-
3
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei, M.S., S. Zemel, and S.M. Tilghman. 1991. Parental imprinting of the mouse H19 gene. Nature 351: 153-155.
-
(1991)
Nature
, vol.351
, pp. 153-155
-
-
Bartolomei, M.S.1
Zemel, S.2
Tilghman, S.M.3
-
4
-
-
0027203606
-
Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
-
Bartolomei, M.S., A.L. Webber, M.E. Brunkow, and S.M. Tilghman. 1993. Epigenetic mechanisms underlying the imprinting of the mouse H19 gene. Genes & Dev. 7; 1663-1673.
-
(1993)
Genes & Dev.
, vol.7
, pp. 1663-1673
-
-
Bartolomei, M.S.1
Webber, A.L.2
Brunkow, M.E.3
Tilghman, S.M.4
-
5
-
-
0028786951
-
Loss of methylation activates Xist in somatic but not in embryonic cells
-
Beard, C., E. Li, and R. Jeanisch. 1995. Loss of methylation activates Xist in somatic but not in embryonic cells. Genes & Dev. 9: 2325-2334.
-
(1995)
Genes & Dev.
, vol.9
, pp. 2325-2334
-
-
Beard, C.1
Li, E.2
Jeanisch, R.3
-
6
-
-
0028901594
-
DNA rearrangements located over 100 kb 5′ of the steel (S1)-coding region in steel-panda and steel-contrasted mice deregulate s1 expression and cause female sterility by disrupting ovarian follicle development
-
Bedell, M.A., C.I. Brannan, E.P. Evans, N.G. Copeland, N.A. Jenkins, and P.J. Donovan. 1995. DNA rearrangements located over 100 kb 5′ of the steel (S1)-coding region in Steel-panda and Steel-contrasted mice deregulate S1 expression and cause female sterility by disrupting ovarian follicle development. Genes & Dev. 9: 455-470.
-
(1995)
Genes & Dev.
, vol.9
, pp. 455-470
-
-
Bedell, M.A.1
Brannan, C.I.2
Evans, E.P.3
Copeland, N.G.4
Jenkins, N.A.5
Donovan, P.J.6
-
7
-
-
0025829449
-
Characterization of a murine gene expressed from the inactive X chromosome
-
Borsani, G., R. Tonlorenzi, M.C. Simmler, L. Dandolo, D. Arnaud, V. Capra, M. Grompe, A. Pizzuti, D. Muzny, C. Lawrence, H.F. Willard, P. Avner, and A. Ballabio. 1991. Characterization of a murine gene expressed from the inactive X chromosome. Nature 351: 325-328.
-
(1991)
Nature
, vol.351
, pp. 325-328
-
-
Borsani, G.1
Tonlorenzi, R.2
Simmler, M.C.3
Dandolo, L.4
Arnaud, D.5
Capra, V.6
Grompe, M.7
Pizzuti, A.8
Muzny, D.9
Lawrence, C.10
Willard, H.F.11
Avner, P.12
Ballabio, A.13
-
8
-
-
0025094358
-
Differential distribution of long and short interspersed element sequences in the mouse genome: Chromosome karyotyping by fluorescence in situ hybridization
-
Boyle, A.L., S.G. Ballard, and D.C. Ward. 1990. Differential distribution of long and short interspersed element sequences in the mouse genome: Chromosome karyotyping by fluorescence in situ hybridization. Proc. Natl. Acad. Sci. 87: 7757-7761.
-
(1990)
Proc. Natl. Acad. Sci.
, vol.87
, pp. 7757-7761
-
-
Boyle, A.L.1
Ballard, S.G.2
Ward, D.C.3
-
9
-
-
0027236694
-
The ontogeny of allele-specific methylation associated with imprinted genes in the mouse
-
Brandeis, M., T. Kafri, M. Ariel, J.R. Chaillet, J. McCarrey, A. Razin, and H. Cedar. 1993. The ontogeny of allele-specific methylation associated with imprinted genes in the mouse. EMBO J. 12: 3669-3677.
-
(1993)
EMBO J.
, vol.12
, pp. 3669-3677
-
-
Brandeis, M.1
Kafri, T.2
Ariel, M.3
Chaillet, J.R.4
McCarrey, J.5
Razin, A.6
Cedar, H.7
-
10
-
-
0025961771
-
A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome
-
Brown, C.J., A. Ballabio, J.L. Rupert, R.G. Lafreniere, M. Grompe, R. Tonlorenzi, and H.F. Willard. 1991. A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosome. Nature 349: 38-44.
-
(1991)
Nature
, vol.349
, pp. 38-44
-
-
Brown, C.J.1
Ballabio, A.2
Rupert, J.L.3
Lafreniere, R.G.4
Grompe, M.5
Tonlorenzi, R.6
Willard, H.F.7
-
11
-
-
0026456701
-
The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus
-
Brown, C.J., B.D. Hendrich, J.L. Rupert, R.G. Lafreniere, Y. Xing, J. Lawrence, and H.F. Willard. 1992. The human XIST gene: Analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus. Cell 71: 527-542.
-
(1992)
Cell
, vol.71
, pp. 527-542
-
-
Brown, C.J.1
Hendrich, B.D.2
Rupert, J.L.3
Lafreniere, R.G.4
Xing, Y.5
Lawrence, J.6
Willard, H.F.7
-
12
-
-
0015356840
-
Evidence of nonrandom X chromosome activity in the mouse
-
Cattanach, B.M. and C.E. Williams. 1972. Evidence of nonrandom X chromosome activity in the mouse. Genet. Res. 19: 229-240.
-
(1972)
Genet. Res.
, vol.19
, pp. 229-240
-
-
Cattanach, B.M.1
Williams, C.E.2
-
13
-
-
0030034051
-
XIST RNA paints the inactive X chromosome at interphase: Evidence for a novel RNA involved in nuclear/chromosome structure
-
Clemson, C.M., J.A. McNeil, H.F. Willard, and J.B. Lawrence. 1996. XIST RNA paints the inactive X chromosome at interphase: Evidence for a novel RNA involved in nuclear/chromosome structure. J. Cell Biol. 132: 259-275.
-
(1996)
J. Cell Biol.
, vol.132
, pp. 259-275
-
-
Clemson, C.M.1
McNeil, J.A.2
Willard, H.F.3
Lawrence, J.B.4
-
14
-
-
0031832579
-
Role of the region 3′ to Xist exon 6 in the counting process of X-chromosome inactivation
-
Clerc, P. and P. Avner. 1998. Role of the region 3′ to Xist exon 6 in the counting process of X-chromosome inactivation. Nat. Genet. 19: 249-253.
-
(1998)
Nat. Genet.
, vol.19
, pp. 249-253
-
-
Clerc, P.1
Avner, P.2
-
15
-
-
0028241961
-
A rosy future for heterochrmatin
-
Cook, K.R. and G.H. Karpen. 1994. A rosy future for heterochrmatin. Proc. Natl. Acad. Sci. 91: 5219-5221.
-
(1994)
Proc. Natl. Acad. Sci.
, vol.91
, pp. 5219-5221
-
-
Cook, K.R.1
Karpen, G.H.2
-
16
-
-
0015207737
-
Directed genetic change model for X chromosome inactivation in eutherian mammals
-
Cooper, D.W. 1971. Directed genetic change model for X chromosome inactivation in eutherian mammals. Nature 230: 292-294.
-
(1971)
Nature
, vol.230
, pp. 292-294
-
-
Cooper, D.W.1
-
17
-
-
0028600585
-
The mouse segmentation gene kr encodes a novel basic domain-leucine zipper transcription factor
-
Cordes, S.P. and G.S. Barsh. 1994. The mouse segmentation gene kr encodes a novel basic domain-leucine zipper transcription factor. Cell 79: 1025-1034.
-
(1994)
Cell
, vol.79
, pp. 1025-1034
-
-
Cordes, S.P.1
Barsh, G.S.2
-
18
-
-
0029937208
-
Genetic modification of heterochromatic association and nuclear organization in Drosophila
-
Csink, A.K. and S. Henikoff. 1996. Genetic modification of heterochromatic association and nuclear organization in Drosophila. Nature 381: 529-531.
-
(1996)
Nature
, vol.381
, pp. 529-531
-
-
Csink, A.K.1
Henikoff, S.2
-
19
-
-
0033546359
-
Dosage compensation proteins targeted to X chromosomes by a determinant of hermaphrodite fate
-
Dawes, H.E., D.S. Berlin, D.M. Lapidus, C. Nusbaum, T.L. Davis, and B.J. Meyer, 1999. Dosage compensation proteins targeted to X chromosomes by a determinant of hermaphrodite fate. Science 284: 1800-1804.
-
(1999)
Science
, vol.284
, pp. 1800-1804
-
-
Dawes, H.E.1
Berlin, D.S.2
Lapidus, D.M.3
Nusbaum, C.4
Davis, T.L.5
Meyer, B.J.6
-
20
-
-
0028789040
-
A duplication/pancreatic inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene
-
de Kok, Y.J.M., G.F.M. Merkx, S.M. van der Maarel, I. Huber, S. Malcolm, H.-H. Ropers, and F.P.M. Cremers. 1995a. A duplication/pancreatic inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene. Hum. Mol. Genet. 4: 2145-2150.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2145-2150
-
-
De Kok, Y.J.M.1
Merkx, G.F.M.2
Van Der Maarel, S.M.3
Huber, I.4
Malcolm, S.5
Ropers, H.-H.6
Cremers, F.P.M.7
-
21
-
-
0028988233
-
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
-
de Kok, Y.J.M., S.M. van der Maarel, M. Bitner-Glindzicz, I. Huber, A.P. Monaco, S. Malcolm, M.E. Pembrey, H.-H. Ropers, and F.P.M. Cremers. 1995b. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. Science 267: 685-688.
-
(1995)
Science
, vol.267
, pp. 685-688
-
-
De Kok, Y.J.M.1
Van Der Maarel, S.M.2
Bitner-Glindzicz, M.3
Huber, I.4
Monaco, A.P.5
Malcolm, S.6
Pembrey, M.E.7
Ropers, H.-H.8
Cremers, F.P.M.9
-
22
-
-
10144238527
-
Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4
-
de Kok, Y.J.M., E.R. Vossenaar, C.W. Cremers, N. Dahl, J. Laporte, L.J. Hu, D. Lacombe, N. Fischel-Ghodsian, R.A. Friedman, L.S. Parnes et al. 1996. Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4. Hum. Mol. Genet. 5: 1229-1235.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1229-1235
-
-
Kok, Y.J.M.1
Vossenaar, E.R.2
Cremers, C.W.3
Dahl, N.4
Laporte, J.5
Hu, L.J.6
Lacombe, D.7
Fischel-Ghodsian, N.8
Friedman, R.A.9
Parnes, L.S.10
-
23
-
-
0032531430
-
Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome
-
DeLorey, T.M., A. Handforth, S.G. Anagnostaras, G.E. Homanics, B.A. Minassian, A. Asatourian, M.S. Fanselow, A. Delgado-Escueta, G.D. Ellison, and R.W. Olsen. 1998. Mice lacking the beta3 subunit of the GABAA 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
-
-
Delorey, T.M.1
Handforth, A.2
Anagnostaras, S.G.3
Homanics, G.E.4
Minassian, B.A.5
Asatourian, A.6
Fanselow, M.S.7
Delgado-Escueta, A.8
Ellison, G.D.9
Olsen, R.W.10
-
24
-
-
0029943141
-
Perturbation of nuclear architecture by long-distance chromosome interactions
-
Dernburg, A.F., K.W. Broman, J.C. Fung, W.F. Marshall, J. Philips, D.A. Agard, and J.W. Sedat. 1996a. Perturbation of nuclear architecture by long-distance chromosome interactions. Cell 85: 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
-
25
-
-
0030581163
-
Direct evidence of a role for heterochromatin in meiotic chromosome segregation
-
Dernburg, A.F., J.W. Sedat, and R.S. Hawley. 1996b. Direct evidence of a role for heterochromatin in meiotic chromosome segregation. Cell 86: 135-146.
-
(1996)
Cell
, vol.86
, pp. 135-146
-
-
Dernburg, A.F.1
Sedat, J.W.2
Hawley, R.S.3
-
26
-
-
0028726492
-
Genomic imprinting in humans
-
Driscoll, D. 1994. Genomic imprinting in humans. Mol. Genet. Med. 4: 37-77.
-
(1994)
Mol. Genet. Med.
, vol.4
, pp. 37-77
-
-
Driscoll, D.1
-
27
-
-
0031914019
-
Imprinting at the mouse Ins2 locus: Evidence for cis- and trans-allelic interactions
-
Duvillie, B., D. Bucchini, T. Tang, J. Jami, and A. Paldi. 1998. Imprinting at the mouse Ins2 locus: Evidence for cis- and trans-allelic interactions. Genomics 47: 52-57.
-
(1998)
Genomics
, vol.47
, pp. 52-57
-
-
Duvillie, B.1
Bucchini, D.2
Tang, T.3
Jami, J.4
Paldi, A.5
-
28
-
-
0027298420
-
The role of heterochromatin in the expression of a heterochromatic gene, the rolled locus of Drosophila melanogaster
-
Eberl, D.F., B.J. Duyf, and A.J. Hilliker. 1993. The role of heterochromatin in the expression of a heterochromatic gene, the rolled locus of Drosophila melanogaster. Genetics 134: 277-292.
-
(1993)
Genetics
, vol.134
, pp. 277-292
-
-
Eberl, D.F.1
Duyf, B.J.2
Hilliker, A.J.3
-
29
-
-
0014920702
-
X-autosome translocations in the mouse: Total inactivation versus partial inactivation of the X chromosome
-
Eicher, E.M. 1970. X-autosome translocations in the mouse: Total inactivation versus partial inactivation of the X chromosome. Adv. Genet. 15: 175-259.
-
(1970)
Adv. Genet.
, vol.15
, pp. 175-259
-
-
Eicher, E.M.1
-
30
-
-
0019823967
-
A preliminary cytogenetic study of X chromosome inactivation in diploid parthenogenetic embryos from LT/Sv mice
-
Endo, S. and N. Takagi. 1981. A preliminary cytogenetic study of X chromosome inactivation in diploid parthenogenetic embryos from LT/Sv mice. Jpn. J. Genet. 56: 349-356.
-
(1981)
Jpn. J. Genet.
, vol.56
, pp. 349-356
-
-
Endo, S.1
Takagi, N.2
-
31
-
-
0019990459
-
The late-replicating X chromosome in digynous mouse triploid embryos
-
Endo, S., N. Takagi, and M. Sasaki. 1982. The late-replicating X chromosome in digynous mouse triploid embryos. Dev. Genet. 3: 165-176.
-
(1982)
Dev. Genet.
, vol.3
, pp. 165-176
-
-
Endo, S.1
Takagi, N.2
Sasaki, M.3
-
32
-
-
0032769062
-
Compact chromatin packaging of inactive X chromosome involves the actively transcribed Xist gene
-
Endo, Y., T. Watanabe, Y. Mishima, A. Yoshimura, N. Takagi, and R. Kominami. 1999. Compact chromatin packaging of inactive X chromosome involves the actively transcribed Xist gene. Mamm Genome 10: 606-610.
-
(1999)
Mamm Genome
, vol.10
, pp. 606-610
-
-
Endo, Y.1
Watanabe, T.2
Mishima, Y.3
Yoshimura, A.4
Takagi, N.5
Kominami, R.6
-
33
-
-
0026492019
-
A question of time: Replication origins of eukaryotic chromosomes
-
Fangman, W.L. and B.J. Brewer. 1992. A question of time: Replication origins of eukaryotic chromosomes. Cell 71: 363-366.
-
(1992)
Cell
, vol.71
, pp. 363-366
-
-
Fangman, W.L.1
Brewer, B.J.2
-
34
-
-
0026428611
-
Embryological and molecular investigations of parental imprinting on mouse chromosome 7
-
Ferguson-Smith, A.C., B.M. Cattanach, S.C. Barton, C.V. Beechey, and M.A. Surani. 1991. Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature 351: 667-670.
-
(1991)
Nature
, vol.351
, pp. 667-670
-
-
Ferguson-Smith, A.C.1
Cattanach, B.M.2
Barton, S.C.3
Beechey, C.V.4
Surani, M.A.5
-
35
-
-
0031984304
-
Repeat-induced gene silencing in mammals
-
Garrick, D., S. Fiering, D.I. Martin, and E. Whitelaw. 1998. Repeat-induced gene silencing in mammals. Nat. Genet. 18: 56-59.
-
(1998)
Nat. Genet.
, vol.18
, pp. 56-59
-
-
Garrick, D.1
Fiering, S.2
Martin, D.I.3
Whitelaw, E.4
-
36
-
-
0033043847
-
The timing of Xist replication: Dominance of the domain
-
Gartler, S.M., L. Goldstein, S.E. Tyler-Freer, and R.S. Hansen. 1999. The timing of Xist replication: dominance of the domain. Hum. Mol. Genetics 8: 1085-1089.
-
(1999)
Hum. Mol. Genetics
, vol.8
, pp. 1085-1089
-
-
Gartler, S.M.1
Goldstein, L.2
Tyler-Freer, S.E.3
Hansen, R.S.4
-
37
-
-
0027169927
-
Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients
-
Glenn, C.C., R.D. Nicholls, W.P. Robinson, S. Saitoh, N. Niikawa, A. Schinzel, B. Horsthemke, and D.J. Driscoll. 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
Nicholls, R.D.2
Robinson, W.P.3
Saitoh, S.4
Niikawa, N.5
Schinzel, A.6
Horsthemke, B.7
Driscoll, D.J.8
-
38
-
-
0030798245
-
Histone acetylation in chromatin structure and transcription
-
Grunstein, M. 1997. Histone acetylation in chromatin structure and transcription. Nature 389: 349-352.
-
(1997)
Nature
, vol.389
, pp. 349-352
-
-
Grunstein, M.1
-
39
-
-
0029042743
-
Reverse replication timing for the XIST gene in human fibroblasts
-
Hansen, R.S., T.K. Canfield, and S.M. Gartler. 1995. Reverse replication timing for the XIST gene in human fibroblasts. Hum. Mol. Genet. 4: 813-820.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 813-820
-
-
Hansen, R.S.1
Canfield, T.K.2
Gartler, S.M.3
-
41
-
-
0032958104
-
Xist yeast artificial chromosome transgenes function as X-inactivation centers only in multicopy arrays and not as single copies
-
Heard, E., F. Mongelard, D. Arnaud, and P. Avner. 1999b. Xist yeast artificial chromosome transgenes function as X-inactivation centers only in multicopy arrays and not as single copies. Mol. Cell. Biol. 19: 3156-3166.
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 3156-3166
-
-
Heard, E.1
Mongelard, F.2
Arnaud, D.3
Avner, P.4
-
42
-
-
0000251397
-
Das heterochromatin der moose
-
Heitz, E. 1928. Das heterochromatin der moose. I Jahrb Wiss Botanik 69: 762-818.
-
(1928)
I Jahrb Wiss Botanik
, vol.69
, pp. 762-818
-
-
Heitz, E.1
-
43
-
-
0031005686
-
Nuclear organization and gene expression: Homologous pairing and long-range interactions
-
Henikoff, S. 1997. Nuclear organization and gene expression: homologous pairing and long-range interactions. Curr. Op. Cell Biol. 9: 388-395.
-
(1997)
Curr. Op. Cell Biol.
, vol.9
, pp. 388-395
-
-
Henikoff, S.1
-
45
-
-
0031001346
-
Xist has properties of the X-chromosome inactivation centre
-
Herzing, L.B.K., J.T. Romer, J.M. Horn, and A. Ashworth. 1997. Xist has properties of the X-chromosome inactivation centre. Nature 386: 272-275.
-
(1997)
Nature
, vol.386
, pp. 272-275
-
-
Herzing, L.B.K.1
Romer, J.T.2
Horn, J.M.3
Ashworth, A.4
-
46
-
-
7144256245
-
Monoallelic expression of the interleukin-2 locus
-
Hollander, G.A., S. Zuklys, C. Morel, E. Mizoguchi, K. Mobisson, S. Simpson, C. Terhorst, W. Wishart, D.E. Golan, A.K. Bhan, and S.J. Burakoff. 1998. Monoallelic expression of the interleukin-2 locus. Science 279: 2118-2121.
-
(1998)
Science
, vol.279
, pp. 2118-2121
-
-
Hollander, G.A.1
Zuklys, S.2
Morel, C.3
Mizoguchi, E.4
Mobisson, K.5
Simpson, S.6
Terhorst, C.7
Wishart, W.8
Golan, D.E.9
Bhan, A.K.10
Burakoff, S.J.11
-
47
-
-
0033535935
-
A new structure for the murine Xist gene and its relationship to chromosome choice/counting during X-chromosome inactivation
-
Hong, Y.K., S.D. Ontiveros, C. Chen, and W.M. Strauss. 1999. A new structure for the murine Xist gene and its relationship to chromosome choice/counting during X-chromosome inactivation. Proc. Natl. Acad. Sci. 96: 6829-6834.
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 6829-6834
-
-
Hong, Y.K.1
Ontiveros, S.D.2
Chen, C.3
Strauss, W.M.4
-
48
-
-
0032954098
-
Taming of transposable elements by homology-dependent gene silencing
-
Jensen, S., M.-P. Gassama, and T. Heidemann. 1999. Taming of transposable elements by homology-dependent gene silencing. Nat. Genet. 21: 209-212.
-
(1999)
Nat. Genet.
, vol.21
, pp. 209-212
-
-
Jensen, S.1
Gassama, M.-P.2
Heidemann, T.3
-
49
-
-
0027183088
-
The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression
-
Jeppesen, P. and B.M. Turner. 1993. The inactive X chromosome in female mammals is distinguished by a lack of histone H4 acetylation, a cytogenetic marker for gene expression. Cell 74: 281-289.
-
(1993)
Cell
, vol.74
, pp. 281-289
-
-
Jeppesen, P.1
Turner, B.M.2
-
50
-
-
0032527755
-
Igf2 imprinting does not require its own DNA methylation or H19 RNA
-
Jones, B.K., J.M. Levorse, and S.M. Tilghman. 1998. Igf2 imprinting does not require its own DNA methylation or H19 RNA. Genes & Dev. 12: 2200-2207.
-
(1998)
Genes & Dev.
, vol.12
, pp. 2200-2207
-
-
Jones, B.K.1
Levorse, J.M.2
Tilghman, S.M.3
-
51
-
-
0028210480
-
Position-effect variegation and the new biology of heterochromatin
-
Karpen, G.H. 1994. Position-effect variegation and the new biology of heterochromatin. Curr. Biol. 4: 281-291.
-
(1994)
Curr. Biol.
, vol.4
, pp. 281-291
-
-
Karpen, G.H.1
-
52
-
-
17344370076
-
The impact of l1 retrotransposons on the human genome
-
Kazazian, H.H.J. and J.V. Moran. 1998. The impact of L1 retrotransposons on the human genome. Nat. Genet. 19: 19-24.
-
(1998)
Nat. Genet.
, vol.19
, pp. 19-24
-
-
Kazazian, H.H.J.1
Moran, J.V.2
-
53
-
-
0027205671
-
Allele-specific replication timing of imprinted gene regions
-
Kitsberg, D., S. Selig, M. Brandeis, I. Simon, I. Keshet, D.J. Driscoll, R.D. Nicholls, and H. Cedar. 1993. Allele-specific replication timing of imprinted gene regions. Nature 364: 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.J.6
Nicholls, R.D.7
Cedar, H.8
-
54
-
-
0030904893
-
DNA methylation, heterochromatin and epigenetic carcinogens
-
Klein, C.B. and M. Costa. 1997. DNA methylation, heterochromatin and epigenetic carcinogens. Mut. Res. 386: 163-180.
-
(1997)
Mut. Res.
, vol.386
, pp. 163-180
-
-
Klein, C.B.1
Costa, M.2
-
55
-
-
0031663782
-
Position effect in human genetic disease
-
Kleinjan, D.-J. and V. van Heyningen. 1998. Position effect in human genetic disease. Hum. Mol. Genet. 7: 1611-1618.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1611-1618
-
-
Kleinjan, D.-J.1
Van Heyningen, V.2
-
56
-
-
0030043993
-
Homologous association of oppositely imprinted chromosomal domains
-
LaSalle, J.M. and M. Lalande. 1996. Homologous association of oppositely imprinted chromosomal domains. Science 272: 725-728.
-
(1996)
Science
, vol.272
, pp. 725-728
-
-
LaSalle, J.M.1
Lalande, M.2
-
58
-
-
0030581152
-
A 450 kb transgene displays properties of the mammalian X-inactivation center
-
Lee, J.T., W.M. Strauss, J.A. Dausman, and R. Jaenisch. 1996. A 450 kb transgene displays properties of the mammalian X-inactivation center. Cell 86: 83-94.
-
(1996)
Cell
, vol.86
, pp. 83-94
-
-
Lee, J.T.1
Strauss, W.M.2
Dausman, J.A.3
Jaenisch, R.4
-
59
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 gene region in mice
-
Leighton, P.A., R.S. Ingram, J. Eggenschwiler, A. Efstratiadis, and S.M. Tilghman. 1995. Disruption of imprinting caused by deletion of the H19 gene region in mice. Nature 375: 34-39.
-
(1995)
Nature
, vol.375
, pp. 34-39
-
-
Leighton, P.A.1
Ingram, R.S.2
Eggenschwiler, J.3
Efstratiadis, A.4
Tilghman, S.M.5
-
60
-
-
0000054724
-
The theory and application of a new method of detecting chromosomal rearrangements in Drosophila melanogaster
-
Lewis, E.B. 1954. The theory and application of a new method of detecting chromosomal rearrangements in Drosophila melanogaster. Am. Nat. 88: 225-239.
-
(1954)
Am. Nat.
, vol.88
, pp. 225-239
-
-
Lewis, E.B.1
-
61
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li, E., C. Beard, and R. Jaenisch. 1993. Role for DNA methylation in genomic imprinting. Nature 366: 362-365.
-
(1993)
Nature
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
62
-
-
0023019631
-
Mouse satellite DNA, centromere structure, and sister chromatid pairing
-
Lica, L.M., S. Narayanswami, and B.A. Hamkalo. 1986. Mouse satellite DNA, centromere structure, and sister chromatid pairing. J. Cell Biol. 103: 1145-1151.
-
(1986)
J. Cell Biol.
, vol.103
, pp. 1145-1151
-
-
Lica, L.M.1
Narayanswami, S.2
Hamkalo, B.A.3
-
63
-
-
0031820331
-
X-chromosome inactivation: A repeat hypothesis
-
Lyon, M.F. 1998. X-chromosome inactivation: A repeat hypothesis. Cytogenet. Cell Genet. 80: 133-137.
-
(1998)
Cytogenet. Cell Genet.
, vol.80
, pp. 133-137
-
-
Lyon, M.F.1
-
64
-
-
0032489426
-
Role of the Xist gene in X chromosome choosing
-
Marahrens, Y., J. Loring, and R. Jaenisch. 1998. Role of the Xist gene in X chromosome choosing. Cell 92: 657-664.
-
(1998)
Cell
, vol.92
, pp. 657-664
-
-
Marahrens, Y.1
Loring, J.2
Jaenisch, R.3
-
65
-
-
0031044166
-
Xist-deficient mice are defective in dosage compensation but not spermatogenesis
-
Marahrens, Y., B. Panning, J. Dausman, W. Strauss, and R. Jaenisch. 1997. Xist-deficient mice are defective in dosage compensation but not spermatogenesis. Genes & Dev. 11: 156-166.
-
(1997)
Genes & Dev.
, vol.11
, pp. 156-166
-
-
Marahrens, Y.1
Panning, B.2
Dausman, J.3
Strauss, W.4
Jaenisch, R.5
-
66
-
-
0028627765
-
Trans-inactivation of homologous sequences in Nicotiana tabacum
-
Matzke, A.J. and M.A. Matzke. 1995a. Trans-inactivation of homologous sequences in Nicotiana tabacum. Curr. Top. Microbiol. Immunol. 197: 1-14.
-
(1995)
Curr. Top. Microbiol. Immunol.
, vol.197
, pp. 1-14
-
-
Matzke, A.J.1
Matzke, M.A.2
-
67
-
-
0002603357
-
Inactivation of repeated genes-DNA-DNA interaction?
-
ed. J. Paszkowski Kluyver Academic Publishers, Netherlands
-
Matzke, M., A.J.M. Matzke, and O.M. Schied. 1994. Inactivation of repeated genes-DNA-DNA interaction? In Homologous recombination and gene silencing in plants (ed. J. Paszkowski) pp. 271-307. Kluyver Academic Publishers, Netherlands.
-
(1994)
Homologous Recombination and Gene Silencing in Plants
, pp. 271-307
-
-
Matzke, M.1
Matzke, A.J.M.2
Schied, O.M.3
-
68
-
-
0028891102
-
Homology-dependent gene silencing in transgenic plants: What does it really tell us?
-
Matzke, M.A. and A.J.M. Matzke. 1995b. Homology-dependent gene silencing in transgenic plants: What does it really tell us? Trends Genet. 11: 1-3.
-
(1995)
Trends Genet.
, vol.11
, pp. 1-3
-
-
Matzke, M.A.1
Matzke, A.J.M.2
-
69
-
-
0029102514
-
How and why do plants inactivate homologous (trans) genes?
-
Matzke, M.A. and A.J.M. Matzke. 1995c. How and why do plants inactivate homologous (trans) genes? Plant Physiol. 107: 679-685.
-
(1995)
Plant Physiol.
, vol.107
, pp. 679-685
-
-
Matzke, M.A.1
Matzke, A.J.M.2
-
70
-
-
0013686676
-
Chromosome studies on the Diptera II. The paired association of chromosomes in the diptera, and its significance
-
Metz, C.W. 1916. Chromosome studies on the Diptera II. The paired association of chromosomes in the diptera, and its significance. J. Exp. Zool. 21: 213-280.
-
(1916)
J. Exp. Zool.
, vol.21
, pp. 213-280
-
-
Metz, C.W.1
-
72
-
-
0025223284
-
Insights into X chromosome inactivation from studies of species variation, DNA methylation and replication, and vice versa
-
Migeon, B.R. 1990. Insights into X chromosome inactivation from studies of species variation, DNA methylation and replication, and vice versa. Genet. Res. 56: 91-98.
-
(1990)
Genet. Res.
, vol.56
, pp. 91-98
-
-
Migeon, B.R.1
-
73
-
-
0028269238
-
x) mutation deletes the S-adenosylhomocysteine hydrolase (Ahcy) gene
-
x) mutation deletes the S-adenosylhomocysteine hydrolase (Ahcy) gene. EMBO J. 13: 1806-1816.
-
(1994)
EMBO J.
, vol.13
, pp. 1806-1816
-
-
Miller, M.W.1
Duhl, D.M.2
Winkes, B.M.3
Arredondo-Vega, F.4
Saxon, P.J.5
Wolff, G.L.6
Epstein, C.J.7
Hershfield, M.S.8
Barsh, G.S.9
-
74
-
-
0019510628
-
Reactivation of an inactive human X chromosome: Evidence for X inactivation by DNA methylation
-
Mohandas, T., R.S. Sparkes, and L.J. Shapiro. 1981. Reactivation of an inactive human X chromosome: Evidence for X inactivation by DNA methylation. Science 211: 393-396.
-
(1981)
Science
, vol.211
, pp. 393-396
-
-
Mohandas, T.1
Sparkes, R.S.2
Shapiro, L.J.3
-
75
-
-
0027787530
-
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene
-
Mutirangura, A., A. Jayakumar, J.S. Sutcliffe, M. Nakao, M.J. McKinney, K. Buiting, B. Horsthemke, A.L. Beaudet, A.C. Chinault, and D.H. Ledbetter. 1993. A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene. Genomics 18: 546-552.
-
(1993)
Genomics
, vol.18
, pp. 546-552
-
-
Mutirangura, A.1
Jayakumar, A.2
Sutcliffe, J.S.3
Nakao, M.4
McKinney, M.J.5
Buiting, K.6
Horsthemke, B.7
Beaudet, A.L.8
Chinault, A.C.9
Ledbetter, D.H.10
-
76
-
-
0027360049
-
Oppositely imprinting genes H19 and insulin-like growth factor 2 are coexpressed in human androgenetic trophoblast
-
Mutter, G.L., C.L. Stewart, M.L. Chaponot, and R.J. Pomponio. 1993. Oppositely imprinting genes H19 and insulin-like growth factor 2 are coexpressed in human androgenetic trophoblast. Am. J. Hum. Genet. 53: 1096-1102.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 1096-1102
-
-
Mutter, G.L.1
Stewart, C.L.2
Chaponot, M.L.3
Pomponio, R.J.4
-
77
-
-
0030750152
-
X chromosome counting mechanisms that determine nematode sex
-
Nicoll, M., C.C. Akerib, and B.J. Meyer. 1997. X chromosome counting mechanisms that determine nematode sex. Nature 388: 200-204.
-
(1997)
Nature
, vol.388
, pp. 200-204
-
-
Nicoll, M.1
Akerib, C.C.2
Meyer, B.J.3
-
78
-
-
0028232839
-
Evidence that random and imprinted Xist expression is controlled by preemptive methylation
-
Norris, D.P., D. Patel, G.F. Kay, G.D. Penny, N. Brockdorff, S.A. Sheardon, and S. Rastan. 1994. Evidence that random and imprinted Xist expression is controlled by preemptive methylation. Cell 77: 41-51.
-
(1994)
Cell
, vol.77
, pp. 41-51
-
-
Norris, D.P.1
Patel, D.2
Kay, G.F.3
Penny, G.D.4
Brockdorff, N.5
Sheardon, S.A.6
Rastan, S.7
-
79
-
-
0033061308
-
Random monoallelic expression of the imprinted Igf2 and H19 genes in the absence of discriminative parental marks
-
Ohlsson, R., F. Flam, R. Fisher, S. Miller, H. Cui, S. Pfeifer, and G.I. Adam. 1999. Random monoallelic expression of the imprinted Igf2 and H19 genes in the absence of discriminative parental marks. Dev. Genes Evol. 209: 113-119.
-
(1999)
Dev. Genes Evol.
, vol.209
, pp. 113-119
-
-
Ohlsson, R.1
Flam, F.2
Fisher, R.3
Miller, S.4
Cui, H.5
Pfeifer, S.6
Adam, G.I.7
-
80
-
-
0000802429
-
Allocycly of the X chromosome in tumors and normal tissues
-
Ohno, S. and T.S. Hauschka. 1960. Allocycly of the X chromosome in tumors and normal tissues. Cancer Res. 20: 541-545.
-
(1960)
Cancer Res.
, vol.20
, pp. 541-545
-
-
Ohno, S.1
Hauschka, T.S.2
-
81
-
-
0033577693
-
A developmental switch in H4 acetylation upstream of Xist plays a role in X chromosome inactivation
-
O'Neill, L.P., A.M. Keohane, J.S. Lavender, V. McCabe, E. Heard, P. Avner, N. Brockdorff, and B.M. Turner. 1999. A developmental switch in H4 acetylation upstream of Xist plays a role in X chromosome inactivation. EMBO J. 18: 2897-2907.
-
(1999)
EMBO J.
, vol.18
, pp. 2897-2907
-
-
O'Neill, L.P.1
Keohane, A.M.2
Lavender, J.S.3
McCabe, V.4
Heard, E.5
Avner, P.6
Brockdorff, N.7
Turner, B.M.8
-
82
-
-
0030835456
-
Cosuppression in Drosophila: Gene silencing of alcohol dehydrogenase by white-ADH transgenes is Polycomb dependent
-
Pal-Bhadra, M., U. Bhadra, and J.A. Birchler. 1997. Cosuppression in Drosophila: Gene silencing of alcohol dehydrogenase by white-ADH transgenes is Polycomb dependent. Cell 90: 479-490.
-
(1997)
Cell
, vol.90
, pp. 479-490
-
-
Pal-Bhadra, M.1
Bhadra, U.2
Birchler, J.A.3
-
83
-
-
0029956442
-
DNA hypomethylation can activate Xist expression and silence X-linked genes
-
Panning, B. and R. Jaenisch. 1996. DNA hypomethylation can activate Xist expression and silence X-linked genes. Genes & Dev. 10: 1991-2002.
-
(1996)
Genes & Dev.
, vol.10
, pp. 1991-2002
-
-
Panning, B.1
Jaenisch, R.2
-
84
-
-
0030026001
-
Requirement for Xist in X chromosome inactivation
-
Penny, G.D., G.F. Kay, S.A. Sheardown, S. Rastan, and N. Brockdorff. 1996. Requirement for Xist in X chromosome inactivation. Nature 379: 131-137.
-
(1996)
Nature
, vol.379
, pp. 131-137
-
-
Penny, G.D.1
Kay, G.F.2
Sheardown, S.A.3
Rastan, S.4
Brockdorff, N.5
-
85
-
-
0027980337
-
Allele-specific gene expression in mammals: The curious case of the imprinted RNAs
-
Pfeifer, K. and S.M. Tilghman. 1994. Allele-specific gene expression in mammals: The curious case of the imprinted RNAs. Genes & Dev. 8: 1867-1874.
-
(1994)
Genes & Dev.
, vol.8
, pp. 1867-1874
-
-
Pfeifer, K.1
Tilghman, S.M.2
-
86
-
-
0026732759
-
Parental imprinting of the human H19 gene
-
Rachmilewitz, J., R. Goshen, I. Ariel, T. Schneider, N. de Groot, and A. Hochberg. 1992. Parental imprinting of the human H19 gene. FEBS Lett. 309: 25-28.
-
(1992)
FEBS Lett.
, vol.309
, pp. 25-28
-
-
Rachmilewitz, J.1
Goshen, R.2
Ariel, I.3
Schneider, T.4
De Groot, N.5
Hochberg, A.6
-
87
-
-
0019131118
-
X chromosome inactivation in extraembryonic membranes of diploid parthenogenetic mouse embryos demonstrated by differential staining
-
Rastan, S., M.H. Kaufman, A.H. Handyside, and M.F. Lyon. 1980. X chromosome inactivation in extraembryonic membranes of diploid parthenogenetic mouse embryos demonstrated by differential staining. Nature 288: 172-173.
-
(1980)
Nature
, vol.288
, pp. 172-173
-
-
Rastan, S.1
Kaufman, M.H.2
Handyside, A.H.3
Lyon, M.F.4
-
88
-
-
84971021823
-
Marsupials and mechanisms of X chromosome inactivation
-
Riggs, A.D. 1990. Marsupials and mechanisms of X chromosome inactivation. Aust. J. Zool. 37: 419-441.
-
(1990)
Aust. J. Zool.
, vol.37
, pp. 419-441
-
-
Riggs, A.D.1
-
89
-
-
0030993133
-
Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element
-
Ripoche, M.A., C. Kress, F. Poirier, and L. Dandolo. 1997. Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element. Genes & Dev. 11: 1596-1604.
-
(1997)
Genes & Dev.
, vol.11
, pp. 1596-1604
-
-
Ripoche, M.A.1
Kress, C.2
Poirier, F.3
Dandolo, L.4
-
90
-
-
0031879856
-
Trans-silencing by P elements inserted in subtelomeric heterochromatin involves the drosophila polycomb group gene, enhancer of zeste
-
Roche, S.E. and D.C. Rio. 1998. Trans-silencing by P elements inserted in subtelomeric heterochromatin involves the drosophila polycomb group gene, enhancer of zeste. Genetics 149: 1839-1855.
-
(1998)
Genetics
, vol.149
, pp. 1839-1855
-
-
Roche, S.E.1
Rio, D.C.2
-
91
-
-
0029589438
-
Temporal and spatial regulation of h19 imprinting in normal and uniparental mouse embryos
-
Sasaki, H., A.C. Ferguson-Smith, A.S.W. Shum, S.C. Barton, and M.A. Surani. 1995. Temporal and spatial regulation of H19 imprinting in normal and uniparental mouse embryos. Development 121: 4195-4202.
-
(1995)
Development
, vol.121
, pp. 4195-4202
-
-
Sasaki, H.1
Ferguson-Smith, A.C.2
Shum, A.S.W.3
Barton, S.C.4
Surani, M.A.5
-
92
-
-
0030903621
-
Many human L1 elements are capable of retrotransposition
-
Sassaman, D.M., B.A. Dombroski, J.V. Moran, M.L. Kimberland, T.P. Naas, R.J. DeBerardinas, A. Gabriel, G.D. Swergold, and H.H.J. Kazazian. 1997. Many human L1 elements are capable of retrotransposition. Nature Genet. 16: 37-43.
-
(1997)
Nature Genet.
, vol.16
, pp. 37-43
-
-
Sassaman, D.M.1
Dombroski, B.A.2
Moran, J.V.3
Kimberland, M.L.4
Naas, T.P.5
DeBerardinas, R.J.6
Gabriel, A.7
Swergold, G.D.8
Kazazian, H.H.J.9
-
93
-
-
0033574570
-
Gene silencing: Repeats that count
-
Selker, E. 1999. Gene silencing: Repeats that count. Cell 97: 157-160.
-
(1999)
Cell
, vol.97
, pp. 157-160
-
-
Selker, E.1
-
94
-
-
0025174641
-
DNA methylation and chromatin structure: A view from below
-
Selker, E.U. 1990. DNA methylation and chromatin structure: A view from below. Trends Biochem. Sci. 15: 103-107.
-
(1990)
Trends Biochem. Sci.
, vol.15
, pp. 103-107
-
-
Selker, E.U.1
-
95
-
-
0025226639
-
An extra maternally derived X chromosome is deleterious to early mouse development
-
Shao, C. and N. Takagi. 1990. An extra maternally derived X chromosome is deleterious to early mouse development. Development 110: 969-975.
-
(1990)
Development
, vol.110
, pp. 969-975
-
-
Shao, C.1
Takagi, N.2
-
96
-
-
0015240843
-
Late DNA replication in the paternally derived X chromosome of female kangaroos
-
Sharman, G.B. 1971. Late DNA replication in the paternally derived X chromosome of female kangaroos. Nature 230: 231-232.
-
(1971)
Nature
, vol.230
, pp. 231-232
-
-
Sharman, G.B.1
-
97
-
-
0030479536
-
The origin of interspersed repeats in the human genome
-
Smit, A.F. 1996. The origin of interspersed repeats in the human genome. Curr. Opin. Genet. Dev. 6: 743-748.
-
(1996)
Curr. Opin. Genet. Dev.
, vol.6
, pp. 743-748
-
-
Smit, A.F.1
-
98
-
-
0028133293
-
Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region
-
Sutcliffe, J.S., M. Nakao, S. Christian, K.H. Orstavik, N. Tommerup, D.H. Ledbetter, and A.L. Beaudet. 1994. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region. Nat. Genet. 8: 52-58.
-
(1994)
Nat. Genet.
, vol.8
, pp. 52-58
-
-
Sutcliffe, J.S.1
Nakao, M.2
Christian, S.3
Orstavik, K.H.4
Tommerup, N.5
Ledbetter, D.H.6
Beaudet, A.L.7
-
99
-
-
0031964299
-
The paternal allele of the H19 gene is progressively silenced during early mouse development: The acetylation status of histones may be involved in the generation of variegated expression patterns
-
Svensson, K., R. Mattsson, T.C. James, P. Wentzel, M. Pilartz, J. MacLaughlin, S.J. Miller, T. Olsson, U.J. Eriksson, and R. Ohlsson. 1998. The paternal allele of the H19 gene is progressively silenced during early mouse development: The acetylation status of histones may be involved in the generation of variegated expression patterns. Development 125: 61-69.
-
(1998)
Development
, vol.125
, pp. 61-69
-
-
Svensson, K.1
Mattsson, R.2
James, T.C.3
Wentzel, P.4
Pilartz, M.5
MacLaughlin, J.6
Miller, S.J.7
Olsson, T.8
Eriksson, U.J.9
Ohlsson, R.10
-
100
-
-
0026589372
-
Early development and X chromosome inactivation in mouse parthenogenetic embryos
-
Tada, T. and N. Takagi. 1992. Early development and X chromosome inactivation in mouse parthenogenetic embryos. Mol. Reprod. Dev. 31: 20-27.
-
(1992)
Mol. Reprod. Dev.
, vol.31
, pp. 20-27
-
-
Tada, T.1
Takagi, N.2
-
101
-
-
0016692463
-
Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse
-
Takagi, N. and M. Sasaki. 1975. Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse. Nature 256: 640-642.
-
(1975)
Nature
, vol.256
, pp. 640-642
-
-
Takagi, N.1
Sasaki, M.2
-
102
-
-
0025857244
-
Trans-sensing effects from Drosophila to humans
-
Tartof, K.D. and S. Henikoff. 1991. Trans-sensing effects from Drosophila to humans. Cell 65: 201-203.
-
(1991)
Cell
, vol.65
, pp. 201-203
-
-
Tartof, K.D.1
Henikoff, S.2
-
103
-
-
0001470477
-
Asynchronous duplication of chromosomes in cultured cells of Chinese hamster
-
Taylor, J.H. 1960. Asynchronous duplication of chromosomes in cultured cells of Chinese hamster. J. Biophys. Biochem. Cytol. 7: 455-464.
-
(1960)
J. Biophys. Biochem. Cytol.
, vol.7
, pp. 455-464
-
-
Taylor, J.H.1
-
104
-
-
0031963718
-
Histone acetylation as an epigenetic determinant of long-term transcriptional competence
-
Turner, B.M. 1998. Histone acetylation as an epigenetic determinant of long-term transcriptional competence. Cell. Mol. Life Sci. 54: 21-31.
-
(1998)
Cell. Mol. Life Sci.
, vol.54
, pp. 21-31
-
-
Turner, B.M.1
-
105
-
-
0028215253
-
The nonviability of uniparental mouse conceptuses correlates with the loss of the products of imprinting genes
-
Walsh, C., A. Glaser, R. Fundele, A. Ferguson-Smith, S. Barton, M.A. Surani, and R. Ohlsson. 1994. The nonviability of uniparental mouse conceptuses correlates with the loss of the products of imprinting genes. Mech. Dev. 46: 55-62.
-
(1994)
Mech. Dev.
, vol.46
, pp. 55-62
-
-
Walsh, C.1
Glaser, A.2
Fundele, R.3
Ferguson-Smith, A.4
Barton, S.5
Surani, M.A.6
Ohlsson, R.7
-
106
-
-
0032231864
-
The spreading of X inactivation into autosomal material of an X autosome translocation: Evidence for a difference between autosomal and X-chromosomal DNA
-
White, W.M., H.F. Willard, D.L. Van Dyke, and D.J. Wolff. 1998. The spreading of X inactivation into autosomal material of an X autosome translocation: Evidence for a difference between autosomal and X-chromosomal DNA. Am. J. Hum. Genet. 63: 20-28.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 20-28
-
-
White, W.M.1
Willard, H.F.2
Van Dyke, D.L.3
Wolff, D.J.4
-
107
-
-
0030840954
-
Cytosine methylation and the ecology of intragenomic parasites
-
Yoder, J.A., C.P. Walsh, and T.H. Bestor. 1997. Cytosine methylation and the ecology of intragenomic parasites. Trends Genet. 13: 335-340.
-
(1997)
Trends Genet.
, vol.13
, pp. 335-340
-
-
Yoder, J.A.1
Walsh, C.P.2
Bestor, T.H.3
-
108
-
-
0026849544
-
Monoallelic expression of the human H19 gene
-
Zhang, Y. and B. Tycko. 1992. Monoallelic expression of the human H19 gene. Nat. Genet. 1: 40-44.
-
(1992)
Nat. Genet.
, vol.1
, pp. 40-44
-
-
Zhang, Y.1
Tycko, B.2
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