnick, L.3    Baumgardner, T.4    Green, K.5    Sozer, A.C.6
  • 143
    • 0031471239 scopus 로고    scopus 로고
    • Fear conditioning induces associative long-term potentiation in the amygdala
    • published erratum appears in Nature 1997; 391: 818
    • Rogan MT, Staubli UV, LeDoux JE. Fear conditioning induces associative long-term potentiation in the amygdala [see comments] [published erratum appears in Nature 1997; 391: 818]. Nature 1997; 390: 604-7. Comment in: Nature 1997; 390: 552-3.
    • (1997) Nature , vol.390 , pp. 604-607
    • Rogan, M.T.1    Staubli, U.V.2    LeDoux, J.E.3
  • 144
    • 0031565083 scopus 로고    scopus 로고
    • Rogan MT, Staubli UV, LeDoux JE. Fear conditioning induces associative long-term potentiation in the amygdala [see comments] [published erratum appears in Nature 1997; 391: 818]. Nature 1997; 390: 604-7. Comment in: Nature 1997; 390: 552-3.
    • (1997) Nature , vol.390 , pp. 552-553
  • 145
    • 0030476713 scopus 로고    scopus 로고
    • Mice expressing activated CaMKII lack low frequency LTP and do not form stable place cells in the CA1 region of the hippocampus
    • Rotenberg A, Mayford M, Hawkins RD, Kandel ER, Muller RU. Mice expressing activated CaMKII lack low frequency LTP and do not form stable place cells in the CA1 region of the hippocampus [see comments]. Cell 1996; 87: 1351-61. Comment in: Cell 1996; 87: 1147-8.
    • (1996) Cell , vol.87 , pp. 1351-1361
    • Rotenberg, A.1    Mayford, M.2    Hawkins, R.D.3    Kandel, E.R.4    Muller, R.U.5
  • 146
    • 0030465053 scopus 로고    scopus 로고
    • Rotenberg A, Mayford M, Hawkins RD, Kandel ER, Muller RU. Mice expressing activated CaMKII lack low frequency LTP and do not form stable place cells in the CA1 region of the hippocampus [see comments]. Cell 1996; 87: 1351-61. Comment in: Cell 1996; 87: 1147-8.
    • (1996) Cell , vol.87 , pp. 1147-1148
  • 147
    • 0019148603 scopus 로고
    • The mental rotation task performance of Turner syndrome subjects
    • Rovet J, Netley C. The mental rotation task performance of Turner syndrome subjects. Behav Genet 1980; 10: 437-43.
    • (1980) Behav Genet , vol.10 , pp. 437-443
    • Rovet, J.1    Netley, C.2
  • 148
    • 0001929207 scopus 로고
    • Processing deficits in Turner's syndrome
    • Rovet J, Netley C. Processing deficits in Turner's syndrome. Dev Psychol 1982; 18: 77-94.
    • (1982) Dev Psychol , vol.18 , pp. 77-94
    • Rovet, J.1    Netley, C.2
  • 149
    • 0026557912 scopus 로고
    • Multiple mRNA isoforms of the transcription activator protein CREB: Generation by alternative splicing and specific expression in primary spermatocytes
    • Ruppert S, Cole TJ, Boshart M, Schmid E, Schutz G. Multiple mRNA isoforms of the transcription activator protein CREB: generation by alternative splicing and specific expression in primary spermatocytes. EMBO J 1992; 11: 1503-12.
    • (1992) EMBO J , vol.11 , pp. 1503-1512
    • Ruppert, S.1    Cole, T.J.2    Boshart, M.3    Schmid, E.4    Schutz, G.5
  • 150
    • 0030582732 scopus 로고    scopus 로고
    • Control of male sexual behavior and sexual orientation in Drosophila by the fruitless gene
    • Ryner LC, Goodwin SF, Castrillon DH, Anand A, Villella A, Baker BS, et al. Control of male sexual behavior and sexual orientation in Drosophila by the fruitless gene. Cell 1996; 87: 1079-89.
    • (1996) Cell , vol.87 , pp. 1079-1089
    • Ryner, L.C.1    Goodwin, S.F.2    Castrillon, D.H.3    Anand, A.4    Villella, A.5    Baker, B.S.6
  • 151
    • 0032475931 scopus 로고    scopus 로고
    • Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions
    • Saudou F, Finkbeiner S, Devys D, Greenberg ME. Huntingtin acts in the nucleus to induce apoptosis but death does not correlate with the formation of intranuclear inclusions. Cell 1998; 95: 55-66.
    • (1998) Cell , vol.95 , pp. 55-66
    • Saudou, F.1    Finkbeiner, S.2    Devys, D.3    Greenberg, M.E.4
  • 152
    • 0027228303 scopus 로고
    • Deletions of human chromosome 22 and associated birth defects
    • Scambler PJ. Deletions of human chromosome 22 and associated birth defects. [Review]. Curr Opin Genet Dev 1993; 3: 432-7.
    • (1993) Curr Opin Genet Dev , vol.3 , pp. 432-437
    • Scambler, P.J.1
  • 153
    • 0027292470 scopus 로고
    • Role of cyclic AMP in the control of cell-specific gene expression
    • Schmid W, Nitsch D, Boshart M, Schutz G. Role of cyclic AMP in the control of cell-specific gene expression. Trends Endocrinol Metab 1993; 4: 204-9.
    • (1993) Trends Endocrinol Metab , vol.4 , pp. 204-209
    • Schmid, W.1    Nitsch, D.2    Boshart, M.3    Schutz, G.4
  • 154
    • 0029004341 scopus 로고
    • Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
    • Sherrington R, Rogaev EI, Liang Y, Rogaeva EA, Levesque G, Ikeda M, et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease [see comments]. Nature 1995; 375: 754-60. Comment in: Nature 1995; 375: 734.
    • (1995) Nature , vol.375 , pp. 754-760
    • Sherrington, R.1    Rogaev, E.I.2    Liang, Y.3    Rogaeva, E.A.4    Levesque, G.5    Ikeda, M.6
  • 155
    • 0029027649 scopus 로고
    • Sherrington R, Rogaev EI, Liang Y, Rogaeva EA, Levesque G, Ikeda M, et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease [see comments]. Nature 1995; 375: 754-60. Comment in: Nature 1995; 375: 734.
    • (1995) Nature , vol.375 , pp. 734
  • 156
    • 0020646121 scopus 로고
    • Cyclic adenosine 3′:5′-monophosphate phosphodiesterase and its role in learning in Drosophila
    • Shotwell SL. Cyclic adenosine 3′:5′-monophosphate phosphodiesterase and its role in learning in Drosophila. J Neurosci 1983; 3: 739-47.
    • (1983) J Neurosci , vol.3 , pp. 739-747
    • Shotwell, S.L.1
  • 157
    • 0031928372 scopus 로고    scopus 로고
    • The psychological consequences of Turner syndrome and review of the national cooperative growth study psychological substudy
    • Siegel PT, Clopper R, Stabler B. The psychological consequences of Turner syndrome and review of the National Cooperative Growth Study psychological substudy. Pediatrics 1998; 102: 488-91.
    • (1998) Pediatrics , vol.102 , pp. 488-491
    • Siegel, P.T.1    Clopper, R.2    Stabler, B.3
  • 158
    • 0026742451 scopus 로고
    • Impaired spatial learning in alpha-calcium-calmodulin kinase II mutant mice
    • Silva AJ, Paylor R, Wehner JM, Tonegawa S. Impaired spatial learning in alpha-calcium-calmodulin kinase II mutant mice [see comments]. Science 1992a; 257: 206-11. Comment in: Science 1992; 257: 162-3, Comment in: Science 1992; 262: 760-3.
    • (1992) Science , vol.257 , pp. 206-211
    • Silva, A.J.1    Paylor, R.2    Wehner, J.M.3    Tonegawa, S.4
  • 159
    • 0026656649 scopus 로고
    • Silva AJ, Paylor R, Wehner JM, Tonegawa S. Impaired spatial learning in alpha-calcium-calmodulin kinase II mutant mice [see comments]. Science 1992a; 257: 206-11. Comment in: Science 1992; 257: 162-3, Comment in: Science 1992; 262: 760-3.
    • (1992) Science , vol.257 , pp. 162-163
  • 160
    • 0026742451 scopus 로고
    • Silva AJ, Paylor R, Wehner JM, Tonegawa S. Impaired spatial learning in alpha-calcium-calmodulin kinase II mutant mice [see comments]. Science 1992a; 257: 206-11. Comment in: Science 1992; 257: 162-3, Comment in: Science 1992; 262: 760-3.
    • (1992) Science , vol.262 , pp. 760-763
  • 161
    • 0026637195 scopus 로고
    • Deficient hippocampal long-term potentiation in alpha-calcium-calmodulin kinase II mutant mice
    • Silva AJ, Stevens CF, Tonegawa S, Wang Y. Deficient hippocampal long-term potentiation in alpha-calcium-calmodulin kinase II mutant mice [see comments]. Science 1992b; 257: 201-6. Comment in: Science 1992; 257: 162-3, Comment in: Science 1992; 262: 760-3.
    • (1992) Science , vol.257 , pp. 201-206
    • Silva, A.J.1    Stevens, C.F.2    Tonegawa, S.3    Wang, Y.4
  • 162
    • 0026656649 scopus 로고
    • Silva AJ, Stevens CF, Tonegawa S, Wang Y. Deficient hippocampal long-term potentiation in alpha-calcium-calmodulin kinase II mutant mice [see comments]. Science 1992b; 257: 201-6. Comment in: Science 1992; 257: 162-3, Comment in: Science 1992; 262: 760-3.
    • (1992) Science , vol.257 , pp. 162-163
  • 163
    • 0026637195 scopus 로고
    • Silva AJ, Stevens CF, Tonegawa S, Wang Y. Deficient hippocampal long-term potentiation in alpha-calcium-calmodulin kinase II mutant mice [see comments]. Science 1992b; 257: 201-6. Comment in: Science 1992; 257: 162-3, Comment in: Science 1992; 262: 760-3.
    • (1992) Science , vol.262 , pp. 760-763
  • 164
    • 0029930884 scopus 로고    scopus 로고
    • Mental retardation: Genetic findings, clinical implications, and research agenda
    • Simonoff EM, Bolton P, Rutter M. Mental retardation: genetic findings, clinical implications, and research agenda. [Review]. J Child Psychol Psychiatry 1996; 37: 259-80.
    • (1996) J Child Psychol Psychiatry , vol.37 , pp. 259-280
    • Simonoff, E.M.1    Bolton, P.2    Rutter, M.3
  • 165
    • 0027214152 scopus 로고
    • Preferential expression in mushroom bodies of the catalytic subunit of protein kinase A and its role in learning and memory
    • Skoulakis EM, Kalderon C, Davis RL. Preferential expression in mushroom bodies of the catalytic subunit of protein kinase A and its role in learning and memory. Neuron 1993; 11: 197-208.
    • (1993) Neuron , vol.11 , pp. 197-208
    • Skoulakis, E.M.1    Kalderon, C.2    Davis, R.L.3
  • 166
    • 16944366964 scopus 로고    scopus 로고
    • Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
    • Skuse DH, James RS, Bishop DV, Coppin B, Dalton P, Aamodt-Leeper G, et al. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function [see comments]. Nature 1997; 387; 705-8. Comment in: Nature 1997; 387: 652-3.
    • (1997) Nature , vol.387 , pp. 705-708
    • Skuse, D.H.1    James, R.S.2    Bishop, D.V.3    Coppin, B.4    Dalton, P.5    Aamodt-Leeper, G.6
  • 167
    • 0031565566 scopus 로고    scopus 로고
    • Skuse DH, James RS, Bishop DV, Coppin B, Dalton P, Aamodt-Leeper G, et al. Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function [see comments]. Nature 1997; 387; 705-8. Comment in: Nature 1997; 387: 652-3.
    • (1997) Nature , vol.387 , pp. 652-653
  • 168
    • 0030915187 scopus 로고    scopus 로고
    • Functional screening of 2Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down's syndrome
    • Smith DJ, Stevens ME, Sudanagunta SP, Bronson RT, Makhinson M, Watanabe AM, et al. Functional screening of 2Mb of human chromosome 21q22.2 in transgenic mice implicates minibrain in learning defects associated with Down's syndrome, Nat Genet 1997; 16: 28-36.
    • (1997) Nat Genet , vol.16 , pp. 28-36
    • Smith, D.J.1    Stevens, M.E.2    Sudanagunta, S.P.3    Bronson, R.T.4    Makhinson, M.5    Watanabe, A.M.6
  • 170
    • 0029026392 scopus 로고
    • The synaptic vesicle cycle: A cascade of protein-protein interactions
    • Sudhof TC. The synaptic vesicle cycle: a cascade of protein-protein interactions. [Review]. Nature 1995; 375: 645-53.
    • (1995) Nature , vol.375 , pp. 645-653
    • Sudhof, T.C.1
  • 171
    • 0027250267 scopus 로고
    • Intellectual functioning of children with Turner syndrome: A comparison of behavioural phenotypes
    • Temple CM, Carney RA. Intellectual functioning of children with Turner syndrome: a comparison of behavioural phenotypes. Dev Med Child Neurol 1993; 35: 691-8.
    • (1993) Dev Med Child Neurol , vol.35 , pp. 691-698
    • Temple, C.M.1    Carney, R.A.2
  • 172
    • 0030982564 scopus 로고    scopus 로고
    • Regulation of dendritic growth and remodeling by Rho, Rac, and Cdc42
    • Threadgill R, Bobb K, Ghosh A. Regulation of dendritic growth and remodeling by Rho, Rac, and Cdc42. Neuron 1997; 19: 625-34.
    • (1997) Neuron , vol.19 , pp. 625-634
    • Threadgill, R.1    Bobb, K.2    Ghosh, A.3
  • 173
    • 0030460425 scopus 로고    scopus 로고
    • Subregion-and cell type-restricted gene knockout in mouse brain
    • Tsien JZ, Chen DF, Gerber D, Tom C, Mercer EH, Anderson DJ, et al. Subregion-and cell type-restricted gene knockout in mouse brain [see comments]. Cell 1996a; 87: 1317-26. Comment in: Cell 1996; 87: 1147-8.
    • (1996) Cell , vol.87 , pp. 1317-1326
    • Tsien, J.Z.1    Chen, D.F.2    Gerber, D.3    Tom, C.4    Mercer, E.H.5    Anderson, D.J.6
  • 174
    • 0030460425 scopus 로고    scopus 로고
    • Tsien JZ, Chen DF, Gerber D, Tom C, Mercer EH, Anderson DJ, et al. Subregion-and cell type-restricted gene knockout in mouse brain [see comments]. Cell 1996a; 87: 1317-26. Comment in: Cell 1996; 87: 1147-8.
    • (1996) , vol.87 , pp. 1147-1148
  • 175
    • 0030446363 scopus 로고    scopus 로고
    • The essential role of hippocampal CAl NMDA receptor-dependent synaptic plasticity in spatial memory
    • Tsien JZ, Huerta PT, Tonegawa S. The essential role of hippocampal CAl NMDA receptor-dependent synaptic plasticity in spatial memory [see comments]. Cell 1996b; 87: 1327-38. Comment in: Cell 1996; 87: 1147-8.
    • (1996) Cell , vol.87 , pp. 1327-1338
    • Tsien, J.Z.1    Huerta, P.T.2    Tonegawa, S.3
  • 176
    • 0030465053 scopus 로고    scopus 로고
    • Tsien JZ, Huerta PT, Tonegawa S. The essential role of hippocampal CAl NMDA receptor-dependent synaptic plasticity in spatial memory [see comments]. Cell 1996b; 87: 1327-38. Comment in: Cell 1996; 87: 1147-8.
    • (1996) Cell , vol.87 , pp. 1147-1148
  • 177
    • 0030447141 scopus 로고    scopus 로고
    • Discovery of genes involved with learning and memory: An experimental synthesis of Hirschian and Benzerian perspectives
    • Tully T. Discovery of genes involved with learning and memory: an experimental synthesis of Hirschian and Benzerian perspectives. [Review], Proc Natl Acad Sci USA 1996; 93: 13460-7.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 13460-13467
    • Tully, T.1
  • 178
    • 0023135739 scopus 로고
    • Cognitive abilities and behavioural characteristics of children with idiopathic infantile hypercalcaemia
    • Udwin O, Yule W, Martin N. Cognitive abilities and behavioural characteristics of children with idiopathic infantile hypercalcaemia. J Child Psychol Psychiatry 1987; 28: 297-309.
    • (1987) J Child Psychol Psychiatry , vol.28 , pp. 297-309
    • Udwin, O.1    Yule, W.2    Martin, N.3
  • 179
    • 0030968580 scopus 로고    scopus 로고
    • Rho GTPases and signaling networks
    • Van Aelst L, D'Souza-Schorey C. Rho GTPases and signaling networks. Genes Dev 1997; 11: 2295-322.
    • (1997) Genes Dev , vol.11 , pp. 2295-2322
    • Van Aelst, L.1    D'Souza-Schorey, C.2
  • 180
    • 0026545863 scopus 로고
    • Wilms' tumour: Reconciling genetics and biology
    • Van Heyningen V, Hastie ND. Wilms' tumour: reconciling genetics and biology. [Review]. Trends Genet 1992; 8: 16-21.
    • (1992) Trends Genet , vol.8 , pp. 16-21
    • Van Heyningen, V.1    Hastie, N.D.2
  • 181
    • 0028870054 scopus 로고
    • Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder
    • Vargha-Khadem F, Watkins K, Alcock K, Fletcher P, Passingham R. Praxic and nonverbal cognitive deficits in a large family with a genetically transmitted speech and language disorder. Proc Natl Acad Sci USA 1995; 92: 930-3.
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 930-933
    • Vargha-Khadem, F.1    Watkins, K.2    Alcock, K.3    Fletcher, P.4    Passingham, R.5
  • 182
    • 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 AJ, Pieretti M, Sutcliffe JS, Fu Y-H, Kuhl DP, Pizzuti A, et al. Identification of a gene (FMR-1 ) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 1991; 65: 905-14.
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.1    Pieretti, M.2    Sutcliffe, J.S.3    Fu, Y.-H.4    Kuhl, D.P.5    Pizzuti, A.6
  • 183
    • 0030666543 scopus 로고    scopus 로고
    • Extended reproductive roles of the fruitless gene in Drosophila melanogaster revealed by behavioral analysis of new fru mutants
    • Villella A, Gailey DA, Berwald B, Ohshima S, Barnes PT, Hall JC. Extended reproductive roles of the fruitless gene in Drosophila melanogaster revealed by behavioral analysis of new fru mutants. Genetics 1997; 147: 1107-30.
    • (1997) Genetics , vol.147 , pp. 1107-1130
    • Villella, A.1    Gailey, D.A.2    Berwald, B.3    Ohshima, S.4    Barnes, P.T.5    Hall, J.C.6
  • 184
    • 0025300216 scopus 로고
    • Gene map of mental retardation
    • Wahlstrom J. Gene map of mental retardation. J Ment Defic Res 1990; 34: 11-27.
    • (1990) J Ment Defic Res , vol.34 , pp. 11-27
    • Wahlstrom, J.1
  • 186
    • 0032493746 scopus 로고    scopus 로고
    • Transmembrane neuregulins interact with LIM kinase 1, a cytoplasmic protein kinase implicated in development of visuospatial cognition
    • Wang JY, Frenzel KE, Wen D, Falls DL. Transmembrane neuregulins interact with LIM kinase 1, a cytoplasmic protein kinase implicated in development of visuospatial cognition. J Biol Chem 1998; 273: 20525-34.
    • (1998) J Biol Chem , vol.273 , pp. 20525-20534
    • Wang, J.Y.1    Frenzel, K.E.2    Wen, D.3    Falls, D.L.4
  • 187
    • 0028351947 scopus 로고
    • Evidence from two genetic syndromes for a dissociation between verbal and visual-spatial short-term memory
    • Wang PP, Bellugi U. Evidence from two genetic syndromes for a dissociation between verbal and visual-spatial short-term memory. J Clin Exp Neuropsychol 1994; 16: 317-22.
    • (1994) J Clin Exp Neuropsychol , vol.16 , pp. 317-322
    • Wang, P.P.1    Bellugi, U.2
  • 188
    • 0026794990 scopus 로고
    • Specific neurobehavioral profile of Williams' syndrome is associated with neocerebellar hemispheric preservation
    • Wang PP, Hesselink JR, Jernigan TL, Doherty S, Bellugi U. Specific neurobehavioral profile of Williams' syndrome is associated with neocerebellar hemispheric preservation. Neurology 1992; 42: 1999-2002.
    • (1992) Neurology , vol.42 , pp. 1999-2002
    • Wang, P.P.1    Hesselink, J.R.2    Jernigan, T.L.3    Doherty, S.4    Bellugi, U.5
  • 190
    • 0023124387 scopus 로고
    • Neuropsychological performance of children with Duchenne muscular dystrophy and spinal muscle atrophy
    • Whelan TB. Neuropsychological performance of children with Duchenne muscular dystrophy and spinal muscle atrophy. Dev Med Child Neurol 1987; 29: 212-20.
    • (1987) Dev Med Child Neurol , vol.29 , pp. 212-220
    • Whelan, T.B.1
  • 191
    • 0027440875 scopus 로고
    • Dynamics of the hippocampal ensemble code for space
    • Wilson MA, McNaughton BL. Dynamics of the hippocampal ensemble code for space [see comments]. Science 1993; 261: 1055-8. Comment in: Science 1993; 261: 993-4.
    • (1993) Science , vol.261 , pp. 1055-1058
    • Wilson, M.A.1    McNaughton, B.L.2
  • 192
    • 0027432517 scopus 로고
    • Wilson MA, McNaughton BL. Dynamics of the hippocampal ensemble code for space [see comments]. Science 1993; 261: 1055-8. Comment in: Science 1993; 261: 993-4.
    • (1993) Science , vol.261 , pp. 993-994
  • 193
    • 0027753184 scopus 로고
    • A role for Fyn tyrosine kinase in the suckling behaviour of neonatal mice
    • Yagi T, Aizawa S, Tokunaga T, Shigetani Y, Takeda N, Ikawa Y. A role for Fyn tyrosine kinase in the suckling behaviour of neonatal mice. Nature 1993; 366: 742-5.
    • (1993) Nature , vol.366 , pp. 742-745
    • Yagi, T.1    Aizawa, S.2    Tokunaga, T.3    Shigetani, Y.4    Takeda, N.5    Ikawa, Y.6
  • 194
    • 0027983479 scopus 로고
    • Induction of a dominant negative CREB transgene specifically blocks long-term memory in Drosophila
    • Yin JC, Wallach JS, Del Vecchio M, Wilder EL, Zhou H, Quinn WG, et al. Induction of a dominant negative CREB transgene specifically blocks long-term memory in Drosophila. Cell 1994; 79: 49-58.
    • (1994) Cell , vol.79 , pp. 49-58
    • Yin, J.C.1    Wallach, J.S.2    Del Vecchio, M.3    Wilder, E.L.4    Zhou, H.5    Quinn, W.G.6
  • 195
    • 0028934097 scopus 로고
    • CREB as a memory modulator: Induced expression of a dCREB2 activator isoform enhances long-term memory in Drosophila
    • Yin JC, Del Vecchio M, Zhou H, Tully T. CREB as a memory modulator: induced expression of a dCREB2 activator isoform enhances long-term memory in Drosophila. Cell 1995; 81: 107-15.
    • (1995) Cell , vol.81 , pp. 107-115
    • Yin, J.C.1    Del Vecchio, M.2    Zhou, H.3    Tully, T.4
  • 196
    • 0018849476 scopus 로고
    • Central nervous system involvement in progressive muscular dystrophy
    • Yoshioka M, Okuno T, Honda Y, Nakano Y. Central nervous system involvement in progressive muscular dystrophy. Arch Dis Childhood 1980; 55: 589-94.
    • (1980) Arch Dis Childhood , vol.55 , pp. 589-594
    • Yoshioka, M.1    Okuno, T.2    Honda, Y.3    Nakano, Y.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.