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220 results
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Microdissecting the genetic events in nephrogenic rests and Wilms' tumor development.
Charles AK, Brown KW, Berry PJ. Charles AK, et al. Among authors: brown kw. Am J Pathol. 1998 Sep;153(3):991-1000. doi: 10.1016/S0002-9440(10)65641-6. Am J Pathol. 1998. PMID: 9736048 Free PMC article.
Wilms' tumor: a paradigm for the new genetics.
Malik K, Yan P, Huang TH, Brown KW. Malik K, et al. Among authors: brown kw. Oncol Res. 2001;12(11-12):441-9. doi: 10.3727/096504001108747440. Oncol Res. 2001. PMID: 11939407 Review.
Identification of differential methylation of the WT1 antisense regulatory region and relaxation of imprinting in Wilms' tumor.
Malik K, Salpekar A, Hancock A, Moorwood K, Jackson S, Charles A, Brown KW. Malik K, et al. Among authors: brown kw. Cancer Res. 2000 May 1;60(9):2356-60. Cancer Res. 2000. PMID: 10811108
Transactivation of the WT1 antisense promoter is unique to the WT1[+/-] isoform.
Moorwood K, Salpekar A, Ivins SM, Hall J, Powlesland RM, Brown KW, Malik K. Moorwood K, et al. Among authors: brown kw. FEBS Lett. 1999 Jul 30;456(1):131-6. doi: 10.1016/s0014-5793(99)00944-8. FEBS Lett. 1999. PMID: 10452544
Antisense WT1 transcription parallels sense mRNA and protein expression in fetal kidney and can elevate protein levels in vitro.
Moorwood K, Charles AK, Salpekar A, Wallace JI, Brown KW, Malik K. Moorwood K, et al. Among authors: brown kw. J Pathol. 1998 Aug;185(4):352-9. doi: 10.1002/(SICI)1096-9896(199808)185:4<352::AID-PATH119>3.0.CO;2-#. J Pathol. 1998. PMID: 9828833
Serum-dependent and cell cycle-dependent expression from a cytomegalovirus-based mammalian expression vector.
Brightwell G, Poirier V, Cole E, Ivins S, Brown KW. Brightwell G, et al. Among authors: brown kw. Gene. 1997 Jul 18;194(1):115-23. doi: 10.1016/s0378-1119(97)00178-9. Gene. 1997. PMID: 9266680
Low frequency of genetic lesions in Wilms tumors by representational difference analysis.
Cummings M, Brown KW. Cummings M, et al. Among authors: brown kw. Cancer Genet Cytogenet. 2001 Jun;127(2):155-60. doi: 10.1016/s0165-4608(01)00387-9. Cancer Genet Cytogenet. 2001. PMID: 11425456
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway.
Brown KW, Villar AJ, Bickmore W, Clayton-Smith J, Catchpoole D, Maher ER, Reik W. Brown KW, et al. Hum Mol Genet. 1996 Dec;5(12):2027-32. doi: 10.1093/hmg/5.12.2027. Hum Mol Genet. 1996. PMID: 8968759
Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature.
Brown KW, Gardner A, Williams JC, Mott MG, McDermott A, Maitland NJ. Brown KW, et al. Cancer Genet Cytogenet. 1992 Jan;58(1):66-70. doi: 10.1016/0165-4608(92)90136-v. Cancer Genet Cytogenet. 1992. PMID: 1728953 Review.
Loss of chromosome 11p alleles in cultured cells derived from Wilms' tumours.
Brown KW, Shaw AP, Poirier V, Tyler SJ, Berry PJ, Mott MG, Maitland NJ. Brown KW, et al. Br J Cancer. 1989 Jul;60(1):25-9. doi: 10.1038/bjc.1989.213. Br J Cancer. 1989. PMID: 2553087 Free PMC article.
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