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The expression of the Wilms' tumour gene, WT1, in the developing mammalian embryo.
Armstrong JF, Pritchard-Jones K, Bickmore WA, Hastie ND, Bard JB. Armstrong JF, et al. Mech Dev. 1993 Jan;40(1-2):85-97. doi: 10.1016/0925-4773(93)90090-k. Mech Dev. 1993. PMID: 8382938
Regarding "expression of the Wilms' tumor gene (WT1) in normal hemopoiesis" by P.N. Baird and P.J. Simmons, Experimental Hematology 25:312-320 (1997).
Pritchard-Jones K, Renshaw J. Pritchard-Jones K, et al. Exp Hematol. 1997 Dec;25(13):1311-2. Exp Hematol. 1997. PMID: 9406989 No abstract available.
Mutations in the Wilms' tumor gene WT1 in leukemias.
King-Underwood L, Renshaw J, Pritchard-Jones K. King-Underwood L, et al. Blood. 1996 Mar 15;87(6):2171-9. Blood. 1996. PMID: 8630376
Controversies and advances in the management of Wilms' tumour.
Pritchard-Jones K. Pritchard-Jones K. Arch Dis Child. 2002 Sep;87(3):241-4. doi: 10.1136/adc.87.3.241. Arch Dis Child. 2002. PMID: 12193442 Free PMC article. Review.
Case of interstitial 12q deletion in association with Wilms tumor.
Rapley EA, Hargrave D, Persinguhe N, Barfoot R, Moore I, Radford M, Stratton MR, Rahman N, Pritchard-Jones K. Rapley EA, et al. Am J Med Genet. 2001 Dec 1;104(3):246-9. Am J Med Genet. 2001. PMID: 11754052
Familial Wilms tumour resulting from WT1 mutation: intronic polymorphism causing artefactual constitutional homozygosity.
Pritchard-Jones K, Rahman N, Gerrard M, Variend D, King-Underwood L. Pritchard-Jones K, et al. J Med Genet. 2000 May;37(5):377-9. doi: 10.1136/jmg.37.5.377. J Med Genet. 2000. PMID: 10905890 Free PMC article. No abstract available.
Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2.
Rapley EA, Barfoot R, Bonaïti-Pellié C, Chompret A, Foulkes W, Perusinghe N, Reeve A, Royer-Pokora B, Schumacher V, Shelling A, Skeen J, de Tourreil S, Weirich A, Pritchard-Jones K, Stratton MR, Rahman N. Rapley EA, et al. Br J Cancer. 2000 Jul;83(2):177-83. doi: 10.1054/bjoc.2000.1283. Br J Cancer. 2000. PMID: 10901367 Free PMC article.
Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene.
Slade I, Stephens P, Douglas J, Barker K, Stebbings L, Abbaszadeh F, Pritchard-Jones K; FACT collaboration, Cole R, Pizer B, Stiller C, Vujanic G, Scott RH, Stratton MR, Rahman N. Slade I, et al. J Med Genet. 2010 May;47(5):342-7. doi: 10.1136/jmg.2009.072983. Epub 2009 Nov 30. J Med Genet. 2010. PMID: 19948536
The Wilms tumour gene, WT1, in normal and abnormal nephrogenesis.
Pritchard-Jones K. Pritchard-Jones K. Pediatr Nephrol. 1999 Sep;13(7):620-5. doi: 10.1007/s004670050757. Pediatr Nephrol. 1999. PMID: 10460515 Review.
Molecular genetic pathways to Wilms tumor.
Pritchard-Jones K. Pritchard-Jones K. Crit Rev Oncog. 1997;8(1):1-27. doi: 10.1615/critrevoncog.v8.i1.10. Crit Rev Oncog. 1997. PMID: 9516084 Review.
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