-
1
-
-
0026720732
-
Modulation of DN'A binding specificity by alternative splicing of the Wilms' tumor WT1 gene transcript
-
Bickmore WA, Oghene K, Little MH, Seawrighl A, Heyningen V van, Mastic ND: Modulation of DN'A binding specificity by alternative splicing of the Wilms' tumor WT1 gene transcript. Science 257:235-237 (1992).
-
(1992)
Science
, vol.257
, pp. 235-237
-
-
Bickmore, W.A.1
Oghene, K.2
Little, M.H.3
Seawrighl, A.4
Van, H.V.5
Mastic, N.D.6
-
2
-
-
0025099787
-
Isolation and characterisation 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 HA, Krai A, Yegcr H, Lewis WH, Jones C, Housman DE: Isolation and characterisation 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, H.A.7
Krai, A.8
Yegcr, H.9
Lewis, W.H.10
Jones, C.11
Housman, D.E.12
-
3
-
-
0022908522
-
Cos-mid vectors for high efficiency DNA-mediated transformation and gene amplification in mammalian cells: Studies with the human growth hormone gene
-
Choo KM, Filhv G, Greco S, Lan V-F, Kan YW: Cos-mid vectors for high efficiency DNA-mediated transformation and gene amplification in mammalian cells: studies with the human growth hormone gene. Gene 46:277-286 (1986).
-
(1986)
Gene
, vol.46
, pp. 277-286
-
-
Choo, K.M.1
Filhv, G.2
Greco, S.3
Lan, V.-F.4
Kan, Y.W.5
-
5
-
-
0025098654
-
Homozygous deletion in Wilms tumours of a zinc-fingcr gene identified by chromosome jumping
-
Gessler M, Poutska A, Cavcnee W, Neve RL, Orkin SH, Bruns GAP: Homozygous deletion in Wilms tumours of a zinc-fingcr gene identified by chromosome jumping. Nature 343:774-778 (1990).
-
(1990)
Nature
, vol.343
, pp. 774-778
-
-
Gessler, M.1
Poutska, A.2
Cavcnee, W.3
Neve, R.L.4
Orkin, S.H.5
Bruns, G.6
-
6
-
-
0023683531
-
Familial predisposition to Wilms’ tumour does not map to the short arm of chromosome 11
-
Grundy P, Koulos A, Morgan K, Li FP, Meadows A, Cavenee WK: Familial predisposition to Wilms’ tumour does not map to the short arm of chromosome 11. Nature 336:374-376 (1988).
-
(1988)
Nature
, vol.336
, pp. 374-376
-
-
Grundy, P.1
Koulos, A.2
Morgan, K.3
Li, F.P.4
Meadows, A.5
Cavenee, W.K.6
-
7
-
-
0025288793
-
An internal deletion w ithin an 11 pi 3 zinc finger gene contributes to the development of Wilms' tumor
-
Haber DA, Buckler AJ, Glaser T, Call KM, Pelletier J, Sohn RL, Douglass EC, Housman DE: An internal deletion w ithin an 11 pi 3 zinc finger gene contributes to the development of Wilms' tumor. Cell 61:1257-1269(1990).
-
(1990)
Cell
, vol.61
, pp. 1257-1269
-
-
Haber, D.A.1
Buckler, A.J.2
Glaser, T.3
Call, K.M.4
Pelletier, J.5
Sohn, R.L.6
Douglass, E.C.7
Housman, D.E.8
-
8
-
-
0025992044
-
Alternative splicing and genomic structure of the Wilms’ tumor gene WTl
-
Haber DA, Sohn RL, Buckler AJ, Pelletier J, Call KM, Housman DE: Alternative splicing and genomic structure of the Wilms’ tumor gene WTl. Proc natl Acad Set. USA 88:9618-9622 (1991).
-
(1991)
Proc Natl Acad Set. 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
-
9
-
-
0023803361
-
Lack of linkage of familial Wilms' tumour to chromosomal band 11 p 13
-
Huff V, Compton DA, Chao LY, Strong LC, Geiser CF, Saunders GF: Lack of linkage of familial Wilms' tumour to chromosomal band 11 p 13. Nature 336:377-378(1988).
-
(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
-
10
-
-
0026457965
-
Nonlinkage of 16q markers to familial predisposition to Wilms' tumor
-
Huff V, Reeve AE, Leppert VI, Strong LC, Douglass EC, Geiser CF, Li FP, Meadows A, Callen DF, Lenoir G, Saunders GF: Nonlinkage of 16q markers to familial predisposition to Wilms' tumor. Cancer Res 52:6117-6120 (1992).
-
(1992)
Cancer Res
, vol.52
, pp. 6117-6120
-
-
Huff, V.1
Reeve, A.E.2
Leppert, V.I.3
Strong, L.C.4
Douglass, E.C.5
Geiser, C.F.6
Li, F.P.7
Meadows, A.8
Callen, D.F.9
Lenoir, G.10
Saunders, G.F.11
-
11
-
-
0015295131
-
Mutation and cancer: A model for Wilms' tumor of the kidney
-
Knudson AG, Strong LC: Mutation and cancer: a model for Wilms' tumor of the kidney. J natl Cancer Inst 48:313-324(1972).
-
(1972)
J Natl Cancer Inst
, vol.48
, pp. 313-324
-
-
Knudson, A.G.1
Strong, L.C.2
-
12
-
-
0027182741
-
WT-I is required for early kidney development
-
Kreidberg JA, Sariola H, Loring JM, Maeda M, Pelletier J, Housman D, Jacnisch R: WT-I is required for early kidney development. Cell 74:679-691 (1993).
-
(1993)
Cell
, vol.74
, pp. 679-691
-
-
Kreidberg, J.A.1
Sariola, H.2
Loring, J.M.3
Maeda, M.4
Pelletier, J.5
Housman, D.6
Jacnisch, R.7
-
13
-
-
0029001463
-
Isolation and mapping of 186 new DNA markers on human chromosome I
-
Kugoh H, Nakagawa Y, Mitsuya K, Mita T, Suzuki M, Suzuki N, Uejima H, Yuasa Y, Oshimura M: Isolation and mapping of 186 new DNA markers on human chromosome I. Genomics 27:207-210 (1995).
-
(1995)
Genomics
, vol.27
, pp. 207-210
-
-
Kugoh, H.1
Nakagawa, Y.2
Mitsuya, K.3
Mita, T.4
Suzuki, M.5
Suzuki, N.6
Uejima, H.7
Yuasa, Y.8
Oshimura, M.9
-
14
-
-
0026669379
-
Allelic loss on chromosome 11 p is a less frequent event in bilateral than in unilateral tumours
-
Little MH, Byrne J, Clarke J, Dunn R, Smith PJ: Allelic loss on chromosome 11 p is a less frequent event in bilateral than in unilateral tumours. Eur J Cancer 28A: 1879-1883(1992a).
-
(1992)
Eur J Cancer
, vol.28A
, pp. 1879-1883
-
-
Little, M.H.1
Byrne, J.2
Clarke, J.3
Dunn, R.4
Smith, P.J.5
-
15
-
-
0026724450
-
Zinc finger point mutations within the WTl gene in Wilms' tumor patients
-
Little MH, Prosser J, Condie A, Smith PJ, Heyningen V van, Hastie ND: Zinc finger point mutations within the WTl gene in Wilms' tumor patients. Proc natl Acad Sei. USA 89:4791-4795 (1992b).
-
(1992)
Proc Natl Acad Sei. USA
, vol.89
, pp. 4791-4795
-
-
Little, M.H.1
Prosser, J.2
Condie, A.3
Smith, P.J.4
Van, H.V.5
Hastie, N.D.6
-
16
-
-
0026691721
-
A third Wilms’ tumor loeus on chromosome 16q
-
Maw M, Grundy P, Millow LJ, Eccles M, Dunn RS, Smith PJ, Feinberg AP, Law DJ, Paterson MC, Telzerow PE, Callen DF, Thompson AD, Richards RL, Reeve AE: A third Wilms’ tumor loeus on chromosome 16q. Cancer Res 52:3094-3098 (1992).
-
(1992)
Cancer Res
, vol.52
, pp. 3094-3098
-
-
Maw, M.1
Grundy, P.2
Millow, L.J.3
Eccles, M.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.L.13
Reeve, A.E.14
-
17
-
-
0025788974
-
WTl mutation contributed abnormal genital system development and hereditary Wilms’ tumor
-
Pelletier J, Bmcning W, Li FP, Haber DA, Glaser T, Housman DE: WTl mutation contributed abnormal genital system development and hereditary Wilms’ tumor. Nature 353:431-434(1991).
-
(1991)
Nature
, vol.353
, pp. 431-434
-
-
Pelletier, J.1
Bmcning, W.2
Li, F.P.3
Haber, D.A.4
Glaser, T.5
Housman, D.E.6
-
18
-
-
0027209712
-
The WTl Wilms’ tumor gene product: A developmentally regulated transacription factor in the kidney that functions as a tuntor suppressor
-
Rauscher FJ III: The WTl Wilms’ tumor gene product: a developmentally regulated transacription factor in the kidney that functions as a tuntor suppressor. FASEB J 7:896-903(1993).
-
(1993)
FASEB J
, vol.7
, pp. 896-903
-
-
Rauscher, F.1
-
19
-
-
0024505754
-
Loss of allelic heterozygosity at a second loeus on chromosome 11 in sporadic Wilms' tumor cells
-
Reeve AE, Sih SV, Raizis AM, Feinherg AP: Loss of allelic heterozygosity at a second loeus 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.V.2
Raizis, A.M.3
Feinherg, A.P.4
-
20
-
-
0024510084
-
The generation of radiolabeled DNA and RNA probes with polymerase chain reaction
-
7:90-94(1989).
-
(1989)
7
, pp. 90-94
-
-
Schowater, D.B.1
Sommer, S.S.2
-
21
-
-
0026689597
-
Y Cytogenetics and molecular genetics of Wilms' tumor of childhood
-
Slater RM, Mannens MM, Y Cytogenetics and molecular genetics of Wilms' tumor of childhood. Cancer Genet Cytogcnel 61:111-121 (1992).
-
(1992)
Cancer Genet Cytogcnel
, vol.61
, pp. 111-121
-
-
Slater, R.M.1
Mannens, M.M.2
-
22
-
-
0021759483
-
Recessive mtation in aetiology of Wilms’ tumour
-
Solomon E: Recessive mtation in aetiology of Wilms’ tumour. Nature 309:111-112(1984).
-
(1984)
Nature
, vol.309
, pp. 111-112
-
-
Solomon, E.1
-
23
-
-
0028958106
-
Hereditary hvper-parathyroidism-jaw tumor syndrome: The endocrine tumor gene HRPT2 maps to chromosome lq2I-.3l
-
Szabo J, Heath B, Hill YM, Jackson CE, Zarbo RJ, Malletle LE, Chew SL, Bcsser GM, Tnakker RY, Huff V, Leppert ME, Heath H: Hereditary hvper-parathyroidism-jaw tumor syndrome: the endocrine tumor gene HRPT2 maps to chromosome lq2I-.3l. Am J hum Genet56:944-950 (1995).
-
(1995)
Am J Hum Genet56
, pp. 944-950
-
-
Szabo, J.1
Heath, B.2
Hill, Y.M.3
Jackson, C.E.4
Zarbo, R.J.5
Malletle, L.E.6
Chew, S.L.7
Bcsser, G.M.8
Tnakker, R.Y.9
Huff, V.10
Leppert, M.E.11
Heath, H.12
-
24
-
-
0028966074
-
The human-growth-spccific gene GAS 1 maps outside the candidate region of the gene for nevoid basal cell carcinoma syndrome
-
Wicking C, Breen M, Negus K, Beikman J, Evdokiou A, Cowled P, Chenmevix-Trcnch G, Wainwright B: The human-growth-spccific gene GAS 1 maps outside the candidate region of the gene for nevoid basal cell carcinoma syndrome. Cylogenet Cell Genet 68:119-121 (1995).
-
(1995)
Cylogenet Cell Genet
, vol.68
, pp. 119-121
-
-
Wicking, C.1
Breen, M.2
Negus, K.3
Beikman, J.4
Evdokiou, A.5
Cowled, P.6
Chenmevix-Trcnch, G.7
Wainwright, B.8
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