메뉴 건너뛰기




Volumn 4, Issue 8, 2000, Pages 309-318

Imprinted genes, cognition and behaviour

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; BEHAVIOR; COGNITION; EPILEPSY; GENE; GENOME IMPRINTING; GILLES DE LA TOURETTE SYNDROME; HAPPY PUPPET SYNDROME; HUMAN; MANIC DEPRESSIVE PSYCHOSIS; MENTAL DISEASE; NONHUMAN; PHENOTYPE; PRADER WILLI SYNDROME; REVIEW; SCHIZOPHRENIA; X CHROMOSOME LINKAGE;

EID: 0034255591     PISSN: 13646613     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1364-6613(00)01504-7     Document Type: Review
Times cited : (103)

References (74)
  • 1
    • 0029587022 scopus 로고
    • Gametic imprinting in mammals
    • Barlow, D.P. (1995) Gametic imprinting in mammals. Science 270, 1610-1613
    • (1995) Science , vol.270 , pp. 1610-1613
    • Barlow, D.P.1
  • 2
    • 0002888528 scopus 로고    scopus 로고
    • Evolutionary theories of genomic imprinting
    • Oxford University Press
    • Hurst, L. (1997) Evolutionary theories of genomic imprinting. In Genomic Imprinting (Vol. 18) (Surani, M.A. and Reik, W., eds), pp. 211-237, Oxford University Press
    • (1997) Genomic Imprinting , vol.18 , pp. 211-237
    • Hurst, L.1
  • 3
    • 0025958320 scopus 로고
    • Genomic imprinting in mammalian development- A parental tug-of-war
    • Moore, T. and Haig, D. (1991) Genomic imprinting in mammalian development- a parental tug-of-war. Trends Genet. 7, 45-49
    • (1991) Trends Genet. , vol.7 , pp. 45-49
    • Moore, T.1    Haig, D.2
  • 4
    • 0030856668 scopus 로고    scopus 로고
    • Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome
    • Reik, W. and Maher, E.R. (1997) Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome. Trends Genet. 13, 330-334
    • (1997) Trends Genet. , vol.13 , pp. 330-334
    • Reik, W.1    Maher, E.R.2
  • 5
    • 0032837374 scopus 로고    scopus 로고
    • Towards a molecular understanding of Prader-Willi and Angelman syndromes
    • Mann, M.R.W. and Bautolomei, M.S. (1999) Towards a molecular understanding of Prader-Willi and Angelman syndromes. Hum. Mol. Genet. 8, 1867-1873
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 1867-1873
    • Mann, M.R.W.1    Bautolomei, M.S.2
  • 6
    • 0032103697 scopus 로고    scopus 로고
    • Imprinting in Angelman and Prader-Willi syndromes
    • Jiang, Y.H. et al. (1998) Imprinting in Angelman and Prader-Willi syndromes. Curr. Opin. Genet. Dev. 8, 334-342
    • (1998) Curr. Opin. Genet. Dev. , vol.8 , pp. 334-342
    • Jiang, Y.H.1
  • 7
    • 0032531430 scopus 로고    scopus 로고
    • a receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome
    • A receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome. J. Neurosci. 18, 8505-8514
    • (1998) J. Neurosci. , vol.18 , pp. 8505-8514
    • Eta, D.T.M.1
  • 8
    • 8544269355 scopus 로고    scopus 로고
    • Linkage analysis between idiopathic generalized epilepsies and the GABA receptor α(5), β(3) and γ(3) subunit gene cluster on chromosome 15
    • Sander, T. et al. (1997) Linkage analysis between idiopathic generalized epilepsies and the GABA receptor α(5), β(3) and γ(3) subunit gene cluster on chromosome 15. Acta Neurol. Scand. 96, 1-7
    • (1997) Acta Neurol. Scand. , vol.96 , pp. 1-7
    • Sander, T.1
  • 9
    • 0033549034 scopus 로고    scopus 로고
    • Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13
    • Gurrieri, F. et al. (1999) Pervasive developmental disorder and epilepsy due to maternally derived duplication of 15q11-q13. Neurology 52, 1694-1697
    • (1999) Neurology , vol.52 , pp. 1694-1697
    • Gurrieri, F.1
  • 10
    • 0025908007 scopus 로고
    • On the parental origin of de novo mutation in man
    • Chandley, A.C. (1991) On the parental origin of de novo mutation in man. J. Med. Genet. 28, 217-223
    • (1991) J. Med. Genet. , vol.28 , pp. 217-223
    • Chandley, A.C.1
  • 11
    • 0030985156 scopus 로고    scopus 로고
    • The complex pathology of trinucleotide repeats
    • Reddy, P.S. and Housman, D.E. (1997) The complex pathology of trinucleotide repeats. Curr. Opin. Cell Biol. 9, 364-372
    • (1997) Curr. Opin. Cell Biol. , vol.9 , pp. 364-372
    • Reddy, P.S.1    Housman, D.E.2
  • 12
    • 0001544409 scopus 로고    scopus 로고
    • Turner's syndrome
    • Sperling, M., Ed.
    • Lippe, B. (1996) Turner's syndrome. In Pediatric Endocrinology (Sperling, M., ed.), pp. 387-421.
    • (1996) Pediatric Endocrinology , pp. 387-421
    • Lippe, B.1
  • 13
    • 16944366964 scopus 로고    scopus 로고
    • Evidence from Turner's syndrome of an imprinted X-l inked locus affecting cognitive function
    • Saunders, W.B., Skuse, D.H. et al. (1997) Evidence from Turner's syndrome of an imprinted X-l inked locus affecting cognitive function. Nature 387, 705-708
    • (1997) Nature , vol.387 , pp. 705-708
    • Saunders, W.B.1    Skuse, D.H.2
  • 14
    • 0033981995 scopus 로고    scopus 로고
    • Distinctive patterns of memory function in subgroups of females with Turner syndrome: Evidence for imprinted loci on the X-chromosome affecting neurodevelopment
    • Bishop, D.V. et al. (2000) Distinctive patterns of memory function in subgroups of females with Turner syndrome: evidence for imprinted loci on the X-chromosome affecting neurodevelopment. Neuropsychologia 38, 712-721
    • (2000) Neuropsychologia , vol.38 , pp. 712-721
    • Bishop, D.V.1
  • 16
    • 0022391691 scopus 로고
    • Differential activity of maternally and paternally derived chromosome regions in mice
    • Cattanach, B.M. and Kirk, M. (1985) Differential activity of maternally and paternally derived chromosome regions in mice. Nature 315,496-498
    • (1985) Nature , vol.315 , pp. 496-498
    • Cattanach, B.M.1    Kirk, M.2
  • 18
    • 0033616719 scopus 로고    scopus 로고
    • A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2
    • Peters, J. et al. (1999) A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2. Proc. Natl. Acad. Sei. U. S. A. 96, 3830-3835
    • (1999) Proc. Natl. Acad. Sei. U.S.A. , vol.96 , pp. 3830-3835
    • Peters, J.1
  • 19
    • 0030742396 scopus 로고    scopus 로고
    • Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse
    • Kagitani, F. et al. (1997) Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse. Nucleic Acids Res. 25, 3428-3432
    • (1997) Nucleic Acids Res. , vol.25 , pp. 3428-3432
    • Kagitani, F.1
  • 20
    • 33646109635 scopus 로고    scopus 로고
    • Investigations into the role of genomic imprinting in olfactory neuron development and function
    • Isles, A. et al. (1998) Investigations into the role of genomic imprinting in olfactory neuron development and function. Development of Sense Organs - BSDB Autumn Meeting
    • (1998) Development of Sense Organs - BSDB Autumn Meeting
    • Isles, A.1
  • 21
    • 0025602064 scopus 로고
    • Genome imprinting and development in the mouse
    • Surani, M.A. et al. (1990) Genome imprinting and development in the mouse. Dev. Suppl. 89-98
    • (1990) Dev. Suppl. , vol.89 , Issue.98
    • Surani, M.A.1
  • 22
    • 0028832361 scopus 로고
    • Distribution of parthenogenetic cells in the mouse-brain and their influence on brain-development and behavior
    • Allen, N.D. et al. (1995) Distribution of parthenogenetic cells in the mouse-brain and their influence on brain-development and behavior. Proc. Natl. Acad. Sei. U. S. A. 92, 10782-10786
    • (1995) Proc. Natl. Acad. Sei. U. S. A. , vol.92 , pp. 10782-10786
    • Allen, N.D.1
  • 23
    • 0029881013 scopus 로고    scopus 로고
    • Genomic imprinting and the differential roles of parental genomes in brain development
    • Keverne, E.B. et al. (1996) Genomic imprinting and the differential roles of parental genomes in brain development. Dev. Brain Res. 92, 91-100
    • (1996) Dev. Brain Res. , vol.92 , pp. 91-100
    • Keverne, E.B.1
  • 24
    • 0032192481 scopus 로고    scopus 로고
    • Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation
    • Jiang, Y.H. et al. (1998) Mutation of the Angelman ubiquitin ligase in mice causes increased cytoplasmic p53 and deficits of contextual learning and long-term potentiation. Neuron 21, 799-811
    • (1998) Neuron , vol.21 , pp. 799-811
    • Jiang, Y.H.1
  • 25
    • 0031706342 scopus 로고    scopus 로고
    • Analysis and identification of imprinted genes
    • Kelsey, G. and Reik, W. (1998) Analysis and identification of imprinted genes. Methods Enzymol. 14, 211-234
    • (1998) Methods Enzymol. , vol.14 , pp. 211-234
    • Kelsey, G.1    Reik, W.2
  • 26
    • 0031426323 scopus 로고    scopus 로고
    • Genomic imprinting in the brain
    • Keverne, E.B. (1997) Genomic imprinting in the brain. Curr. Opin. Neurobiol. 7, 463-468
    • (1997) Curr. Opin. Neurobiol. , vol.7 , pp. 463-468
    • Keverne, E.B.1
  • 27
    • 0029998089 scopus 로고    scopus 로고
    • Genomic imprinting of the human serotonin-receptor (HTR2) gene involved in development of retinoblastoma
    • Kato, M.V. et al. (1996) Genomic imprinting of the human serotonin-receptor (HTR2) gene involved in development of retinoblastoma. Am. J. Hum. Genet. 59, 1084-1090
    • (1996) Am. J. Hum. Genet. , vol.59 , pp. 1084-1090
    • Kato, M.V.1
  • 28
    • 0345628008 scopus 로고    scopus 로고
    • Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain
    • Bunzel, R. et al. (1998) Polymorphic imprinting of the serotonin-2A (5-HT2A) receptor gene in human adult brain. Mol. Brain Res. 59, 90-92
    • (1998) Mol. Brain Res. , vol.59 , pp. 90-92
    • Bunzel, R.1
  • 29
    • 0033519549 scopus 로고    scopus 로고
    • The neuroanatomy of autism: A voxel-based whole brain analysis of structural scans
    • AbelI, F. et al. (1999) The neuroanatomy of autism: a voxel-based whole brain analysis of structural scans. NeuroReport 10, 1647-1651
    • (1999) NeuroReport , vol.10 , pp. 1647-1651
    • Abeli, F.1
  • 30
    • 0032787063 scopus 로고    scopus 로고
    • MRI volumes of amygdala and hippocampus in non-mentally retarded autistic adolescents and adults
    • Aylward, E.H. et al. (1999) MRI volumes of amygdala and hippocampus in non-mentally retarded autistic adolescents and adults. Neurology 53, 2145-2150
    • (1999) Neurology , vol.53 , pp. 2145-2150
    • Aylward, E.H.1
  • 31
    • 0033134860 scopus 로고    scopus 로고
    • Bridging cognition, the brain and molecular genetics: Evidence from Williams syndrome
    • Bellugi, U. et al. (1999) Bridging cognition, the brain and molecular genetics: evidence from Williams syndrome. Trends Neurosci. 22, 197-207
    • (1999) Trends Neurosci. , vol.22 , pp. 197-207
    • Bellugi, U.1
  • 32
    • 0032837072 scopus 로고    scopus 로고
    • A lack of cerebral lateralization in schizophrenia is within the normal variation in brain maturation but indicates late, slow maturation
    • Saugstad, L. (1999) A lack of cerebral lateralization in schizophrenia is within the normal variation in brain maturation but indicates late, slow maturation. Schizophr. Res. 39, 183-196
    • (1999) Schizophr. Res. , vol.39 , pp. 183-196
    • Saugstad, L.1
  • 33
    • 0033537716 scopus 로고    scopus 로고
    • Regulation of maternal behavior and offspring growth by paternally expressed Peg3
    • Li, L.L. et al. (1999) Regulation of maternal behavior and offspring growth by paternally expressed Peg3. Science 284, 330-333
    • (1999) Science , vol.284 , pp. 330-333
    • Li, L.L.1
  • 34
    • 0031687985 scopus 로고    scopus 로고
    • Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
    • Lefebvre, L. et al. (1998) Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest. Nat. Genet. 20, 163-169
    • (1998) Nat. Genet. , vol.20 , pp. 163-169
    • Lefebvre, L.1
  • 35
    • 0031581209 scopus 로고    scopus 로고
    • A role for the Ras signalling pathway in synaptic transmission and long-term memory
    • Brambilla, R. et al. (1997) A role for the Ras signalling pathway in synaptic transmission and long-term memory. Nature 390, 281-286
    • (1997) Nature , vol.390 , pp. 281-286
    • Brambilla, R.1
  • 36
    • 0033590911 scopus 로고    scopus 로고
    • Sex specific X chromosome expression caused by genomic imprinting
    • Iwasa, Y. and Pomiankowski, A. (1999) Sex specific X chromosome expression caused by genomic imprinting. J. Theor. Biol. 197, 487-495
    • (1999) J. Theor. Biol. , vol.197 , pp. 487-495
    • Iwasa, Y.1    Pomiankowski, A.2
  • 37
    • 0033531221 scopus 로고    scopus 로고
    • Mother and father in surprise genetic agreement
    • Pagel, M. (1999) Mother and father in surprise genetic agreement. Nature 397, 19-20
    • (1999) Nature , vol.397 , pp. 19-20
    • Pagel, M.1
  • 38
    • 0032924243 scopus 로고    scopus 로고
    • Genomic imprinting of the X chromosome: A novel mechanism for the evolution of sexual dimorphism
    • Skuse, D.H. (1999) Genomic imprinting of the X chromosome: a novel mechanism for the evolution of sexual dimorphism. J. Lab. Clin. Med. 133, 23-32
    • (1999) J. Lab. Clin. Med. , vol.133 , pp. 23-32
    • Skuse, D.H.1
  • 39
    • 0033963470 scopus 로고    scopus 로고
    • Imprinting, the X-chromsome, and the male brain: Explaining sex differences in the liability to autism
    • Skuse, D. (2000) Imprinting, the X-chromsome, and the male brain: explaining sex differences in the liability to autism. Pediatr. Res. 47,9-16
    • (2000) Pediatr. Res. , vol.47 , pp. 9-16
    • Skuse, D.1
  • 40
    • 0031453213 scopus 로고    scopus 로고
    • Genes and social skills
    • Scourfield, J. et al. (1997) Genes and social skills. BioEssays 19, 1125-1127
    • (1997) BioEssays , vol.19 , pp. 1125-1127
    • Scourfield, J.1
  • 41
  • 43
    • 0027169927 scopus 로고
    • Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients
    • Glenn, C.C. et al. (1993) Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients. Hum. Mol. Genet. 2, 1377-1382
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 1377-1382
    • Glenn, C.C.1
  • 44
    • 16944363776 scopus 로고    scopus 로고
    • The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region
    • Jay, P. et al. (1997) The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region. Wat. Genet. 17, 357-361
    • (1997) Wat. Genet. , vol.17 , pp. 357-361
    • Jay, P.1
  • 45
    • 0027730805 scopus 로고
    • Functional imprinting and epigenetic modification of the human Snrpn gene
    • Glenn, C.C. et al. (1993) Functional imprinting and epigenetic modification of the human Snrpn gene. Hum. Mol. Genet. 2,2001-2005
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 2001-2005
    • Glenn, C.C.1
  • 46
    • 0028124726 scopus 로고
    • Identification of a novel paternally expressed gene in the Prader-Willi syndrome region
    • Wevrick, R. et al. (1994) Identification of a novel paternally expressed gene in the Prader-Willi syndrome region. Hum. Mol. Genet. 3, 1877-1882
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1877-1882
    • Wevrick, R.1
  • 47
    • 0031228039 scopus 로고    scopus 로고
    • The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain
    • Rougeulle, C. et al. (1997) The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain. Wat. Genet. 17, 14-15
    • (1997) Wat. Genet. , vol.17 , pp. 14-15
    • Rougeulle, C.1
  • 48
    • 0030687684 scopus 로고    scopus 로고
    • Evidence for uni parental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer
    • Meguro, M. eta/. (1997) Evidence for uni parental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer. Hum. Mol. Genet. 6, 2127-2133
    • (1997) Hum. Mol. Genet. , vol.6 , pp. 2127-2133
    • Eta, M.M.1
  • 49
    • 0032428381 scopus 로고    scopus 로고
    • A model system to study genomic imprinting of human genes
    • Gabriel, J.M. eta/. (1998) A model system to study genomic imprinting of human genes. Proc. Wat/. Acad. Sei. U. S. A. 95, 14857-14862
    • (1998) Proc. Wat/. Acad. Sei. U. S. A. , vol.95 , pp. 14857-14862
    • Eta, G.J.M.1
  • 50
    • 16944364326 scopus 로고    scopus 로고
    • Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
    • Cook, E.H. et al. (1997) Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am. J. Hum. Genet. 60, 928-934
    • (1997) Am. J. Hum. Genet. , vol.60 , pp. 928-934
    • Cook, E.H.1
  • 51
    • 18344413881 scopus 로고    scopus 로고
    • Autism and maternally derived aberrations of chromosome 15q
    • Schroer, R.J. eta/. (1998) Autism and maternally derived aberrations of chromosome 15q. Am. J. Med. Genet. 76, 327-336
    • (1998) Am. J. Med. Genet. , vol.76 , pp. 327-336
    • Eta, S.R.J.1
  • 52
    • 0032971826 scopus 로고    scopus 로고
    • Xp deletions associated with autism in three females
    • Thomas, M.S. eta/. (1999) Xp deletions associated with autism in three females. Hum. Genet. 104, 43-48
    • (1999) Hum. Genet. , vol.104 , pp. 43-48
    • Eta, T.M.S.1
  • 53
    • 0029021719 scopus 로고
    • Patterns of maternal transmission in bipolar affective-disorder
    • McMahon, F.J. et al. (1995) Patterns of maternal transmission in bipolar affective-disorder. Am. J. Hum. Genet. 56, 1277-1286
    • (1995) Am. J. Hum. Genet. , vol.56 , pp. 1277-1286
    • McMahon, F.J.1
  • 54
    • 13344260701 scopus 로고    scopus 로고
    • A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old order Amish
    • Ginns, E.I. et al. (1996) A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish. Wat. Genet. 12,431-435
    • (1996) Wat. Genet. , vol.12 , pp. 431-435
    • Ginns, E.I.1
  • 55
    • 0024361667 scopus 로고
    • Concordance by sex in sibling pairs with schizophrenia is paternally inherited - Evidence for a pseudoautosomal locus
    • Crow, T.J. et al. (1989) Concordance by sex in sibling pairs with schizophrenia is paternally inherited - evidence for a pseudoautosomal locus. Br. J. Psychiatry 155, 92-97
    • (1989) Br. J. Psychiatry , vol.155 , pp. 92-97
    • Crow, T.J.1
  • 56
    • 0028198920 scopus 로고
    • Imprinting and anticipation - Are they relevant to genetic-studies of schizophrenia
    • Asherson, P. et al. (1994) Imprinting and anticipation - are they relevant to genetic-studies of schizophrenia. Br. J. Psychiatry 164,619-624
    • (1994) Br. J. Psychiatry , vol.164 , pp. 619-624
    • Asherson, P.1
  • 57
    • 0030728102 scopus 로고    scopus 로고
    • Anticipation and imprinting in schizophrenia
    • Ohara, K. et al. (1997) Anticipation and imprinting in schizophrenia. Biol. Psychiatry 42, 760-766
    • (1997) Biol. Psychiatry , vol.42 , pp. 760-766
    • Ohara, K.1
  • 58
    • 12644303225 scopus 로고    scopus 로고
    • Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus
    • Freedman, R. et al. (1997) Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus. Proc. Wat/. Acad. Sei. U. S. A. 94, 587-592
    • (1997) Proc. Wat/. Acad. Sei. U. S. A. , vol.94 , pp. 587-592
    • Freedman, R.1
  • 59
    • 0029039820 scopus 로고
    • Clinical-evidence of genomic imprinting in Tourette's syndrome
    • Lichter, D.G. et al. (1995) Clinical-evidence of genomic imprinting in Tourette's syndrome. Neurology AS, 924-928
    • (1995) Neurology as , pp. 924-928
    • Lichter, D.G.1
  • 60
    • 0031004189 scopus 로고    scopus 로고
    • Sex of parent transmission effect in Tourette's syndrome: Evidence for earlier age at onset in maternally transmitted cases suggests a genomic imprinting effect
    • Eapen, V. et al. (1997) Sex of parent transmission effect in Tourette's syndrome: evidence for earlier age at onset in maternally transmitted cases suggests a genomic imprinting effect. Neurology 48, 934-937
    • (1997) Neurology , vol.48 , pp. 934-937
    • Eapen, V.1
  • 61
    • 0030774928 scopus 로고    scopus 로고
    • Genomic imprinting and audiogenic seizures in mice
    • Banko, M.L. et al. (1997) Genomic imprinting and audiogenic seizures in mice. Behav. Genet 27, 465-475
    • (1997) Behav. Genet , vol.27 , pp. 465-475
    • Banko, M.L.1
  • 62
    • 16044371662 scopus 로고    scopus 로고
    • Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M
    • Plass, C. et al. (1996) Identification of Grf1 on mouse chromosome 9 as an imprinted gene by RLGS-M. Wat. Genet. 14, 106-109
    • (1996) Wat. Genet. , vol.14 , pp. 106-109
    • Plass, C.1
  • 63
    • 0031586329 scopus 로고    scopus 로고
    • The Ras guanine nucleotide exchange factor CDC25Mm is present at the synaptic junction
    • Sturani, E. et al. (1997) The Ras guanine nucleotide exchange factor CDC25Mm is present at the synaptic junction. Exp. Cell Res. 235, 117-123
    • (1997) Exp. Cell Res. , vol.235 , pp. 117-123
    • Sturani, E.1
  • 65
    • 0029114716 scopus 로고
    • Peg1/Mest imprinted gene on chromosome-6 identified by cDNA subtraction hybridization
    • Kanekoishino, T. et al. (1995) Peg1/Mest imprinted gene on chromosome-6 identified by cDNA subtraction hybridization. Nat. Genet. 11, 52-59
    • (1995) Nat. Genet. , vol.11 , pp. 52-59
    • Kanekoishino, T.1
  • 66
    • 0030947270 scopus 로고    scopus 로고
    • Human PEG1/ME5T, an imprinted gene on chromosome 7
    • Kobayashi, S. et al. (1997) Human PEG1/ME5T, an imprinted gene on chromosome 7. Hum. Mol. Genet 6, 781-786
    • (1997) Hum. Mol. Genet , vol.6 , pp. 781-786
    • Kobayashi, S.1
  • 67
    • 9044253328 scopus 로고    scopus 로고
    • Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein
    • Kuroiwa, Y. et al. (1996) Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein. Wat. Genet. 12, 186-190
    • (1996) Wat. Genet. , vol.12 , pp. 186-190
    • Kuroiwa, Y.1
  • 68
    • 0030919534 scopus 로고    scopus 로고
    • The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4
    • Kirn, J. et al. (1997) The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4. Genome Res. 7, 532-540
    • (1997) Genome Res. , vol.7 , pp. 532-540
    • Kirn, J.1
  • 69
    • 0031906851 scopus 로고    scopus 로고
    • Peg3/Pw1 is an imprinted gene involved in the TNF-NF kappa B signal transduction pathway
    • Relaix, F. eta/. (1998) Peg3/Pw1 is an imprinted gene involved in the TNF-NF kappa B signal transduction pathway. Wat. Genet. 18, 287-291
    • (1998) Wat. Genet. , vol.18 , pp. 287-291
    • Eta, R.F.1
  • 70
    • 0030879482 scopus 로고    scopus 로고
    • Imprinted expression of the murine Angel man syndrome gene, Ube3a, in hippocampal and Purkinje neurons
    • Albrecht, U. et al. (1997) Imprinted expression of the murine Angel man syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Wat. Genet. 17, 75-78
    • (1997) Wat. Genet. , vol.17 , pp. 75-78
    • Albrecht, U.1
  • 71
    • 0030887633 scopus 로고    scopus 로고
    • Ubiquitin C-terminal hydrolase is an immediate-early gene essential for long-term facilitation in Aplysia
    • Hegde, A.N. et al. (1997) Ubiquitin C-terminal hydrolase is an immediate-early gene essential for long-term facilitation in Aplysia. Cell 89, 115-126
    • (1997) Cell , vol.89 , pp. 115-126
    • Hegde, A.N.1
  • 72
    • 0031259754 scopus 로고    scopus 로고
    • Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2
    • Kikyo, N. et al. (1997) Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2. Dev. Biol. 190, 66-77
    • (1997) Dev. Biol. , vol.190 , pp. 66-77
    • Kikyo, N.1
  • 73
    • 0029100944 scopus 로고
    • Arrest of cell-growth by necdin, a nuclear-protein expressed in postmitotic neurons
    • Hayashi, Y. et al. (1995) Arrest of cell-growth by necdin, a nuclear-protein expressed in postmitotic neurons. Biochem. Biophys. Res. Commun. 213,317-324
    • (1995) Biochem. Biophys. Res. Commun. , vol.213 , pp. 317-324
    • Hayashi, Y.1
  • 74
    • 0032867020 scopus 로고    scopus 로고
    • Visuospatial attentional functioning in mice: Interactions between cholinergic manipulations and genotype, Eur
    • Humby, T. et al. (1999) Visuospatial attentional functioning in mice: interactions between cholinergic manipulations and genotype, Eur. J. Neurosd. 11, 2813-2823
    • (1999) J. Neurosd. , vol.11 , pp. 2813-2823
    • Humby, T.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.