-
1
-
-
0029587022
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
43
-
-
0027169927
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
|