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A WT1 exon 1 mutation in a child diagnosed with Denys-Drash syndrome.
Little S, Hanks S, King-Underwood L, Picton S, Cullinane C, Rapley E, Rahman N, Pritchard-Jones K. Little S, et al. Pediatr Nephrol. 2005 Jan;20(1):81-5. doi: 10.1007/s00467-004-1649-z. Epub 2004 Oct 21. Pediatr Nephrol. 2005. PMID: 15503171 Review.
Wt1 is not essential for hematopoiesis in the mouse.
King-Underwood L, Little S, Baker M, Clutterbuck R, Delassus S, Enver T, Lebozer C, Min T, Moore A, Schedl A, Pritchard-Jones K. King-Underwood L, et al. Leuk Res. 2005 Jul;29(7):803-12. doi: 10.1016/j.leukres.2004.11.020. Epub 2005 Feb 17. Leuk Res. 2005. PMID: 15927676
EGFRvIII deletion mutations in pediatric high-grade glioma and response to targeted therapy in pediatric glioma cell lines.
Bax DA, Gaspar N, Little SE, Marshall L, Perryman L, Regairaz M, Viana-Pereira M, Vuononvirta R, Sharp SY, Reis-Filho JS, Stávale JN, Al-Sarraj S, Reis RM, Vassal G, Pearson AD, Hargrave D, Ellison DW, Workman P, Jones C. Bax DA, et al. Among authors: little se. Clin Cancer Res. 2009 Sep 15;15(18):5753-61. doi: 10.1158/1078-0432.CCR-08-3210. Epub 2009 Sep 8. Clin Cancer Res. 2009. PMID: 19737945
237 results