-
1
-
-
0025323887
-
Epigenetic control of transgene expression and imprinting by genotype-specific modifiers
-
Allen N., Norris M., Surani M. Epigenetic control of transgene expression and imprinting by genotype-specific modifiers. Cell. 61:1990;853-861.
-
(1990)
Cell
, vol.61
, pp. 853-861
-
-
Allen, N.1
Norris, M.2
Surani, M.3
-
3
-
-
0030595362
-
Interchromosomal transfer of epigenetic states in Ascobolus: Transfer of DNA methylation is mechanistically related to homologous recombination
-
Colot V., Maloisel L., Rossignol J.-L. Interchromosomal transfer of epigenetic states in Ascobolus: Transfer of DNA methylation is mechanistically related to homologous recombination. Cell. 86:1996;855-864.
-
(1996)
Cell
, vol.86
, pp. 855-864
-
-
Colot, V.1
Maloisel, L.2
Rossignol, J.-L.3
-
4
-
-
0025967857
-
Paternal imprinting of the mouse insulin-like growth factor II gene
-
DeChiara T., Robertson E., Efstratiadis A. Paternal imprinting of the mouse insulin-like growth factor II gene. Cell. 64:1991;849-859.
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
Dechiara, T.1
Robertson, E.2
Efstratiadis, A.3
-
5
-
-
0027398295
-
Differential expression of the two nonallelic proinsulin genes in the developing mouse embryo
-
Deltour L., Leduque P., Blume N., Madsen O., Dubois P., Jami J. Differential expression of the two nonallelic proinsulin genes in the developing mouse embryo. Proc. Natl. Acad. Sci. USA. 90:1993;527-531.
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 527-531
-
-
Deltour, L.1
Leduque, P.2
Blume, N.3
Madsen, O.4
Dubois, P.5
Jami, J.6
-
6
-
-
0028958086
-
Tissue- And developmental stage-specific imprinting of the mouse proinsulin gene,Ins2
-
Deltour L., Montagutelli X., Guenet J.-L., Jami J., Pàldi A. Tissue- and developmental stage-specific imprinting of the mouse proinsulin gene,Ins2. Dev. Biol. 168:1995;686-688.
-
(1995)
Dev. Biol.
, vol.168
, pp. 686-688
-
-
Deltour, L.1
Montagutelli, X.2
Guenet, J.-L.3
Jami, J.4
Pàldi, A.5
-
7
-
-
0029943141
-
Perturbation of nuclear architecture by long-distance chromosome interactions
-
Dernburg A. F., Broman K. W., Fung J. C., Marshall W. F., Philips J., Agard D. A., Sedat J. W. Perturbation of nuclear architecture by long-distance chromosome interactions. Cell. 85:1996;745-759.
-
(1996)
Cell
, vol.85
, pp. 745-759
-
-
Dernburg, A.F.1
Broman, K.W.2
Fung, J.C.3
Marshall, W.F.4
Philips, J.5
Agard, D.A.6
Sedat, J.W.7
-
8
-
-
10144234124
-
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
-
Dittrich B., Buiting K., Korn B., Rickard S., Buxton J., Saitoh S., Nicholls R. D., Poustka A., Winterpacht A., Zabel B., Horsthemke B. Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene. Nature Genet. 14:1996;163-170.
-
(1996)
Nature Genet.
, vol.14
, pp. 163-170
-
-
Dittrich, B.1
Buiting, K.2
Korn, B.3
Rickard, S.4
Buxton, J.5
Saitoh, S.6
Nicholls, R.D.7
Poustka, A.8
Winterpacht, A.9
Zabel, B.10
Horsthemke, B.11
-
9
-
-
0031010659
-
Phenotypic alterations in insulin-deficient mutant mice
-
Duvillié B., Cordonnier N., Deltour L., Dandoy-Dron F., Itier J. M., Monthioux E., Jami J., Joshi R. L., Bucchini D. Phenotypic alterations in insulin-deficient mutant mice. Proc. Natl. Acad. Sci. USA. 94:1997;5137-5140.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 5137-5140
-
-
Duvillié, B.1
Cordonnier, N.2
Deltour, L.3
Dandoy-Dron, F.4
Itier, J.M.5
Monthioux, E.6
Jami, J.7
Joshi, R.L.8
Bucchini, D.9
-
10
-
-
0026635880
-
Genetic analysis of genomic imprinting: AnImprintor-1Tme
-
Forejt J., Gregorova S. Genetic analysis of genomic imprinting: AnImprintor-1Tme. Cell. 70:1992;443-450.
-
(1992)
Cell
, vol.70
, pp. 443-450
-
-
Forejt, J.1
Gregorova, S.2
-
11
-
-
0030931672
-
Loss of the maternalH19Igf2
-
Forne T., Oswald J., Dean W., Saam J., Bailleul B., Dandolo L., Tilghman S., Walter J., Reik W. Loss of the maternalH19Igf2. Proc. Natl. Acad. Sci. USA. 94:1997;10243-10248.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 10243-10248
-
-
Forne, T.1
Oswald, J.2
Dean, W.3
Saam, J.4
Bailleul, B.5
Dandolo, L.6
Tilghman, S.7
Walter, J.8
Reik, W.9
-
12
-
-
0028365598
-
Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting
-
Giddings S., King C., Harman K., Flood J., Carnaghi L. Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting. Nature Genet. 6:1994;310-313.
-
(1994)
Nature Genet.
, vol.6
, pp. 310-313
-
-
Giddings, S.1
King, C.2
Harman, K.3
Flood, J.4
Carnaghi, L.5
-
13
-
-
0031005686
-
Nuclear organization and gene expression: Homologous pairing and long-range interaction
-
Henikoff S. Nuclear organization and gene expression: Homologous pairing and long-range interaction. Curr. Opinion Cell Biol. 9:1997;388-395.
-
(1997)
Curr. Opinion Cell Biol.
, vol.9
, pp. 388-395
-
-
Henikoff, S.1
-
15
-
-
0028342915
-
Mosaic and polymorphic imprinting of the WT1 gene in humans
-
Jinno Y., Yun K., Nishiwaki K., Kubota T., Ogawa O., Reeve A., Niikawa N. Mosaic and polymorphic imprinting of the WT1 gene in humans. Nature Genet. 6:1994;305-309.
-
(1994)
Nature Genet.
, vol.6
, pp. 305-309
-
-
Jinno, Y.1
Yun, K.2
Nishiwaki, K.3
Kubota, T.4
Ogawa, O.5
Reeve, A.6
Niikawa, N.7
-
16
-
-
0027205671
-
Allele-specific replication timing of imprinted gene regions
-
Kitsberg D., Selig S., Brandeis M., Simon I., Keshet I., Driscoll D., Nicholls R., Cedar H. Allele-specific replication timing of imprinted gene regions. Nature. 364:1993;459-463.
-
(1993)
Nature
, vol.364
, pp. 459-463
-
-
Kitsberg, D.1
Selig, S.2
Brandeis, M.3
Simon, I.4
Keshet, I.5
Driscoll, D.6
Nicholls, R.7
Cedar, H.8
-
17
-
-
0028260642
-
Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region
-
Knoll J., Cheng S., Lalande M. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region. Nature Genet. 6:1994;41-46.
-
(1994)
Nature Genet.
, vol.6
, pp. 41-46
-
-
Knoll, J.1
Cheng, S.2
Lalande, M.3
-
18
-
-
0030043993
-
Homologous association of oppositely imprinted chromosomal domains
-
LaSalle J. M., Lalande M. Homologous association of oppositely imprinted chromosomal domains. Science. 272:1996;725-728.
-
(1996)
Science
, vol.272
, pp. 725-728
-
-
Lasalle, J.M.1
Lalande, M.2
-
19
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 gene region in mice
-
Leighton P., Ingram R., Eggenschwiler J., Efstratiadis A., Tilghman S. Disruption of imprinting caused by deletion of the H19 gene region in mice. Nature. 375:1995;34-39.
-
(1995)
Nature
, vol.375
, pp. 34-39
-
-
Leighton, P.1
Ingram, R.2
Eggenschwiler, J.3
Efstratiadis, A.4
Tilghman, S.5
-
20
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li E., Beard C., Jaenisch R. Role for DNA methylation in genomic imprinting. Nature. 366:1993;362-365.
-
(1993)
Nature
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
21
-
-
0029985241
-
Multiple roles for DNA methylation in gametic imprinting
-
Neumann B., Barlow D. Multiple roles for DNA methylation in gametic imprinting. Curr. Opinion Genet. Dev. 6:1996;159-163.
-
(1996)
Curr. Opinion Genet. Dev.
, vol.6
, pp. 159-163
-
-
Neumann, B.1
Barlow, D.2
-
22
-
-
0029360421
-
Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies
-
Pàldi A., Gyapay G., Jami J. Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies. Curr. Biol. 5:1995;1030-1035.
-
(1995)
Curr. Biol.
, vol.5
, pp. 1030-1035
-
-
Pàldi, A.1
Gyapay, G.2
Jami, J.3
-
23
-
-
0028862472
-
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in theIGF2-H19
-
Reik W., Brown K., Schneid H., LeBouc Y., Bickmore W., Maher E. Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in theIGF2-H19. Hum. Mol. Genet. 4:1995;2379-2385.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2379-2385
-
-
Reik, W.1
Brown, K.2
Schneid, H.3
Lebouc, Y.4
Bickmore, W.5
Maher, E.6
-
24
-
-
0030993133
-
Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element
-
Ripoche M., Kress C., Poirier F., Dandolo L. Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element. Genes Dev. 11:1997;1596-1604.
-
(1997)
Genes Dev.
, vol.11
, pp. 1596-1604
-
-
Ripoche, M.1
Kress, C.2
Poirier, F.3
Dandolo, L.4
-
25
-
-
0029001828
-
Sex-specific meiotic recombination in the Prader-Willi/Angelman syndrome imprinted region
-
Robinson W. P., Lalande M. Sex-specific meiotic recombination in the Prader-Willi/Angelman syndrome imprinted region. Hum. Mol. Genet. 4:1995;801-806.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 801-806
-
-
Robinson, W.P.1
Lalande, M.2
-
26
-
-
0029811589
-
The mouse Smcx gene exhibits developmental and tissue specific variation in degree of escape from X inactivation
-
Sheardown S., Norris D., Fisher A., Brockdorff N. The mouse Smcx gene exhibits developmental and tissue specific variation in degree of escape from X inactivation. Hum. Mol. Genet. 5:1996;1355-1360.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1355-1360
-
-
Sheardown, S.1
Norris, D.2
Fisher, A.3
Brockdorff, N.4
-
27
-
-
0027400888
-
Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal
-
Stöger R., Kubicka P., Liu C.-G., Kafri T., Razin A., Cedar H., Barlow D. Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal. Cell. 73:1993;1-20.
-
(1993)
Cell
, vol.73
, pp. 1-20
-
-
Stöger, R.1
Kubicka, P.2
Liu, C.-G.3
Kafri, T.4
Razin, A.5
Cedar, H.6
Barlow, D.7
-
28
-
-
0028133293
-
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
-
Sutcliffe J. S., Nakao M., Christian S., Örstavik K. H., Tommerup N., Lebdetter D. H., Beaudet A. L. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Nature Genet. 8:1994;52-58.
-
(1994)
Nature Genet.
, vol.8
, pp. 52-58
-
-
Sutcliffe, J.S.1
Nakao, M.2
Christian, S.3
Örstavik, K.H.4
Tommerup, N.5
Lebdetter, D.H.6
Beaudet, A.L.7
-
29
-
-
0025857244
-
Trans-sensing effects from Drosophila to humans
-
Tartof K., Henikoff S. Trans-sensing effects from Drosophila to humans. Cell. 65:1991;201-203.
-
(1991)
Cell
, vol.65
, pp. 201-203
-
-
Tartof, K.1
Henikoff, S.2
-
30
-
-
0023646810
-
Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells
-
Thomas K. R., Capecchi M. R. Site-directed mutagenesis by gene targeting in mouse embryo-derived stem cells. Cell. 51:1987;503-512.
-
(1987)
Cell
, vol.51
, pp. 503-512
-
-
Thomas, K.R.1
Capecchi, M.R.2
-
31
-
-
0028968205
-
A paternal-specific methylation imprint marks the alleles of the mouseH19
-
Tremblay K. D., Saam J. R., Ingram R. S., Tilghman S. M., Bartolomei M. S. A paternal-specific methylation imprint marks the alleles of the mouseH19. Nature Genet. 9:1995;407-413.
-
(1995)
Nature Genet.
, vol.9
, pp. 407-413
-
-
Tremblay, K.D.1
Saam, J.R.2
Ingram, R.S.3
Tilghman, S.M.4
Bartolomei, M.S.5
|