-
1
-
-
0021237658
-
Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis
-
Surani, M.A., Barton, S.C. and Norris, M.L. (1984) Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis. Nature, 308, 548-550.
-
(1984)
Nature
, vol.308
, pp. 548-550
-
-
Surani, M.A.1
Barton, S.C.2
Norris, M.L.3
-
2
-
-
0021139084
-
Completion of mouse embryogenesis requires both the maternal and paternal genomes
-
McGrath, J. and Solter, D. (1984) Completion of mouse embryogenesis requires both the maternal and paternal genomes. Cell, 37, 179-183.
-
(1984)
Cell
, vol.37
, pp. 179-183
-
-
McGrath, J.1
Solter, D.2
-
3
-
-
0031055223
-
Genomic imprinting: Nature and clinical relevance
-
Hall, J.G. (1997) Genomic imprinting: nature and clinical relevance. Annu. Rev. Med., 48, 35-44.
-
(1997)
Annu. Rev. Med.
, vol.48
, pp. 35-44
-
-
Hall, J.G.1
-
4
-
-
7344254106
-
A catalogue of imprinted genes and parent-of-origin effects in humans and animals
-
Morison, I.M. and Reeve, A.E. (1998) A catalogue of imprinted genes and parent-of-origin effects in humans and animals. Hum. Mol. Genet., 7, 1599-1609.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1599-1609
-
-
Morison, I.M.1
Reeve, A.E.2
-
5
-
-
0002246574
-
Genomic imprinting in the mouse: Possible final analysis
-
Reik, W. and Surani, A. (eds), Oxford University Press, New York, NY
-
Cattanach, B.M. and Beechey, C.V. (1997) Genomic imprinting in the mouse: possible final analysis. In Reik, W. and Surani, A. (eds), Genomic Imprinting. Oxford University Press, New York, NY, pp. 118-145.
-
(1997)
Genomic Imprinting
, pp. 118-145
-
-
Cattanach, B.M.1
Beechey, C.V.2
-
6
-
-
0029162269
-
Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis
-
Ledbetter, D.H. and Engel, E. (1995) Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis. Hum Mol. Genet., 4, 1757-1764.
-
(1995)
Hum Mol. Genet.
, vol.4
, pp. 1757-1764
-
-
Ledbetter, D.H.1
Engel, E.2
-
7
-
-
0031762651
-
Imprinting mechanisms
-
Constância, M., Pickard, B., Kelsey, G. and Reik, W. (1998) Imprinting mechanisms. Genome Res., 8, 881-900.
-
(1998)
Genome Res.
, vol.8
, pp. 881-900
-
-
Constância, M.1
Pickard, B.2
Kelsey, G.3
Reik, W.4
-
8
-
-
0030458551
-
Parental imprinting and human disease
-
Lalande, M. (1997) Parental imprinting and human disease. Annu. Rev. Genet., 30, 173-195.
-
(1997)
Annu. Rev. Genet.
, vol.30
, pp. 173-195
-
-
Lalande, M.1
-
9
-
-
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
-
10
-
-
0029360421
-
Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies
-
Pàldi, A., Gyapay, G. and Jami, J. (1995) Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies. Curr. Biol., 5, 1030-1035.
-
(1995)
Curr. Biol.
, vol.5
, pp. 1030-1035
-
-
Pàldi, A.1
Gyapay, G.2
Jami, J.3
-
11
-
-
0029001828
-
Sex-specific meiotic recombination in the Prader-Willi/Angelman syndrome imprinted region
-
Robinson, W.P. and Lalande, M. (1995) Sex-specific meiotic recombination in the Prader-Willi/Angelman syndrome imprinted region. Hum. Mol. Genet., 4, 801-806.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 801-806
-
-
Robinson, W.P.1
Lalande, M.2
-
12
-
-
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
-
13
-
-
0032067559
-
An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript
-
Rougeulle, C., Cardoso, C., Fontés, M., Colleaux, L. and Lalande, M. (1998) An imprinted antisense RNA overlaps UBE3A and a second maternally expressed transcript. Nature Genet., 19, 15-16.
-
(1998)
Nature Genet.
, vol.19
, pp. 15-16
-
-
Rougeulle, C.1
Cardoso, C.2
Fontés, M.3
Colleaux, L.4
Lalande, M.5
-
14
-
-
0032433682
-
Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally and biallelically derived proteins
-
Hayward, B.E., Moran, V., Strain, L. and Bonthron, D.T. (1998) Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally and biallelically derived proteins. Proc. Natl Acad. Sci. USA, 95, 15475-15480.
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 15475-15480
-
-
Hayward, B.E.1
Moran, V.2
Strain, L.3
Bonthron, D.T.4
-
15
-
-
0030694713
-
Imprinted expression of the Igf2r gene depends on an intronic CpG island
-
Wutz, A., Smrzka, O.W., Schweifer, N., Schellander, K., Wagner, E.F. and Barlow, D.P. (1997) Imprinted expression of the Igf2r gene depends on an intronic CpG island. Nature, 389, 745-749.
-
(1997)
Nature
, vol.389
, pp. 745-749
-
-
Wutz, A.1
Smrzka, O.W.2
Schweifer, N.3
Schellander, K.4
Wagner, E.F.5
Barlow, D.P.6
-
16
-
-
0033531134
-
The imprinting box of the mouse Igf2r gene
-
Birger, Y., Shemer, R., Perk, J. and Razin, A. (1999) The imprinting box of the mouse Igf2r gene. Nature, 397, 84-88.
-
(1999)
Nature
, vol.397
, pp. 84-88
-
-
Birger, Y.1
Shemer, R.2
Perk, J.3
Razin, A.4
-
17
-
-
0030730287
-
Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2
-
Moore, T., Constancia, M., Zubair, M., Bailleul, B., Feil, R., Sasaki, H. and Reik, W. (1997) Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2. Proc. Natl Acad. Sci. USA, 94, 12509-12514.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 12509-12514
-
-
Moore, T.1
Constancia, M.2
Zubair, M.3
Bailleul, B.4
Feil, R.5
Sasaki, H.6
Reik, W.7
-
18
-
-
0030976087
-
Remodelling chromatin with RNA
-
Willard, H.F. and Salz, H.K. (1997) Remodelling chromatin with RNA. Nature, 386, 228-229.
-
(1997)
Nature
, vol.386
, pp. 228-229
-
-
Willard, H.F.1
Salz, H.K.2
-
19
-
-
0030856668
-
Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome
-
Reik, W. and Maher, E.R. (1997) Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome. Trends Genet., 13, 30-334.
-
(1997)
Trends Genet.
, vol.13
, pp. 330-334
-
-
Reik, W.1
Maher, E.R.2
-
20
-
-
0024518392
-
Genetic linkage of Beckwith-Wiedemann syndrome to 11p15
-
Ping, A.J., Reeve, A.E., Law, D.J., Young, M.R., Boehnke, M. and Feinberg, A.P. (1989) Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am. J. Hum. Genet., 44, 720-723.
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 720-723
-
-
Ping, A.J.1
Reeve, A.E.2
Law, D.J.3
Young, M.R.4
Boehnke, M.5
Feinberg, A.P.6
-
21
-
-
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 Chromosomes Cancer, 11, 97-105.
-
(1994)
Genes Chromosomes 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
-
22
-
-
13344278697
-
Multiple genetic loci within llpls defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
-
Hoovers, J.M., Kalikin, L.M., Johnson, L.A., Alders, M., Redeker, B., Law, D.J., Bliek, J., Steenman, M., Benedict, M., Wiegant, J., Lengauer, C., Taillon-Miller, P., Schlessinger, D., Edwards, M.C., Elledge, S.J., Ivens, A., Westerveld, A., Little, P., Mannens, M. and Feinberg, A.P. (1995) Multiple genetic loci within llplS defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc. Natl Acad. Sci. USA, 92, 12456-12460.
-
(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
Redeker, B.5
Law, D.J.6
Bliek, J.7
Steenman, M.8
Benedict, M.9
Wiegant, J.10
Lengauer, C.11
Taillon-Miller, P.12
Schlessinger, D.13
Edwards, M.C.14
Elledge, S.J.15
Ivens, A.16
Westerveld, A.17
Little, P.18
Mannens, M.19
Feinberg, A.P.20
more..
-
23
-
-
0026347794
-
Report of the committee on chromosome and gene loss in human neoplasia
-
Seizinger, B.R., Klinger, H.P., Junien, C., Nakamura, Y., Beau, M.L., Cavenee, W., Emanuel, B., Ponder, B., Naylor, S., Mitelman, F., Louis, D., Menon, A., Newsham, I., Decker, J., Kaelbling, M., Henry, I. and Deimling, A. V. (1991) Report of the committee on chromosome and gene loss in human neoplasia. Cytogenet. Cell Genet., 58, 1080-1096.
-
(1991)
Cytogenet. Cell Genet.
, vol.58
, pp. 1080-1096
-
-
Seizinger, B.R.1
Klinger, H.P.2
Junien, C.3
Nakamura, Y.4
Beau, M.L.5
Cavenee, W.6
Emanuel, B.7
Ponder, B.8
Naylor, S.9
Mitelman, F.10
Louis, D.11
Menon, A.12
Newsham, I.13
Decker, J.14
Kaelbling, M.15
Henry, I.16
Deimling, A.V.17
-
24
-
-
0027231784
-
Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11
-
Koi, M., Johnson, L.A., Kalikin, L.M., Little, P.F., Nakamura, Y. and Feinberg, A.P. (1993) Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11. Science, 260, 361-364.
-
(1993)
Science
, vol.260
, pp. 361-364
-
-
Koi, M.1
Johnson, L.A.2
Kalikin, L.M.3
Little, P.F.4
Nakamura, Y.5
Feinberg, A.P.6
-
25
-
-
0031046285
-
Human KVLQT1 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 KVLQT1 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
-
26
-
-
0028212159
-
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation
-
Brown, C.J. and Willard, H.F. (1994) The human X-inactivation centre is not required for maintenance of X-chromosome inactivation. Nature, 368, 154-156.
-
(1994)
Nature
, vol.368
, pp. 154-156
-
-
Brown, C.J.1
Willard, H.F.2
-
27
-
-
0030952221
-
Expression of genes from the human active and inactive X chromosomes
-
Brown, C.J., Carrel, L. and Willard, H.F. (1997) Expression of genes from the human active and inactive X chromosomes. Am. J. Hum. Genet., 60, 1333-1343.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1333-1343
-
-
Brown, C.J.1
Carrel, L.2
Willard, H.F.3
-
28
-
-
0032555153
-
Chromosomal basis of X chromosome inactivation: Identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation
-
Miller, A.P. and Willard, H.F. (1998) Chromosomal basis of X chromosome inactivation: identification of a multigene domain in Xp11.21-p11.22 that escapes X inactivation. Proc. Natl Acad. Sci. USA, 95, 8709-8714.
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 8709-8714
-
-
Miller, A.P.1
Willard, H.F.2
-
29
-
-
0030687684
-
A receptor subunit genes, using microcell-mediated chromosome transfer
-
A receptor subunit genes, using microcell-mediated chromosome transfer. Hum. Mol. Genet., 6, 2127-2133.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2127-2133
-
-
Meguro, M.1
Mitsuya, K.2
Sui, H.3
Shigenami, K.4
Kugoh, H.5
Nakao, M.6
Oshimura, M.7
-
30
-
-
0031878344
-
Epigenetic reprogramming of the human H19 gene in mouse embryonic cells does not erase the primary parental imprint
-
Mitsuya, K., Meguro, M., Sui, H., Schulz, T.C., Kugoh, H., Hamada, H. and Oshimura, M. (1998) Epigenetic reprogramming of the human H19 gene in mouse embryonic cells does not erase the primary parental imprint. Genes Cells, 3, 245-255.
-
(1998)
Genes Cells
, vol.3
, pp. 245-255
-
-
Mitsuya, K.1
Meguro, M.2
Sui, H.3
Schulz, T.C.4
Kugoh, H.5
Hamada, H.6
Oshimura, M.7
-
31
-
-
0032561502
-
A physical map of 30,000 human genes
-
Deloukas, P. et al. (1998) A physical map of 30,000 human genes. Science, 282, 744-746.
-
(1998)
Science
, vol.282
, pp. 744-746
-
-
Deloukas, P.1
-
32
-
-
0029928454
-
Lack of imprinting of the human dopamine D4 receptor (DRD4) gene
-
Cichon, S., Nöthen, M.M., Wolf, H.K. and Propping, P. (1996) Lack of imprinting of the human dopamine D4 receptor (DRD4) gene. Am. J. Med. Genet., 67, 229-231.
-
(1996)
Am. J. Med. Genet.
, vol.67
, pp. 229-231
-
-
Cichon, S.1
Nöthen, M.M.2
Wolf, H.K.3
Propping, P.4
-
33
-
-
0032054997
-
Imprinting mechanisms in mammals
-
Reik, W. and Walter, J. (1998) Imprinting mechanisms in mammals. Curr. Opin. Genet. Dev., 8, 154-164.
-
(1998)
Curr. Opin. Genet. Dev.
, vol.8
, pp. 154-164
-
-
Reik, W.1
Walter, J.2
-
34
-
-
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
-
35
-
-
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
-
36
-
-
0028862472
-
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain
-
Reik, W., Brown, K.W., Schneid, H., Le Bouc, Y., Bickmore, W. and Maher, E.R. (1995) Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by 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
Le Bouc, Y.4
Bickmore, W.5
Maher, E.R.6
-
37
-
-
0033609117
-
Loss of imprinting of a paternally expressed transcript, with antisense orientation to KvLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
-
Lee, M.P., DeBaun, M.R., Mitsuya, K., Galonek, H.L., Brandenburg, S., Oshimura, M. and Feinberg, A.P. (1999) Loss of imprinting of a paternally expressed transcript, with antisense orientation to KvLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting. Proc. Natl Acad. Sci. USA, 96, 5203-5208.
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 5203-5208
-
-
Lee, M.P.1
DeBaun, M.R.2
Mitsuya, K.3
Galonek, H.L.4
Brandenburg, S.5
Oshimura, M.6
Feinberg, A.P.7
-
38
-
-
0025958320
-
Genomic imprinting in mammalian development: A parental tug-of-war
-
Moore, T. and Haig, D. (1991) Genomic imprinting in mammalian development: a parental tug-of-war. Trends Genet., 7, 45-49.
-
(1991)
Trends Genet.
, vol.7
, pp. 45-49
-
-
Moore, T.1
Haig, D.2
-
39
-
-
10144234124
-
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
-
Dittrich, B., Bulling, 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
-
40
-
-
0031747932
-
A mouse model for Prader-Willi syndrome imprinting-centre mutations
-
Yang, T., Adamson, T.E., Resnick, J.L., Leff, S., Wevrick, R., Francke, U., Jenkins, N.A., Copeland, N.G. and Brannan, C.I. (1998) A mouse model for Prader-Willi syndrome imprinting-centre mutations. Nature Genet., 19, 25-31.
-
(1998)
Nature Genet.
, vol.19
, pp. 25-31
-
-
Yang, T.1
Adamson, T.E.2
Resnick, J.L.3
Leff, S.4
Wevrick, R.5
Francke, U.6
Jenkins, N.A.7
Copeland, N.G.8
Brannan, C.I.9
-
41
-
-
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
-
42
-
-
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
-
43
-
-
0031750223
-
Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5
-
Paulsen, M., Davies, K.R., Bowden, L.M., Villar, A.J., Franck, O., Fuermann, M., Dean, W.L., Moore, T.F., Rodrigues, N., Davies, K.E., Hu, R.J., Feinberg, A.P., Maher, E.R., Reik, W. and Walter, J. (1998) Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5. Hum. Mol. Genet., 7, 1149-1159.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1149-1159
-
-
Paulsen, M.1
Davies, K.R.2
Bowden, L.M.3
Villar, A.J.4
Franck, O.5
Fuermann, M.6
Dean, W.L.7
Moore, T.F.8
Rodrigues, N.9
Davies, K.E.10
Hu, R.J.11
Feinberg, A.P.12
Maher, E.R.13
Reik, W.14
Walter, J.15
-
44
-
-
16044364516
-
KIP2 is mutated in Beckwith-Wiedemann syndrome
-
KIP2 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
-
45
-
-
0030610260
-
KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms' tumors
-
KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms' tumors. Am. J. Hum. Genet., 61, 295-303.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 295-303
-
-
O'Keefe, D.1
Dao, D.2
Zhao, L.3
Sanderson, R.4
Warburton, D.5
Weiss, L.6
Anyane-Yeboa, K.7
Tycko, B.8
-
46
-
-
0030610261
-
KIP2 mutation in Beckwith-Wiedemann syndrome
-
KIP2 mutation in Beckwith-Wiedemann syndrome. Am. J. Hum. Genet., 61, 304-309.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 304-309
-
-
Lee, M.P.1
DeBaun, M.2
Randhawa, G.3
Reichard, B.A.4
Elledge, S.J.5
Feinberg, A.P.6
-
47
-
-
0031952115
-
Imprinting of mouse Kvlqt1 is developmentally regulated
-
Gould, T.D. and Pfeifer, K. (1998) Imprinting of mouse Kvlqt1 is developmentally regulated. Hum. Mol. Genet., 1, 483-487.
-
(1998)
Hum. Mol. Genet.
, vol.1
, pp. 483-487
-
-
Gould, T.D.1
Pfeifer, K.2
-
48
-
-
18744429099
-
Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1
-
Jiang, S., Hemann, M.A., Lee, M.P. and Feinberg, A.P. (1998) Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1. Genomics, 53, 395-399.
-
(1998)
Genomics
, vol.53
, pp. 395-399
-
-
Jiang, S.1
Hemann, M.A.2
Lee, M.P.3
Feinberg, A.P.4
-
49
-
-
0030050208
-
Efficient modification of human chromosomal alleles using recombination-proficient chicken/human microcell hybrids
-
Dieken, E.S., Epner, E.M., Fiering, S., Fournier, R.E. and Groudine, M. (1996) Efficient modification of human chromosomal alleles using recombination-proficient chicken/human microcell hybrids. Nature Genet., 12, 174-182.
-
(1996)
Nature Genet.
, vol.12
, pp. 174-182
-
-
Dieken, E.S.1
Epner, E.M.2
Fiering, S.3
Fournier, R.E.4
Groudine, M.5
-
50
-
-
0030939444
-
Construction of chicken × human microcell hybrids for human gene targeting
-
Koi, M., Lamb, P.W., Filatov, L., Feinberg, A.P. and Barren, J.C. (1997) Construction of chicken × human microcell hybrids for human gene targeting. Cytogenet. Cell Genet., 76, 72-76.
-
(1997)
Cytogenet. Cell Genet.
, vol.76
, pp. 72-76
-
-
Koi, M.1
Lamb, P.W.2
Filatov, L.3
Feinberg, A.P.4
Barren, J.C.5
-
51
-
-
0032528310
-
Efficient modification of a human chromosome by telomere-directed truncation in high homologous recombination-proficient chicken DT40 cells
-
Kuroiwa, Y., Shinohara, T., Notsu, T., Tomizuka, K., Yoshida, H., Takeda, S., Oshimura, M. and Ishida, I. (1998) Efficient modification of a human chromosome by telomere-directed truncation in high homologous recombination-proficient chicken DT40 cells. Nucleic Acids Res., 26, 3447-3448.
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 3447-3448
-
-
Kuroiwa, Y.1
Shinohara, T.2
Notsu, T.3
Tomizuka, K.4
Yoshida, H.5
Takeda, S.6
Oshimura, M.7
Ishida, I.8
-
52
-
-
0028336989
-
Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method
-
Hayashizaki, Y., Shibata, H., Hirotsune, S., Sugino, H., Okazaki, Y., Sasaki, N., Hirose, K., Imoto, H., Okuizumi, H., Muramatsu, M., Komastubara, H., Shiroishi, T., Moriwaki, K., Katsuki, M., Hatano, N., Sasaki, H., Ueda, T., Mise, N., Takagi, N., Plass, C. and Chapman, V.M. (1994) Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method. Nature Genet., 6, 33-40.
-
(1994)
Nature Genet.
, vol.6
, pp. 33-40
-
-
Hayashizaki, Y.1
Shibata, H.2
Hirotsune, S.3
Sugino, H.4
Okazaki, Y.5
Sasaki, N.6
Hirose, K.7
Imoto, H.8
Okuizumi, H.9
Muramatsu, M.10
Komastubara, H.11
Shiroishi, T.12
Moriwaki, K.13
Katsuki, M.14
Hatano, N.15
Sasaki, H.16
Ueda, T.17
Mise, N.18
Takagi, N.19
Plass, C.20
Chapman, V.M.21
more..
-
53
-
-
0027769524
-
A new imprinted gene cloned by a methylation-sensitive genome scanning method
-
Hatada, I., Sugama, T. and Mukai, T. (1993) A new imprinted gene cloned by a methylation-sensitive genome scanning method. Nucleic Acids Res., 21, 5577-5582.
-
(1993)
Nucleic Acids Res.
, vol.21
, pp. 5577-5582
-
-
Hatada, I.1
Sugama, T.2
Mukai, T.3
-
54
-
-
0029114716
-
Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization
-
Kaneko-Ishino, T., Kuroiwa, Y., Miyoshi, N., Kohda, T., Suzuki, R., Yokoyama, M., Viville, S., Barton, S.C., Ishino, F. and Surani, M.A. (1995) Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization. Nature Genet., 11, 52-59.
-
(1995)
Nature Genet.
, vol.11
, pp. 52-59
-
-
Kaneko-Ishino, T.1
Kuroiwa, Y.2
Miyoshi, N.3
Kohda, T.4
Suzuki, R.5
Yokoyama, M.6
Viville, S.7
Barton, S.C.8
Ishino, F.9
Surani, M.A.10
-
55
-
-
0030829364
-
Screening for imprinted genes by allelic message display: Identification of a paternally expressed gene Impact on mouse chromosome 18
-
Hagiwara, Y., Hirai, M., Nishiyama, K., Kanazawa, I., Ueda, T., Sakaki, Y. and Ito, T. (1997) Screening for imprinted genes by allelic message display: identification of a paternally expressed gene Impact on mouse chromosome 18. Proc. Natl Acad. Sci. USA, 94, 9249-9254.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 9249-9254
-
-
Hagiwara, Y.1
Hirai, M.2
Nishiyama, K.3
Kanazawa, I.4
Ueda, T.5
Sakaki, Y.6
Ito, T.7
-
56
-
-
0031259754
-
Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2
-
Kikyo, N., Williamson, C.M., John, R.M., Barton, S.C., Beechey, C.V., Ball, S.T., Cattanach, B.M., Surani, M.A. and Peters, J. (1997) Genetic and functional analysis of neuronatin in mice with maternal or paternal duplication of distal Chr 2. Dev. Biol., 190, 66-77.
-
(1997)
Dev. Biol.
, vol.190
, pp. 66-77
-
-
Kikyo, N.1
Williamson, C.M.2
John, R.M.3
Barton, S.C.4
Beechey, C.V.5
Ball, S.T.6
Cattanach, B.M.7
Surani, M.A.8
Peters, J.9
-
57
-
-
0030746479
-
Duplication 14 (q24.3q31) in a father and daughter: Delineation of a possible imprinted region
-
Robin, N.H., Harari-Shacham, A., Schwartz, S. and Wolff, D.J. (1997) Duplication 14 (q24.3q31) in a father and daughter: delineation of a possible imprinted region. Am. J. Med. Genet., 71, 361-365.
-
(1997)
Am. J. Med. Genet.
, vol.71
, pp. 361-365
-
-
Robin, N.H.1
Harari-Shacham, A.2
Schwartz, S.3
Wolff, D.J.4
-
58
-
-
16944366964
-
Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function
-
Skuse, D.H., James, R.S., Bishop, D.V., Coppin, B., Dalton, P., Aamodt-Leeper, G., Bacarese-Hamilton, M., Creswell, C., McGurk, R. and Jacobs, P.A. (1997) Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function. Nature, 387, 705-708.
-
(1997)
Nature
, vol.387
, pp. 705-708
-
-
Skuse, D.H.1
James, R.S.2
Bishop, D.V.3
Coppin, B.4
Dalton, P.5
Aamodt-Leeper, G.6
Bacarese-Hamilton, M.7
Creswell, C.8
McGurk, R.9
Jacobs, P.A.10
-
59
-
-
0031748497
-
Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome
-
Naumova, A.K., Leppert, M., Barker, D.F., Morgan, K. and Sapienza, C. (1998) Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome. Am. J. Hum Genet., 62, 1493-1499.
-
(1998)
Am. J. Hum Genet.
, vol.62
, pp. 1493-1499
-
-
Naumova, A.K.1
Leppert, M.2
Barker, D.F.3
Morgan, K.4
Sapienza, C.5
-
60
-
-
0030779232
-
Paternal expression of WT1 in human fibroblasts and lymphocytes
-
Mitsuya, K., Sui, H., Meguro, M., Kugoh, H., Jinno, Y., Niikawa, N. and Oshimura, M. (1997) Paternal expression of WT1 in human fibroblasts and lymphocytes. Hum. Mol. Genet., 6, 2243-2246.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2243-2246
-
-
Mitsuya, K.1
Sui, H.2
Meguro, M.3
Kugoh, H.4
Jinno, Y.5
Niikawa, N.6
Oshimura, M.7
-
61
-
-
0020793569
-
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
-
Feinberg, A.P. and Vogelstein, B.A. (1983) A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal. Biochem., 132, 6-13.
-
(1983)
Anal. Biochem.
, vol.132
, pp. 6-13
-
-
Feinberg, A.P.1
Vogelstein, B.A.2
-
62
-
-
0032992678
-
Two novel genes in the center of the 11p1 imprinted domain escape genomic imprinting
-
Lee, M.P., Brandenburg, S., Landes, G.M., Adams, M., Miller, G. and Feinberg, A.P. (1999) Two novel genes in the center of the 11p1 imprinted domain escape genomic imprinting. Hum. Mol. Genet., 8, 683-690.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 683-690
-
-
Lee, M.P.1
Brandenburg, S.2
Landes, G.M.3
Adams, M.4
Miller, G.5
Feinberg, A.P.6
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