-
1
-
-
0029806141
-
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
-
Brown KW, Villar AJ, Bickmore W, Clayton-Smith J, Catchpoole D, Maher ER, Reik W (1996) Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway. Hum Mol Genet 5:2027-2032
-
(1996)
Hum Mol Genet
, vol.5
, pp. 2027-2032
-
-
Brown, K.W.1
Villar, A.J.2
Bickmore, W.3
Clayton-Smith, J.4
Catchpoole, D.5
Maher, E.R.6
Reik, W.7
-
2
-
-
0027158855
-
Parental genomic imprinting of the human IGF2 gene
-
Giannoukakis N, Deal C, Paquette J, Goodyer CG, Polychronakos C (1993) Parental genomic imprinting of the human IGF2 gene. Nat Genet 4:98-101
-
(1993)
Nat Genet
, vol.4
, pp. 98-101
-
-
Giannoukakis, N.1
Deal, C.2
Paquette, J.3
Goodyer, C.G.4
Polychronakos, C.5
-
3
-
-
0027442239
-
Tumor-suppressor activity of H19 RNA
-
Hao Y, Crenshaw T, Moulton T, Newcomb E, Tycko B (1993) Tumor-suppressor activity of H19 RNA. Nature 365:764-767
-
(1993)
Nature
, vol.365
, pp. 764-767
-
-
Hao, Y.1
Crenshaw, T.2
Moulton, T.3
Newcomb, E.4
Tycko, B.5
-
5
-
-
0025738681
-
Uniparental paternal disomy in a genetic cancer-predisposing syndrome
-
Henry I, Bonaiti-Pellie C, Chehensse V, Beldjord C, Schwartz C, Utermann G, Junien C (1991) Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature 351:665-667
-
(1991)
Nature
, vol.351
, pp. 665-667
-
-
Henry, I.1
Bonaiti-Pellie, C.2
Chehensse, V.3
Beldjord, C.4
Schwartz, C.5
Utermann, G.6
Junien, C.7
-
6
-
-
10144230716
-
Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus
-
Jinno Y, Sengoku K, Nakao M, Tamate K, Miyamoto T, Matsuzaka T, Sutcliffe JS, et al (1996) Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus. Hum Mol Genet 5:1155-1161
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1155-1161
-
-
Jinno, Y.1
Sengoku, K.2
Nakao, M.3
Tamate, K.4
Miyamoto, T.5
Matsuzaka, T.6
Sutcliffe, J.S.7
-
7
-
-
0024517062
-
Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5
-
Koufos A, Grundy P, Morgan K, Aleck KA, Hadro T, Lampkin BC, Kalbakji A, et al (1989) Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. Am J Hum Genet 44:711-719
-
(1989)
Am J Hum Genet
, vol.44
, pp. 711-719
-
-
Koufos, A.1
Grundy, P.2
Morgan, K.3
Aleck, K.A.4
Hadro, T.5
Lampkin, B.C.6
Kalbakji, A.7
-
8
-
-
0028988158
-
Cloning of p57/ KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution
-
Lee M-H, Reynisdottir I, Massague J (1995) Cloning of p57/ 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
-
9
-
-
0031046285
-
vLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
-
vLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nat Genet 15:181-185
-
(1997)
Nat Genet
, vol.15
, pp. 181-185
-
-
Lee, M.P.1
Hu, R.-J.2
Johnson, L.A.3
Feinberg, A.P.4
-
10
-
-
0028316620
-
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann Syndrome and various human neoplasia
-
Mannens M, Hoovers JMN, Redeker E, Verjaal M, Feinberg AP, Little P, Boavida M, 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.N.2
Redeker, E.3
Verjaal, M.4
Feinberg, A.P.5
Little, P.6
Boavida, M.7
-
11
-
-
0028988159
-
p57/KIP2, a structurally distinct member of the p21/CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene
-
Matsuoka S, Edwards MC, Bai C, Parker S, Zhang P, Baldini A, Harper JW, et al (1995) p57/KIP2, a structurally distinct member of the p21/CIP1 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
Parker, S.4
Zhang, P.5
Baldini, A.6
Harper, J.W.7
-
12
-
-
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
Barletta, J.M.4
Grundy, P.5
Kalikin, L.M.6
Harper, J.W.7
-
13
-
-
0028227938
-
Epigenetic lesions at the H19 locus in Wilms' tumour patients
-
Moulton T, Crenshaw T, Hao Y, Moosikasuwan J, Lin N, Dembitzer F, Hensle T, et al (1994) Epigenetic lesions at the H19 locus in Wilms' tumour patients. Nat Genet 7:440-447
-
(1994)
Nat Genet
, vol.7
, pp. 440-447
-
-
Moulton, T.1
Crenshaw, T.2
Hao, Y.3
Moosikasuwan, J.4
Lin, N.5
Dembitzer, F.6
Hensle, T.7
-
14
-
-
0027422302
-
Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism
-
Ogawa O, Becroft DM, Morison IM, Eccles MR, Skeen JE, Mauger DC, Reeve AE (1993) Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism. Nat Genet 5:408-412
-
(1993)
Nat Genet
, vol.5
, pp. 408-412
-
-
Ogawa, O.1
Becroft, D.M.2
Morison, I.M.3
Eccles, M.R.4
Skeen, J.E.5
Mauger, D.C.6
Reeve, A.E.7
-
15
-
-
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, et al (1993) IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome. Nat Genet 4:94-97
-
(1993)
Nat Genet
, 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
-
16
-
-
0023011534
-
An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13Xpter: Correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome
-
Okano Y, Osasa Y, Yamamoto H, Hase Y, Tsuruhara T, Fujita H (1986) An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13Xpter: correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome. Jpn J Hum Genet 31:365-372
-
(1986)
Jpn J Hum Genet
, vol.31
, pp. 365-372
-
-
Okano, Y.1
Osasa, Y.2
Yamamoto, H.3
Hase, Y.4
Tsuruhara, T.5
Fujita, H.6
-
17
-
-
0024518392
-
Genetic linkage of Beckwith-Wiedemann syndrome to 11p15
-
Ping AJ, Reeve AE, Law DJ, Young MR, Boehnke M, Feinberg AP (1989) Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. Am J Hum Genet 44:720-723
-
(1989)
Am J Hum Genet
, vol.44
, pp. 720-723
-
-
Ping, A.J.1
Reeve, A.E.2
Law, D.J.3
Young, M.R.4
Boehnke, M.5
Feinberg, A.P.6
-
18
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier S, Johnson LA, Dobry CJ, Ping AJ, Grundy PE, Feinberg AP (1993) Relaxation of imprinted genes in human cancer. Nature 362:747-749
-
(1993)
Nature
, vol.362
, pp. 747-749
-
-
Rainier, S.1
Johnson, L.A.2
Dobry, C.J.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
19
-
-
0028862472
-
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by an altered imprinting pattern in the IGF2-H19 domain
-
Reik W, Brown KW, Schneid H, LeBouc Y, Bickmore W, Maher ER (1995) 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)
Hum Mol Genet
, vol.4
, pp. 2379-2385
-
-
Reik, W.1
Brown, K.W.2
Schneid, H.3
LeBouc, Y.4
Bickmore, W.5
Maher, E.R.6
-
20
-
-
0028356544
-
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumor
-
Steenman MJC, Rainier S, Dobry CJ, Grundy P, Horon IL, Feinberg AP (1994) Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumor. Nat Genet 7:433-439
-
(1994)
Nat 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
-
22
-
-
0029670462
-
KIP2 gene: Alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysis
-
KIP2 gene: alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysis. Hum Genet 97:625-631
-
(1996)
Hum Genet
, vol.97
, pp. 625-631
-
-
Tokino, T.1
Urano, T.2
Furuhata, T.3
Matsushima, M.4
Miyatsu, T.5
Sasaki, S.6
Nakamura, Y.7
-
23
-
-
0021256768
-
Trisomy 11p15 and Beckwith-Wiedemann syndrome: A report of two cases
-
Turleau C, de Grouchy J, Chavin-Colin F, Martelli H, Voyer M, Charlas R (1984) Trisomy 11p15 and Beckwith-Wiedemann syndrome: a report of two cases. Hum Genet 67:219-221
-
(1984)
Hum Genet
, vol.67
, pp. 219-221
-
-
Turleau, C.1
De Grouchy, J.2
Chavin-Colin, F.3
Martelli, H.4
Voyer, M.5
Charlas, R.6
-
24
-
-
0020511170
-
Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome
-
Waziri M, Patil SR, Hanson JW, Bartley JA (1983) Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome. J Pediatr 102:873-876
-
(1983)
J Pediatr
, vol.102
, pp. 873-876
-
-
Waziri, M.1
Patil, S.R.2
Hanson, J.W.3
Bartley, J.A.4
-
25
-
-
0027420362
-
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Weidemann syndrome
-
Weksberg R, Shen DR, Fei YL, Song QL, Squire J (1993) Disruption of insulin-like growth factor 2 imprinting in Beckwith-Weidemann syndrome. Nat Genet 5:143-150
-
(1993)
Nat Genet
, vol.5
, pp. 143-150
-
-
Weksberg, R.1
Shen, D.R.2
Fei, Y.L.3
Song, Q.L.4
Squire, J.5
-
26
-
-
34250134720
-
Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome
-
Wiedemann HR (1983) Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndrome. Eur J Pediatr 141:129
-
(1983)
Eur J Pediatr
, vol.141
, pp. 129
-
-
Wiedemann, H.R.1
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