-
1
-
-
0029587022
-
Garnetic imprinting in mammals
-
Barlow, D. P. 1995, Garnetic imprinting in mammals, Science, 270, 1610-1613.
-
(1995)
Science
, vol.270
, pp. 1610-1613
-
-
Barlow, D.P.1
-
2
-
-
0033593288
-
The sins of the fathers and mothers: Genomic imprinting in mammalian development
-
Tilghman, S. M. 1999, The sins of the fathers and mothers: genomic imprinting in mammalian development, Cell, 96, 185-193.
-
(1999)
Cell
, vol.96
, pp. 185-193
-
-
Tilghman, S.M.1
-
3
-
-
0030856668
-
Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome
-
Reik, W. and Maher, E. R. 1997, Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome, Trends Genet., 13, 330-335.
-
(1997)
Trends Genet.
, vol.13
, pp. 330-335
-
-
Reik, W.1
Maher, E.R.2
-
4
-
-
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. 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
-
5
-
-
0031062973
-
Beckwith-Wiedemann syndrome and Wilms' tumor
-
Ward, A. 1997, Beckwith-Wiedemann syndrome and Wilms' tumor, Mol. Hum. Repro., 3, 157-168.
-
(1997)
Mol. Hum. Repro.
, vol.3
, pp. 157-168
-
-
Ward, A.1
-
6
-
-
0031214796
-
A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region
-
Reid, L. H., Davies, C., Cooper, P. R. et al. 1997, A 1-Mb physical map and PAC contig of the imprinted domain in 11p15.5 that contains TAPA1 and the BWSCR1/WT2 region, Genomics, 43, 366-375.
-
(1997)
Genomics
, vol.43
, pp. 366-375
-
-
Reid, L.H.1
Davies, C.2
Cooper, P.R.3
-
7
-
-
0031573849
-
Novel transcribed sequences within the BWS/WT2 region in 11p15.5: Tissue-specific expression correlates with cancer type
-
Crider-Miller, S. J., Reid, L. H., Higgins, M. J. et al. 1997, Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type, Genomics, 46, 355-363.
-
(1997)
Genomics
, vol.46
, pp. 355-363
-
-
Crider-Miller, S.J.1
Reid, L.H.2
Higgins, M.J.3
-
8
-
-
0031573423
-
A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes
-
Hu, R. J., Lee, M. P., Connors, T. D. et al. 1997, A 2.5-Mb transcript map of a tumor-suppressing subchromosomal transferable fragment from 11p15.5, and isolation and sequence analysis of three novel genes, Genomics, 46, 9-17.
-
(1997)
Genomics
, vol.46
, pp. 9-17
-
-
Hu, R.J.1
Lee, M.P.2
Connors, T.D.3
-
9
-
-
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. et al. 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
-
10
-
-
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
-
11
-
-
0002246574
-
Genomic imprinting in the mouse: Possible final analysis
-
(Reik Wans Surani MA, Eds.), IRL press, Oxford
-
Cattanach, B. M. and Beechey, C. V. 1997, Genomic imprinting in the mouse: possible final analysis. In Genomic Imprinting (Reik Wans Surani MA, Eds.), IRL press, Oxford, pp. 118-145.
-
(1997)
Genomic Imprinting
, pp. 118-145
-
-
Cattanach, B.M.1
Beechey, C.V.2
-
12
-
-
0026872675
-
Beckwith-Wiedemann syndrome, tumourigenesis and imprinting
-
Junien, C. 1992, Beckwith-Wiedemann syndrome, tumourigenesis and imprinting, Curr. Opin. Genet. Dev., 2, 431-438.
-
(1992)
Curr. Opin. Genet. Dev.
, vol.2
, pp. 431-438
-
-
Junien, C.1
-
13
-
-
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
-
14
-
-
9044227621
-
Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms' tumor assay
-
Reid, L. H., West, A., Gioeli, D. G. et al. 1996, Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms' tumor assay, Hum. Mol. Genet., 5, 239-247.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 239-247
-
-
Reid, L.H.1
West, A.2
Gioeli, D.G.3
-
15
-
-
0028356544
-
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumor
-
Steenman, M. J. C., 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.C.1
Rainier, S.2
Dobry, C.J.3
Grundy, P.4
Horon, I.L.5
Feinberg, A.P.6
-
16
-
-
0029774145
-
KIP2 in Wilms' tumor
-
KIP2 in Wilms' tumor, Cancer Res., 56, 5723-5727.
-
(1996)
Cancer Res.
, vol.56
, pp. 5723-5727
-
-
Thompson, J.S.1
Reese, K.J.2
DeBaun, M.R.3
Perlman, E.J.4
Feinberg, A.P.5
-
18
-
-
0029978017
-
KIP2, on chromosome 11p15
-
KIP2, 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
-
19
-
-
0032530827
-
Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5
-
Lee, M. P., Reeves, C., Schmitt, A. et al. 1998, Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5, Cancer Res., 58, 4155-4159.
-
(1998)
Cancer Res.
, vol.58
, pp. 4155-4159
-
-
Lee, M.P.1
Reeves, C.2
Schmitt, A.3
-
20
-
-
13144257678
-
Transcriptional map of 170-kb region at chromosome 11p15.5: Identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples
-
Schwienbacher, C., Sabbioni, S., Campi, M. et al. 1998, Transcriptional map of 170-kb region at chromosome 11p15.5: Identification and mutational analysis of the BWR1A 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
-
21
-
-
0032797231
-
Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: Inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting
-
Dao, D., Walsh, C. P., Yuan, L. et al. 1999, Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting, Hum. Mol. Genet., 8, 1337-1352.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1337-1352
-
-
Dao, D.1
Walsh, C.P.2
Yuan, L.3
-
22
-
-
0025914602
-
Genomic organization and chromosomal localization of the TAPA-1 gene
-
Andria, M. L., Hsieh, C. L., Oren, R., Francke, U., and Levy, S. 1991, Genomic organization and chromosomal localization of the TAPA-1 gene, J. Immunol., 147, 1030-1036.
-
(1991)
J. Immunol.
, vol.147
, pp. 1030-1036
-
-
Andria, M.L.1
Hsieh, C.L.2
Oren, R.3
Francke, U.4
Levy, S.5
-
23
-
-
0028988158
-
KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution
-
KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution, Genes Dev., 9, 639-649.
-
(1995)
Genes Dev.
, vol.9
, pp. 639-649
-
-
Lee, M.H.1
Reynisdottir, I.2
Massague, J.3
-
24
-
-
0028988159
-
CIP Cdk inhibitor family, is a candidate tumor suppressor gene
-
CIP Cdk inhibitor family, is a candidate tumor suppressor gene, Genes Dev., 9, 650-662.
-
(1995)
Genes Dev.
, vol.9
, pp. 650-662
-
-
Matsuoka, S.1
Edwards, M.C.2
Bai, C.3
-
25
-
-
0028980026
-
kip2, a cyclin-dependent kinase inhibitor, in mouse
-
kip2, 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
-
26
-
-
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. et al. 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
-
27
-
-
0032584803
-
KIP2 and IPL, is imprinted in mice
-
KIP2 and IPL, is imprinted in mice, DNA Res., 5, 235-240.
-
(1998)
DNA Res.
, vol.5
, pp. 235-240
-
-
Morisaki, H.1
Hatada, I.2
Morisaki, T.3
Mukai, T.4
-
28
-
-
0031924628
-
IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes
-
Dao, D., Frank, D., Qian, N. et al. 1998, IMPT1, 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
-
29
-
-
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., 7, 483-487.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 483-487
-
-
Gould, T.D.1
Pfeifer, K.2
-
30
-
-
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
-
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. et al. 1995, Multiple genetic loci within 11p15 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
-
32
-
-
0028816879
-
Allele-specific methylation and expression of an imprinted U2af1-rs1 (SP2) gene
-
Hatada, I., Kitagawa, K., Yamaoka, T. et al. 1995, Allele-specific methylation and expression of an imprinted U2af1-rs1 (SP2) gene, Nucleic Acids Res., 23, 36-41.
-
(1995)
Nucleic Acids Res.
, vol.23
, pp. 36-41
-
-
Hatada, I.1
Kitagawa, K.2
Yamaoka, T.3
-
33
-
-
0030825243
-
A novel method for making nested deletions and its application for sequencing of a 300 kb region of human APP locus
-
Hattori, M., Tsukahara, F., Furuhata, Y. et al. 1997, A novel method for making nested deletions and its application for sequencing of a 300 kb region of human APP locus, Nucleic Acids Res., 25, 1802-1808.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 1802-1808
-
-
Hattori, M.1
Tsukahara, F.2
Furuhata, Y.3
-
34
-
-
0030801002
-
Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
-
Altschul, S. F., Madden, T. L., Schaffer, A. A. et al. 1997, Gapped BLAST and PSI-BLAST: a new generation of protein database search programs, Nucleic Acids Res., 25, 3389-3402.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 3389-3402
-
-
Altschul, S.F.1
Madden, T.L.2
Schaffer, A.A.3
-
35
-
-
0033621282
-
Sequence-ready 1-Mb YAC, BAC and cosmid contigs covering the distal imprinted region of mouse chromosome 7
-
Kato, R., Shirohzu, H., Yokomine, T., Mizuno, S., Mukai, T., and Sasaki, H. 1999, Sequence-ready 1-Mb YAC, BAC and cosmid contigs covering the distal imprinted region of mouse chromosome 7, DNA Res., 6, 401-405.
-
(1999)
DNA Res.
, vol.6
, pp. 401-405
-
-
Kato, R.1
Shirohzu, H.2
Yokomine, T.3
Mizuno, S.4
Mukai, T.5
Sasaki, H.6
-
36
-
-
0029975794
-
Retrotransposon reverse-transcriptase-mediated repair of chromosomal breaks
-
Teng, S. C., Kim, B., and Gabriel, A. 1996, Retrotransposon reverse-transcriptase-mediated repair of chromosomal breaks, Nature, 383, 641-644.
-
(1996)
Nature
, vol.383
, pp. 641-644
-
-
Teng, S.C.1
Kim, B.2
Gabriel, A.3
-
37
-
-
0029970701
-
Capture of retrotransposon DNA at the sites of chromosomal double-strand breaks
-
Moore, J. K. and Haber, J. E. 1996, Capture of retrotransposon DNA at the sites of chromosomal double-strand breaks, Nature, 383, 644-646.
-
(1996)
Nature
, vol.383
, pp. 644-646
-
-
Moore, J.K.1
Haber, J.E.2
-
38
-
-
0032813924
-
LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids
-
Mitsuya, K., Meguro, M., Lee, M. P. et al. 1999, LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids, Hum. Mol. Genet., 8, 1209-1217.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1209-1217
-
-
Mitsuya, K.1
Meguro, M.2
Lee, M.P.3
-
39
-
-
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. et al. 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
-
40
-
-
0033529207
-
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome
-
Smilinich, N. J., Day, C. D., Fitzpatrick, G. V. et al. 1999, A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome, Proc. Natl. Acad. Sci. USA., 96, 8064-8069.
-
(1999)
Proc. Natl. Acad. Sci. USA.
, vol.96
, pp. 8064-8069
-
-
Smilinich, N.J.1
Day, C.D.2
Fitzpatrick, G.V.3
-
41
-
-
0032992678
-
Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting
-
Lee, M. P., Brandenburg, S., Landes, G. M., Adams, M., Miller, G., Feinberg, A. P. 1999, Two novel genes in the center of the 11p15 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
-
42
-
-
0033958493
-
Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression
-
Prawitt, D., Enklaar, T., Klemm, G. et al. 2000, Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression, Hum. Mol. Genet., 9, 203-216.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 203-216
-
-
Prawitt, D.1
Enklaar, T.2
Klemm, G.3
-
43
-
-
0032428381
-
A model system to study genomic imprinting of human genes
-
Gabriel, J. M., Higgins, M. J., Gebuhr, T. C., Shows, T. B., Saitoh, S., and Nicholls, R. D. 1998, A model system to study genomic imprinting of human genes, Proc. Natl. Acad. Sci. USA., 95, 14857-14862.
-
(1998)
Proc. Natl. Acad. Sci. USA.
, vol.95
, pp. 14857-14862
-
-
Gabriel, J.M.1
Higgins, M.J.2
Gebuhr, T.C.3
Shows, T.B.4
Saitoh, S.5
Nicholls, R.D.6
-
44
-
-
0034127018
-
Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprinting
-
in press
-
Ishihara, K., Hatano, N., Furuumi, H. et al. Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprinting, Genome Res., (in press).
-
Genome Res.,
-
-
Ishihara, K.1
Hatano, N.2
Furuumi, H.3
-
47
-
-
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
-
48
-
-
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
-
49
-
-
0032749555
-
KIP2 transgene is not activated by passage through the maternal mouse germline
-
KIP2 transgene is not activated by passage through the maternal mouse germline, Hum. Mol. Genet., 8, 2211-2219.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 2211-2219
-
-
John, R.M.1
Hodges, M.2
Little, P.3
Barton, S.C.4
Surani, M.A.5
-
50
-
-
0032419812
-
Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2
-
Thorvaldsen, J. L., Duran, K. L., and Bartolomei, M. S. 1998, Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2, Genes Dev., 12, 3693-3702.
-
(1998)
Genes Dev.
, vol.12
, pp. 3693-3702
-
-
Thorvaldsen, J.L.1
Duran, K.L.2
Bartolomei, M.S.3
|