-
1
-
-
0029587022
-
Gametic imprinting in mammals
-
Barlow,D.P. (1995) Gametic imprinting in mammals. Science, 270, 1610-1613.
-
(1995)
Science
, vol.270
, pp. 1610-1613
-
-
Barlow, D.P.1
-
2
-
-
0025242074
-
Genome imprinting phenomena on mouse chromosome 7
-
Searle,A.G. and Beechey,C.V. (1990) Genome imprinting phenomena on mouse chromosome 7. Genet. Res., 56, 237-244.
-
(1990)
Genet. Res.
, vol.56
, pp. 237-244
-
-
Searle, A.G.1
Beechey, C.V.2
-
3
-
-
0026428611
-
Embryological and molecular investigations of parental imprinting on mouse chromosome 7
-
Ferguson-Smith,A.C., Cattanach,B.A., Barton,S.C., Beechey,C.V. and Surani,M.A. (1993) Embryological and molecular investigations of parental imprinting on mouse chromosome 7. Nature, 351, 667-670.
-
(1993)
Nature
, vol.351
, pp. 667-670
-
-
Ferguson-Smith, A.C.1
Cattanach, B.A.2
Barton, S.C.3
Beechey, C.V.4
Surani, M.A.5
-
4
-
-
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., 8, 21-26.
-
(1995)
J. Natl Cancer Inst. Monogr.
, vol.8
, pp. 21-26
-
-
Feinberg, A.P.1
Rainier, S.2
DeBaun, M.R.3
-
5
-
-
0031054075
-
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
-
Neyroud,N., Tesson,F., Denjoy,I., Leibovici,M., Donger,C., Barhanin,J., Faure,S., Gary,F., Coumel,R., Petit,C., Schwartz,K. and Guicheney,P. (1997) A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Nature Genet., 15, 186-189.
-
(1997)
Nature Genet.
, vol.15
, pp. 186-189
-
-
Neyroud, N.1
Tesson, F.2
Denjoy, I.3
Leibovici, M.4
Donger, C.5
Barhanin, J.6
Faure, S.7
Gary, F.8
Coumel, R.9
Petit, C.10
Schwartz, K.11
Guicheney, P.12
-
6
-
-
0025847714
-
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
-
Keating,M., Atkinson,D., Dunn,C., Timothy,K., Vincent,G.M. and Leppert,M. (1991) Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. Science, 252, 704-706.
-
(1991)
Science
, vol.252
, pp. 704-706
-
-
Keating, M.1
Atkinson, D.2
Dunn, C.3
Timothy, K.4
Vincent, G.M.5
Leppert, M.6
-
7
-
-
49749174698
-
Congenital deaf mutism, functional heart disease with prolongation of the QT interval and sudden death
-
Jervell,A. and Lange-Nielson,F. (1956) Congenital deaf mutism, functional heart disease with prolongation of the QT interval and sudden death. Am. Heart J., 54, 59-68.
-
(1956)
Am. Heart J.
, vol.54
, pp. 59-68
-
-
Jervell, A.1
Lange-Nielson, F.2
-
8
-
-
0016609531
-
The long Q-T syndrome
-
Schwartz,P.J., Periti,M. and Malliani,A. (1975) The long Q-T syndrome. Am. Heart J., 89, 378-390.
-
(1975)
Am. Heart J.
, vol.89
, pp. 378-390
-
-
Schwartz, P.J.1
Periti, M.2
Malliani, A.3
-
9
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
Wang,Q., Curran,M.E., Splawski,I., Burn,T.C., Millholland,J.M., Van-Raay,T.J., Shen,J., Tomothy,K.W., Vincent,G.M., de Jager,T., Schwartz,P.J., Towbin,J.A., Moss,A.J., Atkinson,D.L., Landes,G.M., Connors,T.D. and Keating,M.T. (1996) Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nature Genet., 12, 17-23.
-
(1996)
Nature Genet.
, vol.12
, pp. 17-23
-
-
Wang, Q.1
Curran, M.E.2
Splawski, I.3
Burn, T.C.4
Millholland, J.M.5
Van-Raay, T.J.6
Shen, J.7
Tomothy, K.W.8
Vincent, G.M.9
De Jager, T.10
Schwartz, P.J.11
Towbin, J.A.12
Moss, A.J.13
Atkinson, D.L.14
Landes, G.M.15
Connors, T.D.16
Keating, M.T.17
-
10
-
-
0031046285
-
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beck-with-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 Beck-with-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
-
12
-
-
0029854263
-
KS potassium channel
-
KS potassium channel. Nature., 384, 80-83.
-
(1996)
Nature.
, vol.384
, pp. 80-83
-
-
Sanguinetti, M.C.1
Lesage, F.2
Guillemare, E.3
Fink, M.4
Lazdunski, M.5
Romey, G.6
-
13
-
-
0030890712
-
KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias
-
Yang,W.-P., Levesque,P.C., Little,W.A., Condor,M.L., Shalaby,F.Y. and Blanar,M.A. (1997) KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias. Proc. Natl Acad. Sci. USA, 94, 4017-4021.
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 4017-4021
-
-
Yang, W.-P.1
Levesque, P.C.2
Little, W.A.3
Condor, M.L.4
Shalaby, F.Y.5
Blanar, M.A.6
-
14
-
-
0027203606
-
Epigenetic mechanisms underlying the imprinting of the mouse H19 gene
-
Bartolomei,M.S., Webber,A.L., Brunkow,M.E. and Tilghman,S.M. (1993) Epigenetic mechanisms underlying the imprinting of the mouse H19 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
-
15
-
-
0025809321
-
Parental imprinting of the mouse H19 gene
-
Bartolomei,M.S., Zemel,S. and 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
-
16
-
-
0028815477
-
Genomic imprinting of Mash2, a mouse gene required for trophoblast development
-
Guillemot,F., Caspary,T., Tilghman,S.M., Copeland,N.G., Gilbert,D.J., Jenkins,N.A., Anderson,D.J., Joyner,A.L., Rossant,J. and Nagy,A. (1995) Genomic imprinting of Mash2, a mouse gene required for trophoblast development. Nature Genet., 9, 235-242.
-
(1995)
Nature Genet.
, vol.9
, pp. 235-242
-
-
Guillemot, F.1
Caspary, T.2
Tilghman, S.M.3
Copeland, N.G.4
Gilbert, D.J.5
Jenkins, N.A.6
Anderson, D.J.7
Joyner, A.L.8
Rossant, J.9
Nagy, A.10
-
17
-
-
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
-
18
-
-
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
-
19
-
-
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
-
20
-
-
0030472782
-
The structural gene is required for transgene imprinting
-
Pfeifer,K., Leighton,P.A. and Tilghman,S.M. (1996) The structural gene is required for transgene imprinting. Proc. Natl Acad. Sci. USA, 93, 13876-13883.
-
(1996)
Proc. Natl Acad. Sci. USA
, vol.93
, pp. 13876-13883
-
-
Pfeifer, K.1
Leighton, P.A.2
Tilghman, S.M.3
-
21
-
-
0028968205
-
A paternal-specific methylation imprint marks the alleles of the mouse H19 gene
-
Tremblay,K.D., Saam,J.R., Ingram,R.S., Tilghman,S.M. and Bartolomei,M.S. (1995) A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nature Genet., 9, 407-13.
-
(1995)
Nature Genet.
, vol.9
, pp. 407-413
-
-
Tremblay, K.D.1
Saam, J.R.2
Ingram, R.S.3
Tilghman, S.M.4
Bartolomei, M.S.5
-
22
-
-
0027941535
-
Essential role of Mash-2 in extraembryonic development
-
Guillemot,F., Nagy,A., Auerbach,A., Rossant,J. and Joyner,A.L. (1994) Essential role of Mash-2 in extraembryonic development. Nature, 371, 333-336.
-
(1994)
Nature
, vol.371
, pp. 333-336
-
-
Guillemot, F.1
Nagy, A.2
Auerbach, A.3
Rossant, J.4
Joyner, A.L.5
-
23
-
-
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
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