-
1
-
-
0029765587
-
Identification of novel regions of deletion in familial Wilms' tumor by comparative genome hybridization
-
Altura RA, Valentine M, Li H, Boyett JM, Shearer P, Grundy P, Shapiro DN, Look AT (1996): Identification of novel regions of deletion in familial Wilms' tumor by comparative genome hybridization. Cancer Res 56:3837-3841.
-
(1996)
Cancer Res
, vol.56
, pp. 3837-3841
-
-
Altura, R.A.1
Valentine, M.2
Li, H.3
Boyett, J.M.4
Shearer, P.5
Grundy, P.6
Shapiro, D.N.7
Look, A.T.8
-
2
-
-
0000077851
-
Macroglossia, Omphalocele, Adrenal Cytomegaly, Gigantism, and Hyperplastic Visceromegaly
-
Bergsma D (ed): New York: National Foundation-March of Dimes
-
Beckwith JB (1969): Macroglossia, Omphalocele, Adrenal Cytomegaly, Gigantism, and Hyperplastic Visceromegaly. In Bergsma D (ed): "The Clinical Delineation of Birth Defects, Part II." New York: National Foundation-March of Dimes, pp. 188-190.
-
(1969)
The Clinical Delineation of Birth Defects, Part II
, pp. 188-190
-
-
Beckwith, J.B.1
-
4
-
-
0029796609
-
Familial Wilms' tumor: A descriptive study
-
Breslow NE, Olson J, Moksness J, Beckwith JB, Grundy P (1996): Familial Wilms' tumor: a descriptive study. Med Ped Oncol 27:398-403.
-
(1996)
Med Ped Oncol
, vol.27
, pp. 398-403
-
-
Breslow, N.E.1
Olson, J.2
Moksness, J.3
Beckwith, J.B.4
Grundy, P.5
-
7
-
-
0025762971
-
Ectopic expression of the H19 gene in mice causes prenatal lethality
-
Brunkow ME, Tilghman SM (1991): Ectopic expression of the H19 gene in mice causes prenatal lethality. Genes Devel 5:1092-1101.
-
(1991)
Genes Devel
, vol.5
, pp. 1092-1101
-
-
Brunkow, M.E.1
Tilghman, S.M.2
-
8
-
-
0025099787
-
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
-
Call KM, Glaser T, Ito CY, Buckler AJ, Pelletier J, Haber DA, Rose EA, Kral A, Yeger H, Lewis WH, Jones C, Housman DE (1990): Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell 60:509-520.
-
(1990)
Cell
, vol.60
, pp. 509-520
-
-
Call, K.M.1
Glaser, T.2
Ito, C.Y.3
Buckler, A.J.4
Pelletier, J.5
Haber, D.A.6
Rose, E.A.7
Kral, A.8
Yeger, H.9
Lewis, W.H.10
Jones, C.11
Housman, D.E.12
-
9
-
-
0027465535
-
Genetic mosaicism in normal tissues of Wilms' tumour patients
-
Chao L-Y, Huff V, Tomlinson G, Riccardi VM, Strong LG, Saunders GF (1993): Genetic mosaicism in normal tissues of Wilms' tumour patients. Nature Genet 3:127-131.
-
(1993)
Nature Genet
, vol.3
, pp. 127-131
-
-
Chao, L.-Y.1
Huff, V.2
Tomlinson, G.3
Riccardi, V.M.4
Strong, L.G.5
Saunders, G.F.6
-
10
-
-
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 Mol Genet 5:1101-1108.
-
(1996)
Human Mol Genet
, vol.5
, pp. 1101-1108
-
-
Chung, W.-Y.1
Yuan, L.2
Feng, L.3
Hensle, T.4
Tycko, B.5
-
11
-
-
0030760633
-
Inactivation of H19, an imprinted and putative tumor repressor gene, is a preneoplastic event during Wilms' tumorigenesis
-
Cui H, Hedborg F, He L, Nordenskjold A, Sandstedt B, Pfeifer-Ohlsson S, Ohlsson R (1997): Inactivation of H19, an imprinted and putative tumor repressor gene, is a preneoplastic event during Wilms' tumorigenesis. Cancer Res 57:4469-4473.
-
(1997)
Cancer Res
, vol.57
, pp. 4469-4473
-
-
Cui, H.1
Hedborg, F.2
He, L.3
Nordenskjold, A.4
Sandstedt, B.5
Pfeifer-Ohlsson, S.6
Ohlsson, R.7
-
13
-
-
0014775569
-
A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease
-
Drash A, Sherman F, Hartmann WH, Blizzard RM (1970): A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease. J Pediatr 76:585-593.
-
(1970)
J Pediatr
, vol.76
, pp. 585-593
-
-
Drash, A.1
Sherman, F.2
Hartmann, W.H.3
Blizzard, R.M.4
-
14
-
-
0026669131
-
Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1
-
Drummond IA, Madden SL, Rohwer-Nutter P, Bell GI, Sukhatme VP, Rauscher FJ III (1992): Repression of the insulin-like growth factor II gene by the Wilms tumor suppressor WT1. Science 257:674-678.
-
(1992)
Science
, vol.257
, pp. 674-678
-
-
Drummond, I.A.1
Madden, S.L.2
Rohwer-Nutter, P.3
Bell, G.I.4
Sukhatme, V.P.5
Rauscher III, F.J.6
-
15
-
-
0025098654
-
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
-
Gessler M, Proustka A, Cavenee W, Neve RL, Orkin SH, Bruns GAP (1990): Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping. Nature 343:774-778.
-
(1990)
Nature
, vol.343
, pp. 774-778
-
-
Gessler, M.1
Proustka, A.2
Cavenee, W.3
Neve, R.L.4
Orkin, S.H.5
Bruns, G.A.P.6
-
16
-
-
0026588871
-
The genomic organization and expression of the WT1 gene
-
Gessler M, Konig A, Bruns GAP (1992): The genomic organization and expression of the WT1 gene. Genomics 12:807-813.
-
(1992)
Genomics
, vol.12
, pp. 807-813
-
-
Gessler, M.1
Konig, A.2
Bruns, G.A.P.3
-
17
-
-
0028196679
-
Infrequent mutation of the WT1 gene in 77 Wilms' tumors
-
Gessler M, Konig A, Arden K, Grundy P, Orkin S, Sallan S, Peters C, Ruyle S, Mandell J, Li F, Cavenee W, Bruns F (1994): Infrequent mutation of the WT1 gene in 77 Wilms' tumors. Human Mutat 3:212-222.
-
(1994)
Human Mutat
, vol.3
, pp. 212-222
-
-
Gessler, M.1
Konig, A.2
Arden, K.3
Grundy, P.4
Orkin, S.5
Sallan, S.6
Peters, C.7
Ruyle, S.8
Mandell, J.9
Li, F.10
Cavenee, W.11
Bruns, F.12
-
18
-
-
0023683531
-
Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11
-
Grundy P, Koufos A, Morgan K, Li FP, Meadows AT, Cavenee WK (1988): Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. Nature 336:374-376.
-
(1988)
Nature
, vol.336
, pp. 374-376
-
-
Grundy, P.1
Koufos, A.2
Morgan, K.3
Li, F.P.4
Meadows, A.T.5
Cavenee, W.K.6
-
19
-
-
0030593719
-
Analysis of possible abnormal WT1 RNA processing in primary Wilms tumors
-
Gunning KB, Cohn SL, Tomlinson GE, Strong LC, Huff V (1996): Analysis of possible abnormal WT1 RNA processing in primary Wilms tumors. Oncogene 13:1179-1185.
-
(1996)
Oncogene
, vol.13
, pp. 1179-1185
-
-
Gunning, K.B.1
Cohn, S.L.2
Tomlinson, G.E.3
Strong, L.C.4
Huff, V.5
-
20
-
-
0025992044
-
Alternative splicing and genomic structure of the Wilms tumor gene, WT1
-
Haber DA, Sohn RL, Buckler AJ, Pelletier J, Call KM, Housman DE (1991): Alternative splicing and genomic structure of the Wilms tumor gene, WT1. Proc Natl Acad Sci USA 88:9618-9622.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 9618-9622
-
-
Haber, D.A.1
Sohn, R.L.2
Buckler, A.J.3
Pelletier, J.4
Call, K.M.5
Housman, D.E.6
-
21
-
-
0027771747
-
WT1-mediated growth suppression of Wilms tumor cells expressing a WT1 splicing variant
-
Haber DA, Park S, Maheswaran S, Englert C, Re FF, Hazen-Martin DJ, Sens DA, Garvin AJ (1993): WT1-mediated growth suppression of Wilms tumor cells expressing a WT1 splicing variant. Science 262: 2057-2059.
-
(1993)
Science
, vol.262
, pp. 2057-2059
-
-
Haber, D.A.1
Park, S.2
Maheswaran, S.3
Englert, C.4
Re, F.F.5
Hazen-Martin, D.J.6
Sens, D.A.7
Garvin, A.J.8
-
22
-
-
0027442239
-
Tumour-suppressor activity of H19 gene
-
Hao Y, Crenshaw T, Moulton T, Newcomb E, Tycko B (1993): Tumour-suppressor activity of H19 gene. 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
-
23
-
-
0027212667
-
Wilms' tumor in the Li-Fraumeni family syndrome
-
Hartley AL, Birch JM, Tricker K, Wallace SA, Kelsey AM, Harris M, Morris Jones PH (1993): Wilms' tumor in the Li-Fraumeni family syndrome. Cancer Genet Cytogenet 67:133-135.
-
(1993)
Cancer Genet Cytogenet
, vol.67
, pp. 133-135
-
-
Hartley, A.L.1
Birch, J.M.2
Tricker, K.3
Wallace, S.A.4
Kelsey, A.M.5
Harris, M.6
Morris Jones, P.H.7
-
24
-
-
0029896367
-
KIP2 and its reduced expression in Wilms' tumors
-
KIP2 and its reduced expression in Wilms' tumors. Human Molecular Genet 5: 783-788.
-
(1996)
Human Molecular Genet
, vol.5
, pp. 783-788
-
-
Hatada, I.1
Inazawa, J.2
Abe, T.3
Nakayama, M.4
Kaneko, Y.5
Jinno, Y.6
Niikawa, N.7
Ohashi, H.8
Fukushima, Y.9
Iida, K.10
Yutani, C.11
Takahashi, S.12
Chiba, Y.13
Ohishi, S.14
Mukai, T.15
-
25
-
-
16044364516
-
KIP2 is mutated in Beckwith-Wiedemann syndrome
-
KIP2 is mutated in Beckwith-Wiedemann syndrome. Nature 14:171-173.
-
(1996)
Nature
, vol.14
, pp. 171-173
-
-
Hatada, I.1
Ohashi, H.2
Fukushima, Y.3
Kaneko, Y.4
Inoue, M.5
Komoto, Y.6
Okada, A.7
Ohishi, S.8
Nabetani, A.9
Morisaki, H.10
Nakayama, M.11
Niikawa, N.12
Mukai, T.13
-
26
-
-
0025738681
-
Uniparental paternal disomy in a genetic cancer-predisposing syndrome
-
Henry I, Bonaïti-Pellié 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
Bonaïti-Pellié, C.2
Chehensse, V.3
Beldjord, C.4
Schwartz, C.5
Utermann, G.6
Junien, C.7
-
27
-
-
13344278697
-
Multiple genetic loci within 11p15 defined by Beckwith-Wiedem ann syndrome rearrangement breakpoints and subchromosomal transferable fragments
-
Hoovers JMN, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillon-Miller P, Schlessinger D, Edwards MC, Elledge SJ, Ivens A, Westerveld A, Little P, Mannenes M, Feinberg AP (1995): Multiple genetic loci within 11p15 defined by Beckwith-Wiedem ann 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
Steenman, M.8
Benedict, M.9
Wiegant, J.10
Lengauer, C.11
Taillon-Miller, P.12
Schlessinger, D.13
Edwards, M.C.14
Elledge, S.J.15
Ivens, A.16
Westerveld, A.17
Little, P.18
Mannenes, M.19
Feinberg, A.P.20
more..
-
28
-
-
0023803361
-
Lack of linkage of familial Wilms' tumour to chromosomal band 11p13
-
Huff V, Compton DA, Chao L-Y, Strong LC, Geiser CF, Saunders GF (1988): Lack of linkage of familial Wilms' tumour to chromosomal band 11p13. Nature 336:377-378.
-
(1988)
Nature
, vol.336
, pp. 377-378
-
-
Huff, V.1
Compton, D.A.2
Chao, L.-Y.3
Strong, L.C.4
Geiser, C.F.5
Saunders, G.F.6
-
29
-
-
3342921509
-
Alteration of the WT1 gene in patients with Wilms' tumor and genitourinary anomalies
-
Huff V, Villalba F, Riccardi VM, Strong LC, Saunders GF (1991a): Alteration of the WT1 gene in patients with Wilms' tumor and genitourinary anomalies. Amer J Hum Genet 49:44.
-
(1991)
Amer J Hum Genet
, vol.49
, pp. 44
-
-
Huff, V.1
Villalba, F.2
Riccardi, V.M.3
Strong, L.C.4
Saunders, G.F.5
-
30
-
-
0025828557
-
Evidence for WT1 as a Wilms tumor (WT) gene: Intragenic germinal deletion in bilateral WT
-
Huff V, Miwa H, Haber DA, Call KM, Housman D, Strong LC, Saunders GF (1991b): Evidence for WT1 as a Wilms tumor (WT) gene: Intragenic germinal deletion in bilateral WT. Am J Hum Genet 48:997-1003.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 997-1003
-
-
Huff, V.1
Miwa, H.2
Haber, D.A.3
Call, K.M.4
Housman, D.5
Strong, L.C.6
Saunders, G.F.7
-
31
-
-
0026457965
-
Nonlinkage of 16q markers to familial predisposition to Wilms' tumor
-
Huff V, Reeve AE, Leppert M, Strong LC, Douglass EC, Geiser DF, Li FP, Meadows A, Callen DF, Lenoir G, Saunders GF (1992): Nonlinkage of 16q markers to familial predisposition to Wilms' tumor. Cancer Res 52:6117-6120.
-
(1992)
Cancer Res
, vol.52
, pp. 6117-6120
-
-
Huff, V.1
Reeve, A.E.2
Leppert, M.3
Strong, L.C.4
Douglass, E.C.5
Geiser, D.F.6
Li, F.P.7
Meadows, A.8
Callen, D.F.9
Lenoir, G.10
Saunders, G.F.11
-
32
-
-
0028979148
-
WT1 exon 1 deletion/insertion mutations in Wilms tumor patients associated with di- and trinucleotide repeats and deletion hotspot consensus sequences
-
Huff V, Jaffe N, Saunders GF, Strong LC, Villalba F, Ruteshouser EC (1995): WT1 exon 1 deletion/insertion mutations in Wilms tumor patients associated with di- and trinucleotide repeats and deletion hotspot consensus sequences. Amer J Hum Genet 56:84-90.
-
(1995)
Amer J Hum Genet
, vol.56
, pp. 84-90
-
-
Huff, V.1
Jaffe, N.2
Saunders, G.F.3
Strong, L.C.4
Villalba, F.5
Ruteshouser, E.C.6
-
33
-
-
0030940740
-
Evidence for genetic heterogeneity in familial Wilms tumor
-
Huff V, Amos CI, Douglass ED, Fisher R, Geiser CF, Krill CE, Li FP, Strong LC, McDonald JM (1997): Evidence for genetic heterogeneity in familial Wilms tumor. Cancer Res 57:1859-1862.
-
(1997)
Cancer Res
, vol.57
, pp. 1859-1862
-
-
Huff, V.1
Amos, C.I.2
Douglass, E.D.3
Fisher, R.4
Geiser, C.F.5
Krill, C.E.6
Li, F.P.7
Strong, L.C.8
McDonald, J.M.9
-
34
-
-
2742565105
-
Simpson-Golabi-Behmel syndrome: Genotypc/phenotype analysis of 18 affected males from 7 unrelated families
-
Hughes-Benzie RM, Pilia F, Xuan JY, Hunter AGW, Chen E, Golabi M, Hurst JA, Kobori J, Marymee K, Pagon RA, Punnett HH, Schelley S, Tolmie JL, Wohlferd MM, Grossman T, Schlessinger D, MacKenzie AE (1996): Simpson-Golabi-Behmel syndrome: genotypc/phenotype analysis of 18 affected males from 7 unrelated families. Amer J Med Genet 66:227-234.
-
(1996)
Amer J Med Genet
, vol.66
, pp. 227-234
-
-
Hughes-Benzie, R.M.1
Pilia, F.2
Xuan, J.Y.3
Hunter, A.G.W.4
Chen, E.5
Golabi, M.6
Hurst, J.A.7
Kobori, J.8
Marymee, K.9
Pagon, R.A.10
Punnett, H.H.11
Schelley, S.12
Tolmie, J.L.13
Wohlferd, M.M.14
Grossman, T.15
Schlessinger, D.16
MacKenzie, A.E.17
-
35
-
-
0028376125
-
Familial primary hyperparathyroidism complicated with Wilms' tumor
-
Kakinuma A, Morimoto I, Nakano Y, Fujimoto R, Ishida O, Okada Y, Inokuchi N, Fujihira T, Eto S (1994): Familial primary hyperparathyroidism complicated with Wilms' tumor. Intern Med 33:123-126.
-
(1994)
Intern Med
, vol.33
, pp. 123-126
-
-
Kakinuma, A.1
Morimoto, I.2
Nakano, Y.3
Fujimoto, R.4
Ishida, O.5
Okada, Y.6
Inokuchi, N.7
Fujihira, T.8
Eto, S.9
-
36
-
-
0026341035
-
Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors
-
Kaneko Y, Homma C, Maseki N, Sakurai M, Hata J (1991): Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors. Cancer Res 51:5937-5942.
-
(1991)
Cancer Res
, vol.51
, pp. 5937-5942
-
-
Kaneko, Y.1
Homma, C.2
Maseki, N.3
Sakurai, M.4
Hata, J.5
-
37
-
-
0015295131
-
Mutation and cancer: A model for Wilms' tumor of the kidney
-
Knudson AG, Strong LC (1972): Mutation and cancer: a model for Wilms' tumor of the kidney. J Natl Cancer Instit 48:313-324.
-
(1972)
J Natl Cancer Instit
, vol.48
, pp. 313-324
-
-
Knudson, A.G.1
Strong, L.C.2
-
38
-
-
0021752191
-
Chromosome abnormalities in tumor cells from patients with sporadic Wilms' tumor
-
Kondo K, Chilcote RR, Maurer HS, Rowley JD (1984): Chromosome abnormalities in tumor cells from patients with sporadic Wilms' tumor. Cancer Res 44:5376-5381.
-
(1984)
Cancer Res
, vol.44
, pp. 5376-5381
-
-
Kondo, K.1
Chilcote, R.R.2
Maurer, H.S.3
Rowley, J.D.4
-
39
-
-
0021327569
-
Loss of alleles at loci on human chromosome II during genesis of Wilms' tumour
-
Koufos A, Hansen MF, Lampkin BC, Workman ML, Copeland NG, Jenkins NA, Cavenee WK (1984): Loss of alleles at loci on human chromosome II during genesis of Wilms' tumour. Nature 309:170-172.
-
(1984)
Nature
, vol.309
, pp. 170-172
-
-
Koufos, A.1
Hansen, M.F.2
Lampkin, B.C.3
Workman, M.L.4
Copeland, N.G.5
Jenkins, N.A.6
Cavenee, W.K.7
-
40
-
-
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, Cavenee WK (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
Cavenee, W.K.8
-
41
-
-
0025831010
-
The human ASM (adult skeletal muscle) gene: Expression and chromosomal assignment to 11p15
-
Leibovitch MP, Nguyen VC, Gross MS, Solhonne B, Leibovitch SA, Bernheim A (1991): The human ASM (adult skeletal muscle) gene: expression and chromosomal assignment to 11p15. Biochem Biophys Res Commun 180:1241-1250.
-
(1991)
Biochem Biophys Res Commun
, vol.180
, pp. 1241-1250
-
-
Leibovitch, M.P.1
Nguyen, V.C.2
Gross, M.S.3
Solhonne, B.4
Leibovitch, S.A.5
Bernheim, A.6
-
42
-
-
0029024277
-
Disruption of imprinting caused by deletion of the H19 gene region in mice
-
Leighton PA, Ingram RS, Eggenschwiler J, Efstratiadia 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
Efstratiadia, A.4
Tilghman, S.M.5
-
43
-
-
0029122489
-
Expression, promoter usage and parental imprinting status of insulin-like growth factor II (IGF2) in human hepatoblastoma: Uncoupling of IGF2 and H19 imprinting
-
Li X, Adam G, Cui H, Sandstedt B, Ohlsson R, Ekstrom TJ (1995): Expression, promoter usage and parental imprinting status of insulin-like growth factor II (IGF2) in human hepatoblastoma: uncoupling of IGF2 and H19 imprinting. Oncogene 11:221-229.
-
(1995)
Oncogene
, vol.11
, pp. 221-229
-
-
Li, X.1
Adam, G.2
Cui, H.3
Sandstedt, B.4
Ohlsson, R.5
Ekstrom, T.J.6
-
44
-
-
0026539536
-
Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours
-
Little MH, Dunn R, Byrne JA, Seawright A, Smith PJ, Pritchard-Jones K, van Heyningen V, Hastie ND (1992): Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours. Oncogene 7:635-641.
-
(1992)
Oncogene
, vol.7
, pp. 635-641
-
-
Little, M.H.1
Dunn, R.2
Byrne, J.A.3
Seawright, A.4
Smith, P.J.5
Pritchard-Jones, K.6
Van Heyningen, V.7
Hastie, N.D.8
-
45
-
-
0026006382
-
Transcriptional repression mediated by the WT1 Wilms tumor gene product
-
Madden SL, Cook DM, Morris JF, Gashier A, Sukhatme VP, Rauscher FJ III (1991): Transcriptional repression mediated by the WT1 Wilms tumor gene product. Science 253:1550-1553.
-
(1991)
Science
, vol.253
, pp. 1550-1553
-
-
Madden, S.L.1
Cook, D.M.2
Morris, J.F.3
Gashier, A.4
Sukhatme, V.P.5
Rauscher III, F.J.6
-
46
-
-
0025362975
-
Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11
-
Mannens M, Devilee P, Biliek J, Mandjes I, de Kraker J, Heyting C, Slater RM, Westerveld A (1990): Loss of heterozygosity in Wilms' tumors, studied for six putative tumor suppressor regions, is limited to chromosome 11. Cancer Res 50:3279-3283.
-
(1990)
Cancer Res
, vol.50
, pp. 3279-3283
-
-
Mannens, M.1
Devilee, P.2
Biliek, J.3
Mandjes, I.4
De Kraker, J.5
Heyting, C.6
Slater, R.M.7
Westerveld, A.8
-
47
-
-
0019497899
-
Genetics of Wilms' tumor
-
Matsunaga E (1981): Genetics of Wilms' tumor. Hum Genet 57:231-246.
-
(1981)
Hum Genet
, vol.57
, pp. 231-246
-
-
Matsunaga, E.1
-
48
-
-
0028988159
-
CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene
-
CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene. Genes Devel 9:650-662.
-
(1995)
Genes Devel
, 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
Elledge, S.J.8
-
49
-
-
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
Elledge, S.J.8
Feinberg, A.P.9
-
50
-
-
0026691721
-
A third Wilms' tumor locus on chromosome 16q
-
Maw M, Grundy PE, Millow LJ, Eccels MR, Dunn RS, Smith PJ, Feinberg AP, Law DJ, Paterson MC, Telzerow PE, Callen DF, Thompson AD, Richards RI, Reeve AE (1992): A third Wilms' tumor locus on chromosome 16q. Cancer Res 52:3094-3098.
-
(1992)
Cancer Res
, vol.52
, pp. 3094-3098
-
-
Maw, M.1
Grundy, P.E.2
Millow, L.J.3
Eccels, M.R.4
Dunn, R.S.5
Smith, P.J.6
Feinberg, A.P.7
Law, D.J.8
Paterson, M.C.9
Telzerow, P.E.10
Callen, D.F.11
Thompson, A.D.12
Richards, R.I.13
Reeve, A.E.14
-
51
-
-
0026585964
-
RNA expression of the WT1 gene in Wilms' tumors in relation to histopathology
-
Miwa H, Tomlinson GE, Timmons CS, Huff V, Cohn SL, Strong LC, Saunders GF (1992): RNA expression of the WT1 gene in Wilms' tumors in relation to histopathology. J Natl Cancer Inst 84:181-187.
-
(1992)
J Natl Cancer Inst
, vol.84
, pp. 181-187
-
-
Miwa, H.1
Tomlinson, G.E.2
Timmons, C.S.3
Huff, V.4
Cohn, S.L.5
Strong, L.C.6
Saunders, G.F.7
-
52
-
-
0030297969
-
Mapping of a putative tumor suppressor locus to proximal 7p in Wilms tumors
-
Miozzo M, Perotti D, Minoletti F, Mondini P, Pilotti S, Luksch R, Fassati-Bellani F, Pierotti MA, Sozzi F, Radice P (1996): Mapping of a putative tumor suppressor locus to proximal 7p in Wilms tumors. Genomics 37:310-315.
-
(1996)
Genomics
, vol.37
, pp. 310-315
-
-
Miozzo, M.1
Perotti, D.2
Minoletti, F.3
Mondini, P.4
Pilotti, S.5
Luksch, R.6
Fassati-Bellani, F.7
Pierotti, M.A.8
Sozzi, F.9
Radice, P.10
-
53
-
-
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, Wiess L, McMorrow L, Loew T, Kraus W, Gerald W, Tycko B (1994): Epigenetic lesions at the H19 locus in Wilms' tumour patients. Nature Genet 7:440-447.
-
(1994)
Nature 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
Wiess, L.8
McMorrow, L.9
Loew, T.10
Kraus, W.11
Gerald, W.12
Tycko, B.13
-
54
-
-
0027285258
-
Relaxation of insulin-like growth factor II gene impriting implicated in Wilms' tumor
-
Ogawa O, Eccles MR, Szeto J, McNoe LA, Yun K, Maw MA, Smith PJ, Reeve AE (1993): Relaxation of insulin-like growth factor II gene impriting implicated in Wilms' tumor. Nature 362:749-751.
-
(1993)
Nature
, vol.362
, pp. 749-751
-
-
Ogawa, O.1
Eccles, M.R.2
Szeto, J.3
McNoe, L.A.4
Yun, K.5
Maw, M.A.6
Smith, P.J.7
Reeve, A.E.8
-
55
-
-
0028918615
-
Non-lip constitutional chromosome abnormalities in Wilms' tumor patients
-
Oison JM, Hamlton A, Breslow NE (1995): Non-lip constitutional chromosome abnormalities in Wilms' tumor patients. Medical Fed Oncol 24:305-309.
-
(1995)
Medical Fed Oncol
, vol.24
, pp. 305-309
-
-
Oison, J.M.1
Hamlton, A.2
Breslow, N.E.3
-
56
-
-
0021343902
-
Development of homozygosity of chromosome lip markers in Wilms' tumour
-
Orkin SH, Goldman DS, Sallan SE (1984): Development of homozygosity of chromosome lip markers in Wilms' tumour. Nature 309:172-174.
-
(1984)
Nature
, vol.309
, pp. 172-174
-
-
Orkin, S.H.1
Goldman, D.S.2
Sallan, S.E.3
-
57
-
-
0023730194
-
Differential expression of the human insulin-like growth factor II gene. Characterization of the IGF-II mRNAs and an mRNA encoding a putative IGF-II-associated protein
-
de Pagter-Holthuizen P, Jansen M, van der Kammen RA, van Schaik FMA, Sussenbach JS (1988): Differential expression of the human insulin-like growth factor II gene. Characterization of the IGF-II mRNAs and an mRNA encoding a putative IGF-II-associated protein. Biochim Biophys Acta 950:282-295.
-
(1988)
Biochim Biophys Acta
, vol.950
, pp. 282-295
-
-
De Pagter-Holthuizen, P.1
Jansen, M.2
Van Der Kammen, R.A.3
Van Schaik, F.M.A.4
Sussenbach, J.S.5
-
58
-
-
0026094584
-
Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
-
Pelletier J, Bruening W, Kashtan CD, Mauer SM, Manivel JC, Striegel JE, Houghton DC, Junien C, Habib R, Fouser L, Fine RN, Silverman BL, Haber DA, Housman DE (1991): Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome. Cell 67:437-447.
-
(1991)
Cell
, vol.67
, pp. 437-447
-
-
Pelletier, J.1
Bruening, W.2
Kashtan, C.D.3
Mauer, S.M.4
Manivel, J.C.5
Striegel, J.E.6
Houghton, D.C.7
Junien, C.8
Habib, R.9
Fouser, L.10
Fine, R.N.11
Silverman, B.L.12
Haber, D.A.13
Housman, D.E.14
-
59
-
-
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
-
60
-
-
0026732759
-
Parental imprinting of the human H19 gene
-
Rachmilewitz J, Goshen R, Ariel I, Schneider T, de Groot N, Hochberg A (1992): Parental imprinting of the human H19 gene. FEBS Letters 309:25-28.
-
(1992)
FEBS Letters
, vol.309
, pp. 25-28
-
-
Rachmilewitz, J.1
Goshen, R.2
Ariel, I.3
Schneider, T.4
De Groot, N.5
Hochberg, A.6
-
61
-
-
0030017174
-
Evidence for a familial Wilms' tumor gene (FWT1) on chromosome 17q12-q21
-
Rahman N, Arbour L, Tonin P, Renshaw J, Pelletier J, Baruchel S, Pritchard-Jones K, Stratton MR, Narod SA (1996): Evidence for a familial Wilms' tumor gene (FWT1) on chromosome 17q12-q21. Nat Genet 13:461-462.
-
(1996)
Nat Genet
, vol.13
, pp. 461-462
-
-
Rahman, N.1
Arbour, L.2
Tonin, P.3
Renshaw, J.4
Pelletier, J.5
Baruchel, S.6
Pritchard-Jones, K.7
Stratton, M.R.8
Narod, S.A.9
-
62
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier S, Johnsone 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
Johnsone, L.2
Dobry, C.J.3
Ping, A.J.4
Grundy, P.E.5
Feinberg, A.P.6
-
63
-
-
0025605969
-
Binding of the Wilms' tumor locus zinc finger protein to the EGR-1 consensus sequence
-
Rauscher FJ III, Morris JF, Tournay OE, Cook DM, Curran T (1990): Binding of the Wilms' tumor locus zinc finger protein to the EGR-1 consensus sequence. Science 250:1259-1262.
-
(1990)
Science
, vol.250
, pp. 1259-1262
-
-
Rauscher III, F.J.1
Morris, J.F.2
Tournay, O.E.3
Cook, D.M.4
Curran, T.5
-
64
-
-
0021338485
-
Loss oa a Harvey ras allele in sporadic Wilms' tumour
-
Reeve AE, Housiaux PJ, Gardner RJM, Chewings WE, Grindley RM, Millow LJ (1984): Loss oa a Harvey ras allele in sporadic Wilms' tumour. Nature 309:174-176.
-
(1984)
Nature
, vol.309
, pp. 174-176
-
-
Reeve, A.E.1
Housiaux, P.J.2
Gardner, R.J.M.3
Chewings, W.E.4
Grindley, R.M.5
Millow, L.J.6
-
65
-
-
0017883401
-
Chromosomal imbalance in the aniridia-Wilms' tumor association: Lip interstitial deletion
-
Riccardi VM, Sujansky E, Smith AC, Francke U (1978): Chromosomal imbalance in the aniridia-Wilms' tumor association: lip interstitial deletion. Pediatrics 61:604-610.
-
(1978)
Pediatrics
, vol.61
, pp. 604-610
-
-
Riccardi, V.M.1
Sujansky, E.2
Smith, A.C.3
Francke, U.4
-
66
-
-
33749236339
-
Autosomal dominant inheritance of Wilms' tumor and brachial cleft anomalies. A new syndrome
-
Schimmenti LA, Cich JA, Gorlin RJ, Berry SA (1993): Autosomal dominant inheritance of Wilms' tumor and brachial cleft anomalies. A new syndrome. Amer J Hum Genet 53:503.
-
(1993)
Amer J Hum Genet
, vol.53
, pp. 503
-
-
Schimmenti, L.A.1
Cich, J.A.2
Gorlin, R.J.3
Berry, S.A.4
-
67
-
-
0023256838
-
Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors
-
Schroeder WT, Chao L-Y, Dao DD, Strong LC, Pathak S, Riccardi V, Lewis WH, Saunders GF (1987): Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors. Am J Hum Genet 40:413-420.
-
(1987)
Am J Hum Genet
, vol.40
, pp. 413-420
-
-
Schroeder, W.T.1
Chao, L.-Y.2
Dao, D.D.3
Strong, L.C.4
Pathak, S.5
Riccardi, V.6
Lewis, W.H.7
Saunders, G.F.8
-
68
-
-
0028354829
-
RNA editing in the Wilms' tumor susceptibility gene, WT1
-
Sharma PM, Bowman M, Madden SL, Rauscher FJ III, Sukumar S (1994): RNA editing in the Wilms' tumor susceptibility gene, WT1. Genes Devel 8:720-731.
-
(1994)
Genes Devel
, vol.8
, pp. 720-731
-
-
Sharma, P.M.1
Bowman, M.2
Madden, S.L.3
Rauscher III, F.J.4
Sukumar, S.5
-
69
-
-
0022559675
-
The cytogenetics of Wilms' tumor
-
Slater RM (1986): The cytogenetics of Wilms' tumor. Cancer Genet Cytogenet 19:37-41.
-
(1986)
Cancer Genet Cytogenet
, vol.19
, pp. 37-41
-
-
Slater, R.M.1
-
71
-
-
0018835921
-
Complete and incomplete forms of Beckwith-Wiedemann syndrome: Their oncogenic potential
-
Sotelo-Avila C, Gonzalez-Crussi F, Fowley JW (1980): Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential. J Pediatr 96:47-50.
-
(1980)
J Pediatr
, vol.96
, pp. 47-50
-
-
Sotelo-Avila, C.1
Gonzalez-Crussi, F.2
Fowley, J.W.3
-
72
-
-
0017393712
-
The relationship between nephroblastoma and neurofibromatosis (Von recklinghausen's disease)
-
Stay EJ, Vawter G (1977): The relationship between nephroblastoma and neurofibromatosis (Von recklinghausen's disease). Cancer 39:2550-2555.
-
(1977)
Cancer
, vol.39
, pp. 2550-2555
-
-
Stay, E.J.1
Vawter, G.2
-
73
-
-
0030841547
-
Comparative genomic hybridization analysis of Wilms tumors
-
Steenman M, Redeker B, de Meulemeester M, Wiesmeijer K, Voute PA, Westerveld A, Slater R, Mannens M (1997): Comparative genomic hybridization analysis of Wilms tumors. Cytogenet Cell Genet 77:296-303.
-
(1997)
Cytogenet Cell Genet
, vol.77
, pp. 296-303
-
-
Steenman, M.1
Redeker, B.2
De Meulemeester, M.3
Wiesmeijer, K.4
Voute, P.A.5
Westerveld, A.6
Slater, R.7
Mannens, M.8
-
74
-
-
0028958106
-
The hereditary hyperparathyroidism-jaw tumor syndrome: A new endocrine tumor gene mapping to chromosome 1q21-q31
-
Szabo J, Heath B, Hill VM, Jackson CE, Zarbo RJ, Mallette LE, Chew SL, Besser GM, Thakker RV, Huff V, Leppert MF, Health H (1995): The hereditary hyperparathyroidism-jaw tumor syndrome: a new endocrine tumor gene mapping to chromosome 1q21-q31. Amer J Hum Genet 56:944-950.
-
(1995)
Amer J Hum Genet
, vol.56
, pp. 944-950
-
-
Szabo, J.1
Heath, B.2
Hill, V.M.3
Jackson, C.E.4
Zarbo, R.J.5
Mallette, L.E.6
Chew, S.L.7
Besser, G.M.8
Thakker, R.V.9
Huff, V.10
Leppert, M.F.11
Health, H.12
-
76
-
-
0025796858
-
Smallest region of overlap in Wilms' tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus
-
Ton CCT, Huff V, Call KM, Cohn S, Strong LC, Housman DE, Saunders GF (1991): Smallest region of overlap in Wilms' tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus. Genomics 10:293-297.
-
(1991)
Genomics
, vol.10
, pp. 293-297
-
-
Ton, C.C.T.1
Huff, V.2
Call, K.M.3
Cohn, S.4
Strong, L.C.5
Housman, D.E.6
Saunders, G.F.7
-
77
-
-
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
-
78
-
-
0030479119
-
IGF2 but not H19 shows loss of imprinting in human glioma
-
Uyeno S, Acki Y, Nata M, Sagisaka K, Kayama T, Yoshimoto T, Ono T (1996): IGF2 but not H19 shows loss of imprinting in human glioma. Cancer Res 56:5356-5359.
-
(1996)
Cancer Res
, vol.56
, pp. 5356-5359
-
-
Uyeno, S.1
Acki, Y.2
Nata, M.3
Sagisaka, K.4
Kayama, T.5
Yoshimoto, T.6
Ono, T.7
-
79
-
-
0028298044
-
Fine structure analysis of the WT1 gene in sporadic Wilms tumors
-
Varanasi R, Bardeesy N, Ghahremani M, Petruzzi M-J, Nowak N, Adam MA, Grundy P, Shows TB, Pelletier J (1994): Fine structure analysis of the WT1 gene in sporadic Wilms tumors. Proc Natl Acad Sci USA 91:3554-3558.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 3554-3558
-
-
Varanasi, R.1
Bardeesy, N.2
Ghahremani, M.3
Petruzzi, M.-J.4
Nowak, N.5
Adam, M.A.6
Grundy, P.7
Shows, T.B.8
Pelletier, J.9
-
80
-
-
0027945263
-
Promoter-specific imprinting of the human insulin-like growth factor-II gene
-
Vu TH, Hoffman AR (1994): Promoter-specific imprinting of the human insulin-like growth factor-II gene. Nature 371:714-717.
-
(1994)
Nature
, vol.371
, pp. 714-717
-
-
Vu, T.H.1
Hoffman, A.R.2
-
81
-
-
0025318971
-
Chromosome analysis of 31 wilms' tumors
-
Wang-Wuu S, Soukup S, Bove K, Gotwals B, Lampkin B (1990): Chromosome analysis of 31 wilms' tumors. Cancer Res 50:2786-2793.
-
(1990)
Cancer Res
, vol.50
, pp. 2786-2793
-
-
Wang-Wuu, S.1
Soukup, S.2
Bove, K.3
Gotwals, B.4
Lampkin, B.5
-
82
-
-
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. Nature Genet 5:143-150.
-
(1993)
Nature Genet
, vol.5
, pp. 143-150
-
-
Weksberg, R.1
Shen, D.R.2
Fei, Y.L.3
Song, Q.L.4
Squire, J.5
-
83
-
-
76549164702
-
Complexe malformatif familial avec hernie ombilicale et marcroglossie - Un "syndrome nouveau"?
-
Wiedemann HR (1964): Complexe malformatif familial avec hernie ombilicale et marcroglossie - un "syndrome nouveau"? J Génét Hum 13:223-232.
-
(1964)
J Génét Hum
, vol.13
, pp. 223-232
-
-
Wiedemann, H.R.1
-
84
-
-
34250134720
-
Tumors and hemihypertrophy associated with Wiedemann-Beckwith syndrome
-
Wiedemann HR (1983): Tumors and hemihypertrophy associated with Wiedemann-Beckwith syndrome. Eur J Pediatr 141:129.
-
(1983)
Eur J Pediatr
, vol.141
, pp. 129
-
-
Wiedemann, H.R.1
-
86
-
-
0026849544
-
Monoallelic expression of the human H19 gene
-
Zhang Y, Tycko B (1992): Monoallelic expression of the human H19 gene. Nature Genet 1:40-44.
-
(1992)
Nature Genet
, vol.1
, pp. 40-44
-
-
Zhang, Y.1
Tycko, B.2
|