-
1
-
-
0029765587
-
Identification of novel regions of deletion in familial Wilms' tumor by comparative genomic hybridization
-
Altura RA, Valentine M, Li H, Boyett JM, Shearer P, Grundy P, Shapiro DN, Look AT: Identification of novel regions of deletion in familial Wilms' tumor by comparative genomic hybridization. Cancer Res 56:3837-3841 (1996).
-
(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
-
-
0028839369
-
Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis
-
Austruy E, Candon S, Henry I, Gyapay G, Tournade MF, Mannens M, Callen D, Junien C, Jeanpierre C: Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis. Genes Chrom Cancer 14:285-294 (1995).
-
(1995)
Genes Chrom Cancer
, vol.14
, pp. 285-294
-
-
Austruy, E.1
Candon, S.2
Henry, I.3
Gyapay, G.4
Tournade, M.F.5
Mannens, M.6
Callen, D.7
Junien, C.8
Jeanpierre, C.9
-
3
-
-
0025271523
-
Nephrogenic rests, nephroblastomatosis and the pathogenesis of Wilms' tumour
-
Beckwith JB, Kiviat NB, Bonadio JF: Nephrogenic rests, nephroblastomatosis and the pathogenesis of Wilms' tumour. Pediat Path 10:1-36 (1990).
-
(1990)
Pediat Path
, vol.10
, pp. 1-36
-
-
Beckwith, J.B.1
Kiviat, N.B.2
Bonadio, J.F.3
-
4
-
-
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: Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell 60:509-520 (1990).
-
(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
-
5
-
-
0026685962
-
Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination
-
Coppes MJ, Bonetta L, Huang A, Hoban P, Chilton-MacNeill S, Campbell CE, Weksberg R, Yeger H, Reeve AE, Williams BR: Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination. Genes Chrom Cancer 5:326-334 (1992).
-
(1992)
Genes Chrom Cancer
, vol.5
, pp. 326-334
-
-
Coppes, M.J.1
Bonetta, L.2
Huang, A.3
Hoban, P.4
Chilton-MacNeill, S.5
Campbell, C.E.6
Weksberg, R.7
Yeger, H.8
Reeve, A.E.9
Williams, B.R.10
-
6
-
-
0343262987
-
Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor
-
Dao DD, Schroeder WT, Chao LY, Kikuchi H, Strong LC, Riccardi VM, Pathak S, Nichols WW, Lewis WH, Saunders GF: Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor. Hum Genet 81(1):41-48 (1987).
-
(1987)
Hum Genet
, vol.81
, Issue.1
, pp. 41-48
-
-
Dao, D.D.1
Schroeder, W.T.2
Chao, L.Y.3
Kikuchi, H.4
Strong, L.C.5
Riccardi, V.M.6
Pathak, S.7
Nichols, W.W.8
Lewis, W.H.9
Saunders, G.F.10
-
8
-
-
0026507601
-
Dinucleotide repeat polymorphism at the human hemoglobin alpha-1 pseudo-gene (HBAP1)
-
Fougerousse F, Meloni R, Roudant C, Beckmann JS: Dinucleotide repeat polymorphism at the human hemoglobin alpha-1 pseudo-gene (HBAP1). Nucl Acids Res 20:1165 (1992).
-
(1992)
Nucl Acids Res
, vol.20
, pp. 1165
-
-
Fougerousse, F.1
Meloni, R.2
Roudant, C.3
Beckmann, J.S.4
-
9
-
-
0025098654
-
Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping
-
Gessler M, Poustka A, Cavenee W, Neve RL, Orkin SH, Bruns GAP: Homozygous deletion in Wilms' tumours of a zinc-finger gene identified by chromosome jumping. Nature 343:774-778 (1990).
-
(1990)
Nature
, vol.343
, pp. 774-778
-
-
Gessler, M.1
Poustka, A.2
Cavenee, W.3
Neve, R.L.4
Orkin, S.H.5
Bruns, G.A.P.6
-
10
-
-
0027158855
-
Parental genomic imprinting of the human IGF2 gene
-
Giannoukakis N, Deal C, Paquette J, Goodyer CG, Polychronakos C: Parental genomic imprinting of the human IGF2 gene. Nature Genet 4:98-101 (1993).
-
(1993)
Nature Genet
, vol.4
, pp. 98-101
-
-
Giannoukakis, N.1
Deal, C.2
Paquette, J.3
Goodyer, C.G.4
Polychronakos, C.5
-
11
-
-
0028351728
-
Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome
-
Grundy PE, Telzerow PE, Breslow N, Moksness J, Huff V, Paterson MC: Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome. Cancer Res 54:2331-2333 (1994).
-
(1994)
Cancer Res
, vol.54
, pp. 2331-2333
-
-
Grundy, P.E.1
Telzerow, P.E.2
Breslow, N.3
Moksness, J.4
Huff, V.5
Paterson, M.C.6
-
12
-
-
0023155425
-
Insulin-like growth factor II in human adrenal pheochromocytomas and Wilms tumors: Expression at the mRNA and protein level
-
USA
-
Haselbacher GK, Irminger JC, Zapf J, Ziegler WH, Humbel RE: Insulin-like growth factor II in human adrenal pheochromocytomas and Wilms tumors: expression at the mRNA and protein level. Proc natl Acad Sci, USA 84:1104-1106 (1987).
-
(1987)
Proc Natl Acad Sci
, vol.84
, pp. 1104-1106
-
-
Haselbacher, G.K.1
Irminger, J.C.2
Zapf, J.3
Ziegler, W.H.4
Humbel, R.E.5
-
13
-
-
0021940355
-
Nephroblastomatosis and Wilms' tumor
-
Heidemann RL, Haase GM, Foley CL, Wilson HL, Bailey WC: Nephroblastomatosis and Wilms' tumor. Cancer 55:1446-1451 (1985).
-
(1985)
Cancer
, vol.55
, pp. 1446-1451
-
-
Heidemann, R.L.1
Haase, G.M.2
Foley, C.L.3
Wilson, H.L.4
Bailey, W.C.5
-
14
-
-
0025832872
-
Wilms' tumour and a de novo (1;7) translocation in a child with bilateral radial aplasia
-
Hewitt M, Lunt PW, Oakhill A: Wilms' tumour and a de novo (1;7) translocation in a child with bilateral radial aplasia. J Med Genet 28:411-412 (1991).
-
(1991)
J Med Genet
, vol.28
, pp. 411-412
-
-
Hewitt, M.1
Lunt, P.W.2
Oakhill, A.3
-
15
-
-
4143109093
-
Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome
-
USA
-
van Heyningen V, Boyd PA, Seawright A, Fletcher JM, Fantes JA, Buckton KE, Spowart G, Porteous DJ, Hill RE, Newton MS, Hastie ND: Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome. Proc natl Acad Sci, USA 82:8592-8596 (1985).
-
(1985)
Proc Natl Acad Sci
, vol.82
, pp. 8592-8596
-
-
Van Heyningen, V.1
Boyd, P.A.2
Seawright, A.3
Fletcher, J.M.4
Fantes, J.A.5
Buckton, K.E.6
Spowart, G.7
Porteous, D.J.8
Hill, R.E.9
Newton, M.S.10
Hastie, N.D.11
-
16
-
-
0024542957
-
Structural alteration of the insulin-like growth factor II-gene in Wilms tumour
-
Irminger JC, Schoenle EJ, Briner J, Humbel RE: Structural alteration of the insulin-like growth factor II-gene in Wilms tumour. Eur J Pediat 148:620-623 (1989).
-
(1989)
Eur J Pediat
, vol.148
, pp. 620-623
-
-
Irminger, J.C.1
Schoenle, E.J.2
Briner, J.3
Humbel, R.E.4
-
17
-
-
0023868393
-
Spontaneous mutation rates to new length alleles at tandem repetitive hypervariable loci in human DNA
-
Jeffreys AJ, Royle NJ, Wilson V, Wong Z: Spontaneous mutation rates to new length alleles at tandem repetitive hypervariable loci in human DNA. Nature 332:278-281 (1988).
-
(1988)
Nature
, vol.332
, pp. 278-281
-
-
Jeffreys, A.J.1
Royle, N.J.2
Wilson, V.3
Wong, Z.4
-
18
-
-
0026849704
-
CEB15 detects a VNTR locus (net: 92%) on chromosome 1p
-
Lauthier V, Mariat D, Vergnaud G: CEB15 detects a VNTR locus (net: 92%) on chromosome 1p. Hum molec Genet 1:63 (1992).
-
(1992)
Hum Molec Genet
, vol.1
, pp. 63
-
-
Lauthier, V.1
Mariat, D.2
Vergnaud, G.3
-
19
-
-
0024212964
-
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours
-
Mannens M, Slater RM, Heyting C, Bliek J, de Kraker J, Coad N, de Pagter-Holthuizen P, Pearson PL: Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours. Hum Genet 81:41-48 (1988).
-
(1988)
Hum Genet
, vol.81
, pp. 41-48
-
-
Mannens, M.1
Slater, R.M.2
Heyting, C.3
Bliek, J.4
De Kraker, J.5
Coad, N.6
De Pagter-Holthuizen, P.7
Pearson, P.L.8
-
20
-
-
0025362975
-
Loss of heterozygosity in Wilms' tumours, studied for 6 putative tumour suppressor regions, is limited to chromosome 11
-
Mannens M, Devilee P, Bliek J, Mandjes I, de Kraker J, Heyting C, Slater RM, Westerveld A: Loss of heterozygosity in Wilms' tumours, studied for 6 putative tumour suppressor regions, is limited to chromosome 11. Cancer Res 50:3279-3283 (1990).
-
(1990)
Cancer Res
, vol.50
, pp. 3279-3283
-
-
Mannens, M.1
Devilee, P.2
Bliek, J.3
Mandjes, I.4
De Kraker, J.5
Heyting, C.6
Slater, R.M.7
Westerveld, A.8
-
21
-
-
0026691721
-
A third Wilms' tumor locus on chromosome 16q
-
Maw MA, Grundy PE, Millow LJ, Eccles MR, Dunn RS, Smith PJ, Feinberg AP, Law DJ, Paterson MC, Telzerow PE, Callen DF, Thompson AD, Richards RI, Reeve AE: A third Wilms' tumor locus on chromosome 16q. Cancer Res 52:3094-3098 (1992).
-
(1992)
Cancer Res
, vol.52
, pp. 3094-3098
-
-
Maw, M.A.1
Grundy, P.E.2
Millow, L.J.3
Eccles, 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
-
22
-
-
0030293157
-
The application of microwave denaturation in comparative genomic hybridization
-
de Meulemeester M, Vink A, Jakobs M, Hermsen M, Steenman M, Slater R, Dietrich A, Mannens M: The application of microwave denaturation in comparative genomic hybridization. Genet Anal: Biomolec Engineer 13:129-133 (1996).
-
(1996)
Genet Anal: Biomolec Engineer
, vol.13
, pp. 129-133
-
-
De Meulemeester, M.1
Vink, A.2
Jakobs, M.3
Hermsen, M.4
Steenman, M.5
Slater, R.6
Dietrich, A.7
Mannens, M.8
-
23
-
-
0027285258
-
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
-
Ogawa O, Eccles MR, Szeto J, McNoe LA, Yun K, Maw MA, Smith PJ, Reeve AE: Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour. Nature 362:749-751 (1993).
-
(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
-
24
-
-
0025733733
-
Dinucleotide repeat polymorphism at the D17S514 locus
-
Oliphant AR, Wright EC, Swensen J, Gruis NA, Goldgar D, Skolnick MH: Dinucleotide repeat polymorphism at the D17S514 locus. Nucl Acids Res 19:4794 (1991).
-
(1991)
Nucl Acids Res
, vol.19
, pp. 4794
-
-
Oliphant, A.R.1
Wright, E.C.2
Swensen, J.3
Gruis, N.A.4
Goldgar, D.5
Skolnick, M.H.6
-
25
-
-
0024332040
-
Expression of insulin-like growth factor-II mRNA in fetal kidney and Wilms' tumor. An in situ hybridization study
-
Paik S, Rosen N, Jung W, You JM, Lippman ME, Perdue JF, Yee D: Expression of insulin-like growth factor-II mRNA in fetal kidney and Wilms' tumor. An in situ hybridization study. Lab Invest 61:522-526 (1989).
-
(1989)
Lab Invest
, vol.61
, pp. 522-526
-
-
Paik, S.1
Rosen, N.2
Jung, W.3
You, J.M.4
Lippman, M.E.5
Perdue, J.F.6
Yee, D.7
-
26
-
-
0027172683
-
Relaxation of imprinted genes in human cancer
-
Rainier S, Johnson LA, Dobry CJ, Ping AJ, Grundy PE, Feinberg AP: Relaxation of imprinted genes in human cancer. Nature 362:747-749 (1993).
-
(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
-
28
-
-
0022386613
-
Expression of insulin-like growth factor-II transcripts in Wilms' tumour
-
Reeve AE, Eccles MR, Wilkins RJ, Bell GI, Millow LJ: Expression of insulin-like growth factor-II transcripts in Wilms' tumour. Nature 317:258-260 (1985).
-
(1985)
Nature
, vol.317
, pp. 258-260
-
-
Reeve, A.E.1
Eccles, M.R.2
Wilkins, R.J.3
Bell, G.I.4
Millow, L.J.5
-
29
-
-
0024505754
-
Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells
-
Reeve AE, Sih SA, Raizis AM, Feinberg AP: Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells. Mol cell Biol 9:1799-1803 (1989).
-
(1989)
Mol Cell Biol
, vol.9
, pp. 1799-1803
-
-
Reeve, A.E.1
Sih, S.A.2
Raizis, A.M.3
Feinberg, A.P.4
-
30
-
-
0029011076
-
Constitutional and acquired rearrangements of chromosome 7 in Wilms tumor
-
Rivera H: Constitutional and acquired rearrangements of chromosome 7 in Wilms tumor. Cancer Genet Cytogenet 81:97-98 (1995).
-
(1995)
Cancer Genet Cytogenet
, vol.81
, pp. 97-98
-
-
Rivera, H.1
-
31
-
-
0022414038
-
Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues
-
Scott J, Cavell J, Robertson ME, Priestley LM, Wadey R, Hopkins B, Pritchard J, Bell GI, Rail LB, Graham CF, Knott TJ: Insulin-like growth factor-II gene expression in Wilms' tumour and embryonic tissues. Nature 317:260-262 (1985).
-
(1985)
Nature
, vol.317
, pp. 260-262
-
-
Scott, J.1
Cavell, J.2
Robertson, M.E.3
Priestley, L.M.4
Wadey, R.5
Hopkins, B.6
Pritchard, J.7
Bell, G.I.8
Rail, L.B.9
Graham, C.F.10
Knott, T.J.11
-
33
-
-
0026689597
-
Cytogenetics and molecular genetics of Wilms' tumor of childhood
-
Slater R, Mannens M: Cytogenetics and molecular genetics of Wilms' tumor of childhood. Cancer Genet Cytogenet 61:111-121 (1992).
-
(1992)
Cancer Genet Cytogenet
, vol.61
, pp. 111-121
-
-
Slater, R.1
Mannens, M.2
-
35
-
-
0025346754
-
Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11
-
Wadey RB, Pal N, Buckle B, Yeomans E, Pritchard J, Cowell JK: Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11. Oncogene 5(6):901-907 (1990).
-
(1990)
Oncogene
, vol.5
, Issue.6
, pp. 901-907
-
-
Wadey, R.B.1
Pal, N.2
Buckle, B.3
Yeomans, E.4
Pritchard, J.5
Cowell, J.K.6
-
36
-
-
0024582686
-
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
-
Weber JL, May PE: Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am J hum Genet 44:388-396 (1989).
-
(1989)
Am J Hum Genet
, vol.44
, pp. 388-396
-
-
Weber, J.L.1
May, P.E.2
-
37
-
-
0025293194
-
Dinucleotide repeat polymorphism at the D4S171 locus
-
Weber JL, May PE: Dinucleotide repeat polymorphism at the D4S171 locus. Nucl Acids Res 18:2202 (1990a).
-
(1990)
Nucl Acids Res
, vol.18
, pp. 2202
-
-
Weber, J.L.1
May, P.E.2
-
38
-
-
0025714064
-
Dinucleotide repeat polymorphism at the D9S43 locus
-
Weber JL, May PE: Dinucleotide repeat polymorphism at the D9S43 locus. Nucl Acids Res 18:2203 (1990b).
-
(1990)
Nucl Acids Res
, vol.18
, pp. 2203
-
-
Weber, J.L.1
May, P.E.2
-
39
-
-
0025367977
-
Dinucleotide repeat polymorphisms at the D16S260, D16S261, D16S265, D16S266 and D16S267 loci
-
Weber JL, Kwitek AE, May PE: Dinucleotide repeat polymorphisms at the D16S260, D16S261, D16S265, D16S266 and D16S267 loci. Nucl Acids Res 18:4034 (1990c).
-
(1990)
Nucl Acids Res
, vol.18
, pp. 4034
-
-
Weber, J.L.1
Kwitek, A.E.2
May, P.E.3
-
40
-
-
0025705569
-
Dinucleotide repeat polymorphism at the D10S89 locus
-
Weber JL, May PE: Dinucleotide repeat polymorphism at the D10S89 locus. Nucl Acids Res 18:4637 (1990d).
-
(1990)
Nucl Acids Res
, vol.18
, pp. 4637
-
-
Weber, J.L.1
May, P.E.2
-
42
-
-
0026446099
-
A second generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, Vignal A, Morrisette J, Millasseau P, Vaysseix G, Lathrop M: A second generation linkage map of the human genome. Nature 359:794-801 (1992).
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morrisette, J.5
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.8
-
43
-
-
0026337065
-
Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms
-
Williamson R, Bowcock A, Kidd K, Pearson P, Schmidtke J, Ceverha P, Chipperfield M, Cooper DN, Coutelle C, Hewitt J, Klinger K, Langley K, Beckmann J, Tolley M, Maidak B: Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms. Cytogenet Cell Genet 58:1190-1832 (1991).
-
(1991)
Cytogenet Cell Genet
, vol.58
, pp. 1190-1832
-
-
Williamson, R.1
Bowcock, A.2
Kidd, K.3
Pearson, P.4
Schmidtke, J.5
Ceverha, P.6
Chipperfield, M.7
Cooper, D.N.8
Coutelle, C.9
Hewitt, J.10
Klinger, K.11
Langley, K.12
Beckmann, J.13
Tolley, M.14
Maidak, B.15
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