-
1
-
-
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. Hum Mol Genet 8:1101-1108
-
(1996)
Hum Mol Genet
, vol.8
, pp. 1101-1108
-
-
Chung, W.-Y.1
Yuan, L.2
Feng, L.3
Hensle, T.4
Tycko, B.5
-
2
-
-
0027442239
-
Tumour-suppressor activity of H19 RNA
-
Hao Y, Crenshaw T, Moulton T, Newcomb E, Tycko B (1993) Tumour-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
-
3
-
-
0029896367
-
Genomic imprinting of human pS7KIP2 and its reduced expression in Wilms' tumors
-
Hatada I, Inazawa J, Abe T, Nakayama M, Yasuhiko K, Jinno Y, Niikawa N, et al (1996a) Genomic imprinting of human pS7KIP2 and its reduced expression in Wilms' tumors. Hum Mol Genet 5:783-788
-
(1996)
Hum Mol Genet
, vol.5
, pp. 783-788
-
-
Hatada, I.1
Inazawa, J.2
Abe, T.3
Nakayama, M.4
Yasuhiko, K.5
Jinno, Y.6
Niikawa, N.7
-
4
-
-
0028980026
-
Genomic imprinting of p57Kip2, a cyclin-dependent kinase inhibitor, in mouse
-
Hatada I, Mukai T (1995) Genomic imprinting of p57Kip2, a cyclin-dependent kinase inhibitor, in mouse. Nat Genet 11:204-206
-
(1995)
Nat Genet
, vol.11
, pp. 204-206
-
-
Hatada, I.1
Mukai, T.2
-
5
-
-
16044364516
-
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
-
Hatada I, Ohashi H, Fukushima Y, Kaneko Y, Inoue M, Komoto Y, Okada A, et al (1996b) An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome. Nat Genet 13:171-173
-
(1996)
Nat Genet
, vol.13
, pp. 171-173
-
-
Hatada, I.1
Ohashi, H.2
Fukushima, Y.3
Kaneko, Y.4
Inoue, M.5
Komoto, Y.6
Okada, A.7
-
6
-
-
0025738681
-
Uniparental disomy in a genetic cancer-predisposing syndrome
-
Henry I, Bonaïti-Pellié C, Chehensse V, Beldjord C, Schwartz C, Utermann G, Junien C (1991) Uniparental disomy in a genetic cancer-predisposing syndrome. Nature 351:665-667
-
(1991)
Nature
, vol.351
, pp. 665-667
-
-
Henry, I.1
Bonaïti-Pellié, C.2
Chehensse, V.3
Beldjord, C.4
Schwartz, C.5
Utermann, G.6
Junien, C.7
-
7
-
-
0027793754
-
Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: A post-fertilization event
-
Henry I, Puech A, Riesewijk A, Ahnine L, Mannens M, Beldjord C, Bitoun P, et al (1993) Somatic mosaicism for partial paternal isodisomy in Wiedemann-Beckwith syndrome: a post-fertilization event. Eur J Hum Genet 1:19-29
-
(1993)
Eur J Hum Genet
, vol.1
, pp. 19-29
-
-
Henry, I.1
Puech, A.2
Riesewijk, A.3
Ahnine, L.4
Mannens, M.5
Beldjord, C.6
Bitoun, P.7
-
8
-
-
13344278697
-
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
-
Hoovers JMN, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, et al (1995) Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments. Proc Natl Acad Sci USA 92: 12456-12460
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 12456-12460
-
-
Hoovers, J.M.N.1
Kalikin, L.M.2
Johnson, L.A.3
Alders, M.4
Redeker, B.5
Law, D.J.6
Bliek, J.7
-
9
-
-
0026872675
-
Beckwith-Wiedemann syndrome, tumourigenesis and imprinting
-
Junien C (1992) Beckwith-Wiedemann syndrome, tumourigenesis and imprinting. Curr Opin Genet Dev 2:431-438
-
(1992)
Curr Opin Genet Dev
, vol.2
, pp. 431-438
-
-
Junien, C.1
-
10
-
-
0029869293
-
Selective maternal-allele loss in human lung cancers of the maternally expressed p57KIP2 gene at 11p15.5
-
Kondo M, Matsuoka S, Uchida K, Osada H, Nagatake M, Takagi K, Harper JW, et al (1996) Selective maternal-allele loss in human lung cancers of the maternally expressed p57KIP2 gene at 11p15.5. Oncogene 12:1365-1368
-
(1996)
Oncogene
, vol.12
, pp. 1365-1368
-
-
Kondo, M.1
Matsuoka, S.2
Uchida, K.3
Osada, H.4
Nagatake, M.5
Takagi, K.6
Harper, J.W.7
-
11
-
-
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
-
12
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 gene region in mice
-
Leighton PA, Ingram RS, Eggenschwiler J, Efstratiatis A, Tilghman SM (1995) Disruption of imprinting caused by deletion of the H19 gene region in mice. Nature 375:34-39
-
(1995)
Nature
, vol.375
, pp. 34-39
-
-
Leighton, P.A.1
Ingram, R.S.2
Eggenschwiler, J.3
Efstratiatis, A.4
Tilghman, S.M.5
-
13
-
-
0028316620
-
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia
-
Mannens M, Hoovers JM, 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.2
Redeker, E.3
Verjaal, M.4
Feinberg, A.P.5
Little, P.6
Boavida, M.7
-
14
-
-
0028988159
-
p57KIP2, a structurally distinct member of the p21CIP1 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) p57KIP2, a structurally distinct member of the p21CIP1 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
-
15
-
-
0029978017
-
Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15.5
-
Matsuoka S, Thompson JS, Edwards MC, Barletta JM, Grundy P, Kalikin LM, Harper JW, et al (1996) Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15.5. 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
-
16
-
-
0029939816
-
Somatic overgrowth associated with overexpression of insulin-like growth factor II
-
Morison IM, Becroft DM, Taniguchi T, Woods CG, Reeve AE (1996) Somatic overgrowth associated with overexpression of insulin-like growth factor II. Nat Med 2:311-316
-
(1996)
Nat 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
-
17
-
-
0029818524
-
Genomic imprinting and Wilms' tumor
-
Moulton T, Chung W-Y, Yuan L, Hensle T, Waber P, Nisen P, Tycko B (1996) Genomic imprinting and Wilms' tumor. Med Pediatr Oncol 27:476-483
-
(1996)
Med Pediatr Oncol
, vol.27
, pp. 476-483
-
-
Moulton, T.1
Chung, W.-Y.2
Yuan, L.3
Hensle, T.4
Waber, P.5
Nisen, P.6
Tycko, B.7
-
18
-
-
0028227938
-
Epigenetic lesions at the H19 locus in Wilms' tumor 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' tumor 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
-
19
-
-
0029878892
-
Cyclin-dependent kinase inhibitor p57KIP2 in soft tissue sarcomas and Wilms' tumors
-
Orlow I, Iavarone A, Crider-Miller SJ, Bonilla F, Latres E, Lee M-H, Gerald WL, et al (1996) Cyclin-dependent kinase inhibitor p57KIP2 in soft tissue sarcomas and Wilms' tumors. Cancer Res 56:1219-1221
-
(1996)
Cancer Res
, vol.56
, pp. 1219-1221
-
-
Orlow, I.1
Iavarone, A.2
Crider-Miller, S.J.3
Bonilla, F.4
Latres, E.5
Lee, M.-H.6
Gerald, W.L.7
-
20
-
-
0030226250
-
p57KIP2 is expressed in Wilms' tumor with LOH of 11p15.5
-
Overall ML, Spencer J, Bakker M, Dziadek M, Smith PJ (1996) . p57KIP2 is expressed in Wilms' tumor with LOH of 11p15.5. Genes Chromosom Cancer 17:56-59
-
(1996)
Genes Chromosom Cancer
, vol.17
, pp. 56-59
-
-
Overall, M.L.1
Spencer, J.2
Bakker, M.3
Dziadek, M.4
Smith, P.J.5
-
21
-
-
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
-
22
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier S, Johnson L, 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.2
Dobry, C.J.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
23
-
-
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, Le Bouc 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
Le Bouc, Y.4
Bickmore, W.5
Maher, E.R.6
-
24
-
-
0029665852
-
Crystal structure of the p27KIP1 cyclin-dependent-kinase inhibitor bound to the cyclinA-cdk2 complex
-
Russo AA, Jeffrey PD, Patten AK, Massague J, Pavletich NP (1996) Crystal structure of the p27KIP1 cyclin-dependent-kinase inhibitor bound to the cyclinA-cdk2 complex. Nature 382:325-331
-
(1996)
Nature
, vol.382
, pp. 325-331
-
-
Russo, A.A.1
Jeffrey, P.D.2
Patten, A.K.3
Massague, J.4
Pavletich, N.P.5
-
25
-
-
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
-
26
-
-
0028935017
-
Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor
-
Taniguchi T, Sullivan MJ, Osamu O, Reeve A (1995) Epigenetic changes encompassing the IGF2/H19 locus associated with relaxation of IGF2 imprinting and silencing of H19 in Wilms tumor. Proc Natl Acad Sci USA 92: 2159-2163
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 2159-2163
-
-
Taniguchi, T.1
Sullivan, M.J.2
Osamu, O.3
Reeve, A.4
-
27
-
-
0029670462
-
Characterization of the human p57KIP2 gene: Alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysis
-
Tokino T, Urano T, Furuhata T, Matsushima M, Miyatsu T, Sasaki S, Nakamura Y (1996) Characterization of the human p57KIP2 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
-
28
-
-
10144219962
-
Polymorphisms in the human apolipoprotein-J/clusterin gene: Ethnic variation and distribution in Alzheimer's disease
-
Tycko B, Feng L, Nguyen L, Francis A, Hays A, Chung W-Y, Tang M-X, et al (1996) Polymorphisms in the human apolipoprotein-J/clusterin gene: ethnic variation and distribution in Alzheimer's disease. Hum Genet 98: 430-436
-
(1996)
Hum Genet
, vol.98
, pp. 430-436
-
-
Tycko, B.1
Feng, L.2
Nguyen, L.3
Francis, A.4
Hays, A.5
Chung, W.-Y.6
Tang, M.-X.7
-
29
-
-
0027420362
-
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
-
Weksberg R, Shen DR, Fei YL, Song QL, Squire J (1993) Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann 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
-
30
-
-
0029848437
-
Molecular biology of Beckwith-Wiedemann syndrome
-
Weksberg R, Squire JA (1996) Molecular biology of Beckwith-Wiedemann syndrome. Med Pediatr Oncol 27:462-469
-
(1996)
Med Pediatr Oncol
, vol.27
, pp. 462-469
-
-
Weksberg, R.1
Squire, J.A.2
|