-
1
-
-
0025640017
-
Genomic imprinting and allelic exclusion
-
Holliday, R. (1990) Genomic imprinting and allelic exclusion. Dev. Suppl. 125-129.
-
(1990)
Dev. Suppl.
, pp. 125-129
-
-
Holliday, R.1
-
2
-
-
0032571410
-
Expansion of the allelic exclusion principle?
-
Chess, A. (1998) Expansion of the allelic exclusion principle? Science 279, 2067-2068.
-
(1998)
Science
, vol.279
, pp. 2067-2068
-
-
Chess, A.1
-
3
-
-
0031114837
-
Genomic imprinting: Potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes
-
Glenn, C. C., Driscoll, D. J., Yang, T. P., and Nicholls, R. D. (1997) Genomic imprinting: Potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes. Mol. Hum. Reprod. 3, 321-332.
-
(1997)
Mol. Hum. Reprod.
, vol.3
, pp. 321-332
-
-
Glenn, C.C.1
Driscoll, D.J.2
Yang, T.P.3
Nicholls, R.D.4
-
4
-
-
0030667959
-
Genomic imprinting: Gametic mechanisms and somatic consequences
-
Tycko, B., Trasler, J., and Bestor, T. (1997) Genomic imprinting: Gametic mechanisms and somatic consequences. J. Androl. 18, 480-486.
-
(1997)
J. Androl.
, vol.18
, pp. 480-486
-
-
Tycko, B.1
Trasler, J.2
Bestor, T.3
-
5
-
-
0031469678
-
Genomic imprinting: A chromatin connection
-
Feil, R. and Kelsey, G. (1997) Genomic imprinting: A chromatin connection. Am. J. Hum. Genet. 61, 1213-1219.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 1213-1219
-
-
Feil, R.1
Kelsey, G.2
-
7
-
-
0028365598
-
Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting
-
Giddings, S. J., King, C. D., Harman, K. W., Flood, J. F., and Carnaghi, L. R. (1994) Allele specific inactivation of insulin 1 and 2, in the mouse yolk sac, indicates imprinting. Nature Genet. 6, 310-313.
-
(1994)
Nature Genet
, vol.6
, pp. 310-313
-
-
Giddings, S.J.1
King, C.D.2
Harman, K.W.3
Flood, J.F.4
Carnaghi, L.R.5
-
8
-
-
0028284563
-
Genomic imprinting: Mechanism and role in human pathology
-
Tycko, B. (1994) Genomic imprinting: Mechanism and role in human pathology. Am. J. Pathol. 144, 431-443.
-
(1994)
Am. J. Pathol.
, vol.144
, pp. 431-443
-
-
Tycko, B.1
-
9
-
-
0028776070
-
Genomic imprinting, DNA methylation, and cancer
-
Rainier, S. and Feinberg, A. P. (1994) Genomic imprinting, DNA methylation, and cancer. J. Natl. Cancer Inst. 86, 753-759.
-
(1994)
J. Natl. Cancer Inst.
, vol.86
, pp. 753-759
-
-
Rainier, S.1
Feinberg, A.P.2
-
10
-
-
0027947473
-
Genetics of Wilms' tumor: A blend of aberrant development and genomic imprinting
-
Junien, C. and Henry, I. (1994) Genetics of Wilms' tumor: A blend of aberrant development and genomic imprinting. Kidney Int. 46, 1264-1279.
-
(1994)
Kidney Int.
, vol.46
, pp. 1264-1279
-
-
Junien, C.1
Henry, I.2
-
11
-
-
0028032392
-
Familial paragangliomas of the head and neck
-
McCaffrey, T. V., Meyer, F. B., Michels, V. V., Piepgras, D. G., and Marion, M. S. (1994) Familial paragangliomas of the head and neck. Arch. Otolaryngol. Head Neck Surg. 120, 1211-1216.
-
(1994)
Arch. Otolaryngol. Head Neck Surg.
, vol.120
, pp. 1211-1216
-
-
McCaffrey, T.V.1
Meyer, F.B.2
Michels, V.V.3
Piepgras, D.G.4
Marion, M.S.5
-
12
-
-
0029436208
-
Genomic imprinting, DNA methylation, and cancer
-
Feinberg, A. P., Rainier, S., and DeBaun, M. R. (1995) Genomic imprinting, DNA methylation, and cancer. J. Natl. Cancer Inst. Monogr. 17, 21-26.
-
(1995)
J. Natl. Cancer Inst. Monogr.
, vol.17
, pp. 21-26
-
-
Feinberg, A.P.1
Rainier, S.2
DeBaun, M.R.3
-
13
-
-
0029556759
-
Normal development and neoplasia: The imprinting connection
-
Ohlsson, R. and Franklin, G. (1995) Normal development and neoplasia: The imprinting connection. Int. J. Dev. Biol. 39, 869-876.
-
(1995)
Int. J. Dev. Biol.
, vol.39
, pp. 869-876
-
-
Ohlsson, R.1
Franklin, G.2
-
15
-
-
0029816225
-
Multiple genetic abnormalities of 11p15 in Wilms' tumor
-
Feinberg, A. P. (1996) Multiple genetic abnormalities of 11p15 in Wilms' tumor. Med. Pediatr. Oncol. 27, 484-489.
-
(1996)
Med. Pediatr. Oncol.
, vol.27
, pp. 484-489
-
-
Feinberg, A.P.1
-
16
-
-
0030906349
-
Genetics of renal tumors
-
Fleming, S. (1997) Genetics of renal tumors. Cancer Metast. Rev. 16, 127-140.
-
(1997)
Cancer Metast. Rev.
, vol.16
, pp. 127-140
-
-
Fleming, S.1
-
17
-
-
0028829566
-
DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor
-
Schuffenhauer, S., Bartsch, O., Stumm, M., Buchholz, T., Petropoutou, T., Kraft, S., Belohradsky, B., Hinkel, G. K., Meitinger, T., and Wegner, R. D. (1995) DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factor. Hum. Genet. 96, 562-571.
-
(1995)
Hum. Genet.
, vol.96
, pp. 562-571
-
-
Schuffenhauer, S.1
Bartsch, O.2
Stumm, M.3
Buchholz, T.4
Petropoutou, T.5
Kraft, S.6
Belohradsky, B.7
Hinkel, G.K.8
Meitinger, T.9
Wegner, R.D.10
-
18
-
-
0031452521
-
Molecular genetics of Beckwith-Wiedemann syndrome
-
Li, M., Squire, J. A., and Weksberg, R. (1997) Molecular genetics of Beckwith-Wiedemann syndrome. Curr. Opin. Pediatr. 9, 623-629.
-
(1997)
Curr. Opin. Pediatr.
, vol.9
, pp. 623-629
-
-
Li, M.1
Squire, J.A.2
Weksberg, R.3
-
19
-
-
0024404822
-
Genomic imprinting in hereditary glomus tumors: Evidence for new genetic theory
-
van der Mey, A. G., Maaswinkel-Mooy, P. D., Cornelisse, C. J., Schmidt, P. H., and van de Kamp, J. J. (1989) Genomic imprinting in hereditary glomus tumors: Evidence for new genetic theory. Lancet 2, 1291-1294.
-
(1989)
Lancet
, vol.2
, pp. 1291-1294
-
-
Van der Mey, A.G.1
Maaswinkel-Mooy, P.D.2
Cornelisse, C.J.3
Schmidt, P.H.4
Van de Kamp, J.J.5
-
20
-
-
0026849378
-
A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter
-
Heutink, P., van der Mey, A. G., Sandkuijl, L. A., van Gils, A. P., Bardoel, A., Breedveld, G. J., van Vlict, M., van Ommen, G. J., Cornelisse, C. J., Oostra, B. A., et al. (1992) A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter. Hum. Mol. Genet. 1, 7-10.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 7-10
-
-
Heutink, P.1
Van der Mey, A.G.2
Sandkuijl, L.A.3
Van Gils, A.P.4
Bardoel, A.5
Breedveld, G.J.6
Van Vlict, M.7
Van Ommen, G.J.8
Cornelisse, C.J.9
Oostra, B.A.10
-
21
-
-
0027474137
-
Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: A review
-
Nicholls, R. D. (1993) Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: A review. Am. J. Med. Genet. 46, 16-25.
-
(1993)
Am. J. Med. Genet.
, vol.46
, pp. 16-25
-
-
Nicholls, R.D.1
-
22
-
-
0028240479
-
Mono- and bi-allelic expression of insulin-like growth factor II gene in human muscle tumors
-
Pedone, P. V., Tirabosco, R., Cavazzana, A. O., Ungaro, P., Basso, G., Luksch, R., Carli, M., Bruni, C. B., Frunzio, R., and Riccio, A. (1994) Mono- and bi-allelic expression of insulin-like growth factor II gene in human muscle tumors. Hum. Mol. Genet. 3, 1117-1121.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1117-1121
-
-
Pedone, P.V.1
Tirabosco, R.2
Cavazzana, A.O.3
Ungaro, P.4
Basso, G.5
Luksch, R.6
Carli, M.7
Bruni, C.B.8
Frunzio, R.9
Riccio, A.10
-
23
-
-
0028131720
-
Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFH maternal allele in hepatoblastoma
-
Montagna, M., Menin, C., Chieco-Bianchi, L., and D'Andrea, E. (1994) Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFH maternal allele in hepatoblastoma. J. Cancer Res. Clin. Oncol. 120, 732-736.
-
(1994)
J. Cancer Res. Clin. Oncol.
, vol.120
, pp. 732-736
-
-
Montagna, M.1
Menin, C.2
Chieco-Bianchi, L.3
D'Andrea, E.4
-
24
-
-
0028935151
-
Paternally derived H19 is differentially expressed in malignant and nonmalignant trophoblast
-
Walsh, C., Miller, S. J., Flam, F., Fisher, R. A., and Ohlsson, R. (1995) Paternally derived H19 is differentially expressed in malignant and nonmalignant trophoblast. Cancer Res. 55, 1111-1116.
-
(1995)
Cancer Res.
, vol.55
, pp. 1111-1116
-
-
Walsh, C.1
Miller, S.J.2
Flam, F.3
Fisher, R.A.4
Ohlsson, R.5
-
25
-
-
0029039059
-
Insulin-like growth factor II in uterine smooth-muscle tumors: Maintenance of genomic imprinting in leiomyomata and loss of imprinting in leiomyosarcomata
-
Vu, T. H., Yballe, C., Boonyanit, S., and Hoffman, A. R. (1995) Insulin-like growth factor II in uterine smooth-muscle tumors: Maintenance of genomic imprinting in leiomyomata and loss of imprinting in leiomyosarcomata. J. Clin. Endocrinol. Metab. 80, 1670-1676.
-
(1995)
J. Clin. Endocrinol. Metab.
, vol.80
, pp. 1670-1676
-
-
Vu, T.H.1
Yballe, C.2
Boonyanit, S.3
Hoffman, A.R.4
-
26
-
-
0029848437
-
Molecular biology of Beckwith-Wiedemann syndrome
-
Weksberg, R. and Squire, J.A. (1996) Molecular biology of Beckwith-Wiedemann syndrome. Med. Pediatr. Oncol. 27, 462-469.
-
(1996)
Med. Pediatr. Oncol.
, vol.27
, pp. 462-469
-
-
Weksberg, R.1
Squire, J.A.2
-
27
-
-
0021338485
-
Loss of a Harvey ras allele in sporadic Wilms' tumor
-
Reeve, A. E., Housiaux, P. J., Gardner, R. J., Chewings, W. E., Grindley, R. M., and Millow, L. J. (1984) Loss of a Harvey ras allele in sporadic Wilms' tumor. Nature 309, 174-176.
-
(1984)
Nature
, vol.309
, pp. 174-176
-
-
Reeve, A.E.1
Housiaux, P.J.2
Gardner, R.J.3
Chewings, W.E.4
Grindley, R.M.5
Millow, L.J.6
-
28
-
-
0027289089
-
Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted
-
Weksberg, R., Teshima, I., Williams, B. R., Greenberg, C. R., Pueschel, S. M., Chernos, J. E., Fowlow, S. B., Hoyme, E., Anderson, I. J., Whiteman, D. A., et al. (1993) Molecular characterization of cytogenetic alterations associated with the Beckwith-Wiedemann syndrome (BWS) phenotype refines the localization and suggests the gene for BWS is imprinted. Hum. Mol. Genet. 2, 549-556.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 549-556
-
-
Weksberg, R.1
Teshima, I.2
Williams, B.R.3
Greenberg, C.R.4
Pueschel, S.M.5
Chernos, J.E.6
Fowlow, S.B.7
Hoyme, E.8
Anderson, I.J.9
Whiteman, D.A.10
-
29
-
-
0028147055
-
Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5
-
Sait, S. N., Nowak, N. J., Singh-Kahlon, P., Weksberg, R., Squire, J., Shows, T. B., and Higgins, M.J. (1994) Localization of Beckwith-Wiedemann and rhabdoid tumor chromosome rearrangements to a defined interval in chromosome band 11p15.5. Genes Chrom. Cancer 11, 97-105.
-
(1994)
Genes Chrom. Cancer
, vol.11
, pp. 97-105
-
-
Sait, S.N.1
Nowak, N.J.2
Singh-Kahlon, P.3
Weksberg, R.4
Squire, J.5
Shows, T.B.6
Higgins, M.J.7
-
30
-
-
0028316620
-
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
-
Mannens, M., Hoovers, J. M., Redeker, E., Verjaal, M., Feinberg, A. P., Little, P., Boavida, M., Coad, N., Steenman, M., Blick, J., et al. (1994) Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia. Eur. J. Hum. Genet. 2, 3-23.
-
(1994)
Eur. J. Hum. Genet.
, vol.2
, pp. 3-23
-
-
Mannens, M.1
Hoovers, J.M.2
Redeker, E.3
Verjaal, M.4
Feinberg, A.P.5
Little, P.6
Boavida, M.7
Coad, N.8
Steenman, M.9
Blick, J.10
-
31
-
-
13344278697
-
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
-
Hoovers, J. M., Kalikin, L. M., Johnson, L. A., Alders, M, Redeker, Law, D. J., Bliek, J., Steenman, M., Benedict, M., and Wiegant, J. (1995) Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc. Natl. Acad. Sci. USA 92, 12,456-12,460.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 12456-12460
-
-
Hoovers, J.M.1
Kalikin, L.M.2
Johnson, L.A.3
Alders, M.4
Redeker5
Law, D.J.6
Bliek, J.7
Steenman, M.8
Benedict, M.9
Wiegant, J.10
-
32
-
-
16044364516
-
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
-
Hatada, I., Ohashi, H., Fukushima, Y., Kaneko, Y., Inoue, M., Komoto, Y., Okada, A., Ohishi, S., Nabetani, A., Morisaki, H., Nakayama, M., Niikawa, N., and Mukai, T. (1996) An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome. Nature Genet. 14, 171-173.
-
(1996)
Nature Genet.
, vol.14
, pp. 171-173
-
-
Hatada, I.1
Ohashi, H.2
Fukushima, Y.3
Kaneko, Y.4
Inoue, M.5
Komoto, Y.6
Okada, A.7
Ohishi, S.8
Nabetani, A.9
Morisaki, H.10
Nakayama, M.11
Niikawa, N.12
Mukai, T.13
-
33
-
-
0028988159
-
p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene
-
Malsuoka, S., Edwards, M. C., Bai, C., Parker, S., Zhang, P., Baldini, A., Harper, J. W., and Elledge, S. J. (1995) p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. Genes Dev. 9, 650-662.
-
(1995)
Genes Dev.
, vol.9
, pp. 650-662
-
-
Malsuoka, S.1
Edwards, M.C.2
Bai, C.3
Parker, S.4
Zhang, P.5
Baldini, A.6
Harper, J.W.7
Elledge, S.J.8
-
34
-
-
1842335753
-
Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith-Wiedemann syndrome
-
Zhang, P., Liegeois, N. J., Wong, C., Finegold, M., Hou, H., Thompson, J. C., Silverman, A., Harper, J. W., DePinho, R. A., and Elledge, S. J. (1997) Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith-Wiedemann syndrome. Nature 387, 151-158.
-
(1997)
Nature
, vol.387
, pp. 151-158
-
-
Zhang, P.1
Liegeois, N.J.2
Wong, C.3
Finegold, M.4
Hou, H.5
Thompson, J.C.6
Silverman, A.7
Harper, J.W.8
DePinho, R.A.9
Elledge, S.J.10
-
35
-
-
0030955563
-
Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development
-
Yan, Y., Frisen, J., Lee, M. H., Massague, J., and Barbacid, M. (1997) Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development. Genes Dev. 11, 973-983.
-
(1997)
Genes Dev
, vol.11
, pp. 973-983
-
-
Yan, Y.1
Frisen, J.2
Lee, M.H.3
Massague, J.4
Barbacid, M.5
-
36
-
-
0030660180
-
Mouse mutant embryos overexprcssing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes
-
Eggenschwiler, J., Ludwig, T., Fisher, P., Leighton, P. A., Tilghman, S. M., and Efstratiadis, A. (1997) Mouse mutant embryos overexprcssing IGF-II exhibit phenotypic features of the Beckwith-Wiedemann and Simpson-Golabi-Behmel syndromes. Genes Dev. 11, 3128-3142.
-
(1997)
Genes Dev.
, vol.11
, pp. 3128-3142
-
-
Eggenschwiler, J.1
Ludwig, T.2
Fisher, P.3
Leighton, P.A.4
Tilghman, S.M.5
Efstratiadis, A.6
-
37
-
-
0025320906
-
A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting
-
DeChiara, T. M., Efstratiadis, A., and Robertson, E. J. (1990) A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting. Nature 345, 78-80.
-
(1990)
Nature
, vol.345
, pp. 78-80
-
-
DeChiara, T.M.1
Efstratiadis, A.2
Robertson, E.J.3
-
38
-
-
0027420362
-
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
-
Weksberg, R., Shen, D. R., Fei, Y. L., Song, Q. L., and Squire, J. (1993) Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome. Nature Genet. 5, 143-150.
-
(1993)
Nature Genet.
, vol.5
, pp. 143-150
-
-
Weksberg, R.1
Shen, D.R.2
Fei, Y.L.3
Song, Q.L.4
Squire, J.5
-
39
-
-
0027422302
-
Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumor and gigantism
-
Ogawa, O., Becroft, D. M., Morison, I. M., Eccles, M. R., Skeen, J. E., Mauger, D. C., and Reeve, A. E. (1993) Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumor and gigantism. Nature Genet. 5, 408-412.
-
(1993)
Nature Genet.
, vol.5
, pp. 408-412
-
-
Ogawa, O.1
Becroft, D.M.2
Morison, I.M.3
Eccles, M.R.4
Skeen, J.E.5
Mauger, D.C.6
Reeve, A.E.7
-
40
-
-
0029806141
-
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
-
Brown, K. W., Villar, A. J., Bickmore, W., Clayton-Smith, J., Catchpoole, D., Maher, E. R., and Reik, W. (1996) Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway. Hum. Mol. Genet. 5, 2027-2032.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 2027-2032
-
-
Brown, K.W.1
Villar, A.J.2
Bickmore, W.3
Clayton-Smith, J.4
Catchpoole, D.5
Maher, E.R.6
Reik, W.7
-
41
-
-
0030827119
-
Imprinting of IGF2 and H19: Lack of reciprocity in sporadic Beckwith-Wiedemann syndrome
-
Joyce, J. A., Lam, W. K., Catchpoole, D. J., Jenks, P., Reik, W., Maher, E. R., and Schofield, P. N. (1997) Imprinting of IGF2 and H19: Lack of reciprocity in sporadic Beckwith-Wiedemann syndrome. Hum. Mol. Genet. 6, 1543-1548.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1543-1548
-
-
Joyce, J.A.1
Lam, W.K.2
Catchpoole, D.J.3
Jenks, P.4
Reik, W.5
Maher, E.R.6
Schofield, P.N.7
-
42
-
-
0029039059
-
Insulin-like growth factor II in uterine smooth-muscle tumors: Maintenance of genomic imprinting in leiomyomata and loss of imprinting in leiomyosarcomata
-
Vu, T. H., Yballe, C., Boonyanit, S., and Hoffman, A.R. (1995) Insulin-like growth factor II in uterine smooth-muscle tumors: Maintenance of genomic imprinting in leiomyomata and loss of imprinting in leiomyosarcomata. J. Clin. Endocrinol. Metab. 80, 1670-1676.
-
(1995)
J. Clin. Endocrinol. Metab.
, vol.80
, pp. 1670-1676
-
-
Vu, T.H.1
Yballe, C.2
Boonyanit, S.3
Hoffman, A.R.4
-
43
-
-
0029588595
-
Loss of imprinting of IGF2 in Ewing's sarcoma
-
Zhan, S., Shapiro, D. N., and Helman, L. J. (1995) Loss of imprinting of IGF2 in Ewing's sarcoma. Oncogene 11, 2503-2507.
-
(1995)
Oncogene
, vol.11
, pp. 2503-2507
-
-
Zhan, S.1
Shapiro, D.N.2
Helman, L.J.3
-
44
-
-
0030053512
-
High incidente of loss of heterozygosity and abnormal imprinting of H19 and IGF2 genes in invasive cervical carcinomas. Uncoupling of H19 and IGF2 expression and biallelic hypomethylation of H19
-
Doue-Rasy, S., Barrois, M., Fogel, S., Ahomadegbe, J. C., Stehelin, D., Coll, J., and Riou, G. (1996) High incidente of loss of heterozygosity and abnormal imprinting of H19 and IGF2 genes in invasive cervical carcinomas. Uncoupling of H19 and IGF2 expression and biallelic hypomethylation of H19. Oncogene 12, 423-430.
-
(1996)
Oncogene
, vol.12
, pp. 423-430
-
-
Doue-Rasy, S.1
Barrois, M.2
Fogel, S.3
Ahomadegbe, J.C.4
Stehelin, D.5
Coll, J.6
Riou, G.7
-
45
-
-
0029797635
-
Biallelic expression of the IGF2 gene in human breast disease
-
McCann, A. H., Miller, N., O'Meara, A., Pedersen, I., Keogh, K., Gorey, T., and Dervan, P. A. (1996) Biallelic expression of the IGF2 gene in human breast disease. Hum. Mol. Genet. 5, 1123-1127.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1123-1127
-
-
McCann, A.H.1
Miller, N.2
O'Meara, A.3
Pedersen, I.4
Keogh, K.5
Gorey, T.6
Dervan, P.A.7
-
46
-
-
0030271691
-
Relaxation of imprinting of the insulin-like growth factor II gene in colorectal cancer
-
Kinouchi, Y., Hiwatashi, N., Higashioka, S., Nagashima, F., Chida, M., and Toyota, T. (1996) Relaxation of imprinting of the insulin-like growth factor II gene in colorectal cancer. Cancer Lett. 107, 105-108.
-
(1996)
Cancer Lett
, vol.107
, pp. 105-108
-
-
Kinouchi, Y.1
Hiwatashi, N.2
Higashioka, S.3
Nagashima, F.4
Chida, M.5
Toyota, T.6
-
47
-
-
0030479119
-
IGF2 but not H19 shows loss of imprinting in human glioma
-
Uyeno, S., Aoki, Y., Nata, M., Sagisaka, K., Kayama, T., Yoshimoto, T., and Ono, T. (1996) IGF2 but not H19 shows loss of imprinting in human glioma. Cancer Res. 56, 5356-5359.
-
(1996)
Cancer Res.
, vol.56
, pp. 5356-5359
-
-
Uyeno, S.1
Aoki, Y.2
Nata, M.3
Sagisaka, K.4
Kayama, T.5
Yoshimoto, T.6
Ono, T.7
-
48
-
-
0031566230
-
Loss of imprinting of human insulin-like growth factor II gene, IGF2, in acute myeloid leukemia
-
Wu, H. K., Weksberg, R., Minden, M. D., and Squire, J. A. (1997) Loss of imprinting of human insulin-like growth factor II gene, IGF2, in acute myeloid leukemia. Biochem. Biophys. Res. Commun. 231, 466-472.
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.231
, pp. 466-472
-
-
Wu, H.K.1
Weksberg, R.2
Minden, M.D.3
Squire, J.A.4
-
49
-
-
0030970061
-
Altered imprinting of the H19 and insulin-like growth factor II genes in testicular tumors
-
Nonomura, N., Miki, T., Nishimura, K., Kanno, N., Kojima, Y., and Okuyama, A. (1997) Altered imprinting of the H19 and insulin-like growth factor II genes in testicular tumors. J. Urol. 157, 1977-1979.
-
(1997)
J. Urol.
, vol.157
, pp. 1977-1979
-
-
Nonomura, N.1
Miki, T.2
Nishimura, K.3
Kanno, N.4
Kojima, Y.5
Okuyama, A.6
-
50
-
-
0031560899
-
Relaxation of imprinting of human insulin-like growth factor II gene, IGF2, in sporadic breast carcinomas
-
Wu, H. K., Squire, J. A., Catzavelos, C. G., and Weksberg, R. (1997) Relaxation of imprinting of human insulin-like growth factor II gene, IGF2, in sporadic breast carcinomas. Biochem. Biophys. Res. Commun. 235, 123-129.
-
(1997)
Biochem. Biophys. Res. Commun.
, vol.235
, pp. 123-129
-
-
Wu, H.K.1
Squire, J.A.2
Catzavelos, C.G.3
Weksberg, R.4
-
51
-
-
0032579364
-
Loss of imprinting of IGF2 in renal-cell carcinomas
-
Oda, H., Kume, H., Shimizu, Y., Inoue, T. and Ishikawa, T. (1998) Loss of imprinting of IGF2 in renal-cell carcinomas. Int. J. Cancer 75, 343-346.
-
(1998)
Int. J. Cancer
, vol.75
, pp. 343-346
-
-
Oda, H.1
Kume, H.2
Shimizu, Y.3
Inoue, T.4
Ishikawa, T.5
-
52
-
-
0030715240
-
Biallelic expression of the H19 and IGF2 genes in hepatocellular carcinoma
-
Kim, K. S. and Lee, Y. I. (1997) Biallelic expression of the H19 and IGF2 genes in hepatocellular carcinoma. Cancer Lett. 119, 143-148.
-
(1997)
Cancer Lett.
, vol.119
, pp. 143-148
-
-
Kim, K.S.1
Lee, Y.I.2
-
53
-
-
0030862361
-
Loss of imprinting and overexpression of IGF2 gene in gastric adenocarcinoma
-
Wu, M. S., Wang, H. P., Lin, C. C., Sheu, J. C., Shun, C. T., Lee, W. J., and Lin, J. T. (1997) Loss of imprinting and overexpression of IGF2 gene in gastric adenocarcinoma. Cancer Lett. 120, 9-14.
-
(1997)
Cancer Lett.
, vol.120
, pp. 9-14
-
-
Wu, M.S.1
Wang, H.P.2
Lin, C.C.3
Sheu, J.C.4
Shun, C.T.5
Lee, W.J.6
Lin, J.T.7
-
54
-
-
0032080161
-
Loss of imprinting in disease progression in chronic myelogenous leukemia
-
Randhawa, G. S., Cui, H., Barletta, J. A., Strichman-Almashanu, L. Z., Talpaz, M., Kantarjian, H., Deisseroth, A. B., Champlin, R. C., and Feinberg, A. P. (1998) Loss of imprinting in disease progression in chronic myelogenous leukemia. Blood 91, 3144-3147.
-
(1998)
Blood
, vol.91
, pp. 3144-3147
-
-
Randhawa, G.S.1
Cui, H.2
Barletta, J.A.3
Strichman-Almashanu, L.Z.4
Talpaz, M.5
Kantarjian, H.6
Deisseroth, A.B.7
Champlin, R.C.8
Feinberg, A.P.9
-
55
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier, S., Johnson, L. A., Dobry, C. J., Ping, A. J., Grundy, P. E., and Feinberg, A. P. (1993) Relaxation of imprinted genes in human cancer. Nature 362, 747-749.
-
(1993)
Nature
, vol.362
, pp. 747-749
-
-
Rainier, S.1
Johnson, L.A.2
Dobry, C.J.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
56
-
-
0030735169
-
Transactivation of IGF2 in a mouse model of Beckwith-Wiedemann syndrome
-
Sun, F. L., Dean, W. L., Kelsey, G., Allen, N. D., and Reik, W. (1997) Transactivation of IGF2 in a mouse model of Beckwith-Wiedemann syndrome. Nature 389, 809-815.
-
(1997)
Nature
, vol.389
, pp. 809-815
-
-
Sun, F.L.1
Dean, W.L.2
Kelsey, G.3
Allen, N.D.4
Reik, W.5
-
57
-
-
13344261391
-
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
-
Pilia, G., Hughes-Benzie, R. M., MacKenzie, A., Baybayan, P., Chen, E. Y., Huber, R., Neri, G., Cao, A., Forabosco, A., and Schlessinger, D. (1996) Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome. Nature Genet. 12, 241-247.
-
(1996)
Nature Genet.
, vol.12
, pp. 241-247
-
-
Pilia, G.1
Hughes-Benzie, R.M.2
MacKenzie, A.3
Baybayan, P.4
Chen, E.Y.5
Huber, R.6
Neri, G.7
Cao, A.8
Forabosco, A.9
Schlessinger, D.10
-
58
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor II gene
-
DeChiara, T. M., Robertson, E. J., and Efstratiadis, A. (1991) Parental imprinting of the mouse insulin-like growth factor II gene. Cell 64, 849-859.
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
DeChiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
59
-
-
0028980026
-
Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse
-
Hatada, I. and Mukai, T. (1995) Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse. Nature Genet. 11, 204-206.
-
(1995)
Nature Genet.
, vol.11
, pp. 204-206
-
-
Hatada, I.1
Mukai, T.2
-
60
-
-
0029978017
-
Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15
-
Matsuoka, S., Thompson, J. S., Edwards, M. C., Bartletta, J. M., Grundy, P., Kalikin, L. M., Harper, J. W., Elledge, S. J., and Feinberg, A. P. (1996) Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15. Proc. Natl. Acad. Sci. USA 93, 3026-3030.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 3026-3030
-
-
Matsuoka, S.1
Thompson, J.S.2
Edwards, M.C.3
Bartletta, J.M.4
Grundy, P.5
Kalikin, L.M.6
Harper, J.W.7
Elledge, S.J.8
Feinberg, A.P.9
-
61
-
-
0027205671
-
Allele-specific replication timing of imprinted gene regions
-
Kitsberg, D., Selig, S., Brandeis, M., Simon, I., Keshet, I., Driscoll, D. J., Nicholls, R. D., and Cedar, H. (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
-
62
-
-
0028912476
-
Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development
-
Zhou, Q. Y., Quaife, C. J., and Palmiter, R. D. (1995) Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development. Nature 374, 640-643.
-
(1995)
Nature
, vol.374
, pp. 640-643
-
-
Zhou, Q.Y.1
Quaife, C.J.2
Palmiter, R.D.3
-
63
-
-
0028858477
-
Targeted disruption of the tyrosine hydroxylase locus results in severe catecholamine depletion and perinatal lethality in mice
-
Kobayashi, K., Morita, S., Sawada, H., Mizuguchi, T., Yamada, K., Nagatsu, I., Hata, T., Watanabe, Y., Fujita, K., and Nagatsu, T. (1995) Targeted disruption of the tyrosine hydroxylase locus results in severe catecholamine depletion and perinatal lethality in mice. J. Biol. Chem. 270, 27,235-27,243.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 27235-27243
-
-
Kobayashi, K.1
Morita, S.2
Sawada, H.3
Mizuguchi, T.4
Yamada, K.5
Nagatsu, I.6
Hata, T.7
Watanabe, Y.8
Fujita, K.9
Nagatsu, T.10
-
64
-
-
0031844688
-
Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster
-
Caspary, T., Cleary, M. A., Baker, C. C., Guan, X.-J., and Tilghman, S. M. (1998) Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster. Mol. Cell. Biol. 18, 3466-3474.
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 3466-3474
-
-
Caspary, T.1
Cleary, M.A.2
Baker, C.C.3
Guan, X.-J.4
Tilghman, S.M.5
-
65
-
-
0028209550
-
New insights reveal complex mechanisms involved in genomic imprinting
-
Nicholls, R. D. (1994) New insights reveal complex mechanisms involved in genomic imprinting. Am. J. Hum. Genet. 54, 733-740.
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 733-740
-
-
Nicholls, R.D.1
-
66
-
-
0030879482
-
Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons
-
Albrecht, U., Sutcliffe, J. S., Cattanach, B. M., Beechey, C. V., Armstrong, D., Eichele, G., and Beaudet, A. L. (1997) Imprinted expression of the murine Angelman syndrome gene, Ube3a, in hippocampal and Purkinje neurons. Nature Genet. 17, 75-78.
-
(1997)
Nature Genet
, vol.17
, pp. 75-78
-
-
Albrecht, U.1
Sutcliffe, J.S.2
Cattanach, B.M.3
Beechey, C.V.4
Armstrong, D.5
Eichele, G.6
Beaudet, A.L.7
-
67
-
-
0031228039
-
The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain
-
Rougeulle, C., Glatt, H., and Lalande, M. (1997) The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain. Nature Genet. 17, 14-15.
-
(1997)
Nature Genet.
, vol.17
, pp. 14-15
-
-
Rougeulle, C.1
Glatt, H.2
Lalande, M.3
-
68
-
-
0031230614
-
Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain
-
Vu, T. H. and Hoffman, A. R. (1997) Imprinting of the Angelman syndrome gene, UBE3A, is restricted to brain. Nature Genet. 17, 12-13.
-
(1997)
Nature Genet.
, vol.17
, pp. 12-13
-
-
Vu, T.H.1
Hoffman, A.R.2
-
69
-
-
9844265406
-
The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis
-
Qian, N., Frank, D., O'Keefe, D., Dao, D., Zhao, L., Yuan, L., Wang, Q., Keating, M., Walsh, C., and Tycko, B. (1997) The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis. Hum. Mol. Genet. 6, 2021-2029.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2021-2029
-
-
Qian, N.1
Frank, D.2
O'Keefe, D.3
Dao, D.4
Zhao, L.5
Yuan, L.6
Wang, Q.7
Keating, M.8
Walsh, C.9
Tycko, B.10
-
70
-
-
0032032697
-
Genomic imprinting of a human apoptosis gene homologue, TSSC3
-
Lee, M. P. and Feinberg, A. P. (1998) Genomic imprinting of a human apoptosis gene homologue, TSSC3. Cancer Res. 58, 1052-1056.
-
(1998)
Cancer Res.
, vol.58
, pp. 1052-1056
-
-
Lee, M.P.1
Feinberg, A.P.2
-
71
-
-
0031924628
-
IMPTI, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes
-
Dao, D., Frank, D., Qian, N., O'Keefe, D., Vosatka, R. J., Walsh, C. P., and Tycko, B. (1998) IMPTI, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes. Hum. Mol. Genet. 7, 597-608.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 597-608
-
-
Dao, D.1
Frank, D.2
Qian, N.3
O'Keefe, D.4
Vosatka, R.J.5
Walsh, C.P.6
Tycko, B.7
-
72
-
-
13144257678
-
Transcriptional map of 170-kb region at chromosome 11p15.5: Identification and mutational analyzis of the BWR1 A gene reveals the presence of mutations in tumor samples
-
Schwienbacher, C., Sabbioni, S., Campi, M., Veronese, A., Bernardi, G., Menegatti, A., Hatada, I., Mukai, T., Ohashi, H., Barbanti-Brodano, G., Croce, C. M., and Negrini, M. (1998) Transcriptional map of 170-kb region at chromosome 11p15.5: Identification and mutational analyzis of the BWR1 A gene reveals the presence of mutations in tumor samples. Proc. Natl. Acad. Sci. USA 95, 3873-3878.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 3873-3878
-
-
Schwienbacher, C.1
Sabbioni, S.2
Campi, M.3
Veronese, A.4
Bernardi, G.5
Menegatti, A.6
Hatada, I.7
Mukai, T.8
Ohashi, H.9
Barbanti-Brodano, G.10
Croce, C.M.11
Negrini, M.12
-
73
-
-
0030784857
-
Structure and function of the human chromosome 15 imprinting center
-
Horsthemke, B. (1997) Structure and function of the human chromosome 15 imprinting center. J. Cell Physiol. 173, 237-241.
-
(1997)
J. Cell Physiol.
, vol.173
, pp. 237-241
-
-
Horsthemke, B.1
-
74
-
-
0030833487
-
Imprinting mutations on human chromosome 15
-
Horsthemke, B., Dittrich, B., and Buiting, K. (1997) Imprinting mutations on human chromosome 15. Hum. Mutat. 10, 329-337.
-
(1997)
Hum. Mutat.
, vol.10
, pp. 329-337
-
-
Horsthemke, B.1
Dittrich, B.2
Buiting, K.3
-
75
-
-
0028862472
-
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domain
-
Reik, W., Brown, K. W., Schneid, H., Lebouc, Y., Bickmore, W., and Maher, E. W. (1995) Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domain. Hum. Mol. Genet. 4, 2379-2385.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2379-2385
-
-
Reik, W.1
Brown, K.W.2
Schneid, H.3
Lebouc, Y.4
Bickmore, W.5
Maher, E.W.6
-
76
-
-
0029165883
-
An enhancer deletion affects both H19 and IGF2 expression
-
Leighton, P. A., Saam, J. R., Ingram, R. S., Stewart, C. L., and Tilghman, S. M. (1995) An enhancer deletion affects both H19 and IGF2 expression. Genes Dev. 9, 2079-2089.
-
(1995)
Genes Dev.
, vol.9
, pp. 2079-2089
-
-
Leighton, P.A.1
Saam, J.R.2
Ingram, R.S.3
Stewart, C.L.4
Tilghman, S.M.5
-
77
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 gene region in mice
-
Leighton, P. A., Ingram, R. S., Eggenschwiler, J., Efstratiadis, A., and Tilghman, S. M. (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
-
78
-
-
0030931672
-
Loss of the maternal H19 gene induces changes in IGF2 methylation in both cis and trans
-
Forné, T., Oswald, J., Dean, W., Saam, J. R., Bailleul, B., Dandolo, L., Tilghman, S. M., Walter, J., and Reik, W. (1997) Loss of the maternal H19 gene induces changes in IGF2 methylation in both cis and trans. Proc. Natl. Acad. Sci. USA 94, 10,243-10,248.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 10243-10248
-
-
Forné, T.1
Oswald, J.2
Dean, W.3
Saam, J.R.4
Bailleul, B.5
Dandolo, L.6
Tilghman, S.M.7
Walter, J.8
Reik, W.9
-
79
-
-
0030993133
-
Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element
-
Ripoche, M. A., Kress, C., Poirier, F., and Dandolo, L. (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
-
80
-
-
10144227776
-
Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors
-
Mannens, M., Alders, M., Redeker, B., Blick, J., Steenman, M., Wiesmeyer, C., de Meulemeester, M., Ryan, A., Kalikin, L., Voute, T., De Kraker, J., Hoovers, J., Slater, R., Feinberg, A., Little, P., and Westerveld, A. (1996) Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors. Med. Pediatr. Oncol. 27, 490-494.
-
(1996)
Med. Pediatr. Oncol.
, vol.27
, pp. 490-494
-
-
Mannens, M.1
Alders, M.2
Redeker, B.3
Blick, J.4
Steenman, M.5
Wiesmeyer, C.6
De Meulemeester, M.7
Ryan, A.8
Kalikin, L.9
Voute, T.10
De Kraker, J.11
Hoovers, J.12
Slater, R.13
Feinberg, A.14
Little, P.15
Westerveld, A.16
-
81
-
-
0031046285
-
Human KVLQTI gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
-
Lee, M. P., Hu, R. J., Johnson, L. A., and Feinberg, A. P. (1997) Human KVLQTI gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nature Genet. 15, 181-185.
-
(1997)
Nature Genet.
, vol.15
, pp. 181-185
-
-
Lee, M.P.1
Hu, R.J.2
Johnson, L.A.3
Feinberg, A.P.4
-
82
-
-
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., and Horsthemke, B. (1996) Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene. Nature Genet. 14, 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
-
83
-
-
0029918828
-
Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint
-
Schulze, A., Hansen, C., Skakkeback, N. E., Brondum-Nielsen, K., Ledbeter, D. H., and Tommerup, N. (1996) Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint. Nature Genet. 12, 452-454.
-
(1996)
Nature Genet.
, vol.12
, pp. 452-454
-
-
Schulze, A.1
Hansen, C.2
Skakkeback, N.E.3
Brondum-Nielsen, K.4
Ledbeter, D.H.5
Tommerup, N.6
-
84
-
-
0029868661
-
Familial cryptic translocation resulting in Angelman syndrome: Implications for imprinting or location of the Angelman gene?
-
Burke, L. W., Wiley, J. E., Glenn, C. C., Driscoll, D. J., Loud, K. M., Smith, A. J., and Kushnick, T. (1996) Familial cryptic translocation resulting in Angelman syndrome: Implications for imprinting or location of the Angelman gene? Am. J. Hum. Genet. 58, 777-784.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 777-784
-
-
Burke, L.W.1
Wiley, J.E.2
Glenn, C.C.3
Driscoll, D.J.4
Loud, K.M.5
Smith, A.J.6
Kushnick, T.7
-
85
-
-
0029985822
-
Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient
-
Sun, Y., Nicholls, R. D., Butler, M. G., Saitoh, S., Hainline, B. E., and Palmer, C. G. (1996) Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient. Hum. Mol. Genet. 5, 517-524.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 517-524
-
-
Sun, Y.1
Nicholls, R.D.2
Butler, M.G.3
Saitoh, S.4
Hainline, B.E.5
Palmer, C.G.6
-
86
-
-
0031020198
-
Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3
-
Greger, V., Knoll, J. H., Wagstaff, J., Woolf, E., Lieske, P., Glatt, H., Benn, P. A., Rosengren, S. S., and Lalande, M. (1997) Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3. Am. J. Hum. Genet. 60, 574-580.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 574-580
-
-
Greger, V.1
Knoll, J.H.2
Wagstaff, J.3
Woolf, E.4
Lieske, P.5
Glatt, H.6
Benn, P.A.7
Rosengren, S.S.8
Lalande, M.9
-
87
-
-
0030761243
-
Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome
-
Conroy, J. M., Grebe, T. A., Becker, L. A., Tsuchiya, K., Nicholls, R. D., Buiting, K., Horsthemke, B., Cassidy, S. B., and Schwartz, S. (1997) Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome. Am. J. Hum. Genet. 61, 388-394.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 388-394
-
-
Conroy, J.M.1
Grebe, T.A.2
Becker, L.A.3
Tsuchiya, K.4
Nicholls, R.D.5
Buiting, K.6
Horsthemke, B.7
Cassidy, S.B.8
Schwartz, S.9
-
88
-
-
0029126018
-
A novel L23-related gent 40 kb downstream of the imprinted H19 gene is biallelically expressed in mid-fetal and adult human tissues
-
Tsang, P., Gilles, F., Yuan, L., Kuo, Y.-H., Lupu, F., Samara, G., Moosikasuwan, J., Goye, A., Zelenetz, A.D., Selleri, L., and Tycko, B. (1995) A novel L23-related gent 40 kb downstream of the imprinted H19 gene is biallelically expressed in mid-fetal and adult human tissues. Hum. Mol. Genet. 4, 1499-1507.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1499-1507
-
-
Tsang, P.1
Gilles, F.2
Yuan, L.3
Kuo, Y.-H.4
Lupu, F.5
Samara, G.6
Moosikasuwan, J.7
Goye, A.8
Zelenetz, A.D.9
Selleri, L.10
Tycko, B.11
-
89
-
-
0029803501
-
An extended region of biallelic gene expression and rodenthuman synteny downstream of the imprinted H19 gene on chromosome 11p15.5
-
Yuan, L., Qian, N., and Tycko, B. (1996) An extended region of biallelic gene expression and rodenthuman synteny downstream of the imprinted H19 gene on chromosome 11p15.5. Hum. Mol. Genet. 5, 1931-1937.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1931-1937
-
-
Yuan, L.1
Qian, N.2
Tycko, B.3
-
90
-
-
0031965478
-
The mouse H19 locus mediates a transition between imprinted and non- imprinted DNA replication patterns
-
Greally, J. M., Starr, D. J., Hwang, S., Song, L., Jaarola, M., and Zemel, S. (1998) The mouse H19 locus mediates a transition between imprinted and non- imprinted DNA replication patterns. Hum. Mol. Genet. 7, 91-96.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 91-96
-
-
Greally, J.M.1
Starr, D.J.2
Hwang, S.3
Song, L.4
Jaarola, M.5
Zemel, S.6
-
91
-
-
0032559794
-
Replicon clusters are stable units of chromosome structure: Evidence that nuclear organization contributes to the efficient activation and propagation of S phase in human cells
-
Jackson, D. A. and Pombo, A. (1998) Replicon clusters are stable units of chromosome structure: Evidence that nuclear organization contributes to the efficient activation and propagation of S phase in human cells. J. Cell Biol. 140, 1285-1295.
-
(1998)
J. Cell Biol.
, vol.140
, pp. 1285-1295
-
-
Jackson, D.A.1
Pombo, A.2
-
92
-
-
0026842288
-
Scaffold-associated regions: Cis-acting determinants of chromatin structural loops and functional domains
-
Laemnlli, U. K., Kas, E., Poljak, L., and Adachi, Y. (1992) Scaffold-associated regions: Cis-acting determinants of chromatin structural loops and functional domains. Curr. Opin. Genet. Dev. 2, 275-285.
-
(1992)
Curr. Opin. Genet. Dev.
, vol.2
, pp. 275-285
-
-
Laemnlli, U.K.1
Kas, E.2
Poljak, L.3
Adachi, Y.4
-
93
-
-
0026711089
-
A group of scs elements function as domain boundaries in an enhancer-blocking assay
-
Kellum, R. and Schedl, P. (1992) A group of scs elements function as domain boundaries in an enhancer-blocking assay. Mol. Cell. Biol. 12, 2424-2431.
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 2424-2431
-
-
Kellum, R.1
Schedl, P.2
-
94
-
-
0022553738
-
Chromosomal loop anchorage of the kappa immunoglobulin gene occurs next to the enhancer in a region containing topoisomerase II sites
-
Cockerill, P. N. and Garrard, W. T. (1986) Chromosomal loop anchorage of the kappa immunoglobulin gene occurs next to the enhancer in a region containing topoisomerase II sites. Cell 44, 273-282.
-
(1986)
Cell
, vol.44
, pp. 273-282
-
-
Cockerill, P.N.1
Garrard, W.T.2
-
95
-
-
0028150972
-
SARs stimulate but do not confer position independent gene expression
-
Poljak, L., Seum, C., Mattioni, T., and Laemmli, U.K. (1994) SARs stimulate but do not confer position independent gene expression. Nucleic Acids Res. 22, 4386-4394.
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 4386-4394
-
-
Poljak, L.1
Seum, C.2
Mattioni, T.3
Laemmli, U.K.4
-
96
-
-
0030779367
-
Matrix-attachment regions in the mouse chromosome 7F imprinted domain
-
Greally, J. M., Guinness, M. E., McGrath, J., and Zemel, S. (1997) Matrix-attachment regions in the mouse chromosome 7F imprinted domain. Mamm. Genome 8, 805-810.
-
(1997)
Mamm. Genome
, vol.8
, pp. 805-810
-
-
Greally, J.M.1
Guinness, M.E.2
McGrath, J.3
Zemel, S.4
-
97
-
-
0030472782
-
The structural H19 gene is required for transgene imprinting
-
Pfeifer, K., Leighton, P. A., and Tilghman, S. M. (1996) The structural H19 gene is required for transgene imprinting. Proc. Natl. Acad. Sci. USA 93, 13,876-13,883.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 13876-13883
-
-
Pfeifer, K.1
Leighton, P.A.2
Tilghman, S.M.3
-
98
-
-
0031014601
-
A 5′ differentially methylated sequence and the 3′-flanking region are necessary for H19 transgene imprinting
-
Elson, D. A. and Bartolomei, M. S. (1997) A 5′ differentially methylated sequence and the 3′-flanking region are necessary for H19 transgene imprinting. Mol. Cell Biol. 17, 309-317.
-
(1997)
Mol. Cell Biol.
, vol.17
, pp. 309-317
-
-
Elson, D.A.1
Bartolomei, M.S.2
-
99
-
-
0026027982
-
A position-effect assay for boundaries of higher order chromosomal domains
-
Kellum, R. and Schedl, P. (1991) A position-effect assay for boundaries of higher order chromosomal domains. Cell 64, 941-950.
-
(1991)
Cell
, vol.64
, pp. 941-950
-
-
Kellum, R.1
Schedl, P.2
-
100
-
-
0026922595
-
Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2
-
Zemel, S., Bartolomei, M. S., and Tilghman, S. M. (1992) Physical linkage of two mammalian imprinted genes, H19 and insulin-like growth factor 2. Nature Genet. 2, 61-65.
-
(1992)
Nature Genet.
, vol.2
, pp. 61-65
-
-
Zemel, S.1
Bartolomei, M.S.2
Tilghman, S.M.3
-
101
-
-
0023806622
-
Two regulatory domains flank the mouse H19 gene
-
Yoo-Warren, H., Pachnis, V., Ingram, R. S., and Tilghman, S. M. (1988) Two regulatory domains flank the mouse H19 gene. Mol. Cell. Biol. 8, 4707-4715.
-
(1988)
Mol. Cell. Biol.
, vol.8
, pp. 4707-4715
-
-
Yoo-Warren, H.1
Pachnis, V.2
Ingram, R.S.3
Tilghman, S.M.4
-
102
-
-
0032509990
-
Location of enhancers is essential for the imprinting of H19 and IGF2 genes
-
Webber, A. L., Ingrain, R. S., Levorse, J. M., and Tilghman, S. M. (1998) Location of enhancers is essential for the imprinting of H19 and IGF2 genes. Nature 391, 711-715.
-
(1998)
Nature
, vol.391
, pp. 711-715
-
-
Webber, A.L.1
Ingrain, R.S.2
Levorse, J.M.3
Tilghman, S.M.4
-
103
-
-
0030880815
-
X chromosome inactivation is mediated by Xist RNA stabilization
-
Panning, B., Dausman, J., and Jaenisch, R. (1997) X chromosome inactivation is mediated by Xist RNA stabilization. Cell 90, 907-916.
-
(1997)
Cell
, vol.90
, pp. 907-916
-
-
Panning, B.1
Dausman, J.2
Jaenisch, R.3
-
104
-
-
0025012640
-
The product of the H19 gene may function as an RNA
-
Brannan, C. I., Dees, E. C., Ingram, R. S., and Tilghman, S. M. (1990) The product of the H19 gene may function as an RNA. Mol. Cell. Biol. 10, 28-36.
-
(1990)
Mol. Cell. Biol.
, vol.10
, pp. 28-36
-
-
Brannan, C.I.1
Dees, E.C.2
Ingram, R.S.3
Tilghman, S.M.4
-
105
-
-
10144230716
-
Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus
-
Jinno, Y., Sengoku, K., Nakao, M., Tamate, K., Miyamoto, T., Matsuzaka, T., Sutcliffe, J. S., Anan, T., Takuma, N., Nishiwaki, K., Ikeda, Y., Ishimaru, T., Ishikawa, M., and Niikawa, N. (1996) Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus. Hum. Mol. Genet. 5, 1155-1161.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1155-1161
-
-
Jinno, Y.1
Sengoku, K.2
Nakao, M.3
Tamate, K.4
Miyamoto, T.5
Matsuzaka, T.6
Sutcliffe, J.S.7
Anan, T.8
Takuma, N.9
Nishiwaki, K.10
Ikeda, Y.11
Ishimaru, T.12
Ishikawa, M.13
Niikawa, N.14
-
106
-
-
0030950759
-
An imprinting element from the mouse H19 locus functions as a silcncer in Drosophila
-
Lyko, F., Brenton, J. D., Surani, M. A., and Paro, R. (1997) An imprinting element from the mouse H19 locus functions as a silcncer in Drosophila. Nature Genet. 16, 171-173.
-
(1997)
Nature Genet.
, vol.16
, pp. 171-173
-
-
Lyko, F.1
Brenton, J.D.2
Surani, M.A.3
Paro, R.4
-
107
-
-
0030043038
-
Introduction of a DNA methyltransferase into Drosophila to probe chromatin structure in vivo
-
Wines, D. R., Talbert, P. B., Clark, D. V., and Henikoff, S. (1996) Introduction of a DNA methyltransferase into Drosophila to probe chromatin structure in vivo. Chromosoma 104, 332-340.
-
(1996)
Chromosoma
, vol.104
, pp. 332-340
-
-
Wines, D.R.1
Talbert, P.B.2
Clark, D.V.3
Henikoff, S.4
-
108
-
-
0027980337
-
Allele-specific gene expression in mammals: The curious case of the imprinted RNAs
-
Pfeifer, K. and Tilghman, S. M. (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
-
109
-
-
0030463741
-
Fab-7 functions as a chromatin domain boundary to ensure proper segment specification by the Drosophila bithorax complex
-
Hagstrom, K., Muller, M., and Schedl, P. (1996) Fab-7 functions as a chromatin domain boundary to ensure proper segment specification by the Drosophila bithorax complex. Genes Dev. 10, 3202-3215.
-
(1996)
Genes Dev.
, vol.10
, pp. 3202-3215
-
-
Hagstrom, K.1
Muller, M.2
Schedl, P.3
-
110
-
-
0027402685
-
The su(Hw) protein insulates expression of the Drosophila melanogaster white gene from chromosomal position-effects
-
Roseman, R. R., Pirrotta, V., and Geyer, P. K. (1993) The su(Hw) protein insulates expression of the Drosophila melanogaster white gene from chromosomal position-effects. EMBO J. 12, 435-442.
-
(1993)
EMBO J.
, vol.12
, pp. 435-442
-
-
Roseman, R.R.1
Pirrotta, V.2
Geyer, P.K.3
-
111
-
-
0027254748
-
A 5′ element of the chicken beta-globin domain serves as an insulator in human erythroid cells and protects against position effect in Drosophila
-
Chung, J. H., Whiteley, M., and Felsenfeld, G. (1993) A 5′ element of the chicken beta-globin domain serves as an insulator in human erythroid cells and protects against position effect in Drosophila. Cell 74, 505-514.
-
(1993)
Cell
, vol.74
, pp. 505-514
-
-
Chung, J.H.1
Whiteley, M.2
Felsenfeld, G.3
-
112
-
-
0030992767
-
An enhancer-blocking element between α and δ gene segments within the human T cell receptor α/δ locus
-
Zhong, X.-P. and Krangel, M. S. (1997) An enhancer-blocking element between α and δ gene segments within the human T cell receptor α/δ locus. Proc. Natl. Acad. Sci. USA 94, 5219-5224.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 5219-5224
-
-
Zhong, X.-P.1
Krangel, M.S.2
-
113
-
-
0030922269
-
The role of insulator elements in defining domains of gene expression
-
Geyer, P. K. (1997) The role of insulator elements in defining domains of gene expression. Curr. Opm. Genet. Dev. 7, 242-248.
-
(1997)
Curr. Opm. Genet. Dev.
, vol.7
, pp. 242-248
-
-
Geyer, P.K.1
-
114
-
-
0032548927
-
Polycomb and trithorax group proteins mediate the function of a chromatin insulator
-
Gerasimova, T. I. and Corces, V. G. (1998) Polycomb and trithorax group proteins mediate the function of a chromatin insulator. Cell 92, 511-521.
-
(1998)
Cell
, vol.92
, pp. 511-521
-
-
Gerasimova, T.I.1
Corces, V.G.2
-
115
-
-
0028978180
-
A Drosophila protein that imparts directionality on a chromatin insulator is an enhancer of position-effect variegation
-
Gerasimova, T. I., Gdula, D. A., Gerasimov, D. V., Simonova, O., and Corces, V. G. (1995) A Drosophila protein that imparts directionality on a chromatin insulator is an enhancer of position-effect variegation. Cell 82, 587-597.
-
(1995)
Cell
, vol.82
, pp. 587-597
-
-
Gerasimova, T.I.1
Gdula, D.A.2
Gerasimov, D.V.3
Simonova, O.4
Corces, V.G.5
-
116
-
-
0031019177
-
Characterization of the chicken beta-globin insulator
-
Chung, J. H., Bell, A. C., and Felsenfeld, G. (1997) Characterization of the chicken beta-globin insulator. Proc. Natl. Acad. Sci. USA 94, 575-580.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 575-580
-
-
Chung, J.H.1
Bell, A.C.2
Felsenfeld, G.3
-
117
-
-
0030965628
-
Ligand-inducible and liver-specific target gene expression in transgenic mice
-
Wang, Y., DeMayo, F. J., Tsai, S. Y., and O'Malley, B. W. (1997) Ligand-inducible and liver-specific target gene expression in transgenic mice. Nature Biotech. 15, 239-243.
-
(1997)
Nature Biotech.
, vol.15
, pp. 239-243
-
-
Wang, Y.1
DeMayo, F.J.2
Tsai, S.Y.3
O'Malley, B.W.4
-
118
-
-
0028600559
-
Sequences required for enhancer blocking activity of ses are located within two nuclease-hypersensitive regions
-
Vazquez, J. and Schedl, P. (1994) Sequences required for enhancer blocking activity of ses are located within two nuclease-hypersensitive regions. EMBO J. 13, 5984-5993.
-
(1994)
EMBO J.
, vol.13
, pp. 5984-5993
-
-
Vazquez, J.1
Schedl, P.2
-
119
-
-
0030802395
-
A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development
-
Tremblay, K. D., Duran, K. L., and Bartolomei, M. S. (1997) A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development. Mol. Cell. Biol. 17, 4322-4329.
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 4322-4329
-
-
Tremblay, K.D.1
Duran, K.L.2
Bartolomei, M.S.3
-
120
-
-
0027172684
-
Parental-origin-specific epigenetic modification of the mouse H19 gene
-
Ferguson-Smith, A. C., Sasaki, H., Cattanach, B. M., and Surani, M. A. (1993) Parental-origin-specific epigenetic modification of the mouse H19 gene. Nature 362, 751-755.
-
(1993)
Nature
, vol.362
, pp. 751-755
-
-
Ferguson-Smith, A.C.1
Sasaki, H.2
Cattanach, B.M.3
Surani, M.A.4
-
121
-
-
0028356544
-
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumor
-
Steenman, M. J., Rainier, S., Dobry, C. J., Grundy, P., Horon, I. L., and Feinberg, A. P. (1994) Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumor. Nature Genet. 7, 433-439.
-
(1994)
Nature Genet.
, vol.7
, pp. 433-439
-
-
Steenman, M.J.1
Rainier, S.2
Dobry, C.J.3
Grundy, P.4
Horon, I.L.5
Feinberg, A.P.6
-
122
-
-
0028935017
-
Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor
-
Taniguchi, T., Sullivan, M. J., Ogawa, O., and Reeve, A. E. (1995) Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor. Proc. Natl. Acad. Sci. USA 92, 2159-2163.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 2159-2163
-
-
Taniguchi, T.1
Sullivan, M.J.2
Ogawa, O.3
Reeve, A.E.4
-
123
-
-
0030840328
-
Imprinting of IGF2 and H19 from a 130 kb YAC transgene
-
Ainscough, J. F., Koide, T., Tada, M., Barton, S., and Surani, M. A. (1997) Imprinting of IGF2 and H19 from a 130 kb YAC transgene. Development 124, 3621-3632.
-
(1997)
Development
, vol.124
, pp. 3621-3632
-
-
Ainscough, J.F.1
Koide, T.2
Tada, M.3
Barton, S.4
Surani, M.A.5
-
124
-
-
0027203606
-
Epigenetic mechanisms underlying the imprinting of the mouse HI9 gene
-
Bartolomei, M. S., Webber, A. L., Brunkow, M. E., and Tilghman, S. M. (1993) Epigenetic mechanisms underlying the imprinting of the mouse HI9 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
-
125
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0031214796
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A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPAI and the BWSCRI/WT2 region
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Reid, L. H., Davies, C., Cooper, P. R., Crider-Miller, S. J., Sait, S. N., Nowak, N. J., Evans, G., Stanbridge, E. J., deJong, P., Shows, T. B., Weissman, B. E., and Higgins, M. J. (1997) A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPAI and the BWSCRI/WT2 region. Genomics 43, 366-375.
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(1997)
Genomics
, vol.43
, pp. 366-375
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Reid, L.H.1
Davies, C.2
Cooper, P.R.3
Crider-Miller, S.J.4
Sait, S.N.5
Nowak, N.J.6
Evans, G.7
Stanbridge, E.J.8
DeJong, P.9
Shows, T.B.10
Weissman, B.E.11
Higgins, M.J.12
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