-
1
-
-
0000142302
-
Organisation and control of imprinted genes: The common features
-
ed. V. E. A. Russo, R. A. Martienssen & A. D. Riggs, CSHL Press. (Cold Spring Harbor Laboratory Press, USA)
-
Ainscough, J. F-X. & Surani, M. A. (1996). Organisation and control of imprinted genes: the common features. In Epigenetic Mechanisms of Gene Regulation (ed. V. E. A. Russo, R. A. Martienssen & A. D. Riggs), pp. 173-194. CSHL Press. (Cold Spring Harbor Laboratory Press, USA).
-
(1996)
Epigenetic Mechanisms of Gene Regulation
, pp. 173-194
-
-
Ainscough, J.F.-X.1
Surani, M.A.2
-
2
-
-
0030840328
-
Imprinting of Igf2 and H19 from a 130 kb YAC transgene
-
Ainscough, J. F-X., Koide, T., Tada, M., Barton, S. & 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.-X.1
Koide, T.2
Tada, M.3
Barton, S.4
Surani, M.A.5
-
3
-
-
8244224533
-
The human Achaete-Scute homologue 2 (ASCL2, HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillous trophoblasts
-
Alders, M., Hodges, M., Hadjantonakis, A., Postmus, J., van Wijk, I., Bliek, J., de Meulemeester, M., Westerveld, A., Guillemot, F., Oudejans, C., Little, P. & Mannens, M. (1997). The human Achaete-Scute homologue 2 (ASCL2, HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillous trophoblasts. Human Molecular Genetics 6, 859-867.
-
(1997)
Human Molecular Genetics
, vol.6
, pp. 859-867
-
-
Alders, M.1
Hodges, M.2
Hadjantonakis, A.3
Postmus, J.4
Van Wijk, I.5
Bliek, J.6
De Meulemeester, M.7
Westerveld, A.8
Guillemot, F.9
Oudejans, C.10
Little, P.11
Mannens, M.12
-
4
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei, M. S., Zemel, S. & Tilghman, S. M. (1991). Parental imprinting of the mouse H19 gene. Nature 351, 153-155.
-
(1991)
Nature
, vol.351
, pp. 153-155
-
-
Bartolomei, M.S.1
Zemel, S.2
Tilghman, S.M.3
-
5
-
-
0027203606
-
Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
-
Bartolomei, M. S., Webber, A. L., Brunkow, M. E. & Tilghman, S. M. (1993). Epigenetic mechanisms underlying the imprinting of the mouse H19 gene. Genes and Development 7, 1663-1673.
-
(1993)
Genes and Development
, vol.7
, pp. 1663-1673
-
-
Bartolomei, M.S.1
Webber, A.L.2
Brunkow, M.E.3
Tilghman, S.M.4
-
6
-
-
0029089444
-
Factors affecting the timing and imprinting of replication on a mammalian chromosome
-
Bickmore, W. A. & Carothers, A. D. (1995). Factors affecting the timing and imprinting of replication on a mammalian chromosome. Journal of Cell Science 108, 2801-9533.
-
(1995)
Journal of Cell Science
, vol.108
, pp. 2801-9533
-
-
Bickmore, W.A.1
Carothers, A.D.2
-
7
-
-
0028939902
-
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15
-
Buiting, K., Saitoh, S., Gross, S., Dittrich, B., Schwartz, S., Nicholls, R. D. & Horsthemke, B. (1995). Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nature Genetics 9, 395-400.
-
(1995)
Nature Genetics
, vol.9
, pp. 395-400
-
-
Buiting, K.1
Saitoh, S.2
Gross, S.3
Dittrich, B.4
Schwartz, S.5
Nicholls, R.D.6
Horsthemke, B.7
-
8
-
-
0022391691
-
Differential activity of maternally and paternally derived chromosome regions in mice
-
Cattanach, B. M. & Kirk, M. (1985). Differential activity of maternally and paternally derived chromosome regions in mice. Nature 315, 496-498.
-
(1985)
Nature
, vol.315
, pp. 496-498
-
-
Cattanach, B.M.1
Kirk, M.2
-
9
-
-
0027017879
-
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
-
Cattanach, B. M., Barr, J. A., Evans, E. P., Burtenshaw, M., Beechey, C. V., Leff, S. E., Brannan, C. I., Copeland, N. G., Jenkins, N. A. & Jones, J. (1992). A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression. Nature Genetics 2, 270-274.
-
(1992)
Nature Genetics
, vol.2
, pp. 270-274
-
-
Cattanach, B.M.1
Barr, J.A.2
Evans, E.P.3
Burtenshaw, M.4
Beechey, C.V.5
Leff, S.E.6
Brannan, C.I.7
Copeland, N.G.8
Jenkins, N.A.9
Jones, J.10
-
10
-
-
0003092366
-
Use of chromosome rearrangements for investigations into imprinting in the mouse
-
ed. R. Ohlsson, K. Hall & M. Ritzen, Cambridge: Cambridge University Press
-
Cattanach, B., Barr, J. & Jones, J. (1995). Use of chromosome rearrangements for investigations into imprinting in the mouse. Genomic Imprinting: Causes and Consequences (ed. R. Ohlsson, K. Hall & M. Ritzen), pp. 327-341. Cambridge: Cambridge University Press.
-
(1995)
Genomic Imprinting: Causes and Consequences
, pp. 327-341
-
-
Cattanach, B.1
Barr, J.2
Jones, J.3
-
11
-
-
0029847299
-
Chromosome 11p15.5 regional imprinting: Comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors
-
Chung, W.-Y., Yuan, L., Feng, L., Hensle, T. & Tycko, B. (1996). Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors. Human Molecular Genetics 5, 1101-1108.
-
(1996)
Human Molecular Genetics
, vol.5
, pp. 1101-1108
-
-
Chung, W.-Y.1
Yuan, L.2
Feng, L.3
Hensle, T.4
Tycko, B.5
-
12
-
-
0031924628
-
IMPT1, 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. & Tycko, B. (1998). IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes. Human Molecular Genetics 7, 597-608.
-
(1998)
Human Molecular Genetics
, 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
-
13
-
-
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. & Reik, W. (1997). Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2. Proceedings of the National Academy of Sciences of the USA 94, 12509-12514.
-
(1997)
Proceedings of the National Academy of Sciences of the 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
-
14
-
-
0027997318
-
Insulin-like growth factor 2 cannot be linked to a familial form of Beckwith-Wiedemann syndrome
-
Nystrom, A., Hedborg, F. & Ohlsson, R. (1994). Insulin-like growth factor 2 cannot be linked to a familial form of Beckwith-Wiedemann syndrome. European Journal of Paediatrics 153, 574-580.
-
(1994)
European Journal of Paediatrics
, vol.153
, pp. 574-580
-
-
Nystrom, A.1
Hedborg, F.2
Ohlsson, R.3
-
15
-
-
0031813176
-
Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis
-
Obata, Y., Kaneko-Ishino, T., Koide, T., Takai, Y., Ueda, T., Domeki, I., Shiroishi, T., Ishino, F. & Kono, T. (1998). Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis. Development 125, 1553-1560.
-
(1998)
Development
, vol.125
, pp. 1553-1560
-
-
Obata, Y.1
Kaneko-Ishino, T.2
Koide, T.3
Takai, Y.4
Ueda, T.5
Domeki, I.6
Shiroishi, T.7
Ishino, F.8
Kono, T.9
-
16
-
-
0027322519
-
IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome
-
Ohlsson, R., Nystrom, A., Pfeifer-Ohlsson, S., Tohonen, V., Hedborg, F., Schofield, P., Flam, F. & Ekstrom, J. (1993). IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome. Nature Genetics 4, 94-97.
-
(1993)
Nature Genetics
, vol.4
, pp. 94-97
-
-
Ohlsson, R.1
Nystrom, A.2
Pfeifer-Ohlsson, S.3
Tohonen, V.4
Hedborg, F.5
Schofield, P.6
Flam, F.7
Ekstrom, J.8
-
17
-
-
0030610260
-
Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors
-
O'Keefe, D., Dao, D., Zhao, L., Sanderson, R., Warburton, D., Wiess, L., Anyane-Yeboa, K. & Tycko, B. (1997). Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors. American Journal of Human Genetics 61, 295-303.
-
(1997)
American Journal of Human Genetics
, vol.61
, pp. 295-303
-
-
O'Keefe, D.1
Dao, D.2
Zhao, L.3
Sanderson, R.4
Warburton, D.5
Wiess, L.6
Anyane-Yeboa, K.7
Tycko, B.8
-
18
-
-
0030472782
-
The structural H19 gene is required for transgene imprinting
-
Pfeifer, K., Leighton, P. A. & Tilghman, S. M. (1996). The structural H19 gene is required for transgene imprinting. Proceedings of the National Academy of Sciences of the USA 93, 13876-13883.
-
(1996)
Proceedings of the National Academy of Sciences of the USA
, vol.93
, pp. 13876-13883
-
-
Pfeifer, K.1
Leighton, P.A.2
Tilghman, S.M.3
-
19
-
-
0024518392
-
Genetic linkage of Beckwith-Wiedemann syndrome to 11p15
-
Ping, A. J., Reeve, A. E., Law, D. J., Young, M. R., Boehnke, M. & Freiberg, A. P. (1989). Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. American Journal of Human Genetics 44, 720-723.
-
(1989)
American Journal of Human Genetics
, vol.44
, pp. 720-723
-
-
Ping, A.J.1
Reeve, A.E.2
Law, D.J.3
Young, M.R.4
Boehnke, M.5
Freiberg, A.P.6
-
20
-
-
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. & 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. Human Molecular Genetics 6, 2021-2029.
-
(1997)
Human Molecular Genetics
, 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
-
21
-
-
0028101171
-
Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome
-
Reik, W., Brown, K. W., Slatter, R. E., Sartori, P., Elliot, M. & Maher, E. R. (1994). Allelic methylation of H19 and IGF2 in the Beckwith-Wiedemann syndrome. Human Molecular Genetics 3, 1297-1301.
-
(1994)
Human Molecular Genetics
, vol.3
, pp. 1297-1301
-
-
Reik, W.1
Brown, K.W.2
Slatter, R.E.3
Sartori, P.4
Elliot, M.5
Maher, E.R.6
|