-
5
-
-
0035895513
-
Gene number. What if there are only 30,000 human genes?
-
(2001)
Science
, vol.291
, pp. 1255-1257
-
-
Claverie, J.M.1
-
7
-
-
0034326859
-
Sequence and functional comparison in the Beckwith-Wiedemann region: Implications for a novel imprinting centre and extended imprinting
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2691-2706
-
-
Engemann, S.1
Strodicke, M.2
Paulsen, M.3
Franck, O.4
Reinhardt, R.5
Lane, N.6
Reik, W.7
Walter, J.8
-
8
-
-
0026635880
-
Genetic analysis of genomic imprinting: An imprintor-1 gene controls inactivation of the paternal copy of the mouse Tme locus
-
(1992)
Cell
, vol.70
, pp. 443-450
-
-
Forejt, J.1
Gregorova, S.2
-
9
-
-
0034284693
-
Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2075-2083
-
-
Horike, S.1
Mitsuya, K.2
Meguro, M.3
Kotobuki, N.4
Kashiwagi, A.5
Notsu, T.6
Schulz, T.C.7
Shirayoshi, Y.8
Oshimura, M.9
-
10
-
-
0033551109
-
Lack of reciprocal genomic imprinting of sense and antisense RNA of mouse insulin-like growth factor II receptor in the central nervous system
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.257
, pp. 604-608
-
-
Hu, J.F.1
Balaguru, K.A.2
Ivaturi, R.D.3
Oruganti, H.4
Li, T.5
Nguyen, B.T.6
Vu, T.H.7
Hoffman, A.R.8
-
11
-
-
0035158704
-
Loss of genomic methylation causes p53-dependent apoptosis and epigenetic deregulation
-
(2001)
Nat. Genet.
, vol.27
, pp. 31-39
-
-
Jackson-Grusby, L.1
Beard, C.2
Possemato, R.3
Tudor, M.4
Fambrough, D.5
Csankovszki, G.6
Dausman, J.7
Lee, P.8
Wilson, C.9
Lander, E.10
-
14
-
-
0034724647
-
Mit1/Lb9 and Copg2, new members of mouse imprinted genes closely linked to Peg1/Mest(1)
-
(2000)
FEBS Lett.
, vol.472
, pp. 230-234
-
-
Lee, Y.J.1
Park, C.W.2
Hahn, Y.3
Park, J.4
Lee, J.5
Yun, J.H.6
Hyun, B.7
Chung, J.H.8
-
16
-
-
0034118382
-
The imprinted antisense RNA at the Igf2r locus overlaps but does not imprint Masl
-
(2000)
Nat. Genet.
, vol.25
, pp. 19-21
-
-
Lyle, R.1
Watanabe, D.2
Te Vruchte, D.3
Lerchner, W.4
Smrzka, O.W.5
Wutz, A.6
Schageman, J.7
Hahner, L.8
Davies, C.9
Barlow, D.P.10
-
18
-
-
0031813176
-
Disruption of primary imprinting during oocyte growth leads to the modified expression of imprinted genes during embryogenesis
-
(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
-
19
-
-
0033073395
-
Imprinting-mutation mechanisms in Prader-Willi syndrome
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 397-413
-
-
Ohta, T.1
Gray, T.A.2
Rogan, P.K.3
Buiting, K.4
Gabriel, J.M.5
Saitoh, S.6
Muralidhar, B.7
Bilienska, B.8
Krajewska-Walasek, M.9
Driscoll, D.J.10
-
20
-
-
0033858005
-
Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1829-1841
-
-
Paulsen, M.1
El-Maarri, O.2
Engemann, S.3
Strodicke, M.4
Franck, O.5
Davies, K.6
Reinhardt, R.7
Reik, W.8
Walter, J.9
-
23
-
-
0031214583
-
Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene
-
(1997)
Genomics
, vol.43
, pp. 285-297
-
-
Schweifer, N.1
Valk, P.J.2
Delwel, R.3
Cox, R.4
Francis, F.5
Meier-Ewert, S.6
Lehrach, H.7
Barlow, D.P.8
-
26
-
-
0033529207
-
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome
-
(1999)
Proc. Natl. Acad. Sci.
, vol.96
, pp. 8064-8069
-
-
Smilinich, N.J.1
Day, C.D.2
Fitzpatrick, G.V.3
Caldwell, G.M.4
Lossie, A.C.5
Cooper, P.R.6
Smallwood, A.C.7
Joyce, J.A.8
Schofield, P.N.9
Reik, W.10
-
30
-
-
0034724290
-
An imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locus
-
(2000)
Proc. Natl. Acad. Sci.
, vol.97
, pp. 3342-3346
-
-
Wroe, S.F.1
Kelsey, G.2
Skinner, J.A.3
Bodle, D.4
Ball, S.T.5
Beechey, C.V.6
Peters, J.7
Williamson, C.M.8
-
33
-
-
0031747932
-
A mouse model for Prader-Willi syndrome imprinting-centre mutations
-
(1998)
Nat. 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
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