| 1 | H19, WT2
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| Constitutional 11p15 abnormalities, including heritable imprinting center mutations, cause nonsyndromic Wilms tumor.
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| Scott RH, Douglas J, Baskcomb L, Huxter N, Barker K, Hanks S, Craft A, Gerrard M, Kohler JA, Levitt GA, Picton S, Pizer B, Ronghe MD, Williams D; Factors Associated with Childhood Tumours (FACT) Collaboration, Cook JA, Pujol P, Maher ER, Birch JM, Stiller CA, Pritchard-Jones K, Rahman N.
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| Nat Genet 40(11):1329-34. Epub 2008 Oct 5.
2008
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| 2 | WT2, ZNF195
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| Multipoint analysis of human chromosome 11p15/mouse distal chromosome 7: inclusion of H19/IGF2 in the minimal WT2 region, gene specificity of H19 silencing in Wilms' tumorigenesis and methylation hyper-dependence of H19 imprinting.
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| Dao D, Walsh CP, Yuan L, Gorelov D, Feng L, Hensle T, Nisen P, Yamashiro DJ, Bestor TH, Tycko B.
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| Hum Mol Genet 8(7):1337-52. 1999
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| 3 | TSG11D, WT2
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| Loss of heterozygosity at chromosome 11p15 in Wilms tumors : identification of two independent region.
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| Karnik P, et al.
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| Oncogene 17 : 237-240. 1998
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| 4 | IGF2, H19, WT2
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| Epigenetic changes at the insulin-like growth factor II/H19 locus in developing kidney is an early event in Wilms tumorigenesis.
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| Okamoto K, et al.
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| Proc Natl Acad Sci U S A 94 : 5367-5371. 1997
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| 5 | BWS, WT2
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| Novel transcribed sequences within the BWS/WT2 region in 11p15.5 : tissue-specific expression correlates with cancer type.
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| Crider-Miller SJ, Reid LH, Higgins MJ, Nowak NJ, Shows TB, Futreal PA, Weissman BE.
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| Genomics 46(3):355-63. 1997
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| 6 | WT2, ST5
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| A common region of loss of heterozygosity in Wilms'tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5.
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| Besnard-Guˇrin C, et al.
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| Hum Genet 97 : 163-170. 1996
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| 7 | ST5, WT2
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| Localization of a tumor suppressor gene in 11p15.5 using the G401 Wilms'tumor assay.
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| Reid LH, et al.
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| Hum Mol Genet 5 : 239-247. 1996
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| 8 | H19, ST5, WT2
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| Epigenetic lesions at the H19 locus in Wilms'tumour patients.
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| Moulton T, et al.
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| Nat Genet 7 : 440-447. 1994
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| 9 | H19, IGF2, WT2
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| Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms'tumour.
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| Steenman MJC, et al.
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| Nat Genet 7 : 433-439. 1994
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| 10 | WT1, WT2
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| Molecular genetic analysis of chromosome 11p in familial Wilms tumor.
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| Baird PN, et al.
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| Br J Cancer 69 : 1072-1077. 1994
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| 11 | WT1, WT2
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| The genetics of Wilms' tumor-A case of disrupted development.
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| Hastie ND.
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| Annu Rev Genet 28 : 523-558. 1994
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| 12 | WT1, WT2, TSG11A, ST5
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| Deletion of WT1 and WIT1 genes and loss of heterozygosity on chromosome 11p in Wilms tumors in Japan.
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| Kaneko Y, et al.
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| Jpn J Cancer Res 84 : 616-624. 1993
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| 13 | WT1, WT2, TSG11A, ST5
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| Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination.
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| Coppes MJ, et al.
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| Genes Chromosomes Cancer 5 : 326-334. 1992
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| 14 | WT1, WT2
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| Loss of heterozygosity in Wilms' tumour involves two distinct regions of chromosome 11.
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| Wadey RB, et al.
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| Oncogene 5 : 901-907. 1990
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| 15 | BWS, WT2
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| Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
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| Koufos A, et al.
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| Am J Hum Genet 44 : 711-719. 1989
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| 16 | WT1, WT2
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| Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilm's tumours.
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| Mannens M, et al.
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| Hum Genet 81 : 41-48. 1988
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