-
1
-
-
0025320906
-
A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor-II gene disrupted by targeting
-
De Chiara, T. M., Efstratiadis, A. & Robertson, E. J. A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor-II gene disrupted by targeting. Nature 345, 78-80 (1990).
-
(1990)
Nature
, vol.345
, pp. 78-80
-
-
De Chiara, T.M.1
Efstratiadis, A.2
Robertson, E.J.3
-
2
-
-
0025967857
-
Parental imprinting of the mouse insulin-like growth factor-II gene
-
DeChiara, T. M., Robertson, E. J. & Efstratiadis, A. Parental imprinting of the mouse insulin-like growth factor-II gene. Cell 64, 849-859 (1991).
-
(1991)
Cell
, vol.64
, pp. 849-859
-
-
DeChiara, T.M.1
Robertson, E.J.2
Efstratiadis, A.3
-
3
-
-
0030856668
-
Imprinting in clusters: Lessons from Beckwith-Wiedemann syndrome
-
Reik, W. & Maher, E. R. Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome. Trends Genet. 13, 330-334 (1997).
-
(1997)
Trends Genet.
, vol.13
, pp. 330-334
-
-
Reik, W.1
Maher, E.R.2
-
4
-
-
0029165883
-
An enhancer deletion affects both H19 and IGF2 expression
-
Leighton, R A., Saam, J. R., Ingram, R. S., Stewart, C. L. & Tilghman, S. M. An enhancer deletion affects both H19 and IGF2 expression. Genes Dev. 9, 2079-2089 (1995).
-
(1995)
Genes Dev.
, vol.9
, pp. 2079-2089
-
-
Leighton, R.A.1
Saam, J.R.2
Ingram, R.S.3
Stewart, C.L.4
Tilghman, S.M.5
-
5
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 region in mice
-
Leighton, P. A., Ingram, R. S., Eggenschwiler, J., Efstratiadis, A. & Tilghman, S. M. Disruption of imprinting caused by deletion of the H19 region in mice. Nature 375, 34-39 (1995).
-
(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
-
6
-
-
0030993133
-
Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element
-
Ripoche, M. A., Kress, C., Pirier, F. & Dandolo, L. Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element. Genes. Dev. 11, 1596-1604 (1997).
-
(1997)
Genes. Dev.
, vol.11
, pp. 1596-1604
-
-
Ripoche, M.A.1
Kress, C.2
Pirier, F.3
Dandolo, L.4
-
7
-
-
0026781474
-
Parental imprinting-potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor-II (IGF2) gene
-
Sasaki, H. et al. Parental imprinting-potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor-II (IGF2) gene. Genes Dev. 6, 1843-1856 (1992).
-
(1992)
Genes Dev.
, vol.6
, pp. 1843-1856
-
-
Sasaki, H.1
-
8
-
-
0027937839
-
Development control of allelic methylation in the imprinted mouse IGF2 and H19 genes
-
Feil, R., Walter, J., Allen, N. D. & Reik, W. Development control of allelic methylation in the imprinted mouse IGF2 and H19 genes. Development 120, 2933-2943 (1994).
-
(1994)
Development
, vol.120
, pp. 2933-2943
-
-
Feil, R.1
Walter, J.2
Allen, N.D.3
Reik, W.4
-
9
-
-
0001443162
-
-
eds Russo, V. E. A., Martienssen, R. A. & Riggs, A. D. (Cold Spring Harbor Laboratory Press, NY)
-
Walter, J. et al. in Epigenetic Mechanisms of Gene Regulation (eds Russo, V. E. A., Martienssen, R. A. & Riggs, A. D.) 195-213 (Cold Spring Harbor Laboratory Press, NY, 1996).
-
(1996)
Epigenetic Mechanisms of Gene Regulation
, pp. 195-213
-
-
Walter, J.1
-
10
-
-
0031061679
-
Genomic regions regulating imprinting and insulin-like growth factor-II promoter 3 activity in transgenics: Novel enhancer and silencer elements
-
Ward, A. et al. Genomic regions regulating imprinting and insulin-like growth factor-II promoter 3 activity in transgenics: novel enhancer and silencer elements. Genes Funct. 1, 25-36 (1997).
-
(1997)
Genes Funct.
, vol.1
, pp. 25-36
-
-
Ward, A.1
-
11
-
-
0027287437
-
Genomic imprinting and gene activation in cancer
-
Feinberg, A. P. Genomic imprinting and gene activation in cancer Nature Genet 4, 110-113 (1993).
-
(1993)
Nature Genet
, vol.4
, pp. 110-113
-
-
Feinberg, A.P.1
-
12
-
-
0028880017
-
Mammary-cancer in transgenic mice expressing insulin-like growth-factor II (IGFII)
-
Bates, P. et al. Mammary-cancer in transgenic mice expressing insulin-like growth-factor II (IGFII). Brit. J. Cancer 72, 1189-1193 (1995).
-
(1995)
Brit. J. Cancer
, vol.72
, pp. 1189-1193
-
-
Bates, P.1
-
13
-
-
0028356419
-
A second signal supplied by insulin-like growth factor II in oncogene-induced tumorigenesis
-
Christofori, G., Naik, P. & Hanahan, D. A. A second signal supplied by insulin-like growth factor II in oncogene-induced tumorigenesis. Nature 369, 414-418 (1994).
-
(1994)
Nature
, vol.369
, pp. 414-418
-
-
Christofori, G.1
Naik, P.2
Hanahan, D.A.3
-
14
-
-
0028318189
-
Altered body composition and increased frequency of diverse malignancies in insulin-like growth factor II transgenic mice
-
Rogler, C. E. et al. Altered body composition and increased frequency of diverse malignancies in insulin-like growth factor II transgenic mice. J. Biol. Chem. 269, 13779-13784 (1994).
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 13779-13784
-
-
Rogler, C.E.1
-
15
-
-
0028470672
-
Beckwith-Wiedemann syndrome
-
Elliott, M. & Maher, E. R. Beckwith-Wiedemann syndrome. J. Med. Genet. 31, 560-564 (1994).
-
(1994)
J. Med. Genet.
, vol.31
, pp. 560-564
-
-
Elliott, M.1
Maher, E.R.2
-
16
-
-
0027420362
-
Disruption of insulin-like growth factor-II imprinting in Beckwith-Weidemann syndrome
-
Weksberg, R., Shen, D. R., Fei, Y. L., Song, Q. L. & Squire, J. Disruption of insulin-like growth factor-II imprinting in Beckwith-Weidemann syndrome. Nature Genet. 5, 143-150 (1994).
-
(1994)
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
-
17
-
-
0030827119
-
Imprinting of Igf2 and H19: Lack of reciprocity in sporadic Beckwith-Wiedemann syndrome
-
Joyce, J. A. et al. Imprinting of Igf2 and H19: Lack of reciprocity in sporadic Beckwith-Wiedemann syndrome. Hum. Mol. Genet. 6, 1543-1548 (1997).
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1543-1548
-
-
Joyce, J.A.1
-
18
-
-
0028862472
-
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domain
-
Reik, W. et al. 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).
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2379-2385
-
-
Reik, W.1
-
19
-
-
0029806141
-
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
-
Brown, K. W. et al. Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway. Hum. Mol. Genet. 5, 2027-2032 (1996).
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 2027-2032
-
-
Brown, K.W.1
-
20
-
-
0031046285
-
Human KvLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
-
Lee, M. P., Hu, R. J., Johnson, L. A. & Feinberg, A. P. Human KvLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nature Genet. 15, 181-185 (1997).
-
(1997)
Nature Genet.
, vol.15
, pp. 181-185
-
-
Lee, M.P.1
Hu, R.J.2
Johnson, L.A.3
Feinberg, A.P.4
-
21
-
-
16044364516
-
Kip2 is mutated in Beckwith-Wiedemann syndrome
-
Kip2 is mutated in Beckwith-Wiedemann syndrome. Nature Genet. 14, 171-173 (1996).
-
(1996)
Nature Genet.
, vol.14
, pp. 171-173
-
-
Hatada, I.1
-
22
-
-
1842335753
-
Kip2 indicates a role in Beckwith-Wiedemann syndrome
-
Kip2 indicates a role in Beckwith-Wiedemann syndrome. Nature 387, 151-158 (1997).
-
(1997)
Nature
, vol.387
, pp. 151-158
-
-
Zhang, P.1
-
24
-
-
0028575985
-
Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality
-
Lau, M. M. H. et al. Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality. Genes Dev. 8, 2953-2963 (1994).
-
(1994)
Genes Dev.
, vol.8
, pp. 2953-2963
-
-
Lau, M.M.H.1
-
25
-
-
0027999284
-
Regulation of embryonic growth and lysosomal targeting by the imprinted IGF2/MPR gene
-
Wang, Z. Q., Fun, M. R., Barlow, D. P. & Wagner, E. F. Regulation of embryonic growth and lysosomal targeting by the imprinted IGF2/MPR gene. Nature 372, 464-467 (1994).
-
(1994)
Nature
, vol.372
, pp. 464-467
-
-
Wang, Z.Q.1
Fun, M.R.2
Barlow, D.P.3
Wagner, E.F.4
-
26
-
-
0030221121
-
Mouse mutants lacking the type-2 IGF receptor (IGF2R) are rescued from perinatal lethality in IGF2 and IGF1R null backgrounds
-
Ludwig, T. et al. Mouse mutants lacking the type-2 IGF receptor (IGF2R) are rescued from perinatal lethality in IGF2 and IGF1R null backgrounds. Dev. Biol. 177, 517-535 (1996).
-
(1996)
Dev. Biol.
, vol.177
, pp. 517-535
-
-
Ludwig, T.1
-
27
-
-
0026428611
-
Embryological and molecular investigations of parental imprinting on mouse chromosome 7
-
Ferguson-Smith, A. C., Cattanach, B. M., Barton, S. C., Beechey, C. V. & Surani, M. A. Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature 351, 667-670 (1991).
-
(1991)
Nature
, vol.351
, pp. 667-670
-
-
Ferguson-Smith, A.C.1
Cattanach, B.M.2
Barton, S.C.3
Beechey, C.V.4
Surani, M.A.5
-
28
-
-
0027303619
-
Parental imprinting of an IGF2 transgene
-
Lee, J. E., Trantrahavi, U., Boyle, A. L. & Efstratiadis, A. Parental imprinting of an IGF2 transgene. Mol. Reprod. Dev. 35, 382-390 (1993).
-
(1993)
Mol. Reprod. Dev.
, vol.35
, pp. 382-390
-
-
Lee, J.E.1
Trantrahavi, U.2
Boyle, A.L.3
Efstratiadis, A.4
-
29
-
-
0028046891
-
The cell-type specific IGF2 expression during early human development correlates to the pattern of overgrowth and neoplasia in the Beckwith-Wiedemann syndrome
-
Hedborg, F., Holmgren, L., Sandstedt, B. & Ohlsson, R. The cell-type specific IGF2 expression during early human development correlates to the pattern of overgrowth and neoplasia in the Beckwith-Wiedemann syndrome. Am. J. Pathol. 145, 802-817 (1994).
-
(1994)
Am. J. Pathol.
, vol.145
, pp. 802-817
-
-
Hedborg, F.1
Holmgren, L.2
Sandstedt, B.3
Ohlsson, R.4
-
30
-
-
0027231511
-
Parental allele-specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome
-
Schneid, H. et al. Parental allele-specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome. J. Med. Genet. 30, 353-362 (1993).
-
(1993)
J. Med. Genet.
, vol.30
, pp. 353-362
-
-
Schneid, H.1
-
31
-
-
0027999665
-
Mosaic uniparental disomy in Beckwith-Wiedemann syndrome
-
Slatter, R. E. et al. Mosaic uniparental disomy in Beckwith-Wiedemann syndrome. J. Med. Genet. 31, 749-753 (1994).
-
(1994)
J. Med. Genet.
, vol.31
, pp. 749-753
-
-
Slatter, R.E.1
-
32
-
-
0029939816
-
Somatic overgrowth associated with overexpression of insulin-like growth factor II
-
Morison, I. M., Becroft, D. M., Taniguchi, T., Woods, C. G. & Reeve, A. E. Somatic overgrowth associated with overexpression of insulin-like growth factor II. Nature Med. 2, 311-316 (1996).
-
(1996)
Nature Med.
, vol.2
, pp. 311-316
-
-
Morison, I.M.1
Becroft, D.M.2
Taniguchi, T.3
Woods, C.G.4
Reeve, A.E.5
-
33
-
-
13344261391
-
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
-
Pilia, G. et al. Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome. Nature Genet. 12, 241-247 (1996).
-
(1996)
Nature Genet.
, vol.12
, pp. 241-247
-
-
Pilia, G.1
-
34
-
-
0030032278
-
Mouse embryos with paternal duplication of an imprinted chromosome 7 region die at midgestation and lack placental spongiotrophoblast
-
McLaughlin, K. J., Szabo, P., Haegel, H. & Mann, J. R. Mouse embryos with paternal duplication of an imprinted chromosome 7 region die at midgestation and lack placental spongiotrophoblast. Development 122, 265-270 (1996).
-
(1996)
Development
, vol.122
, pp. 265-270
-
-
McLaughlin, K.J.1
Szabo, P.2
Haegel, H.3
Mann, J.R.4
-
35
-
-
0030015418
-
Dynamic methylation adjustment and counting as part of imprinting mechanisms
-
Shemer, R. et al. Dynamic methylation adjustment and counting as part of imprinting mechanisms. Proc. Natl Acad. Sci. USA 93, 6371-6376 (1996).
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 6371-6376
-
-
Shemer, R.1
-
36
-
-
0030903760
-
Aberrant methylation of an imprinted gene U2af1-rs1 caused by its own transgene
-
Hatada, I. et al. Aberrant methylation of an imprinted gene U2af1-rs1 caused by its own transgene. J. Biol. Chem. 272, 9120-9122 (1997).
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 9120-9122
-
-
Hatada, I.1
-
37
-
-
0030895047
-
Long-range cis effects of ectopic X-inactivation centres on a mouse autosome
-
Lee, J. T. & Jaenisch, R. Long-range cis effects of ectopic X-inactivation centres on a mouse autosome. Nature 386, 272-275 (1997).
-
(1997)
Nature
, vol.386
, pp. 272-275
-
-
Lee, J.T.1
Jaenisch, R.2
-
38
-
-
0031001346
-
Xist has properties of the X-chromosome inactivation centre
-
Herzing, L. B. K., Romer, J. T., Horn, J. M. & Ashworth, A. Xist has properties of the X-chromosome inactivation centre. Nature 386, 272-275 (1997).
-
(1997)
Nature
, vol.386
, pp. 272-275
-
-
Herzing, L.B.K.1
Romer, J.T.2
Horn, J.M.3
Ashworth, A.4
-
39
-
-
0030608276
-
Nucleotide sequence of a 28 kb mouse genomic region comprising the imprinted Igf2 gene
-
Sasaki, H. et al. Nucleotide sequence of a 28 kb mouse genomic region comprising the imprinted Igf2 gene. DNA Res. 3, 331-335 (1996).
-
(1996)
DNA Res.
, vol.3
, pp. 331-335
-
-
Sasaki, H.1
-
40
-
-
0025600899
-
Evolution of insulin-like growth factor II: Characterisation of the mouse Igf2 gene and identification of two pseudo-exons
-
Rotwein, P. & Hall, L. J. Evolution of insulin-like growth factor II: characterisation of the mouse Igf2 gene and identification of two pseudo-exons. DNA Cell Biol. 9, 725-735 (1990).
-
(1990)
DNA Cell Biol.
, vol.9
, pp. 725-735
-
-
Rotwein, P.1
Hall, L.J.2
-
41
-
-
0004136246
-
-
Cold Spring Harbor Laboratory Press, NY
-
Sambrook, J., Fritsch, E. F. & Maniatis, T. Molecular Cloning: A Laboratory Manual (Cold Spring Harbor Laboratory Press, NY, 1989).
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
43
-
-
0021770917
-
Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter
-
Melton, D. A. et al. Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. Nucleic Acids Res. 12, 7035-7056 (1984).
-
(1984)
Nucleic Acids Res.
, vol.12
, pp. 7035-7056
-
-
Melton, D.A.1
|