摘要: Nephroblastoma, or Wilms tumor (WT), is a childhood of the kidney that was described and characterized in several case reports reviews during 19th century. It acquired its commonly used eponym after Max published monograph on subject 1899. Occurring with frequency roughly 1 10,000 live births (Matsunaga, 1981; Breslow et al., 1983), WT one most common solid tumors children. Fortunately, it also successfully treated cancers; triple modality therapy surgery, chemotherapy, radiotherapy, overall 2-yr, disease-free survival rate now 85% (D’Angio 1989).
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W. T. Schroeder, V. Riccardi, G. F. Saunders, Louise C Strong, S. Pathak, W. H. Lewis, L. Y. Chao, D. D. Dao, Nonrandom loss of maternal chromosome 11 alleles in Wilms' tumors American Journal of Human Genetics. ,vol. 40, pp. 413- 420 ,(1987)
Philippa Lloyd, An anniversary for atmospheric ozone Nature. ,vol. 338, pp. 113- 113 ,(1989) , 10.1038/338113A0
Nick Hastie, M H Little, J A Byrne, R Dunn, Paul Smith, A Seawright, Veronica Van Heyningen, K Pritchard-Jones, Equivalent expression of paternally and maternally inherited WT1 alleles in normal fetal tissue and Wilms' tumours. Oncogene. ,vol. 7, pp. 635- 641 ,(1992)
A P Feinberg, M Boehnke, M R Young, D J Law, A E Reeve, A J Ping, Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. American Journal of Human Genetics. ,vol. 44, pp. 720- 723 ,(1989)
G. F. Saunders, S. Pathak, H. Kikuchi, W. H. Lewis, W. W. Nichols, D. D. Dao, L. Y. Chao, W. T. Schroeder, V. M. Riccardi, L. C. Strong, Genetic mechanisms of tumor-specific loss of 11p DNA sequences in Wilms tumor. American Journal of Human Genetics. ,vol. 41, pp. 202- 217 ,(1987)
Daniel A. Haber, Vicki Huff, Louise C. Strong, David Housman, Grady F. Saunders, Katherine M. Call, Hiroshi Miwa, Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT. American Journal of Human Genetics. ,vol. 48, pp. 997- 1003 ,(1991)
A Koufos, K Morgan, A Kalbakji, K A Aleck, W K Cavenee, T Hadro, P Grundy, B C Lampkin, Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. American Journal of Human Genetics. ,vol. 44, pp. 711- 719 ,(1989)
Gilbert Lenoir, Vicki Huff, Grady F. Saunders, Mark Leppert, Anna Meadows, Frederick P. Li, Louise C. Strong, Anthony E. Reeve, Clementina F. Geiser, David F. Callen, Edwin C. Douglass, Nonlinkage of 16q markers to familial predisposition to Wilms' tumor. Cancer Research. ,vol. 52, pp. 6117- 6120 ,(1992)
Vicki Huff, Grady F. Saunders, Louise C. Strong, Vincent M. Riccardi, Anna Meadows, Parental origin of de novo constitutional deletions of chromosomal band 11p13. American Journal of Human Genetics. ,vol. 47, pp. 155- 160 ,(1990)
Perry E. Telzerow, Andrew P. Feinberg, Michael R. Eccles, Paul E. Grundy, Marion A. Maw, Roseanne S. Dunn, Robert I. Richards, Malcolm C. Paterson, Lynn J. Millow, Anthony E. Reeve, Andrew D. Thompson, David F. Callen, Dave J. Law, Peter J. Smith, A Third Wilms' Tumor Locus on Chromosome 16q Cancer Research. ,vol. 52, pp. 3094- 3098 ,(1992)